Item | Value |
---|---|
geneid | 9132 |
ensemblid | ENSG00000117013.17 |
hgncid | 6298 |
symbol | KCNQ4 |
name | potassium voltage-gated channel subfamily Q member 4 |
refseq_nuc | NM_004700.4 |
refseq_prot | NP_004691.2 |
ensembl_nuc | ENST00000347132.10 |
ensembl_prot | ENSP00000262916.6 |
mane_status | MANE Select |
chr | chr1 |
start | 40783787 |
end | 40840452 |
strand | + |
ver | v1.2 |
region | chr1:40783787-40840452 |
region5000 | chr1:40778787-40845452 |
regionname0 | KCNQ4_chr1_40783787_40840452 |
regionname5000 | KCNQ4_chr1_40778787_40845452 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 695 | 343 | 85 | 64 | 133 | 16 | 43 | 105 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | MAEAP others(690): Show |
chr1 | 40778787 | 40845452 |
a0002 | 0/0 | 695 | 19 | 0 | 7 | 5 | 2 | 5 | 4 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | MAEAP others(690): Show |
chr1 | 40778787 | 40845452 |
a0003 | 0/0 | 695 | 4 | 0 | 0 | 4 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | MAEAP others(690): Show |
chr1 | 40778787 | 40845452 |
a0004 | 0/0 | 695 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | MAEAP others(690): Show |
chr1 | 40778787 | 40845452 |
a0005 | 0/0 | 695 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | MAEAP others(690): Show |
chr1 | 40778787 | 40845452 |
a0006 | 0/0 | 695 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | MAEAP others(690): Show |
chr1 | 40778787 | 40845452 |
a0007 | 0/0 | 695 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | MAEAP others(690): Show |
chr1 | 40778787 | 40845452 |
a0008 | 0/0 | 695 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | MAEAP others(690): Show |
chr1 | 40778787 | 40845452 |
a0009 | 0/0 | 695 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | MAEAP others(690): Show |
chr1 | 40778787 | 40845452 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2085 | 156 | 34 | 31 | 68 | 4 | 18 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | ATGGC others(2080): Show |
chr1 | 40778787 | 40845452 | ||
a0001c0002 | 0/1 | 2085 | 108 | 47 | 17 | 18 | 10 | 15 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | ATGGC others(2080): Show |
chr1 | 40778787 | 40845452 | ||
a0001c0003 | 0/0 | 2085 | 51 | 1 | 8 | 35 | 1 | 6 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | ATGGC others(2080): Show |
chr1 | 40778787 | 40845452 | ||
a0001c0004 | 0/0 | 2085 | 15 | 1 | 7 | 6 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | ATGGC others(2080): Show |
chr1 | 40778787 | 40845452 | ||
a0001c0006 | 0/0 | 2085 | 4 | 0 | 0 | 4 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | ATGGC others(2080): Show |
chr1 | 40778787 | 40845452 | ||
a0001c0008 | 0/0 | 2085 | 3 | 0 | 1 | 0 | 1 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | ATGGC others(2080): Show |
chr1 | 40778787 | 40845452 | ||
a0001c0009 | 0/0 | 2085 | 2 | 0 | 0 | 2 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | ATGGC others(2080): Show |
chr1 | 40778787 | 40845452 | ||
a0001c0011 | 0/0 | 2085 | 2 | 0 | 0 | 0 | 0 | 2 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | ATGGC others(2080): Show |
chr1 | 40778787 | 40845452 | ||
a0001c0013 | 0/0 | 2085 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | ATGGC others(2080): Show |
chr1 | 40778787 | 40845452 | ||
a0001c0016 | 0/0 | 2085 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | ATGGC others(2080): Show |
chr1 | 40778787 | 40845452 | ||
a0002c0005 | 0/0 | 2085 | 14 | 0 | 5 | 4 | 1 | 4 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | ATGGC others(2080): Show |
chr1 | 40778787 | 40845452 | ||
a0002c0010 | 0/0 | 2085 | 2 | 0 | 1 | 0 | 1 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | ATGGC others(2080): Show |
chr1 | 40778787 | 40845452 | ||
a0002c0012 | 0/0 | 2085 | 2 | 0 | 0 | 1 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | ATGGC others(2080): Show |
chr1 | 40778787 | 40845452 | ||
a0002c0014 | 0/0 | 2085 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | ATGGC others(2080): Show |
chr1 | 40778787 | 40845452 | ||
a0003c0007 | 0/0 | 2085 | 3 | 0 | 0 | 3 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | ATGGC others(2080): Show |
chr1 | 40778787 | 40845452 | ||
a0003c0019 | 0/0 | 2085 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | ATGGC others(2080): Show |
chr1 | 40778787 | 40845452 | ||
a0004c0015 | 0/0 | 2085 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | ATGGC others(2080): Show |
chr1 | 40778787 | 40845452 | ||
a0005c0020 | 0/0 | 2085 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | ATGGC others(2080): Show |
chr1 | 40778787 | 40845452 | ||
a0006c0021 | 0/0 | 2085 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | ATGGC others(2080): Show |
chr1 | 40778787 | 40845452 | ||
a0007c0022 | 0/0 | 2085 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | ATGGC others(2080): Show |
chr1 | 40778787 | 40845452 | ||
a0008c0018 | 0/0 | 2085 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | ATGGC others(2080): Show |
chr1 | 40778787 | 40845452 | ||
a0009c0017 | 0/0 | 2085 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | ATGGC others(2080): Show |
chr1 | 40778787 | 40845452 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4324 | 91 | 30 | 11 | 38 | 1 | 11 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0001c0001t0002 | 1/0 | 4324 | 24 | 1 | 7 | 9 | 0 | 6 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0001c0001t0003 | 0/0 | 4324 | 26 | 2 | 13 | 9 | 1 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0001c0001t0004 | 0/0 | 4320 | 8 | 0 | 0 | 8 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4315): Show |
chr1 | 40778787 | 40845452 |
a0001c0001t0005 | 0/0 | 4324 | 2 | 0 | 0 | 0 | 2 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0001c0001t0007 | 0/0 | 4324 | 2 | 0 | 0 | 2 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0001c0001t0011 | 0/0 | 4324 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0001c0001t0012 | 0/0 | 4324 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0001c0001t0020 | 0/0 | 4324 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0001c0002t0001 | 0/1 | 4324 | 75 | 32 | 10 | 15 | 9 | 8 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0001c0002t0002 | 0/0 | 4324 | 16 | 4 | 4 | 2 | 1 | 5 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0001c0002t0003 | 0/0 | 4324 | 5 | 2 | 2 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0001c0002t0006 | 0/0 | 4323 | 3 | 3 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4318): Show |
chr1 | 40778787 | 40845452 |
a0001c0002t0008 | 0/0 | 4324 | 2 | 0 | 0 | 0 | 0 | 2 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0001c0002t0013 | 0/0 | 4311 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4306): Show |
chr1 | 40778787 | 40845452 |
a0001c0002t0014 | 0/0 | 4324 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0001c0002t0015 | 0/0 | 4324 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0001c0002t0016 | 0/0 | 4324 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0001c0002t0017 | 0/0 | 4324 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0001c0002t0018 | 0/0 | 4324 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0001c0002t0019 | 0/0 | 4324 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0001c0003t0001 | 0/0 | 4324 | 36 | 1 | 7 | 23 | 0 | 5 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0001c0003t0002 | 0/0 | 4324 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0001c0003t0003 | 0/0 | 4324 | 5 | 0 | 0 | 3 | 1 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0001c0003t0004 | 0/0 | 4320 | 8 | 0 | 0 | 8 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4315): Show |
chr1 | 40778787 | 40845452 |
a0001c0003t0009 | 0/0 | 4324 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0001c0004t0001 | 0/0 | 4324 | 7 | 1 | 2 | 3 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0001c0004t0002 | 0/0 | 4324 | 2 | 0 | 2 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0001c0004t0003 | 0/0 | 4324 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0001c0004t0004 | 0/0 | 4320 | 2 | 0 | 0 | 2 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4315): Show |
chr1 | 40778787 | 40845452 |
a0001c0004t0005 | 0/0 | 4324 | 3 | 0 | 3 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0001c0006t0001 | 0/0 | 4324 | 4 | 0 | 0 | 4 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0001c0008t0003 | 0/0 | 4324 | 3 | 0 | 1 | 0 | 1 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0001c0009t0001 | 0/0 | 4324 | 2 | 0 | 0 | 2 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0001c0011t0002 | 0/0 | 4324 | 2 | 0 | 0 | 0 | 0 | 2 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0001c0013t0002 | 0/0 | 4324 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0001c0016t0010 | 0/0 | 4324 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0002c0005t0001 | 0/0 | 4324 | 9 | 0 | 2 | 4 | 0 | 3 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0002c0005t0002 | 0/0 | 4324 | 4 | 0 | 2 | 0 | 1 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0002c0005t0005 | 0/0 | 4324 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0002c0010t0001 | 0/0 | 4324 | 2 | 0 | 1 | 0 | 1 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0002c0012t0001 | 0/0 | 4324 | 2 | 0 | 0 | 1 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0002c0014t0001 | 0/0 | 4324 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0003c0007t0001 | 0/0 | 4324 | 3 | 0 | 0 | 3 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0003c0019t0001 | 0/0 | 4324 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0004c0015t0001 | 0/0 | 4324 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0005c0020t0001 | 0/0 | 4324 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0006c0021t0001 | 0/0 | 4324 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0007c0022t0001 | 0/0 | 4324 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0008c0018t0001 | 0/0 | 4324 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
a0009c0017t0001 | 0/0 | 4324 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | GACAT others(4319): Show |
chr1 | 40778787 | 40845452 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0002g0069 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0003g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0003g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0003g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0003g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0004g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0005g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0007g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0007g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0011g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0012g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0001t0020g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0249 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0002g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0002g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0006g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0006g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0008g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0008g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0013g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0014g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0015g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0016g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0017g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0018g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0002t0019g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0003t0009g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0004t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0004t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0004t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0004t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0004t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0004t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0004t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0004t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0004t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0004t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0004t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0004t0005g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0004t0005g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0004t0005g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0006t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0006t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0006t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0006t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0008t0003g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0008t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0009t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0009t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0011t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0011t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0013t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0001c0016t0010g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0002c0005t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0002c0005t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0002c0005t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0002c0005t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0002c0005t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0002c0005t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0002c0005t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0002c0005t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0002c0005t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0002c0005t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0002c0005t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0002c0005t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0002c0005t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0002c0005t0005g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0002c0010t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0002c0010t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0002c0012t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0002c0012t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0002c0014t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0003c0007t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0003c0007t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0003c0019t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0004c0015t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0005c0020t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0006c0021t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0007c0022t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0008c0018t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
a0009c0017t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0322 | EUR | GBR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0049 | EUR | GBR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG00140 | hp1 | a0001 | c0003 | t0003 | g0087 | EUR | GBR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0038 | EUR | GBR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG00280 | hp1 | a0002 | c0005 | t0002 | g0315 | EUR | FIN | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0224 | EUR | FIN | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG00323 | hp1 | a0001 | c0002 | t0002 | g0186 | EUR | FIN | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0296 | EUR | FIN | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG00408 | hp1 | a0002 | c0005 | t0001 | g0324 | EAS | CHS | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG00558 | hp1 | a0001 | c0001 | t0004 | g0095 | EAS | CHS | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0156 | EAS | CHS | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG00597 | hp2 | a0001 | c0003 | t0001 | g0294 | EAS | CHS | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG00609 | hp1 | a0003 | c0007 | t0001 | g0004 | EAS | CHS | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG00621 | hp1 | a0001 | c0003 | t0001 | g0314 | EAS | CHS | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG00621 | hp2 | a0001 | c0004 | t0001 | g0270 | EAS | CHS | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0114 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0334 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0035 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG00735 | hp2 | a0002 | c0005 | t0005 | g0227 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG00738 | hp1 | a0002 | c0005 | t0001 | g0220 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0127 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG00741 | hp1 | a0001 | c0003 | t0001 | g0228 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0110 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0336 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01070 | hp1 | a0001 | c0004 | t0002 | g0134 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01070 | hp2 | a0001 | c0003 | t0001 | g0174 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01071 | hp2 | a0001 | c0004 | t0002 | g0135 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01081 | hp1 | a0001 | c0008 | t0003 | g0009 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01081 | hp2 | a0002 | c0005 | t0002 | g0199 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0115 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01106 | hp1 | a0002 | c0005 | t0001 | g0128 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0108 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01167 | hp1 | a0001 | c0003 | t0001 | g0157 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01168 | hp1 | a0001 | c0003 | t0001 | g0267 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01175 | hp1 | a0001 | c0004 | t0001 | g0288 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01175 | hp2 | a0001 | c0004 | t0005 | g0214 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01192 | hp1 | a0002 | c0010 | t0001 | g0299 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01192 | hp2 | a0001 | c0003 | t0001 | g0167 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0129 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01255 | hp1 | a0001 | c0002 | t0003 | g0109 | AMR | CLM | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01255 | hp2 | a0001 | c0004 | t0005 | g0165 | AMR | CLM | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01256 | hp1 | a0001 | c0003 | t0001 | g0293 | AMR | CLM | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01256 | hp2 | a0004 | c0015 | t0001 | g0014 | AMR | CLM | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01257 | hp1 | a0001 | c0004 | t0005 | g0071 | AMR | CLM | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0308 | AMR | CLM | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01261 | hp1 | a0001 | c0002 | t0003 | g0140 | AMR | CLM | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01346 | hp1 | a0002 | c0005 | t0002 | g0307 | AMR | CLM | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0112 | AMR | CLM | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01358 | hp1 | a0001 | c0004 | t0001 | g0321 | AMR | CLM | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0111 | AMR | CLM | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0223 | AMR | CLM | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0246 | AMR | CLM | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0209 | EUR | IBS | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0215 | EUR | IBS | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01516 | hp1 | a0001 | c0001 | t0005 | g0116 | EUR | IBS | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0014 | EUR | IBS | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01517 | hp1 | a0001 | c0001 | t0005 | g0119 | EUR | IBS | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0213 | EUR | IBS | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0212 | AFR | ACB | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01934 | hp1 | a0001 | c0003 | t0002 | g0283 | AMR | PEL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01943 | hp1 | a0001 | c0002 | t0018 | g0057 | AMR | PEL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01943 | hp2 | a0001 | c0002 | t0002 | g0301 | AMR | PEL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | PEL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PEL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0070 | AMR | PEL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01978 | hp2 | a0001 | c0002 | t0002 | g0138 | AMR | PEL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0036 | AMR | PEL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01981 | hp2 | a0001 | c0003 | t0001 | g0173 | AMR | PEL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0317 | AMR | PEL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01993 | hp2 | a0002 | c0014 | t0001 | g0313 | AMR | PEL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02015 | hp1 | a0001 | c0003 | t0001 | g0176 | EAS | KHV | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | KHV | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02027 | hp1 | a0001 | c0003 | t0004 | g0251 | EAS | KHV | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | KHV | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02040 | hp1 | a0003 | c0007 | t0001 | g0004 | EAS | KHV | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02040 | hp2 | a0001 | c0003 | t0001 | g0261 | EAS | KHV | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0152 | AFR | ACB | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02071 | hp1 | a0005 | c0020 | t0001 | g0117 | EAS | KHV | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02071 | hp2 | a0003 | c0019 | t0001 | g0039 | EAS | KHV | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | KHV | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02080 | hp2 | a0001 | c0003 | t0003 | g0312 | EAS | KHV | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02083 | hp1 | a0001 | c0002 | t0003 | g0268 | EAS | KHV | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02083 | hp2 | a0001 | c0003 | t0001 | g0155 | EAS | KHV | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02132 | hp1 | a0001 | c0001 | t0020 | g0042 | EAS | KHV | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02132 | hp2 | a0001 | c0003 | t0001 | g0295 | EAS | KHV | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02135 | hp1 | a0001 | c0003 | t0001 | g0092 | EAS | KHV | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02135 | hp2 | a0001 | c0003 | t0001 | g0122 | EAS | KHV | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | ACB | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0302 | AMR | PEL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0139 | AMR | PEL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02155 | hp1 | a0001 | c0004 | t0001 | g0269 | EAS | CDX | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CDX | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02165 | hp1 | a0001 | c0003 | t0001 | g0255 | EAS | CDX | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02165 | hp2 | a0003 | c0007 | t0001 | g0022 | EAS | CDX | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0347 | AFR | ACB | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0048 | AFR | ACB | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0243 | AMR | PEL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0088 | AMR | PEL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0303 | AMR | PEL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0207 | AFR | ACB | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0191 | EAS | KHV | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02572 | hp2 | a0001 | c0002 | t0006 | g0170 | AFR | GWD | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02602 | hp1 | a0001 | c0003 | t0001 | g0284 | SAS | PJL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0337 | AFR | GWD | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02615 | hp2 | a0001 | c0002 | t0003 | g0219 | AFR | GWD | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0335 | AFR | GWD | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0046 | AFR | GWD | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0333 | AFR | GWD | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0225 | AFR | GWD | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0250 | SAS | PJL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02683 | hp2 | a0002 | c0005 | t0002 | g0013 | SAS | PJL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02698 | hp1 | a0001 | c0011 | t0002 | g0233 | SAS | PJL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0273 | SAS | PJL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02723 | hp1 | a0001 | c0002 | t0019 | g0056 | AFR | GWD | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02723 | hp2 | a0001 | c0002 | t0014 | g0162 | AFR | GWD | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02735 | hp1 | a0002 | c0005 | t0001 | g0013 | SAS | PJL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0238 | SAS | PJL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0168 | SAS | PJL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0355 | AFR | GWD | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02818 | hp1 | a0001 | c0002 | t0013 | g0053 | AFR | GWD | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02818 | hp2 | a0006 | c0021 | t0001 | g0354 | AFR | GWD | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02886 | hp1 | a0001 | c0002 | t0006 | g0184 | AFR | GWD | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0350 | AFR | GWD | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02895 | hp1 | a0001 | c0002 | t0002 | g0340 | AFR | GWD | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0016 | AFR | GWD | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0040 | AFR | ESN | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0158 | AFR | ESN | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0338 | AFR | ESN | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | ESN | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02970 | hp2 | a0001 | c0002 | t0016 | g0045 | AFR | ESN | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0023 | AFR | ESN | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03017 | hp1 | a0001 | c0003 | t0003 | g0175 | SAS | PJL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0291 | SAS | PJL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03098 | hp1 | a0001 | c0002 | t0001 | g0161 | AFR | MSL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03098 | hp2 | a0001 | c0002 | t0006 | g0229 | AFR | MSL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0052 | AFR | ESN | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03130 | hp2 | a0001 | c0004 | t0001 | g0300 | AFR | ESN | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | ESN | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | MSL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03209 | hp2 | a0001 | c0002 | t0015 | g0346 | AFR | MSL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0034 | AFR | MSL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03225 | hp2 | a0001 | c0013 | t0002 | g0343 | AFR | MSL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03239 | hp1 | a0001 | c0011 | t0002 | g0239 | SAS | PJL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03453 | hp1 | a0001 | c0016 | t0010 | g0160 | AFR | MSL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0348 | AFR | MSL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03486 | hp2 | a0001 | c0002 | t0001 | g0062 | AFR | MSL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0005 | SAS | PJL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0221 | SAS | PJL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03491 | hp2 | a0001 | c0002 | t0008 | g0178 | SAS | PJL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03492 | hp1 | a0001 | c0002 | t0008 | g0179 | SAS | PJL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03492 | hp2 | a0001 | c0002 | t0002 | g0005 | SAS | PJL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03516 | hp2 | a0001 | c0002 | t0002 | g0341 | AFR | ESN | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | GWD | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0349 | AFR | MSL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0351 | AFR | MSL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03654 | hp1 | a0001 | c0003 | t0001 | g0137 | SAS | PJL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0325 | SAS | PJL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03669 | hp2 | a0001 | c0002 | t0002 | g0258 | SAS | PJL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03704 | hp1 | a0001 | c0008 | t0003 | g0032 | SAS | PJL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03704 | hp2 | a0002 | c0005 | t0001 | g0050 | SAS | PJL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03710 | hp2 | a0001 | c0002 | t0002 | g0151 | SAS | PJL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0259 | SAS | BEB | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0125 | SAS | BEB | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03834 | hp1 | a0001 | c0003 | t0001 | g0126 | SAS | BEB | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | BEB | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03927 | hp1 | a0001 | c0004 | t0001 | g0289 | SAS | BEB | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0328 | SAS | BEB | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0198 | SAS | BEB | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | BEB | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0327 | SAS | STU | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0195 | SAS | STU | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG04199 | hp1 | a0002 | c0005 | t0001 | g0309 | SAS | STU | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0166 | SAS | STU | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG04204 | hp1 | a0001 | c0003 | t0001 | g0236 | SAS | STU | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0030 | SAS | STU | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG04228 | hp1 | a0001 | c0003 | t0001 | g0298 | SAS | STU | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0075 | SAS | STU | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18522 | hp1 | a0001 | c0002 | t0002 | g0342 | AFR | YRI | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | YRI | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | CHB | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18747 | hp2 | a0001 | c0002 | t0002 | g0196 | EAS | CHB | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0028 | AFR | YRI | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | YRI | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18944 | hp1 | a0001 | c0003 | t0001 | g0274 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18945 | hp2 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18948 | hp1 | a0001 | c0003 | t0004 | g0306 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18949 | hp1 | a0007 | c0022 | t0001 | g0079 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18949 | hp2 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18950 | hp1 | a0001 | c0003 | t0001 | g0287 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18950 | hp2 | a0001 | c0001 | t0004 | g0077 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18952 | hp1 | a0001 | c0003 | t0004 | g0272 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0330 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18962 | hp1 | a0001 | c0006 | t0001 | g0121 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18962 | hp2 | a0001 | c0003 | t0003 | g0281 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18967 | hp1 | a0008 | c0018 | t0001 | g0097 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18970 | hp2 | a0002 | c0005 | t0001 | g0082 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18971 | hp1 | a0009 | c0017 | t0001 | g0200 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18973 | hp1 | a0001 | c0001 | t0004 | g0265 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18973 | hp2 | a0001 | c0003 | t0001 | g0136 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18975 | hp2 | a0001 | c0003 | t0001 | g0275 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18977 | hp2 | a0002 | c0005 | t0001 | g0304 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18985 | hp1 | a0001 | c0003 | t0001 | g0260 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18990 | hp2 | a0001 | c0003 | t0004 | g0311 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18993 | hp1 | a0001 | c0006 | t0001 | g0244 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18995 | hp1 | a0001 | c0003 | t0004 | g0271 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18998 | hp2 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19000 | hp1 | a0001 | c0001 | t0007 | g0085 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19002 | hp2 | a0001 | c0003 | t0001 | g0285 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19004 | hp1 | a0002 | c0012 | t0001 | g0018 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19005 | hp1 | a0001 | c0003 | t0001 | g0290 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19005 | hp2 | a0001 | c0003 | t0004 | g0256 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19007 | hp1 | a0001 | c0006 | t0001 | g0078 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19007 | hp2 | a0001 | c0003 | t0009 | g0280 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19009 | hp1 | a0001 | c0003 | t0004 | g0305 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19010 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19012 | hp1 | a0001 | c0004 | t0003 | g0329 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19012 | hp2 | a0001 | c0001 | t0011 | g0060 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | LWK | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19030 | hp2 | a0001 | c0003 | t0001 | g0024 | AFR | LWK | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19043 | hp1 | a0001 | c0002 | t0017 | g0132 | AFR | LWK | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19043 | hp2 | a0001 | c0001 | t0012 | g0159 | AFR | LWK | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19057 | hp1 | a0001 | c0003 | t0001 | g0310 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19060 | hp2 | a0001 | c0004 | t0004 | g0067 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19064 | hp1 | a0001 | c0004 | t0004 | g0257 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19065 | hp1 | a0001 | c0003 | t0001 | g0278 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19067 | hp1 | a0001 | c0009 | t0001 | g0185 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19067 | hp2 | a0001 | c0003 | t0001 | g0276 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19074 | hp1 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19074 | hp2 | a0001 | c0003 | t0003 | g0279 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19077 | hp1 | a0001 | c0003 | t0001 | g0154 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19077 | hp2 | a0001 | c0001 | t0007 | g0094 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19079 | hp1 | a0001 | c0003 | t0001 | g0282 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0331 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19082 | hp2 | a0001 | c0006 | t0001 | g0237 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19083 | hp1 | a0001 | c0004 | t0001 | g0019 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19083 | hp2 | a0001 | c0009 | t0001 | g0113 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19084 | hp2 | a0001 | c0003 | t0001 | g0277 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19087 | hp2 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19088 | hp2 | a0001 | c0003 | t0001 | g0093 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19090 | hp1 | a0002 | c0005 | t0001 | g0245 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19090 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0153 | AFR | YRI | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | YRI | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | TSI | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA20752 | hp2 | a0002 | c0010 | t0001 | g0232 | EUR | TSI | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA20805 | hp1 | a0001 | c0008 | t0003 | g0009 | EUR | TSI | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0141 | EUR | TSI | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | GIH | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA20905 | hp2 | a0002 | c0012 | t0001 | g0323 | SAS | GIH | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG01123 | hp2 | a0001 | c0002 | t0002 | g0319 | AMR | CLM | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0163 | AFR | ACB | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | ACB | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0344 | AFR | MSL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0352 | AFR | MSL | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0061 | AFR | USA | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | USA | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA18955 | hp2 | a0001 | c0003 | t0004 | g0286 | EAS | JPT | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0345 | AFR | USA | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0353 | AFR | USA | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA21309 | hp1 | a0001 | c0002 | t0002 | g0226 | AFR | LWK | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
NA21309 | hp2 | a0001 | c0002 | t0003 | g0222 | AFR | LWK | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0249 | REF | REF | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0069 | REF | REF | KCNQ4_chr1_40778787_40845452 | KCNQ4 | chr1 | 40778787 | 40845452 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:40818518 | C | G | 1 | a0007 | 1 | NA18949.hp1 | missense_variant | MODERATE | c.546C>G | p.Phe182Leu | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 4/14 | 853/4324 | 546/2088 | 182/695 | chr1 | 40818518 | |||
chr1:40820232 | G | A | 1 | a0004 | 1 | HG01256.hp2 | missense_variant | MODERATE | c.1013G>A | p.Arg338Gln | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 7/14 | 1320/4324 | 1013/2088 | 338/695 | chr1 | 40820232 | |||
chr1:40831133 | C | T | 1 | a0006 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.1342C>T | p.Arg448Trp | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 10/14 | 1649/4324 | 1342/2088 | 448/695 | chr1 | 40831133 | |||
chr1:40831156 | T | G | 1 | a0002 | 19 | HG00280.hp1 HG00408.hp1 HG00735.hp2 others(16): Show |
missense_variant | MODERATE | c.1365T>G | p.His455Gln | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 10/14 | 1672/4324 | 1365/2088 | 455/695 | chr1 | 40831156 | |||
chr1:40831277 | A | G | 1 | a0005 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.1486A>G | p.Arg496Gly | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 10/14 | 1793/4324 | 1486/2088 | 496/695 | chr1 | 40831277 | |||
chr1:40837737 | C | G | 1 | a0003 | 4 | HG00609.hp1 HG02040.hp1 HG02071.hp2 others(1): Show |
missense_variant | MODERATE | c.1818C>G | p.Asp606Glu | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 13/14 | 2125/4324 | 1818/2088 | 606/695 | chr1 | 40837737 | |||
chr1:40837767 | G | A | 1 | a0009 | 1 | NA18971.hp1 | missense_variant | MODERATE | c.1848G>A | p.Met616Ile | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 13/14 | 2155/4324 | 1848/2088 | 616/695 | chr1 | 40837767 | |||
chr1:40838506 | A | G | 1 | a0008 | 1 | NA18967.hp1 | missense_variant | MODERATE | c.2071A>G | p.Ser691Gly | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 14/14 | 2378/4324 | 2071/2088 | 691/695 | chr1 | 40838506 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:40784183 | G | A | 1 | a0001c0013 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.90G>A | p.Gln30Gln | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/14 | 397/4324 | 90/2088 | 30/695 | chr1 | 40784183 | |||
chr1:40819415 | T | C | 10 | a0001c0002 a0001c0003 a0001c0004 others(7): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
synonymous_variant | LOW | c.777T>C | p.Ala259Ala | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 5/14 | 1084/4324 | 777/2088 | 259/695 | chr1 | 40819415 | |||
chr1:40819881 | T | C | 2 | a0001c0004 a0001c0009 |
17 | HG00621.hp2 HG01070.hp1 HG01071.hp2 others(14): Show |
synonymous_variant | LOW | c.841T>C | p.Leu281Leu | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 6/14 | 1148/4324 | 841/2088 | 281/695 | chr1 | 40819881 | |||
chr1:40819913 | G | A | 2 | a0001c0003 a0002c0014 |
52 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(49): Show |
synonymous_variant | LOW | c.873G>A | p.Pro291Pro | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 6/14 | 1180/4324 | 873/2088 | 291/695 | chr1 | 40819913 | |||
chr1:40819919 | A | G | 3 | a0001c0003 a0001c0009 a0002c0014 |
54 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(51): Show |
synonymous_variant | LOW | c.879A>G | p.Thr293Thr | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 6/14 | 1186/4324 | 879/2088 | 293/695 | chr1 | 40819919 | |||
chr1:40820191 | G | A | 1 | a0001c0011 | 2 | HG02698.hp1 HG03239.hp1 |
synonymous_variant | LOW | c.972G>A | p.Leu324Leu | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 7/14 | 1279/4324 | 972/2088 | 324/695 | chr1 | 40820191 | |||
chr1:40835010 | C | T | 1 | a0001c0008 | 3 | HG01081.hp1 HG03704.hp1 NA20805.hp1 |
synonymous_variant | LOW | c.1657C>T | p.Leu553Leu | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 12/14 | 1964/4324 | 1657/2088 | 553/695 | chr1 | 40835010 | |||
chr1:40835018 | G | A | 2 | a0001c0016 a0002c0010 |
3 | HG01192.hp1 HG03453.hp1 NA20752.hp2 |
synonymous_variant | LOW | c.1665G>A | p.Pro555Pro | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 12/14 | 1972/4324 | 1665/2088 | 555/695 | chr1 | 40835018 | |||
chr1:40838421 | C | G | 1 | a0001c0006 | 4 | NA18962.hp1 NA18993.hp1 NA19007.hp1 others(1): Show |
synonymous_variant | LOW | c.1986C>G | p.Pro662Pro | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 14/14 | 2293/4324 | 1986/2088 | 662/695 | chr1 | 40838421 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:40783792 | G | A | 1 | a0001c0003t0009 | 1 | NA19007.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-302G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/14 | chr1 | 40783792 | |||||||
chr1:40783800 | C | T | 1 | a0001c0001t0020 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-294C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/14 | 294 | chr1 | 40783800 | ||||||
chr1:40784080 | G | T | 3 | a0001c0002t0017 a0001c0002t0018 a0001c0002t0019 |
3 | HG01943.hp1 HG02723.hp1 NA19043.hp1 |
5_prime_UTR_variant | MODIFIER | c.-14G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/14 | 14 | chr1 | 40784080 | ||||||
chr1:40838634 | A | G | 3 | a0001c0001t0005 a0001c0004t0005 a0002c0005t0005 |
6 | HG00735.hp2 HG01175.hp2 HG01255.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*111A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 14/14 | 111 | chr1 | 40838634 | ||||||
chr1:40838761 | C | T | 3 | a0001c0001t0004 a0001c0003t0004 a0001c0004t0004 |
18 | HG00558.hp1 HG02027.hp1 NA18945.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*238C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 14/14 | 238 | chr1 | 40838761 | ||||||
chr1:40838853 | C | T | 1 | a0001c0002t0016 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*330C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 14/14 | 330 | chr1 | 40838853 | ||||||
chr1:40838936 | C | T | 1 | a0001c0002t0015 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*413C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 14/14 | 413 | chr1 | 40838936 | ||||||
chr1:40839214 | C | T | 8 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0014 others(5): Show |
43 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*691C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 14/14 | 691 | chr1 | 40839214 | ||||||
chr1:40839228 | A | G | 1 | a0001c0002t0008 | 2 | HG03491.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*705A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 14/14 | 705 | chr1 | 40839228 | ||||||
chr1:40839517 | GCCAGTGG others(6): Show |
G | 1 | a0001c0002t0013 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*996_*1008delCAGTG others(8): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 14/14 | 996 | INFO_REALIGN_3_PRIME | chr1 | 40839517 | |||||
chr1:40839545 | A | T | 41 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(38): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
3_prime_UTR_variant | MODIFIER | c.*1022A>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 14/14 | 1022 | chr1 | 40839545 | ||||||
chr1:40839630 | C | T | 1 | a0001c0002t0014 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1107C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 14/14 | 1107 | chr1 | 40839630 | ||||||
chr1:40839639 | G | A | 1 | a0001c0001t0011 | 1 | NA19012.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1116G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 14/14 | 1116 | chr1 | 40839639 | ||||||
chr1:40839643 | C | T | 1 | a0001c0001t0007 | 2 | NA19000.hp1 NA19077.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1120C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 14/14 | 1120 | chr1 | 40839643 | ||||||
chr1:40839706 | C | T | 2 | a0001c0001t0012 a0001c0002t0018 |
2 | HG01943.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1183C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 14/14 | 1183 | chr1 | 40839706 | ||||||
chr1:40839868 | C | T | 1 | a0001c0016t0010 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1345C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 14/14 | 1345 | chr1 | 40839868 | ||||||
chr1:40840142 | TACTC | T | 3 | a0001c0001t0004 a0001c0003t0004 a0001c0004t0004 |
18 | HG00558.hp1 HG02027.hp1 NA18945.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1621_*1624delCTCA | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 14/14 | 1621 | INFO_REALIGN_3_PRIME | chr1 | 40840142 | |||||
chr1:40840200 | GC | G | 1 | a0001c0002t0006 | 3 | HG02572.hp2 HG02886.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1680delC | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 14/14 | 1680 | INFO_REALIGN_3_PRIME | chr1 | 40840200 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:40784445 | C | T | 1 | a0001c0001t0001g0355 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.314+38C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40784445 | |||||||
chr1:40784473 | G | A | 7 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(4): Show |
8 | HG02559.hp2 HG02895.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.314+66G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40784473 | |||||||
chr1:40784973 | G | C | 1 | a0003c0007t0001g0022 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.314+566G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40784973 | |||||||
chr1:40785008 | T | C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0027 others(3): Show |
