Item | Value |
---|---|
geneid | 113510 |
ensemblid | ENSG00000163312.11 |
hgncid | 18536 |
symbol | HELQ |
name | helicase, POLQ like |
refseq_nuc | NM_133636.5 |
refseq_prot | NP_598375.3 |
ensembl_nuc | ENST00000295488.8 |
ensembl_prot | ENSP00000295488.3 |
mane_status | MANE Select |
chr | chr4 |
start | 83407346 |
end | 83455823 |
strand | - |
ver | v1.2 |
region | chr4:83407346-83455823 |
region5000 | chr4:83402346-83460823 |
regionname0 | HELQ_chr4_83407346_83455823 |
regionname5000 | HELQ_chr4_83402346_83460823 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1101 | 147 | 21 | 29 | 74 | 4 | 19 | 51 | HELQ_chr4_83402346_83460823 | HELQ | MDECG others(1096): Show |
chr4 | 83402346 | 83460823 |
a0002 | 1/0 | 1101 | 100 | 14 | 20 | 46 | 5 | 14 | 39 | HELQ_chr4_83402346_83460823 | HELQ | MDECG others(1096): Show |
chr4 | 83402346 | 83460823 |
a0003 | 0/0 | 1101 | 29 | 28 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | MDECG others(1096): Show |
chr4 | 83402346 | 83460823 |
a0004 | 0/0 | 1101 | 20 | 18 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | MDECG others(1096): Show |
chr4 | 83402346 | 83460823 |
a0005 | 0/0 | 1101 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | MDECG others(1096): Show |
chr4 | 83402346 | 83460823 |
a0006 | 0/0 | 1101 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | MDECG others(1096): Show |
chr4 | 83402346 | 83460823 |
a0007 | 0/0 | 1101 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | MDECG others(1096): Show |
chr4 | 83402346 | 83460823 |
a0008 | 0/0 | 1101 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | MDECG others(1096): Show |
chr4 | 83402346 | 83460823 |
a0009 | 0/0 | 1101 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | MDECG others(1096): Show |
chr4 | 83402346 | 83460823 |
a0010 | 0/0 | 1101 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | MDECG others(1096): Show |
chr4 | 83402346 | 83460823 |
a0011 | 0/0 | 1101 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | MDECG others(1096): Show |
chr4 | 83402346 | 83460823 |
a0012 | 0/0 | 1101 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | MDECG others(1096): Show |
chr4 | 83402346 | 83460823 |
a0013 | 0/0 | 1101 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | MDECG others(1096): Show |
chr4 | 83402346 | 83460823 |
a0014 | 0/0 | 1101 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HELQ_chr4_83402346_83460823 | HELQ | MDECG others(1096): Show |
chr4 | 83402346 | 83460823 |
a0015 | 0/1 | 1101 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | MDECG others(1096): Show |
chr4 | 83402346 | 83460823 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3303 | 124 | 10 | 24 | 73 | 2 | 15 | HELQ_chr4_83402346_83460823 | HELQ | ATGGA others(3298): Show |
chr4 | 83402346 | 83460823 | ||
a0001c0004 | 0/0 | 3303 | 17 | 7 | 5 | 0 | 2 | 3 | HELQ_chr4_83402346_83460823 | HELQ | ATGGA others(3298): Show |
chr4 | 83402346 | 83460823 | ||
a0001c0006 | 0/0 | 3303 | 4 | 2 | 0 | 1 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | ATGGA others(3298): Show |
chr4 | 83402346 | 83460823 | ||
a0001c0020 | 0/0 | 3303 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | ATGGA others(3298): Show |
chr4 | 83402346 | 83460823 | ||
a0001c0021 | 0/0 | 3303 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | ATGGA others(3298): Show |
chr4 | 83402346 | 83460823 | ||
a0002c0002 | 1/0 | 3303 | 99 | 14 | 20 | 46 | 5 | 13 | HELQ_chr4_83402346_83460823 | HELQ | ATGGA others(3298): Show |
chr4 | 83402346 | 83460823 | ||
a0002c0022 | 0/0 | 3303 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | ATGGA others(3298): Show |
chr4 | 83402346 | 83460823 | ||
a0003c0003 | 0/0 | 3303 | 27 | 26 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | ATGGA others(3298): Show |
chr4 | 83402346 | 83460823 | ||
a0003c0016 | 0/0 | 3303 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | ATGGA others(3298): Show |
chr4 | 83402346 | 83460823 | ||
a0003c0017 | 0/0 | 3303 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | ATGGA others(3298): Show |
chr4 | 83402346 | 83460823 | ||
a0004c0005 | 0/0 | 3303 | 15 | 13 | 2 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | ATGGA others(3298): Show |
chr4 | 83402346 | 83460823 | ||
a0004c0010 | 0/0 | 3303 | 3 | 3 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | ATGGA others(3298): Show |
chr4 | 83402346 | 83460823 | ||
a0004c0011 | 0/0 | 3303 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | ATGGA others(3298): Show |
chr4 | 83402346 | 83460823 | ||
a0005c0007 | 0/0 | 3303 | 4 | 4 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | ATGGA others(3298): Show |
chr4 | 83402346 | 83460823 | ||
a0006c0008 | 0/0 | 3303 | 4 | 4 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | ATGGA others(3298): Show |
chr4 | 83402346 | 83460823 | ||
a0007c0009 | 0/0 | 3303 | 3 | 3 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | ATGGA others(3298): Show |
chr4 | 83402346 | 83460823 | ||
a0008c0012 | 0/0 | 3303 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | ATGGA others(3298): Show |
chr4 | 83402346 | 83460823 | ||
a0009c0019 | 0/0 | 3303 | 1 | 0 | 0 | 0 | 1 | 0 | HELQ_chr4_83402346_83460823 | HELQ | ATGGA others(3298): Show |
chr4 | 83402346 | 83460823 | ||
a0010c0024 | 0/0 | 3303 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | ATGGA others(3298): Show |
chr4 | 83402346 | 83460823 | ||
a0011c0023 | 0/0 | 3303 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | ATGGA others(3298): Show |
chr4 | 83402346 | 83460823 | ||
a0012c0014 | 0/0 | 3303 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | ATGGA others(3298): Show |
chr4 | 83402346 | 83460823 | ||
a0013c0015 | 0/0 | 3303 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | ATGGA others(3298): Show |
chr4 | 83402346 | 83460823 | ||
a0014c0018 | 0/0 | 3303 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | ATGGA others(3298): Show |
chr4 | 83402346 | 83460823 | ||
a0015c0013 | 0/1 | 3303 | 1 | 0 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | ATGGA others(3298): Show |
chr4 | 83402346 | 83460823 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3543 | 124 | 10 | 24 | 73 | 2 | 15 | HELQ_chr4_83402346_83460823 | HELQ | GAGAG others(3538): Show |
chr4 | 83402346 | 83460823 |
a0001c0004t0001 | 0/0 | 3543 | 17 | 7 | 5 | 0 | 2 | 3 | HELQ_chr4_83402346_83460823 | HELQ | GAGAG others(3538): Show |
chr4 | 83402346 | 83460823 |
a0001c0006t0001 | 0/0 | 3543 | 4 | 2 | 0 | 1 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | GAGAG others(3538): Show |
chr4 | 83402346 | 83460823 |
a0001c0020t0001 | 0/0 | 3543 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | GAGAG others(3538): Show |
chr4 | 83402346 | 83460823 |
a0001c0021t0001 | 0/0 | 3543 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | GAGAG others(3538): Show |
chr4 | 83402346 | 83460823 |
a0002c0002t0001 | 1/0 | 3543 | 99 | 14 | 20 | 46 | 5 | 13 | HELQ_chr4_83402346_83460823 | HELQ | GAGAG others(3538): Show |
chr4 | 83402346 | 83460823 |
a0002c0022t0001 | 0/0 | 3543 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | GAGAG others(3538): Show |
chr4 | 83402346 | 83460823 |
a0003c0003t0002 | 0/0 | 3540 | 27 | 26 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | GAGAG others(3535): Show |
chr4 | 83402346 | 83460823 |
a0003c0016t0001 | 0/0 | 3543 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | GAGAG others(3538): Show |
chr4 | 83402346 | 83460823 |
a0003c0017t0001 | 0/0 | 3543 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | GAGAG others(3538): Show |
chr4 | 83402346 | 83460823 |
a0004c0005t0001 | 0/0 | 3543 | 11 | 10 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | GAGAG others(3538): Show |
chr4 | 83402346 | 83460823 |
a0004c0005t0002 | 0/0 | 3540 | 4 | 3 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | GAGAG others(3535): Show |
chr4 | 83402346 | 83460823 |
a0004c0010t0001 | 0/0 | 3543 | 3 | 3 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | GAGAG others(3538): Show |
chr4 | 83402346 | 83460823 |
a0004c0011t0002 | 0/0 | 3540 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | GAGAG others(3535): Show |
chr4 | 83402346 | 83460823 |
a0005c0007t0001 | 0/0 | 3543 | 4 | 4 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | GAGAG others(3538): Show |
chr4 | 83402346 | 83460823 |
a0006c0008t0001 | 0/0 | 3543 | 4 | 4 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | GAGAG others(3538): Show |
chr4 | 83402346 | 83460823 |
a0007c0009t0002 | 0/0 | 3540 | 3 | 3 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | GAGAG others(3535): Show |
chr4 | 83402346 | 83460823 |
a0008c0012t0001 | 0/0 | 3543 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | GAGAG others(3538): Show |
chr4 | 83402346 | 83460823 |
a0009c0019t0001 | 0/0 | 3543 | 1 | 0 | 0 | 0 | 1 | 0 | HELQ_chr4_83402346_83460823 | HELQ | GAGAG others(3538): Show |
chr4 | 83402346 | 83460823 |
a0010c0024t0001 | 0/0 | 3543 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | GAGAG others(3538): Show |
chr4 | 83402346 | 83460823 |
a0011c0023t0001 | 0/0 | 3543 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | GAGAG others(3538): Show |
chr4 | 83402346 | 83460823 |
a0012c0014t0002 | 0/0 | 3540 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | GAGAG others(3535): Show |
chr4 | 83402346 | 83460823 |
a0013c0015t0002 | 0/0 | 3540 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | GAGAG others(3535): Show |
chr4 | 83402346 | 83460823 |
a0014c0018t0001 | 0/0 | 3543 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | GAGAG others(3538): Show |
chr4 | 83402346 | 83460823 |
a0015c0013t0001 | 0/1 | 3543 | 1 | 0 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | GAGAG others(3538): Show |
chr4 | 83402346 | 83460823 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0004t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0004t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0004t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0004t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0004t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0004t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0004t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0004t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0004t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0004t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0004t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0004t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0004t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0004t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0004t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0006t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0006t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0006t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0020t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0001c0021t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0001 | 0/0 | 12 | 1 | 1 | 7 | 0 | 3 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0002 | 1/0 | 5 | 0 | 2 | 2 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0002c0022t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0003t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0016t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0003c0017t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0005t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0005t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0005t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0005t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0005t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0005t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0005t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0005t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0005t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0005t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0005t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0005t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0005t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0010t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0010t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0010t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0011t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0004c0011t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0005c0007t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0005c0007t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0005c0007t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0006c0008t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0006c0008t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0006c0008t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0006c0008t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0007c0009t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0007c0009t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0008c0012t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0008c0012t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0009c0019t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0010c0024t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0011c0023t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0012c0014t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0013c0015t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0014c0018t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
a0015c0013t0001g0033 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0111 | EUR | GBR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0078 | EUR | GBR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00140 | hp1 | a0001 | c0004 | t0001 | g0013 | EUR | GBR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0125 | EUR | GBR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00280 | hp1 | a0001 | c0004 | t0001 | g0013 | EUR | FIN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00280 | hp2 | a0009 | c0019 | t0001 | g0144 | EUR | FIN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | CHS | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00642 | hp1 | a0001 | c0004 | t0001 | g0048 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0123 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00733 | hp1 | a0001 | c0004 | t0001 | g0045 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00733 | hp2 | a0002 | c0002 | t0001 | g0122 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0087 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00735 | hp2 | a0001 | c0004 | t0001 | g0050 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00741 | hp1 | a0001 | c0004 | t0001 | g0049 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0101 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0097 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0019 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01106 | hp1 | a0010 | c0024 | t0001 | g0228 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01109 | hp1 | a0003 | c0003 | t0002 | g0233 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01167 | hp2 | a0004 | c0005 | t0002 | g0256 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01243 | hp1 | a0002 | c0002 | t0001 | g0113 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01243 | hp2 | a0004 | c0005 | t0001 | g0039 | AMR | PUR | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01255 | hp1 | a0001 | c0004 | t0001 | g0047 | AMR | CLM | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0110 | AMR | CLM | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0015 | AMR | CLM | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0070 | AMR | CLM | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0015 | AMR | CLM | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0109 | AMR | CLM | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0124 | AMR | CLM | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0096 | EUR | IBS | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0100 | EUR | IBS | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01884 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01891 | hp1 | a0002 | c0002 | t0001 | g0083 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0092 | AMR | PEL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG01981 | hp2 | a0011 | c0023 | t0001 | g0227 | AMR | PEL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0093 | AMR | PEL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02055 | hp1 | a0004 | c0005 | t0001 | g0035 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02055 | hp2 | a0012 | c0014 | t0002 | g0254 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02080 | hp1 | a0001 | c0006 | t0001 | g0177 | EAS | KHV | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | KHV | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | KHV | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02145 | hp2 | a0003 | c0003 | t0002 | g0234 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | CDX | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CDX | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CDX | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02258 | hp1 | a0001 | c0021 | t0001 | g0063 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02258 | hp2 | a0003 | c0003 | t0002 | g0248 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0089 | AMR | PEL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02451 | hp1 | a0003 | c0017 | t0001 | g0044 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02451 | hp2 | a0004 | c0010 | t0001 | g0224 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0103 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02572 | hp2 | a0003 | c0003 | t0002 | g0236 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02615 | hp1 | a0004 | c0005 | t0001 | g0012 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02615 | hp2 | a0003 | c0003 | t0002 | g0030 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02622 | hp1 | a0008 | c0012 | t0001 | g0084 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02622 | hp2 | a0003 | c0003 | t0002 | g0011 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02630 | hp1 | a0003 | c0003 | t0002 | g0246 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02630 | hp2 | a0004 | c0005 | t0001 | g0012 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0072 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02717 | hp1 | a0004 | c0010 | t0001 | g0225 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02717 | hp2 | a0004 | c0011 | t0002 | g0231 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02723 | hp1 | a0003 | c0003 | t0002 | g0251 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02723 | hp2 | a0001 | c0020 | t0001 | g0158 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02738 | hp2 | a0014 | c0018 | t0001 | g0146 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02809 | hp2 | a0004 | c0005 | t0002 | g0032 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0086 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02818 | hp2 | a0004 | c0005 | t0001 | g0034 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0102 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02895 | hp1 | a0003 | c0003 | t0002 | g0257 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02895 | hp2 | a0004 | c0005 | t0001 | g0037 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02896 | hp1 | a0001 | c0006 | t0001 | g0022 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02896 | hp2 | a0004 | c0005 | t0001 | g0038 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02897 | hp1 | a0001 | c0006 | t0001 | g0022 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02897 | hp2 | a0003 | c0003 | t0002 | g0245 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02922 | hp1 | a0003 | c0003 | t0002 | g0250 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02922 | hp2 | a0001 | c0004 | t0001 | g0014 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02965 | hp1 | a0003 | c0003 | t0002 | g0235 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02965 | hp2 | a0001 | c0004 | t0001 | g0060 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02970 | hp1 | a0001 | c0004 | t0001 | g0061 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02970 | hp2 | a0003 | c0003 | t0002 | g0030 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02976 | hp1 | a0001 | c0004 | t0001 | g0014 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02976 | hp2 | a0003 | c0003 | t0002 | g0011 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0120 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03041 | hp1 | a0002 | c0002 | t0001 | g0082 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03041 | hp2 | a0005 | c0007 | t0001 | g0028 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03098 | hp1 | a0005 | c0007 | t0001 | g0223 | AFR | MSL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03098 | hp2 | a0007 | c0009 | t0002 | g0255 | AFR | MSL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03130 | hp1 | a0003 | c0003 | t0002 | g0011 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03130 | hp2 | a0003 | c0003 | t0002 | g0239 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03139 | hp1 | a0003 | c0003 | t0002 | g0253 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03139 | hp2 | a0004 | c0005 | t0002 | g0229 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03195 | hp1 | a0005 | c0007 | t0001 | g0054 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03195 | hp2 | a0003 | c0003 | t0002 | g0249 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03209 | hp1 | a0007 | c0009 | t0002 | g0031 | AFR | MSL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03209 | hp2 | a0004 | c0005 | t0001 | g0043 | AFR | MSL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0073 | AFR | MSL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03225 | hp2 | a0003 | c0003 | t0002 | g0237 | AFR | MSL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03239 | hp2 | a0001 | c0006 | t0001 | g0179 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03453 | hp1 | a0004 | c0005 | t0002 | g0032 | AFR | MSL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03453 | hp2 | a0005 | c0007 | t0001 | g0028 | AFR | MSL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03486 | hp1 | a0003 | c0003 | t0002 | g0238 | AFR | MSL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03486 | hp2 | a0004 | c0005 | t0001 | g0041 | AFR | MSL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0108 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0019 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03516 | hp1 | a0006 | c0008 | t0001 | g0064 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03540 | hp1 | a0006 | c0008 | t0001 | g0062 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03540 | hp2 | a0004 | c0005 | t0001 | g0036 | AFR | GWD | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0117 | AFR | MSL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03579 | hp2 | a0004 | c0005 | t0001 | g0040 | AFR | MSL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03654 | hp2 | a0002 | c0022 | t0001 | g0053 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0016 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03669 | hp2 | a0001 | c0004 | t0001 | g0051 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | STU | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03688 | hp2 | a0001 | c0004 | t0001 | g0046 | SAS | STU | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03704 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03710 | hp1 | a0001 | c0004 | t0001 | g0052 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | BEB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0016 | SAS | BEB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0116 | SAS | BEB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0112 | SAS | STU | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | STU | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | STU | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0121 | SAS | STU | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | STU | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0065 | SAS | STU | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | YRI | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0105 | AFR | YRI | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18906 | hp1 | a0003 | c0003 | t0002 | g0243 | AFR | YRI | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18906 | hp2 | a0006 | c0008 | t0001 | g0057 | AFR | YRI | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18939 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18942 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18965 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18982 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18985 | hp2 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18988 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18990 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18993 | hp1 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | LWK | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19030 | hp2 | a0003 | c0003 | t0002 | g0241 | AFR | LWK | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19043 | hp1 | a0007 | c0009 | t0002 | g0031 | AFR | LWK | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19043 | hp2 | a0001 | c0004 | t0001 | g0056 | AFR | LWK | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19078 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19086 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19240 | hp1 | a0003 | c0003 | t0002 | g0244 | AFR | YRI | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA19240 | hp2 | a0004 | c0011 | t0002 | g0230 | AFR | YRI | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA20129 | hp1 | a0003 | c0003 | t0002 | g0252 | AFR | ASW | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ASW | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0114 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02486 | hp1 | a0013 | c0015 | t0002 | g0232 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02486 | hp2 | a0001 | c0004 | t0001 | g0055 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02559 | hp1 | a0002 | c0002 | t0001 | g0104 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG02559 | hp2 | a0003 | c0003 | t0002 | g0242 | AFR | ACB | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03471 | hp1 | a0003 | c0003 | t0002 | g0240 | AFR | MSL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG03471 | hp2 | a0006 | c0008 | t0001 | g0059 | AFR | MSL | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG06807 | hp1 | a0001 | c0004 | t0001 | g0058 | AFR | USA | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
HG06807 | hp2 | a0004 | c0010 | t0001 | g0226 | AFR | USA | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA20300 | hp1 | a0008 | c0012 | t0001 | g0085 | AFR | USA | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0066 | AFR | USA | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA21309 | hp1 | a0003 | c0003 | t0002 | g0247 | AFR | LWK | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
NA21309 | hp2 | a0003 | c0016 | t0001 | g0042 | AFR | LWK | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
homoSapiens | chm13v2 | a0015 | c0013 | t0001 | g0033 | REF | REF | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0002 | REF | REF | HELQ_chr4_83402346_83460823 | HELQ | chr4 | 83402346 | 83460823 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:83407479 | C | T | 2 | a0006 a0013 |
5 | HG02486.hp1 HG03471.hp2 HG03516.hp1 others(2): Show |
missense_variant | MODERATE | c.3280G>A | p.Val1094Met | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 18/18 | 3410/3543 | 3280/3306 | 1094/1101 | chr4 | 83407479 | |||
chr4:83427592 | T | C | 1 | a0009 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.2647A>G | p.Asn883Asp | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/18 | 2777/3543 | 2647/3306 | 883/1101 | chr4 | 83427592 | |||
chr4:83427612 | T | A | 1 | a0005 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
missense_variant | MODERATE | c.2627A>T | p.Tyr876Phe | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/18 | 2757/3543 | 2627/3306 | 876/1101 | chr4 | 83427612 | |||
chr4:83429586 | T | C | 1 | a0007 | 3 | HG03098.hp2 HG03209.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.2456A>G | p.Lys819Arg | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/18 | 2586/3543 | 2456/3306 | 819/1101 | chr4 | 83429586 | |||
chr4:83437005 | C | T | 1 | a0005 | 4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
missense_variant | MODERATE | c.1901G>A | p.Arg634His | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/18 | 2031/3543 | 1901/3306 | 634/1101 | chr4 | 83437005 | |||
chr4:83437074 | T | C | 1 | a0007 | 3 | HG03098.hp2 HG03209.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.1832A>G | p.Lys611Arg | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/18 | 1962/3543 | 1832/3306 | 611/1101 | chr4 | 83437074 | |||
chr4:83439918 | G | A | 2 | a0003 a0013 |
30 | HG01109.hp1 HG02145.hp2 HG02258.hp2 others(27): Show |
missense_variant | MODERATE | c.1753C>T | p.Pro585Ser | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/18 | 1883/3543 | 1753/3306 | 585/1101 | chr4 | 83439918 | |||
chr4:83441313 | T | G | 1 | a0008 | 2 | HG02622.hp1 NA20300.hp1 |
missense_variant | MODERATE | c.1654A>C | p.Asn552His | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/18 | 1784/3543 | 1654/3306 | 552/1101 | chr4 | 83441313 | |||
chr4:83441321 | C | T | 1 | a0008 | 2 | HG02622.hp1 NA20300.hp1 |
missense_variant | MODERATE | c.1646G>A | p.Arg549His | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/18 | 1776/3543 | 1646/3306 | 549/1101 | chr4 | 83441321 | |||
chr4:83443597 | C | T | 1 | a0014 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.1483G>A | p.Gly495Ser | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/18 | 1613/3543 | 1483/3306 | 495/1101 | chr4 | 83443597 | |||
chr4:83453327 | C | T | 12 | a0001 a0003 a0004 others(9): Show |
213 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
missense_variant | MODERATE | c.916G>A | p.Val306Ile | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/18 | 1046/3543 | 916/3306 | 306/1101 | chr4 | 83453327 | |||
chr4:83453539 | A | G | 5 | a0003 a0004 a0007 others(2): Show |
54 | HG01109.hp1 HG01167.hp2 HG01243.hp2 others(51): Show |
missense_variant | MODERATE | c.704T>C | p.Leu235Pro | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/18 | 834/3543 | 704/3306 | 235/1101 | chr4 | 83453539 | |||
chr4:83453873 | C | G | 1 | a0012 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.370G>C | p.Asp124His | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/18 | 500/3543 | 370/3306 | 124/1101 | chr4 | 83453873 | |||
chr4:83455594 | G | A | 1 | a0011 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.100C>T | p.Leu34Phe | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/18 | 230/3543 | 100/3306 | 34/1101 | chr4 | 83455594 | |||
chr4:83455641 | T | C | 1 | a0010 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.53A>G | p.Asn18Ser | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/18 | 183/3543 | 53/3306 | 18/1101 | chr4 | 83455641 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:83429717 | A | G | 7 | a0001c0021 a0003c0003 a0003c0016 others(4): Show |
37 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(34): Show |
synonymous_variant | LOW | c.2325T>C | p.His775His | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/18 | 2455/3543 | 2325/3306 | 775/1101 | chr4 | 83429717 | |||
chr4:83443598 | A | G | 11 | a0001c0001 a0001c0020 a0002c0022 others(8): Show |
163 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(160): Show |
synonymous_variant | LOW | c.1482T>C | p.Ile494Ile | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/18 | 1612/3543 | 1482/3306 | 494/1101 | chr4 | 83443598 | |||
chr4:83448938 | A | G | 6 | a0001c0001 a0001c0006 a0009c0019 others(3): Show |
132 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(129): Show |
synonymous_variant | LOW | c.1036T>C | p.Leu346Leu | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/18 | 1166/3543 | 1036/3306 | 346/1101 | chr4 | 83448938 | |||
chr4:83453538 | C | A | 1 | a0003c0017 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.705G>T | p.Leu235Leu | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/18 | 835/3543 | 705/3306 | 235/1101 | chr4 | 83453538 | |||
chr4:83455586 | G | C | 1 | a0004c0010 | 3 | HG02451.hp2 HG02717.hp1 HG06807.hp2 |
synonymous_variant | LOW | c.108C>G | p.Pro36Pro | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/18 | 238/3543 | 108/3306 | 36/1101 | chr4 | 83455586 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:83455719 | ACGT | A | 6 | a0003c0003t0002 a0004c0005t0002 a0004c0011t0002 others(3): Show |
38 | HG01109.hp1 HG01167.hp2 HG02055.hp2 others(35): Show |
5_prime_UTR_variant | MODIFIER | c.-29_-27delACG | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/18 | 27 | chr4 | 83455719 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:83407581 | G | A | 6 | a0002c0002t0001g0096 a0002c0002t0001g0108 a0002c0002t0001g0109 others(3): Show |
6 | HG00099.hp1 HG00733.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.3199-21C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83407581 | |||||||
chr4:83407700 | G | A | 1 | a0002c0002t0001g0124 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3199-140C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83407700 | |||||||
chr4:83407748 | T | G | 1 | a0003c0017t0001g0044 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3199-188A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83407748 | |||||||
chr4:83407906 | A | G | 1 | a0001c0020t0001g0158 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3199-346T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83407906 | |||||||
chr4:83407929 | G | A | 16 | a0001c0004t0001g0013 a0001c0004t0001g0045 a0001c0004t0001g0046 others(13): Show |
19 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.3199-369C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83407929 | |||||||
chr4:83407951 | T | G | 5 | a0006c0008t0001g0057 a0006c0008t0001g0059 a0006c0008t0001g0062 others(2): Show |
5 | HG02486.hp1 HG03471.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.3199-391A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83407951 | |||||||
chr4:83408046 | A | G | 31 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(28): Show |
34 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(31): Show |
intron_variant | MODIFIER | c.3199-486T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83408046 | |||||||
chr4:83408134 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3199-574A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83408134 | |||||||
chr4:83408197 | T | C | 22 | a0001c0001t0001g0024 a0001c0001t0001g0156 a0001c0001t0001g0207 others(19): Show |
26 | HG01081.hp2 HG01106.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.3199-637A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83408197 | |||||||
chr4:83408291 | C | T | 1 | a0001c0001t0001g0027 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.3199-731G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83408291 | |||||||
chr4:83408494 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3199-934C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83408494 | |||||||
chr4:83408652 | G | A | 1 | a0001c0004t0001g0058 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3199-1092C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83408652 | |||||||
chr4:83408701 | C | T | 5 | a0006c0008t0001g0057 a0006c0008t0001g0059 a0006c0008t0001g0062 others(2): Show |
5 | HG02486.hp1 HG03471.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.3199-1141G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83408701 | |||||||
chr4:83408762 | G | C | 2 | a0007c0009t0002g0031 a0007c0009t0002g0255 |
3 | HG03098.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3199-1202C>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83408762 | |||||||
chr4:83408906 | A | G | 16 | a0001c0004t0001g0013 a0001c0004t0001g0045 a0001c0004t0001g0046 others(13): Show |
19 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.3199-1346T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83408906 | |||||||
chr4:83408961 | G | A | 3 | a0006c0008t0001g0057 a0006c0008t0001g0059 a0006c0008t0001g0064 |
3 | HG03471.hp2 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3199-1401C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83408961 | |||||||
chr4:83409047 | A | C | 5 | a0006c0008t0001g0057 a0006c0008t0001g0059 a0006c0008t0001g0062 others(2): Show |
5 | HG02486.hp1 HG03471.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.3199-1487T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83409047 | |||||||
chr4:83409054 | T | C | 7 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0141 others(4): Show |
7 | NA18952.hp1 NA18954.hp2 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.3199-1494A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83409054 | |||||||
chr4:83409201 | T | C | 6 | a0001c0006t0001g0022 a0002c0002t0001g0029 a0002c0002t0001g0086 others(3): Show |
8 | HG01243.hp1 HG01884.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.3199-1641A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83409201 | |||||||
chr4:83409322 | G | A | 14 | a0001c0001t0001g0024 a0001c0001t0001g0156 a0001c0001t0001g0207 others(11): Show |
16 | HG01081.hp2 HG01106.hp1 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.3199-1762C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83409322 | |||||||
chr4:83409424 | G | A | 1 | a0004c0005t0001g0038 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3199-1864C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83409424 | |||||||
chr4:83409550 | T | C | 5 | a0006c0008t0001g0057 a0006c0008t0001g0059 a0006c0008t0001g0062 others(2): Show |
5 | HG02486.hp1 HG03471.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.3199-1990A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83409550 | |||||||
chr4:83409553 | CA | C | 23 | a0001c0004t0001g0013 a0001c0004t0001g0045 a0001c0004t0001g0046 others(20): Show |
26 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.3199-1994delT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83409553 | |||||||
chr4:83409578 | C | A | 53 | a0001c0004t0001g0013 a0001c0004t0001g0045 a0001c0004t0001g0046 others(50): Show |
59 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.3199-2018G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83409578 | |||||||
chr4:83409830 | C | T | 1 | a0008c0012t0001g0084 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3199-2270G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83409830 | |||||||
