Item | Value |
---|---|
geneid | 6596 |
ensemblid | ENSG00000071794.16 |
hgncid | 11099 |
symbol | HLTF |
name | helicase like transcription factor |
refseq_nuc | NM_003071.4 |
refseq_prot | NP_003062.2 |
ensembl_nuc | ENST00000310053.10 |
ensembl_prot | ENSP00000308944.5 |
mane_status | MANE Select |
chr | chr3 |
start | 149030127 |
end | 149086533 |
strand | - |
ver | v1.2 |
region | chr3:149030127-149086533 |
region5000 | chr3:149025127-149091533 |
regionname0 | HLTF_chr3_149030127_149086533 |
regionname5000 | HLTF_chr3_149025127_149091533 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1009 | 354 | 71 | 54 | 170 | 16 | 41 | 135 | HLTF_chr3_149025127_149091533 | HLTF | MSWMF others(1004): Show |
chr3 | 149025127 | 149091533 |
a0002 | 0/0 | 1009 | 15 | 0 | 2 | 10 | 2 | 1 | 9 | HLTF_chr3_149025127_149091533 | HLTF | MSWMF others(1004): Show |
chr3 | 149025127 | 149091533 |
a0003 | 0/0 | 1009 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | MSWMF others(1004): Show |
chr3 | 149025127 | 149091533 |
a0004 | 0/0 | 1009 | 6 | 4 | 1 | 1 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | MSWMF others(1004): Show |
chr3 | 149025127 | 149091533 |
a0005 | 0/0 | 1009 | 4 | 0 | 3 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | MSWMF others(1004): Show |
chr3 | 149025127 | 149091533 |
a0006 | 0/0 | 1009 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | MSWMF others(1004): Show |
chr3 | 149025127 | 149091533 |
a0007 | 0/0 | 1009 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | MSWMF others(1004): Show |
chr3 | 149025127 | 149091533 |
a0008 | 0/0 | 1009 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | MSWMF others(1004): Show |
chr3 | 149025127 | 149091533 |
a0009 | 0/0 | 1009 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | MSWMF others(1004): Show |
chr3 | 149025127 | 149091533 |
a0010 | 0/0 | 1009 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | HLTF_chr3_149025127_149091533 | HLTF | MSWMF others(1004): Show |
chr3 | 149025127 | 149091533 |
a0011 | 0/0 | 1009 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | MSWMF others(1004): Show |
chr3 | 149025127 | 149091533 |
a0012 | 0/0 | 1009 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | MSWMF others(1004): Show |
chr3 | 149025127 | 149091533 |
a0013 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | MSWMF others(1004): Show |
chr3 | 149025127 | 149091533 |
a0014 | 0/0 | 1009 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | MSWMF others(1004): Show |
chr3 | 149025127 | 149091533 |
a0015 | 0/0 | 1009 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | MSWMF others(1004): Show |
chr3 | 149025127 | 149091533 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3027 | 123 | 26 | 15 | 65 | 6 | 11 | HLTF_chr3_149025127_149091533 | HLTF | ATGTC others(3022): Show |
chr3 | 149025127 | 149091533 | ||
a0001c0002 | 0/0 | 3027 | 112 | 20 | 23 | 57 | 3 | 9 | HLTF_chr3_149025127_149091533 | HLTF | ATGTC others(3022): Show |
chr3 | 149025127 | 149091533 | ||
a0001c0003 | 1/1 | 3027 | 97 | 11 | 10 | 47 | 6 | 21 | HLTF_chr3_149025127_149091533 | HLTF | ATGTC others(3022): Show |
chr3 | 149025127 | 149091533 | ||
a0001c0005 | 0/0 | 3027 | 13 | 12 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | ATGTC others(3022): Show |
chr3 | 149025127 | 149091533 | ||
a0001c0007 | 0/0 | 3027 | 6 | 1 | 4 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | ATGTC others(3022): Show |
chr3 | 149025127 | 149091533 | ||
a0001c0017 | 0/0 | 3027 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | ATGTC others(3022): Show |
chr3 | 149025127 | 149091533 | ||
a0001c0021 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | ATGTC others(3022): Show |
chr3 | 149025127 | 149091533 | ||
a0001c0023 | 0/0 | 3027 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | ATGTC others(3022): Show |
chr3 | 149025127 | 149091533 | ||
a0002c0004 | 0/0 | 3027 | 15 | 0 | 2 | 10 | 2 | 1 | HLTF_chr3_149025127_149091533 | HLTF | ATGTC others(3022): Show |
chr3 | 149025127 | 149091533 | ||
a0003c0006 | 0/0 | 3027 | 8 | 8 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | ATGTC others(3022): Show |
chr3 | 149025127 | 149091533 | ||
a0004c0008 | 0/0 | 3027 | 5 | 4 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | ATGTC others(3022): Show |
chr3 | 149025127 | 149091533 | ||
a0004c0018 | 0/0 | 3027 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | ATGTC others(3022): Show |
chr3 | 149025127 | 149091533 | ||
a0005c0009 | 0/0 | 3027 | 4 | 0 | 3 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | ATGTC others(3022): Show |
chr3 | 149025127 | 149091533 | ||
a0006c0010 | 0/0 | 3027 | 4 | 4 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | ATGTC others(3022): Show |
chr3 | 149025127 | 149091533 | ||
a0007c0014 | 0/0 | 3027 | 2 | 0 | 2 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | ATGTC others(3022): Show |
chr3 | 149025127 | 149091533 | ||
a0008c0012 | 0/0 | 3027 | 2 | 2 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | ATGTC others(3022): Show |
chr3 | 149025127 | 149091533 | ||
a0009c0013 | 0/0 | 3027 | 2 | 2 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | ATGTC others(3022): Show |
chr3 | 149025127 | 149091533 | ||
a0010c0011 | 0/0 | 3027 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | ATGTC others(3022): Show |
chr3 | 149025127 | 149091533 | ||
a0011c0019 | 0/0 | 3027 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | ATGTC others(3022): Show |
chr3 | 149025127 | 149091533 | ||
a0012c0020 | 0/0 | 3027 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | ATGTC others(3022): Show |
chr3 | 149025127 | 149091533 | ||
a0013c0015 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | ATGTC others(3022): Show |
chr3 | 149025127 | 149091533 | ||
a0014c0022 | 0/0 | 3027 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | ATGTC others(3022): Show |
chr3 | 149025127 | 149091533 | ||
a0015c0016 | 0/0 | 3027 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | ATGTC others(3022): Show |
chr3 | 149025127 | 149091533 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5320 | 116 | 22 | 14 | 63 | 6 | 11 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5315): Show |
chr3 | 149025127 | 149091533 |
a0001c0001t0011 | 0/0 | 5318 | 2 | 2 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5313): Show |
chr3 | 149025127 | 149091533 |
a0001c0001t0014 | 0/0 | 5320 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5315): Show |
chr3 | 149025127 | 149091533 |
a0001c0001t0015 | 0/0 | 5318 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5313): Show |
chr3 | 149025127 | 149091533 |
a0001c0001t0018 | 0/0 | 5320 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5315): Show |
chr3 | 149025127 | 149091533 |
a0001c0001t0020 | 0/0 | 5320 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5315): Show |
chr3 | 149025127 | 149091533 |
a0001c0002t0003 | 0/0 | 5323 | 85 | 0 | 20 | 55 | 2 | 8 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5318): Show |
chr3 | 149025127 | 149091533 |
a0001c0002t0004 | 0/0 | 5320 | 16 | 13 | 2 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5315): Show |
chr3 | 149025127 | 149091533 |
a0001c0002t0006 | 0/0 | 5320 | 5 | 5 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5315): Show |
chr3 | 149025127 | 149091533 |
a0001c0002t0010 | 0/0 | 5324 | 3 | 2 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5319): Show |
chr3 | 149025127 | 149091533 |
a0001c0002t0013 | 0/0 | 5323 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5318): Show |
chr3 | 149025127 | 149091533 |
a0001c0002t0021 | 0/0 | 5323 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5318): Show |
chr3 | 149025127 | 149091533 |
a0001c0003t0002 | 1/1 | 5320 | 94 | 11 | 10 | 45 | 6 | 20 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5315): Show |
chr3 | 149025127 | 149091533 |
a0001c0003t0012 | 0/0 | 5323 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5318): Show |
chr3 | 149025127 | 149091533 |
a0001c0003t0016 | 0/0 | 5320 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5315): Show |
chr3 | 149025127 | 149091533 |
a0001c0005t0002 | 0/0 | 5320 | 12 | 11 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5315): Show |
chr3 | 149025127 | 149091533 |
a0001c0005t0019 | 0/0 | 5320 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5315): Show |
chr3 | 149025127 | 149091533 |
a0001c0007t0003 | 0/0 | 5323 | 6 | 1 | 4 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5318): Show |
chr3 | 149025127 | 149091533 |
a0001c0017t0001 | 0/0 | 5320 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5315): Show |
chr3 | 149025127 | 149091533 |
a0001c0021t0002 | 0/0 | 5320 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5315): Show |
chr3 | 149025127 | 149091533 |
a0001c0023t0002 | 0/0 | 5320 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5315): Show |
chr3 | 149025127 | 149091533 |
a0002c0004t0001 | 0/0 | 5320 | 12 | 0 | 1 | 10 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5315): Show |
chr3 | 149025127 | 149091533 |
a0002c0004t0009 | 0/0 | 5320 | 3 | 0 | 1 | 0 | 1 | 1 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5315): Show |
chr3 | 149025127 | 149091533 |
a0003c0006t0005 | 0/0 | 5320 | 8 | 8 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5315): Show |
chr3 | 149025127 | 149091533 |
