Item | Value |
---|---|
geneid | 133060 |
ensemblid | ENSG00000163982.6 |
hgncid | 19656 |
symbol | OTOP1 |
name | otopetrin 1 |
refseq_nuc | NM_177998.3 |
refseq_prot | NP_819056.1 |
ensembl_nuc | ENST00000296358.5 |
ensembl_prot | ENSP00000296358.4 |
mane_status | MANE Select |
chr | chr4 |
start | 4188726 |
end | 4226929 |
strand | - |
ver | v1.2 |
region | chr4:4188726-4226929 |
region5000 | chr4:4183726-4231929 |
regionname0 | OTOP1_chr4_4188726_4226929 |
regionname5000 | OTOP1_chr4_4183726_4231929 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 612 | 226 | 36 | 38 | 118 | 8 | 26 | 87 | OTOP1_chr4_4183726_4231929 | OTOP1 | MLEGL others(607): Show |
chr4 | 4183726 | 4231929 |
a0002 | 1/0 | 612 | 119 | 21 | 25 | 63 | 2 | 7 | 53 | OTOP1_chr4_4183726_4231929 | OTOP1 | MLEGL others(607): Show |
chr4 | 4183726 | 4231929 |
a0003 | 0/1 | 612 | 17 | 0 | 7 | 6 | 1 | 2 | 5 | OTOP1_chr4_4183726_4231929 | OTOP1 | MLEGL others(607): Show |
chr4 | 4183726 | 4231929 |
a0004 | 0/0 | 610 | 12 | 4 | 4 | 0 | 2 | 2 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | MLEGL others(605): Show |
chr4 | 4183726 | 4231929 |
a0005 | 0/0 | 610 | 10 | 0 | 10 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | MLEGL others(605): Show |
chr4 | 4183726 | 4231929 |
a0006 | 0/0 | 612 | 8 | 7 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | MLEGL others(607): Show |
chr4 | 4183726 | 4231929 |
a0007 | 0/0 | 612 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | MLEGL others(607): Show |
chr4 | 4183726 | 4231929 |
a0008 | 0/0 | 612 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | MLEGL others(607): Show |
chr4 | 4183726 | 4231929 |
a0009 | 0/0 | 610 | 5 | 3 | 0 | 0 | 0 | 2 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | MLEGL others(605): Show |
chr4 | 4183726 | 4231929 |
a0010 | 0/0 | 612 | 4 | 0 | 1 | 0 | 1 | 2 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | MLEGL others(607): Show |
chr4 | 4183726 | 4231929 |
a0011 | 0/0 | 610 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | MLEGL others(605): Show |
chr4 | 4183726 | 4231929 |
a0012 | 0/0 | 612 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | MLEGL others(607): Show |
chr4 | 4183726 | 4231929 |
a0013 | 0/0 | 612 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | MLEGL others(607): Show |
chr4 | 4183726 | 4231929 |
a0014 | 0/0 | 612 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | MLEGL others(607): Show |
chr4 | 4183726 | 4231929 |
a0015 | 0/0 | 612 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | MLEGL others(607): Show |
chr4 | 4183726 | 4231929 |
a0016 | 0/0 | 610 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | MLEGL others(605): Show |
chr4 | 4183726 | 4231929 |
a0017 | 0/0 | 612 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | MLEGL others(607): Show |
chr4 | 4183726 | 4231929 |
a0018 | 0/0 | 612 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | MLEGL others(607): Show |
chr4 | 4183726 | 4231929 |
a0019 | 0/0 | 610 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | MLEGL others(605): Show |
chr4 | 4183726 | 4231929 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1836 | 204 | 35 | 30 | 115 | 7 | 17 | OTOP1_chr4_4183726_4231929 | OTOP1 | ATGCT others(1831): Show |
chr4 | 4183726 | 4231929 | ||
a0001c0004 | 0/0 | 1836 | 22 | 1 | 8 | 3 | 1 | 9 | OTOP1_chr4_4183726_4231929 | OTOP1 | ATGCT others(1831): Show |
chr4 | 4183726 | 4231929 | ||
a0002c0002 | 1/0 | 1836 | 85 | 5 | 22 | 48 | 2 | 7 | OTOP1_chr4_4183726_4231929 | OTOP1 | ATGCT others(1831): Show |
chr4 | 4183726 | 4231929 | ||
a0002c0003 | 0/0 | 1836 | 27 | 10 | 3 | 14 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | ATGCT others(1831): Show |
chr4 | 4183726 | 4231929 | ||
a0002c0013 | 0/0 | 1836 | 4 | 4 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | ATGCT others(1831): Show |
chr4 | 4183726 | 4231929 | ||
a0002c0020 | 0/0 | 1836 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | ATGCT others(1831): Show |
chr4 | 4183726 | 4231929 | ||
a0002c0023 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | ATGCT others(1831): Show |
chr4 | 4183726 | 4231929 | ||
a0002c0028 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | ATGCT others(1831): Show |
chr4 | 4183726 | 4231929 | ||
a0003c0005 | 0/1 | 1836 | 17 | 0 | 7 | 6 | 1 | 2 | OTOP1_chr4_4183726_4231929 | OTOP1 | ATGCT others(1831): Show |
chr4 | 4183726 | 4231929 | ||
a0004c0006 | 0/0 | 1830 | 12 | 4 | 4 | 0 | 2 | 2 | OTOP1_chr4_4183726_4231929 | OTOP1 | ATGCT others(1825): Show |
chr4 | 4183726 | 4231929 | ||
a0005c0007 | 0/0 | 1830 | 10 | 0 | 10 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | ATGCT others(1825): Show |
chr4 | 4183726 | 4231929 | ||
a0006c0010 | 0/0 | 1836 | 7 | 6 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | ATGCT others(1831): Show |
chr4 | 4183726 | 4231929 | ||
a0006c0025 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | ATGCT others(1831): Show |
chr4 | 4183726 | 4231929 | ||
a0007c0008 | 0/0 | 1836 | 8 | 8 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | ATGCT others(1831): Show |
chr4 | 4183726 | 4231929 | ||
a0008c0009 | 0/0 | 1836 | 7 | 7 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | ATGCT others(1831): Show |
chr4 | 4183726 | 4231929 | ||
a0008c0026 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | ATGCT others(1831): Show |
chr4 | 4183726 | 4231929 | ||
a0009c0012 | 0/0 | 1830 | 4 | 2 | 0 | 0 | 0 | 2 | OTOP1_chr4_4183726_4231929 | OTOP1 | ATGCT others(1825): Show |
chr4 | 4183726 | 4231929 | ||
a0009c0018 | 0/0 | 1830 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | ATGCT others(1825): Show |
chr4 | 4183726 | 4231929 | ||
a0010c0011 | 0/0 | 1836 | 4 | 0 | 1 | 0 | 1 | 2 | OTOP1_chr4_4183726_4231929 | OTOP1 | ATGCT others(1831): Show |
chr4 | 4183726 | 4231929 | ||
a0011c0014 | 0/0 | 1830 | 2 | 2 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | ATGCT others(1825): Show |
chr4 | 4183726 | 4231929 | ||
a0012c0015 | 0/0 | 1836 | 2 | 2 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | ATGCT others(1831): Show |
chr4 | 4183726 | 4231929 | ||
a0013c0027 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | ATGCT others(1831): Show |
chr4 | 4183726 | 4231929 | ||
a0014c0024 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | ATGCT others(1831): Show |
chr4 | 4183726 | 4231929 | ||
a0015c0019 | 0/0 | 1836 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | ATGCT others(1831): Show |
chr4 | 4183726 | 4231929 | ||
a0016c0016 | 0/0 | 1830 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | ATGCT others(1825): Show |
chr4 | 4183726 | 4231929 | ||
a0017c0017 | 0/0 | 1836 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | ATGCT others(1831): Show |
chr4 | 4183726 | 4231929 | ||
a0018c0022 | 0/0 | 1836 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | ATGCT others(1831): Show |
chr4 | 4183726 | 4231929 | ||
a0019c0021 | 0/0 | 1830 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | ATGCT others(1825): Show |
chr4 | 4183726 | 4231929 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1981 | 203 | 35 | 30 | 114 | 7 | 17 | OTOP1_chr4_4183726_4231929 | OTOP1 | AGGAG others(1976): Show |
chr4 | 4183726 | 4231929 |
a0001c0001t0002 | 0/0 | 1981 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | AGGAG others(1976): Show |
chr4 | 4183726 | 4231929 |
a0001c0004t0001 | 0/0 | 1981 | 22 | 1 | 8 | 3 | 1 | 9 | OTOP1_chr4_4183726_4231929 | OTOP1 | AGGAG others(1976): Show |
chr4 | 4183726 | 4231929 |
a0002c0002t0001 | 1/0 | 1981 | 85 | 5 | 22 | 48 | 2 | 7 | OTOP1_chr4_4183726_4231929 | OTOP1 | AGGAG others(1976): Show |
chr4 | 4183726 | 4231929 |
a0002c0003t0001 | 0/0 | 1981 | 27 | 10 | 3 | 14 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | AGGAG others(1976): Show |
chr4 | 4183726 | 4231929 |
a0002c0013t0001 | 0/0 | 1981 | 4 | 4 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | AGGAG others(1976): Show |
chr4 | 4183726 | 4231929 |
a0002c0020t0001 | 0/0 | 1981 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | AGGAG others(1976): Show |
chr4 | 4183726 | 4231929 |
a0002c0023t0001 | 0/0 | 1981 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | AGGAG others(1976): Show |
chr4 | 4183726 | 4231929 |
a0002c0028t0001 | 0/0 | 1981 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | AGGAG others(1976): Show |
chr4 | 4183726 | 4231929 |
a0003c0005t0001 | 0/1 | 1981 | 17 | 0 | 7 | 6 | 1 | 2 | OTOP1_chr4_4183726_4231929 | OTOP1 | AGGAG others(1976): Show |
chr4 | 4183726 | 4231929 |
a0004c0006t0001 | 0/0 | 1975 | 12 | 4 | 4 | 0 | 2 | 2 | OTOP1_chr4_4183726_4231929 | OTOP1 | AGGAG others(1970): Show |
chr4 | 4183726 | 4231929 |
a0005c0007t0001 | 0/0 | 1975 | 10 | 0 | 10 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | AGGAG others(1970): Show |
chr4 | 4183726 | 4231929 |
a0006c0010t0001 | 0/0 | 1981 | 7 | 6 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | AGGAG others(1976): Show |
chr4 | 4183726 | 4231929 |
a0006c0025t0001 | 0/0 | 1981 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | AGGAG others(1976): Show |
chr4 | 4183726 | 4231929 |
a0007c0008t0001 | 0/0 | 1981 | 8 | 8 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | AGGAG others(1976): Show |
chr4 | 4183726 | 4231929 |
a0008c0009t0001 | 0/0 | 1981 | 7 | 7 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | AGGAG others(1976): Show |
chr4 | 4183726 | 4231929 |
a0008c0026t0001 | 0/0 | 1981 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | AGGAG others(1976): Show |
chr4 | 4183726 | 4231929 |
a0009c0012t0001 | 0/0 | 1975 | 4 | 2 | 0 | 0 | 0 | 2 | OTOP1_chr4_4183726_4231929 | OTOP1 | AGGAG others(1970): Show |
chr4 | 4183726 | 4231929 |
a0009c0018t0001 | 0/0 | 1975 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | AGGAG others(1970): Show |
chr4 | 4183726 | 4231929 |
a0010c0011t0001 | 0/0 | 1981 | 4 | 0 | 1 | 0 | 1 | 2 | OTOP1_chr4_4183726_4231929 | OTOP1 | AGGAG others(1976): Show |
chr4 | 4183726 | 4231929 |
a0011c0014t0001 | 0/0 | 1975 | 2 | 2 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | AGGAG others(1970): Show |
chr4 | 4183726 | 4231929 |
a0012c0015t0001 | 0/0 | 1981 | 2 | 2 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | AGGAG others(1976): Show |
chr4 | 4183726 | 4231929 |
a0013c0027t0001 | 0/0 | 1981 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | AGGAG others(1976): Show |
chr4 | 4183726 | 4231929 |
a0014c0024t0001 | 0/0 | 1981 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | AGGAG others(1976): Show |
chr4 | 4183726 | 4231929 |
a0015c0019t0001 | 0/0 | 1981 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | AGGAG others(1976): Show |
chr4 | 4183726 | 4231929 |
a0016c0016t0001 | 0/0 | 1975 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | AGGAG others(1970): Show |
chr4 | 4183726 | 4231929 |
a0017c0017t0001 | 0/0 | 1981 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | AGGAG others(1976): Show |
chr4 | 4183726 | 4231929 |
a0018c0022t0001 | 0/0 | 1981 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | AGGAG others(1976): Show |
chr4 | 4183726 | 4231929 |
a0019c0021t0001 | 0/0 | 1975 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | AGGAG others(1970): Show |
chr4 | 4183726 | 4231929 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0004t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0004t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0004t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0004t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0004t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0004t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0004t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0004t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0004t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0004t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0004t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0004t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0004t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0004t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0004t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0004t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0004t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0004t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0004t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0004t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0004t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0001c0004t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0299 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0002t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0003t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0003t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0003t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0003t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0003t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0003t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0003t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0003t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0003t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0003t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0003t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0003t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0003t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0003t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0003t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0013t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0013t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0013t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0013t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0020t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0023t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0002c0028t0001g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0003c0005t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0003c0005t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0003c0005t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0003c0005t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0003c0005t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0003c0005t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0003c0005t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0003c0005t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0003c0005t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0003c0005t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0003c0005t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0003c0005t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0003c0005t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0003c0005t0001g0245 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0003c0005t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0003c0005t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0004c0006t0001g0007 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0004c0006t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0004c0006t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0004c0006t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0004c0006t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0004c0006t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0004c0006t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0004c0006t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0004c0006t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0004c0006t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0005c0007t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0005c0007t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0005c0007t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0005c0007t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0005c0007t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0005c0007t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0005c0007t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0005c0007t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0006c0010t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0006c0010t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0006c0010t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0006c0010t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0006c0010t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0006c0010t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0006c0010t0001g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0006c0025t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0007c0008t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0007c0008t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0007c0008t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0007c0008t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0007c0008t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0007c0008t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0007c0008t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0007c0008t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0008c0009t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0008c0009t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0008c0009t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0008c0009t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0008c0009t0001g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0008c0009t0001g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0008c0009t0001g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0008c0026t0001g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0009c0012t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0009c0012t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0009c0012t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0009c0012t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0009c0018t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0010c0011t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0010c0011t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0010c0011t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0011c0014t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0011c0014t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0012c0015t0001g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0012c0015t0001g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0013c0027t0001g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0014c0024t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0015c0019t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0016c0016t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0017c0017t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0018c0022t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
a0019c0021t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0293 | EUR | GBR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG00099 | hp2 | a0004 | c0006 | t0001 | g0059 | EUR | GBR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG00140 | hp1 | a0001 | c0004 | t0001 | g0242 | EUR | GBR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | GBR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG00280 | hp1 | a0010 | c0011 | t0001 | g0027 | EUR | FIN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0152 | EUR | FIN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | FIN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG00323 | hp2 | a0003 | c0005 | t0001 | g0237 | EUR | FIN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | CHS | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG00544 | hp1 | a0002 | c0002 | t0001 | g0311 | EAS | CHS | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG00544 | hp2 | a0003 | c0005 | t0001 | g0140 | EAS | CHS | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0344 | EAS | CHS | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG00609 | hp1 | a0002 | c0003 | t0001 | g0307 | EAS | CHS | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG00642 | hp2 | a0001 | c0004 | t0001 | g0274 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG00673 | hp1 | a0002 | c0003 | t0001 | g0255 | EAS | CHS | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG00733 | hp1 | a0005 | c0007 | t0001 | g0351 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG00733 | hp2 | a0002 | c0002 | t0001 | g0106 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG00738 | hp1 | a0001 | c0004 | t0001 | g0135 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG00738 | hp2 | a0003 | c0005 | t0001 | g0258 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0112 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG00741 | hp2 | a0001 | c0004 | t0001 | g0275 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0321 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0342 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0315 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01099 | hp2 | a0001 | c0004 | t0001 | g0243 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01106 | hp1 | a0004 | c0006 | t0001 | g0294 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01109 | hp1 | a0006 | c0010 | t0001 | g0372 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0249 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01167 | hp1 | a0002 | c0003 | t0001 | g0098 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01167 | hp2 | a0003 | c0005 | t0001 | g0023 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01168 | hp2 | a0004 | c0006 | t0001 | g0007 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01169 | hp1 | a0003 | c0005 | t0001 | g0023 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01169 | hp2 | a0004 | c0006 | t0001 | g0007 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0291 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01175 | hp2 | a0004 | c0006 | t0001 | g0240 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0250 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01192 | hp2 | a0003 | c0005 | t0001 | g0227 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01243 | hp1 | a0002 | c0003 | t0001 | g0127 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01243 | hp2 | a0002 | c0002 | t0001 | g0122 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01255 | hp1 | a0002 | c0003 | t0001 | g0187 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01257 | hp2 | a0005 | c0007 | t0001 | g0024 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01258 | hp1 | a0005 | c0007 | t0001 | g0024 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0325 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01261 | hp2 | a0003 | c0005 | t0001 | g0235 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0251 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01346 | hp2 | a0010 | c0011 | t0001 | g0027 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0300 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01358 | hp2 | a0001 | c0004 | t0001 | g0283 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01361 | hp1 | a0005 | c0007 | t0001 | g0032 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0309 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01433 | hp1 | a0003 | c0005 | t0001 | g0226 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01433 | hp2 | a0001 | c0004 | t0001 | g0244 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0348 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0335 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0159 | EUR | IBS | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0257 | EUR | IBS | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01891 | hp1 | a0007 | c0008 | t0001 | g0129 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01891 | hp2 | a0011 | c0014 | t0001 | g0361 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01928 | hp2 | a0005 | c0007 | t0001 | g0032 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01943 | hp2 | a0005 | c0007 | t0001 | g0343 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0312 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01975 | hp1 | a0005 | c0007 | t0001 | g0345 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0301 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01978 | hp1 | a0003 | c0005 | t0001 | g0236 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01978 | hp2 | a0005 | c0007 | t0001 | g0346 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0288 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0323 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0330 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02004 | hp2 | a0001 | c0004 | t0001 | g0137 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02040 | hp1 | a0002 | c0003 | t0001 | g0025 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0305 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0308 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02145 | hp2 | a0007 | c0008 | t0001 | g0103 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02148 | hp1 | a0005 | c0007 | t0001 | g0046 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0338 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CDX | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CDX | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CDX | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0297 | EAS | CDX | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02257 | hp1 | a0012 | c0015 | t0001 | g0377 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02257 | hp2 | a0002 | c0003 | t0001 | g0110 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0340 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02258 | hp2 | a0006 | c0025 | t0001 | g0370 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02273 | hp2 | a0005 | c0007 | t0001 | g0347 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02280 | hp1 | a0002 | c0003 | t0001 | g0128 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0302 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0341 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0304 