chr4:83410034 | T | C | 1 | a0004c0005t0001g0040 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3199-2474A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410034 | |||||||
chr4:83410051 | G | A | 6 | a0001c0006t0001g0022 a0002c0002t0001g0029 a0002c0002t0001g0086 others(3): Show |
8 | HG01243.hp1 HG01884.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.3199-2491C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410051 | |||||||
chr4:83410153 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3199-2593T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410153 | |||||||
chr4:83410221 | C | T | 2 | a0001c0004t0001g0056 a0004c0011t0002g0231 |
2 | HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3199-2661G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410221 | |||||||
chr4:83410230 | C | CA | 6 | a0001c0006t0001g0022 a0002c0002t0001g0029 a0002c0002t0001g0086 others(3): Show |
8 | HG01243.hp1 HG01884.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.3199-2671dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410230 | |||||||
chr4:83410289 | A | C | 55 | a0001c0004t0001g0013 a0001c0004t0001g0045 a0001c0004t0001g0046 others(52): Show |
62 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.3199-2729T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410289 | |||||||
chr4:83410290 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3199-2730A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410290 | |||||||
chr4:83410392 | T | C | 3 | a0006c0008t0001g0057 a0006c0008t0001g0059 a0006c0008t0001g0064 |
3 | HG03471.hp2 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3199-2832A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410392 | |||||||
chr4:83410458 | G | T | 3 | a0006c0008t0001g0057 a0006c0008t0001g0059 a0006c0008t0001g0064 |
3 | HG03471.hp2 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3199-2898C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410458 | |||||||
chr4:83410518 | C | CAG | 53 | a0001c0004t0001g0013 a0001c0004t0001g0045 a0001c0004t0001g0046 others(50): Show |
59 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.3199-2960_3199-295 others(6): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410518 | |||||||
chr4:83410542 | G | A | 2 | a0003c0016t0001g0042 a0003c0017t0001g0044 |
2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3199-2982C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410542 | |||||||
chr4:83410572 | G | A | 1 | a0003c0003t0002g0247 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3199-3012C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410572 | |||||||
chr4:83410615 | T | C | 181 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(178): Show |
214 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.3199-3055A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410615 | |||||||
chr4:83410645 | G | A | 5 | a0006c0008t0001g0057 a0006c0008t0001g0059 a0006c0008t0001g0062 others(2): Show |
5 | HG02486.hp1 HG03471.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.3199-3085C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410645 | |||||||
chr4:83410712 | G | A | 1 | a0002c0002t0001g0097 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.3199-3152C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410712 | |||||||
chr4:83410836 | T | C | 90 | a0001c0001t0001g0156 a0001c0001t0001g0207 a0001c0001t0001g0208 others(87): Show |
101 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.3199-3276A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410836 | |||||||
chr4:83410960 | G | A | 1 | a0003c0003t0002g0236 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3199-3400C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410960 | |||||||
chr4:83410985 | T | TA | 6 | a0001c0001t0001g0187 a0001c0001t0001g0191 a0001c0001t0001g0219 others(3): Show |
6 | HG01109.hp1 HG01168.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.3199-3426dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83410985 | |||||||
chr4:83411087 | G | T | 1 | a0001c0001t0001g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3199-3527C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83411087 | |||||||
chr4:83411157 | C | CA | 40 | a0001c0001t0001g0131 a0001c0001t0001g0154 a0001c0001t0001g0156 others(37): Show |
44 | HG01081.hp2 HG01106.hp1 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.3199-3598dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83411157 | |||||||
chr4:83411157 | CA | C | 53 | a0001c0001t0001g0149 a0001c0004t0001g0013 a0001c0004t0001g0045 others(50): Show |
60 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.3199-3598delT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83411157 | |||||||
chr4:83411206 | T | C | 3 | a0006c0008t0001g0057 a0006c0008t0001g0059 a0006c0008t0001g0064 |
3 | HG03471.hp2 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3199-3646A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83411206 | |||||||
chr4:83411251 | T | C | 52 | a0001c0004t0001g0013 a0001c0004t0001g0045 a0001c0004t0001g0046 others(49): Show |
59 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.3199-3691A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83411251 | |||||||
chr4:83411310 | A | T | 2 | a0002c0002t0001g0100 a0002c0002t0001g0101 |
2 | HG01070.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.3199-3750T>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83411310 | |||||||
chr4:83411321 | T | C | 1 | a0002c0002t0001g0070 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3199-3761A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83411321 | |||||||
chr4:83411604 | A | AAAAT | 31 | a0001c0006t0001g0022 a0001c0020t0001g0158 a0002c0002t0001g0029 others(28): Show |
36 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.3199-4048_3199-404 others(8): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83411604 | |||||||
chr4:83411625 | A | AAATAAAT others(4): Show |
1 | a0003c0016t0001g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3199-4066_3199-406 others(15): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83411625 | |||||||
chr4:83411630 | T | A | 1 | a0003c0016t0001g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3199-4070A>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83411630 | |||||||
chr4:83411637 | T | A | 3 | a0002c0002t0001g0112 a0002c0002t0001g0120 a0002c0002t0001g0121 |
3 | HG03017.hp1 HG04115.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.3199-4077A>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83411637 | |||||||
chr4:83411953 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3199-4393C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83411953 | |||||||
chr4:83412178 | T | G | 5 | a0004c0005t0001g0036 a0004c0005t0001g0037 a0004c0010t0001g0224 others(2): Show |
5 | HG02451.hp2 HG02717.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.3198+4553A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83412178 | |||||||
chr4:83412185 | T | C | 1 | a0004c0005t0002g0229 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3198+4546A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83412185 | |||||||
chr4:83412311 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.3198+4420G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83412311 | |||||||
chr4:83412314 | G | A | 3 | a0006c0008t0001g0057 a0006c0008t0001g0059 a0006c0008t0001g0064 |
3 | HG03471.hp2 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3198+4417C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83412314 | |||||||
chr4:83412395 | G | A | 13 | a0004c0005t0001g0012 a0004c0005t0001g0034 a0004c0005t0001g0035 others(10): Show |
14 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.3198+4336C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83412395 | |||||||
chr4:83412726 | A | T | 1 | a0002c0002t0001g0100 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.3198+4005T>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83412726 | |||||||
chr4:83412817 | C | G | 12 | a0001c0004t0001g0055 a0001c0006t0001g0022 a0002c0002t0001g0029 others(9): Show |
14 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.3198+3914G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83412817 | |||||||
chr4:83412912 | G | C | 6 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0027 others(3): Show |
9 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.3198+3819C>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83412912 | |||||||
chr4:83413135 | C | G | 2 | a0003c0016t0001g0042 a0003c0017t0001g0044 |
2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3198+3596G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83413135 | |||||||
chr4:83413153 | T | C | 27 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(24): Show |
30 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(27): Show |
intron_variant | MODIFIER | c.3198+3578A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83413153 | |||||||
chr4:83413365 | C | T | 1 | a0013c0015t0002g0232 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3198+3366G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83413365 | |||||||
chr4:83413566 | T | C | 1 | a0003c0016t0001g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3198+3165A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83413566 | |||||||
chr4:83413593 | C | T | 1 | a0001c0004t0001g0052 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3198+3138G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83413593 | |||||||
chr4:83413614 | C | G | 51 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0045 others(48): Show |
57 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.3198+3117G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83413614 | |||||||
chr4:83413818 | A | G | 33 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(30): Show |
38 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(35): Show |
intron_variant | MODIFIER | c.3198+2913T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83413818 | |||||||
chr4:83413860 | G | T | 10 | a0001c0006t0001g0022 a0002c0002t0001g0029 a0002c0002t0001g0082 others(7): Show |
12 | HG01243.hp1 HG01884.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.3198+2871C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83413860 | |||||||
chr4:83414003 | T | C | 1 | a0002c0002t0001g0099 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3198+2728A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83414003 | |||||||
chr4:83414064 | C | T | 1 | a0002c0002t0001g0095 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3198+2667G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83414064 | |||||||
chr4:83414324 | A | C | 6 | a0001c0001t0001g0024 a0001c0001t0001g0156 a0001c0001t0001g0207 others(3): Show |
7 | HG01081.hp2 HG01106.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.3198+2407T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83414324 | |||||||
chr4:83414421 | A | G | 4 | a0005c0007t0001g0028 a0005c0007t0001g0223 a0007c0009t0002g0031 others(1): Show |
6 | HG03041.hp2 HG03098.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.3198+2310T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83414421 | |||||||
chr4:83414441 | C | T | 2 | a0007c0009t0002g0031 a0007c0009t0002g0255 |
3 | HG03098.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3198+2290G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83414441 | |||||||
chr4:83414487 | GC | G | 3 | a0001c0021t0001g0063 a0008c0012t0001g0084 a0008c0012t0001g0085 |
3 | HG02258.hp1 HG02622.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3198+2243delG | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83414487 | |||||||
chr4:83414827 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3198+1904C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83414827 | |||||||
chr4:83414844 | C | G | 1 | a0004c0011t0002g0230 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3198+1887G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83414844 | |||||||
chr4:83415128 | C | T | 33 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(30): Show |
38 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(35): Show |
intron_variant | MODIFIER | c.3198+1603G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415128 | |||||||
chr4:83415130 | C | T | 84 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0045 others(81): Show |
95 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.3198+1601G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415130 | |||||||
chr4:83415329 | T | C | 2 | a0003c0016t0001g0042 a0003c0017t0001g0044 |
2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3198+1402A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415329 | |||||||
chr4:83415388 | A | G | 4 | a0005c0007t0001g0028 a0005c0007t0001g0223 a0007c0009t0002g0031 others(1): Show |
6 | HG03041.hp2 HG03098.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.3198+1343T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415388 | |||||||
chr4:83415495 | C | T | 4 | a0005c0007t0001g0028 a0005c0007t0001g0223 a0007c0009t0002g0031 others(1): Show |
6 | HG03041.hp2 HG03098.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.3198+1236G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415495 | |||||||
chr4:83415636 | C | CT | 31 | a0001c0001t0001g0155 a0001c0001t0001g0183 a0001c0004t0001g0056 others(28): Show |
34 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(31): Show |
intron_variant | MODIFIER | c.3198+1094dupA | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415636 | |||||||
chr4:83415676 | A | G | 14 | a0001c0004t0001g0013 a0001c0004t0001g0045 a0001c0004t0001g0046 others(11): Show |
16 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.3198+1055T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415676 | |||||||
chr4:83415686 | G | A | 5 | a0004c0005t0001g0035 a0004c0005t0001g0039 a0004c0005t0001g0040 others(2): Show |
5 | HG01243.hp2 HG02055.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3198+1045C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415686 | |||||||
chr4:83415767 | G | T | 1 | a0001c0001t0001g0181 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3198+964C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415767 | |||||||
chr4:83415810 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3198+921G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415810 | |||||||
chr4:83415922 | T | C | 84 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0045 others(81): Show |
95 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.3198+809A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415922 | |||||||
chr4:83415941 | C | T | 1 | a0002c0002t0001g0066 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3198+790G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415941 | |||||||
chr4:83415946 | CA | C | 13 | a0001c0004t0001g0013 a0001c0004t0001g0045 a0001c0004t0001g0046 others(10): Show |
15 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.3198+784delT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415946 | |||||||
chr4:83415947 | A | AT | 12 | a0001c0001t0001g0147 a0001c0001t0001g0166 a0001c0001t0001g0180 others(9): Show |
13 | HG01109.hp1 HG02080.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.3198+783dupA | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415947 | |||||||
chr4:83415947 | A | T | 1 | a0012c0014t0002g0254 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3198+784T>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415947 | |||||||
chr4:83415947 | AT | A | 30 | a0001c0004t0001g0014 a0001c0004t0001g0055 a0001c0004t0001g0056 others(27): Show |
32 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.3198+783delA | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415947 | |||||||
chr4:83415947 | ATT | A | 7 | a0001c0006t0001g0022 a0002c0002t0001g0029 a0002c0002t0001g0086 others(4): Show |
9 | HG01243.hp1 HG01884.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.3198+782_3198+783d others(4): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83415947 | |||||||
chr4:83416015 | C | T | 13 | a0004c0005t0001g0012 a0004c0005t0001g0034 a0004c0005t0001g0035 others(10): Show |
14 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.3198+716G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83416015 | |||||||
chr4:83416072 | G | A | 29 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(26): Show |
32 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.3198+659C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83416072 | |||||||
chr4:83416092 | G | A | 5 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0161 others(2): Show |
7 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.3198+639C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83416092 | |||||||
chr4:83416250 | T | G | 1 | a0001c0001t0001g0139 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3198+481A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83416250 | |||||||
chr4:83416255 | T | G | 3 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0010c0024t0001g0228 |
3 | HG01081.hp2 HG01106.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3198+476A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83416255 | |||||||
chr4:83416463 | C | T | 1 | a0002c0002t0001g0072 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3198+268G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83416463 | |||||||
chr4:83416579 | C | A | 1 | a0001c0001t0001g0027 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.3198+152G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83416579 | |||||||
chr4:83416594 | C | T | 1 | a0004c0005t0001g0043 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3198+137G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 17/17 | chr4 | 83416594 | |||||||
chr4:83416923 | T | C | 14 | a0001c0004t0001g0013 a0001c0004t0001g0045 a0001c0004t0001g0046 others(11): Show |
16 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.3064-58A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 16/17 | chr4 | 83416923 | |||||||
chr4:83416994 | C | T | 2 | a0001c0001t0001g0145 a0009c0019t0001g0144 |
2 | HG00280.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.3064-129G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 16/17 | chr4 | 83416994 | |||||||
chr4:83417078 | C | G | 29 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(26): Show |
32 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.3064-213G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 16/17 | chr4 | 83417078 | |||||||
chr4:83417149 | T | C | 4 | a0005c0007t0001g0028 a0005c0007t0001g0223 a0007c0009t0002g0031 others(1): Show |
6 | HG03041.hp2 HG03098.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.3064-284A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 16/17 | chr4 | 83417149 | |||||||
chr4:83417348 | G | T | 1 | a0002c0002t0001g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3064-483C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 16/17 | chr4 | 83417348 | |||||||
chr4:83417560 | C | G | 29 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(26): Show |
32 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.3063+533G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 16/17 | chr4 | 83417560 | |||||||
chr4:83417572 | G | A | 1 | a0001c0004t0001g0056 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3063+521C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 16/17 | chr4 | 83417572 | |||||||