a0004c0008t0002 | 0/0 | 5320 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5315): Show |
chr3 | 149025127 | 149091533 |
a0004c0008t0008 | 0/0 | 5320 | 3 | 3 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5315): Show |
chr3 | 149025127 | 149091533 |
a0004c0008t0017 | 0/0 | 5320 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5315): Show |
chr3 | 149025127 | 149091533 |
a0004c0018t0001 | 0/0 | 5320 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5315): Show |
chr3 | 149025127 | 149091533 |
a0005c0009t0002 | 0/0 | 5320 | 4 | 0 | 3 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5315): Show |
chr3 | 149025127 | 149091533 |
a0006c0010t0007 | 0/0 | 5321 | 4 | 4 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5316): Show |
chr3 | 149025127 | 149091533 |
a0007c0014t0002 | 0/0 | 5320 | 2 | 0 | 2 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5315): Show |
chr3 | 149025127 | 149091533 |
a0008c0012t0001 | 0/0 | 5320 | 2 | 2 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5315): Show |
chr3 | 149025127 | 149091533 |
a0009c0013t0002 | 0/0 | 5320 | 2 | 2 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5315): Show |
chr3 | 149025127 | 149091533 |
a0010c0011t0001 | 0/0 | 5320 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5315): Show |
chr3 | 149025127 | 149091533 |
a0011c0019t0003 | 0/0 | 5323 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5318): Show |
chr3 | 149025127 | 149091533 |
a0012c0020t0003 | 0/0 | 5323 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5318): Show |
chr3 | 149025127 | 149091533 |
a0013c0015t0006 | 0/0 | 5320 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5315): Show |
chr3 | 149025127 | 149091533 |
a0014c0022t0002 | 0/0 | 5320 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5315): Show |
chr3 | 149025127 | 149091533 |
a0015c0016t0003 | 0/0 | 5323 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | AGATT others(5318): Show |
chr3 | 149025127 | 149091533 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0011g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0011g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0014g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0014g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0015g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0018g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0020g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0002 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0004 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0004g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0004g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0004g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0004g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0004g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0010g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0010g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0010g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0013g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0013g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0021g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0001 | 1/0 | 5 | 0 | 0 | 0 | 2 | 2 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0329 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0012g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0012g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0016g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0005t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0005t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0005t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0005t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0005t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0005t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0005t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0005t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0005t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0005t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0005t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0005t0019g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0007t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0007t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0007t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0007t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0007t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0007t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0017t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0021t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0023t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0002c0004t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0002c0004t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0002c0004t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0002c0004t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0002c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0002c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0002c0004t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0002c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0002c0004t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0002c0004t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0002c0004t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0002c0004t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0002c0004t0009g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0002c0004t0009g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0003c0006t0005g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0003c0006t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0003c0006t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0003c0006t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0003c0006t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0003c0006t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0003c0006t0005g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0004c0008t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0004c0008t0008g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0004c0008t0008g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0004c0008t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0004c0008t0017g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0004c0018t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0005c0009t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0005c0009t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0005c0009t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0005c0009t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0006c0010t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0006c0010t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0006c0010t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0006c0010t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0007c0014t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0007c0014t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0008c0012t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0008c0012t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0009c0013t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0009c0013t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0010c0011t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0010c0011t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0011c0019t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0012c0020t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0013c0015t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0014c0022t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0015c0016t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0003 | g0065 | EUR | GBR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00099 | hp2 | a0001 | c0003 | t0002 | g0308 | EUR | GBR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0169 | EUR | GBR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00140 | hp2 | a0001 | c0003 | t0002 | g0290 | EUR | GBR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00280 | hp2 | a0002 | c0004 | t0001 | g0201 | EUR | FIN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00323 | hp1 | a0001 | c0003 | t0002 | g0336 | EUR | FIN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00323 | hp2 | a0002 | c0004 | t0009 | g0016 | EUR | FIN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00423 | hp1 | a0001 | c0002 | t0003 | g0100 | EAS | CHS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00438 | hp1 | a0001 | c0002 | t0003 | g0110 | EAS | CHS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00438 | hp2 | a0001 | c0003 | t0002 | g0348 | EAS | CHS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00558 | hp2 | a0001 | c0003 | t0002 | g0345 | EAS | CHS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00597 | hp2 | a0001 | c0002 | t0003 | g0058 | EAS | CHS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00621 | hp1 | a0001 | c0003 | t0002 | g0298 | EAS | CHS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00621 | hp2 | a0001 | c0002 | t0003 | g0102 | EAS | CHS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00673 | hp1 | a0001 | c0002 | t0003 | g0086 | EAS | CHS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00733 | hp2 | a0001 | c0002 | t0003 | g0124 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00735 | hp2 | a0001 | c0002 | t0003 | g0123 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00738 | hp1 | a0001 | c0002 | t0003 | g0070 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00738 | hp2 | a0001 | c0002 | t0010 | g0048 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01069 | hp1 | a0007 | c0014 | t0002 | g0282 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01069 | hp2 | a0001 | c0002 | t0003 | g0002 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01070 | hp2 | a0001 | c0003 | t0002 | g0331 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01071 | hp1 | a0007 | c0014 | t0002 | g0281 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01074 | hp1 | a0001 | c0002 | t0003 | g0072 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01074 | hp2 | a0001 | c0003 | t0002 | g0339 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01081 | hp1 | a0002 | c0004 | t0009 | g0016 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01081 | hp2 | a0001 | c0002 | t0003 | g0002 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01106 | hp1 | a0001 | c0002 | t0003 | g0069 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01106 | hp2 | a0001 | c0003 | t0002 | g0332 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01109 | hp1 | a0001 | c0007 | t0003 | g0108 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01167 | hp1 | a0001 | c0002 | t0004 | g0256 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01167 | hp2 | a0005 | c0009 | t0002 | g0032 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01169 | hp1 | a0001 | c0002 | t0003 | g0255 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01169 | hp2 | a0001 | c0007 | t0003 | g0097 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01175 | hp1 | a0001 | c0002 | t0003 | g0091 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01175 | hp2 | a0001 | c0003 | t0002 | g0316 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01243 | hp1 | a0001 | c0003 | t0002 | g0272 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01243 | hp2 | a0001 | c0005 | t0002 | g0145 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01255 | hp1 | a0001 | c0003 | t0002 | g0312 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01255 | hp2 | a0004 | c0008 | t0002 | g0029 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01256 | hp1 | a0001 | c0002 | t0004 | g0262 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01256 | hp2 | a0001 | c0007 | t0003 | g0095 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01257 | hp1 | a0001 | c0002 | t0003 | g0087 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01261 | hp1 | a0001 | c0002 | t0003 | g0113 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01261 | hp2 | a0011 | c0019 | t0003 | g0116 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01346 | hp2 | a0005 | c0009 | t0002 | g0031 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01358 | hp1 | a0001 | c0007 | t0003 | g0093 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01358 | hp2 | a0005 | c0009 | t0002 | g0033 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01433 | hp1 | a0001 | c0003 | t0002 | g0271 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01433 | hp2 | a0001 | c0003 | t0002 | g0311 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01496 | hp2 | a0001 | c0002 | t0003 | g0111 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01515 | hp1 | a0001 | c0007 | t0003 | g0066 | EUR | IBS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01515 | hp2 | a0001 | c0003 | t0002 | g0001 | EUR | IBS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01516 | hp1 | a0001 | c0002 | t0004 | g0259 | EUR | IBS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0227 | EUR | IBS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | IBS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01517 | hp2 | a0001 | c0003 | t0002 | g0001 | EUR | IBS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01891 | hp1 | a0008 | c0012 | t0001 | g0183 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01891 | hp2 | a0004 | c0008 | t0008 | g0028 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01928 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01952 | hp2 | a0001 | c0002 | t0003 | g0106 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01975 | hp1 | a0012 | c0020 | t0003 | g0083 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01975 | hp2 | a0001 | c0003 | t0002 | g0304 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01978 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01978 | hp2 | a0001 | c0017 | t0001 | g0158 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01981 | hp1 | a0001 | c0002 | t0003 | g0090 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02015 | hp2 | a0001 | c0002 | t0003 | g0063 | EAS | KHV | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02055 | hp1 | a0008 | c0012 | t0001 | g0238 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02055 | hp2 | a0003 | c0006 | t0005 | g0043 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02074 | hp1 | a0001 | c0003 | t0012 | g0300 | EAS | KHV | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02080 | hp1 | a0001 | c0003 | t0002 | g0291 | EAS | KHV | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02080 | hp2 | a0001 | c0002 | t0003 | g0081 | EAS | KHV | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02083 | hp1 | a0001 | c0003 | t0002 | g0352 | EAS | KHV | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02129 | hp1 | a0002 | c0004 | t0001 | g0199 | EAS | KHV | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02129 | hp2 | a0001 | c0003 | t0002 | g0292 | EAS | KHV | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02132 | hp1 | a0001 | c0002 | t0003 | g0059 | EAS | KHV | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02135 | hp1 | a0001 | c0002 | t0003 | g0109 | EAS | KHV | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02135 | hp2 | a0001 | c0003 | t0012 | g0324 | EAS | KHV | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02145 | hp1 | a0001 | c0002 | t0006 | g0042 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02148 | hp1 | a0001 | c0003 | t0002 | g0315 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02148 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CDX | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02155 | hp2 | a0001 | c0002 | t0003 | g0067 | EAS | CDX | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02165 | hp1 | a0001 | c0002 | t0003 | g0062 | EAS | CDX | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02257 | hp1 | a0001 | c0002 | t0004 | g0355 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02258 | hp1 | a0001 | c0001 | t0011 | g0129 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02273 | hp1 | a0001 | c0001 | t0018 | g0163 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02280 | hp1 | a0009 | c0013 | t0002 | g0035 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02280 | hp2 | a0001 | c0005 | t0002 | g0137 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02293 | hp1 | a0001 | c0002 | t0003 | g0084 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02300 | hp1 | a0001 | c0002 | t0003 | g0085 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02300 | hp2 | a0001 | c0002 | t0003 | g0112 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02451 | hp2 | a0001 | c0002 | t0010 | g0047 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02572 | hp1 | a0001 | c0002 | t0006 | g0050 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02572 | hp2 | a0006 | c0010 | t0007 | g0040 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02602 | hp1 | a0002 | c0004 | t0009 | g0153 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02602 | hp2 | a0001 | c0003 | t0002 | g0296 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02615 | hp1 | a0001 | c0001 | t0011 | g0131 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02615 | hp2 | a0001 | c0002 | t0006 | g0052 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02622 | hp1 | a0001 | c0003 | t0002 | g0268 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02622 | hp2 | a0001 | c0005 | t0019 | g0136 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02630 | hp1 | a0001 | c0002 | t0004 | g0267 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02647 | hp1 | a0001 | c0005 | t0002 | g0142 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02647 | hp2 | a0001 | c0001 | t0015 | g0130 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02683 | hp1 | a0001 | c0002 | t0003 | g0004 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02717 | hp1 | a0001 | c0003 | t0002 | g0279 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02717 | hp2 | a0001 | c0002 | t0004 | g0261 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02723 | hp1 | a0006 | c0010 | t0007 | g0039 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02723 | hp2 | a0004 | c0008 | t0008 | g0027 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02738 | hp1 | a0001 | c0002 | t0003 | g0120 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02738 | hp2 | a0001 | c0003 | t0002 | g0288 