7 | HG02559.hp1 HG02896.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.314+601T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40785008 | |||||||
chr1:40785302 | C | T | 5 | a0001c0002t0001g0015 a0001c0002t0001g0351 a0001c0002t0001g0352 others(2): Show |
6 | HG02818.hp2 HG03471.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.314+895C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40785302 | |||||||
chr1:40785554 | G | T | 19 | a0001c0001t0001g0339 a0001c0001t0001g0344 a0001c0001t0001g0345 others(16): Show |
19 | HG00639.hp2 HG01069.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.314+1147G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40785554 | |||||||
chr1:40785592 | G | T | 3 | a0001c0001t0001g0332 a0001c0001t0003g0330 a0001c0001t0003g0331 |
3 | NA18957.hp2 NA18966.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.314+1185G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40785592 | |||||||
chr1:40785750 | C | T | 1 | a0001c0004t0003g0329 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.314+1343C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40785750 | |||||||
chr1:40785841 | A | C | 1 | a0001c0002t0001g0156 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.314+1434A>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40785841 | |||||||
chr1:40785843 | G | T | 89 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0253 others(86): Show |
91 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.314+1436G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40785843 | |||||||
chr1:40786019 | T | C | 1 | a0001c0002t0001g0028 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.314+1612T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40786019 | |||||||
chr1:40786073 | A | G | 4 | a0001c0001t0001g0349 a0001c0001t0003g0347 a0001c0001t0003g0348 others(1): Show |
4 | HG02258.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+1666A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40786073 | |||||||
chr1:40786250 | G | A | 5 | a0001c0001t0001g0029 a0001c0002t0001g0333 a0001c0002t0001g0334 others(2): Show |
5 | HG00639.hp2 HG01069.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+1843G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40786250 | |||||||
chr1:40786349 | G | A | 4 | a0001c0001t0001g0349 a0001c0001t0003g0347 a0001c0001t0003g0348 others(1): Show |
4 | HG02258.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+1942G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40786349 | |||||||
chr1:40786437 | T | C | 12 | a0001c0001t0001g0031 a0001c0001t0002g0037 a0001c0001t0003g0036 others(9): Show |
12 | HG00140.hp2 HG00642.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.314+2030T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40786437 | |||||||
chr1:40786496 | G | A | 5 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0020g0042 others(2): Show |
5 | HG02132.hp1 HG02165.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+2089G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40786496 | |||||||
chr1:40786537 | A | G | 1 | a0001c0001t0001g0003 | 2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.314+2130A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40786537 | |||||||
chr1:40786745 | G | A | 1 | a0001c0001t0001g0043 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.314+2338G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40786745 | |||||||
chr1:40786754 | G | A | 2 | a0001c0001t0001g0044 a0001c0004t0003g0329 |
2 | HG02155.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.314+2347G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40786754 | |||||||
chr1:40786844 | G | A | 12 | a0001c0001t0001g0029 a0001c0001t0001g0339 a0001c0002t0001g0015 others(9): Show |
13 | HG00639.hp2 HG01069.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.314+2437G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40786844 | |||||||
chr1:40786981 | A | G | 1 | a0001c0001t0003g0252 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.314+2574A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40786981 | |||||||
chr1:40787057 | G | C | 2 | a0001c0002t0001g0016 a0001c0002t0001g0017 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.314+2650G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40787057 | |||||||
chr1:40787110 | G | C | 136 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0027 others(133): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.314+2703G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40787110 | |||||||
chr1:40787114 | C | T | 1 | a0001c0003t0004g0251 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.314+2707C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40787114 | |||||||
chr1:40787513 | A | G | 270 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0020 others(267): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.314+3106A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40787513 | |||||||
chr1:40787587 | G | A | 10 | a0001c0001t0001g0031 a0001c0001t0002g0037 a0001c0001t0003g0036 others(7): Show |
10 | HG00140.hp2 HG00642.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.314+3180G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40787587 | |||||||
chr1:40787636 | T | A | 2 | a0001c0002t0001g0127 a0002c0005t0001g0128 |
2 | HG00738.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.314+3229T>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40787636 | |||||||
chr1:40787668 | G | A | 270 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0020 others(267): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.314+3261G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40787668 | |||||||
chr1:40787704 | C | CTA | 138 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0027 others(135): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.314+3299_314+3300d others(4): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40787704 | ||||||
chr1:40787749 | T | G | 1 | a0001c0002t0001g0333 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.314+3342T>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40787749 | |||||||
chr1:40787750 | G | A | 1 | a0001c0004t0004g0257 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.314+3343G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40787750 | |||||||
chr1:40787750 | G | C | 1 | a0001c0002t0001g0333 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.314+3343G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40787750 | |||||||
chr1:40787779 | G | A | 2 | a0001c0002t0001g0259 a0001c0002t0002g0258 |
2 | HG03669.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.314+3372G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40787779 | |||||||
chr1:40787819 | G | A | 1 | a0001c0002t0001g0133 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.314+3412G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40787819 | |||||||
chr1:40787979 | A | T | 1 | a0001c0002t0001g0250 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.314+3572A>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40787979 | |||||||
chr1:40788083 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0344 a0001c0001t0001g0345 |
4 | HG02976.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+3676C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40788083 | |||||||
chr1:40788152 | G | C | 2 | a0001c0001t0003g0330 a0001c0001t0003g0331 |
2 | NA18957.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.314+3745G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40788152 | |||||||
chr1:40788172 | G | A | 1 | a0001c0002t0001g0030 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.314+3765G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40788172 | |||||||
chr1:40788209 | G | A | 1 | a0001c0002t0001g0129 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.314+3802G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40788209 | |||||||
chr1:40788361 | T | C | 146 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0026 others(143): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.314+3954T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40788361 | |||||||
chr1:40788443 | T | A | 1 | a0001c0002t0001g0141 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.314+4036T>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40788443 | |||||||
chr1:40788611 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.314+4204C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40788611 | |||||||
chr1:40788747 | G | A | 3 | a0001c0002t0001g0142 a0001c0002t0001g0143 a0001c0002t0001g0144 |
3 | NA19002.hp1 NA19057.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.314+4340G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40788747 | |||||||
chr1:40788831 | C | T | 2 | a0001c0001t0001g0355 a0001c0002t0001g0129 |
2 | HG01243.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.314+4424C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40788831 | |||||||
chr1:40789217 | C | A | 1 | a0001c0001t0001g0145 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.314+4810C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40789217 | |||||||
chr1:40789448 | A | C | 74 | a0001c0001t0001g0029 a0001c0001t0001g0054 a0001c0001t0001g0145 others(71): Show |
76 | HG00280.hp2 HG00639.hp2 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.314+5041A>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40789448 | |||||||
chr1:40789457 | T | C | 1 | a0001c0001t0011g0060 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.314+5050T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40789457 | |||||||
chr1:40789559 | T | C | 41 | a0001c0001t0001g0029 a0001c0001t0001g0044 a0001c0001t0001g0054 others(38): Show |
42 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.314+5152T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40789559 | |||||||
chr1:40789656 | C | T | 1 | a0001c0003t0001g0126 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.314+5249C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40789656 | |||||||
chr1:40789715 | C | T | 38 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(35): Show |
40 | HG00639.hp2 HG01069.hp1 HG01123.hp1 others(37): Show |
intron_variant | MODIFIER | c.314+5308C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40789715 | |||||||
chr1:40789804 | A | G | 17 | a0001c0001t0001g0349 a0001c0001t0001g0355 a0001c0001t0002g0037 others(14): Show |
17 | HG00140.hp2 HG00642.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.314+5397A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40789804 | |||||||
chr1:40790079 | G | A | 4 | a0001c0001t0001g0063 a0001c0001t0003g0064 a0001c0001t0003g0065 others(1): Show |
4 | NA18943.hp2 NA18979.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+5672G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40790079 | |||||||
chr1:40790242 | A | G | 1 | a0001c0002t0017g0132 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.314+5835A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40790242 | |||||||
chr1:40790407 | G | A | 1 | a0001c0003t0001g0260 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.314+6000G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40790407 | |||||||
chr1:40790488 | G | A | 3 | a0001c0001t0001g0054 a0001c0001t0001g0326 a0001c0003t0004g0256 |
3 | HG02015.hp2 NA18946.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.314+6081G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40790488 | |||||||
chr1:40790541 | A | C | 13 | a0001c0001t0001g0029 a0001c0001t0001g0339 a0001c0002t0001g0015 others(10): Show |
14 | HG00639.hp2 HG01069.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.314+6134A>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40790541 | |||||||
chr1:40790541 | A | G | 39 | a0001c0001t0001g0044 a0001c0001t0001g0054 a0001c0001t0001g0058 others(36): Show |
39 | HG00140.hp2 HG00642.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.314+6134A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40790541 | |||||||
chr1:40790762 | C | T | 1 | a0001c0001t0002g0125 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.314+6355C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40790762 | |||||||
chr1:40790835 | C | T | 9 | a0001c0001t0002g0055 a0001c0002t0001g0061 a0001c0002t0001g0062 others(6): Show |
9 | HG02723.hp1 HG02818.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.314+6428C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40790835 | |||||||
chr1:40790852 | T | G | 1 | a0001c0001t0001g0149 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.314+6445T>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40790852 | |||||||
chr1:40790874 | G | C | 1 | a0001c0002t0001g0141 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.314+6467G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40790874 | |||||||
chr1:40790951 | G | A | 1 | a0001c0002t0001g0150 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.314+6544G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40790951 | |||||||
chr1:40791000 | C | T | 1 | a0001c0002t0001g0212 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.314+6593C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40791000 | |||||||
chr1:40791052 | C | T | 1 | a0001c0002t0001g0325 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.314+6645C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40791052 | |||||||
chr1:40791252 | G | A | 2 | a0001c0001t0001g0355 a0001c0002t0001g0129 |
2 | HG01243.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.314+6845G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40791252 | |||||||
chr1:40791267 | G | A | 4 | a0001c0001t0001g0029 a0001c0002t0001g0333 a0001c0002t0001g0334 others(1): Show |
4 | HG00639.hp2 HG02109.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+6860G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40791267 | |||||||
chr1:40791320 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.314+6913A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40791320 | |||||||
chr1:40791533 | G | T | 1 | a0001c0002t0001g0353 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.314+7126G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40791533 | |||||||
chr1:40791537 | A | G | 41 | a0001c0001t0001g0029 a0001c0001t0001g0058 a0001c0001t0001g0339 others(38): Show |
42 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.314+7130A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40791537 | |||||||
chr1:40791771 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.314+7364G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40791771 | |||||||
chr1:40791938 | G | A | 2 | a0001c0002t0001g0030 a0001c0008t0003g0032 |
2 | HG03704.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.314+7531G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40791938 | |||||||
chr1:40791969 | C | T | 2 | a0001c0002t0001g0210 a0001c0002t0001g0211 |
2 | NA18967.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.314+7562C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40791969 | |||||||
chr1:40792068 | T | C | 13 | a0001c0001t0001g0349 a0001c0001t0002g0055 a0001c0001t0003g0347 others(10): Show |
13 | HG02258.hp1 HG02723.hp1 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.314+7661T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40792068 | |||||||
chr1:40792145 | G | C | 1 | a0001c0002t0017g0132 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.314+7738G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40792145 | |||||||
chr1:40792145 | G | T | 1 | a0001c0002t0006g0229 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.314+7738G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40792145 | |||||||
chr1:40792240 | A | G | 28 | a0001c0001t0001g0029 a0001c0001t0001g0058 a0001c0001t0001g0339 others(25): Show |
29 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.314+7833A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40792240 | |||||||
chr1:40792454 | G | A | 1 | a0001c0002t0001g0127 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.314+8047G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40792454 | |||||||
chr1:40792540 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.314+8133G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40792540 | |||||||
chr1:40792648 | G | A | 6 | a0001c0001t0002g0055 a0001c0002t0002g0340 a0001c0002t0002g0341 others(3): Show |
6 | HG02818.hp2 HG02895.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.314+8241G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40792648 | |||||||
chr1:40792677 | C | T | 1 | a0002c0005t0001g0324 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.314+8270C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40792677 | |||||||
chr1:40792739 | G | A | 1 | a0001c0003t0001g0261 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.314+8332G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40792739 | |||||||
chr1:40792894 | G | T | 1 | a0002c0012t0001g0323 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.314+8487G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40792894 | |||||||
chr1:40792989 | T | C | 19 | a0001c0001t0001g0029 a0001c0001t0001g0058 a0001c0001t0001g0339 others(16): Show |
20 | HG00639.hp2 HG01069.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.314+8582T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40792989 | |||||||
chr1:40793004 | C | CT | 79 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0044 others(76): Show |
81 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(78): Show |
intron_variant | MODIFIER | c.314+8617dupT | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40793004 | ||||||
chr1:40793004 | C | CTT | 59 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0031 others(56): Show |
60 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.314+8616_314+8617d others(4): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40793004 | ||||||
chr1:40793004 | C | CTTT | 6 | a0001c0001t0001g0339 a0001c0001t0001g0349 a0001c0002t0001g0133 others(3): Show |
6 | HG01978.hp2 HG02615.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.314+8615_314+8617d others(5): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40793004 | ||||||
chr1:40793004 | C | T | 2 | a0001c0001t0001g0332 a0001c0001t0003g0331 |
2 | NA18966.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.314+8597C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40793004 | |||||||
chr1:40793004 | CT | C | 6 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0002t0001g0052 others(3): Show |
6 | HG01517.hp2 HG02818.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.314+8617delT | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40793004 | ||||||
chr1:40793004 | CTTTTTTT others(4): Show |
C | 1 | a0001c0003t0002g0283 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.314+8607_314+8617d others(13): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40793004 | ||||||
chr1:40793008 | T | C | 8 | a0001c0001t0001g0262 a0001c0001t0001g0264 a0001c0001t0004g0011 others(5): Show |
9 | HG00408.hp2 HG02922.hp2 NA18973.hp1 others(6): Show |
intron_variant | MODIFIER | c.314+8601T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40793008 | |||||||
chr1:40793047 | C | G | 2 | a0001c0002t0001g0352 a0001c0002t0001g0353 |
2 | HG03471.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.314+8640C>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40793047 | |||||||
chr1:40793049 | C | A | 1 | a0001c0001t0003g0330 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.314+8642C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40793049 | |||||||
chr1:40793312 | C | T | 101 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0021 others(98): Show |
104 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.314+8905C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40793312 | |||||||
chr1:40793348 | T | C | 8 | a0001c0001t0002g0055 a0001c0002t0001g0061 a0001c0002t0001g0062 others(5): Show |
8 | HG02818.hp2 HG02895.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.314+8941T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40793348 | |||||||
chr1:40793520 | G | A | 2 | a0001c0001t0001g0044 a0001c0004t0003g0329 |
2 | HG02155.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.314+9113G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40793520 | |||||||
chr1:40793606 | TC | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0344 a0001c0001t0001g0345 |
4 | HG02976.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+9201delC | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40793606 | ||||||
chr1:40793629 | T | C | 1 | a0001c0002t0001g0156 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.314+9222T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40793629 | |||||||
chr1:40793917 | G | C | 3 | a0001c0001t0001g0044 a0001c0001t0001g0063 a0001c0004t0003g0329 |
3 | HG02155.hp2 NA19009.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.314+9510G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40793917 | |||||||
chr1:40793921 | G | A | 2 | a0001c0002t0001g0040 a0001c0002t0001g0041 |
2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.314+9514G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40793921 | |||||||
chr1:40793946 | A | G | 1 | a0001c0004t0001g0321 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.314+9539A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40793946 | |||||||
chr1:40793955 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.314+9548G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40793955 | |||||||
chr1:40794289 | A | T | 1 | a0001c0002t0019g0056 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.314+9882A>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40794289 | |||||||
chr1:40794294 | C | T | 1 | a0001c0002t0001g0209 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.314+9887C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40794294 | |||||||
chr1:40794374 | C | T | 1 | a0001c0002t0002g0226 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.314+9967C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40794374 | |||||||
chr1:40794394 | C | T | 2 | a0001c0002t0001g0052 a0001c0002t0013g0053 |
2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.314+9987C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40794394 | |||||||
chr1:40794439 | A | C | 2 | a0001c0002t0001g0040 a0001c0002t0001g0041 |
2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.314+10032A>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40794439 | |||||||
chr1:40794456 | G | A | 1 | a0001c0002t0001g0016 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.314+10049G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40794456 | |||||||
chr1:40794496 | C | T | 208 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(205): Show |
219 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.314+10089C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40794496 | |||||||
chr1:40794520 | G | A | 2 | a0001c0002t0001g0061 a0001c0002t0001g0062 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.314+10113G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40794520 | |||||||
chr1:40794555 | C | T | 4 | a0001c0001t0001g0029 a0001c0002t0001g0333 a0001c0002t0001g0334 others(1): Show |
4 | HG00639.hp2 HG02109.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+10148C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40794555 | |||||||
chr1:40794727 | T | C | 8 | a0001c0001t0001g0072 a0001c0003t0001g0282 a0001c0003t0001g0284 others(5): Show |
9 | HG00609.hp1 HG01934.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.314+10320T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40794727 | |||||||
chr1:40794946 | G | A | 1 | a0001c0002t0001g0052 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.314+10539G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40794946 | |||||||
chr1:40794963 | G | GGCAAA | 3 | a0001c0001t0001g0339 a0001c0002t0001g0337 a0001c0002t0001g0338 |