chr4:83417818 | C | T | 27 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(24): Show |
30 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(27): Show |
intron_variant | MODIFIER | c.3063+275G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 16/17 | chr4 | 83417818 | |||||||
chr4:83417833 | C | T | 29 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(26): Show |
32 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.3063+260G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 16/17 | chr4 | 83417833 | |||||||
chr4:83418059 | A | C | 1 | a0001c0006t0001g0179 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3063+34T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 16/17 | chr4 | 83418059 | |||||||
chr4:83418357 | G | C | 1 | a0001c0001t0001g0026 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2950-151C>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83418357 | |||||||
chr4:83418454 | T | C | 2 | a0005c0007t0001g0028 a0005c0007t0001g0223 |
3 | HG03041.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2950-248A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83418454 | |||||||
chr4:83418673 | A | G | 1 | a0002c0002t0001g0116 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2950-467T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83418673 | |||||||
chr4:83418809 | C | T | 1 | a0001c0004t0001g0048 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2950-603G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83418809 | |||||||
chr4:83418923 | T | C | 1 | a0002c0002t0001g0119 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2950-717A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83418923 | |||||||
chr4:83418972 | G | A | 2 | a0005c0007t0001g0028 a0005c0007t0001g0223 |
3 | HG03041.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2950-766C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83418972 | |||||||
chr4:83419083 | CCACAGGC others(2): Show |
C | 4 | a0001c0004t0001g0056 a0004c0005t0002g0229 a0006c0008t0001g0062 others(1): Show |
4 | HG02486.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2950-886_2950-878d others(11): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419083 | |||||||
chr4:83419093 | C | T | 4 | a0001c0004t0001g0056 a0004c0005t0002g0229 a0006c0008t0001g0062 others(1): Show |
4 | HG02486.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2950-887G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419093 | |||||||
chr4:83419094 | A | G | 4 | a0001c0004t0001g0056 a0004c0005t0002g0229 a0006c0008t0001g0062 others(1): Show |
4 | HG02486.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2950-888T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419094 | |||||||
chr4:83419161 | A | AT | 32 | a0001c0001t0001g0195 a0001c0021t0001g0063 a0003c0003t0002g0011 others(29): Show |
36 | HG01109.hp1 HG01175.hp2 HG02145.hp2 others(33): Show |
intron_variant | MODIFIER | c.2950-956dupA | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419161 | |||||||
chr4:83419161 | AT | A | 39 | a0001c0004t0001g0013 a0001c0004t0001g0045 a0001c0004t0001g0046 others(36): Show |
44 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.2950-956delA | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419161 | |||||||
chr4:83419161 | ATT | A | 11 | a0001c0004t0001g0014 a0001c0004t0001g0056 a0001c0004t0001g0058 others(8): Show |
12 | HG02486.hp1 HG02922.hp2 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.2950-957_2950-956d others(4): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419161 | |||||||
chr4:83419192 | G | A | 1 | a0003c0003t0002g0253 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2950-986C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419192 | |||||||
chr4:83419198 | G | C | 6 | a0001c0006t0001g0022 a0002c0002t0001g0029 a0002c0002t0001g0086 others(3): Show |
8 | HG01243.hp1 HG01884.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2950-992C>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419198 | |||||||
chr4:83419392 | A | G | 1 | a0006c0008t0001g0059 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2950-1186T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419392 | |||||||
chr4:83419395 | C | T | 1 | a0004c0005t0001g0038 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2950-1189G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419395 | |||||||
chr4:83419478 | T | C | 2 | a0003c0016t0001g0042 a0003c0017t0001g0044 |
2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2950-1272A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419478 | |||||||
chr4:83419726 | C | T | 7 | a0004c0005t0001g0012 a0004c0005t0001g0034 a0004c0005t0001g0035 others(4): Show |
8 | HG01243.hp2 HG02055.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2950-1520G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419726 | |||||||
chr4:83419743 | T | G | 1 | a0001c0001t0001g0141 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2950-1537A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419743 | |||||||
chr4:83419768 | C | T | 12 | a0001c0004t0001g0013 a0001c0004t0001g0045 a0001c0004t0001g0046 others(9): Show |
14 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.2950-1562G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419768 | |||||||
chr4:83419804 | C | G | 3 | a0005c0007t0001g0028 a0005c0007t0001g0054 a0005c0007t0001g0223 |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2950-1598G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419804 | |||||||
chr4:83419988 | A | C | 29 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(26): Show |
32 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.2949+1575T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83419988 | |||||||
chr4:83420028 | G | A | 26 | a0001c0021t0001g0063 a0003c0003t0002g0030 a0003c0003t0002g0233 others(23): Show |
28 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(25): Show |
intron_variant | MODIFIER | c.2949+1535C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83420028 | |||||||
chr4:83420075 | A | G | 2 | a0005c0007t0001g0054 a0005c0007t0001g0223 |
2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2949+1488T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83420075 | |||||||
chr4:83420343 | G | A | 6 | a0002c0002t0001g0029 a0002c0002t0001g0086 a0002c0002t0001g0102 others(3): Show |
7 | HG01243.hp1 HG01884.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2949+1220C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83420343 | |||||||
chr4:83420413 | G | A | 3 | a0001c0001t0001g0148 a0001c0004t0001g0046 a0001c0004t0001g0047 |
3 | HG01255.hp1 HG03688.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.2949+1150C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83420413 | |||||||
chr4:83420434 | C | T | 5 | a0001c0004t0001g0014 a0001c0004t0001g0058 a0001c0004t0001g0061 others(2): Show |
6 | HG02922.hp2 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2949+1129G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83420434 | |||||||
chr4:83420468 | C | T | 1 | a0005c0007t0001g0054 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2949+1095G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83420468 | |||||||
chr4:83420684 | T | C | 44 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0045 others(41): Show |
50 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.2949+879A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83420684 | |||||||
chr4:83420704 | G | A | 29 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0045 others(26): Show |
33 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.2949+859C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83420704 | |||||||
chr4:83420710 | G | A | 27 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0045 others(24): Show |
30 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.2949+853C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83420710 | |||||||
chr4:83420712 | G | A | 3 | a0005c0007t0001g0028 a0005c0007t0001g0054 a0005c0007t0001g0223 |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2949+851C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83420712 | |||||||
chr4:83420717 | G | A | 2 | a0005c0007t0001g0028 a0005c0007t0001g0223 |
3 | HG03041.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2949+846C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83420717 | |||||||
chr4:83420983 | T | C | 1 | a0003c0016t0001g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2949+580A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83420983 | |||||||
chr4:83420996 | T | C | 3 | a0005c0007t0001g0028 a0005c0007t0001g0054 a0005c0007t0001g0223 |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2949+567A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83420996 | |||||||
chr4:83421116 | T | C | 1 | a0002c0002t0001g0098 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2949+447A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83421116 | |||||||
chr4:83421132 | G | A | 1 | a0002c0002t0001g0122 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2949+431C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83421132 | |||||||
chr4:83421161 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2949+402T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83421161 | |||||||
chr4:83421189 | C | CAA | 3 | a0001c0001t0001g0193 a0002c0002t0001g0007 a0002c0002t0001g0069 |
5 | NA18959.hp2 NA18968.hp2 NA19077.hp1 others(2): Show |
intron_variant | MODIFIER | c.2949+372_2949+373d others(4): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83421189 | |||||||
chr4:83421232 | T | G | 1 | a0002c0002t0001g0078 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2949+331A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83421232 | |||||||
chr4:83421359 | G | T | 7 | a0001c0004t0001g0014 a0001c0004t0001g0058 a0001c0004t0001g0060 others(4): Show |
8 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.2949+204C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83421359 | |||||||
chr4:83421461 | C | A | 1 | a0002c0002t0001g0077 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2949+102G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83421461 | |||||||
chr4:83421543 | C | T | 1 | a0001c0006t0001g0022 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2949+20G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 15/17 | chr4 | 83421543 | |||||||
chr4:83422351 | C | T | 30 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(27): Show |
33 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.2776-615G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83422351 | |||||||
chr4:83422411 | C | T | 84 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0045 others(81): Show |
95 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.2776-675G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83422411 | |||||||
chr4:83422460 | A | G | 13 | a0001c0001t0001g0003 a0001c0001t0001g0134 a0001c0001t0001g0143 others(10): Show |
17 | HG00609.hp1 HG02165.hp1 NA18939.hp1 others(14): Show |
intron_variant | MODIFIER | c.2776-724T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83422460 | |||||||
chr4:83422504 | A | G | 10 | a0001c0004t0001g0014 a0001c0004t0001g0056 a0001c0004t0001g0058 others(7): Show |
11 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.2776-768T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83422504 | |||||||
chr4:83422776 | G | A | 28 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(25): Show |
31 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.2776-1040C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83422776 | |||||||
chr4:83422857 | A | G | 30 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(27): Show |
33 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.2776-1121T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83422857 | |||||||
chr4:83422942 | G | A | 3 | a0005c0007t0001g0028 a0005c0007t0001g0054 a0005c0007t0001g0223 |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2776-1206C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83422942 | |||||||
chr4:83423094 | T | C | 2 | a0007c0009t0002g0031 a0007c0009t0002g0255 |
3 | HG03098.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2776-1358A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423094 | |||||||
chr4:83423164 | A | G | 3 | a0005c0007t0001g0028 a0005c0007t0001g0054 a0005c0007t0001g0223 |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2776-1428T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423164 | |||||||
chr4:83423210 | A | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0140 a0001c0001t0001g0210 others(1): Show |
6 | HG00558.hp2 HG01952.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.2776-1474T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423210 | |||||||
chr4:83423245 | C | T | 1 | a0006c0008t0001g0064 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2776-1509G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423245 | |||||||
chr4:83423263 | T | C | 2 | a0005c0007t0001g0028 a0005c0007t0001g0223 |
3 | HG03041.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2776-1527A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423263 | |||||||
chr4:83423273 | A | T | 1 | a0002c0002t0001g0074 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2776-1537T>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423273 | |||||||
chr4:83423500 | T | A | 1 | a0001c0001t0001g0221 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2776-1764A>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423500 | |||||||
chr4:83423614 | G | A | 29 | a0001c0001t0001g0005 a0001c0001t0001g0126 a0001c0001t0001g0127 others(26): Show |
32 | HG00280.hp2 HG00609.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.2776-1878C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423614 | |||||||
chr4:83423651 | T | C | 33 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(30): Show |
37 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(34): Show |
intron_variant | MODIFIER | c.2776-1915A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423651 | |||||||
chr4:83423685 | C | T | 1 | a0001c0004t0001g0056 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2776-1949G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423685 | |||||||
chr4:83423723 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2776-1987G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423723 | |||||||
chr4:83423727 | A | G | 12 | a0001c0004t0001g0055 a0001c0006t0001g0022 a0002c0002t0001g0029 others(9): Show |
14 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.2776-1991T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423727 | |||||||
chr4:83423763 | T | G | 8 | a0001c0004t0001g0014 a0001c0004t0001g0055 a0001c0004t0001g0058 others(5): Show |
9 | HG02486.hp2 HG02922.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.2776-2027A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423763 | |||||||
chr4:83423780 | G | A | 1 | a0005c0007t0001g0054 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2776-2044C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423780 | |||||||
chr4:83423800 | A | T | 3 | a0001c0021t0001g0063 a0008c0012t0001g0084 a0008c0012t0001g0085 |
3 | HG02258.hp1 HG02622.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2776-2064T>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423800 | |||||||
chr4:83423902 | G | A | 3 | a0005c0007t0001g0028 a0005c0007t0001g0054 a0005c0007t0001g0223 |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2775+2092C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423902 | |||||||
chr4:83423996 | A | C | 2 | a0001c0001t0001g0157 a0001c0001t0001g0213 |
2 | HG01884.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2775+1998T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83423996 | |||||||
chr4:83424020 | T | C | 2 | a0004c0005t0002g0229 a0006c0008t0001g0062 |
2 | HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2775+1974A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83424020 | |||||||
chr4:83424054 | C | A | 1 | a0002c0002t0001g0083 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2775+1940G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83424054 | |||||||
chr4:83424112 | T | C | 1 | a0002c0002t0001g0110 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2775+1882A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83424112 | |||||||
chr4:83424167 | A | G | 3 | a0005c0007t0001g0028 a0005c0007t0001g0054 a0005c0007t0001g0223 |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2775+1827T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83424167 | |||||||
chr4:83424273 | T | C | 3 | a0005c0007t0001g0028 a0005c0007t0001g0054 a0005c0007t0001g0223 |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2775+1721A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83424273 | |||||||
chr4:83424362 | C | G | 1 | a0001c0001t0001g0027 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2775+1632G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83424362 | |||||||
chr4:83424381 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2775+1613G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83424381 | |||||||
chr4:83424403 | C | T | 1 | a0002c0002t0001g0015 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2775+1591G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83424403 | |||||||
chr4:83424463 | G | A | 3 | a0002c0002t0001g0109 a0002c0002t0001g0110 a0002c0002t0001g0111 |
3 | HG00099.hp1 HG01256.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.2775+1531C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83424463 | |||||||
chr4:83424543 | G | A | 2 | a0002c0002t0001g0123 a0002c0002t0001g0124 |
2 | HG00642.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.2775+1451C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83424543 | |||||||
chr4:83424582 | A | G | 2 | a0001c0001t0001g0208 a0010c0024t0001g0228 |
2 | HG01081.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.2775+1412T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83424582 | |||||||
chr4:83424958 | T | G | 1 | a0001c0001t0001g0186 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2775+1036A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83424958 | |||||||
chr4:83424982 | A | G | 33 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(30): Show |
37 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(34): Show |
intron_variant | MODIFIER | c.2775+1012T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83424982 | |||||||
chr4:83425050 | C | G | 30 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(27): Show |
33 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.2775+944G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83425050 | |||||||
chr4:83425152 | C | T | 1 | a0002c0002t0001g0087 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2775+842G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83425152 | |||||||
chr4:83425258 | C | T | 2 | a0006c0008t0001g0057 a0006c0008t0001g0064 |
2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2775+736G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83425258 | |||||||
chr4:83425279 | C | CA | 8 | a0001c0001t0001g0172 a0001c0001t0001g0194 a0001c0001t0001g0195 others(5): Show |
8 | HG01175.hp2 HG02109.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2775+714dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83425279 | |||||||
chr4:83425279 | C | CAA | 26 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(23): Show |