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02809 | hp1 | a0001 | c0002 | t0004 | g0265 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02809 | hp2 | a0001 | c0002 | t0006 | g0051 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02818 | hp1 | a0001 | c0002 | t0006 | g0046 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02886 | hp1 | a0004 | c0008 | t0017 | g0026 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02886 | hp2 | a0001 | c0002 | t0004 | g0264 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02895 | hp1 | a0001 | c0002 | t0004 | g0253 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02895 | hp2 | a0001 | c0005 | t0002 | g0140 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02922 | hp1 | a0003 | c0006 | t0005 | g0012 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02965 | hp1 | a0003 | c0006 | t0005 | g0362 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02965 | hp2 | a0001 | c0005 | t0002 | g0143 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02970 | hp1 | a0009 | c0013 | t0002 | g0036 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02970 | hp2 | a0003 | c0006 | t0005 | g0012 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02976 | hp2 | a0001 | c0021 | t0002 | g0254 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03041 | hp1 | a0001 | c0003 | t0002 | g0356 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03041 | hp2 | a0001 | c0007 | t0003 | g0064 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03098 | hp1 | a0001 | c0005 | t0002 | g0135 | AFR | MSL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03130 | hp1 | a0001 | c0005 | t0002 | g0015 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03130 | hp2 | a0001 | c0002 | t0010 | g0049 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03139 | hp1 | a0003 | c0006 | t0005 | g0053 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03195 | hp1 | a0001 | c0002 | t0004 | g0257 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | MSL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03209 | hp2 | a0001 | c0002 | t0004 | g0266 | AFR | MSL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03225 | hp1 | a0001 | c0002 | t0004 | g0260 | AFR | MSL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03239 | hp1 | a0005 | c0009 | t0002 | g0034 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03239 | hp2 | a0001 | c0003 | t0002 | g0001 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03453 | hp2 | a0003 | c0006 | t0005 | g0045 | AFR | MSL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03486 | hp1 | a0001 | c0002 | t0004 | g0263 | AFR | MSL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03486 | hp2 | a0013 | c0015 | t0006 | g0041 | AFR | MSL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03491 | hp1 | a0001 | c0002 | t0003 | g0014 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03491 | hp2 | a0001 | c0003 | t0002 | g0001 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03492 | hp1 | a0001 | c0002 | t0003 | g0014 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03516 | hp2 | a0003 | c0006 | t0005 | g0054 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03540 | hp1 | a0001 | c0003 | t0002 | g0277 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03540 | hp2 | a0001 | c0005 | t0002 | g0138 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03579 | hp1 | a0003 | c0006 | t0005 | g0044 | AFR | MSL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03654 | hp1 | a0001 | c0002 | t0021 | g0365 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03654 | hp2 | a0001 | c0003 | t0002 | g0286 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03669 | hp1 | a0001 | c0003 | t0002 | g0360 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03669 | hp2 | a0001 | c0003 | t0002 | g0278 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03688 | hp1 | a0001 | c0002 | t0003 | g0094 | SAS | STU | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03688 | hp2 | a0001 | c0003 | t0002 | g0317 | SAS | STU | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03704 | hp1 | a0001 | c0003 | t0002 | g0128 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03704 | hp2 | a0001 | c0003 | t0002 | g0335 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03710 | hp1 | a0001 | c0003 | t0002 | g0310 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03710 | hp2 | a0001 | c0003 | t0002 | g0269 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03834 | hp1 | a0001 | c0003 | t0002 | g0327 | SAS | BEB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03927 | hp1 | a0001 | c0003 | t0002 | g0346 | SAS | BEB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03927 | hp2 | a0001 | c0003 | t0002 | g0354 | SAS | BEB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03942 | hp1 | a0001 | c0002 | t0003 | g0361 | SAS | BEB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03942 | hp2 | a0001 | c0003 | t0002 | g0284 | SAS | BEB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG04115 | hp1 | a0001 | c0003 | t0002 | g0337 | SAS | STU | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | STU | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG04184 | hp2 | a0001 | c0003 | t0002 | g0295 | SAS | BEB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG04199 | hp1 | a0001 | c0003 | t0002 | g0322 | SAS | STU | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG04199 | hp2 | a0001 | c0002 | t0003 | g0114 | SAS | STU | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | STU | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG04204 | hp2 | a0001 | c0002 | t0003 | g0013 | SAS | STU | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG04228 | hp1 | a0001 | c0003 | t0002 | g0273 | SAS | STU | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG04228 | hp2 | a0014 | c0022 | t0002 | g0325 | SAS | STU | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18522 | hp1 | a0001 | c0002 | t0004 | g0023 | AFR | YRI | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18522 | hp2 | a0001 | c0005 | t0002 | g0144 | AFR | YRI | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18612 | hp2 | a0001 | c0003 | t0002 | g0299 | EAS | CHB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CHB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18747 | hp2 | a0001 | c0002 | t0003 | g0088 | EAS | CHB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18906 | hp1 | a0001 | c0003 | t0002 | g0274 | AFR | YRI | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18906 | hp2 | a0006 | c0010 | t0007 | g0038 | AFR | YRI | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18939 | hp1 | a0001 | c0003 | t0002 | g0306 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18941 | hp1 | a0001 | c0002 | t0003 | g0098 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18943 | hp2 | a0001 | c0001 | t0014 | g0363 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18944 | hp1 | a0001 | c0002 | t0003 | g0079 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18944 | hp2 | a0001 | c0003 | t0002 | g0330 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18945 | hp2 | a0001 | c0002 | t0013 | g0077 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18946 | hp2 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18947 | hp1 | a0001 | c0003 | t0002 | g0347 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18947 | hp2 | a0001 | c0002 | t0003 | g0121 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18948 | hp1 | a0001 | c0003 | t0002 | g0302 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18948 | hp2 | a0001 | c0002 | t0003 | g0068 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18951 | hp1 | a0001 | c0003 | t0002 | g0353 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18951 | hp2 | a0001 | c0002 | t0003 | g0115 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18952 | hp1 | a0002 | c0004 | t0001 | g0200 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18952 | hp2 | a0001 | c0002 | t0003 | g0078 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18953 | hp1 | a0002 | c0004 | t0001 | g0197 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18953 | hp2 | a0015 | c0016 | t0003 | g0056 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18954 | hp1 | a0002 | c0004 | t0001 | g0229 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18954 | hp2 | a0001 | c0003 | t0002 | g0305 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18956 | hp1 | a0001 | c0002 | t0003 | g0118 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18957 | hp1 | a0001 | c0002 | t0003 | g0107 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18960 | hp1 | a0001 | c0023 | t0002 | g0357 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18960 | hp2 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18961 | hp2 | a0001 | c0002 | t0003 | g0013 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18962 | hp1 | a0001 | c0003 | t0002 | g0307 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18963 | hp1 | a0001 | c0002 | t0003 | g0104 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18964 | hp1 | a0001 | c0002 | t0003 | g0082 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18964 | hp2 | a0001 | c0003 | t0002 | g0321 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18965 | hp2 | a0001 | c0003 | t0002 | g0340 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18967 | hp1 | a0001 | c0002 | t0003 | g0127 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18967 | hp2 | a0001 | c0003 | t0002 | g0343 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18968 | hp1 | a0001 | c0003 | t0002 | g0319 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18968 | hp2 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18969 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18970 | hp1 | a0001 | c0002 | t0003 | g0073 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18971 | hp1 | a0001 | c0002 | t0003 | g0096 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18971 | hp2 | a0001 | c0003 | t0002 | g0289 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18972 | hp1 | a0001 | c0003 | t0002 | g0313 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18972 | hp2 | a0001 | c0002 | t0003 | g0103 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18973 | hp1 | a0004 | c0018 | t0001 | g0155 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18973 | hp2 | a0001 | c0002 | t0003 | g0122 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18974 | hp1 | a0001 | c0003 | t0002 | g0318 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18978 | hp1 | a0001 | c0001 | t0014 | g0364 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18978 | hp2 | a0001 | c0002 | t0003 | g0101 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18979 | hp1 | a0001 | c0003 | t0002 | g0344 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18979 | hp2 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18980 | hp1 | a0001 | c0002 | t0003 | g0071 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18980 | hp2 | a0002 | c0004 | t0001 | g0196 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18984 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18984 | hp2 | a0001 | c0003 | t0002 | g0293 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18985 | hp1 | a0001 | c0003 | t0002 | g0351 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18986 | hp1 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18986 | hp2 | a0010 | c0011 | t0001 | g0133 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18989 | hp1 | a0002 | c0004 | t0001 | g0202 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18989 | hp2 | a0001 | c0002 | t0003 | g0076 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18990 | hp1 | a0001 | c0003 | t0002 | g0297 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18991 | hp2 | a0002 | c0004 | t0001 | g0241 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18992 | hp2 | a0001 | c0003 | t0002 | g0349 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18993 | hp1 | a0001 | c0003 | t0002 | g0342 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18998 | hp1 | a0001 | c0003 | t0002 | g0024 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18998 | hp2 | a0001 | c0002 | t0003 | g0126 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18999 | hp1 | a0001 | c0002 | t0003 | g0060 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18999 | hp2 | a0001 | c0003 | t0002 | g0350 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19000 | hp1 | a0001 | c0003 | t0002 | g0341 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19002 | hp1 | a0001 | c0002 | t0003 | g0075 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19005 | hp2 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19006 | hp1 | a0001 | c0003 | t0002 | g0303 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19006 | hp2 | a0001 | c0002 | t0003 | g0105 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19007 | hp1 | a0001 | c0002 | t0013 | g0080 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19007 | hp2 | a0001 | c0003 | t0002 | g0309 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19009 | hp1 | a0001 | c0003 | t0002 | g0338 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19010 | hp2 | a0001 | c0002 | t0003 | g0074 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19012 | hp2 | a0001 | c0003 | t0002 | g0333 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | LWK | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19030 | hp2 | a0001 | c0003 | t0002 | g0287 | AFR | LWK | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19043 | hp1 | a0001 | c0005 | t0002 | g0141 | AFR | LWK | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19043 | hp2 | a0001 | c0002 | t0004 | g0023 | AFR | LWK | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19056 | hp2 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19057 | hp1 | a0001 | c0003 | t0002 | g0301 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19057 | hp2 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19058 | hp2 | a0001 | c0003 | t0002 | g0323 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19059 | hp1 | a0001 | c0003 | t0002 | g0326 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19060 | hp2 | a0001 | c0003 | t0002 | g0328 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19063 | hp1 | a0001 | c0003 | t0002 | g0025 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19064 | hp1 | a0001 | c0002 | t0003 | g0061 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19064 | hp2 | a0002 | c0004 | t0001 | g0204 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19066 | hp2 | a0001 | c0003 | t0002 | g0025 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19074 | hp2 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19076 | hp1 | a0001 | c0002 | t0003 | g0125 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19077 | hp1 | a0001 | c0002 | t0003 | g0117 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19078 | hp1 | a0002 | c0004 | t0001 | g0242 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19078 | hp2 | a0001 | c0002 | t0003 | g0057 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19079 | hp1 | a0002 | c0004 | t0001 | g0205 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19082 | hp1 | a0001 | c0002 | t0003 | g0099 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19083 | hp1 | a0001 | c0002 | t0003 | g0092 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19083 | hp2 | a0010 | c0011 | t0001 | g0194 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19084 | hp1 | a0001 | c0002 | t0003 | g0089 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19085 | hp1 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19086 | hp1 | a0001 | c0003 | t0002 | g0024 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19088 | hp2 | a0001 | c0003 | t0002 | g0314 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19090 | hp2 | a0001 | c0003 | t0002 | g0334 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19091 | hp1 | a0001 | c0003 | t0002 | g0358 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19240 | hp1 | a0001 | c0005 | t0002 | g0015 | AFR | YRI | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | TSI | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA20752 | hp2 | a0001 | c0003 | t0002 | g0283 | EUR | TSI | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0228 | EUR | TSI | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA20805 | hp2 | a0001 | c0002 | t0003 | g0119 | EUR | TSI | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA20905 | hp1 | a0001 | c0003 | t0016 | g0285 | SAS | GIH | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | GIH | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01123 | hp2 | a0002 | c0004 | t0001 | g0203 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02109 | hp1 | a0006 | c0010 | t0007 | g0037 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02109 | hp2 | a0004 | c0008 | t0008 | g0030 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02486 | hp1 | a0001 | c0003 | t0002 | g0275 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02559 | hp2 | a0001 | c0005 | t0002 | g0139 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | MSL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03471 | hp2 | a0001 | c0003 | t0002 | g0280 | AFR | MSL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG06807 | hp1 | a0001 | c0001 | t0020 | g0221 | AFR | USA | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG06807 | hp2 | a0001 | c0002 | t0004 | g0258 | AFR | USA | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18955 | hp1 | a0001 | c0003 | t0002 | g0294 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA20300 | hp1 | a0001 | c0003 | t0002 | g0270 | AFR | USA | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA20300 | hp2 | a0001 | c0003 | t0002 | g0320 | AFR | USA | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | LWK | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA21309 | hp2 | a0001 | c0003 | t0002 | g0276 | AFR | LWK | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
homoSapiens | chm13v2 | a0001 | c0003 | t0002 | g0329 | REF | REF | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
homoSapiens | grch38p0 | a0001 | c0003 | t0002 | g0001 | REF | REF | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:149040077 | C | T | 1 | a0005 | 4 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(1): Show |
missense_variant | MODERATE | c.2456G>A | p.Arg819His | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 21/25 | 2653/5320 | 2456/3030 | 819/1009 | chr3 | 149040077 | |||