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0094 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02615 | hp1 | a0002 | c0003 | t0001 | g0189 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02622 | hp1 | a0008 | c0026 | t0001 | g0371 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02630 | hp1 | a0002 | c0003 | t0001 | g0097 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02683 | hp1 | a0010 | c0011 | t0001 | g0048 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02683 | hp2 | a0003 | c0005 | t0001 | g0230 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02698 | hp1 | a0001 | c0004 | t0001 | g0061 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02717 | hp1 | a0008 | c0009 | t0001 | g0358 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02717 | hp2 | a0013 | c0027 | t0001 | g0378 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02723 | hp1 | a0007 | c0008 | t0001 | g0105 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02723 | hp2 | a0002 | c0003 | t0001 | g0223 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0295 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02735 | hp2 | a0001 | c0004 | t0001 | g0092 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02809 | hp1 | a0009 | c0018 | t0001 | g0036 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02809 | hp2 | a0008 | c0009 | t0001 | g0374 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02818 | hp1 | a0002 | c0003 | t0001 | g0225 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02818 | hp2 | a0002 | c0013 | t0001 | g0102 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02886 | hp1 | a0008 | c0009 | t0001 | g0359 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02895 | hp2 | a0007 | c0008 | t0001 | g0124 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02896 | hp1 | a0002 | c0002 | t0001 | g0328 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02896 | hp2 | a0002 | c0003 | t0001 | g0143 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02897 | hp1 | a0007 | c0008 | t0001 | g0130 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02897 | hp2 | a0002 | c0002 | t0001 | g0324 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02922 | hp1 | a0006 | c0010 | t0001 | g0364 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02922 | hp2 | a0002 | c0028 | t0001 | g0379 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02965 | hp1 | a0009 | c0012 | t0001 | g0138 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02965 | hp2 | a0004 | c0006 | t0001 | g0125 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02970 | hp2 | a0012 | c0015 | t0001 | g0376 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0317 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03041 | hp2 | a0004 | c0006 | t0001 | g0182 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03098 | hp1 | a0006 | c0010 | t0001 | g0365 | AFR | MSL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03130 | hp2 | a0002 | c0013 | t0001 | g0224 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0354 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03195 | hp2 | a0002 | c0013 | t0001 | g0123 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03209 | hp1 | a0014 | c0024 | t0001 | g0357 | AFR | MSL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0350 | AFR | MSL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03239 | hp2 | a0004 | c0006 | t0001 | g0273 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03453 | hp2 | a0007 | c0008 | t0001 | g0100 | AFR | MSL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03486 | hp1 | a0008 | c0009 | t0001 | g0375 | AFR | MSL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0356 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03490 | hp2 | a0001 | c0004 | t0001 | g0134 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0045 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03491 | hp2 | a0001 | c0004 | t0001 | g0150 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03516 | hp1 | a0006 | c0010 | t0001 | g0369 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03516 | hp2 | a0002 | c0003 | t0001 | g0190 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03540 | hp1 | a0008 | c0009 | t0001 | g0373 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03540 | hp2 | a0002 | c0003 | t0001 | g0037 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0216 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03654 | hp2 | a0010 | c0011 | t0001 | g0270 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | STU | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03688 | hp2 | a0015 | c0019 | t0001 | g0327 | SAS | STU | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03704 | hp1 | a0003 | c0005 | t0001 | g0238 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03710 | hp1 | a0009 | c0012 | t0001 | g0195 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0326 | SAS | BEB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03834 | hp2 | a0001 | c0004 | t0001 | g0060 | SAS | BEB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03927 | hp1 | a0016 | c0016 | t0001 | g0034 | SAS | BEB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03942 | hp1 | a0017 | c0017 | t0001 | g0035 | SAS | BEB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03942 | hp2 | a0004 | c0006 | t0001 | g0038 | SAS | BEB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | STU | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0313 | SAS | STU | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG04184 | hp1 | a0009 | c0012 | t0001 | g0162 | SAS | BEB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG04184 | hp2 | a0001 | c0004 | t0001 | g0108 | SAS | BEB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | STU | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | STU | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | STU | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG04204 | hp2 | a0001 | c0004 | t0001 | g0133 | SAS | STU | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG04228 | hp1 | a0001 | c0004 | t0001 | g0229 | SAS | STU | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG04228 | hp2 | a0001 | c0004 | t0001 | g0171 | SAS | STU | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | YRI | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18522 | hp2 | a0008 | c0009 | t0001 | g0362 | AFR | YRI | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | CHB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | CHB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CHB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0349 | AFR | YRI | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18906 | hp2 | a0001 | c0004 | t0001 | g0191 | AFR | YRI | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18939 | hp2 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0290 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0303 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18952 | hp2 | a0003 | c0005 | t0001 | g0166 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18954 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18957 | hp1 | a0002 | c0003 | t0001 | g0026 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0320 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18962 | hp2 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18965 | hp2 | a0002 | c0020 | t0001 | g0289 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18968 | hp2 | a0002 | c0003 | t0001 | g0005 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18969 | hp1 | a0001 | c0004 | t0001 | g0049 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18970 | hp2 | a0002 | c0003 | t0001 | g0201 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0316 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18979 | hp2 | a0018 | c0022 | t0001 | g0082 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18981 | hp2 | a0003 | c0005 | t0001 | g0262 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18982 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18985 | hp1 | a0002 | c0002 | t0001 | g0332 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18986 | hp2 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18988 | hp1 | a0003 | c0005 | t0001 | g0113 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18989 | hp1 | a0002 | c0003 | t0001 | g0005 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18989 | hp2 | a0001 | c0004 | t0001 | g0041 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18992 | hp2 | a0001 | c0004 | t0001 | g0040 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18993 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18999 | hp1 | a0002 | c0003 | t0001 | g0025 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0322 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19012 | hp2 | a0002 | c0003 | t0001 | g0206 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19030 | hp1 | a0002 | c0013 | t0001 | g0099 | AFR | LWK | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19030 | hp2 | a0011 | c0014 | t0001 | g0363 | AFR | LWK | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | LWK | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19043 | hp2 | a0019 | c0021 | t0001 | g0136 | AFR | LWK | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19056 | hp2 | a0002 | c0003 | t0001 | g0256 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0318 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19058 | hp1 | a0003 | c0005 | t0001 | g0167 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19066 | hp1 | a0002 | c0003 | t0001 | g0026 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0353 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19067 | hp1 | a0003 | c0005 | t0001 | g0239 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19070 | hp2 | a0002 | c0003 | t0001 | g0005 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0298 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19077 | hp2 | a0002 | c0003 | t0001 | g0005 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19083 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0329 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0319 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0314 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19240 | hp1 | a0006 | c0010 | t0001 | g0367 | AFR | YRI | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA19240 | hp2 | a0007 | c0008 | t0001 | g0101 | AFR | YRI | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ASW | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0184 | AFR | ASW | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0149 | EUR | TSI | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0054 | EUR | TSI | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA20805 | hp1 | a0004 | c0006 | t0001 | g0007 | EUR | TSI | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0151 | EUR | TSI | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01123 | hp1 | a0001 | c0004 | t0001 | g0247 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0165 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02109 | hp2 | a0009 | c0012 | t0001 | g0126 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02486 | hp1 | a0004 | c0006 | t0001 | g0272 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02486 | hp2 | a0002 | c0023 | t0001 | g0104 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG02559 | hp2 | a0008 | c0009 | t0001 | g0360 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG03471 | hp2 | a0002 | c0003 | t0001 | g0116 | AFR | MSL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG06807 | hp1 | a0004 | c0006 | t0001 | g0271 | AFR | USA | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
HG06807 | hp2 | a0006 | c0010 | t0001 | g0366 | AFR | USA | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA18955 | hp2 | a0002 | c0003 | t0001 | g0215 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA20300 | hp1 | a0006 | c0010 | t0001 | g0368 | AFR | USA | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | USA | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA21309 | hp1 | a0007 | c0008 | t0001 | g0222 | AFR | LWK | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0355 | AFR | LWK | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
homoSapiens | chm13v2 | a0003 | c0005 | t0001 | g0245 | REF | REF | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0299 | REF | REF | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:4197180 | G | A | 1 | a0005 | 10 | HG00733.hp1 HG01257.hp2 HG01258.hp1 others(7): Show |
missense_variant | MODERATE | c.1654C>T | p.Leu552Phe | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/6 | 1719/1981 | 1654/1839 | 552/612 | chr4 | 4197180 | |||
chr4:4197221 | GCGTTGC | G | 6 | a0004 a0005 a0009 others(3): Show |
31 | HG00099.hp2 HG00733.hp1 HG01106.hp1 others(28): Show |
disruptive_inframe_deletion | MODERATE | c.1607_1612delGCAACG | p.Gly536_Asn537del | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/6 | 1677/1981 | 1607/1839 | 536/612 | chr4 | 4197221 | |||
chr4:4197356 | T | G | 1 | a0003 | 16 | HG00323.hp2 HG00544.hp2 HG00738.hp2 others(13): Show |
missense_variant | MODERATE | c.1478A>C | p.Lys493Thr | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/6 | 1543/1981 | 1478/1839 | 493/612 | chr4 | 4197356 | |||
chr4:4197534 | C | T | 1 | a0010 | 4 | HG00280.hp1 HG01346.hp2 HG02683.hp1 others(1): Show |
missense_variant | MODERATE | c.1300G>A | p.Val434Met | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/6 | 1365/1981 | 1300/1839 | 434/612 | chr4 | 4197534 | |||
chr4:4197638 | G | C | 1 | a0018 | 1 | NA18979.hp2 | missense_variant | MODERATE | c.1196C>G | p.Ser399Trp | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/6 | 1261/1981 | 1196/1839 | 399/612 | chr4 | 4197638 | |||
chr4:4197788 | A | G | 1 | a0017 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.1046T>C | p.Met349Thr | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/6 | 1111/1981 | 1046/1839 | 349/612 | chr4 | 4197788 | |||
chr4:4197907 | A | T | 10 | a0001 a0003 a0007 others(7): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
missense_variant | MODERATE | c.927T>A | p.Asp309Glu | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/6 | 992/1981 | 927/1839 | 309/612 | chr4 | 4197907 | |||
chr4:4202457 | T | C | 1 | a0007 | 8 | HG01891.hp1 HG02145.hp2 HG02723.hp1 others(5): Show |
missense_variant | MODERATE | c.721A>G | p.Ile241Val | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/6 | 786/1981 | 721/1839 | 241/612 | chr4 | 4202457 | |||
chr4:4202526 | C | T | 1 | a0019 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.652G>A | p.Val218Ile | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/6 | 717/1981 | 652/1839 | 218/612 | chr4 | 4202526 | |||
chr4:4202556 | A | T | 1 | a0015 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.622T>A | p.Phe208Ile | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/6 | 687/1981 | 622/1839 | 208/612 | chr4 | 4202556 | |||
chr4:4226480 | C | T | 1 | a0013 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.385G>A | p.Gly129Ser | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/6 | 450/1981 | 385/1839 | 129/612 | chr4 | 4226480 | |||
chr4:4226524 | C | G | 1 | a0016 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.341G>C | p.Ser114Thr | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/6 | 406/1981 | 341/1839 | 114/612 | chr4 | 4226524 | |||
chr4:4226570 | G | A | 1 | a0014 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.295C>T | p.Leu99Phe | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/6 | 360/1981 | 295/1839 | 99/612 | chr4 | 4226570 | |||
chr4:4226650 | G | T | 1 | a0017 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.215C>A | p.Ala72Glu | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/6 | 280/1981 | 215/1839 | 72/612 | chr4 | 4226650 | |||
chr4:4226737 | G | A | 3 | a0006 a0008 a0011 |
18 | HG01109.hp1 HG01891.hp2 HG02258.hp2 others(15): Show |
missense_variant | MODERATE | c.128C>T | p.Ala43Val | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/6 | 193/1981 | 128/1839 | 43/612 | chr4 | 4226737 | |||
chr4:4226786 | C | A | 1 | a0012 | 2 | HG02257.hp1 HG02970.hp2 |
missense_variant | MODERATE | c.79G>T | p.Ala27Ser | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/6 | 144/1981 | 79/1839 | 27/612 | chr4 | 4226786 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:4197490 | G | A | 4 | a0002c0013 a0002c0023 a0006c0025 others(1): Show |
7 | HG02258.hp2 HG02486.hp2 HG02717.hp2 others(4): Show |
synonymous_variant | LOW | c.1344C>T | p.His448His | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/6 | 1409/1981 | 1344/1839 | 448/612 | chr4 | 4197490 | |||
chr4:4198033 | G | A | 2 | a0001c0004 a0008c0026 |
23 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(20): Show |
synonymous_variant | LOW | c.801C>T | p.Ile267Ile | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/6 | 866/1981 | 801/1839 | 267/612 | chr4 | 4198033 | |||
chr4:4198042 | G | A | 1 | a0002c0020 | 1 | NA18965.hp2 | synonymous_variant | LOW | c.792C>T | p.Ser264Ser | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/6 | 857/1981 | 792/1839 | 264/612 | chr4 | 4198042 | |||
chr4:4202527 | G | A | 1 | a0002c0023 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.651C>T | p.Gly217Gly | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/6 | 716/1981 | 651/1839 | 217/612 | chr4 | 4202527 | |||
chr4:4202572 | T | C | 25 | a0001c0001 a0001c0004 a0002c0003 others(22): Show |
340 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(337): Show |
synonymous_variant | LOW | c.606A>G | p.Gly202Gly | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/6 | 671/1981 | 606/1839 | 202/612 | chr4 | 4202572 | |||
chr4:4226481 | C | G | 3 | a0002c0028 a0009c0018 a0013c0027 |
3 | HG02717.hp2 HG02809.hp1 HG02922.hp2 |
synonymous_variant | LOW | c.384G>C | p.Ala128Ala | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/6 | 449/1981 | 384/1839 | 128/612 | chr4 | 4226481 | |||
chr4:4226736 | G | T | 1 | a0016c0016 | 1 | HG03927.hp1 | synonymous_variant | LOW | c.129C>A | p.Ala43Ala | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/6 | 194/1981 | 129/1839 | 43/612 | chr4 | 4226736 | |||
chr4:4226859 | G | A | 2 | a0002c0028 a0013c0027 |
2 | HG02717.hp2 HG02922.hp2 |
synonymous_variant | LOW | c.6C>T | p.Leu2Leu | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/6 | 71/1981 | 6/1839 | 2/612 | chr4 | 4226859 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:4226915 | C | G | 1 | a0001c0001t0002 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-51G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/6 | 51 | chr4 | 4226915 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:4189049 | G | T | 1 | a0008c0009t0001g0362 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1669-76C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4189049 | |||||||
chr4:4189065 | A | C | 282 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(279): Show |
320 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.1669-92T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4189065 | |||||||
chr4:4189120 | C | T | 1 | a0001c0001t0001g0017 | 2 | HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1669-147G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4189120 | |||||||
chr4:4189184 | C | A | 27 | a0002c0013t0001g0099 a0002c0013t0001g0102 a0002c0013t0001g0123 others(24): Show |
31 | HG00099.hp2 HG00733.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.1669-211G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4189184 | |||||||
chr4:4189187 | C | G | 22 | a0001c0004t0001g0040 a0001c0004t0001g0041 a0001c0004t0001g0049 others(19): Show |
22 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.1669-214G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4189187 | |||||||
chr4:4189215 | A | G | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
137 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(134): Show |
intron_variant | MODIFIER | c.1669-242T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4189215 | |||||||
chr4:4189368 | T | C | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1669-395A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4189368 | |||||||
chr4:4189372 | C | T | 11 | a0002c0002t0001g0106 a0002c0002t0001g0122 a0002c0003t0001g0037 others(8): Show |
11 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.1669-399G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4189372 | |||||||
chr4:4189511 | T | C | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1669-538A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4189511 | |||||||
chr4:4189539 | C | A | 282 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(279): Show |
320 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.1669-566G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4189539 | |||||||
chr4:4189737 | G | T | 1 | a0002c0003t0001g0127 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1669-764C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4189737 | |||||||
chr4:4189771 | C | T | 70 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(67): Show |
84 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.1669-798G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4189771 | |||||||
chr4:4189787 | G | T | 1 | a0002c0002t0001g0132 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1669-814C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4189787 | |||||||
chr4:4190126 | C | T | 3 | a0001c0001t0001g0178 a0001c0001t0001g0231 a0002c0002t0001g0045 |
3 | HG03491.hp1 HG03669.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1669-1153G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4190126 | |||||||
chr4:4190128 | C | T | 1 | a0002c0002t0001g0301 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1669-1155G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4190128 | |||||||
chr4:4190164 | G | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(90): Show |
106 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1669-1191C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4190164 | |||||||
chr4:4190219 | T | A | 73 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0019 others(70): Show |
81 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.1669-1246A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4190219 | |||||||
chr4:4190228 | T | C | 1 | a0001c0004t0001g0150 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1669-1255A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4190228 | |||||||
chr4:4190259 | G | A | 20 | a0001c0004t0001g0040 a0001c0004t0001g0041 a0001c0004t0001g0049 others(17): Show |
20 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1669-1286C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4190259 | |||||||
chr4:4190339 | C | T | 12 | a0002c0002t0001g0106 a0002c0002t0001g0122 a0002c0003t0001g0037 others(9): Show |
12 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.1669-1366G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4190339 | |||||||
chr4:4190405 | C | T | 4 | a0001c0001t0001g0172 a0009c0012t0001g0162 a0009c0012t0001g0195 others(1): Show |
4 | HG03710.hp1 HG03927.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1669-1432G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4190405 | |||||||
chr4:4190512 | G | A | 28 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(25): Show |
38 | HG00438.hp1 HG00673.hp2 HG01496.hp1 others(35): Show |
intron_variant | MODIFIER | c.1669-1539C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4190512 | |||||||
chr4:4190525 | G | C | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(290): Show |
331 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.1669-1552C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4190525 | |||||||
chr4:4190721 | C | A | 3 | a0001c0001t0001g0284 a0001c0001t0001g0352 a0001c0001t0002g0033 |
3 | HG02083.hp1 NA18993.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1669-1748G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4190721 | |||||||
chr4:4190810 | G | C | 1 | a0001c0001t0001g0071 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1669-1837C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4190810 | |||||||
chr4:4190869 | G | C | 1 | a0003c0005t0001g0140 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1669-1896C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4190869 | |||||||
chr4:4190974 | C | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0070 |
4 | HG02145.hp1 HG02622.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1669-2001G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4190974 | |||||||
chr4:4190979 | T | A | 78 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(75): Show |
92 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.1669-2006A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4190979 | |||||||
chr4:4191102 | C | T | 55 | a0001c0004t0001g0040 a0001c0004t0001g0041 a0001c0004t0001g0049 others(52): Show |
59 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.1669-2129G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191102 | |||||||
chr4:4191105 | C | G | 12 | a0002c0002t0001g0106 a0002c0002t0001g0122 a0002c0003t0001g0037 others(9): Show |
12 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.1669-2132G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191105 | |||||||
chr4:4191113 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1669-2140G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191113 | |||||||
chr4:4191177 | C | T | 3 | a0001c0004t0001g0092 a0001c0004t0001g0150 a0001c0004t0001g0171 |
3 | HG02735.hp2 HG03491.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1669-2204G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191177 | |||||||
chr4:4191298 | C | T | 69 | a0001c0001t0001g0009 a0001c0001t0001g0192 a0001c0001t0001g0194 others(66): Show |
75 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.1669-2325G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191298 | |||||||