29 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(26): Show |
intron_variant | MODIFIER | c.2775+713_2775+714d others(4): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83425279 | |||||||
chr4:83425279 | CA | C | 52 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0045 others(49): Show |
60 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.2775+714delT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83425279 | |||||||
chr4:83425365 | GA | G | 12 | a0004c0005t0001g0012 a0004c0005t0001g0034 a0004c0005t0001g0035 others(9): Show |
13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2775+628delT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83425365 | |||||||
chr4:83425539 | T | C | 3 | a0005c0007t0001g0028 a0005c0007t0001g0054 a0005c0007t0001g0223 |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2775+455A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83425539 | |||||||
chr4:83425575 | T | G | 2 | a0004c0011t0002g0230 a0004c0011t0002g0231 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2775+419A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83425575 | |||||||
chr4:83425859 | G | A | 33 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(30): Show |
37 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(34): Show |
intron_variant | MODIFIER | c.2775+135C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83425859 | |||||||
chr4:83425958 | A | G | 5 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0161 others(2): Show |
7 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2775+36T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 14/17 | chr4 | 83425958 | |||||||
chr4:83426126 | C | A | 1 | a0001c0004t0001g0056 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2677-34G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83426126 | |||||||
chr4:83426210 | A | G | 109 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(106): Show |
130 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.2677-118T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83426210 | |||||||
chr4:83426247 | TAGGATAT others(4): Show |
T | 1 | a0001c0001t0001g0169 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2677-166_2677-156d others(13): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83426247 | |||||||
chr4:83426270 | C | T | 145 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(142): Show |
170 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(167): Show |
intron_variant | MODIFIER | c.2677-178G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83426270 | |||||||
chr4:83426572 | G | GT | 84 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(81): Show |
102 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.2677-481dupA | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83426572 | |||||||
chr4:83426583 | TG | T | 28 | a0001c0001t0001g0005 a0001c0001t0001g0126 a0001c0001t0001g0127 others(25): Show |
31 | HG00280.hp2 HG00609.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.2677-492delC | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83426583 | |||||||
chr4:83426585 | A | T | 28 | a0001c0001t0001g0005 a0001c0001t0001g0126 a0001c0001t0001g0127 others(25): Show |
31 | HG00280.hp2 HG00609.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.2677-493T>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83426585 | |||||||
chr4:83426650 | G | A | 1 | a0002c0002t0001g0083 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2677-558C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83426650 | |||||||
chr4:83426772 | C | G | 145 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(142): Show |
170 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(167): Show |
intron_variant | MODIFIER | c.2677-680G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83426772 | |||||||
chr4:83426796 | C | T | 110 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(107): Show |
131 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.2677-704G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83426796 | |||||||
chr4:83426824 | C | T | 3 | a0005c0007t0001g0028 a0005c0007t0001g0054 a0005c0007t0001g0223 |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2677-732G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83426824 | |||||||
chr4:83426920 | T | G | 3 | a0005c0007t0001g0028 a0005c0007t0001g0054 a0005c0007t0001g0223 |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2676+643A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83426920 | |||||||
chr4:83426941 | T | C | 1 | a0002c0002t0001g0105 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2676+622A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83426941 | |||||||
chr4:83427043 | G | A | 3 | a0005c0007t0001g0028 a0005c0007t0001g0054 a0005c0007t0001g0223 |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2676+520C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83427043 | |||||||
chr4:83427074 | A | G | 2 | a0004c0011t0002g0230 a0004c0011t0002g0231 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2676+489T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83427074 | |||||||
chr4:83427154 | T | C | 1 | a0001c0001t0001g0025 | 2 | NA18959.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.2676+409A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83427154 | |||||||
chr4:83427188 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2676+375T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83427188 | |||||||
chr4:83427249 | A | G | 4 | a0002c0002t0001g0093 a0002c0002t0001g0112 a0002c0002t0001g0120 others(1): Show |
4 | HG02004.hp1 HG03017.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.2676+314T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83427249 | |||||||
chr4:83427376 | C | T | 30 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(27): Show |
33 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.2676+187G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 13/17 | chr4 | 83427376 | |||||||
chr4:83427957 | G | A | 2 | a0004c0005t0002g0229 a0006c0008t0001g0062 |
2 | HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2519-237C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83427957 | |||||||
chr4:83428074 | T | C | 110 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(107): Show |
131 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.2519-354A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83428074 | |||||||
chr4:83428089 | T | G | 1 | a0013c0015t0002g0232 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2519-369A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83428089 | |||||||
chr4:83428334 | C | A | 1 | a0013c0015t0002g0232 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2519-614G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83428334 | |||||||
chr4:83428378 | T | C | 12 | a0004c0005t0001g0012 a0004c0005t0001g0034 a0004c0005t0001g0035 others(9): Show |
13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2519-658A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83428378 | |||||||
chr4:83428434 | C | A | 144 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
169 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(166): Show |
intron_variant | MODIFIER | c.2519-714G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83428434 | |||||||
chr4:83428601 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2519-881T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83428601 | |||||||
chr4:83428712 | C | G | 33 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(30): Show |
37 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(34): Show |
intron_variant | MODIFIER | c.2518+812G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83428712 | |||||||
chr4:83428782 | T | C | 2 | a0002c0002t0001g0109 a0002c0002t0001g0110 |
2 | HG01256.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.2518+742A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83428782 | |||||||
chr4:83428799 | T | A | 1 | a0001c0001t0001g0176 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2518+725A>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83428799 | |||||||
chr4:83428833 | AAATG | A | 10 | a0001c0004t0001g0014 a0001c0004t0001g0056 a0001c0004t0001g0058 others(7): Show |
11 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.2518+687_2518+690d others(6): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83428833 | |||||||
chr4:83428903 | G | T | 3 | a0003c0003t0002g0245 a0003c0003t0002g0246 a0003c0003t0002g0257 |
3 | HG02630.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2518+621C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83428903 | |||||||
chr4:83428953 | A | G | 1 | a0001c0001t0001g0024 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2518+571T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83428953 | |||||||
chr4:83429019 | T | C | 2 | a0002c0002t0001g0102 a0002c0002t0001g0103 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2518+505A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83429019 | |||||||
chr4:83429056 | CT | C | 30 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(27): Show |
33 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.2518+467delA | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83429056 | |||||||
chr4:83429176 | C | T | 2 | a0007c0009t0002g0031 a0007c0009t0002g0255 |
3 | HG03098.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2518+348G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83429176 | |||||||
chr4:83429217 | A | G | 1 | a0005c0007t0001g0054 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2518+307T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83429217 | |||||||
chr4:83429292 | A | G | 2 | a0003c0016t0001g0042 a0003c0017t0001g0044 |
2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2518+232T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83429292 | |||||||
chr4:83429434 | C | T | 1 | a0001c0001t0001g0026 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2518+90G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83429434 | |||||||
chr4:83429501 | A | G | 12 | a0004c0005t0001g0012 a0004c0005t0001g0034 a0004c0005t0001g0035 others(9): Show |
13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2518+23T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 12/17 | chr4 | 83429501 | |||||||
chr4:83429763 | T | C | 33 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(30): Show |
37 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(34): Show |
intron_variant | MODIFIER | c.2296-17A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83429763 | |||||||
chr4:83429832 | C | T | 1 | a0002c0002t0001g0078 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2296-86G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83429832 | |||||||
chr4:83429900 | T | C | 1 | a0004c0005t0001g0043 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2296-154A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83429900 | |||||||
chr4:83430000 | G | A | 182 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
212 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.2296-254C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83430000 | |||||||
chr4:83430131 | C | T | 12 | a0004c0005t0001g0012 a0004c0005t0001g0034 a0004c0005t0001g0035 others(9): Show |
13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2296-385G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83430131 | |||||||
chr4:83430146 | A | C | 2 | a0003c0003t0002g0245 a0003c0003t0002g0257 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2296-400T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83430146 | |||||||
chr4:83430156 | TA | T | 12 | a0004c0005t0001g0012 a0004c0005t0001g0034 a0004c0005t0001g0035 others(9): Show |
13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2296-411delT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83430156 | |||||||
chr4:83430175 | A | G | 2 | a0003c0016t0001g0042 a0003c0017t0001g0044 |
2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2296-429T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83430175 | |||||||
chr4:83430274 | T | TA | 29 | a0001c0001t0001g0185 a0001c0021t0001g0063 a0003c0003t0002g0011 others(26): Show |
32 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.2296-529dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83430274 | |||||||
chr4:83430274 | T | TAA | 5 | a0003c0016t0001g0042 a0003c0017t0001g0044 a0005c0007t0001g0028 others(2): Show |
6 | HG02451.hp1 HG03041.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2296-530_2296-529d others(4): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83430274 | |||||||
chr4:83430315 | GA | G | 143 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(140): Show |
168 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(165): Show |
intron_variant | MODIFIER | c.2296-570delT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83430315 | |||||||
chr4:83430348 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2296-602C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83430348 | |||||||
chr4:83430406 | G | T | 1 | a0013c0015t0002g0232 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2296-660C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83430406 | |||||||
chr4:83430451 | C | T | 1 | a0012c0014t0002g0254 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2296-705G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83430451 | |||||||
chr4:83430569 | C | T | 1 | a0001c0004t0001g0046 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2296-823G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83430569 | |||||||
chr4:83430754 | T | C | 1 | a0001c0001t0001g0141 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2295+910A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83430754 | |||||||
chr4:83431020 | T | A | 1 | a0003c0017t0001g0044 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2295+644A>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83431020 | |||||||
chr4:83431108 | A | AAAAC | 29 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(26): Show |
32 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.2295+552_2295+555d others(6): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83431108 | |||||||
chr4:83431197 | G | GT | 32 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(29): Show |
36 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(33): Show |
intron_variant | MODIFIER | c.2295+466dupA | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83431197 | |||||||
chr4:83431267 | A | G | 1 | a0001c0001t0001g0027 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2295+397T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83431267 | |||||||
chr4:83431548 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2295+116A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83431548 | |||||||
chr4:83431580 | T | C | 1 | a0002c0002t0001g0079 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2295+84A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83431580 | |||||||
chr4:83431597 | T | C | 109 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(106): Show |
130 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.2295+67A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 11/17 | chr4 | 83431597 | |||||||
chr4:83432001 | T | C | 108 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(105): Show |
129 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.2190+125A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 10/17 | chr4 | 83432001 | |||||||
chr4:83432020 | T | C | 1 | a0002c0002t0001g0117 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2190+106A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 10/17 | chr4 | 83432020 | |||||||
chr4:83432073 | A | G | 6 | a0001c0001t0001g0025 a0001c0001t0001g0187 a0001c0001t0001g0191 others(3): Show |
7 | HG01168.hp2 HG01169.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.2190+53T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 10/17 | chr4 | 83432073 | |||||||
chr4:83432367 | C | T | 30 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(27): Show |
33 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.2049-100G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83432367 | |||||||
chr4:83432453 | ACT | A | 12 | a0004c0005t0001g0012 a0004c0005t0001g0034 a0004c0005t0001g0035 others(9): Show |
13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2049-188_2049-187d others(4): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83432453 | |||||||
chr4:83432642 | C | T | 1 | a0001c0020t0001g0158 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2049-375G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83432642 | |||||||
chr4:83432886 | A | AAACAAC | 3 | a0001c0001t0001g0130 a0001c0001t0001g0164 a0001c0001t0001g0205 |
3 | NA18947.hp1 NA18971.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.2049-625_2049-620d others(8): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83432886 | |||||||
chr4:83432971 | G | A | 1 | a0002c0002t0001g0065 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2049-704C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83432971 | |||||||
chr4:83433061 | T | TA | 26 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(23): Show |
29 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(26): Show |
intron_variant | MODIFIER | c.2049-795dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433061 | |||||||
chr4:83433102 | A | T | 1 | a0006c0008t0001g0064 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2049-835T>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433102 | |||||||
chr4:83433139 | G | A | 3 | a0005c0007t0001g0028 a0005c0007t0001g0054 a0005c0007t0001g0223 |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2049-872C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433139 | |||||||
chr4:83433212 | T | G | 110 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(107): Show |
131 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.2049-945A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433212 | |||||||
chr4:83433392 | G | A | 28 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(25): Show |
31 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.2049-1125C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433392 | |||||||
chr4:83433441 | G | A | 12 | a0001c0004t0001g0013 a0001c0004t0001g0045 a0001c0004t0001g0046 others(9): Show |
14 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.2049-1174C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433441 | |||||||
chr4:83433542 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2049-1275A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433542 | |||||||
chr4:83433558 | C | T | 1 | a0001c0006t0001g0022 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2049-1291G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433558 | |||||||
chr4:83433665 | C | CA | 26 | a0001c0001t0001g0128 a0001c0001t0001g0152 a0001c0001t0001g0200 others(23): Show |
29 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.2049-1399dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433665 | |||||||
chr4:83433665 | CA | C | 36 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0206 others(33): Show |
39 | HG01109.hp1 HG01168.hp2 HG01169.hp2 others(36): Show |
intron_variant | MODIFIER | c.2049-1399delT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433665 | |||||||