chr3:149040122 | A | G | 1 | a0012 | 1 | HG01975.hp1 | missense_variant | MODERATE | c.2411T>C | p.Ile804Thr | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 21/25 | 2608/5320 | 2411/3030 | 804/1009 | chr3 | 149040122 | |||
chr3:149041582 | T | C | 1 | a0008 | 2 | HG01891.hp1 HG02055.hp1 |
missense_variant | MODERATE | c.2284A>G | p.Ile762Val | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 20/25 | 2481/5320 | 2284/3030 | 762/1009 | chr3 | 149041582 | |||
chr3:149042174 | C | T | 1 | a0007 | 2 | HG01069.hp1 HG01071.hp1 |
missense_variant | MODERATE | c.2189G>A | p.Gly730Asp | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 19/25 | 2386/5320 | 2189/3030 | 730/1009 | chr3 | 149042174 | |||
chr3:149046257 | C | T | 1 | a0010 | 2 | NA18986.hp2 NA19083.hp2 |
missense_variant&splice_region_variant | MODERATE | c.1895G>A | p.Arg632His | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/25 | 2092/5320 | 1895/3030 | 632/1009 | chr3 | 149046257 | |||
chr3:149063459 | A | T | 1 | a0011 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.1132T>A | p.Ser378Thr | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/25 | 1329/5320 | 1132/3030 | 378/1009 | chr3 | 149063459 | |||
chr3:149063464 | C | T | 1 | a0006 | 4 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
missense_variant | MODERATE | c.1127G>A | p.Arg376His | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/25 | 1324/5320 | 1127/3030 | 376/1009 | chr3 | 149063464 | |||
chr3:149063507 | C | G | 1 | a0003 | 8 | HG02055.hp2 HG02922.hp1 HG02965.hp1 others(5): Show |
missense_variant | MODERATE | c.1084G>C | p.Glu362Gln | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/25 | 1281/5320 | 1084/3030 | 362/1009 | chr3 | 149063507 | |||
chr3:149063522 | C | T | 1 | a0014 | 1 | HG04228.hp2 | missense_variant&splice_region_variant | MODERATE | c.1069G>A | p.Ala357Thr | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/25 | 1266/5320 | 1069/3030 | 357/1009 | chr3 | 149063522 | |||
chr3:149064862 | T | C | 2 | a0006 a0009 |
6 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
missense_variant | MODERATE | c.995A>G | p.Tyr332Cys | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 9/25 | 1192/5320 | 995/3030 | 332/1009 | chr3 | 149064862 | |||
chr3:149068298 | T | C | 1 | a0002 | 15 | HG00280.hp2 HG00323.hp2 HG01081.hp1 others(12): Show |
missense_variant | MODERATE | c.932A>G | p.Asn311Ser | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/25 | 1129/5320 | 932/3030 | 311/1009 | chr3 | 149068298 | |||
chr3:149071340 | T | C | 1 | a0004 | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
missense_variant | MODERATE | c.806A>G | p.Asp269Gly | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/25 | 1003/5320 | 806/3030 | 269/1009 | chr3 | 149071340 | |||
chr3:149071341 | C | T | 1 | a0004 | 1 | NA18973.hp1 | missense_variant | MODERATE | c.805G>A | p.Asp269Asn | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/25 | 1002/5320 | 805/3030 | 269/1009 | chr3 | 149071341 | |||
chr3:149084684 | C | T | 1 | a0015 | 1 | NA18953.hp2 | missense_variant&splice_region_variant | MODERATE | c.226G>A | p.Val76Ile | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/25 | 423/5320 | 226/3030 | 76/1009 | chr3 | 149084684 | |||
chr3:149084782 | A | G | 1 | a0013 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.128T>C | p.Ile43Thr | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/25 | 325/5320 | 128/3030 | 43/1009 | chr3 | 149084782 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:149041538 | T | C | 6 | a0001c0001 a0001c0017 a0002c0004 others(3): Show |
144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
synonymous_variant | LOW | c.2328A>G | p.Ala776Ala | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 20/25 | 2525/5320 | 2328/3030 | 776/1009 | chr3 | 149041538 | |||
chr3:149048879 | T | C | 1 | a0001c0007 | 6 | HG01109.hp1 HG01169.hp2 HG01256.hp2 others(3): Show |
synonymous_variant | LOW | c.1740A>G | p.Arg580Arg | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 16/25 | 1937/5320 | 1740/3030 | 580/1009 | chr3 | 149048879 | |||
chr3:149048882 | T | C | 1 | a0001c0021 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.1737A>G | p.Glu579Glu | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 16/25 | 1934/5320 | 1737/3030 | 579/1009 | chr3 | 149048882 | |||
chr3:149050343 | T | C | 1 | a0001c0005 | 13 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(10): Show |
synonymous_variant | LOW | c.1506A>G | p.Val502Val | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 15/25 | 1703/5320 | 1506/3030 | 502/1009 | chr3 | 149050343 | |||
chr3:149068321 | C | T | 19 | a0001c0001 a0001c0002 a0001c0005 others(16): Show |
303 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(300): Show |
synonymous_variant | LOW | c.909G>A | p.Thr303Thr | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/25 | 1106/5320 | 909/3030 | 303/1009 | chr3 | 149068321 | |||
chr3:149073279 | A | T | 1 | a0001c0017 | 1 | HG01978.hp2 | synonymous_variant | LOW | c.573T>A | p.Ala191Ala | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 5/25 | 770/5320 | 573/3030 | 191/1009 | chr3 | 149073279 | |||
chr3:149084739 | G | A | 1 | a0001c0023 | 1 | NA18960.hp1 | synonymous_variant | LOW | c.171C>T | p.Ser57Ser | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/25 | 368/5320 | 171/3030 | 57/1009 | chr3 | 149084739 | |||
chr3:149084826 | G | A | 1 | a0004c0008 | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
synonymous_variant | LOW | c.84C>T | p.Leu28Leu | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/25 | 281/5320 | 84/3030 | 28/1009 | chr3 | 149084826 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:149030292 | C | CT | 1 | a0006c0010t0007 | 4 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1927dupA | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 1927 | chr3 | 149030292 | ||||||
chr3:149030415 | A | AACTT | 1 | a0001c0002t0010 | 3 | HG00738.hp2 HG02451.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1801_*1804dupAAGT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 1804 | chr3 | 149030415 | ||||||
chr3:149030453 | A | C | 1 | a0004c0008t0017 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1767T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 1767 | chr3 | 149030453 | ||||||
chr3:149030475 | T | TGTC | 8 | a0001c0002t0003 a0001c0002t0013 a0001c0002t0021 others(5): Show |
99 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*1742_*1744dupGAC | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 1744 | chr3 | 149030475 | ||||||
chr3:149030579 | C | T | 1 | a0003c0006t0005 | 8 | HG02055.hp2 HG02922.hp1 HG02965.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1641G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 1641 | chr3 | 149030579 | ||||||
chr3:149030593 | T | C | 10 | a0001c0001t0001 a0001c0001t0014 a0001c0001t0018 others(7): Show |
141 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*1627A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 1627 | chr3 | 149030593 | ||||||
chr3:149030681 | G | A | 1 | a0001c0001t0018 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1539C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 1539 | chr3 | 149030681 | ||||||
chr3:149030713 | C | G | 1 | a0002c0004t0009 | 3 | HG00323.hp2 HG01081.hp1 HG02602.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1507G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 1507 | chr3 | 149030713 | ||||||
chr3:149030729 | T | C | 4 | a0001c0002t0006 a0001c0002t0010 a0003c0006t0005 others(1): Show |
17 | HG00738.hp2 HG02055.hp2 HG02145.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1491A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 1491 | chr3 | 149030729 | ||||||
chr3:149030894 | A | G | 1 | a0004c0008t0008 | 3 | HG01891.hp2 HG02109.hp2 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1326T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 1326 | chr3 | 149030894 | ||||||
chr3:149031224 | T | G | 1 | a0001c0003t0016 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*996A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 996 | chr3 | 149031224 | ||||||
chr3:149031252 | A | G | 1 | a0001c0003t0016 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*968T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 968 | chr3 | 149031252 | ||||||
chr3:149031379 | T | G | 1 | a0001c0001t0015 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*841A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 841 | chr3 | 149031379 | ||||||
chr3:149031418 | TTA | T | 2 | a0001c0001t0011 a0001c0001t0015 |
3 | HG02258.hp1 HG02615.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*800_*801delTA | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 800 | chr3 | 149031418 | ||||||
chr3:149031421 | T | C | 1 | a0001c0005t0019 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*799A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 799 | chr3 | 149031421 | ||||||
chr3:149031566 | A | G | 1 | a0001c0002t0013 | 2 | NA18945.hp2 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*654T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 654 | chr3 | 149031566 | ||||||
chr3:149031834 | T | C | 8 | a0001c0002t0003 a0001c0002t0004 a0001c0002t0013 others(5): Show |