3 | HG02615.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.314+10557_314+1055 others(9): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40794963 | ||||||
chr1:40794965 | T | C | 1 | a0001c0001t0002g0012 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.314+10558T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40794965 | |||||||
chr1:40795226 | G | A | 1 | a0001c0002t0001g0048 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.314+10819G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40795226 | |||||||
chr1:40795255 | C | CT | 18 | a0001c0001t0001g0074 a0001c0001t0001g0262 a0001c0001t0001g0264 others(15): Show |
18 | HG00140.hp2 HG00408.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.314+10866dupT | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40795255 | ||||||
chr1:40795255 | C | CTT | 219 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(216): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.314+10865_314+1086 others(6): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40795255 | ||||||
chr1:40795343 | C | T | 1 | a0001c0002t0001g0156 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.314+10936C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40795343 | |||||||
chr1:40795373 | TGCCTCA | T | 5 | a0001c0003t0004g0271 a0001c0003t0004g0272 a0001c0004t0001g0269 others(2): Show |
5 | HG00621.hp2 HG02155.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+10971_314+1097 others(10): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40795373 | ||||||
chr1:40795400 | C | T | 119 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0021 others(116): Show |
123 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.314+10993C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40795400 | |||||||
chr1:40795515 | G | A | 2 | a0001c0003t0001g0157 a0001c0003t0001g0267 |
2 | HG01167.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.314+11108G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40795515 | |||||||
chr1:40795662 | C | T | 1 | a0001c0006t0001g0121 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.314+11255C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40795662 | |||||||
chr1:40795786 | C | G | 2 | a0001c0002t0001g0061 a0001c0002t0001g0062 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.314+11379C>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40795786 | |||||||
chr1:40795858 | T | C | 3 | a0001c0003t0003g0279 a0001c0003t0003g0281 a0001c0003t0009g0280 |
3 | NA18962.hp2 NA19007.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.314+11451T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40795858 | |||||||
chr1:40796025 | T | C | 1 | a0001c0001t0003g0075 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.314+11618T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40796025 | |||||||
chr1:40796040 | G | C | 25 | a0001c0001t0001g0021 a0001c0001t0001g0130 a0001c0001t0001g0131 others(22): Show |
26 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.314+11633G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40796040 | |||||||
chr1:40796108 | G | A | 2 | a0001c0002t0001g0061 a0001c0002t0001g0062 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.314+11701G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40796108 | |||||||
chr1:40796214 | G | A | 224 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(221): Show |
235 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.314+11807G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40796214 | |||||||
chr1:40796264 | T | C | 4 | a0001c0001t0001g0029 a0001c0002t0001g0333 a0001c0002t0001g0334 others(1): Show |
4 | HG00639.hp2 HG02109.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+11857T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40796264 | |||||||
chr1:40796315 | T | C | 1 | a0001c0002t0019g0056 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.314+11908T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40796315 | |||||||
chr1:40796346 | C | T | 97 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0026 others(94): Show |
100 | HG00323.hp1 HG00558.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.314+11939C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40796346 | |||||||
chr1:40796459 | G | C | 3 | a0001c0002t0001g0015 a0001c0002t0001g0336 a0001c0002t0001g0351 |
4 | HG01069.hp1 HG03540.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.314+12052G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40796459 | |||||||
chr1:40796534 | T | C | 6 | a0001c0002t0001g0161 a0001c0002t0002g0340 a0001c0002t0002g0341 others(3): Show |
6 | HG02818.hp2 HG02895.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.314+12127T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40796534 | |||||||
chr1:40796601 | T | G | 354 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(351): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.314+12194T>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40796601 | |||||||
chr1:40796643 | G | A | 2 | a0001c0002t0001g0040 a0001c0002t0001g0041 |
2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.314+12236G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40796643 | |||||||
chr1:40796685 | G | A | 2 | a0001c0002t0001g0163 a0001c0002t0014g0162 |
2 | HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.314+12278G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40796685 | |||||||
chr1:40796769 | T | G | 5 | a0001c0003t0004g0271 a0001c0003t0004g0272 a0001c0004t0001g0269 others(2): Show |
5 | HG00621.hp2 HG02155.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+12362T>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40796769 | |||||||
chr1:40796833 | G | C | 4 | a0001c0001t0001g0054 a0001c0001t0001g0326 a0001c0002t0003g0268 others(1): Show |
4 | HG02015.hp2 HG02083.hp1 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.314+12426G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40796833 | |||||||
chr1:40796868 | A | T | 1 | a0001c0002t0001g0120 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.314+12461A>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40796868 | |||||||
chr1:40796915 | C | CAAAT | 171 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(168): Show |
180 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.314+12542_314+1254 others(8): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40796915 | ||||||
chr1:40796915 | C | CAAATAAA others(1): Show |
55 | a0001c0001t0001g0068 a0001c0001t0001g0074 a0001c0001t0001g0076 others(52): Show |
57 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.314+12538_314+1254 others(12): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40796915 | ||||||
chr1:40796915 | CAAAT | C | 73 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0026 others(70): Show |
75 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.314+12542_314+1254 others(8): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40796915 | ||||||
chr1:40796915 | CAAATAAA others(1): Show |
C | 9 | a0001c0001t0001g0118 a0001c0001t0001g0146 a0001c0001t0001g0147 others(6): Show |
9 | HG00642.hp2 HG00735.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.314+12538_314+1254 others(12): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40796915 | ||||||
chr1:40796992 | G | A | 5 | a0001c0002t0001g0133 a0001c0002t0001g0142 a0001c0002t0001g0143 others(2): Show |
5 | NA18747.hp1 NA19002.hp1 NA19057.hp2 others(2): Show |
intron_variant | MODIFIER | c.314+12585G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40796992 | |||||||
chr1:40797045 | T | G | 1 | a0001c0001t0002g0166 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.314+12638T>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40797045 | |||||||
chr1:40797141 | G | A | 2 | a0001c0001t0001g0292 a0001c0002t0001g0291 |
2 | HG01106.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.314+12734G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40797141 | |||||||
chr1:40797155 | A | G | 2 | a0001c0002t0001g0061 a0001c0002t0001g0062 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.314+12748A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40797155 | |||||||
chr1:40797776 | C | T | 1 | a0001c0002t0001g0052 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.314+13369C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40797776 | |||||||
chr1:40797954 | G | T | 2 | a0001c0001t0001g0058 a0001c0002t0018g0057 |
2 | HG01884.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.314+13547G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40797954 | |||||||
chr1:40798122 | T | C | 111 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0026 others(108): Show |
115 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.314+13715T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40798122 | |||||||
chr1:40798340 | C | T | 108 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0026 others(105): Show |
112 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.314+13933C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40798340 | |||||||
chr1:40798436 | A | T | 4 | a0001c0001t0001g0349 a0001c0001t0003g0347 a0001c0001t0003g0348 others(1): Show |
4 | HG02258.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+14029A>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40798436 | |||||||
chr1:40798456 | G | A | 1 | a0001c0003t0001g0293 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.314+14049G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40798456 | |||||||
chr1:40798520 | A | G | 112 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0026 others(109): Show |
116 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.314+14113A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40798520 | |||||||
chr1:40798692 | G | A | 1 | a0002c0005t0001g0324 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.314+14285G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40798692 | |||||||
chr1:40798826 | C | T | 5 | a0001c0001t0001g0054 a0001c0001t0001g0145 a0001c0001t0001g0326 others(2): Show |
5 | HG02015.hp2 HG02083.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+14419C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40798826 | |||||||
chr1:40798961 | G | T | 221 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(218): Show |
232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.314+14554G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40798961 | |||||||
chr1:40799159 | C | G | 3 | a0001c0002t0001g0014 a0001c0002t0002g0319 a0004c0015t0001g0014 |
3 | HG01123.hp2 HG01256.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.314+14752C>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40799159 | |||||||
chr1:40799286 | G | A | 2 | a0001c0002t0001g0210 a0001c0002t0001g0211 |
2 | NA18967.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.314+14879G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40799286 | |||||||
chr1:40799338 | T | C | 1 | a0001c0001t0001g0328 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.314+14931T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40799338 | |||||||
chr1:40799432 | G | GC | 104 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0026 others(101): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.314+15034dupC | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40799432 | ||||||
chr1:40799432 | G | GCC | 17 | a0001c0001t0001g0205 a0001c0001t0002g0055 a0001c0001t0002g0166 others(14): Show |
17 | HG00597.hp1 HG01192.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.314+15033_314+1503 others(6): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40799432 | ||||||
chr1:40799437 | C | G | 2 | a0001c0001t0003g0114 a0001c0002t0019g0056 |
2 | HG00639.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.314+15030C>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40799437 | |||||||
chr1:40799437 | C | T | 3 | a0001c0001t0001g0149 a0001c0002t0001g0052 a0001c0002t0013g0053 |
3 | HG02451.hp1 HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.314+15030C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40799437 | |||||||
chr1:40799438 | C | A | 6 | a0001c0001t0001g0349 a0001c0001t0003g0347 a0001c0001t0003g0348 others(3): Show |
6 | HG02258.hp1 HG02886.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.314+15031C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40799438 | |||||||
chr1:40799439 | C | G | 4 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0011t0002g0233 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+15032C>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40799439 | |||||||
chr1:40799440 | C | G | 4 | a0001c0001t0001g0002 a0001c0004t0001g0019 a0001c0009t0001g0113 others(1): Show |
5 | NA18952.hp2 NA18995.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+15033C>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40799440 | |||||||
chr1:40799569 | T | G | 127 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0021 others(124): Show |
131 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.314+15162T>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40799569 | |||||||
chr1:40799578 | T | C | 225 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(222): Show |
236 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.314+15171T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40799578 | |||||||
chr1:40799579 | G | A | 1 | a0001c0003t0001g0295 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.314+15172G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40799579 | |||||||
chr1:40799620 | C | T | 2 | a0001c0001t0001g0248 a0001c0001t0002g0247 |
2 | NA19085.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.314+15213C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40799620 | |||||||
chr1:40799621 | G | A | 2 | a0001c0002t0001g0061 a0001c0002t0001g0062 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.314+15214G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40799621 | |||||||
chr1:40799669 | C | G | 1 | a0001c0002t0001g0015 | 2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.314+15262C>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40799669 | |||||||
chr1:40799728 | C | T | 1 | a0001c0001t0003g0064 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.314+15321C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40799728 | |||||||
chr1:40799745 | G | T | 1 | a0001c0001t0001g0149 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.314+15338G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40799745 | |||||||
chr1:40799781 | A | G | 127 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0021 others(124): Show |
131 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.314+15374A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40799781 | |||||||
chr1:40799954 | C | T | 102 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0051 others(99): Show |
106 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.314+15547C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40799954 | |||||||
chr1:40800005 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.314+15598G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40800005 | |||||||
chr1:40800236 | A | G | 127 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0021 others(124): Show |
131 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.314+15829A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40800236 | |||||||
chr1:40800264 | G | A | 2 | a0001c0001t0003g0036 a0001c0001t0003g0038 |
2 | HG00140.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.314+15857G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40800264 | |||||||
chr1:40800276 | C | G | 7 | a0001c0001t0003g0001 a0001c0001t0003g0108 a0001c0001t0003g0110 others(4): Show |
10 | HG00639.hp1 HG00741.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.314+15869C>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40800276 | |||||||
chr1:40800438 | T | C | 4 | a0001c0001t0001g0349 a0001c0001t0003g0347 a0001c0001t0003g0348 others(1): Show |
4 | HG02258.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+16031T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40800438 | |||||||
chr1:40800727 | T | C | 2 | a0001c0002t0001g0209 a0001c0002t0001g0322 |
2 | HG00099.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.314+16320T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40800727 | |||||||
chr1:40800848 | G | C | 127 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0021 others(124): Show |
131 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.315-16417G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40800848 | |||||||
chr1:40800877 | G | A | 3 | a0001c0002t0001g0015 a0001c0002t0001g0336 a0001c0002t0001g0351 |
4 | HG01069.hp1 HG03540.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.315-16388G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40800877 | |||||||
chr1:40801059 | G | A | 1 | a0002c0012t0001g0018 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.315-16206G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40801059 | |||||||
chr1:40801097 | G | T | 1 | a0001c0006t0001g0121 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.315-16168G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40801097 | |||||||
chr1:40801397 | C | A | 1 | a0001c0001t0003g0115 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.315-15868C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40801397 | |||||||
chr1:40801553 | T | C | 4 | a0001c0001t0001g0029 a0001c0002t0001g0333 a0001c0002t0001g0334 others(1): Show |
4 | HG00639.hp2 HG02109.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-15712T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40801553 | |||||||
chr1:40801586 | C | T | 222 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(219): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.315-15679C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40801586 | |||||||
chr1:40801807 | G | T | 1 | a0001c0002t0002g0196 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.315-15458G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40801807 | |||||||
chr1:40801963 | G | T | 1 | a0001c0002t0001g0333 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.315-15302G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40801963 | |||||||
chr1:40802104 | C | T | 2 | a0001c0002t0001g0141 a0001c0004t0005g0165 |
2 | HG01255.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.315-15161C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40802104 | |||||||
chr1:40802154 | CTG | C | 5 | a0001c0003t0004g0271 a0001c0003t0004g0272 a0001c0004t0001g0269 others(2): Show |
5 | HG00621.hp2 HG02155.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.315-15110_315-1510 others(6): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40802154 | |||||||
chr1:40802405 | C | T | 8 | a0001c0001t0001g0021 a0001c0001t0001g0130 a0001c0001t0001g0131 others(5): Show |
8 | HG01069.hp2 HG01071.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.315-14860C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40802405 | |||||||
chr1:40802406 | G | C | 2 | a0001c0001t0001g0054 a0001c0002t0006g0170 |
2 | HG02572.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.315-14859G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40802406 | |||||||
chr1:40802428 | T | C | 354 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(351): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.315-14837T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40802428 | |||||||
chr1:40802430 | G | C | 1 | a0001c0001t0003g0036 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.315-14835G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40802430 | |||||||
chr1:40802471 | T | C | 1 | a0009c0017t0001g0200 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.315-14794T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40802471 | |||||||
chr1:40802477 | T | A | 1 | a0001c0001t0003g0036 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.315-14788T>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40802477 | |||||||
chr1:40802612 | G | C | 4 | a0001c0001t0001g0349 a0001c0001t0003g0347 a0001c0001t0003g0348 others(1): Show |
4 | HG02258.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-14653G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40802612 | |||||||
chr1:40802642 | G | A | 101 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0021 others(98): Show |
104 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.315-14623G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40802642 | |||||||
chr1:40802853 | C | T | 85 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0043 others(82): Show |
90 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.315-14412C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40802853 | |||||||
chr1:40802894 | A | G | 344 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(341): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.315-14371A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40802894 | |||||||
chr1:40802901 | C | G | 1 | a0001c0002t0001g0195 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.315-14364C>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40802901 | |||||||
chr1:40802970 | C | T | 1 | a0001c0003t0004g0286 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.315-14295C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40802970 | |||||||
chr1:40803081 | T | C | 5 | a0001c0003t0004g0271 a0001c0003t0004g0272 a0001c0004t0001g0269 others(2): Show |
5 | HG00621.hp2 HG02155.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.315-14184T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40803081 | |||||||
chr1:40803135 | T | C | 15 | a0001c0001t0001g0029 a0001c0001t0001g0349 a0001c0001t0003g0347 others(12): Show |
15 | HG00639.hp2 HG00642.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.315-14130T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40803135 | |||||||
chr1:40803231 | C | A | 1 | a0001c0001t0001g0145 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.315-14034C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40803231 | |||||||
chr1:40803373 | C | T | 2 | a0001c0002t0013g0053 a0001c0002t0017g0132 |
2 | HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.315-13892C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40803373 | |||||||
chr1:40803567 | A | G | 160 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0021 others(157): Show |
164 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.315-13698A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40803567 | |||||||
chr1:40803594 | C | T | 3 | a0001c0001t0001g0058 a0001c0002t0016g0045 a0001c0002t0018g0057 |
3 | HG01884.hp2 HG01943.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.315-13671C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40803594 | |||||||
chr1:40804148 | T | G | 1 | a0001c0003t0001g0293 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.315-13117T>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40804148 | |||||||
chr1:40804410 | A | G | 9 | a0001c0001t0001g0021 a0001c0001t0001g0130 a0001c0001t0001g0131 others(6): Show |
9 | HG01069.hp2 HG01071.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.315-12855A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40804410 | |||||||
chr1:40804491 | T | A | 84 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0026 others(81): Show |
86 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.315-12774T>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40804491 | |||||||
chr1:40804570 | C | A | 5 | a0001c0003t0004g0271 a0001c0003t0004g0272 a0001c0004t0001g0269 others(2): Show |
5 | HG00621.hp2 HG02155.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.315-12695C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40804570 | |||||||