chr4:83433710 | T | C | 1 | a0003c0016t0001g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2049-1443A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433710 | |||||||
chr4:83433840 | A | G | 1 | a0004c0005t0001g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2049-1573T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433840 | |||||||
chr4:83433843 | T | C | 3 | a0005c0007t0001g0028 a0005c0007t0001g0054 a0005c0007t0001g0223 |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2049-1576A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433843 | |||||||
chr4:83433888 | G | A | 28 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(25): Show |
31 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.2049-1621C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433888 | |||||||
chr4:83433895 | C | T | 30 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(27): Show |
33 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.2049-1628G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433895 | |||||||
chr4:83433979 | C | CA | 45 | a0001c0001t0001g0151 a0001c0021t0001g0063 a0002c0002t0001g0091 others(42): Show |
50 | HG00099.hp1 HG01109.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.2049-1713dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433979 | |||||||
chr4:83433985 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2049-1718T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433985 | |||||||
chr4:83433997 | G | T | 1 | a0001c0001t0001g0190 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2049-1730C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83433997 | |||||||
chr4:83434091 | C | T | 1 | a0002c0002t0001g0070 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2049-1824G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83434091 | |||||||
chr4:83434129 | G | A | 2 | a0007c0009t0002g0031 a0007c0009t0002g0255 |
3 | HG03098.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2049-1862C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83434129 | |||||||
chr4:83434192 | G | A | 3 | a0005c0007t0001g0028 a0005c0007t0001g0054 a0005c0007t0001g0223 |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2049-1925C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83434192 | |||||||
chr4:83434471 | A | AT | 33 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(30): Show |
36 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(33): Show |
intron_variant | MODIFIER | c.2049-2205dupA | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83434471 | |||||||
chr4:83434619 | T | G | 12 | a0001c0004t0001g0013 a0001c0004t0001g0045 a0001c0004t0001g0046 others(9): Show |
14 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.2048+2239A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83434619 | |||||||
chr4:83434788 | T | C | 1 | a0002c0002t0001g0080 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2048+2070A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83434788 | |||||||
chr4:83434848 | G | A | 3 | a0005c0007t0001g0028 a0005c0007t0001g0054 a0005c0007t0001g0223 |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2048+2010C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83434848 | |||||||
chr4:83434858 | T | C | 12 | a0004c0005t0001g0012 a0004c0005t0001g0034 a0004c0005t0001g0035 others(9): Show |
13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2048+2000A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83434858 | |||||||
chr4:83434922 | A | G | 30 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(27): Show |
33 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.2048+1936T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83434922 | |||||||
chr4:83434997 | T | C | 35 | a0001c0006t0001g0179 a0002c0002t0001g0001 a0002c0002t0001g0004 others(32): Show |
52 | HG00099.hp1 HG00408.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.2048+1861A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83434997 | |||||||
chr4:83435207 | A | G | 33 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(30): Show |
37 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(34): Show |
intron_variant | MODIFIER | c.2048+1651T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83435207 | |||||||
chr4:83435256 | A | G | 33 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(30): Show |
37 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(34): Show |
intron_variant | MODIFIER | c.2048+1602T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83435256 | |||||||
chr4:83435301 | A | G | 33 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(30): Show |
37 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(34): Show |
intron_variant | MODIFIER | c.2048+1557T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83435301 | |||||||
chr4:83435538 | C | T | 1 | a0004c0005t0001g0035 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2048+1320G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83435538 | |||||||
chr4:83435575 | TA | T | 34 | a0001c0001t0001g0209 a0001c0021t0001g0063 a0003c0003t0002g0011 others(31): Show |
38 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(35): Show |
intron_variant | MODIFIER | c.2048+1282delT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83435575 | |||||||
chr4:83435585 | A | G | 30 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(27): Show |
33 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.2048+1273T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83435585 | |||||||
chr4:83435637 | A | C | 3 | a0005c0007t0001g0028 a0005c0007t0001g0054 a0005c0007t0001g0223 |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2048+1221T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83435637 | |||||||
chr4:83435925 | G | C | 143 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(140): Show |
168 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(165): Show |
intron_variant | MODIFIER | c.2048+933C>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83435925 | |||||||
chr4:83435935 | A | C | 1 | a0002c0002t0001g0069 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2048+923T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83435935 | |||||||
chr4:83435955 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2048+903T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83435955 | |||||||
chr4:83435973 | C | CA | 28 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(25): Show |
31 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.2048+884dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83435973 | |||||||
chr4:83435973 | CA | C | 145 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(142): Show |
171 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.2048+884delT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83435973 | |||||||
chr4:83435987 | G | A | 2 | a0004c0011t0002g0230 a0004c0011t0002g0231 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2048+871C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83435987 | |||||||
chr4:83436202 | T | C | 1 | a0013c0015t0002g0232 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2048+656A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83436202 | |||||||
chr4:83436241 | C | T | 143 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(140): Show |
168 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(165): Show |
intron_variant | MODIFIER | c.2048+617G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83436241 | |||||||
chr4:83436307 | A | C | 2 | a0007c0009t0002g0031 a0007c0009t0002g0255 |
3 | HG03098.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2048+551T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83436307 | |||||||
chr4:83436380 | T | C | 2 | a0003c0016t0001g0042 a0003c0017t0001g0044 |
2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2048+478A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83436380 | |||||||
chr4:83436662 | G | A | 12 | a0004c0005t0001g0012 a0004c0005t0001g0034 a0004c0005t0001g0035 others(9): Show |
13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2048+196C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83436662 | |||||||
chr4:83436823 | G | C | 3 | a0005c0007t0001g0028 a0005c0007t0001g0054 a0005c0007t0001g0223 |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2048+35C>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 9/17 | chr4 | 83436823 | |||||||
chr4:83437261 | C | A | 2 | a0002c0002t0001g0104 a0002c0002t0001g0105 |
2 | HG02559.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1809-164G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83437261 | |||||||
chr4:83437333 | C | A | 3 | a0002c0002t0001g0020 a0002c0002t0001g0099 a0002c0002t0001g0118 |
4 | HG02132.hp1 NA18969.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.1809-236G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83437333 | |||||||
chr4:83437361 | T | C | 33 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(30): Show |
37 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(34): Show |
intron_variant | MODIFIER | c.1809-264A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83437361 | |||||||
chr4:83437369 | T | A | 1 | a0001c0001t0001g0153 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1809-272A>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83437369 | |||||||
chr4:83437603 | T | TA | 28 | a0001c0001t0001g0188 a0001c0001t0001g0196 a0001c0001t0001g0218 others(25): Show |
31 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1809-507dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83437603 | |||||||
chr4:83437603 | TA | T | 62 | a0001c0001t0001g0005 a0001c0001t0001g0126 a0001c0001t0001g0127 others(59): Show |
69 | HG00280.hp2 HG00609.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.1809-507delT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83437603 | |||||||
chr4:83437604 | A | T | 1 | a0002c0002t0001g0111 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1809-507T>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83437604 | |||||||
chr4:83437650 | A | T | 3 | a0005c0007t0001g0028 a0005c0007t0001g0054 a0005c0007t0001g0223 |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1809-553T>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83437650 | |||||||
chr4:83437744 | T | C | 1 | a0003c0003t0002g0244 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1809-647A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83437744 | |||||||
chr4:83437815 | T | C | 3 | a0005c0007t0001g0028 a0005c0007t0001g0054 a0005c0007t0001g0223 |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1809-718A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83437815 | |||||||
chr4:83437852 | T | C | 1 | a0001c0001t0001g0173 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1809-755A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83437852 | |||||||
chr4:83437866 | C | T | 33 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(30): Show |
37 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(34): Show |
intron_variant | MODIFIER | c.1809-769G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83437866 | |||||||
chr4:83437991 | G | C | 2 | a0002c0002t0001g0074 a0002c0002t0001g0075 |
2 | NA18953.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1809-894C>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83437991 | |||||||
chr4:83438272 | T | C | 30 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(27): Show |
33 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.1809-1175A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83438272 | |||||||
chr4:83438577 | T | A | 28 | a0001c0021t0001g0063 a0003c0003t0002g0011 a0003c0003t0002g0030 others(25): Show |
31 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.1808+1286A>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83438577 | |||||||
chr4:83438634 | T | C | 1 | a0004c0005t0001g0043 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1808+1229A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83438634 | |||||||
chr4:83438641 | C | G | 1 | a0002c0002t0001g0115 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1808+1222G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83438641 | |||||||
chr4:83438747 | G | T | 1 | a0004c0005t0001g0043 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1808+1116C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83438747 | |||||||
chr4:83438748 | G | GAAAAAA | 15 | a0001c0004t0001g0013 a0001c0004t0001g0045 a0001c0004t0001g0046 others(12): Show |
18 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.1808+1109_1808+111 others(10): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83438748 | |||||||
chr4:83438748 | G | GAAAAAAA | 32 | a0001c0004t0001g0056 a0003c0003t0002g0011 a0003c0003t0002g0030 others(29): Show |
36 | HG01243.hp2 HG02055.hp1 HG02451.hp1 others(33): Show |
intron_variant | MODIFIER | c.1808+1108_1808+111 others(11): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83438748 | |||||||
chr4:83438748 | G | GAAAAAAA others(1): Show |
17 | a0001c0004t0001g0014 a0001c0004t0001g0055 a0001c0004t0001g0058 others(14): Show |
18 | HG01109.hp1 HG02258.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.1808+1107_1808+111 others(12): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83438748 | |||||||
chr4:83438748 | GAA | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(104): Show |
128 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.1808+1113_1808+111 others(6): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83438748 | |||||||
chr4:83438931 | G | A | 144 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
169 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(166): Show |
intron_variant | MODIFIER | c.1808+932C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83438931 | |||||||
chr4:83439192 | C | A | 25 | a0003c0003t0002g0011 a0003c0003t0002g0030 a0003c0003t0002g0233 others(22): Show |
28 | HG01109.hp1 HG02145.hp2 HG02258.hp2 others(25): Show |
intron_variant | MODIFIER | c.1808+671G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83439192 | |||||||
chr4:83439267 | ATGTTGGC others(287): Show |
A | 2 | a0003c0003t0002g0239 a0003c0003t0002g0243 |
2 | HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1808+302_1808+595d others(2): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83439267 | |||||||
chr4:83439313 | C | T | 1 | a0004c0005t0001g0043 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1808+550G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83439313 | |||||||
chr4:83439367 | C | CT | 109 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(106): Show |
130 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.1808+495dupA | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83439367 | |||||||
chr4:83439401 | G | A | 5 | a0003c0016t0001g0042 a0003c0017t0001g0044 a0005c0007t0001g0028 others(2): Show |
6 | HG02451.hp1 HG03041.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1808+462C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83439401 | |||||||
chr4:83439420 | T | G | 1 | a0005c0007t0001g0054 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1808+443A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83439420 | |||||||
chr4:83439448 | C | T | 3 | a0005c0007t0001g0028 a0005c0007t0001g0054 a0005c0007t0001g0223 |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1808+415G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83439448 | |||||||
chr4:83439452 | C | A | 12 | a0001c0004t0001g0013 a0001c0004t0001g0045 a0001c0004t0001g0046 others(9): Show |
14 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.1808+411G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83439452 | |||||||
chr4:83439545 | G | A | 1 | a0003c0003t0002g0244 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1808+318C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83439545 | |||||||
chr4:83439561 | G | A | 4 | a0003c0003t0002g0238 a0005c0007t0001g0028 a0005c0007t0001g0054 others(1): Show |
5 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1808+302C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83439561 | |||||||
chr4:83439687 | C | T | 1 | a0002c0002t0001g0092 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1808+176G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83439687 | |||||||
chr4:83439838 | G | A | 1 | a0003c0016t0001g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1808+25C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 8/17 | chr4 | 83439838 | |||||||
chr4:83440297 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1663-289A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/17 | chr4 | 83440297 | |||||||
chr4:83440312 | T | A | 3 | a0005c0007t0001g0028 a0005c0007t0001g0054 a0005c0007t0001g0223 |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-304A>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/17 | chr4 | 83440312 | |||||||
chr4:83440387 | C | T | 2 | a0005c0007t0001g0028 a0005c0007t0001g0223 |
3 | HG03041.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1663-379G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/17 | chr4 | 83440387 | |||||||
chr4:83440388 | G | A | 2 | a0003c0003t0002g0245 a0003c0003t0002g0257 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1663-380C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/17 | chr4 | 83440388 | |||||||
chr4:83440792 | G | T | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
165 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.1662+513C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/17 | chr4 | 83440792 | |||||||
chr4:83440800 | G | T | 3 | a0005c0007t0001g0028 a0005c0007t0001g0054 a0005c0007t0001g0223 |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1662+505C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/17 | chr4 | 83440800 | |||||||
chr4:83440902 | C | T | 25 | a0003c0003t0002g0011 a0003c0003t0002g0030 a0003c0003t0002g0233 others(22): Show |
28 | HG01109.hp1 HG02145.hp2 HG02258.hp2 others(25): Show |
intron_variant | MODIFIER | c.1662+403G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/17 | chr4 | 83440902 | |||||||
chr4:83441106 | G | A | 3 | a0005c0007t0001g0028 a0005c0007t0001g0054 a0005c0007t0001g0223 |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1662+199C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/17 | chr4 | 83441106 | |||||||
chr4:83441248 | T | G | 8 | a0001c0004t0001g0014 a0001c0004t0001g0055 a0001c0004t0001g0058 others(5): Show |
9 | HG02486.hp2 HG02922.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1662+57A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/17 | chr4 | 83441248 | |||||||
chr4:83441281 | G | A | 2 | a0002c0002t0001g0100 a0002c0002t0001g0101 |
2 | HG01070.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1662+24C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/17 | chr4 | 83441281 | |||||||
chr4:83441290 | T | C | 50 | a0001c0004t0001g0013 a0001c0004t0001g0014 a0001c0004t0001g0046 others(47): Show |
57 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.1662+15A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/17 | chr4 | 83441290 | |||||||
chr4:83441290 | T | G | 141 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(138): Show |
166 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(163): Show |
intron_variant | MODIFIER | c.1662+15A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/17 | chr4 | 83441290 | |||||||
chr4:83441298 | A | G | 12 | a0004c0005t0001g0012 a0004c0005t0001g0034 a0004c0005t0001g0035 others(9): Show |
13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