chr4:4191333 | T | C | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(278): Show |
319 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.1669-2360A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191333 | |||||||
chr4:4191337 | C | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0192 a0001c0001t0001g0194 others(2): Show |
7 | HG02109.hp1 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1669-2364G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191337 | |||||||
chr4:4191482 | C | T | 2 | a0004c0006t0001g0125 a0004c0006t0001g0182 |
2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1669-2509G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191482 | |||||||
chr4:4191492 | C | T | 1 | a0006c0010t0001g0364 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1669-2519G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191492 | |||||||
chr4:4191549 | C | T | 13 | a0003c0005t0001g0023 a0003c0005t0001g0113 a0003c0005t0001g0140 others(10): Show |
14 | HG00323.hp2 HG00544.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1669-2576G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191549 | |||||||
chr4:4191612 | C | T | 1 | a0003c0005t0001g0237 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1669-2639G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191612 | |||||||
chr4:4191617 | C | T | 2 | a0001c0004t0001g0150 a0001c0004t0001g0171 |
2 | HG03491.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1669-2644G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191617 | |||||||
chr4:4191638 | A | C | 1 | a0003c0005t0001g0235 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1669-2665T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191638 | |||||||
chr4:4191640 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0157 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1669-2667G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191640 | |||||||
chr4:4191650 | T | C | 52 | a0001c0001t0001g0131 a0001c0004t0001g0040 a0001c0004t0001g0041 others(49): Show |
56 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.1669-2677A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191650 | |||||||
chr4:4191754 | T | C | 13 | a0003c0005t0001g0023 a0003c0005t0001g0113 a0003c0005t0001g0140 others(10): Show |
14 | HG00323.hp2 HG00544.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1669-2781A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191754 | |||||||
chr4:4191789 | G | T | 28 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(25): Show |
38 | HG00438.hp1 HG00673.hp2 HG01496.hp1 others(35): Show |
intron_variant | MODIFIER | c.1669-2816C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191789 | |||||||
chr4:4191813 | G | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0259 |
4 | NA18940.hp2 NA18945.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.1669-2840C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191813 | |||||||
chr4:4191846 | C | A | 68 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(65): Show |
82 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.1669-2873G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191846 | |||||||
chr4:4192130 | T | G | 1 | a0001c0004t0001g0243 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1669-3157A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192130 | |||||||
chr4:4192172 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1669-3199G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192172 | |||||||
chr4:4192277 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(83): Show |
97 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1669-3304G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192277 | |||||||
chr4:4192309 | C | T | 2 | a0009c0012t0001g0126 a0009c0012t0001g0138 |
2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1669-3336G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192309 | |||||||
chr4:4192439 | A | G | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(232): Show |
268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1669-3466T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192439 | |||||||
chr4:4192526 | A | G | 4 | a0001c0001t0001g0172 a0009c0012t0001g0162 a0009c0012t0001g0195 others(1): Show |
4 | HG03710.hp1 HG03927.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1669-3553T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192526 | |||||||
chr4:4192535 | A | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.1669-3562T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192535 | |||||||
chr4:4192656 | A | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1669-3683T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192656 | |||||||
chr4:4192682 | C | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0259 |
4 | NA18940.hp2 NA18945.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.1669-3709G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192682 | |||||||
chr4:4192735 | C | T | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.1669-3762G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192735 | |||||||
chr4:4192852 | G | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.1669-3879C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192852 | |||||||
chr4:4192855 | T | C | 4 | a0001c0001t0001g0172 a0009c0012t0001g0162 a0009c0012t0001g0195 others(1): Show |
4 | HG03710.hp1 HG03927.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1669-3882A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192855 | |||||||
chr4:4192864 | G | T | 83 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0017 others(80): Show |
91 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.1669-3891C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192864 | |||||||
chr4:4192934 | C | T | 177 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(174): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.1669-3961G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192934 | |||||||
chr4:4192951 | T | C | 23 | a0001c0004t0001g0040 a0001c0004t0001g0041 a0001c0004t0001g0049 others(20): Show |
23 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.1669-3978A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192951 | |||||||
chr4:4192980 | C | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(238): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.1669-4007G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192980 | |||||||
chr4:4193087 | C | T | 1 | a0003c0005t0001g0258 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1668+4079G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193087 | |||||||
chr4:4193126 | C | T | 2 | a0001c0001t0001g0205 a0001c0001t0001g0212 |
2 | HG02015.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.1668+4040G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193126 | |||||||
chr4:4193208 | G | A | 7 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0070 others(4): Show |
8 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1668+3958C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193208 | |||||||
chr4:4193286 | T | C | 11 | a0001c0001t0001g0131 a0001c0001t0001g0193 a0007c0008t0001g0100 others(8): Show |
11 | HG01891.hp1 HG02145.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1668+3880A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193286 | |||||||
chr4:4193292 | A | C | 3 | a0001c0001t0001g0193 a0007c0008t0001g0222 a0008c0009t0001g0375 |
3 | HG03471.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1668+3874T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193292 | |||||||
chr4:4193347 | A | G | 12 | a0001c0001t0001g0131 a0001c0001t0001g0193 a0006c0010t0001g0364 others(9): Show |
12 | HG01891.hp1 HG02145.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1668+3819T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193347 | |||||||
chr4:4193362 | G | C | 8 | a0001c0001t0001g0172 a0001c0001t0001g0193 a0006c0010t0001g0364 others(5): Show |
8 | HG02922.hp1 HG03471.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1668+3804C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193362 | |||||||
chr4:4193417 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1668+3749C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193417 | |||||||
chr4:4193443 | T | A | 9 | a0002c0003t0001g0116 a0002c0003t0001g0143 a0002c0003t0001g0187 others(6): Show |
9 | HG01255.hp1 HG02615.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1668+3723A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193443 | |||||||
chr4:4193554 | CA | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
245 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.1668+3611delT | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193554 | |||||||
chr4:4193587 | C | T | 2 | a0002c0003t0001g0206 a0002c0003t0001g0215 |
2 | NA18955.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1668+3579G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193587 | |||||||
chr4:4193640 | C | T | 1 | a0002c0002t0001g0308 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1668+3526G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193640 | |||||||
chr4:4193657 | C | T | 1 | a0002c0002t0001g0045 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1668+3509G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193657 | |||||||
chr4:4193673 | A | G | 47 | a0001c0001t0001g0172 a0001c0004t0001g0040 a0001c0004t0001g0041 others(44): Show |
51 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.1668+3493T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193673 | |||||||
chr4:4193693 | G | T | 8 | a0002c0013t0001g0099 a0002c0013t0001g0102 a0002c0013t0001g0123 others(5): Show |
8 | HG02258.hp2 HG02486.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1668+3473C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193693 | |||||||
chr4:4193809 | G | T | 2 | a0009c0012t0001g0126 a0009c0012t0001g0138 |
2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1668+3357C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193809 | |||||||
chr4:4193856 | G | A | 1 | a0003c0005t0001g0227 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1668+3310C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193856 | |||||||
chr4:4193897 | A | AG | 20 | a0004c0006t0001g0007 a0004c0006t0001g0038 a0004c0006t0001g0059 others(17): Show |
24 | HG00099.hp2 HG00733.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1668+3268_1668+326 others(5): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193897 | |||||||
chr4:4193916 | G | A | 1 | a0001c0004t0001g0171 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1668+3250C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193916 | |||||||
chr4:4193929 | C | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
226 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.1668+3237G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193929 | |||||||
chr4:4193930 | G | A | 1 | a0002c0020t0001g0289 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1668+3236C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193930 | |||||||
chr4:4194013 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1668+3153G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194013 | |||||||
chr4:4194014 | C | T | 3 | a0001c0001t0001g0154 a0001c0001t0001g0176 a0001c0001t0001g0177 |
3 | HG02056.hp2 NA18966.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1668+3152G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194014 | |||||||
chr4:4194081 | C | T | 23 | a0001c0004t0001g0040 a0001c0004t0001g0041 a0001c0004t0001g0049 others(20): Show |
23 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.1668+3085G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194081 | |||||||
chr4:4194138 | A | G | 2 | a0009c0012t0001g0126 a0009c0012t0001g0138 |
2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1668+3028T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194138 | |||||||
chr4:4194158 | C | A | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
310 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.1668+3008G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194158 | |||||||
chr4:4194244 | A | C | 19 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(16): Show |
22 | HG00735.hp2 HG01884.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1668+2922T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194244 | |||||||
chr4:4194301 | C | G | 27 | a0001c0001t0001g0172 a0001c0004t0001g0040 a0001c0004t0001g0041 others(24): Show |
27 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.1668+2865G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194301 | |||||||
chr4:4194315 | C | T | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(265): Show |
306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.1668+2851G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194315 | |||||||
chr4:4194318 | A | C | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(265): Show |
306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.1668+2848T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194318 | |||||||
chr4:4194359 | C | T | 1 | a0002c0013t0001g0123 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1668+2807G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194359 | |||||||
chr4:4194486 | T | C | 1 | a0001c0004t0001g0274 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1668+2680A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194486 | |||||||
chr4:4194509 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1668+2657C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194509 | |||||||
chr4:4194636 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1668+2530A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194636 | |||||||
chr4:4194656 | G | A | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1668+2510C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194656 | |||||||
chr4:4194658 | C | T | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1668+2508G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194658 | |||||||
chr4:4194699 | G | C | 1 | a0006c0010t0001g0364 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1668+2467C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194699 | |||||||
chr4:4194719 | A | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1668+2447T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194719 | |||||||
chr4:4194750 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1668+2416C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194750 | |||||||
chr4:4194766 | G | A | 1 | a0006c0010t0001g0364 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1668+2400C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194766 | |||||||
chr4:4194814 | G | T | 3 | a0010c0011t0001g0027 a0010c0011t0001g0048 a0010c0011t0001g0270 |
4 | HG00280.hp1 HG01346.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1668+2352C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194814 | |||||||
chr4:4194835 | C | T | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1668+2331G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194835 | |||||||
chr4:4195038 | T | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(217): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1668+2128A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4195038 | |||||||
chr4:4195076 | A | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(209): Show |
240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1668+2090T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4195076 | |||||||
chr4:4195228 | G | T | 1 | a0001c0001t0001g0241 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1668+1938C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4195228 | |||||||
chr4:4195254 | C | G | 2 | a0001c0001t0001g0248 a0001c0001t0001g0253 |
2 | HG02135.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1668+1912G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4195254 | |||||||
chr4:4195349 | T | C | 8 | a0002c0003t0001g0037 a0002c0003t0001g0127 a0002c0003t0001g0128 others(5): Show |
8 | HG01109.hp1 HG01243.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1668+1817A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4195349 | |||||||
chr4:4195562 | G | A | 7 | a0002c0013t0001g0099 a0002c0013t0001g0102 a0002c0013t0001g0123 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1668+1604C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4195562 | |||||||
chr4:4195649 | A | C | 292 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(289): Show |
330 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.1668+1517T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4195649 | |||||||
chr4:4195710 | A | T | 1 | a0001c0001t0001g0246 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1668+1456T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4195710 | |||||||
chr4:4195897 | G | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1668+1269C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4195897 | |||||||
chr4:4195926 | T | C | 26 | a0001c0001t0001g0193 a0001c0004t0001g0040 a0001c0004t0001g0041 others(23): Show |
26 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.1668+1240A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4195926 | |||||||
chr4:4196171 | C | T | 1 | a0005c0007t0001g0345 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1668+995G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4196171 | |||||||
chr4:4196177 | G | T | 3 | a0010c0011t0001g0027 a0010c0011t0001g0048 a0010c0011t0001g0270 |
4 | HG00280.hp1 HG01346.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1668+989C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4196177 | |||||||
chr4:4196186 | A | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
180 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.1668+980T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4196186 | |||||||
chr4:4196349 | C | T | 15 | a0003c0005t0001g0023 a0003c0005t0001g0113 a0003c0005t0001g0140 others(12): Show |
16 | HG00323.hp2 HG00544.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1668+817G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4196349 | |||||||
chr4:4196350 | G | A | 3 | a0001c0001t0001g0085 a0001c0001t0001g0204 a0001c0001t0001g0218 |
3 | HG02129.hp2 NA18944.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1668+816C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4196350 | |||||||
chr4:4196469 | A | G | 1 | a0002c0002t0001g0353 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1668+697T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4196469 | |||||||
chr4:4196481 | C | T | 12 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0050 others(9): Show |
15 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1668+685G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4196481 | |||||||
chr4:4196507 | A | G | 15 | a0003c0005t0001g0023 a0003c0005t0001g0113 a0003c0005t0001g0140 others(12): Show |
16 | HG00323.hp2 HG00544.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1668+659T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4196507 | |||||||
chr4:4196678 | T | G | 1 | a0001c0001t0001g0115 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1668+488A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4196678 | |||||||
chr4:4196764 | C | T | 5 | a0002c0003t0001g0127 a0002c0003t0001g0128 a0002c0003t0001g0190 others(2): Show |
5 | HG01109.hp1 HG01243.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1668+402G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4196764 | |||||||
chr4:4196857 | C | G | 10 | a0002c0013t0001g0099 a0002c0013t0001g0102 a0002c0013t0001g0123 others(7): Show |
10 | HG02258.hp2 HG02486.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1668+309G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4196857 | |||||||
chr4:4197088 | C | G | 18 | a0001c0001t0001g0178 a0001c0001t0001g0231 a0003c0005t0001g0023 others(15): Show |
19 | HG00323.hp2 HG00544.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1668+78G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4197088 | |||||||
chr4:4197089 | T | C | 1 | a0006c0010t0001g0369 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1668+77A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4197089 | |||||||
chr4:4197124 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1668+42T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4197124 | |||||||
chr4:4197154 | G | C | 1 | a0001c0001t0001g0087 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1668+12C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4197154 | |||||||
chr4:4198232 | G | A | 1 | a0002c0002t0001g0309 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.731-129C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4198232 | |||||||
chr4:4198254 | A | G | 42 | a0002c0003t0001g0037 a0002c0003t0001g0097 a0002c0003t0001g0098 others(39): Show |
46 | HG00099.hp2 HG00733.hp1 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.731-151T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4198254 | |||||||
chr4:4198270 | T | C | 1 | a0002c0003t0001g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.731-167A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4198270 | |||||||
chr4:4198359 | T | C | 2 | a0008c0009t0001g0373 a0008c0009t0001g0374 |
2 | HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.731-256A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4198359 | |||||||
chr4:4198373 | A | T | 59 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(56): Show |
66 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.731-270T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4198373 | |||||||
chr4:4198384 | T | TGATA | 16 | a0001c0001t0001g0231 a0003c0005t0001g0023 a0003c0005t0001g0113 others(13): Show |
17 | HG00323.hp2 HG00544.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.731-285_731-282dup others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4198384 | |||||||
chr4:4198492 | T | C | 16 | a0001c0001t0001g0231 a0003c0005t0001g0023 a0003c0005t0001g0113 others(13): Show |
17 | HG00323.hp2 HG00544.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.731-389A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4198492 | |||||||
chr4:4198527 | A | G | 1 | a0001c0001t0001g0335 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.731-424T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4198527 | |||||||
chr4:4198560 | A | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(82): Show |
96 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.731-457T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4198560 | |||||||
chr4:4198659 | G | A | 41 | a0002c0003t0001g0037 a0002c0003t0001g0110 a0002c0003t0001g0127 others(38): Show |
45 | HG00099.hp2 HG00733.hp1 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.731-556C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4198659 | |||||||
chr4:4198684 | G | T | 1 | a0002c0002t0001g0011 | 3 | HG01069.hp1 HG01071.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.731-581C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4198684 | |||||||
chr4:4198740 | G | A | 2 | a0001c0001t0001g0336 a0002c0002t0001g0054 |
2 | NA19088.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.731-637C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4198740 | |||||||
chr4:4198894 | C | A | 1 | a0002c0002t0001g0106 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.731-791G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4198894 | |||||||
chr4:4198919 | G | A | 11 | a0001c0001t0001g0009 a0001c0001t0001g0192 a0001c0001t0001g0194 others(8): Show |
13 | HG02109.hp1 HG02109.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.731-816C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4198919 | |||||||
chr4:4199059 | C | T | 9 | a0002c0003t0001g0097 a0002c0003t0001g0098 a0002c0013t0001g0099 others(6): Show |
9 | HG01167.hp1 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.731-956G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199059 | |||||||
chr4:4199125 | G | A | 1 | a0004c0006t0001g0240 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.731-1022C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199125 | |||||||
chr4:4199220 | T | TTGTGTG | 4 | a0001c0001t0001g0009 a0001c0001t0001g0192 a0001c0001t0001g0194 others(1): Show |
6 | HG02109.hp1 HG02630.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.731-1123_731-1118d others(8): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199220 | |||||||
chr4:4199220 | T | TTGTGTGT others(1): Show |
23 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0017 others(20): Show |
31 | HG00735.hp2 HG01069.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.731-1125_731-1118d others(10): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199220 | |||||||
chr4:4199220 | T | TTGTGTGT others(3): Show |
24 | a0001c0001t0001g0163 a0001c0001t0001g0231 a0001c0004t0001g0133 others(21): Show |
26 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.731-1127_731-1118d others(12): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199220 | |||||||
chr4:4199220 | T | TTGTGTGT others(5): Show |
96 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(93): Show |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.731-1129_731-1118d others(14): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199220 | |||||||
chr4:4199220 | T | TTGTGTGT others(7): Show |
25 | a0001c0001t0001g0066 a0001c0001t0001g0070 a0001c0001t0001g0093 others(22): Show |
25 | HG00544.hp2 HG00639.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.731-1131_731-1118d others(16): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199220 | |||||||
chr4:4199220 | T | TTGTGTGT others(9): Show |
6 | a0001c0001t0001g0039 a0001c0001t0001g0146 a0001c0004t0001g0041 others(3): Show |
6 | HG00140.hp1 HG01433.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.731-1118_731-1117i others(18): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199220 | |||||||
chr4:4199220 | T | TTGTGTGT others(11): Show |