chr1:40804642 | C | A | 84 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0026 others(81): Show |
86 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.315-12623C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40804642 | |||||||
chr1:40804674 | C | T | 83 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0026 others(80): Show |
85 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.315-12591C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40804674 | |||||||
chr1:40804733 | G | A | 1 | a0001c0002t0001g0127 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.315-12532G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40804733 | |||||||
chr1:40804817 | C | CA | 141 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0027 others(138): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.315-12428dupA | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40804817 | ||||||
chr1:40804817 | C | CAA | 10 | a0001c0001t0001g0146 a0001c0001t0002g0241 a0001c0003t0001g0274 others(7): Show |
10 | HG00642.hp2 HG02071.hp2 NA18944.hp1 others(7): Show |
intron_variant | MODIFIER | c.315-12429_315-1242 others(6): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40804817 | ||||||
chr1:40804817 | CA | C | 7 | a0001c0001t0001g0107 a0001c0001t0001g0204 a0001c0002t0001g0025 others(4): Show |
7 | HG00323.hp2 HG01257.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.315-12428delA | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40804817 | ||||||
chr1:40805044 | C | T | 1 | a0001c0001t0003g0036 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.315-12221C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40805044 | |||||||
chr1:40805127 | C | T | 1 | a0001c0002t0001g0158 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.315-12138C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40805127 | |||||||
chr1:40805159 | AAAAC | A | 109 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0058 others(106): Show |
114 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.315-12090_315-1208 others(8): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40805159 | ||||||
chr1:40805265 | A | G | 86 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0026 others(83): Show |
88 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.315-12000A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40805265 | |||||||
chr1:40805330 | C | A | 1 | a0001c0001t0001g0181 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.315-11935C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40805330 | |||||||
chr1:40805481 | T | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(117): Show |
127 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.315-11784T>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40805481 | |||||||
chr1:40805579 | T | C | 95 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0026 others(92): Show |
97 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.315-11686T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40805579 | |||||||
chr1:40805634 | G | C | 1 | a0001c0003t0001g0278 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.315-11631G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40805634 | |||||||
chr1:40805635 | GA | G | 128 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0027 others(125): Show |
134 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.315-11629delA | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40805635 | |||||||
chr1:40805636 | A | G | 2 | a0001c0001t0001g0253 a0001c0002t0016g0045 |
2 | HG02970.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.315-11629A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40805636 | |||||||
chr1:40805650 | C | T | 86 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0026 others(83): Show |
88 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.315-11615C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40805650 | |||||||
chr1:40805716 | G | C | 1 | a0001c0004t0001g0269 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.315-11549G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40805716 | |||||||
chr1:40805761 | T | C | 1 | a0001c0002t0014g0162 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.315-11504T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40805761 | |||||||
chr1:40805768 | G | T | 1 | a0001c0001t0001g0076 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.315-11497G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40805768 | |||||||
chr1:40805844 | AT | A | 8 | a0001c0001t0001g0230 a0001c0001t0002g0089 a0001c0002t0001g0142 others(5): Show |
8 | HG01168.hp2 HG03239.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.315-11406delT | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40805844 | ||||||
chr1:40805852 | T | C | 21 | a0001c0001t0001g0054 a0001c0001t0001g0145 a0001c0001t0001g0171 others(18): Show |
21 | HG00140.hp1 HG00735.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.315-11413T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40805852 | |||||||
chr1:40805942 | C | T | 3 | a0001c0002t0001g0014 a0001c0002t0002g0319 a0004c0015t0001g0014 |
3 | HG01123.hp2 HG01256.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.315-11323C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40805942 | |||||||
chr1:40806032 | G | A | 1 | a0001c0003t0001g0176 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.315-11233G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40806032 | |||||||
chr1:40806043 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | NA18993.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.315-11222G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40806043 | |||||||
chr1:40806077 | G | A | 84 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0026 others(81): Show |
86 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.315-11188G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40806077 | |||||||
chr1:40806084 | G | A | 68 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0001g0292 others(65): Show |
70 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.315-11181G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40806084 | |||||||
chr1:40806296 | C | T | 116 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(113): Show |
123 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.315-10969C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40806296 | |||||||
chr1:40806577 | G | A | 63 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0026 others(60): Show |
65 | HG00099.hp1 HG00323.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.315-10688G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40806577 | |||||||
chr1:40806587 | A | T | 65 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0026 others(62): Show |
67 | HG00099.hp1 HG00323.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.315-10678A>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40806587 | |||||||
chr1:40806676 | A | G | 1 | a0001c0002t0019g0056 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.315-10589A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40806676 | |||||||
chr1:40806699 | G | GAGA | 218 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0020 others(215): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.315-10564_315-1056 others(7): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40806699 | ||||||
chr1:40806861 | C | T | 83 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0026 others(80): Show |
85 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.315-10404C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40806861 | |||||||
chr1:40807110 | T | G | 1 | a0001c0002t0002g0168 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.315-10155T>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40807110 | |||||||
chr1:40807131 | C | T | 1 | a0001c0002t0001g0106 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.315-10134C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40807131 | |||||||
chr1:40807233 | A | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0043 others(74): Show |
82 | HG00408.hp1 HG00558.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.315-10032A>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40807233 | |||||||
chr1:40807291 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.315-9974G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40807291 | |||||||
chr1:40807391 | C | A | 2 | a0001c0004t0002g0134 a0001c0004t0002g0135 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.315-9874C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40807391 | |||||||
chr1:40807473 | T | TC | 20 | a0001c0001t0001g0218 a0001c0002t0001g0016 a0001c0002t0001g0017 others(17): Show |
20 | HG00280.hp2 HG00323.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.315-9792_315-9791i others(3): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40807473 | |||||||
chr1:40807962 | C | CA | 94 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0026 others(91): Show |
96 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.315-9295dupA | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40807962 | ||||||
chr1:40808007 | TGAGGCAG others(44): Show |
T | 5 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 others(2): Show |
5 | HG00639.hp2 HG00642.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.315-9257_315-9207d others(53): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40808007 | |||||||
chr1:40808257 | C | T | 1 | a0001c0001t0001g0339 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.315-9008C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40808257 | |||||||
chr1:40808509 | T | C | 1 | a0001c0003t0003g0087 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.315-8756T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40808509 | |||||||
chr1:40808750 | C | T | 83 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0026 others(80): Show |
85 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.315-8515C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40808750 | |||||||
chr1:40808781 | TCTC | T | 7 | a0001c0001t0001g0029 a0001c0002t0001g0033 a0001c0002t0001g0034 others(4): Show |
7 | HG00639.hp2 HG00642.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.315-8481_315-8479d others(5): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40808781 | ||||||
chr1:40808815 | G | A | 2 | a0001c0002t0001g0337 a0001c0002t0001g0338 |
2 | HG02615.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.315-8450G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40808815 | |||||||
chr1:40808875 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.315-8390C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40808875 | |||||||
chr1:40808999 | CT | C | 7 | a0001c0001t0001g0029 a0001c0002t0001g0033 a0001c0002t0001g0034 others(4): Show |
7 | HG00639.hp2 HG00642.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.315-8264delT | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40808999 | ||||||
chr1:40809017 | C | A | 7 | a0001c0001t0001g0029 a0001c0002t0001g0033 a0001c0002t0001g0034 others(4): Show |
7 | HG00639.hp2 HG00642.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.315-8248C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40809017 | |||||||
chr1:40809059 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.315-8206A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40809059 | |||||||
chr1:40809073 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.315-8192G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40809073 | |||||||
chr1:40809322 | C | G | 1 | a0001c0001t0003g0112 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.315-7943C>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40809322 | |||||||
chr1:40809422 | C | T | 5 | a0001c0002t0001g0015 a0001c0002t0001g0040 a0001c0002t0001g0041 others(2): Show |
6 | HG01069.hp1 HG02145.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.315-7843C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40809422 | |||||||
chr1:40809440 | C | T | 1 | a0002c0005t0002g0315 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.315-7825C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40809440 | |||||||
chr1:40809466 | G | A | 1 | a0001c0002t0001g0127 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.315-7799G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40809466 | |||||||
chr1:40809494 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.315-7771A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40809494 | |||||||
chr1:40809647 | G | C | 116 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0058 others(113): Show |
121 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.315-7618G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40809647 | |||||||
chr1:40809802 | C | G | 124 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0027 others(121): Show |
129 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.315-7463C>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40809802 | |||||||
chr1:40809818 | A | G | 1 | a0001c0002t0019g0056 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.315-7447A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40809818 | |||||||
chr1:40809926 | G | A | 1 | a0001c0003t0001g0155 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.315-7339G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40809926 | |||||||
chr1:40809936 | G | T | 124 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0027 others(121): Show |
129 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.315-7329G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40809936 | |||||||
chr1:40809957 | C | T | 16 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0002g0198 others(13): Show |
16 | HG00140.hp1 HG00735.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.315-7308C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40809957 | |||||||
chr1:40810059 | C | CA | 218 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(215): Show |
228 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.315-7195dupA | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40810059 | ||||||
chr1:40810059 | C | CAA | 127 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0027 others(124): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.315-7196_315-7195d others(4): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40810059 | ||||||
chr1:40810392 | C | T | 1 | a0001c0004t0001g0289 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.315-6873C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40810392 | |||||||
chr1:40810401 | C | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(117): Show |
127 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.315-6864C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40810401 | |||||||
chr1:40810516 | A | G | 218 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0020 others(215): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.315-6749A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40810516 | |||||||
chr1:40810543 | G | A | 1 | a0001c0002t0001g0322 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.315-6722G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40810543 | |||||||
chr1:40810567 | AC | A | 13 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0181 others(10): Show |
14 | HG01243.hp2 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.315-6693delC | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40810567 | ||||||
chr1:40810624 | A | G | 3 | a0001c0002t0001g0224 a0001c0002t0001g0296 a0001c0002t0002g0223 |
3 | HG00280.hp2 HG00323.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.315-6641A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40810624 | |||||||
chr1:40810703 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.315-6562G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40810703 | |||||||
chr1:40810746 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.315-6519C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40810746 | |||||||
chr1:40810747 | G | A | 2 | a0001c0003t0001g0274 a0001c0003t0001g0275 |
2 | NA18944.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.315-6518G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40810747 | |||||||
chr1:40810987 | T | A | 1 | a0001c0003t0001g0236 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.315-6278T>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40810987 | |||||||
chr1:40811222 | A | G | 346 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(343): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.315-6043A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40811222 | |||||||
chr1:40811315 | G | A | 9 | a0001c0001t0001g0029 a0001c0002t0001g0033 a0001c0002t0001g0034 others(6): Show |
9 | HG00639.hp2 HG00642.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.315-5950G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40811315 | |||||||
chr1:40811320 | T | C | 1 | a0001c0002t0001g0322 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.315-5945T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40811320 | |||||||
chr1:40811602 | T | A | 3 | a0001c0002t0001g0040 a0001c0002t0001g0041 a0001c0002t0018g0057 |
3 | HG01943.hp1 HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.315-5663T>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40811602 | |||||||
chr1:40811653 | T | C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0027 others(129): Show |
137 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.315-5612T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40811653 | |||||||
chr1:40811702 | T | G | 1 | a0001c0003t0001g0290 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.315-5563T>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40811702 | |||||||
chr1:40811759 | G | C | 3 | a0001c0002t0001g0040 a0001c0002t0001g0041 a0001c0002t0018g0057 |
3 | HG01943.hp1 HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.315-5506G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40811759 | |||||||
chr1:40811877 | C | G | 91 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(88): Show |
98 | HG00408.hp1 HG00558.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.315-5388C>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40811877 | |||||||
chr1:40811902 | T | A | 5 | a0001c0001t0001g0027 a0001c0001t0001g0355 a0001c0002t0001g0337 others(2): Show |
5 | HG02572.hp2 HG02615.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.315-5363T>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40811902 | |||||||
chr1:40811929 | G | A | 108 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(105): Show |
115 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.315-5336G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40811929 | |||||||
chr1:40811960 | T | A | 148 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0020 others(145): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.315-5305T>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40811960 | |||||||
chr1:40812004 | C | A | 1 | a0001c0002t0001g0049 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.315-5261C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40812004 | |||||||
chr1:40812197 | C | T | 3 | a0001c0003t0001g0285 a0001c0003t0001g0294 a0001c0003t0001g0295 |
3 | HG00597.hp2 HG02132.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.315-5068C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40812197 | |||||||
chr1:40812360 | G | A | 3 | a0001c0002t0001g0152 a0001c0002t0001g0153 a0001c0002t0001g0212 |
3 | HG01891.hp1 HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.315-4905G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40812360 | |||||||
chr1:40812415 | C | A | 1 | a0001c0002t0001g0052 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.315-4850C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40812415 | |||||||
chr1:40812551 | C | T | 2 | a0001c0002t0001g0040 a0001c0002t0001g0041 |
2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.315-4714C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40812551 | |||||||
chr1:40812552 | G | A | 42 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0177 others(39): Show |
46 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.315-4713G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40812552 | |||||||
chr1:40812559 | G | A | 1 | a0001c0002t0018g0057 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.315-4706G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40812559 | |||||||
chr1:40812615 | C | T | 1 | a0001c0002t0001g0221 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.315-4650C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40812615 | |||||||
chr1:40813254 | C | T | 3 | a0001c0001t0004g0011 a0001c0001t0004g0265 a0001c0001t0004g0266 |
4 | NA18973.hp1 NA19010.hp2 NA19087.hp2 others(1): Show |
intron_variant | MODIFIER | c.315-4011C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40813254 | |||||||
chr1:40813365 | G | A | 76 | a0001c0001t0001g0029 a0001c0001t0001g0171 a0001c0001t0001g0172 others(73): Show |
76 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.315-3900G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40813365 | |||||||
chr1:40813456 | G | C | 1 | a0001c0002t0019g0056 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.315-3809G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40813456 | |||||||
chr1:40813634 | C | T | 2 | a0001c0001t0001g0091 a0001c0002t0002g0196 |
2 | NA18747.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.315-3631C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40813634 | |||||||
chr1:40813760 | G | T | 155 | a0001c0001t0001g0029 a0001c0001t0001g0171 a0001c0001t0001g0172 others(152): Show |
157 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.315-3505G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40813760 | |||||||
chr1:40813809 | G | A | 82 | a0001c0001t0001g0029 a0001c0001t0001g0171 a0001c0001t0001g0172 others(79): Show |
82 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.315-3456G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40813809 | |||||||
chr1:40813896 | C | T | 5 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 others(2): Show |
5 | HG00639.hp2 HG00642.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.315-3369C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40813896 | |||||||
chr1:40813948 | C | T | 1 | a0001c0003t0001g0290 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.315-3317C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40813948 | |||||||
chr1:40814011 | T | C | 1 | a0001c0002t0001g0061 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.315-3254T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40814011 | |||||||
chr1:40814026 | C | T | 1 | a0001c0001t0003g0038 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.315-3239C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40814026 | |||||||
chr1:40814046 | C | CT | 60 | a0001c0001t0001g0066 a0001c0001t0001g0072 a0001c0001t0001g0190 others(57): Show |
61 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.315-3195dupT | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40814046 | ||||||
chr1:40814046 | C | CTT | 25 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0349 others(22): Show |
25 | HG00639.hp2 HG00642.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.315-3196_315-3195d others(4): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40814046 | ||||||
chr1:40814046 | C | CTTT | 41 | a0001c0002t0001g0014 a0001c0002t0001g0025 a0001c0002t0001g0028 others(38): Show |
43 | HG00099.hp1 HG00323.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.315-3197_315-3195d others(5): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40814046 | ||||||
chr1:40814046 | C | CTTTT | 12 | a0001c0002t0001g0030 a0001c0002t0001g0062 a0001c0002t0001g0123 others(9): Show |