splice_region_variant&intron_variant | LOW | c.1662+7T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/17 | chr4 | 83441298 | |||||||
chr4:83441299 | T | C | 30 | a0003c0003t0002g0011 a0003c0003t0002g0030 a0003c0003t0002g0233 others(27): Show |
34 | HG01109.hp1 HG02145.hp2 HG02258.hp2 others(31): Show |
splice_region_variant&intron_variant | LOW | c.1662+6A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 7/17 | chr4 | 83441299 | |||||||
chr4:83441435 | G | A | 3 | a0001c0004t0001g0048 a0001c0004t0001g0049 a0001c0004t0001g0051 |
3 | HG00642.hp1 HG00741.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1564-32C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83441435 | |||||||
chr4:83441770 | C | T | 2 | a0007c0009t0002g0031 a0007c0009t0002g0255 |
3 | HG03098.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1564-367G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83441770 | |||||||
chr4:83441770 | CT | C | 55 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(52): Show |
69 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.1564-368delA | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83441770 | |||||||
chr4:83441922 | C | T | 1 | a0001c0020t0001g0158 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1564-519G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83441922 | |||||||
chr4:83442047 | G | A | 1 | a0002c0002t0001g0076 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1564-644C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442047 | |||||||
chr4:83442259 | A | G | 3 | a0005c0007t0001g0028 a0005c0007t0001g0054 a0005c0007t0001g0223 |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1564-856T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442259 | |||||||
chr4:83442260 | A | AT | 49 | a0001c0001t0001g0005 a0001c0001t0001g0126 a0001c0001t0001g0127 others(46): Show |
54 | HG00609.hp2 HG00735.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.1564-858dupA | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442260 | |||||||
chr4:83442260 | A | ATT | 89 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(86): Show |
109 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1564-859_1564-858d others(4): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442260 | |||||||
chr4:83442260 | A | ATTT | 31 | a0001c0001t0001g0159 a0001c0001t0001g0164 a0001c0001t0001g0165 others(28): Show |
34 | HG01109.hp1 HG01433.hp1 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.1564-860_1564-858d others(5): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442260 | |||||||
chr4:83442260 | AT | A | 6 | a0002c0002t0001g0017 a0002c0002t0001g0020 a0002c0002t0001g0080 others(3): Show |
8 | HG00140.hp2 HG01168.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1564-858delA | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442260 | |||||||
chr4:83442423 | ATGCTCTA others(222): Show |
A | 1 | a0003c0003t0002g0244 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1563+865_1564-1021 others(3): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442423 | |||||||
chr4:83442426 | C | G | 11 | a0001c0004t0001g0014 a0001c0004t0001g0056 a0001c0004t0001g0058 others(8): Show |
12 | HG02258.hp1 HG02922.hp2 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.1564-1023G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442426 | |||||||
chr4:83442448 | C | G | 29 | a0003c0003t0002g0011 a0003c0003t0002g0030 a0003c0003t0002g0233 others(26): Show |
33 | HG01109.hp1 HG02145.hp2 HG02258.hp2 others(30): Show |
intron_variant | MODIFIER | c.1564-1045G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442448 | |||||||
chr4:83442485 | G | T | 1 | a0014c0018t0001g0146 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1563+1032C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442485 | |||||||
chr4:83442496 | C | T | 1 | a0002c0002t0001g0098 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1563+1021G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442496 | |||||||
chr4:83442659 | C | T | 27 | a0003c0003t0002g0011 a0003c0003t0002g0030 a0003c0003t0002g0233 others(24): Show |
30 | HG01109.hp1 HG02145.hp2 HG02258.hp2 others(27): Show |
intron_variant | MODIFIER | c.1563+858G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442659 | |||||||
chr4:83442702 | C | T | 111 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(108): Show |
132 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.1563+815G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442702 | |||||||
chr4:83442800 | C | T | 2 | a0003c0016t0001g0042 a0003c0017t0001g0044 |
2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1563+717G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442800 | |||||||
chr4:83442844 | A | C | 1 | a0001c0001t0001g0129 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1563+673T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442844 | |||||||
chr4:83442956 | G | C | 114 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(111): Show |
136 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.1563+561C>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442956 | |||||||
chr4:83442995 | A | G | 1 | a0002c0002t0001g0065 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1563+522T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83442995 | |||||||
chr4:83443091 | T | C | 1 | a0004c0010t0001g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1563+426A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83443091 | |||||||
chr4:83443340 | C | A | 3 | a0003c0003t0002g0245 a0003c0003t0002g0246 a0003c0003t0002g0257 |
3 | HG02630.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1563+177G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83443340 | |||||||
chr4:83443413 | C | T | 1 | a0004c0005t0001g0043 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1563+104G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83443413 | |||||||
chr4:83443443 | T | A | 1 | a0004c0010t0001g0226 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1563+74A>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83443443 | |||||||
chr4:83443451 | C | T | 12 | a0001c0004t0001g0013 a0001c0004t0001g0045 a0001c0004t0001g0046 others(9): Show |
14 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.1563+66G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 6/17 | chr4 | 83443451 | |||||||
chr4:83443655 | T | C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(129): Show |
156 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.1466-41A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83443655 | |||||||
chr4:83443684 | T | C | 1 | a0001c0004t0001g0051 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1466-70A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83443684 | |||||||
chr4:83443807 | G | A | 7 | a0001c0004t0001g0014 a0001c0004t0001g0058 a0001c0004t0001g0060 others(4): Show |
8 | HG02922.hp2 HG02965.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1466-193C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83443807 | |||||||
chr4:83443871 | C | T | 1 | a0004c0005t0001g0043 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1466-257G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83443871 | |||||||
chr4:83443959 | C | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(100): Show |
124 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.1466-345G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83443959 | |||||||
chr4:83444052 | G | A | 2 | a0001c0004t0001g0055 a0002c0002t0001g0083 |
2 | HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1466-438C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83444052 | |||||||
chr4:83444475 | G | A | 1 | a0003c0003t0002g0253 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1466-861C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83444475 | |||||||
chr4:83444491 | CT | C | 153 | a0001c0001t0001g0005 a0001c0001t0001g0126 a0001c0001t0001g0127 others(150): Show |
184 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1466-878delA | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83444491 | |||||||
chr4:83444585 | T | C | 27 | a0003c0003t0002g0011 a0003c0003t0002g0030 a0003c0003t0002g0233 others(24): Show |
30 | HG01109.hp1 HG02145.hp2 HG02258.hp2 others(27): Show |
intron_variant | MODIFIER | c.1466-971A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83444585 | |||||||
chr4:83444652 | T | C | 2 | a0003c0016t0001g0042 a0003c0017t0001g0044 |
2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1466-1038A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83444652 | |||||||
chr4:83444875 | T | C | 6 | a0002c0002t0001g0117 a0004c0005t0002g0032 a0004c0005t0002g0256 others(3): Show |
8 | HG01167.hp2 HG02055.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1465+1139A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83444875 | |||||||
chr4:83444998 | G | A | 1 | a0005c0007t0001g0054 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1465+1016C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83444998 | |||||||
chr4:83445005 | A | T | 1 | a0002c0002t0001g0086 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1465+1009T>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83445005 | |||||||
chr4:83445144 | C | T | 1 | a0009c0019t0001g0144 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1465+870G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83445144 | |||||||
chr4:83445214 | G | A | 169 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(166): Show |
199 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(196): Show |
intron_variant | MODIFIER | c.1465+800C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83445214 | |||||||
chr4:83445257 | A | T | 2 | a0001c0004t0001g0055 a0002c0002t0001g0083 |
2 | HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1465+757T>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83445257 | |||||||
chr4:83445426 | G | A | 12 | a0004c0005t0001g0012 a0004c0005t0001g0034 a0004c0005t0001g0035 others(9): Show |
13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1465+588C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83445426 | |||||||
chr4:83445470 | A | T | 15 | a0003c0016t0001g0042 a0003c0017t0001g0044 a0004c0005t0001g0012 others(12): Show |
16 | HG01243.hp2 HG02055.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1465+544T>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83445470 | |||||||
chr4:83445584 | T | C | 12 | a0004c0005t0001g0012 a0004c0005t0001g0034 a0004c0005t0001g0035 others(9): Show |
13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1465+430A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83445584 | |||||||
chr4:83445602 | A | G | 15 | a0003c0016t0001g0042 a0003c0017t0001g0044 a0004c0005t0001g0012 others(12): Show |
16 | HG01243.hp2 HG02055.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1465+412T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83445602 | |||||||
chr4:83445897 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(129): Show |
156 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.1465+117C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83445897 | |||||||
chr4:83446006 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG02074.hp1 | splice_region_variant&intron_variant | LOW | c.1465+8T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 5/17 | chr4 | 83446006 | |||||||
chr4:83446133 | G | A | 150 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(147): Show |
176 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.1393-47C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 4/17 | chr4 | 83446133 | |||||||
chr4:83446139 | A | G | 1 | a0002c0002t0001g0019 | 2 | HG01099.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1393-53T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 4/17 | chr4 | 83446139 | |||||||
chr4:83446151 | C | T | 4 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0204 others(1): Show |
4 | HG01255.hp2 HG01346.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1393-65G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 4/17 | chr4 | 83446151 | |||||||
chr4:83446314 | AT | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(129): Show |
156 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.1393-229delA | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 4/17 | chr4 | 83446314 | |||||||
chr4:83446315 | T | A | 3 | a0002c0002t0001g0083 a0008c0012t0001g0084 a0008c0012t0001g0085 |
3 | HG01891.hp1 HG02622.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1393-229A>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 4/17 | chr4 | 83446315 | |||||||
chr4:83446354 | T | G | 12 | a0001c0004t0001g0014 a0001c0004t0001g0055 a0001c0004t0001g0056 others(9): Show |
13 | HG02258.hp1 HG02486.hp2 HG02922.hp2 others(10): Show |
intron_variant | MODIFIER | c.1393-268A>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 4/17 | chr4 | 83446354 | |||||||
chr4:83446368 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0210 a0001c0001t0001g0214 others(1): Show |
6 | HG00558.hp2 HG01952.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.1393-282C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 4/17 | chr4 | 83446368 | |||||||
chr4:83446451 | C | T | 3 | a0003c0016t0001g0042 a0003c0017t0001g0044 a0004c0005t0001g0043 |
3 | HG02451.hp1 HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1393-365G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 4/17 | chr4 | 83446451 | |||||||
chr4:83446452 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(129): Show |
156 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.1393-366C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 4/17 | chr4 | 83446452 | |||||||
chr4:83446606 | A | T | 147 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(144): Show |
172 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.1392+229T>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 4/17 | chr4 | 83446606 | |||||||
chr4:83446687 | T | C | 4 | a0002c0002t0001g0108 a0002c0002t0001g0109 a0002c0002t0001g0110 others(1): Show |
4 | HG00099.hp1 HG01256.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1392+148A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 4/17 | chr4 | 83446687 | |||||||
chr4:83447072 | GCATTGTG others(17): Show |
G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(129): Show |
156 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.1192-61_1192-38del others(24): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83447072 | |||||||
chr4:83447077 | G | T | 2 | a0003c0016t0001g0042 a0003c0017t0001g0044 |
2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1192-42C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83447077 | |||||||
chr4:83447477 | G | A | 32 | a0003c0003t0002g0011 a0003c0003t0002g0030 a0003c0003t0002g0233 others(29): Show |
37 | HG01109.hp1 HG01167.hp2 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.1192-442C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83447477 | |||||||
chr4:83447496 | C | G | 15 | a0003c0016t0001g0042 a0003c0017t0001g0044 a0004c0005t0001g0012 others(12): Show |
16 | HG01243.hp2 HG02055.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1192-461G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83447496 | |||||||
chr4:83447761 | G | A | 32 | a0003c0003t0002g0011 a0003c0003t0002g0030 a0003c0003t0002g0233 others(29): Show |
37 | HG01109.hp1 HG01167.hp2 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.1192-726C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83447761 | |||||||
chr4:83447859 | C | CA | 17 | a0001c0001t0001g0180 a0001c0001t0001g0199 a0001c0001t0001g0200 others(14): Show |
20 | HG00140.hp2 HG01243.hp1 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.1192-825dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83447859 | |||||||
chr4:83447859 | C | CAAAA | 12 | a0004c0005t0001g0012 a0004c0005t0001g0034 a0004c0005t0001g0035 others(9): Show |
13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1192-828_1192-825d others(6): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83447859 | |||||||
chr4:83447884 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1192-849T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83447884 | |||||||
chr4:83447931 | C | T | 1 | a0001c0004t0001g0013 | 2 | HG00140.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.1191+852G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83447931 | |||||||
chr4:83447964 | C | T | 35 | a0003c0003t0002g0011 a0003c0003t0002g0030 a0003c0003t0002g0233 others(32): Show |
41 | HG01109.hp1 HG01167.hp2 HG02055.hp2 others(38): Show |
intron_variant | MODIFIER | c.1191+819G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83447964 | |||||||
chr4:83447997 | G | A | 3 | a0005c0007t0001g0028 a0005c0007t0001g0054 a0005c0007t0001g0223 |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1191+786C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83447997 | |||||||
chr4:83448039 | A | C | 1 | a0003c0003t0002g0237 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1191+744T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83448039 | |||||||
chr4:83448396 | G | A | 1 | a0002c0002t0001g0015 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1191+387C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83448396 | |||||||
chr4:83448441 | G | A | 3 | a0005c0007t0001g0028 a0005c0007t0001g0054 a0005c0007t0001g0223 |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1191+342C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83448441 | |||||||
chr4:83448489 | G | A | 1 | a0002c0002t0001g0078 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1191+294C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83448489 | |||||||
chr4:83448584 | C | T | 1 | a0003c0003t0002g0236 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1191+199G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83448584 | |||||||
chr4:83448669 | C | CA | 138 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(135): Show |
163 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(160): Show |
intron_variant | MODIFIER | c.1191+113dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83448669 | |||||||
chr4:83448670 | A | AG | 2 | a0001c0001t0001g0008 a0001c0001t0001g0221 |
4 | HG00741.hp2 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.1191+112_1191+113i others(3): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83448670 | |||||||
chr4:83448684 | AG | A | 12 | a0004c0005t0001g0012 a0004c0005t0001g0034 a0004c0005t0001g0035 others(9): Show |
13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1191+98delC | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 3/17 | chr4 | 83448684 | |||||||
chr4:83448971 | TA | T | 182 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
213 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.1013-11delT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83448971 | |||||||
chr4:83449154 | C | T | 2 | a0003c0016t0001g0042 a0003c0017t0001g0044 |
2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1013-193G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83449154 | |||||||
chr4:83449191 | C | T | 1 | a0004c0005t0001g0043 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1013-230G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83449191 | |||||||
chr4:83449230 | T | C | 69 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(66): Show |
84 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1013-269A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83449230 | |||||||