3 | a0001c0001t0001g0058 a0001c0004t0001g0049 a0001c0004t0001g0061 |
3 | HG02698.hp1 NA18967.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.731-1118_731-1117i others(20): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199220 | |||||||
chr4:4199233 | T | TGA | 23 | a0002c0002t0001g0011 a0002c0002t0001g0028 a0002c0002t0001g0091 others(20): Show |
26 | HG01069.hp1 HG01071.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.731-1132_731-1131d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199233 | |||||||
chr4:4199233 | T | TGAGA | 15 | a0002c0002t0001g0200 a0002c0002t0001g0213 a0002c0002t0001g0250 others(12): Show |
15 | HG00544.hp1 HG01192.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.731-1134_731-1131d others(6): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199233 | |||||||
chr4:4199233 | T | TGAGAGAG others(3): Show |
4 | a0002c0002t0001g0094 a0002c0003t0001g0110 a0002c0028t0001g0379 others(1): Show |
4 | HG02257.hp2 HG02602.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.731-1140_731-1131d others(12): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199233 | |||||||
chr4:4199233 | T | TGAGAGAG others(5): Show |
1 | a0008c0009t0001g0374 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.731-1142_731-1131d others(14): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199233 | |||||||
chr4:4199233 | TGA | T | 5 | a0002c0002t0001g0031 a0002c0002t0001g0056 a0002c0002t0001g0318 others(2): Show |
6 | HG02818.hp1 NA18959.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.731-1132_731-1131d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199233 | |||||||
chr4:4199233 | TGAGA | T | 3 | a0002c0002t0001g0055 a0005c0007t0001g0024 a0014c0024t0001g0357 |
4 | HG01257.hp2 HG01258.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.731-1134_731-1131d others(6): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199233 | |||||||
chr4:4199233 | TGAGAGA | T | 7 | a0001c0001t0001g0077 a0001c0001t0001g0081 a0001c0001t0001g0088 others(4): Show |
7 | HG00099.hp2 HG01928.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.731-1136_731-1131d others(8): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199233 | |||||||
chr4:4199233 | TGAGAGAG others(1): Show |
T | 60 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(57): Show |
76 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.731-1138_731-1131d others(10): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199233 | |||||||
chr4:4199235 | A | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(179): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.731-1132T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199235 | |||||||
chr4:4199237 | A | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(178): Show |
199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.731-1134T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199237 | |||||||
chr4:4199239 | A | T | 180 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(177): Show |
198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.731-1136T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199239 | |||||||
chr4:4199241 | A | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(166): Show |
187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.731-1138T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199241 | |||||||
chr4:4199243 | A | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
186 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.731-1140T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199243 | |||||||
chr4:4199245 | A | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(61): Show |
75 | HG00323.hp2 HG00544.hp2 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.731-1142T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199245 | |||||||
chr4:4199247 | A | T | 47 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0017 others(44): Show |
54 | HG00323.hp2 HG00544.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.731-1144T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199247 | |||||||
chr4:4199249 | A | T | 9 | a0001c0001t0001g0009 a0001c0001t0001g0192 a0001c0001t0001g0194 others(6): Show |
11 | HG02109.hp1 HG02559.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.731-1146T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199249 | |||||||
chr4:4199251 | A | T | 6 | a0001c0001t0001g0009 a0001c0001t0001g0192 a0001c0001t0001g0194 others(3): Show |
8 | HG02109.hp1 HG02559.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.731-1148T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199251 | |||||||
chr4:4199253 | A | T | 1 | a0001c0001t0001g0350 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.731-1150T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199253 | |||||||
chr4:4199295 | C | T | 3 | a0001c0001t0001g0281 a0009c0012t0001g0162 a0016c0016t0001g0034 |
3 | HG03927.hp1 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.731-1192G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199295 | |||||||
chr4:4199378 | C | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(178): Show |
199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.731-1275G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199378 | |||||||
chr4:4199389 | G | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(178): Show |
199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.731-1286C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199389 | |||||||
chr4:4199490 | T | G | 1 | a0002c0002t0001g0266 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.731-1387A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199490 | |||||||
chr4:4199552 | A | G | 16 | a0001c0001t0001g0231 a0003c0005t0001g0023 a0003c0005t0001g0113 others(13): Show |
17 | HG00323.hp2 HG00544.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.731-1449T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199552 | |||||||
chr4:4199560 | G | A | 1 | a0001c0004t0001g0049 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.731-1457C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199560 | |||||||
chr4:4199566 | C | T | 18 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(15): Show |
21 | HG00735.hp2 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.731-1463G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199566 | |||||||
chr4:4199570 | G | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(178): Show |
199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.731-1467C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199570 | |||||||
chr4:4199586 | C | A | 23 | a0001c0004t0001g0040 a0001c0004t0001g0041 a0001c0004t0001g0049 others(20): Show |
23 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.731-1483G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199586 | |||||||
chr4:4199615 | G | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(178): Show |
199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.731-1512C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199615 | |||||||
chr4:4199655 | C | T | 1 | a0012c0015t0001g0377 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.731-1552G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199655 | |||||||
chr4:4199656 | G | A | 23 | a0001c0004t0001g0040 a0001c0004t0001g0041 a0001c0004t0001g0049 others(20): Show |
23 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.731-1553C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199656 | |||||||
chr4:4199709 | G | A | 3 | a0001c0001t0001g0281 a0009c0012t0001g0162 a0016c0016t0001g0034 |
3 | HG03927.hp1 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.731-1606C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199709 | |||||||
chr4:4199838 | G | A | 206 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(203): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.731-1735C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199838 | |||||||
chr4:4199852 | T | C | 1 | a0002c0002t0001g0298 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.731-1749A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199852 | |||||||
chr4:4199980 | A | T | 1 | a0001c0001t0001g0280 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.731-1877T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199980 | |||||||
chr4:4200018 | C | T | 25 | a0002c0003t0001g0110 a0002c0028t0001g0379 a0004c0006t0001g0007 others(22): Show |
29 | HG00099.hp2 HG00733.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.731-1915G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200018 | |||||||
chr4:4200154 | C | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(81): Show |
94 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.731-2051G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200154 | |||||||
chr4:4200165 | T | A | 207 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(204): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.731-2062A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200165 | |||||||
chr4:4200197 | T | TA | 3 | a0001c0001t0001g0281 a0009c0012t0001g0162 a0016c0016t0001g0034 |
3 | HG03927.hp1 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.731-2095dupT | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200197 | |||||||
chr4:4200222 | G | A | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0326 |
3 | HG01517.hp1 HG02300.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.731-2119C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200222 | |||||||
chr4:4200233 | C | T | 79 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(76): Show |
102 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.731-2130G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200233 | |||||||
chr4:4200335 | C | G | 1 | a0001c0001t0001g0209 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.730+2113G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200335 | |||||||
chr4:4200401 | G | A | 2 | a0001c0001t0001g0207 a0001c0001t0001g0254 |
2 | HG02155.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.730+2047C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200401 | |||||||
chr4:4200425 | G | A | 1 | a0001c0001t0001g0020 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.730+2023C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200425 | |||||||
chr4:4200434 | C | T | 2 | a0002c0002t0001g0029 a0002c0002t0001g0292 |
3 | NA18943.hp1 NA18983.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.730+2014G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200434 | |||||||
chr4:4200473 | T | TA | 195 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(192): Show |
217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.730+1974dupT | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200473 | |||||||
chr4:4200473 | T | TAA | 13 | a0001c0001t0001g0039 a0001c0001t0001g0067 a0001c0001t0001g0193 others(10): Show |
13 | HG01891.hp1 HG02145.hp2 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.730+1973_730+1974d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200473 | |||||||
chr4:4200504 | A | G | 23 | a0001c0004t0001g0040 a0001c0004t0001g0041 a0001c0004t0001g0049 others(20): Show |
23 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.730+1944T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200504 | |||||||
chr4:4200590 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.730+1858C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200590 | |||||||
chr4:4200623 | A | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(168): Show |
187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.730+1825T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200623 | |||||||
chr4:4200662 | A | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(172): Show |
191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.730+1786T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200662 | |||||||
chr4:4200723 | C | CT | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(97): Show |
123 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(120): Show |
intron_variant | MODIFIER | c.730+1724dupA | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200723 | |||||||
chr4:4200723 | C | CTT | 26 | a0001c0001t0001g0194 a0002c0003t0001g0110 a0002c0028t0001g0379 others(23): Show |
30 | HG00099.hp2 HG00733.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.730+1723_730+1724d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200723 | |||||||
chr4:4200723 | C | CTTT | 54 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0019 others(51): Show |
59 | HG00323.hp2 HG00544.hp2 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.730+1722_730+1724d others(5): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200723 | |||||||
chr4:4200723 | C | CTTTT | 108 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(105): Show |
119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.730+1721_730+1724d others(6): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200723 | |||||||
chr4:4200723 | C | CTTTTT | 9 | a0001c0001t0001g0144 a0001c0001t0001g0151 a0001c0001t0001g0152 others(6): Show |
9 | HG00280.hp2 HG00642.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.730+1720_730+1724d others(7): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200723 | |||||||
chr4:4200810 | G | A | 16 | a0002c0003t0001g0037 a0002c0003t0001g0127 a0002c0003t0001g0128 others(13): Show |
16 | HG01109.hp1 HG01243.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.730+1638C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200810 | |||||||
chr4:4200810 | G | T | 1 | a0001c0001t0001g0006 | 3 | NA18944.hp1 NA18948.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.730+1638C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200810 | |||||||
chr4:4200873 | A | G | 206 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(203): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.730+1575T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200873 | |||||||
chr4:4200905 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.730+1543G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200905 | |||||||
chr4:4200906 | G | A | 2 | a0001c0001t0001g0208 a0001c0001t0001g0210 |
2 | HG03669.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.730+1542C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200906 | |||||||
chr4:4200966 | A | G | 18 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(15): Show |
21 | HG00735.hp2 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.730+1482T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200966 | |||||||
chr4:4200967 | G | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(203): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.730+1481C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200967 | |||||||
chr4:4201004 | C | G | 4 | a0001c0001t0001g0009 a0001c0001t0001g0192 a0001c0001t0001g0194 others(1): Show |
6 | HG02109.hp1 HG02630.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.730+1444G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201004 | |||||||
chr4:4201074 | G | A | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(87): Show |
111 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.730+1374C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201074 | |||||||
chr4:4201093 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(109): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.730+1355A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201093 | |||||||
chr4:4201097 | C | T | 10 | a0001c0001t0001g0193 a0007c0008t0001g0100 a0007c0008t0001g0101 others(7): Show |
10 | HG01891.hp1 HG02145.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.730+1351G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201097 | |||||||
chr4:4201294 | G | A | 4 | a0008c0009t0001g0358 a0009c0012t0001g0126 a0009c0012t0001g0138 others(1): Show |
4 | HG02109.hp2 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.730+1154C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201294 | |||||||
chr4:4201363 | G | A | 18 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(15): Show |
21 | HG00735.hp2 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.730+1085C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201363 | |||||||
chr4:4201435 | T | A | 3 | a0009c0012t0001g0126 a0009c0012t0001g0138 a0012c0015t0001g0376 |
3 | HG02109.hp2 HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.730+1013A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201435 | |||||||
chr4:4201459 | AAT | A | 6 | a0001c0001t0001g0009 a0001c0001t0001g0192 a0001c0001t0001g0194 others(3): Show |
8 | HG02109.hp1 HG02559.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.730+987_730+988del others(2): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201459 | |||||||
chr4:4201463 | T | TAC | 14 | a0004c0006t0001g0007 a0004c0006t0001g0059 a0004c0006t0001g0240 others(11): Show |
18 | HG00099.hp2 HG00733.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.730+984_730+985ins others(2): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201463 | |||||||
chr4:4201463 | T | TACACAC | 5 | a0002c0003t0001g0110 a0004c0006t0001g0294 a0008c0009t0001g0373 others(2): Show |
5 | HG01106.hp1 HG02257.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.730+984_730+985ins others(6): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201463 | |||||||
chr4:4201463 | T | TACACACA others(1): Show |
4 | a0004c0006t0001g0125 a0004c0006t0001g0182 a0008c0009t0001g0374 others(1): Show |
4 | HG01891.hp2 HG02809.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.730+984_730+985ins others(8): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201463 | |||||||
chr4:4201465 | T | C | 25 | a0002c0003t0001g0110 a0002c0028t0001g0379 a0004c0006t0001g0007 others(22): Show |
29 | HG00099.hp2 HG00733.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.730+983A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201465 | |||||||
chr4:4201465 | T | TACACACA others(5): Show |
2 | a0007c0008t0001g0124 a0007c0008t0001g0130 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.730+982_730+983ins others(12): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201465 | |||||||
chr4:4201467 | T | C | 30 | a0001c0001t0001g0193 a0001c0001t0001g0267 a0001c0001t0001g0269 others(27): Show |
34 | HG00099.hp2 HG00609.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.730+981A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201467 | |||||||
chr4:4201467 | T | TAC | 31 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0039 others(28): Show |
34 | HG00280.hp1 HG00621.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.730+980_730+981ins others(2): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201467 | |||||||
chr4:4201467 | T | TACAC | 4 | a0001c0001t0001g0268 a0002c0003t0001g0206 a0002c0003t0001g0215 others(1): Show |
4 | HG02970.hp2 NA18955.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.730+980_730+981ins others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201467 | |||||||
chr4:4201467 | T | TACACACA others(1): Show |
7 | a0001c0004t0001g0049 a0007c0008t0001g0101 a0007c0008t0001g0103 others(4): Show |
7 | HG01891.hp1 HG02145.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.730+980_730+981ins others(8): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201467 | |||||||
chr4:4201467 | T | TACACACA others(3): Show |
6 | a0001c0004t0001g0060 a0001c0004t0001g0061 a0001c0004t0001g0243 others(3): Show |
6 | HG01099.hp2 HG01123.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.730+980_730+981ins others(10): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201467 | |||||||
chr4:4201467 | T | TACACACA others(5): Show |
16 | a0001c0004t0001g0040 a0001c0004t0001g0041 a0001c0004t0001g0092 others(13): Show |
16 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.730+980_730+981ins others(12): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201467 | |||||||
chr4:4201469 | T | C | 99 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0039 others(96): Show |
106 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.730+979A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201469 | |||||||
chr4:4201469 | T | TAC | 41 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0018 others(38): Show |
49 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.730+978_730+979ins others(2): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201469 | |||||||
chr4:4201469 | T | TACAC | 3 | a0001c0001t0001g0263 a0001c0001t0001g0355 a0009c0012t0001g0126 |
3 | HG02109.hp2 HG02698.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.730+978_730+979ins others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201469 | |||||||
chr4:4201469 | T | TACACAC | 6 | a0001c0001t0001g0144 a0001c0001t0001g0151 a0001c0001t0001g0152 others(3): Show |
6 | HG00280.hp2 HG00642.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.730+978_730+979ins others(6): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201469 | |||||||
chr4:4201469 | T | TACACACA others(1): Show |
4 | a0001c0001t0001g0231 a0002c0003t0001g0097 a0003c0005t0001g0230 others(1): Show |
4 | HG02630.hp1 HG02683.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.730+978_730+979ins others(8): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201469 | |||||||
chr4:4201469 | T | TACACACA others(3): Show |
2 | a0002c0013t0001g0102 a0013c0027t0001g0378 |
2 | HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.730+978_730+979ins others(10): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201469 | |||||||
chr4:4201469 | T | TACACACA others(5): Show |
5 | a0002c0003t0001g0098 a0002c0013t0001g0099 a0002c0013t0001g0224 others(2): Show |
5 | HG01167.hp1 HG02258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.730+978_730+979ins others(12): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201469 | |||||||
chr4:4201469 | T | TACACACA others(7): Show |
1 | a0002c0013t0001g0123 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.730+978_730+979ins others(14): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201469 | |||||||
chr4:4201471 | T | C | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(235): Show |
277 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.730+977A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201471 | |||||||
chr4:4201471 | T | TAC | 21 | a0001c0001t0001g0145 a0001c0001t0001g0161 a0001c0001t0001g0241 others(18): Show |
21 | HG00140.hp2 HG01070.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.730+975_730+976dup others(2): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201471 | |||||||
chr4:4201471 | T | TACACACA others(1): Show |
14 | a0001c0001t0001g0021 a0003c0005t0001g0023 a0003c0005t0001g0113 others(11): Show |
16 | HG00323.hp2 HG00544.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.730+969_730+976dup others(8): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201471 | |||||||
chr4:4201471 | T | TACACACA others(3): Show |
2 | a0003c0005t0001g0236 a0008c0009t0001g0362 |
2 | HG01978.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.730+967_730+976dup others(10): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201471 | |||||||
chr4:4201471 | T | TATATATA others(3): Show |
1 | a0009c0012t0001g0162 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.730+976_730+977ins others(10): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201471 | |||||||
chr4:4201473 | C | T | 1 | a0002c0002t0001g0094 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.730+975G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201473 | |||||||
chr4:4201501 | T | C | 9 | a0002c0003t0001g0097 a0002c0003t0001g0098 a0002c0013t0001g0099 others(6): Show |
9 | HG01167.hp1 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.730+947A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201501 | |||||||
chr4:4201515 | T | A | 2 | a0008c0009t0001g0358 a0012c0015t0001g0376 |
2 | HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.730+933A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201515 | |||||||
chr4:4201597 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.730+851G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201597 | |||||||
chr4:4201690 | A | G | 1 | a0002c0002t0001g0342 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.730+758T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201690 | |||||||
chr4:4201893 | A | C | 27 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0019 others(24): Show |
31 | HG00735.hp2 HG01884.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.730+555T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201893 | |||||||
chr4:4201951 | G | A | 9 | a0002c0003t0001g0097 a0002c0003t0001g0098 a0002c0013t0001g0099 others(6): Show |
9 | HG01167.hp1 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.730+497C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201951 | |||||||
chr4:4202013 | A | G | 1 | a0002c0002t0001g0216 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.730+435T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4202013 | |||||||
chr4:4202163 | T | C | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(294): Show |
340 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.730+285A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4202163 | |||||||
chr4:4202207 | C | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0073 a0001c0001t0001g0285 others(1): Show |
5 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.730+241G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4202207 | |||||||
chr4:4202248 | A | T | 1 | a0009c0018t0001g0036 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.730+200T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4202248 | |||||||
chr4:4202262 | A | T | 1 | a0001c0001t0001g0257 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.730+186T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4202262 | |||||||
chr4:4202275 | G | A | 1 | a0009c0018t0001g0036 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.730+173C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4202275 | |||||||