12 | HG01123.hp2 HG01192.hp2 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.315-3198_315-3195d others(6): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40814046 | ||||||
chr1:40814046 | C | CTTTTT | 48 | a0001c0001t0001g0172 a0001c0001t0001g0218 a0001c0001t0001g0254 others(45): Show |
48 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.315-3199_315-3195d others(7): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40814046 | ||||||
chr1:40814046 | C | CTTTTTT | 13 | a0001c0001t0001g0253 a0001c0003t0001g0024 a0001c0003t0001g0092 others(10): Show |
13 | HG01070.hp2 HG01934.hp1 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.315-3200_315-3195d others(8): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40814046 | ||||||
chr1:40814046 | C | CTTTTTTT others(3): Show |
2 | a0001c0004t0002g0135 a0001c0004t0005g0071 |
2 | HG01071.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.315-3204_315-3195d others(12): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40814046 | ||||||
chr1:40814046 | C | CTTTTTTT others(4): Show |
5 | a0001c0004t0001g0288 a0001c0004t0001g0289 a0001c0004t0001g0321 others(2): Show |
5 | HG01175.hp1 HG01175.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.315-3205_315-3195d others(13): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40814046 | ||||||
chr1:40814046 | C | CTTTTTTT others(20): Show |
1 | a0001c0002t0006g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.315-3195_315-3194i others(29): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40814046 | ||||||
chr1:40814046 | C | CTTTTTTT others(21): Show |
2 | a0001c0002t0003g0219 a0001c0002t0006g0229 |
2 | HG02615.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.315-3195_315-3194i others(30): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40814046 | ||||||
chr1:40814046 | C | CTTTTTTT others(25): Show |
1 | a0001c0001t0001g0029 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.315-3195_315-3194i others(34): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40814046 | ||||||
chr1:40814046 | CT | C | 11 | a0001c0001t0001g0058 a0001c0001t0001g0149 a0001c0001t0001g0187 others(8): Show |
12 | HG01081.hp1 HG01168.hp2 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.315-3195delT | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40814046 | ||||||
chr1:40814208 | C | T | 4 | a0001c0002t0001g0213 a0001c0002t0001g0215 a0002c0005t0001g0050 others(1): Show |
4 | HG01515.hp2 HG01517.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.315-3057C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40814208 | |||||||
chr1:40814211 | G | A | 1 | a0001c0001t0001g0008 | 2 | HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.315-3054G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40814211 | |||||||
chr1:40814211 | G | T | 1 | a0001c0001t0001g0355 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.315-3054G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40814211 | |||||||
chr1:40814256 | G | A | 8 | a0001c0002t0001g0152 a0001c0002t0001g0153 a0001c0002t0001g0161 others(5): Show |
8 | HG02055.hp2 HG02895.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.315-3009G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40814256 | |||||||
chr1:40814277 | C | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0058 a0001c0001t0001g0183 |
3 | HG01884.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.315-2988C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40814277 | |||||||
chr1:40814330 | A | G | 1 | a0001c0003t0001g0277 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.315-2935A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40814330 | |||||||
chr1:40814475 | G | A | 5 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 others(2): Show |
5 | HG00639.hp2 HG00642.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.315-2790G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40814475 | |||||||
chr1:40814493 | C | T | 1 | a0001c0002t0001g0336 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.315-2772C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40814493 | |||||||
chr1:40814577 | G | T | 82 | a0001c0001t0001g0029 a0001c0001t0001g0172 a0001c0001t0001g0218 others(79): Show |
82 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.315-2688G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40814577 | |||||||
chr1:40814653 | G | A | 6 | a0001c0001t0001g0029 a0001c0002t0003g0219 a0001c0002t0003g0222 others(3): Show |
6 | HG02109.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.315-2612G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40814653 | |||||||
chr1:40814703 | C | CA | 23 | a0001c0001t0001g0029 a0001c0002t0001g0046 a0001c0002t0003g0219 others(20): Show |
23 | HG00621.hp2 HG01070.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.315-2553dupA | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40814703 | ||||||
chr1:40814704 | A | AG | 58 | a0001c0001t0001g0172 a0001c0001t0001g0218 a0001c0001t0001g0253 others(55): Show |
58 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.315-2561_315-2560i others(3): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40814704 | |||||||
chr1:40814708 | A | AC | 14 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(11): Show |
14 | HG00639.hp2 HG00642.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.315-2557_315-2556i others(3): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40814708 | |||||||
chr1:40814708 | A | ACAAAAC | 63 | a0001c0002t0001g0014 a0001c0002t0001g0016 a0001c0002t0001g0017 others(60): Show |
65 | HG00099.hp1 HG00323.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.315-2557_315-2556i others(8): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40814708 | |||||||
chr1:40814708 | A | C | 2 | a0001c0001t0004g0266 a0002c0005t0002g0199 |
2 | HG01081.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.315-2557A>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40814708 | |||||||
chr1:40814775 | T | A | 1 | a0001c0001t0001g0063 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.315-2490T>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40814775 | |||||||
chr1:40814884 | TC | T | 63 | a0001c0002t0001g0014 a0001c0002t0001g0016 a0001c0002t0001g0017 others(60): Show |
65 | HG00099.hp1 HG00323.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.315-2379delC | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40814884 | ||||||
chr1:40814886 | C | T | 91 | a0001c0001t0001g0029 a0001c0001t0001g0172 a0001c0001t0001g0218 others(88): Show |
91 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.315-2379C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40814886 | |||||||
chr1:40814979 | C | T | 82 | a0001c0001t0001g0029 a0001c0001t0001g0172 a0001c0001t0001g0218 others(79): Show |
82 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.315-2286C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40814979 | |||||||
chr1:40814981 | C | T | 1 | a0001c0004t0004g0067 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.315-2284C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40814981 | |||||||
chr1:40815165 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.315-2100G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40815165 | |||||||
chr1:40815176 | G | C | 1 | a0001c0001t0001g0355 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.315-2089G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40815176 | |||||||
chr1:40815238 | C | CA | 96 | a0001c0001t0001g0029 a0001c0001t0001g0066 a0001c0001t0001g0084 others(93): Show |
98 | HG00099.hp1 HG00323.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.315-2013dupA | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40815238 | ||||||
chr1:40815238 | C | CAA | 63 | a0001c0001t0001g0172 a0001c0001t0001g0218 a0001c0001t0001g0253 others(60): Show |
63 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.315-2014_315-2013d others(4): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40815238 | ||||||
chr1:40815295 | A | G | 82 | a0001c0001t0001g0029 a0001c0001t0001g0172 a0001c0001t0001g0218 others(79): Show |
82 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.315-1970A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40815295 | |||||||
chr1:40815387 | A | T | 74 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0002t0001g0014 others(71): Show |
76 | HG00099.hp1 HG00323.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.315-1878A>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40815387 | |||||||
chr1:40815459 | C | T | 1 | a0001c0002t0019g0056 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.315-1806C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40815459 | |||||||
chr1:40815535 | G | A | 6 | a0001c0001t0001g0029 a0001c0002t0003g0219 a0001c0002t0003g0222 others(3): Show |
6 | HG02109.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.315-1730G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40815535 | |||||||
chr1:40815538 | G | T | 1 | a0001c0001t0001g0118 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.315-1727G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40815538 | |||||||
chr1:40815539 | A | T | 1 | a0001c0001t0001g0118 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.315-1726A>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40815539 | |||||||
chr1:40815680 | A | T | 6 | a0001c0002t0001g0052 a0001c0002t0001g0163 a0001c0002t0001g0338 others(3): Show |
6 | HG01943.hp1 HG02109.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.315-1585A>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40815680 | |||||||
chr1:40815812 | C | T | 5 | a0001c0002t0001g0040 a0001c0002t0001g0041 a0001c0002t0001g0129 others(2): Show |
5 | HG01243.hp1 HG01891.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.315-1453C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40815812 | |||||||
chr1:40815829 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0058 others(1): Show |
5 | HG01884.hp2 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.315-1436G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40815829 | |||||||
chr1:40815922 | C | T | 3 | a0001c0002t0001g0040 a0001c0002t0001g0041 a0001c0002t0001g0337 |
3 | HG02145.hp2 HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.315-1343C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40815922 | |||||||
chr1:40815923 | G | A | 82 | a0001c0001t0001g0029 a0001c0001t0001g0172 a0001c0001t0001g0218 others(79): Show |
82 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.315-1342G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40815923 | |||||||
chr1:40816047 | CT | C | 156 | a0001c0001t0001g0029 a0001c0001t0001g0172 a0001c0001t0001g0218 others(153): Show |
158 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.315-1215delT | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40816047 | ||||||
chr1:40816099 | G | A | 1 | a0001c0003t0001g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.315-1166G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40816099 | |||||||
chr1:40816203 | T | C | 1 | a0001c0003t0001g0310 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.315-1062T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40816203 | |||||||
chr1:40816449 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0103 a0001c0001t0001g0104 |
4 | NA18945.hp1 NA19004.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-816C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40816449 | |||||||
chr1:40816492 | C | T | 1 | a0001c0001t0001g0297 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.315-773C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40816492 | |||||||
chr1:40816894 | TC | T | 56 | a0001c0001t0001g0172 a0001c0001t0001g0253 a0001c0001t0001g0254 others(53): Show |
56 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.315-368delC | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 40816894 | ||||||
chr1:40816897 | C | T | 56 | a0001c0001t0001g0172 a0001c0001t0001g0253 a0001c0001t0001g0254 others(53): Show |
56 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.315-368C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40816897 | |||||||
chr1:40817201 | A | C | 1 | a0001c0002t0001g0325 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.315-64A>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40817201 | |||||||
chr1:40817247 | C | T | 88 | a0001c0001t0001g0029 a0001c0001t0001g0172 a0001c0001t0001g0218 others(85): Show |
88 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.315-18C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40817247 | |||||||
chr1:40817249 | C | T | 87 | a0001c0001t0001g0029 a0001c0001t0001g0172 a0001c0001t0001g0218 others(84): Show |
87 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.315-16C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 1/13 | chr1 | 40817249 | |||||||
chr1:40817361 | T | TGCTGGGA others(40): Show |
1 | a0001c0001t0003g0112 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.405+73_405+119dupG others(46): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 40817361 | ||||||
chr1:40817428 | G | GGGGGGCT others(40): Show |
1 | a0001c0002t0017g0132 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.405+105_405+106ins others(47): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 40817428 | ||||||
chr1:40817428 | G | GGGGGGCT others(87): Show |
6 | a0001c0001t0001g0029 a0001c0002t0003g0219 a0001c0002t0003g0222 others(3): Show |
6 | HG02109.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.405+119_405+120ins others(94): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 40817428 | ||||||
chr1:40817428 | GGGGGGCT others(40): Show |
G | 17 | a0001c0004t0001g0019 a0001c0004t0001g0269 a0001c0004t0001g0270 others(14): Show |
17 | HG00621.hp2 HG01070.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.405+120_405+166del others(47): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 40817428 | ||||||
chr1:40817475 | A | AGGGGGCT others(40): Show |
63 | a0001c0001t0001g0172 a0001c0001t0001g0218 a0001c0001t0001g0253 others(60): Show |
63 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.405+127_405+173dup others(47): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 40817475 | ||||||
chr1:40817475 | A | G | 7 | a0001c0001t0001g0029 a0001c0002t0003g0219 a0001c0002t0003g0222 others(4): Show |
7 | HG02109.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.405+120A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 2/13 | chr1 | 40817475 | |||||||
chr1:40817492 | A | AGCACCTC others(40): Show |
1 | a0001c0002t0019g0056 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.405+162_405+163ins others(47): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 40817492 | ||||||
chr1:40817691 | A | G | 1 | a0001c0002t0019g0056 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.405+336A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 2/13 | chr1 | 40817691 | |||||||
chr1:40817737 | C | A | 1 | a0001c0001t0001g0197 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.405+382C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 2/13 | chr1 | 40817737 | |||||||
chr1:40818386 | C | A | 1 | a0001c0002t0018g0057 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.532+96C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 3/13 | chr1 | 40818386 | |||||||
chr1:40818406 | C | T | 1 | a0002c0005t0001g0082 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.533-99C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 3/13 | chr1 | 40818406 | |||||||
chr1:40818415 | C | T | 3 | a0001c0002t0002g0341 a0001c0002t0002g0342 a0001c0013t0002g0343 |
3 | HG03225.hp2 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.533-90C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 3/13 | chr1 | 40818415 | |||||||
chr1:40818447 | C | G | 87 | a0001c0001t0001g0029 a0001c0001t0001g0172 a0001c0001t0001g0218 others(84): Show |
87 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.533-58C>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 3/13 | chr1 | 40818447 | |||||||
chr1:40818462 | G | A | 1 | a0001c0002t0018g0057 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.533-43G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 3/13 | chr1 | 40818462 | |||||||
chr1:40818471 | G | A | 1 | a0002c0012t0001g0018 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.533-34G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 3/13 | chr1 | 40818471 | |||||||
chr1:40818694 | G | C | 195 | a0001c0001t0001g0029 a0001c0001t0001g0172 a0001c0001t0001g0216 others(192): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.708+14G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 4/13 | chr1 | 40818694 | |||||||
chr1:40818734 | A | G | 195 | a0001c0001t0001g0029 a0001c0001t0001g0172 a0001c0001t0001g0216 others(192): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.708+54A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 4/13 | chr1 | 40818734 | |||||||
chr1:40818743 | A | T | 2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | NA18957.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.708+63A>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 4/13 | chr1 | 40818743 | |||||||
chr1:40818791 | G | T | 2 | a0001c0001t0007g0085 a0001c0001t0007g0094 |
2 | NA19000.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.708+111G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 4/13 | chr1 | 40818791 | |||||||
chr1:40818801 | C | T | 2 | a0002c0005t0001g0128 a0002c0010t0001g0232 |
2 | HG01106.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.708+121C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 4/13 | chr1 | 40818801 | |||||||
chr1:40818819 | C | G | 2 | a0001c0002t0001g0161 a0001c0002t0016g0045 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.708+139C>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 4/13 | chr1 | 40818819 | |||||||
chr1:40818837 | C | G | 193 | a0001c0001t0001g0029 a0001c0001t0001g0172 a0001c0001t0001g0216 others(190): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.708+157C>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 4/13 | chr1 | 40818837 | |||||||
chr1:40818848 | A | G | 192 | a0001c0001t0001g0029 a0001c0001t0001g0172 a0001c0001t0001g0216 others(189): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.708+168A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 4/13 | chr1 | 40818848 | |||||||
chr1:40818855 | T | G | 193 | a0001c0001t0001g0029 a0001c0001t0001g0172 a0001c0001t0001g0216 others(190): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.708+175T>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 4/13 | chr1 | 40818855 | |||||||
chr1:40818888 | G | T | 1 | a0001c0002t0019g0056 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.708+208G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 4/13 | chr1 | 40818888 | |||||||
chr1:40819059 | T | G | 1 | a0001c0002t0002g0226 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.709-288T>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 4/13 | chr1 | 40819059 | |||||||
chr1:40819131 | T | TG | 3 | a0001c0001t0001g0262 a0001c0001t0004g0266 a0001c0003t0003g0281 |
3 | NA18962.hp2 NA19060.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.709-215dupG | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 40819131 | ||||||
chr1:40819133 | A | G | 257 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0027 others(254): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.709-214A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 4/13 | chr1 | 40819133 | |||||||
chr1:40819138 | G | C | 7 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(4): Show |
7 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.709-209G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 4/13 | chr1 | 40819138 | |||||||
chr1:40819162 | A | T | 59 | a0001c0002t0001g0014 a0001c0002t0001g0016 a0001c0002t0001g0017 others(56): Show |
61 | HG00099.hp1 HG00323.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.709-185A>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 4/13 | chr1 | 40819162 | |||||||
chr1:40819192 | G | A | 33 | a0001c0002t0001g0015 a0001c0002t0001g0048 a0001c0002t0001g0049 others(30): Show |
34 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.709-155G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 4/13 | chr1 | 40819192 | |||||||
chr1:40819499 | C | A | 45 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0027 others(42): Show |
49 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.834+27C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 5/13 | chr1 | 40819499 | |||||||
chr1:40819506 | C | G | 1 | a0001c0001t0001g0218 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.834+34C>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 5/13 | chr1 | 40819506 | |||||||
chr1:40819620 | C | A | 44 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0027 others(41): Show |
48 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.834+148C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 5/13 | chr1 | 40819620 | |||||||
chr1:40819623 | A | G | 13 | a0001c0001t0001g0029 a0001c0001t0001g0187 a0001c0001t0001g0188 others(10): Show |
13 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.834+151A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 5/13 | chr1 | 40819623 | |||||||
chr1:40819714 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.835-161A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 5/13 | chr1 | 40819714 | |||||||
chr1:40820064 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.945+79G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 6/13 | chr1 | 40820064 | |||||||
chr1:40820130 | C | T | 1 | a0001c0001t0012g0159 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.946-35C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 6/13 | chr1 | 40820130 | |||||||
chr1:40820153 | C | G | 2 | a0001c0003t0001g0092 a0001c0003t0001g0093 |
2 | HG02135.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.946-12C>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 6/13 | chr1 | 40820153 | |||||||
chr1:40820276 | G | A | 1 | a0002c0005t0001g0245 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1041+16G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 7/13 | chr1 | 40820276 | |||||||
chr1:40820437 | C | A | 2 | a0001c0002t0001g0046 a0001c0002t0017g0132 |
2 | HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1041+177C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 7/13 | chr1 | 40820437 | |||||||
chr1:40820655 | C | G | 6 | a0001c0002t0001g0052 a0001c0002t0001g0163 a0001c0002t0001g0338 others(3): Show |
6 | HG01943.hp1 HG02109.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1041+395C>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 7/13 | chr1 | 40820655 | |||||||
chr1:40820664 | TCA | T | 7 | a0001c0004t0001g0019 a0001c0004t0001g0269 a0001c0004t0001g0270 others(4): Show |
7 | HG00621.hp2 HG02155.hp1 NA19012.hp1 others(4): Show |
intron_variant | MODIFIER | c.1041+409_1041+410d others(4): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 40820664 | ||||||
chr1:40820681 | G | A | 203 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0021 others(200): Show |
210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1041+421G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 7/13 | chr1 | 40820681 | |||||||
chr1:40820713 | A | G | 1 | a0001c0003t0009g0280 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1041+453A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 7/13 | chr1 | 40820713 | |||||||
chr1:40820811 | G | C | 1 | a0001c0003t0001g0293 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1041+551G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 7/13 | chr1 | 40820811 | |||||||
chr1:40820824 | C | T | 1 | a0001c0002t0001g0169 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1041+564C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 7/13 | chr1 | 40820824 | |||||||