chr4:83449239 | C | T | 1 | a0004c0005t0001g0043 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1013-278G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83449239 | |||||||
chr4:83449240 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1013-279C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83449240 | |||||||
chr4:83449263 | A | G | 2 | a0008c0012t0001g0084 a0008c0012t0001g0085 |
2 | HG02622.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1013-302T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83449263 | |||||||
chr4:83449306 | C | T | 1 | a0002c0002t0001g0067 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1013-345G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83449306 | |||||||
chr4:83449307 | G | A | 28 | a0001c0001t0001g0005 a0001c0001t0001g0126 a0001c0001t0001g0127 others(25): Show |
31 | HG00609.hp2 HG01109.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.1013-346C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83449307 | |||||||
chr4:83449307 | G | T | 50 | a0003c0003t0002g0011 a0003c0003t0002g0030 a0003c0003t0002g0233 others(47): Show |
57 | HG01109.hp1 HG01167.hp2 HG01243.hp2 others(54): Show |
intron_variant | MODIFIER | c.1013-346C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83449307 | |||||||
chr4:83449350 | C | T | 6 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(3): Show |
6 | HG02056.hp2 HG02165.hp2 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.1013-389G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83449350 | |||||||
chr4:83449391 | G | A | 2 | a0001c0001t0001g0145 a0009c0019t0001g0144 |
2 | HG00280.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1013-430C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83449391 | |||||||
chr4:83449736 | G | GGCAAATG others(34): Show |
1 | a0005c0007t0001g0054 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1013-816_1013-776d others(43): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83449736 | |||||||
chr4:83449868 | C | CA | 94 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(91): Show |
114 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.1013-908dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83449868 | |||||||
chr4:83449943 | G | A | 25 | a0003c0003t0002g0011 a0003c0003t0002g0030 a0003c0003t0002g0233 others(22): Show |
28 | HG01109.hp1 HG02145.hp2 HG02258.hp2 others(25): Show |
intron_variant | MODIFIER | c.1013-982C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83449943 | |||||||
chr4:83449990 | T | C | 2 | a0004c0011t0002g0230 a0004c0011t0002g0231 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1013-1029A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83449990 | |||||||
chr4:83450006 | A | C | 12 | a0004c0005t0001g0012 a0004c0005t0001g0034 a0004c0005t0001g0035 others(9): Show |
13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1013-1045T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450006 | |||||||
chr4:83450007 | C | T | 25 | a0003c0003t0002g0011 a0003c0003t0002g0030 a0003c0003t0002g0233 others(22): Show |
28 | HG01109.hp1 HG02145.hp2 HG02258.hp2 others(25): Show |
intron_variant | MODIFIER | c.1013-1046G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450007 | |||||||
chr4:83450057 | C | T | 1 | a0001c0006t0001g0022 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1013-1096G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450057 | |||||||
chr4:83450128 | C | T | 3 | a0005c0007t0001g0028 a0005c0007t0001g0054 a0005c0007t0001g0223 |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1013-1167G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450128 | |||||||
chr4:83450203 | T | C | 3 | a0005c0007t0001g0028 a0005c0007t0001g0054 a0005c0007t0001g0223 |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1013-1242A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450203 | |||||||
chr4:83450218 | A | G | 35 | a0003c0003t0002g0011 a0003c0003t0002g0030 a0003c0003t0002g0233 others(32): Show |
41 | HG01109.hp1 HG01167.hp2 HG02055.hp2 others(38): Show |
intron_variant | MODIFIER | c.1013-1257T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450218 | |||||||
chr4:83450222 | T | TA | 13 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0020t0001g0158 others(10): Show |
16 | HG01168.hp1 HG02109.hp1 HG02723.hp2 others(13): Show |
intron_variant | MODIFIER | c.1013-1262dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450222 | |||||||
chr4:83450222 | T | TAA | 24 | a0001c0001t0001g0005 a0001c0001t0001g0126 a0001c0001t0001g0129 others(21): Show |
27 | HG00280.hp2 HG00609.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1013-1263_1013-126 others(6): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450222 | |||||||
chr4:83450222 | T | TAAA | 35 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(32): Show |
44 | HG00609.hp1 HG00639.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.1013-1264_1013-126 others(7): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450222 | |||||||
chr4:83450222 | T | TAAAA | 30 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(27): Show |
36 | HG00408.hp2 HG00673.hp2 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1013-1265_1013-126 others(8): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450222 | |||||||
chr4:83450222 | T | TAAAAA | 12 | a0001c0001t0001g0026 a0001c0001t0001g0201 a0001c0001t0001g0202 others(9): Show |
13 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.1013-1266_1013-126 others(9): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450222 | |||||||
chr4:83450222 | T | TAAAAAA | 7 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0211 others(4): Show |
10 | HG00558.hp2 HG01106.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1013-1267_1013-126 others(10): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450222 | |||||||
chr4:83450222 | TAAA | T | 8 | a0001c0004t0001g0013 a0001c0004t0001g0045 a0001c0004t0001g0046 others(5): Show |
9 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.1013-1264_1013-126 others(7): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450222 | |||||||
chr4:83450222 | TAAAA | T | 9 | a0001c0004t0001g0014 a0001c0004t0001g0055 a0001c0004t0001g0056 others(6): Show |
10 | HG02486.hp2 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.1013-1265_1013-126 others(8): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450222 | |||||||
chr4:83450222 | TAAAAAAA others(3): Show |
T | 27 | a0003c0003t0002g0011 a0003c0003t0002g0233 a0003c0003t0002g0234 others(24): Show |
31 | HG01109.hp1 HG01167.hp2 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.1013-1271_1013-126 others(14): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450222 | |||||||
chr4:83450222 | TAAAAAAA others(4): Show |
T | 3 | a0003c0003t0002g0030 a0003c0003t0002g0235 a0012c0014t0002g0254 |
4 | HG02055.hp2 HG02615.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1013-1272_1013-126 others(15): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450222 | |||||||
chr4:83450222 | TAAAAAAA others(5): Show |
T | 1 | a0003c0017t0001g0044 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1013-1273_1013-126 others(16): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450222 | |||||||
chr4:83450222 | TAAAAAAA others(7): Show |
T | 13 | a0002c0002t0001g0066 a0004c0005t0001g0012 a0004c0005t0001g0034 others(10): Show |
14 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1013-1275_1013-126 others(18): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450222 | |||||||
chr4:83450364 | T | TA | 5 | a0003c0016t0001g0042 a0003c0017t0001g0044 a0004c0005t0002g0032 others(2): Show |
6 | HG01167.hp2 HG02055.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1013-1404dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450364 | |||||||
chr4:83450542 | C | T | 4 | a0001c0001t0001g0126 a0005c0007t0001g0028 a0005c0007t0001g0054 others(1): Show |
5 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1013-1581G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450542 | |||||||
chr4:83450664 | C | CA | 9 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0002c0002t0001g0018 others(6): Show |
10 | HG03516.hp1 HG03704.hp2 NA18943.hp1 others(7): Show |
intron_variant | MODIFIER | c.1013-1704dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450664 | |||||||
chr4:83450664 | CA | C | 50 | a0001c0001t0001g0155 a0002c0002t0001g0082 a0002c0002t0001g0083 others(47): Show |
57 | HG01167.hp2 HG01243.hp2 HG01891.hp1 others(54): Show |
intron_variant | MODIFIER | c.1013-1704delT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450664 | |||||||
chr4:83450688 | G | A | 2 | a0002c0002t0001g0120 a0002c0002t0001g0121 |
2 | HG03017.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1013-1727C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450688 | |||||||
chr4:83450693 | C | A | 12 | a0004c0005t0001g0012 a0004c0005t0001g0034 a0004c0005t0001g0035 others(9): Show |
13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1013-1732G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450693 | |||||||
chr4:83450719 | C | A | 2 | a0004c0011t0002g0230 a0004c0011t0002g0231 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1013-1758G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450719 | |||||||
chr4:83450773 | C | G | 1 | a0003c0003t0002g0234 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1013-1812G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450773 | |||||||
chr4:83450792 | C | A | 1 | a0003c0003t0002g0247 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1013-1831G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450792 | |||||||
chr4:83450871 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1013-1910A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450871 | |||||||
chr4:83450909 | T | C | 2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1013-1948A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450909 | |||||||
chr4:83450999 | A | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(108): Show |
133 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.1013-2038T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83450999 | |||||||
chr4:83451050 | C | T | 182 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
213 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.1013-2089G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83451050 | |||||||
chr4:83451106 | T | C | 50 | a0003c0003t0002g0011 a0003c0003t0002g0030 a0003c0003t0002g0233 others(47): Show |
57 | HG01109.hp1 HG01167.hp2 HG01243.hp2 others(54): Show |
intron_variant | MODIFIER | c.1012+2125A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83451106 | |||||||
chr4:83451242 | C | CA | 32 | a0003c0003t0002g0011 a0003c0003t0002g0030 a0003c0003t0002g0233 others(29): Show |
37 | HG01109.hp1 HG01167.hp2 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.1012+1988dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83451242 | |||||||
chr4:83451286 | A | C | 12 | a0004c0005t0001g0012 a0004c0005t0001g0034 a0004c0005t0001g0035 others(9): Show |
13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1012+1945T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83451286 | |||||||
chr4:83451296 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1012+1935A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83451296 | |||||||
chr4:83451324 | G | A | 2 | a0004c0011t0002g0230 a0004c0011t0002g0231 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1012+1907C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83451324 | |||||||
chr4:83451506 | C | CA | 32 | a0003c0003t0002g0011 a0003c0003t0002g0030 a0003c0003t0002g0233 others(29): Show |
37 | HG01109.hp1 HG01167.hp2 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.1012+1724dupT | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83451506 | |||||||
chr4:83451523 | G | A | 7 | a0003c0003t0002g0011 a0003c0003t0002g0248 a0003c0003t0002g0249 others(4): Show |
9 | HG02258.hp2 HG02622.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1012+1708C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83451523 | |||||||
chr4:83451553 | C | T | 1 | a0004c0005t0001g0034 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1012+1678G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83451553 | |||||||
chr4:83451584 | C | T | 3 | a0003c0016t0001g0042 a0003c0017t0001g0044 a0004c0005t0001g0043 |
3 | HG02451.hp1 HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1012+1647G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83451584 | |||||||
chr4:83451672 | AC | A | 33 | a0003c0003t0002g0011 a0003c0003t0002g0030 a0003c0003t0002g0234 others(30): Show |
39 | HG01167.hp2 HG02145.hp2 HG02258.hp2 others(36): Show |
intron_variant | MODIFIER | c.1012+1558delG | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83451672 | |||||||
chr4:83451673 | C | A | 17 | a0003c0003t0002g0233 a0003c0016t0001g0042 a0004c0005t0001g0012 others(14): Show |
18 | HG01109.hp1 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1012+1558G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83451673 | |||||||
chr4:83451675 | A | C | 3 | a0005c0007t0001g0028 a0005c0007t0001g0054 a0005c0007t0001g0223 |
4 | HG03041.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1012+1556T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83451675 | |||||||
chr4:83451845 | T | C | 229 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(226): Show |
278 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.1012+1386A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83451845 | |||||||
chr4:83451994 | G | A | 25 | a0003c0003t0002g0011 a0003c0003t0002g0030 a0003c0003t0002g0233 others(22): Show |
28 | HG01109.hp1 HG02145.hp2 HG02258.hp2 others(25): Show |
intron_variant | MODIFIER | c.1012+1237C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83451994 | |||||||
chr4:83452415 | C | G | 2 | a0004c0011t0002g0230 a0004c0011t0002g0231 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1012+816G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83452415 | |||||||
chr4:83452457 | G | A | 1 | a0001c0004t0001g0052 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1012+774C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83452457 | |||||||
chr4:83452469 | A | G | 183 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(180): Show |
214 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.1012+762T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83452469 | |||||||
chr4:83452473 | G | A | 1 | a0003c0016t0001g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1012+758C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83452473 | |||||||
chr4:83452682 | G | C | 1 | a0001c0001t0001g0222 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1012+549C>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83452682 | |||||||
chr4:83452738 | T | C | 1 | a0004c0005t0001g0043 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1012+493A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83452738 | |||||||
chr4:83452901 | A | G | 1 | a0005c0007t0001g0054 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1012+330T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83452901 | |||||||
chr4:83452966 | C | T | 1 | a0002c0002t0001g0065 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1012+265G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83452966 | |||||||
chr4:83452974 | TGAGGAAT others(2): Show |
T | 48 | a0003c0003t0002g0011 a0003c0003t0002g0030 a0003c0003t0002g0233 others(45): Show |
54 | HG01109.hp1 HG01167.hp2 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.1012+248_1012+256d others(11): Show |
HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83452974 | |||||||
chr4:83453076 | G | A | 48 | a0003c0003t0002g0011 a0003c0003t0002g0030 a0003c0003t0002g0233 others(45): Show |
54 | HG01109.hp1 HG01167.hp2 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.1012+155C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 2/17 | chr4 | 83453076 | |||||||
chr4:83453964 | C | T | 1 | a0002c0022t0001g0053 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.298-19G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/17 | chr4 | 83453964 | |||||||
chr4:83454033 | G | T | 1 | a0005c0007t0001g0028 | 2 | HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.298-88C>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/17 | chr4 | 83454033 | |||||||
chr4:83454132 | A | G | 9 | a0001c0004t0001g0013 a0001c0004t0001g0045 a0001c0004t0001g0046 others(6): Show |
10 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.298-187T>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/17 | chr4 | 83454132 | |||||||
chr4:83454134 | C | T | 12 | a0004c0005t0001g0012 a0004c0005t0001g0034 a0004c0005t0001g0035 others(9): Show |
13 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.298-189G>A | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/17 | chr4 | 83454134 | |||||||
chr4:83454136 | C | G | 48 | a0003c0003t0002g0011 a0003c0003t0002g0030 a0003c0003t0002g0233 others(45): Show |
54 | HG01109.hp1 HG01167.hp2 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.298-191G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/17 | chr4 | 83454136 | |||||||
chr4:83454155 | A | C | 30 | a0001c0001t0001g0005 a0001c0001t0001g0126 a0001c0001t0001g0127 others(27): Show |
33 | HG00280.hp2 HG00609.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.298-210T>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/17 | chr4 | 83454155 | |||||||
chr4:83454196 | C | G | 1 | a0004c0005t0002g0229 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.298-251G>C | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/17 | chr4 | 83454196 | |||||||
chr4:83454367 | T | A | 4 | a0002c0002t0001g0122 a0002c0002t0001g0123 a0002c0002t0001g0124 others(1): Show |
4 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(1): Show |
intron_variant | MODIFIER | c.298-422A>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/17 | chr4 | 83454367 | |||||||
chr4:83454405 | T | C | 5 | a0004c0005t0002g0032 a0004c0005t0002g0256 a0007c0009t0002g0031 others(2): Show |
7 | HG01167.hp2 HG02055.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.298-460A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/17 | chr4 | 83454405 | |||||||
chr4:83454581 | G | A | 181 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(178): Show |
212 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.298-636C>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/17 | chr4 | 83454581 | |||||||
chr4:83454591 | T | A | 1 | a0003c0003t0002g0257 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.298-646A>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/17 | chr4 | 83454591 | |||||||
chr4:83454644 | C | A | 111 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(108): Show |
133 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.298-699G>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/17 | chr4 | 83454644 | |||||||
chr4:83455086 | T | A | 2 | a0005c0007t0001g0028 a0005c0007t0001g0223 |
3 | HG03041.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.297+311A>T | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/17 | chr4 | 83455086 | |||||||
chr4:83455290 | T | C | 34 | a0002c0002t0001g0029 a0003c0003t0002g0011 a0003c0003t0002g0030 others(31): Show |
40 | HG01109.hp1 HG01167.hp2 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.297+107A>G | HELQ | ENSG00000163312.11 | transcript | ENST00000295488.8 | protein_coding | 1/17 | chr4 | 83455290 |