113 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*386A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 386 | chr3 | 149031834 | ||||||
chr3:149032000 | T | C | 1 | a0001c0001t0020 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*220A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 220 | chr3 | 149032000 | ||||||
chr3:149086458 | T | A | 1 | a0001c0001t0014 | 2 | NA18943.hp2 NA18978.hp1 |
5_prime_UTR_variant | MODIFIER | c.-122A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/25 | 122 | chr3 | 149086458 | ||||||
chr3:149086493 | G | C | 1 | a0001c0001t0014 | 2 | NA18943.hp2 NA18978.hp1 |
5_prime_UTR_variant | MODIFIER | c.-157C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/25 | 157 | chr3 | 149086493 | ||||||
chr3:149086507 | C | A | 1 | a0001c0002t0021 | 1 | HG03654.hp1 | 5_prime_UTR_variant | MODIFIER | c.-171G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/25 | 171 | chr3 | 149086507 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:149032513 | A | T | 6 | a0006c0010t0007g0037 a0006c0010t0007g0038 a0006c0010t0007g0039 others(3): Show |
6 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2878-141T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149032513 | |||||||
chr3:149032571 | G | A | 4 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(1): Show |
4 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.2878-199C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149032571 | |||||||
chr3:149032734 | G | A | 2 | a0001c0002t0006g0042 a0013c0015t0006g0041 |
2 | HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2878-362C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149032734 | |||||||
chr3:149032909 | G | A | 2 | a0001c0002t0006g0042 a0013c0015t0006g0041 |
2 | HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2878-537C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149032909 | |||||||
chr3:149032957 | C | CA | 43 | a0001c0002t0006g0042 a0001c0003t0002g0128 a0001c0003t0002g0268 others(40): Show |
44 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.2878-586dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149032957 | |||||||
chr3:149032957 | C | CAA | 7 | a0001c0003t0002g0271 a0001c0003t0002g0273 a0003c0006t0005g0045 others(4): Show |
7 | HG01255.hp2 HG01433.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.2878-587_2878-586d others(4): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149032957 | |||||||
chr3:149032967 | A | C | 12 | a0001c0005t0002g0015 a0001c0005t0002g0135 a0001c0005t0002g0137 others(9): Show |
13 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.2878-595T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149032967 | |||||||
chr3:149032968 | A | C | 2 | a0001c0001t0001g0055 a0001c0001t0001g0247 |
2 | NA19076.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.2878-596T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149032968 | |||||||
chr3:149032971 | A | AC | 3 | a0001c0002t0003g0118 a0001c0002t0003g0125 a0001c0002t0003g0361 |
3 | HG03942.hp1 NA18956.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.2878-600_2878-599i others(3): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149032971 | |||||||
chr3:149032971 | A | C | 95 | a0001c0002t0003g0002 a0001c0002t0003g0004 a0001c0002t0003g0005 others(92): Show |
110 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.2878-599T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149032971 | |||||||
chr3:149032974 | A | C | 128 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(125): Show |
145 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.2878-602T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149032974 | |||||||
chr3:149032975 | A | C | 11 | a0001c0001t0001g0134 a0001c0001t0001g0146 a0001c0001t0001g0173 others(8): Show |
11 | HG02818.hp2 HG03225.hp2 HG03516.hp1 others(8): Show |
intron_variant | MODIFIER | c.2878-603T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149032975 | |||||||
chr3:149032976 | AAC | A | 129 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(126): Show |
146 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.2878-606_2878-605d others(4): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149032976 | |||||||
chr3:149032977 | AC | A | 11 | a0001c0001t0001g0134 a0001c0001t0001g0146 a0001c0001t0001g0173 others(8): Show |
11 | HG02818.hp2 HG03225.hp2 HG03516.hp1 others(8): Show |
intron_variant | MODIFIER | c.2878-606delG | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149032977 | |||||||
chr3:149032978 | C | A | 5 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2878-606G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149032978 | |||||||
chr3:149033026 | C | T | 22 | a0001c0003t0002g0128 a0001c0003t0002g0268 a0001c0003t0002g0269 others(19): Show |
22 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.2878-654G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149033026 | |||||||
chr3:149033109 | A | G | 1 | a0001c0002t0013g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2878-737T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149033109 | |||||||
chr3:149033217 | G | A | 4 | a0001c0003t0002g0321 a0001c0003t0002g0340 a0001c0003t0002g0342 others(1): Show |
4 | NA18964.hp2 NA18965.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.2878-845C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149033217 | |||||||
chr3:149033328 | C | G | 4 | a0006c0010t0007g0037 a0006c0010t0007g0038 a0006c0010t0007g0039 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2878-956G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149033328 | |||||||
chr3:149033370 | TA | T | 125 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(122): Show |
141 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.2878-999delT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149033370 | |||||||
chr3:149033468 | C | A | 293 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(290): Show |
326 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.2878-1096G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149033468 | |||||||
chr3:149033816 | C | T | 1 | a0001c0003t0002g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2877+1102G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149033816 | |||||||
chr3:149033893 | CT | C | 3 | a0001c0003t0002g0269 a0001c0003t0002g0278 a0001c0003t0002g0286 |
3 | HG03654.hp2 HG03669.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2877+1024delA | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149033893 | |||||||
chr3:149034043 | G | A | 1 | a0001c0002t0003g0361 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2877+875C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149034043 | |||||||
chr3:149034186 | T | A | 1 | a0001c0001t0001g0234 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2877+732A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149034186 | |||||||
chr3:149034354 | A | G | 1 | a0001c0003t0002g0128 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2877+564T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149034354 | |||||||
chr3:149034363 | T | C | 128 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(125): Show |
144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.2877+555A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149034363 | |||||||
chr3:149034395 | A | G | 4 | a0006c0010t0007g0037 a0006c0010t0007g0038 a0006c0010t0007g0039 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2877+523T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149034395 | |||||||
chr3:149034620 | T | A | 1 | a0001c0005t0002g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2877+298A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149034620 | |||||||
chr3:149034651 | G | A | 125 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(122): Show |
141 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.2877+267C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149034651 | |||||||
chr3:149034728 | A | C | 2 | a0002c0004t0009g0016 a0002c0004t0009g0153 |
3 | HG00323.hp2 HG01081.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.2877+190T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149034728 | |||||||
chr3:149034764 | A | G | 2 | a0009c0013t0002g0035 a0009c0013t0002g0036 |
2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2877+154T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149034764 | |||||||
chr3:149035095 | T | C | 1 | a0001c0003t0002g0323 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2797-97A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035095 | |||||||
chr3:149035146 | G | C | 2 | a0001c0002t0006g0042 a0013c0015t0006g0041 |
2 | HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2797-148C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035146 | |||||||
chr3:149035298 | A | T | 2 | a0001c0002t0003g0014 a0001c0002t0003g0114 |
3 | HG03491.hp1 HG03492.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2797-300T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035298 | |||||||
chr3:149035435 | G | GAAATAAA others(5): Show |
1 | a0001c0002t0003g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2797-449_2797-438d others(14): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035435 | |||||||