chr1:40820847 | T | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0103 |
3 | NA18945.hp1 NA19068.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1041+587T>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 7/13 | chr1 | 40820847 | |||||||
chr1:40820851 | C | T | 1 | a0001c0002t0001g0338 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1041+591C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 7/13 | chr1 | 40820851 | |||||||
chr1:40820936 | C | A | 35 | a0001c0001t0001g0007 a0001c0001t0001g0344 a0001c0001t0001g0345 others(32): Show |
36 | HG00621.hp2 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.1041+676C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 7/13 | chr1 | 40820936 | |||||||
chr1:40820951 | G | A | 98 | a0001c0001t0001g0007 a0001c0001t0001g0344 a0001c0001t0001g0345 others(95): Show |
101 | HG00099.hp1 HG00323.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.1041+691G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 7/13 | chr1 | 40820951 | |||||||
chr1:40821030 | T | C | 99 | a0001c0001t0001g0007 a0001c0001t0001g0344 a0001c0001t0001g0345 others(96): Show |
102 | HG00099.hp1 HG00323.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.1041+770T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 7/13 | chr1 | 40821030 | |||||||
chr1:40821062 | C | T | 7 | a0001c0004t0001g0019 a0001c0004t0001g0269 a0001c0004t0001g0270 others(4): Show |
7 | HG00621.hp2 HG02155.hp1 NA19012.hp1 others(4): Show |
intron_variant | MODIFIER | c.1041+802C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 7/13 | chr1 | 40821062 | |||||||
chr1:40821122 | G | A | 1 | a0002c0005t0001g0309 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1041+862G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 7/13 | chr1 | 40821122 | |||||||
chr1:40821204 | G | A | 1 | a0001c0003t0001g0092 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1041+944G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 7/13 | chr1 | 40821204 | |||||||
chr1:40821211 | A | G | 143 | a0001c0001t0001g0007 a0001c0001t0001g0234 a0001c0001t0001g0235 others(140): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1041+951A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 7/13 | chr1 | 40821211 | |||||||
chr1:40821218 | T | C | 65 | a0001c0002t0001g0014 a0001c0002t0001g0016 a0001c0002t0001g0017 others(62): Show |
67 | HG00099.hp1 HG00323.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.1041+958T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 7/13 | chr1 | 40821218 | |||||||
chr1:40821355 | G | A | 1 | a0001c0002t0001g0338 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1042-959G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 7/13 | chr1 | 40821355 | |||||||
chr1:40821382 | G | A | 29 | a0001c0001t0001g0007 a0001c0001t0001g0344 a0001c0001t0001g0345 others(26): Show |
30 | HG00621.hp2 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.1042-932G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 7/13 | chr1 | 40821382 | |||||||
chr1:40821484 | A | AG | 60 | a0001c0002t0001g0023 a0001c0002t0001g0033 a0001c0002t0001g0034 others(57): Show |
60 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.1042-827dupG | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 40821484 | ||||||
chr1:40821689 | A | G | 14 | a0001c0003t0001g0136 a0001c0003t0001g0274 a0001c0003t0001g0275 others(11): Show |
14 | HG00597.hp2 HG00621.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.1042-625A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 7/13 | chr1 | 40821689 | |||||||
chr1:40821764 | G | C | 4 | a0001c0002t0001g0127 a0001c0002t0001g0158 a0001c0002t0001g0352 others(1): Show |
4 | HG00738.hp2 HG02965.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1042-550G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 7/13 | chr1 | 40821764 | |||||||
chr1:40821776 | T | A | 118 | a0001c0001t0001g0029 a0001c0001t0001g0187 a0001c0001t0001g0188 others(115): Show |
119 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.1042-538T>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 7/13 | chr1 | 40821776 | |||||||
chr1:40822262 | G | A | 2 | a0001c0001t0001g0194 a0001c0002t0014g0162 |
2 | HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1042-52G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 7/13 | chr1 | 40822262 | |||||||
chr1:40822430 | T | G | 2 | a0001c0003t0001g0157 a0001c0003t0001g0267 |
2 | HG01167.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.1130+28T>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 8/13 | chr1 | 40822430 | |||||||
chr1:40822433 | G | C | 5 | a0001c0002t0001g0014 a0001c0002t0001g0238 a0001c0002t0001g0250 others(2): Show |
6 | HG01256.hp2 HG01516.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1130+31G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 8/13 | chr1 | 40822433 | |||||||
chr1:40822443 | G | A | 1 | a0007c0022t0001g0079 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1130+41G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 8/13 | chr1 | 40822443 | |||||||
chr1:40822493 | A | AG | 11 | a0001c0001t0001g0076 a0001c0001t0001g0103 a0001c0001t0001g0124 others(8): Show |
11 | HG00621.hp2 HG00741.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.1130+96dupG | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 40822493 | ||||||
chr1:40822723 | G | A | 1 | a0003c0007t0001g0022 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1130+321G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 8/13 | chr1 | 40822723 | |||||||
chr1:40822743 | G | C | 1 | a0001c0001t0002g0316 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1130+341G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 8/13 | chr1 | 40822743 | |||||||
chr1:40822809 | C | G | 1 | a0001c0002t0013g0053 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1130+407C>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 8/13 | chr1 | 40822809 | |||||||
chr1:40822858 | G | A | 4 | a0001c0001t0001g0172 a0001c0001t0004g0059 a0001c0001t0004g0095 others(1): Show |
4 | HG00558.hp1 NA18945.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.1130+456G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 8/13 | chr1 | 40822858 | |||||||
chr1:40822986 | C | T | 1 | a0001c0001t0001g0349 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1130+584C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 8/13 | chr1 | 40822986 | |||||||
chr1:40823053 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1130+651C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 8/13 | chr1 | 40823053 | |||||||
chr1:40823102 | C | G | 1 | a0001c0002t0018g0057 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1130+700C>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 8/13 | chr1 | 40823102 | |||||||
chr1:40823150 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1130+748G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 8/13 | chr1 | 40823150 | |||||||
chr1:40823299 | C | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0074 a0001c0001t0001g0081 others(2): Show |
5 | HG00597.hp1 HG00609.hp2 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.1131-798C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 8/13 | chr1 | 40823299 | |||||||
chr1:40823533 | G | C | 336 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(333): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1131-564G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 8/13 | chr1 | 40823533 | |||||||
chr1:40823542 | G | A | 189 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0020 others(186): Show |
198 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.1131-555G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 8/13 | chr1 | 40823542 | |||||||
chr1:40823692 | G | A | 1 | a0001c0002t0013g0053 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1131-405G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 8/13 | chr1 | 40823692 | |||||||
chr1:40823703 | C | A | 1 | a0001c0008t0003g0009 | 2 | HG01081.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1131-394C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 8/13 | chr1 | 40823703 | |||||||
chr1:40823713 | C | T | 46 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0074 others(43): Show |
48 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.1131-384C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 8/13 | chr1 | 40823713 | |||||||
chr1:40823809 | C | T | 1 | a0001c0002t0001g0052 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1131-288C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 8/13 | chr1 | 40823809 | |||||||
chr1:40823816 | G | T | 4 | a0001c0001t0001g0054 a0001c0001t0001g0326 a0001c0002t0001g0169 others(1): Show |
4 | HG00621.hp1 HG02015.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.1131-281G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 8/13 | chr1 | 40823816 | |||||||
chr1:40823843 | G | C | 2 | a0001c0011t0002g0233 a0001c0011t0002g0239 |
2 | HG02698.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1131-254G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 8/13 | chr1 | 40823843 | |||||||
chr1:40823907 | C | T | 77 | a0001c0001t0001g0006 a0001c0001t0001g0043 a0001c0001t0001g0047 others(74): Show |
80 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.1131-190C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 8/13 | chr1 | 40823907 | |||||||
chr1:40823924 | G | T | 1 | a0001c0001t0003g0114 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1131-173G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 8/13 | chr1 | 40823924 | |||||||
chr1:40823969 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1131-128C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 8/13 | chr1 | 40823969 | |||||||
chr1:40824321 | T | C | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(115): Show |
122 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1292+63T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40824321 | |||||||
chr1:40824351 | C | T | 1 | a0001c0003t0001g0284 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1292+93C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40824351 | |||||||
chr1:40824411 | C | G | 1 | a0001c0002t0018g0057 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1292+153C>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40824411 | |||||||
chr1:40824563 | C | T | 122 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0026 others(119): Show |
129 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.1292+305C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40824563 | |||||||
chr1:40825153 | G | A | 1 | a0001c0002t0001g0334 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1292+895G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40825153 | |||||||
chr1:40825170 | T | A | 1 | a0001c0002t0002g0341 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1292+912T>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40825170 | |||||||
chr1:40825240 | T | A | 1 | a0001c0001t0001g0355 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1292+982T>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40825240 | |||||||
chr1:40825311 | C | T | 5 | a0001c0001t0002g0055 a0001c0002t0002g0340 a0001c0002t0002g0341 others(2): Show |
5 | HG02895.hp1 HG03209.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1292+1053C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40825311 | |||||||
chr1:40825392 | C | T | 1 | a0001c0002t0018g0057 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1292+1134C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40825392 | |||||||
chr1:40825546 | AGGAAGTG | A | 3 | a0001c0002t0001g0127 a0001c0002t0001g0152 a0001c0002t0001g0153 |
3 | HG00738.hp2 HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1292+1291_1292+129 others(11): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr1 | 40825546 | ||||||
chr1:40825714 | C | T | 4 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0262 others(1): Show |
4 | HG00408.hp2 NA18957.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292+1456C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40825714 | |||||||
chr1:40825794 | G | A | 2 | a0001c0002t0001g0129 a0001c0002t0001g0212 |
2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1292+1536G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40825794 | |||||||
chr1:40825859 | A | G | 174 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0020 others(171): Show |
183 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.1292+1601A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40825859 | |||||||
chr1:40825948 | G | A | 4 | a0001c0001t0001g0029 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG01069.hp2 HG01071.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1292+1690G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40825948 | |||||||
chr1:40825974 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0103 a0001c0001t0001g0104 |
4 | NA18945.hp1 NA19004.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.1292+1716G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40825974 | |||||||
chr1:40826038 | G | A | 4 | a0001c0001t0001g0172 a0001c0001t0004g0059 a0001c0001t0004g0095 others(1): Show |
4 | HG00558.hp1 NA18945.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.1292+1780G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40826038 | |||||||
chr1:40826086 | G | A | 334 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(331): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1292+1828G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40826086 | |||||||
chr1:40826090 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1292+1832C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40826090 | |||||||
chr1:40826112 | C | T | 69 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0074 others(66): Show |
71 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1292+1854C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40826112 | |||||||
chr1:40826293 | T | C | 6 | a0001c0002t0001g0023 a0001c0002t0001g0033 a0001c0002t0001g0034 others(3): Show |
6 | HG00639.hp2 HG00642.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1292+2035T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40826293 | |||||||
chr1:40826351 | A | G | 335 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(332): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1292+2093A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40826351 | |||||||
chr1:40826396 | C | G | 2 | a0001c0001t0007g0085 a0001c0001t0007g0094 |
2 | NA19000.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1292+2138C>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40826396 | |||||||
chr1:40826600 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1292+2342C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40826600 | |||||||
chr1:40826660 | A | C | 1 | a0001c0002t0013g0053 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1292+2402A>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40826660 | |||||||
chr1:40826705 | G | A | 15 | a0001c0001t0001g0172 a0001c0001t0004g0059 a0001c0001t0004g0095 others(12): Show |
15 | HG00558.hp1 HG00621.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1292+2447G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40826705 | |||||||
chr1:40826713 | C | T | 3 | a0001c0002t0001g0127 a0001c0002t0001g0152 a0001c0002t0001g0153 |
3 | HG00738.hp2 HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1292+2455C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40826713 | |||||||
chr1:40826960 | T | G | 1 | a0001c0002t0001g0192 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1292+2702T>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40826960 | |||||||
chr1:40826961 | G | C | 1 | a0001c0002t0001g0192 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1292+2703G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40826961 | |||||||
chr1:40826962 | C | T | 1 | a0001c0002t0001g0192 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1292+2704C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40826962 | |||||||
chr1:40827022 | C | T | 1 | a0001c0001t0003g0100 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1292+2764C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40827022 | |||||||
chr1:40827297 | C | T | 21 | a0001c0002t0001g0023 a0001c0002t0001g0033 a0001c0002t0001g0034 others(18): Show |
21 | HG00639.hp2 HG00642.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1292+3039C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40827297 | |||||||
chr1:40827329 | G | A | 79 | a0001c0001t0001g0006 a0001c0001t0001g0043 a0001c0001t0001g0054 others(76): Show |
82 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.1292+3071G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40827329 | |||||||
chr1:40827473 | C | G | 1 | a0001c0002t0001g0127 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1292+3215C>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40827473 | |||||||
chr1:40827517 | C | T | 92 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0026 others(89): Show |
99 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1292+3259C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40827517 | |||||||
chr1:40827523 | G | A | 5 | a0001c0003t0001g0274 a0001c0003t0001g0275 a0001c0003t0001g0276 others(2): Show |
5 | NA18944.hp1 NA18975.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.1292+3265G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40827523 | |||||||
chr1:40827747 | G | A | 91 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0026 others(88): Show |
98 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.1293-3337G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40827747 | |||||||
chr1:40827766 | A | G | 6 | a0001c0001t0005g0116 a0001c0001t0005g0119 a0001c0004t0002g0134 others(3): Show |
6 | HG01070.hp1 HG01071.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.1293-3318A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40827766 | |||||||
chr1:40827773 | C | T | 1 | a0001c0002t0018g0057 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1293-3311C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40827773 | |||||||
chr1:40827817 | T | C | 92 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0026 others(89): Show |
99 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1293-3267T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40827817 | |||||||
chr1:40827881 | T | A | 4 | a0001c0001t0001g0172 a0001c0001t0004g0059 a0001c0001t0004g0095 others(1): Show |
4 | HG00558.hp1 NA18945.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.1293-3203T>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40827881 | |||||||
chr1:40827909 | T | TA | 142 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0020 others(139): Show |
151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.1293-3171dupA | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr1 | 40827909 | ||||||
chr1:40827947 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1293-3137G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40827947 | |||||||
chr1:40827977 | C | T | 81 | a0001c0001t0001g0006 a0001c0001t0001g0043 a0001c0001t0001g0047 others(78): Show |
84 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.1293-3107C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40827977 | |||||||
chr1:40827992 | G | A | 81 | a0001c0001t0001g0006 a0001c0001t0001g0043 a0001c0001t0001g0047 others(78): Show |
84 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.1293-3092G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40827992 | |||||||
chr1:40828055 | G | T | 1 | a0001c0001t0001g0345 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1293-3029G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40828055 | |||||||
chr1:40828064 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1293-3020C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40828064 | |||||||
chr1:40828185 | C | A | 24 | a0001c0001t0002g0055 a0001c0002t0001g0023 a0001c0002t0001g0033 others(21): Show |
24 | HG00639.hp2 HG00642.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.1293-2899C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40828185 | |||||||
chr1:40828262 | C | T | 4 | a0001c0001t0001g0172 a0001c0001t0004g0059 a0001c0001t0004g0095 others(1): Show |
4 | HG00558.hp1 NA18945.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.1293-2822C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40828262 | |||||||
chr1:40828362 | C | T | 1 | a0001c0002t0018g0057 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1293-2722C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40828362 | |||||||
chr1:40828447 | C | A | 1 | a0001c0003t0001g0287 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1293-2637C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40828447 | |||||||
chr1:40828560 | T | C | 5 | a0001c0002t0003g0219 a0001c0002t0003g0222 a0001c0002t0006g0170 others(2): Show |
5 | HG02572.hp2 HG02615.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1293-2524T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40828560 | |||||||
chr1:40828569 | C | T | 2 | a0001c0002t0001g0338 a0001c0002t0019g0056 |
2 | HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1293-2515C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40828569 | |||||||
chr1:40828591 | CTTGGCCA others(5): Show |
C | 2 | a0001c0003t0001g0276 a0001c0003t0001g0278 |
2 | NA19065.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1293-2491_1293-248 others(16): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr1 | 40828591 | ||||||
chr1:40828805 | A | T | 2 | a0001c0001t0005g0116 a0001c0001t0005g0119 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1293-2279A>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40828805 | |||||||
chr1:40829092 | T | C | 6 | a0001c0001t0002g0105 a0001c0002t0001g0302 a0001c0002t0001g0303 others(3): Show |
6 | HG00323.hp1 HG01943.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1293-1992T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40829092 | |||||||
chr1:40829225 | G | A | 15 | a0001c0001t0001g0172 a0001c0001t0004g0059 a0001c0001t0004g0095 others(12): Show |
15 | HG00558.hp1 HG00621.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1293-1859G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40829225 | |||||||
chr1:40829457 | C | A | 5 | a0001c0001t0002g0055 a0001c0002t0002g0340 a0001c0002t0002g0341 others(2): Show |
5 | HG02895.hp1 HG03209.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1293-1627C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40829457 | |||||||
chr1:40829503 | G | T | 1 | a0001c0001t0001g0297 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1293-1581G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40829503 | |||||||
chr1:40829665 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1293-1419G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40829665 | |||||||
chr1:40829782 | G | A | 13 | a0001c0001t0002g0055 a0001c0002t0001g0023 a0001c0002t0001g0033 others(10): Show |
13 | HG00639.hp2 HG00642.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1293-1302G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40829782 | |||||||
chr1:40829843 | A | C | 1 | a0001c0008t0003g0009 | 2 | HG01081.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1293-1241A>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40829843 | |||||||
chr1:40829844 | C | A | 1 | a0001c0008t0003g0009 | 2 | HG01081.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1293-1240C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40829844 | |||||||
chr1:40829870 | A | G | 50 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0074 others(47): Show |
52 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.1293-1214A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40829870 | |||||||