chr4:4202308 | CG | C | 6 | a0001c0001t0001g0009 a0001c0001t0001g0192 a0001c0001t0001g0194 others(3): Show |
8 | HG02109.hp1 HG02559.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.730+139delC | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4202308 | |||||||
chr4:4202309 | G | A | 8 | a0007c0008t0001g0100 a0007c0008t0001g0101 a0007c0008t0001g0103 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.730+139C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4202309 | |||||||
chr4:4202343 | G | A | 9 | a0002c0003t0001g0097 a0002c0003t0001g0098 a0002c0013t0001g0099 others(6): Show |
9 | HG01167.hp1 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.730+105C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4202343 | |||||||
chr4:4202396 | T | C | 1 | a0009c0018t0001g0036 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.730+52A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4202396 | |||||||
chr4:4202622 | C | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0164 |
4 | NA18939.hp1 NA18970.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.600-44G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4202622 | |||||||
chr4:4202649 | G | A | 1 | a0009c0018t0001g0036 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.600-71C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4202649 | |||||||
chr4:4202852 | G | A | 1 | a0003c0005t0001g0230 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.600-274C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4202852 | |||||||
chr4:4202976 | A | C | 3 | a0001c0001t0001g0281 a0009c0012t0001g0162 a0016c0016t0001g0034 |
3 | HG03927.hp1 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.600-398T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4202976 | |||||||
chr4:4202986 | T | C | 1 | a0001c0001t0001g0058 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.600-408A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4202986 | |||||||
chr4:4203114 | C | T | 1 | a0002c0002t0001g0091 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.600-536G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4203114 | |||||||
chr4:4203379 | G | A | 21 | a0002c0003t0001g0110 a0002c0028t0001g0379 a0004c0006t0001g0007 others(18): Show |
25 | HG00099.hp2 HG00733.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.600-801C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4203379 | |||||||
chr4:4203403 | A | G | 2 | a0008c0009t0001g0373 a0008c0009t0001g0374 |
2 | HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.600-825T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4203403 | |||||||
chr4:4203452 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.600-874G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4203452 | |||||||
chr4:4203524 | G | C | 1 | a0002c0002t0001g0091 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.600-946C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4203524 | |||||||
chr4:4203533 | T | C | 1 | a0002c0003t0001g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.600-955A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4203533 | |||||||
chr4:4203534 | A | G | 1 | a0008c0009t0001g0359 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.600-956T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4203534 | |||||||
chr4:4203626 | C | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(174): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.600-1048G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4203626 | |||||||
chr4:4203707 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.600-1129C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4203707 | |||||||
chr4:4203722 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.600-1144G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4203722 | |||||||
chr4:4203838 | C | A | 8 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0070 others(5): Show |
9 | HG02055.hp2 HG02145.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.600-1260G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4203838 | |||||||
chr4:4204060 | C | T | 1 | a0008c0009t0001g0362 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.600-1482G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204060 | |||||||
chr4:4204061 | G | A | 1 | a0001c0001t0001g0335 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.600-1483C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204061 | |||||||
chr4:4204079 | G | A | 2 | a0008c0009t0001g0359 a0008c0009t0001g0360 |
2 | HG02559.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.600-1501C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204079 | |||||||
chr4:4204218 | G | C | 1 | a0001c0001t0001g0241 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.600-1640C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204218 | |||||||
chr4:4204238 | G | A | 4 | a0008c0009t0001g0358 a0009c0012t0001g0126 a0009c0012t0001g0138 others(1): Show |
4 | HG02109.hp2 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.600-1660C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204238 | |||||||
chr4:4204277 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.600-1699A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204277 | |||||||
chr4:4204341 | A | G | 23 | a0001c0004t0001g0040 a0001c0004t0001g0041 a0001c0004t0001g0049 others(20): Show |
23 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.599+1731T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204341 | |||||||
chr4:4204533 | G | A | 1 | a0003c0005t0001g0237 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.599+1539C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204533 | |||||||
chr4:4204559 | T | C | 3 | a0001c0001t0001g0154 a0001c0001t0001g0176 a0001c0001t0001g0177 |
3 | HG02056.hp2 NA18966.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.599+1513A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204559 | |||||||
chr4:4204599 | G | A | 6 | a0001c0001t0001g0193 a0007c0008t0001g0124 a0007c0008t0001g0129 others(3): Show |
6 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.599+1473C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204599 | |||||||
chr4:4204712 | C | CTG | 17 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0002c0002t0001g0106 others(14): Show |
21 | HG00544.hp1 HG00609.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.599+1358_599+1359d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204712 | |||||||
chr4:4204712 | CTG | C | 49 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0015 others(46): Show |
54 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.599+1358_599+1359d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204712 | |||||||
chr4:4204712 | CTGTG | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(22): Show |
36 | HG00621.hp2 HG01993.hp1 HG02015.hp2 others(33): Show |
intron_variant | MODIFIER | c.599+1356_599+1359d others(6): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204712 | |||||||
chr4:4204712 | CTGTGTG | C | 3 | a0001c0001t0001g0261 a0001c0001t0001g0338 a0001c0001t0001g0339 |
3 | HG01928.hp1 HG02148.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.599+1354_599+1359d others(8): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204712 | |||||||
chr4:4204712 | CTGTGTGT others(3): Show |
C | 3 | a0002c0002t0001g0291 a0002c0002t0001g0340 a0002c0002t0001g0341 |
3 | HG01175.hp1 HG02258.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.599+1350_599+1359d others(12): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204712 | |||||||
chr4:4204712 | CTGTGTGT others(9): Show |
C | 9 | a0001c0001t0001g0001 a0001c0001t0001g0107 a0001c0001t0001g0163 others(6): Show |
13 | HG00438.hp1 HG01496.hp1 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.599+1344_599+1359d others(18): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204712 | |||||||
chr4:4204712 | CTGTGTGT others(11): Show |
C | 197 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(194): Show |
215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.599+1342_599+1359d others(20): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204712 | |||||||
chr4:4204749 | T | TGTGC | 2 | a0002c0002t0001g0028 a0002c0002t0001g0319 |
3 | NA18954.hp2 NA19011.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.599+1322_599+1323i others(6): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204749 | |||||||
chr4:4204751 | C | T | 1 | a0002c0002t0001g0091 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.599+1321G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204751 | |||||||
chr4:4204895 | G | A | 1 | a0008c0009t0001g0359 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.599+1177C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204895 | |||||||
chr4:4205134 | T | G | 3 | a0008c0009t0001g0358 a0009c0012t0001g0126 a0009c0012t0001g0138 |
3 | HG02109.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.599+938A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205134 | |||||||
chr4:4205137 | C | T | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0334 |
3 | NA18971.hp2 NA18985.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.599+935G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205137 | |||||||
chr4:4205226 | G | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(144): Show |
162 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.599+846C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205226 | |||||||
chr4:4205309 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.599+763G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205309 | |||||||
chr4:4205370 | C | T | 56 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(53): Show |
65 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.599+702G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205370 | |||||||
chr4:4205393 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0204 a0001c0001t0001g0209 |
6 | HG02071.hp2 HG02602.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.599+679C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205393 | |||||||
chr4:4205395 | T | C | 3 | a0001c0001t0001g0281 a0009c0012t0001g0162 a0016c0016t0001g0034 |
3 | HG03927.hp1 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.599+677A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205395 | |||||||
chr4:4205416 | G | C | 1 | a0009c0012t0001g0162 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.599+656C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205416 | |||||||
chr4:4205436 | T | C | 9 | a0001c0001t0001g0144 a0001c0001t0001g0148 a0001c0001t0001g0149 others(6): Show |
9 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.599+636A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205436 | |||||||
chr4:4205488 | C | G | 23 | a0001c0004t0001g0040 a0001c0004t0001g0041 a0001c0004t0001g0049 others(20): Show |
23 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.599+584G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205488 | |||||||
chr4:4205592 | G | T | 201 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(198): Show |
223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.599+480C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205592 | |||||||
chr4:4205639 | T | G | 296 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(293): Show |
339 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.599+433A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205639 | |||||||
chr4:4205660 | G | A | 3 | a0008c0009t0001g0358 a0009c0012t0001g0126 a0009c0012t0001g0138 |
3 | HG02109.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.599+412C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205660 | |||||||
chr4:4205710 | G | C | 1 | a0001c0001t0001g0154 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.599+362C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205710 | |||||||
chr4:4205766 | A | G | 2 | a0002c0003t0001g0025 a0002c0003t0001g0255 |
3 | HG00673.hp1 HG02040.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.599+306T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205766 | |||||||
chr4:4205800 | G | A | 1 | a0002c0003t0001g0037 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.599+272C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205800 | |||||||
chr4:4205888 | C | G | 1 | a0008c0009t0001g0358 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.599+184G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205888 | |||||||
chr4:4205963 | G | A | 15 | a0001c0001t0001g0021 a0001c0001t0001g0231 a0003c0005t0001g0023 others(12): Show |
17 | HG00544.hp2 HG00738.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.599+109C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205963 | |||||||
chr4:4206793 | T | C | 14 | a0004c0006t0001g0007 a0004c0006t0001g0038 a0004c0006t0001g0059 others(11): Show |
18 | HG00099.hp2 HG00733.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.541-663A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4206793 | |||||||
chr4:4206851 | G | A | 7 | a0002c0003t0001g0110 a0002c0028t0001g0379 a0008c0009t0001g0362 others(4): Show |
7 | HG01891.hp2 HG02257.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.541-721C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4206851 | |||||||
chr4:4206897 | C | T | 3 | a0001c0001t0001g0281 a0009c0012t0001g0162 a0016c0016t0001g0034 |
3 | HG03927.hp1 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.541-767G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4206897 | |||||||
chr4:4207015 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.541-885C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4207015 | |||||||
chr4:4207074 | G | C | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(286): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.541-944C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4207074 | |||||||
chr4:4207134 | T | C | 183 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(180): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.541-1004A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4207134 | |||||||
chr4:4207204 | GCAGT | G | 203 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(200): Show |
225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.541-1078_541-1075d others(6): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4207204 | |||||||
chr4:4207386 | C | A | 203 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(200): Show |
225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.541-1256G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4207386 | |||||||
chr4:4207573 | G | T | 1 | a0001c0001t0001g0246 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.541-1443C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4207573 | |||||||
chr4:4207595 | GTA | G | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(81): Show |
97 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.541-1467_541-1466d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4207595 | |||||||
chr4:4207595 | GTATA | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(206): Show |
234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.541-1469_541-1466d others(6): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4207595 | |||||||
chr4:4207630 | G | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(205): Show |
233 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.541-1500C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4207630 | |||||||
chr4:4207687 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.541-1557C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4207687 | |||||||
chr4:4207810 | A | G | 1 | a0002c0003t0001g0037 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.541-1680T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4207810 | |||||||
chr4:4207823 | G | C | 1 | a0002c0002t0001g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.541-1693C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4207823 | |||||||
chr4:4207853 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.541-1723A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4207853 | |||||||
chr4:4207864 | G | C | 2 | a0001c0001t0001g0193 a0008c0009t0001g0375 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.541-1734C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4207864 | |||||||
chr4:4207888 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.541-1758C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4207888 | |||||||
chr4:4208069 | G | A | 207 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(204): Show |
232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.541-1939C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4208069 | |||||||
chr4:4208108 | C | T | 206 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(203): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.541-1978G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4208108 | |||||||
chr4:4208340 | C | T | 3 | a0001c0001t0001g0144 a0001c0001t0001g0156 a0001c0001t0001g0157 |
3 | HG01106.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.541-2210G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4208340 | |||||||
chr4:4208373 | T | A | 1 | a0011c0014t0001g0361 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.541-2243A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4208373 | |||||||
chr4:4208532 | C | T | 14 | a0004c0006t0001g0007 a0004c0006t0001g0038 a0004c0006t0001g0059 others(11): Show |
18 | HG00099.hp2 HG00733.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.541-2402G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4208532 | |||||||
chr4:4208733 | G | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(165): Show |
189 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.541-2603C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4208733 | |||||||
chr4:4208736 | C | T | 1 | a0002c0002t0001g0297 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.541-2606G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4208736 | |||||||
chr4:4208737 | G | A | 1 | a0012c0015t0001g0376 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.541-2607C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4208737 | |||||||
chr4:4208738 | C | T | 1 | a0014c0024t0001g0357 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.541-2608G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4208738 | |||||||
chr4:4208762 | G | A | 22 | a0001c0004t0001g0040 a0001c0004t0001g0041 a0001c0004t0001g0049 others(19): Show |
22 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.541-2632C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4208762 | |||||||
chr4:4208780 | TA | T | 168 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(165): Show |
189 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.541-2651delT | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4208780 | |||||||
chr4:4208780 | TAAA | T | 25 | a0001c0001t0001g0281 a0001c0004t0001g0040 a0001c0004t0001g0041 others(22): Show |
25 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.541-2653_541-2651d others(5): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4208780 | |||||||
chr4:4208915 | G | A | 1 | a0002c0002t0001g0317 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.541-2785C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4208915 | |||||||
chr4:4209051 | T | C | 1 | a0013c0027t0001g0378 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.541-2921A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4209051 | |||||||
chr4:4209170 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG00639.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.541-3040C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4209170 | |||||||
chr4:4209331 | C | CAT | 3 | a0008c0009t0001g0358 a0009c0012t0001g0126 a0009c0012t0001g0138 |
3 | HG02109.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.541-3203_541-3202d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4209331 | |||||||
chr4:4209398 | G | C | 2 | a0008c0009t0001g0373 a0008c0009t0001g0374 |
2 | HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.541-3268C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4209398 | |||||||
chr4:4209408 | G | T | 15 | a0002c0002t0001g0028 a0002c0002t0001g0031 a0002c0002t0001g0055 others(12): Show |
17 | HG00597.hp2 HG01346.hp1 HG02148.hp1 others(14): Show |
intron_variant | MODIFIER | c.541-3278C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4209408 | |||||||
chr4:4209615 | C | G | 3 | a0002c0002t0001g0291 a0002c0002t0001g0340 a0002c0002t0001g0341 |
3 | HG01175.hp1 HG02258.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.540+3253G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4209615 | |||||||
chr4:4209722 | G | A | 3 | a0001c0001t0001g0281 a0009c0012t0001g0162 a0016c0016t0001g0034 |
3 | HG03927.hp1 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.540+3146C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4209722 | |||||||
chr4:4209730 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.540+3138C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4209730 | |||||||
chr4:4209768 | T | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(184): Show |
207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.540+3100A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4209768 | |||||||
chr4:4209782 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.540+3086A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4209782 | |||||||
chr4:4209838 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.540+3030C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4209838 | |||||||
chr4:4209963 | T | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(184): Show |
207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.540+2905A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4209963 | |||||||
chr4:4210069 | G | A | 2 | a0001c0001t0001g0193 a0008c0009t0001g0375 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.540+2799C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210069 | |||||||
chr4:4210110 | C | T | 3 | a0008c0009t0001g0358 a0009c0012t0001g0126 a0009c0012t0001g0138 |
3 | HG02109.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.540+2758G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210110 | |||||||
chr4:4210114 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.540+2754T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210114 | |||||||
chr4:4210162 | C | T | 1 | a0005c0007t0001g0351 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.540+2706G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210162 | |||||||
chr4:4210169 | C | T | 2 | a0009c0012t0001g0126 a0009c0012t0001g0138 |
2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.540+2699G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210169 | |||||||
chr4:4210199 | A | AAATG | 7 | a0002c0003t0001g0110 a0002c0028t0001g0379 a0008c0009t0001g0362 others(4): Show |
7 | HG01891.hp2 HG02257.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.540+2665_540+2668d others(6): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210199 | |||||||
chr4:4210354 | C | A | 3 | a0001c0001t0001g0281 a0009c0012t0001g0162 a0016c0016t0001g0034 |
3 | HG03927.hp1 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.540+2514G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210354 | |||||||
chr4:4210396 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.540+2472G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210396 | |||||||
chr4:4210397 | G | C | 1 | a0001c0001t0001g0210 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.540+2471C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210397 | |||||||
chr4:4210422 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.540+2446T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210422 | |||||||
chr4:4210483 | G | A | 14 | a0001c0001t0001g0009 a0001c0001t0001g0185 a0001c0001t0001g0186 others(11): Show |
16 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.540+2385C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210483 | |||||||
chr4:4210558 | C | T | 3 | a0007c0008t0001g0124 a0007c0008t0001g0129 a0007c0008t0001g0130 |
3 | HG01891.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.540+2310G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210558 | |||||||
chr4:4210581 | A | T | 1 | a0002c0002t0001g0318 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2287T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210581 | |||||||
chr4:4210586 | T | A | 1 | a0002c0002t0001g0318 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2282A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210586 | |||||||
chr4:4210588 | T | A | 1 | a0002c0002t0001g0318 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2280A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210588 | |||||||
chr4:4210589 | G | C | 1 | a0002c0002t0001g0318 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2279C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210589 | |||||||
chr4:4210590 | G | C | 1 | a0002c0002t0001g0318 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2278C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210590 | |||||||
chr4:4210591 | G | A | 1 | a0002c0002t0001g0318 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2277C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210591 | |||||||
chr4:4210592 | A | C | 1 | a0002c0002t0001g0318 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2276T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210592 | |||||||
chr4:4210593 | G | T | 1 | a0002c0002t0001g0318 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2275C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210593 | |||||||
chr4:4210594 | G | T | 1 | a0002c0002t0001g0318 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2274C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210594 | |||||||
chr4:4210596 | C | T | 1 | a0002c0002t0001g0318 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2272G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210596 | |||||||
chr4:4210597 | G | A | 1 | a0002c0002t0001g0318 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2271C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210597 | |||||||