chr1:40830008 | C | T | 18 | a0001c0001t0005g0116 a0001c0001t0005g0119 a0001c0002t0001g0129 others(15): Show |
18 | HG00621.hp2 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.1293-1076C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40830008 | |||||||
chr1:40830009 | G | A | 90 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0026 others(87): Show |
97 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.1293-1075G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40830009 | |||||||
chr1:40830058 | G | A | 3 | a0001c0002t0001g0127 a0001c0002t0001g0152 a0001c0002t0001g0153 |
3 | HG00738.hp2 HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1293-1026G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40830058 | |||||||
chr1:40830070 | G | A | 1 | a0001c0002t0001g0338 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1293-1014G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40830070 | |||||||
chr1:40830128 | C | G | 334 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(331): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1293-956C>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40830128 | |||||||
chr1:40830245 | T | C | 17 | a0001c0001t0002g0055 a0001c0002t0001g0023 a0001c0002t0001g0033 others(14): Show |
17 | HG00639.hp2 HG00642.hp1 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.1293-839T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40830245 | |||||||
chr1:40830340 | A | G | 249 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(246): Show |
261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.1293-744A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40830340 | |||||||
chr1:40830416 | G | A | 1 | a0001c0002t0001g0161 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1293-668G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40830416 | |||||||
chr1:40830509 | C | T | 4 | a0001c0002t0001g0141 a0001c0002t0001g0213 a0001c0002t0001g0215 others(1): Show |
4 | HG01515.hp2 HG01517.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.1293-575C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40830509 | |||||||
chr1:40830554 | G | T | 66 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0031 others(63): Show |
68 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.1293-530G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40830554 | |||||||
chr1:40830559 | C | T | 1 | a0002c0005t0005g0227 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1293-525C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40830559 | |||||||
chr1:40830866 | T | C | 1 | a0001c0001t0001g0355 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1293-218T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40830866 | |||||||
chr1:40830970 | C | T | 2 | a0001c0002t0001g0127 a0001c0002t0013g0053 |
2 | HG00738.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1293-114C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 9/13 | chr1 | 40830970 | |||||||
chr1:40831315 | G | A | 1 | a0001c0003t0001g0284 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1513+11G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 10/13 | chr1 | 40831315 | |||||||
chr1:40831332 | C | G | 1 | a0001c0002t0013g0053 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1513+28C>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 10/13 | chr1 | 40831332 | |||||||
chr1:40831340 | G | A | 6 | a0001c0001t0001g0182 a0001c0001t0001g0187 a0001c0001t0001g0339 others(3): Show |
6 | HG01243.hp2 HG02818.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1513+36G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 10/13 | chr1 | 40831340 | |||||||
chr1:40831411 | A | G | 1 | a0001c0002t0013g0053 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1513+107A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 10/13 | chr1 | 40831411 | |||||||
chr1:40831662 | A | G | 1 | a0001c0002t0001g0127 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1513+358A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 10/13 | chr1 | 40831662 | |||||||
chr1:40831690 | T | G | 11 | a0001c0002t0001g0023 a0001c0002t0001g0033 a0001c0002t0001g0034 others(8): Show |
11 | HG00639.hp2 HG00642.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.1513+386T>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 10/13 | chr1 | 40831690 | |||||||
chr1:40831739 | G | T | 192 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0020 others(189): Show |
202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.1513+435G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 10/13 | chr1 | 40831739 | |||||||
chr1:40831899 | G | A | 1 | a0001c0002t0013g0053 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1513+595G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 10/13 | chr1 | 40831899 | |||||||
chr1:40831926 | A | G | 2 | a0001c0002t0018g0057 a0001c0016t0010g0160 |
2 | HG01943.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1513+622A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 10/13 | chr1 | 40831926 | |||||||
chr1:40831932 | A | G | 1 | a0001c0001t0002g0243 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1513+628A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 10/13 | chr1 | 40831932 | |||||||
chr1:40831983 | T | G | 330 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(327): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1513+679T>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 10/13 | chr1 | 40831983 | |||||||
chr1:40832008 | G | C | 6 | a0001c0002t0001g0023 a0001c0002t0001g0033 a0001c0002t0001g0034 others(3): Show |
6 | HG00639.hp2 HG00642.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1513+704G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 10/13 | chr1 | 40832008 | |||||||
chr1:40832072 | C | T | 1 | a0002c0005t0005g0227 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1513+768C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 10/13 | chr1 | 40832072 | |||||||
chr1:40832396 | A | G | 2 | a0001c0002t0001g0052 a0001c0002t0001g0333 |
2 | HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1514-618A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 10/13 | chr1 | 40832396 | |||||||
chr1:40832418 | T | C | 13 | a0001c0001t0001g0096 a0001c0003t0001g0136 a0001c0003t0001g0274 others(10): Show |
13 | HG00597.hp2 HG02132.hp2 NA18944.hp1 others(10): Show |
intron_variant | MODIFIER | c.1514-596T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 10/13 | chr1 | 40832418 | |||||||
chr1:40832488 | G | A | 1 | a0001c0001t0002g0242 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1514-526G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 10/13 | chr1 | 40832488 | |||||||
chr1:40832576 | C | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1514-438C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 10/13 | chr1 | 40832576 | |||||||
chr1:40832711 | C | A | 3 | a0001c0002t0001g0046 a0001c0002t0001g0061 a0001c0002t0001g0062 |
3 | HG02622.hp2 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1514-303C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 10/13 | chr1 | 40832711 | |||||||
chr1:40832786 | CAG | C | 11 | a0001c0001t0001g0029 a0001c0001t0001g0130 a0001c0001t0001g0131 others(8): Show |
12 | HG00558.hp1 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.1514-226_1514-225d others(4): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 40832786 | ||||||
chr1:40832817 | G | A | 1 | a0001c0002t0001g0259 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1514-197G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 10/13 | chr1 | 40832817 | |||||||
chr1:40832819 | T | C | 1 | a0001c0008t0003g0032 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1514-195T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 10/13 | chr1 | 40832819 | |||||||
chr1:40832838 | G | A | 95 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0026 others(92): Show |
103 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1514-176G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 10/13 | chr1 | 40832838 | |||||||
chr1:40832874 | G | GC | 330 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(327): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1514-136dupC | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 40832874 | ||||||
chr1:40832927 | C | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG01069.hp2 HG01071.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1514-87C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 10/13 | chr1 | 40832927 | |||||||
chr1:40832980 | T | C | 264 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(261): Show |
277 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.1514-34T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 10/13 | chr1 | 40832980 | |||||||
chr1:40833186 | A | G | 20 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0026 others(17): Show |
22 | HG00639.hp2 HG01884.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1613+73A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 11/13 | chr1 | 40833186 | |||||||
chr1:40833228 | G | T | 1 | a0001c0001t0001g0020 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1613+115G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 11/13 | chr1 | 40833228 | |||||||
chr1:40833237 | C | T | 1 | a0001c0002t0002g0226 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1613+124C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 11/13 | chr1 | 40833237 | |||||||
chr1:40833238 | G | A | 18 | a0001c0001t0004g0011 a0001c0001t0004g0059 a0001c0001t0004g0077 others(15): Show |
19 | HG00558.hp1 HG00621.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1613+125G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 11/13 | chr1 | 40833238 | |||||||
chr1:40833408 | A | T | 128 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0043 others(125): Show |
131 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.1613+295A>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 11/13 | chr1 | 40833408 | |||||||
chr1:40833437 | G | A | 21 | a0001c0001t0001g0029 a0001c0001t0001g0130 a0001c0001t0001g0131 others(18): Show |
22 | HG00558.hp1 HG00621.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.1613+324G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 11/13 | chr1 | 40833437 | |||||||
chr1:40833528 | C | A | 5 | a0001c0001t0005g0116 a0001c0001t0005g0119 a0001c0004t0005g0071 others(2): Show |
5 | HG00735.hp2 HG01255.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1613+415C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 11/13 | chr1 | 40833528 | |||||||
chr1:40833591 | G | T | 1 | a0001c0002t0001g0152 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1613+478G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 11/13 | chr1 | 40833591 | |||||||
chr1:40833624 | C | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG01069.hp2 HG01071.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1613+511C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 11/13 | chr1 | 40833624 | |||||||
chr1:40833748 | C | A | 263 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(260): Show |
276 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.1613+635C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 11/13 | chr1 | 40833748 | |||||||
chr1:40833833 | C | CA | 139 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0029 others(136): Show |
143 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1613+738dupA | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 40833833 | ||||||
chr1:40833833 | C | CAA | 6 | a0001c0001t0001g0043 a0001c0002t0001g0046 a0001c0002t0001g0211 others(3): Show |
6 | HG00621.hp1 HG02622.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.1613+737_1613+738d others(4): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 40833833 | ||||||
chr1:40833854 | A | T | 3 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0035 |
3 | HG00642.hp1 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1613+741A>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 11/13 | chr1 | 40833854 | |||||||
chr1:40833987 | T | A | 2 | a0001c0003t0001g0173 a0001c0003t0001g0174 |
2 | HG01070.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1613+874T>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 11/13 | chr1 | 40833987 | |||||||
chr1:40834236 | G | A | 15 | a0001c0001t0001g0044 a0001c0002t0001g0142 a0001c0002t0001g0191 others(12): Show |
15 | HG02027.hp1 HG02040.hp2 HG02155.hp2 others(12): Show |
intron_variant | MODIFIER | c.1614-731G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 11/13 | chr1 | 40834236 | |||||||
chr1:40834567 | G | A | 326 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(323): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.1614-400G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 11/13 | chr1 | 40834567 | |||||||
chr1:40834569 | A | AC | 5 | a0001c0001t0002g0055 a0001c0002t0002g0340 a0001c0002t0002g0341 others(2): Show |
5 | HG02895.hp1 HG03209.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1614-393dupC | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 40834569 | ||||||
chr1:40834596 | T | TA | 11 | a0001c0001t0002g0012 a0001c0001t0002g0105 a0001c0001t0002g0273 others(8): Show |
13 | HG01081.hp2 HG01123.hp2 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.1614-357dupA | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 40834596 | ||||||
chr1:40834596 | TA | T | 6 | a0001c0001t0001g0043 a0001c0001t0007g0094 a0001c0002t0001g0215 others(3): Show |
6 | HG01515.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1614-357delA | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 40834596 | ||||||
chr1:40834622 | A | T | 2 | a0001c0002t0001g0302 a0001c0002t0001g0303 |
2 | HG02148.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1614-345A>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 11/13 | chr1 | 40834622 | |||||||
chr1:40834638 | A | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0344 a0001c0001t0001g0345 |
4 | HG02976.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1614-329A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 11/13 | chr1 | 40834638 | |||||||
chr1:40834698 | C | T | 3 | a0001c0001t0001g0029 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG01069.hp2 HG01071.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1614-269C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 11/13 | chr1 | 40834698 | |||||||
chr1:40834750 | C | T | 14 | a0001c0001t0001g0145 a0001c0001t0002g0012 a0001c0001t0002g0055 others(11): Show |
15 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1614-217C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 11/13 | chr1 | 40834750 | |||||||
chr1:40834754 | C | T | 41 | a0001c0001t0003g0001 a0001c0001t0003g0036 a0001c0001t0003g0038 others(38): Show |
45 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.1614-213C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 11/13 | chr1 | 40834754 | |||||||
chr1:40834755 | AC | A | 7 | a0001c0001t0001g0339 a0001c0002t0001g0017 a0001c0002t0001g0025 others(4): Show |
7 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1614-208delC | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 40834755 | ||||||
chr1:40834829 | C | T | 9 | a0001c0001t0001g0043 a0001c0001t0001g0090 a0001c0001t0001g0091 others(6): Show |
9 | HG02071.hp1 NA18942.hp1 NA18993.hp2 others(6): Show |
intron_variant | MODIFIER | c.1614-138C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 11/13 | chr1 | 40834829 | |||||||
chr1:40834864 | G | A | 7 | a0001c0001t0003g0036 a0001c0001t0003g0038 a0001c0001t0003g0075 others(4): Show |
8 | HG00140.hp1 HG00140.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.1614-103G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 11/13 | chr1 | 40834864 | |||||||
chr1:40835173 | A | G | 1 | a0001c0009t0001g0185 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1745+75A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 12/13 | chr1 | 40835173 | |||||||
chr1:40835280 | C | A | 44 | a0001c0001t0001g0047 a0001c0001t0003g0001 a0001c0001t0003g0036 others(41): Show |
48 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.1745+182C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 12/13 | chr1 | 40835280 | |||||||
chr1:40835347 | T | C | 189 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(186): Show |
193 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1745+249T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 12/13 | chr1 | 40835347 | |||||||
chr1:40835354 | G | C | 22 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0026 others(19): Show |
24 | HG00639.hp2 HG01884.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.1745+256G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 12/13 | chr1 | 40835354 | |||||||
chr1:40835362 | G | C | 47 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0002g0010 others(44): Show |
50 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.1745+264G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 12/13 | chr1 | 40835362 | |||||||
chr1:40835662 | G | T | 3 | a0001c0001t0001g0218 a0001c0002t0001g0352 a0001c0002t0001g0353 |
3 | HG03471.hp2 HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1745+564G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 12/13 | chr1 | 40835662 | |||||||
chr1:40835701 | G | A | 1 | a0001c0002t0001g0351 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1745+603G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 12/13 | chr1 | 40835701 | |||||||
chr1:40835812 | G | A | 1 | a0001c0001t0012g0159 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1745+714G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 12/13 | chr1 | 40835812 | |||||||
chr1:40835822 | G | C | 1 | a0001c0002t0018g0057 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1745+724G>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 12/13 | chr1 | 40835822 | |||||||
chr1:40835989 | T | C | 1 | a0001c0002t0013g0053 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1745+891T>C | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 12/13 | chr1 | 40835989 | |||||||
chr1:40836001 | C | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(18): Show |
23 | HG00639.hp2 HG01884.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.1745+903C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 12/13 | chr1 | 40836001 | |||||||
chr1:40836039 | G | A | 3 | a0001c0001t0001g0218 a0001c0002t0001g0352 a0001c0002t0001g0353 |
3 | HG03471.hp2 HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1745+941G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 12/13 | chr1 | 40836039 | |||||||
chr1:40836158 | G | A | 1 | a0001c0016t0010g0160 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1745+1060G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 12/13 | chr1 | 40836158 | |||||||
chr1:40836529 | A | G | 3 | a0001c0004t0001g0019 a0001c0004t0001g0269 a0001c0004t0001g0270 |
3 | HG00621.hp2 HG02155.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1746-1136A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 12/13 | chr1 | 40836529 | |||||||
chr1:40836711 | A | G | 1 | a0001c0002t0001g0338 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1746-954A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 12/13 | chr1 | 40836711 | |||||||
chr1:40836913 | G | A | 26 | a0001c0001t0004g0011 a0001c0001t0004g0059 a0001c0001t0004g0077 others(23): Show |
27 | HG00558.hp1 HG00621.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1746-752G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 12/13 | chr1 | 40836913 | |||||||
chr1:40836917 | G | T | 1 | a0001c0001t0001g0029 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1746-748G>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 12/13 | chr1 | 40836917 | |||||||
chr1:40837025 | C | T | 1 | a0001c0002t0001g0035 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1746-640C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 12/13 | chr1 | 40837025 | |||||||
chr1:40837069 | A | ATCTTT | 49 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0021 others(46): Show |
52 | HG00558.hp1 HG00621.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.1746-574_1746-570d others(7): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 40837069 | ||||||
chr1:40837069 | ATCTTT | A | 7 | a0001c0002t0001g0033 a0001c0002t0001g0052 a0001c0002t0001g0169 others(4): Show |
7 | HG00408.hp1 HG02630.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1746-574_1746-570d others(7): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 40837069 | ||||||
chr1:40837069 | ATCTTTTC others(3): Show |
A | 28 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0076 others(25): Show |
29 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1746-579_1746-570d others(12): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 40837069 | ||||||
chr1:40837081 | CTTTTCTT others(4): Show |
C | 1 | a0001c0006t0001g0121 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1746-579_1746-569d others(13): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 40837081 | ||||||
chr1:40837087 | TTTTC | T | 61 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0026 others(58): Show |
67 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.1746-574_1746-571d others(6): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 40837087 | ||||||
chr1:40837091 | C | CT | 5 | a0001c0001t0001g0318 a0001c0001t0002g0012 a0001c0001t0002g0105 others(2): Show |
6 | HG01167.hp2 HG01169.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1746-560dupT | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 40837091 | ||||||
chr1:40837091 | C | CTTTTCT | 7 | a0001c0001t0005g0116 a0001c0001t0005g0119 a0001c0001t0012g0159 others(4): Show |
7 | HG00735.hp2 HG01175.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.1746-570_1746-569i others(8): Show |
KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 40837091 | ||||||
chr1:40837233 | A | G | 17 | a0001c0001t0004g0011 a0001c0001t0004g0059 a0001c0001t0004g0077 others(14): Show |
18 | HG00558.hp1 HG02027.hp1 NA18945.hp2 others(15): Show |
intron_variant | MODIFIER | c.1746-432A>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 12/13 | chr1 | 40837233 | |||||||
chr1:40837381 | C | A | 1 | a0001c0002t0013g0053 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1746-284C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 12/13 | chr1 | 40837381 | |||||||
chr1:40837382 | T | G | 1 | a0001c0002t0013g0053 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1746-283T>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 12/13 | chr1 | 40837382 | |||||||
chr1:40837578 | C | A | 1 | a0001c0002t0015g0346 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1746-87C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 12/13 | chr1 | 40837578 | |||||||
chr1:40837945 | C | T | 1 | a0002c0014t0001g0313 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1875+151C>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 13/13 | chr1 | 40837945 | |||||||
chr1:40838017 | C | A | 1 | a0001c0001t0001g0327 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1875+223C>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 13/13 | chr1 | 40838017 | |||||||
chr1:40838151 | C | G | 1 | a0001c0002t0003g0140 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1876-160C>G | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 13/13 | chr1 | 40838151 | |||||||
chr1:40838232 | G | A | 39 | a0001c0001t0003g0001 a0001c0001t0003g0036 a0001c0001t0003g0038 others(36): Show |
43 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1876-79G>A | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 13/13 | chr1 | 40838232 | |||||||
chr1:40838240 | A | T | 1 | a0001c0003t0001g0293 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1876-71A>T | KCNQ4 | ENSG00000117013.17 | transcript | ENST00000347132.10 | protein_coding | 13/13 | chr1 | 40838240 |