chr4:4210603 | G | A | 1 | a0002c0002t0001g0318 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2265C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210603 | |||||||
chr4:4210604 | G | T | 1 | a0002c0002t0001g0318 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2264C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210604 | |||||||
chr4:4210606 | G | C | 1 | a0002c0002t0001g0318 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2262C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210606 | |||||||
chr4:4210607 | G | T | 1 | a0002c0002t0001g0318 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2261C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210607 | |||||||
chr4:4210608 | A | C | 1 | a0002c0002t0001g0318 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2260T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210608 | |||||||
chr4:4210609 | T | C | 1 | a0002c0002t0001g0318 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2259A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210609 | |||||||
chr4:4210610 | T | A | 1 | a0002c0002t0001g0318 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2258A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210610 | |||||||
chr4:4210611 | G | T | 1 | a0002c0002t0001g0318 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2257C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210611 | |||||||
chr4:4210613 | C | T | 1 | a0002c0002t0001g0318 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2255G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210613 | |||||||
chr4:4210615 | G | C | 1 | a0002c0002t0001g0318 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2253C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210615 | |||||||
chr4:4210616 | A | T | 1 | a0002c0002t0001g0318 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2252T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210616 | |||||||
chr4:4210617 | G | A | 1 | a0002c0002t0001g0318 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2251C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210617 | |||||||
chr4:4210623 | G | A | 1 | a0002c0002t0001g0318 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2245C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210623 | |||||||
chr4:4210625 | G | A | 1 | a0002c0002t0001g0318 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2243C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210625 | |||||||
chr4:4210626 | T | A | 1 | a0002c0002t0001g0318 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2242A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210626 | |||||||
chr4:4210627 | T | A | 1 | a0002c0002t0001g0318 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2241A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210627 | |||||||
chr4:4210629 | G | T | 1 | a0002c0002t0001g0318 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2239C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210629 | |||||||
chr4:4210631 | G | A | 1 | a0002c0002t0001g0318 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2237C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210631 | |||||||
chr4:4210633 | C | G | 3 | a0001c0001t0001g0281 a0009c0012t0001g0162 a0016c0016t0001g0034 |
3 | HG03927.hp1 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.540+2235G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210633 | |||||||
chr4:4210635 | A | C | 1 | a0002c0002t0001g0318 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2233T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210635 | |||||||
chr4:4210636 | G | C | 1 | a0002c0002t0001g0318 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2232C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210636 | |||||||
chr4:4210787 | C | T | 7 | a0002c0003t0001g0110 a0002c0028t0001g0379 a0008c0009t0001g0362 others(4): Show |
7 | HG01891.hp2 HG02257.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.540+2081G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210787 | |||||||
chr4:4210869 | G | C | 3 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0354 |
3 | HG02451.hp2 HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.540+1999C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210869 | |||||||
chr4:4210911 | C | T | 1 | a0003c0005t0001g0230 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.540+1957G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210911 | |||||||
chr4:4210997 | C | T | 3 | a0008c0009t0001g0358 a0009c0012t0001g0126 a0009c0012t0001g0138 |
3 | HG02109.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.540+1871G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210997 | |||||||
chr4:4211066 | T | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(186): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.540+1802A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211066 | |||||||
chr4:4211140 | T | C | 6 | a0002c0028t0001g0379 a0008c0009t0001g0362 a0008c0009t0001g0373 others(3): Show |
6 | HG01891.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+1728A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211140 | |||||||
chr4:4211204 | C | A | 13 | a0001c0001t0001g0144 a0001c0001t0001g0148 a0001c0001t0001g0149 others(10): Show |
13 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.540+1664G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211204 | |||||||
chr4:4211207 | G | A | 19 | a0001c0004t0001g0049 a0001c0004t0001g0060 a0001c0004t0001g0061 others(16): Show |
19 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.540+1661C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211207 | |||||||
chr4:4211292 | C | G | 7 | a0002c0003t0001g0110 a0002c0028t0001g0379 a0008c0009t0001g0362 others(4): Show |
7 | HG01891.hp2 HG02257.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.540+1576G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211292 | |||||||
chr4:4211348 | C | T | 5 | a0003c0005t0001g0113 a0003c0005t0001g0140 a0003c0005t0001g0166 others(2): Show |
5 | HG00544.hp2 NA18952.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.540+1520G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211348 | |||||||
chr4:4211361 | G | A | 20 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0019 others(17): Show |
24 | HG00735.hp2 HG01884.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.540+1507C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211361 | |||||||
chr4:4211385 | C | T | 2 | a0001c0004t0001g0191 a0008c0026t0001g0371 |
2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.540+1483G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211385 | |||||||
chr4:4211438 | ACTT | A | 19 | a0001c0004t0001g0049 a0001c0004t0001g0060 a0001c0004t0001g0061 others(16): Show |
19 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.540+1427_540+1429d others(5): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211438 | |||||||
chr4:4211477 | T | C | 1 | a0009c0018t0001g0036 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.540+1391A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211477 | |||||||
chr4:4211496 | T | C | 13 | a0001c0001t0001g0144 a0001c0001t0001g0148 a0001c0001t0001g0149 others(10): Show |
13 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.540+1372A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211496 | |||||||
chr4:4211583 | C | T | 15 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(12): Show |
18 | HG00735.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.540+1285G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211583 | |||||||
chr4:4211612 | A | G | 186 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(183): Show |
206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.540+1256T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211612 | |||||||
chr4:4211647 | C | T | 3 | a0001c0001t0001g0281 a0009c0012t0001g0162 a0016c0016t0001g0034 |
3 | HG03927.hp1 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.540+1221G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211647 | |||||||
chr4:4211666 | G | C | 14 | a0001c0001t0001g0009 a0001c0001t0001g0185 a0001c0001t0001g0186 others(11): Show |
16 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.540+1202C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211666 | |||||||
chr4:4211767 | T | G | 3 | a0001c0001t0001g0281 a0009c0012t0001g0162 a0016c0016t0001g0034 |
3 | HG03927.hp1 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.540+1101A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211767 | |||||||
chr4:4211881 | A | T | 1 | a0002c0002t0001g0314 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.540+987T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211881 | |||||||
chr4:4211938 | A | T | 2 | a0002c0002t0001g0304 a0002c0002t0001g0305 |
2 | HG02056.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.540+930T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211938 | |||||||
chr4:4212005 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.540+863T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4212005 | |||||||
chr4:4212118 | T | C | 3 | a0008c0009t0001g0358 a0009c0012t0001g0126 a0009c0012t0001g0138 |
3 | HG02109.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.540+750A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4212118 | |||||||
chr4:4212138 | T | C | 3 | a0002c0002t0001g0291 a0002c0002t0001g0340 a0002c0002t0001g0341 |
3 | HG01175.hp1 HG02258.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.540+730A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4212138 | |||||||
chr4:4212226 | T | C | 3 | a0008c0009t0001g0362 a0011c0014t0001g0361 a0011c0014t0001g0363 |
3 | HG01891.hp2 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.540+642A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4212226 | |||||||
chr4:4212307 | G | T | 7 | a0002c0003t0001g0110 a0002c0028t0001g0379 a0008c0009t0001g0362 others(4): Show |
7 | HG01891.hp2 HG02257.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.540+561C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4212307 | |||||||
chr4:4212381 | C | T | 3 | a0001c0001t0001g0144 a0001c0001t0001g0156 a0001c0001t0001g0157 |
3 | HG01106.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.540+487G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4212381 | |||||||
chr4:4212448 | A | G | 3 | a0001c0001t0001g0281 a0009c0012t0001g0162 a0016c0016t0001g0034 |
3 | HG03927.hp1 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.540+420T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4212448 | |||||||
chr4:4212557 | T | C | 3 | a0001c0001t0001g0281 a0009c0012t0001g0162 a0016c0016t0001g0034 |
3 | HG03927.hp1 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.540+311A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4212557 | |||||||
chr4:4212822 | A | G | 3 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0218 |
3 | HG02129.hp2 NA18968.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.540+46T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4212822 | |||||||
chr4:4213043 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.404-39A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213043 | |||||||
chr4:4213208 | G | A | 3 | a0001c0001t0001g0017 a0001c0004t0001g0191 a0008c0026t0001g0371 |
4 | HG02280.hp2 HG02622.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-204C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213208 | |||||||
chr4:4213329 | G | T | 1 | a0001c0001t0001g0085 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.404-325C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213329 | |||||||
chr4:4213445 | G | A | 185 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(182): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.404-441C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213445 | |||||||
chr4:4213450 | G | A | 1 | a0004c0006t0001g0059 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.404-446C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213450 | |||||||
chr4:4213453 | A | G | 2 | a0001c0004t0001g0191 a0008c0026t0001g0371 |
2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.404-449T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213453 | |||||||
chr4:4213460 | A | G | 45 | a0001c0001t0001g0009 a0001c0001t0001g0131 a0001c0001t0001g0164 others(42): Show |
47 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.404-456T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213460 | |||||||
chr4:4213580 | T | C | 12 | a0002c0003t0001g0097 a0002c0003t0001g0098 a0002c0013t0001g0099 others(9): Show |
12 | HG01167.hp1 HG02145.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.404-576A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213580 | |||||||
chr4:4213597 | C | T | 2 | a0009c0012t0001g0126 a0009c0012t0001g0138 |
2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.404-593G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213597 | |||||||
chr4:4213601 | T | A | 1 | a0002c0013t0001g0224 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.404-597A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213601 | |||||||
chr4:4213647 | C | T | 1 | a0002c0002t0001g0313 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.404-643G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213647 | |||||||
chr4:4213730 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.404-726G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213730 | |||||||
chr4:4213731 | G | A | 1 | a0002c0002t0001g0298 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.404-727C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213731 | |||||||
chr4:4213816 | A | T | 2 | a0009c0012t0001g0162 a0016c0016t0001g0034 |
2 | HG03927.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.404-812T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213816 | |||||||
chr4:4213868 | T | C | 32 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(29): Show |
39 | HG01109.hp1 HG01243.hp1 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.404-864A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213868 | |||||||
chr4:4213963 | G | T | 1 | a0001c0004t0001g0229 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.404-959C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213963 | |||||||
chr4:4214006 | CT | C | 6 | a0001c0001t0001g0043 a0001c0001t0001g0072 a0001c0001t0001g0080 others(3): Show |
6 | HG00438.hp2 HG02074.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.404-1003delA | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214006 | |||||||
chr4:4214041 | G | A | 1 | a0002c0003t0001g0187 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.404-1037C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214041 | |||||||
chr4:4214329 | T | C | 2 | a0001c0004t0001g0191 a0008c0026t0001g0371 |
2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.404-1325A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214329 | |||||||
chr4:4214417 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.404-1413G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214417 | |||||||
chr4:4214461 | A | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0259 |
4 | NA18940.hp2 NA18945.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-1457T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214461 | |||||||
chr4:4214490 | A | C | 1 | a0001c0001t0001g0070 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.404-1486T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214490 | |||||||
chr4:4214511 | T | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(122): Show |
139 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.404-1507A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214511 | |||||||
chr4:4214531 | T | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(122): Show |
139 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.404-1527A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214531 | |||||||
chr4:4214769 | A | C | 15 | a0001c0001t0001g0009 a0001c0001t0001g0131 a0001c0001t0001g0185 others(12): Show |
17 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.404-1765T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214769 | |||||||
chr4:4214800 | A | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(175): Show |
198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.404-1796T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214800 | |||||||
chr4:4214834 | G | C | 20 | a0002c0002t0001g0028 a0002c0002t0001g0031 a0002c0002t0001g0055 others(17): Show |
27 | HG00609.hp1 HG00673.hp1 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.404-1830C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214834 | |||||||
chr4:4214851 | C | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(122): Show |
139 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.404-1847G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214851 | |||||||
chr4:4214871 | G | C | 1 | a0002c0013t0001g0224 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.404-1867C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214871 | |||||||
chr4:4214953 | G | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(183): Show |
206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.404-1949C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214953 | |||||||
chr4:4214966 | CA | C | 4 | a0002c0003t0001g0110 a0002c0028t0001g0379 a0008c0009t0001g0373 others(1): Show |
4 | HG02257.hp2 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-1963delT | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214966 | |||||||
chr4:4214969 | A | G | 19 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0019 others(16): Show |
23 | HG00735.hp2 HG01884.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.404-1965T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214969 | |||||||
chr4:4214972 | T | TAAAAATA others(344): Show |
1 | a0002c0002t0001g0344 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.404-1969_404-1968i others(353): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214972 | |||||||
chr4:4214991 | T | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(80): Show |
93 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.404-1987A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214991 | |||||||
chr4:4215068 | G | A | 1 | a0017c0017t0001g0035 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.404-2064C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215068 | |||||||
chr4:4215224 | G | C | 24 | a0001c0001t0001g0193 a0001c0004t0001g0049 a0001c0004t0001g0060 others(21): Show |
24 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.404-2220C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215224 | |||||||
chr4:4215235 | C | A | 2 | a0002c0002t0001g0312 a0002c0002t0001g0323 |
2 | HG01952.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.404-2231G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215235 | |||||||
chr4:4215263 | C | A | 7 | a0002c0003t0001g0110 a0002c0028t0001g0379 a0008c0009t0001g0358 others(4): Show |
7 | HG02109.hp2 HG02257.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.404-2259G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215263 | |||||||
chr4:4215385 | G | A | 3 | a0002c0002t0001g0091 a0002c0002t0001g0219 a0002c0002t0001g0220 |
3 | NA18966.hp2 NA19005.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.404-2381C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215385 | |||||||
chr4:4215427 | T | C | 60 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0017 others(57): Show |
66 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.404-2423A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215427 | |||||||
chr4:4215433 | G | A | 13 | a0001c0001t0001g0144 a0001c0001t0001g0148 a0001c0001t0001g0149 others(10): Show |
13 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.404-2429C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215433 | |||||||
chr4:4215459 | C | T | 1 | a0002c0002t0001g0304 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.404-2455G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215459 | |||||||
chr4:4215468 | C | G | 2 | a0001c0004t0001g0191 a0008c0026t0001g0371 |
2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.404-2464G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215468 | |||||||
chr4:4215493 | C | A | 1 | a0002c0002t0001g0298 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.404-2489G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215493 | |||||||
chr4:4215521 | T | C | 61 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0017 others(58): Show |
67 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.404-2517A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215521 | |||||||
chr4:4215550 | C | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(122): Show |
139 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.404-2546G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215550 | |||||||
chr4:4215589 | A | G | 61 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0017 others(58): Show |
67 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.404-2585T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215589 | |||||||
chr4:4215686 | T | TA | 61 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0017 others(58): Show |
67 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.404-2683dupT | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215686 | |||||||
chr4:4215724 | A | G | 61 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0017 others(58): Show |
67 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.404-2720T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215724 | |||||||
chr4:4215987 | T | G | 1 | a0008c0009t0001g0362 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.404-2983A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215987 | |||||||
chr4:4216054 | T | C | 122 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(119): Show |
140 | HG00140.hp1 HG00438.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.404-3050A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216054 | |||||||
chr4:4216078 | C | A | 80 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0012 others(77): Show |
96 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.404-3074G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216078 | |||||||
chr4:4216084 | T | A | 15 | a0001c0001t0001g0009 a0001c0001t0001g0131 a0001c0001t0001g0185 others(12): Show |
17 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.404-3080A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216084 | |||||||
chr4:4216091 | G | A | 15 | a0001c0001t0001g0009 a0001c0001t0001g0131 a0001c0001t0001g0185 others(12): Show |
17 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.404-3087C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216091 | |||||||
chr4:4216193 | C | A | 31 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(28): Show |
38 | HG01109.hp1 HG01243.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.404-3189G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216193 | |||||||
chr4:4216257 | T | G | 3 | a0001c0001t0001g0281 a0009c0012t0001g0162 a0016c0016t0001g0034 |
3 | HG03927.hp1 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.404-3253A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216257 | |||||||
chr4:4216309 | G | A | 6 | a0001c0001t0001g0043 a0001c0001t0001g0072 a0001c0001t0001g0080 others(3): Show |
6 | HG00438.hp2 HG02074.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.404-3305C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216309 | |||||||
chr4:4216315 | T | A | 11 | a0001c0001t0001g0017 a0001c0001t0001g0047 a0001c0001t0001g0114 others(8): Show |
12 | HG01884.hp2 HG02055.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.404-3311A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216315 | |||||||
chr4:4216357 | G | A | 15 | a0001c0001t0001g0009 a0001c0001t0001g0131 a0001c0001t0001g0185 others(12): Show |
17 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.404-3353C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216357 | |||||||
chr4:4216382 | T | G | 1 | a0002c0002t0001g0320 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.404-3378A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216382 | |||||||
chr4:4216395 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.404-3391A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216395 | |||||||
chr4:4216423 | C | T | 2 | a0002c0003t0001g0127 a0006c0010t0001g0372 |
2 | HG01109.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.404-3419G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216423 | |||||||
chr4:4216443 | C | T | 1 | a0014c0024t0001g0357 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.404-3439G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216443 | |||||||
chr4:4216518 | C | T | 3 | a0001c0001t0001g0281 a0009c0012t0001g0162 a0016c0016t0001g0034 |
3 | HG03927.hp1 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.404-3514G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216518 | |||||||
chr4:4216525 | C | G | 372 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(369): Show |
419 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(416): Show |
intron_variant | MODIFIER | c.404-3521G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216525 | |||||||
chr4:4216571 | C | T | 2 | a0001c0001t0001g0231 a0003c0005t0001g0230 |
2 | HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.404-3567G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216571 | |||||||
chr4:4216603 | C | G | 3 | a0008c0009t0001g0358 a0009c0012t0001g0126 a0009c0012t0001g0138 |
3 | HG02109.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.404-3599G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216603 | |||||||
chr4:4216775 | A | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(109): Show |
128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.404-3771T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216775 | |||||||
chr4:4216780 | A | T | 1 | a0004c0006t0001g0271 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.404-3776T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216780 | |||||||
chr4:4216804 | G | A | 2 | a0001c0001t0001g0193 a0008c0009t0001g0375 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.404-3800C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216804 | |||||||
chr4:4216942 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(114): Show |
133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.404-3938G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216942 | |||||||
chr4:4216974 | A | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(238): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.404-3970T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216974 | |||||||
chr4:4217151 | G | A | 1 | a0001c0004t0001g0171 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.404-4147C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4217151 | |||||||
chr4:4217221 | T | C | 2 | a0001c0004t0001g0191 a0008c0026t0001g0371 |
2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.404-4217A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4217221 | |||||||
chr4:4217225 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.404-4221A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4217225 | |||||||
chr4:4217361 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(114): Show |
133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.404-4357G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4217361 | |||||||
chr4:4217495 | T | C | 1 | a0006c0010t0001g0369 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.404-4491A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4217495 | |||||||
chr4:4217556 | T | C | 2 | a0001c0004t0001g0191 a0008c0026t0001g0371 |
2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.404-4552A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4217556 | |||||||
chr4:4217651 | T | C | 2 | a0001c0001t0001g0193 a0008c0009t0001g0375 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.404-4647A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4217651 | |||||||
chr4:4217712 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.404-4708C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4217712 | |||||||
chr4:4217746 | G | A | 18 | a0001c0001t0001g0009 a0001c0001t0001g0131 a0001c0001t0001g0185 others(15): Show |
20 | HG01255.hp1 HG01891.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.404-4742C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4217746 | |||||||
chr4:4217782 | T | A | 1 | a0001c0001t0001g0349 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.404-4778A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4217782 | |||||||
chr4:4217819 | A | G | 5 | a0001c0001t0001g0193 a0008c0009t0001g0358 a0008c0009t0001g0375 others(2): Show |
5 | HG02109.hp2 HG02717.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.404-4815T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4217819 | |||||||
chr4:4217852 | G | C | 1 | a0003c0005t0001g0258 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.404-4848C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4217852 | |||||||
chr4:4217863 | A | G | 19 | a0001c0001t0001g0193 a0001c0001t0001g0281 a0001c0004t0001g0049 others(16): Show |
19 | HG00738.hp1 HG01123.hp1 HG02004.hp2 others(16): Show |
intron_variant | MODIFIER | c.404-4859T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4217863 | |||||||
chr4:4217878 | T | C | 4 | a0002c0003t0001g0110 a0002c0028t0001g0379 a0008c0009t0001g0373 others(1): Show |
4 | HG02257.hp2 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-4874A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4217878 | |||||||
chr4:4217883 | A | G | 4 | a0002c0003t0001g0110 a0002c0028t0001g0379 a0008c0009t0001g0373 others(1): Show |
4 | HG02257.hp2 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-4879T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4217883 | |||||||
chr4:4218003 | T | G | 1 | a0002c0002t0001g0321 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.404-4999A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218003 | |||||||
chr4:4218076 | T | C | 3 | a0008c0009t0001g0358 a0009c0012t0001g0126 a0009c0012t0001g0138 |
3 | HG02109.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.404-5072A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218076 | |||||||
chr4:4218088 | T | C | 21 | a0001c0001t0001g0009 a0001c0001t0001g0131 a0001c0001t0001g0185 others(18): Show |
23 | HG01255.hp1 HG01891.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.404-5084A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218088 | |||||||
chr4:4218305 | T | C | 3 | a0008c0009t0001g0358 a0009c0012t0001g0126 a0009c0012t0001g0138 |
3 | HG02109.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.404-5301A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218305 | |||||||
chr4:4218349 | G | A | 2 | a0008c0009t0001g0359 a0008c0009t0001g0360 |
2 | HG02559.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.404-5345C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218349 | |||||||
chr4:4218378 | C | T | 3 | a0008c0009t0001g0362 a0011c0014t0001g0361 a0011c0014t0001g0363 |
3 | HG01891.hp2 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.404-5374G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218378 | |||||||
chr4:4218379 | G | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | NA18747.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.404-5375C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218379 | |||||||
chr4:4218391 | C | CA | 217 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(214): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.404-5388dupT | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218391 | |||||||
chr4:4218391 | C | CAA | 22 | a0001c0001t0001g0009 a0001c0001t0001g0118 a0001c0001t0001g0131 others(19): Show |
24 | HG01192.hp2 HG01255.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.404-5389_404-5388d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218391 | |||||||
chr4:4218456 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.404-5452G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218456 | |||||||
chr4:4218533 | C | A | 3 | a0008c0009t0001g0362 a0011c0014t0001g0361 a0011c0014t0001g0363 |
3 | HG01891.hp2 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.404-5529G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218533 | |||||||
chr4:4218549 | G | A | 1 | a0001c0001t0001g0014 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.404-5545C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218549 | |||||||
chr4:4218599 | G | A | 3 | a0008c0009t0001g0362 a0011c0014t0001g0361 a0011c0014t0001g0363 |
3 | HG01891.hp2 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.404-5595C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218599 | |||||||
chr4:4218648 | C | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(134): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.404-5644G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218648 | |||||||
chr4:4218717 | C | G | 7 | a0002c0003t0001g0187 a0002c0003t0001g0225 a0007c0008t0001g0124 others(4): Show |
7 | HG01255.hp1 HG01891.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.404-5713G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218717 | |||||||
chr4:4218735 | C | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(153): Show |
176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.404-5731G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218735 | |||||||
chr4:4218747 | G | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG00280.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.404-5743C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218747 | |||||||
chr4:4218748 | T | C | 1 | a0002c0002t0001g0308 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.404-5744A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218748 | |||||||
chr4:4218778 | C | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(154): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.404-5774G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218778 | |||||||
chr4:4218798 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.404-5794C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218798 | |||||||
chr4:4218877 | C | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(130): Show |
151 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.404-5873G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218877 | |||||||
chr4:4218878 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(133): Show |
154 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.404-5874T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218878 | |||||||
chr4:4218879 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(133): Show |
154 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.404-5875T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218879 | |||||||
chr4:4218885 | T | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(133): Show |
154 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.404-5881A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218885 | |||||||
chr4:4218890 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(133): Show |
154 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.404-5886G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218890 | |||||||
chr4:4218891 | T | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(133): Show |
154 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.404-5887A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218891 | |||||||
chr4:4218925 | T | C | 1 | a0008c0009t0001g0358 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.404-5921A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218925 | |||||||
chr4:4218933 | A | G | 2 | a0001c0004t0001g0191 a0008c0026t0001g0371 |
2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.404-5929T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218933 | |||||||
chr4:4218975 | G | A | 3 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0001g0188 |
3 | HG01884.hp2 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.404-5971C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218975 | |||||||
chr4:4218998 | G | C | 1 | a0001c0001t0001g0264 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.404-5994C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218998 | |||||||
chr4:4219118 | CAAAA | C | 5 | a0001c0001t0001g0193 a0008c0009t0001g0362 a0008c0009t0001g0375 others(2): Show |
5 | HG01891.hp2 HG03471.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.404-6118_404-6115d others(6): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219118 | |||||||
chr4:4219158 | T | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0131 a0001c0001t0001g0192 others(2): Show |
7 | HG02109.hp1 HG02630.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.404-6154A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219158 | |||||||
chr4:4219199 | G | C | 1 | a0013c0027t0001g0378 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.404-6195C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219199 | |||||||
chr4:4219243 | T | C | 3 | a0008c0009t0001g0362 a0011c0014t0001g0361 a0011c0014t0001g0363 |
3 | HG01891.hp2 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.404-6239A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219243 | |||||||
chr4:4219390 | C | T | 1 | a0001c0001t0001g0331 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.404-6386G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219390 | |||||||
chr4:4219395 | T | A | 1 | a0001c0001t0001g0241 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.404-6391A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219395 | |||||||
chr4:4219428 | G | A | 2 | a0001c0001t0001g0074 a0009c0018t0001g0036 |
2 | HG02083.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.404-6424C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219428 | |||||||
chr4:4219429 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.404-6425G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219429 | |||||||
chr4:4219472 | C | T | 1 | a0002c0002t0001g0132 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.404-6468G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219472 | |||||||
chr4:4219498 | G | C | 1 | a0001c0001t0001g0071 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.404-6494C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219498 | |||||||
chr4:4219512 | C | T | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.404-6508G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219512 | |||||||
chr4:4219518 | G | A | 1 | a0009c0012t0001g0162 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.404-6514C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219518 | |||||||
chr4:4219571 | G | A | 1 | a0002c0002t0001g0106 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.404-6567C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219571 | |||||||
chr4:4219574 | T | C | 3 | a0008c0009t0001g0362 a0011c0014t0001g0361 a0011c0014t0001g0363 |
3 | HG01891.hp2 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.404-6570A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219574 | |||||||
chr4:4219592 | T | G | 2 | a0001c0001t0001g0119 a0001c0001t0001g0145 |
2 | HG01070.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.404-6588A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219592 | |||||||
chr4:4219669 | C | G | 1 | a0002c0013t0001g0224 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.404-6665G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219669 | |||||||
chr4:4219684 | G | A | 1 | a0002c0002t0001g0342 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.404-6680C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219684 | |||||||
chr4:4219692 | G | A | 1 | a0014c0024t0001g0357 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.404-6688C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219692 | |||||||
chr4:4219696 | C | CAA | 135 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(132): Show |
154 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.404-6694_404-6693d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219696 | |||||||
chr4:4219798 | A | C | 2 | a0002c0002t0001g0342 a0003c0005t0001g0236 |
2 | HG01081.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.403+6664T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219798 | |||||||
chr4:4219809 | G | A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0287 a0001c0001t0001g0333 |
7 | HG00438.hp1 NA18946.hp1 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.403+6653C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219809 | |||||||
chr4:4219809 | G | GTGTATAT others(39): Show |
1 | a0001c0001t0001g0083 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.403+6607_403+6652d others(48): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219809 | |||||||
chr4:4219836 | C | CAT | 129 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(126): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.403+6624_403+6625d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219836 | |||||||
chr4:4219837 | A | ATATATAT others(33): Show |
1 | a0002c0003t0001g0223 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.403+6585_403+6624d others(42): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219837 | |||||||
chr4:4219856 | T | C | 1 | a0002c0002t0001g0342 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.403+6606A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219856 | |||||||
chr4:4219884 | T | C | 14 | a0004c0006t0001g0007 a0004c0006t0001g0038 a0004c0006t0001g0059 others(11): Show |
17 | HG00099.hp2 HG00733.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.403+6578A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219884 | |||||||
chr4:4219895 | G | GTATACAC others(35): Show |
3 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0164 |
6 | NA18939.hp1 NA18970.hp1 NA19063.hp1 others(3): Show |
intron_variant | MODIFIER | c.403+6566_403+6567i others(44): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219895 | |||||||
chr4:4219913 | G | GTATATAC others(25): Show |
2 | a0001c0004t0001g0191 a0008c0026t0001g0371 |
2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.403+6517_403+6548d others(34): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219913 | |||||||
chr4:4219915 | A | G | 131 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(128): Show |
150 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.403+6547T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219915 | |||||||
chr4:4219935 | A | G | 1 | a0001c0004t0001g0092 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.403+6527T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219935 | |||||||
chr4:4219940 | T | C | 4 | a0002c0003t0001g0127 a0002c0003t0001g0190 a0009c0012t0001g0126 others(1): Show |
4 | HG01243.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.403+6522A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219940 | |||||||
chr4:4219952 | C | T | 1 | a0001c0001t0001g0310 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.403+6510G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219952 | |||||||
chr4:4219967 | A | G | 1 | a0001c0004t0001g0060 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.403+6495T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219967 | |||||||
chr4:4219985 | G | A | 5 | a0001c0001t0001g0331 a0002c0002t0001g0332 a0008c0009t0001g0362 others(2): Show |
5 | HG01891.hp2 NA18522.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.403+6477C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219985 | |||||||
chr4:4220009 | A | ATGTATAT others(41): Show |
4 | a0001c0004t0001g0247 a0002c0002t0001g0295 a0002c0002t0001g0309 others(1): Show |
4 | HG01123.hp1 HG01361.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.403+6405_403+6452d others(50): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220009 | |||||||
chr4:4220010 | T | G | 1 | a0013c0027t0001g0378 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.403+6452A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220010 | |||||||
chr4:4220011 | GTA | G | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(287): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.403+6449_403+6450d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220011 | |||||||
chr4:4220020 | T | C | 1 | a0005c0007t0001g0347 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.403+6442A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220020 | |||||||
chr4:4220024 | TATACGTA others(19): Show |
T | 2 | a0004c0006t0001g0125 a0004c0006t0001g0182 |
2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.403+6412_403+6437d others(28): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220024 | |||||||
chr4:4220029 | G | A | 292 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(289): Show |
331 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.403+6433C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220029 | |||||||
chr4:4220048 | TAC | T | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(233): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.403+6412_403+6413d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220048 | |||||||
chr4:4220050 | C | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(51): Show |
63 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.403+6412G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220050 | |||||||
chr4:4220067 | A | ATGTATAT others(3): Show |
1 | a0002c0002t0001g0328 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.403+6394_403+6395i others(12): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220067 | |||||||
chr4:4220080 | CAT | C | 164 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(161): Show |
188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.403+6380_403+6381d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220080 | |||||||
chr4:4220080 | CATAT | C | 60 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(57): Show |
68 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.403+6378_403+6381d others(6): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220080 | |||||||
chr4:4220080 | CATATAT | C | 5 | a0001c0001t0001g0090 a0002c0028t0001g0379 a0008c0009t0001g0362 others(2): Show |
5 | HG01891.hp2 HG02922.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.403+6376_403+6381d others(8): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220080 | |||||||
chr4:4220084 | T | TATACATA others(27): Show |
1 | a0002c0002t0001g0328 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.403+6377_403+6378i others(36): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220084 | |||||||
chr4:4220084 | T | TATATATA others(27): Show |
1 | a0001c0001t0001g0084 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.403+6377_403+6378i others(36): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220084 | |||||||
chr4:4220098 | TA | T | 9 | a0002c0003t0001g0189 a0002c0003t0001g0223 a0006c0010t0001g0365 others(6): Show |
9 | HG02109.hp2 HG02615.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.403+6363delT | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220098 | |||||||
chr4:4220098 | TATA | T | 20 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0114 others(17): Show |
24 | HG01884.hp2 HG02015.hp2 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.403+6361_403+6363d others(5): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220098 | |||||||
chr4:4220098 | TATATA | T | 21 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0044 others(18): Show |
23 | HG00597.hp1 HG00621.hp2 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.403+6359_403+6363d others(7): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220098 | |||||||
chr4:4220099 | A | T | 18 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0192 others(15): Show |
21 | HG01167.hp1 HG01255.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.403+6363T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220099 | |||||||
chr4:4220100 | TATA | T | 12 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0001t0001g0337 others(9): Show |
12 | HG00609.hp1 HG02056.hp1 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.403+6359_403+6361d others(5): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220100 | |||||||
chr4:4220100 | TATATA | T | 8 | a0001c0001t0001g0014 a0001c0001t0001g0072 a0001c0001t0001g0073 others(5): Show |
9 | HG00438.hp2 HG01069.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.403+6357_403+6361d others(7): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220100 | |||||||
chr4:4220101 | A | T | 56 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(53): Show |
62 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.403+6361T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220101 | |||||||
chr4:4220102 | TATA | T | 16 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0051 others(13): Show |
18 | HG00323.hp2 HG00544.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.403+6357_403+6359d others(5): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220102 | |||||||
chr4:4220103 | A | T | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(107): Show |
130 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(127): Show |
intron_variant | MODIFIER | c.403+6359T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220103 | |||||||
chr4:4220103 | ATAT | A | 7 | a0001c0001t0001g0310 a0001c0004t0001g0191 a0001c0004t0001g0247 others(4): Show |
7 | HG00099.hp1 HG01123.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.403+6356_403+6358d others(5): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220103 | |||||||
chr4:4220104 | TA | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0062 others(2): Show |
6 | HG00673.hp2 HG00735.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.403+6357delT | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220104 | |||||||
chr4:4220105 | A | T | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(262): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.403+6357T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220105 | |||||||
chr4:4220105 | ATT | A | 7 | a0001c0001t0001g0071 a0001c0001t0001g0248 a0001c0001t0001g0253 others(4): Show |
7 | HG01952.hp2 HG02129.hp1 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.403+6355_403+6356d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220105 | |||||||
chr4:4220107 | T | A | 2 | a0002c0002t0001g0322 a0002c0002t0001g0323 |
2 | HG01993.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.403+6355A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220107 | |||||||
chr4:4220120 | G | A | 2 | a0002c0002t0001g0094 a0002c0002t0001g0165 |
2 | HG01123.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.403+6342C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220120 | |||||||
chr4:4220141 | C | T | 1 | a0002c0002t0001g0141 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.403+6321G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220141 | |||||||
chr4:4220181 | T | C | 373 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(370): Show |
420 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(417): Show |
intron_variant | MODIFIER | c.403+6281A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220181 | |||||||
chr4:4220188 | C | T | 3 | a0001c0001t0001g0193 a0008c0009t0001g0375 a0009c0018t0001g0036 |
3 | HG02809.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.403+6274G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220188 | |||||||
chr4:4220327 | T | C | 40 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(37): Show |
47 | HG00621.hp1 HG01243.hp1 HG02015.hp2 others(44): Show |
intron_variant | MODIFIER | c.403+6135A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220327 | |||||||
chr4:4220332 | C | T | 25 | a0001c0001t0001g0017 a0001c0001t0001g0114 a0001c0001t0001g0115 others(22): Show |
26 | HG00733.hp2 HG01167.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.403+6130G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220332 | |||||||
chr4:4220351 | G | A | 4 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0354 others(1): Show |
4 | HG02451.hp2 HG02886.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.403+6111C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220351 | |||||||
chr4:4220394 | A | G | 51 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0014 others(48): Show |
60 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.403+6068T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220394 | |||||||
chr4:4220400 | G | A | 3 | a0001c0001t0001g0193 a0008c0009t0001g0375 a0009c0018t0001g0036 |
3 | HG02809.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.403+6062C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220400 | |||||||
chr4:4220650 | T | C | 1 | a0001c0001t0001g0175 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.403+5812A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220650 | |||||||
chr4:4220852 | C | T | 11 | a0001c0001t0001g0017 a0001c0001t0001g0114 a0001c0001t0001g0115 others(8): Show |
12 | HG01884.hp2 HG02055.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.403+5610G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220852 | |||||||
chr4:4220868 | A | G | 1 | a0014c0024t0001g0357 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.403+5594T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220868 | |||||||
chr4:4220970 | G | T | 1 | a0004c0006t0001g0294 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.403+5492C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220970 | |||||||
chr4:4220979 | T | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(203): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.403+5483A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220979 | |||||||
chr4:4220992 | G | T | 1 | a0014c0024t0001g0357 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.403+5470C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220992 | |||||||
chr4:4221038 | T | G | 6 | a0001c0001t0001g0131 a0002c0003t0001g0128 a0007c0008t0001g0124 others(3): Show |
6 | HG01891.hp1 HG02280.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.403+5424A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221038 | |||||||
chr4:4221043 | C | CTATTT | 27 | a0001c0001t0001g0017 a0001c0001t0001g0093 a0001c0001t0001g0114 others(24): Show |
28 | HG01243.hp2 HG01433.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.403+5414_403+5418d others(7): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221043 | |||||||
chr4:4221043 | C | CTATTTTA others(3): Show |
15 | a0001c0001t0001g0069 a0001c0001t0001g0115 a0001c0001t0001g0178 others(12): Show |
16 | HG01167.hp1 HG01257.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.403+5409_403+5418d others(12): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221043 | |||||||
chr4:4221043 | C | CTATTTTA others(8): Show |
9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(6): Show |
9 | HG02735.hp2 HG03491.hp2 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.403+5404_403+5418d others(17): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221043 | |||||||
chr4:4221043 | C | CTATTTTA others(13): Show |
3 | a0001c0001t0001g0062 a0001c0004t0001g0171 a0002c0013t0001g0123 |
3 | HG03195.hp2 HG04228.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.403+5399_403+5418d others(22): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221043 | |||||||
chr4:4221043 | C | CTATTTTA others(18): Show |
1 | a0011c0014t0001g0361 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.403+5394_403+5418d others(27): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221043 | |||||||
chr4:4221043 | CTATTT | C | 126 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(123): Show |
150 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.403+5414_403+5418d others(7): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221043 | |||||||
chr4:4221043 | CTATTTTA others(3): Show |
C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(90): Show |
109 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.403+5409_403+5418d others(12): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221043 | |||||||
chr4:4221043 | CTATTTTA others(8): Show |
C | 19 | a0001c0001t0001g0131 a0001c0001t0001g0185 a0001c0001t0001g0186 others(16): Show |
19 | HG01175.hp1 HG01891.hp1 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.403+5404_403+5418d others(17): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221043 | |||||||
chr4:4221043 | CTATTTTA others(13): Show |
C | 9 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0051 others(6): Show |
10 | HG00738.hp1 HG02004.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.403+5399_403+5418d others(22): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221043 | |||||||
chr4:4221295 | C | T | 3 | a0008c0009t0001g0362 a0011c0014t0001g0361 a0011c0014t0001g0363 |
3 | HG01891.hp2 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.403+5167G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221295 | |||||||
chr4:4221349 | A | G | 1 | a0002c0002t0001g0295 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.403+5113T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221349 | |||||||
chr4:4221350 | G | C | 1 | a0001c0001t0001g0233 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.403+5112C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221350 | |||||||
chr4:4221355 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.403+5107A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221355 | |||||||
chr4:4221384 | C | T | 20 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(17): Show |
20 | HG01891.hp2 HG02257.hp2 HG02698.hp1 others(17): Show |
intron_variant | MODIFIER | c.403+5078G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221384 | |||||||
chr4:4221467 | AG | A | 25 | a0001c0001t0001g0017 a0001c0001t0001g0114 a0001c0001t0001g0115 others(22): Show |
26 | HG00733.hp2 HG01167.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.403+4994delC | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221467 | |||||||
chr4:4221535 | C | T | 1 | a0004c0006t0001g0294 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.403+4927G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221535 | |||||||
chr4:4221895 | T | C | 28 | a0001c0001t0001g0017 a0001c0001t0001g0114 a0001c0001t0001g0115 others(25): Show |
29 | HG00733.hp2 HG01167.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.403+4567A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221895 | |||||||
chr4:4222082 | G | T | 1 | a0008c0009t0001g0358 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.403+4380C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4222082 | |||||||
chr4:4222285 | G | A | 1 | a0006c0010t0001g0364 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.403+4177C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4222285 | |||||||
chr4:4222388 | G | A | 1 | a0006c0025t0001g0370 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.403+4074C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4222388 | |||||||
chr4:4222522 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.403+3940G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4222522 | |||||||
chr4:4222550 | G | A | 2 | a0012c0015t0001g0376 a0012c0015t0001g0377 |
2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.403+3912C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4222550 | |||||||
chr4:4222669 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.403+3793G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4222669 | |||||||
chr4:4222744 | G | C | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(294): Show |
336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.403+3718C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4222744 | |||||||
chr4:4222816 | C | T | 1 | a0002c0002t0001g0293 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.403+3646G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4222816 | |||||||
chr4:4222986 | T | A | 126 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(123): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.403+3476A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4222986 | |||||||
chr4:4223014 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.403+3448C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223014 | |||||||
chr4:4223099 | A | G | 10 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0051 others(7): Show |
11 | HG00738.hp1 HG02004.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.403+3363T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223099 | |||||||
chr4:4223197 | C | T | 1 | a0009c0018t0001g0036 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.403+3265G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223197 | |||||||
chr4:4223216 | T | C | 10 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0051 others(7): Show |
11 | HG00738.hp1 HG02004.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.403+3246A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223216 | |||||||
chr4:4223408 | CAGAT | C | 10 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0051 others(7): Show |
11 | HG00738.hp1 HG02004.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.403+3050_403+3053d others(6): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223408 | |||||||
chr4:4223409 | A | AGATG | 219 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(216): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.403+3049_403+3052d others(6): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223409 | |||||||
chr4:4223409 | A | AGATGGAT others(1): Show |
60 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(57): Show |
69 | HG00621.hp1 HG01433.hp2 HG01891.hp2 others(66): Show |
intron_variant | MODIFIER | c.403+3045_403+3052d others(10): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223409 | |||||||
chr4:4223409 | A | AGATGGAT others(5): Show |
2 | a0001c0001t0001g0205 a0001c0001t0001g0212 |
2 | HG02015.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.403+3041_403+3052d others(14): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223409 | |||||||
chr4:4223409 | A | AGATGGAT others(9): Show |
1 | a0008c0009t0001g0375 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.403+3037_403+3052d others(18): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223409 | |||||||
chr4:4223409 | AGATGGAT others(1): Show |
A | 3 | a0001c0001t0001g0214 a0002c0002t0001g0213 a0002c0002t0001g0311 |
3 | HG00544.hp1 NA19068.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.403+3045_403+3052d others(10): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223409 | |||||||
chr4:4223441 | G | A | 10 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0051 others(7): Show |
11 | HG00738.hp1 HG02004.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.403+3021C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223441 | |||||||
chr4:4223443 | A | T | 10 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0051 others(7): Show |
11 | HG00738.hp1 HG02004.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.403+3019T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223443 | |||||||
chr4:4223444 | T | G | 10 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0051 others(7): Show |
11 | HG00738.hp1 HG02004.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.403+3018A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223444 | |||||||
chr4:4223522 | G | A | 10 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0051 others(7): Show |
11 | HG00738.hp1 HG02004.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.403+2940C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223522 | |||||||
chr4:4223558 | A | G | 11 | a0001c0001t0001g0017 a0001c0001t0001g0114 a0001c0001t0001g0115 others(8): Show |
12 | HG01884.hp2 HG02055.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.403+2904T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223558 | |||||||
chr4:4223572 | G | A | 10 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0051 others(7): Show |
11 | HG00738.hp1 HG02004.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.403+2890C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223572 | |||||||
chr4:4223578 | C | G | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(292): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.403+2884G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223578 | |||||||
chr4:4223622 | G | A | 1 | a0008c0009t0001g0360 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.403+2840C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223622 | |||||||
chr4:4223634 | C | T | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(292): Show |
334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.403+2828G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223634 | |||||||
chr4:4223757 | T | G | 1 | a0002c0002t0001g0091 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.403+2705A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223757 | |||||||
chr4:4223769 | C | T | 1 | a0002c0002t0001g0292 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.403+2693G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223769 | |||||||
chr4:4223800 | G | A | 1 | a0008c0009t0001g0359 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.403+2662C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223800 | |||||||
chr4:4223888 | TCAAAAA | T | 120 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(117): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.403+2568_403+2573d others(8): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223888 | |||||||
chr4:4224050 | A | C | 1 | a0009c0012t0001g0195 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.403+2412T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224050 | |||||||
chr4:4224219 | C | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG00280.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.403+2243G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224219 | |||||||
chr4:4224271 | C | T | 1 | a0001c0004t0001g0247 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.403+2191G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224271 | |||||||
chr4:4224278 | T | C | 10 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0051 others(7): Show |
11 | HG00738.hp1 HG02004.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.403+2184A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224278 | |||||||
chr4:4224280 | G | A | 1 | a0001c0004t0001g0243 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.403+2182C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224280 | |||||||
chr4:4224288 | A | G | 10 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0051 others(7): Show |
11 | HG00738.hp1 HG02004.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.403+2174T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224288 | |||||||
chr4:4224346 | C | CA | 33 | a0001c0001t0001g0131 a0001c0001t0001g0146 a0001c0001t0001g0147 others(30): Show |
33 | HG01175.hp1 HG01891.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.403+2115dupT | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224346 | |||||||
chr4:4224346 | C | CAA | 61 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0014 others(58): Show |
70 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.403+2114_403+2115d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224346 | |||||||
chr4:4224389 | C | G | 38 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(35): Show |
38 | HG01175.hp1 HG01891.hp1 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.403+2073G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224389 | |||||||
chr4:4224620 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.403+1842T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224620 | |||||||
chr4:4224642 | C | CTAAAACA others(5): Show |
1 | a0001c0004t0001g0060 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.403+1808_403+1819d others(14): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224642 | |||||||
chr4:4224764 | G | A | 33 | a0001c0001t0001g0017 a0001c0001t0001g0114 a0001c0001t0001g0115 others(30): Show |
34 | HG00733.hp2 HG01167.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.403+1698C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224764 | |||||||
chr4:4224821 | G | A | 3 | a0008c0009t0001g0362 a0011c0014t0001g0361 a0011c0014t0001g0363 |
3 | HG01891.hp2 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.403+1641C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224821 | |||||||
chr4:4224835 | G | A | 1 | a0001c0004t0001g0244 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.403+1627C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224835 | |||||||
chr4:4224853 | G | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(136): Show |
155 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.403+1609C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224853 | |||||||
chr4:4224854 | AAGTGAGG others(3): Show |
A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(136): Show |
155 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.403+1598_403+1607d others(12): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224854 | |||||||
chr4:4224885 | G | A | 287 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(284): Show |
326 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.403+1577C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224885 | |||||||
chr4:4224976 | T | C | 288 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(285): Show |
329 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.403+1486A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224976 | |||||||
chr4:4225232 | G | A | 2 | a0012c0015t0001g0376 a0012c0015t0001g0377 |
2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.403+1230C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225232 | |||||||
chr4:4225296 | A | C | 3 | a0002c0002t0001g0288 a0002c0002t0001g0290 a0002c0020t0001g0289 |
3 | HG01981.hp2 NA18941.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.403+1166T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225296 | |||||||
chr4:4225297 | C | T | 2 | a0012c0015t0001g0376 a0012c0015t0001g0377 |
2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.403+1165G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225297 | |||||||
chr4:4225338 | G | A | 1 | a0002c0003t0001g0225 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.403+1124C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225338 | |||||||
chr4:4225413 | A | T | 1 | a0001c0001t0001g0287 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.403+1049T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225413 | |||||||
chr4:4225456 | C | A | 5 | a0001c0001t0001g0193 a0006c0010t0001g0372 a0008c0009t0001g0373 others(2): Show |
5 | HG01109.hp1 HG02809.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.403+1006G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225456 | |||||||
chr4:4225560 | T | C | 1 | a0002c0002t0001g0142 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.403+902A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225560 | |||||||
chr4:4225566 | C | CA | 16 | a0001c0001t0001g0197 a0001c0001t0001g0348 a0001c0001t0001g0349 others(13): Show |
17 | HG00597.hp2 HG01081.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.403+895dupT | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225566 | |||||||
chr4:4225566 | C | CAA | 33 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0022 others(30): Show |
40 | HG00621.hp1 HG00733.hp1 HG02015.hp2 others(37): Show |
intron_variant | MODIFIER | c.403+894_403+895dup others(2): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225566 | |||||||
chr4:4225566 | C | CAAA | 9 | a0001c0001t0001g0218 a0001c0004t0001g0191 a0002c0002t0001g0142 others(6): Show |
9 | HG02622.hp1 HG03654.hp1 NA18612.hp2 others(6): Show |
intron_variant | MODIFIER | c.403+893_403+895dup others(3): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225566 | |||||||
chr4:4225566 | C | CAAAA | 27 | a0001c0001t0001g0009 a0001c0001t0001g0047 a0001c0001t0001g0192 others(24): Show |
29 | HG00738.hp1 HG01192.hp2 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.403+892_403+895dup others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225566 | |||||||
chr4:4225566 | C | CAAAAA | 34 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0050 others(31): Show |
39 | HG00140.hp1 HG00323.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.403+891_403+895dup others(5): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225566 | |||||||
chr4:4225566 | C | CAAAAAA | 138 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(135): Show |
161 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.403+890_403+895dup others(6): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225566 | |||||||
chr4:4225566 | C | CAAAAAAA | 36 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0021 others(33): Show |
40 | HG00544.hp2 HG00673.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.403+889_403+895dup others(7): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225566 | |||||||
chr4:4225566 | C | CAAAAAAA others(1): Show |
8 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(5): Show |
8 | HG02080.hp1 HG02895.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.403+888_403+895dup others(8): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225566 | |||||||
chr4:4225566 | C | CAAAAAAA others(2): Show |
6 | a0002c0003t0001g0127 a0002c0003t0001g0128 a0004c0006t0001g0125 others(3): Show |
6 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.403+887_403+895dup others(9): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225566 | |||||||
chr4:4225566 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.403+886_403+895dup others(10): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225566 | |||||||
chr4:4225667 | C | G | 3 | a0008c0009t0001g0362 a0011c0014t0001g0361 a0011c0014t0001g0363 |
3 | HG01891.hp2 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.403+795G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225667 | |||||||
chr4:4225691 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0183 |
5 | HG00735.hp2 HG01884.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.403+771C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225691 | |||||||
chr4:4225711 | A | C | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
312 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.403+751T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225711 | |||||||
chr4:4225713 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.403+749G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225713 | |||||||
chr4:4225717 | T | C | 1 | a0001c0004t0001g0108 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.403+745A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225717 | |||||||
chr4:4225730 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.403+732T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225730 | |||||||
chr4:4225828 | C | G | 1 | a0002c0002t0001g0196 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.403+634G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225828 | |||||||
chr4:4225848 | T | C | 1 | a0001c0004t0001g0247 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.403+614A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225848 | |||||||
chr4:4225854 | C | T | 1 | a0001c0004t0001g0247 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.403+608G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225854 | |||||||
chr4:4225916 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.403+546C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225916 | |||||||
chr4:4226038 | G | T | 1 | a0008c0009t0001g0360 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.403+424C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4226038 | |||||||
chr4:4226047 | C | G | 2 | a0001c0001t0001g0139 a0003c0005t0001g0140 |
2 | HG00544.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.403+415G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4226047 | |||||||
chr4:4226048 | G | C | 3 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0354 |
3 | HG02451.hp2 HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.403+414C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4226048 | |||||||
chr4:4226110 | G | A | 156 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(153): Show |
173 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.403+352C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4226110 | |||||||
chr4:4226281 | A | G | 197 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(194): Show |
215 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.403+181T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4226281 | |||||||
chr4:4226301 | G | T | 83 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(80): Show |
89 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.403+161C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4226301 | |||||||
chr4:4226302 | A | AAAG | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
288 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.403+157_403+159dup others(3): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4226302 | |||||||
chr4:4226335 | G | T | 82 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(79): Show |
91 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.403+127C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4226335 | |||||||
chr4:4226366 | G | GGGAAGAC others(26): Show |
1 | a0001c0001t0001g0354 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.403+63_403+95dupTG others(31): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4226366 | |||||||
chr4:4226447 | G | A | 2 | a0001c0001t0001g0355 a0002c0002t0001g0356 |
2 | HG03490.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.403+15C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4226447 |