chr3:149035523 | T | A | 4 | a0001c0002t0006g0050 a0001c0002t0010g0047 a0001c0002t0010g0048 others(1): Show |
4 | HG00738.hp2 HG02451.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.2797-525A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035523 | |||||||
chr3:149035576 | T | G | 1 | a0005c0009t0002g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2797-578A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035576 | |||||||
chr3:149035607 | C | G | 12 | a0001c0005t0002g0015 a0001c0005t0002g0135 a0001c0005t0002g0137 others(9): Show |
13 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.2797-609G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035607 | |||||||
chr3:149035614 | G | C | 1 | a0001c0002t0006g0051 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2797-616C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035614 | |||||||
chr3:149035656 | C | CA | 13 | a0001c0003t0002g0288 a0001c0003t0002g0289 a0001c0003t0002g0290 others(10): Show |
13 | HG00140.hp2 HG01175.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.2797-659dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035656 | |||||||
chr3:149035656 | CAAA | C | 10 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0184 others(7): Show |
10 | HG00423.hp2 HG00597.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.2797-661_2797-659d others(5): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035656 | |||||||
chr3:149035656 | CAAAA | C | 141 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(138): Show |
160 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.2797-662_2797-659d others(6): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035656 | |||||||
chr3:149035656 | CAAAAA | C | 76 | a0001c0001t0001g0149 a0001c0001t0011g0129 a0001c0001t0011g0131 others(73): Show |
87 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.2797-663_2797-659d others(7): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035656 | |||||||
chr3:149035656 | CAAAAAA | C | 42 | a0001c0002t0003g0087 a0001c0002t0003g0125 a0001c0002t0004g0253 others(39): Show |
42 | HG00738.hp2 HG01071.hp1 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.2797-664_2797-659d others(8): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035656 | |||||||
chr3:149035656 | CAAAAAAA | C | 7 | a0001c0002t0006g0051 a0004c0008t0002g0029 a0004c0008t0008g0027 others(4): Show |
7 | HG01069.hp1 HG01255.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.2797-665_2797-659d others(9): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035656 | |||||||
chr3:149035673 | A | G | 1 | a0001c0002t0003g0361 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2797-675T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035673 | |||||||
chr3:149035674 | A | G | 1 | a0001c0002t0003g0361 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2797-676T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035674 | |||||||
chr3:149035675 | A | G | 1 | a0001c0002t0003g0361 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2797-677T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035675 | |||||||
chr3:149035676 | A | T | 1 | a0001c0002t0003g0361 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2797-678T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035676 | |||||||
chr3:149035677 | A | T | 1 | a0001c0002t0003g0361 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2797-679T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035677 | |||||||
chr3:149035678 | A | AGGGGGTT others(1): Show |
12 | a0001c0002t0003g0006 a0001c0002t0003g0013 a0001c0002t0003g0059 others(9): Show |
13 | HG01169.hp1 HG01169.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.2797-681_2797-680i others(10): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035678 | |||||||
chr3:149035678 | A | T | 4 | a0001c0002t0003g0361 a0001c0002t0004g0260 a0001c0002t0004g0262 others(1): Show |
4 | HG01256.hp1 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2797-680T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035678 | |||||||
chr3:149035679 | A | T | 16 | a0001c0002t0003g0006 a0001c0002t0003g0013 a0001c0002t0003g0059 others(13): Show |
17 | HG01169.hp1 HG01169.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.2797-681T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035679 | |||||||
chr3:149035682 | A | G | 18 | a0001c0002t0003g0006 a0001c0002t0003g0013 a0001c0002t0003g0059 others(15): Show |
19 | HG01169.hp1 HG01169.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.2797-684T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035682 | |||||||
chr3:149035683 | A | G | 5 | a0001c0001t0001g0210 a0001c0002t0006g0050 a0001c0002t0010g0047 others(2): Show |
5 | HG00738.hp2 HG02451.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2797-685T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035683 | |||||||
chr3:149035685 | G | T | 18 | a0001c0002t0003g0006 a0001c0002t0003g0013 a0001c0002t0003g0059 others(15): Show |
19 | HG01169.hp1 HG01169.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.2797-687C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035685 | |||||||
chr3:149035686 | G | C | 18 | a0001c0002t0003g0006 a0001c0002t0003g0013 a0001c0002t0003g0059 others(15): Show |
19 | HG01169.hp1 HG01169.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.2797-688C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035686 | |||||||
chr3:149035687 | G | A | 18 | a0001c0002t0003g0006 a0001c0002t0003g0013 a0001c0002t0003g0059 others(15): Show |
19 | HG01169.hp1 HG01169.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.2797-689C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035687 | |||||||
chr3:149035690 | T | C | 18 | a0001c0002t0003g0006 a0001c0002t0003g0013 a0001c0002t0003g0059 others(15): Show |
19 | HG01169.hp1 HG01169.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.2797-692A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035690 | |||||||
chr3:149035690 | T | TTTAAGAG others(6): Show |
81 | a0001c0002t0003g0002 a0001c0002t0003g0004 a0001c0002t0003g0005 others(78): Show |
93 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.2797-693_2797-692i others(15): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035690 | |||||||
chr3:149035776 | G | C | 5 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2797-778C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035776 | |||||||
chr3:149035840 | A | G | 5 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2797-842T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035840 | |||||||
chr3:149035874 | G | A | 12 | a0001c0002t0003g0011 a0001c0002t0003g0061 a0001c0002t0003g0072 others(9): Show |
13 | HG00621.hp2 HG01074.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.2797-876C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035874 | |||||||
chr3:149035971 | T | C | 1 | a0001c0002t0006g0050 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2797-973A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035971 | |||||||
chr3:149035993 | G | T | 1 | a0001c0002t0003g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2797-995C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035993 | |||||||
chr3:149036035 | T | C | 1 | a0001c0002t0003g0085 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2797-1037A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036035 | |||||||
chr3:149036177 | T | G | 1 | a0001c0002t0003g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2797-1179A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036177 | |||||||
chr3:149036196 | G | T | 4 | a0006c0010t0007g0037 a0006c0010t0007g0038 a0006c0010t0007g0039 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2797-1198C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036196 | |||||||
chr3:149036297 | G | GTTTTTTT others(3): Show |
6 | a0001c0002t0003g0060 a0001c0002t0003g0073 a0001c0002t0003g0255 others(3): Show |
7 | HG01167.hp1 HG01169.hp1 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.2797-1309_2797-130 others(14): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036297 | |||||||
chr3:149036297 | G | GTTTTTTT others(4): Show |
92 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(89): Show |
104 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.2797-1300_2797-129 others(15): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036297 | |||||||
chr3:149036297 | G | GTTTTTTT others(5): Show |
127 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(124): Show |
143 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.2797-1300_2797-129 others(16): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036297 | |||||||
chr3:149036297 | G | GTTTTTTT others(6): Show |
40 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0132 others(37): Show |
44 | HG00280.hp1 HG00408.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.2797-1300_2797-129 others(17): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036297 | |||||||
chr3:149036297 | G | GTTTTTTT others(7): Show |
5 | a0001c0001t0018g0163 a0003c0006t0005g0044 a0003c0006t0005g0053 others(2): Show |
5 | HG02273.hp1 HG02572.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2797-1300_2797-129 others(18): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036297 | |||||||
chr3:149036376 | C | T | 3 | a0001c0002t0003g0060 a0001c0002t0003g0112 a0001c0002t0003g0113 |
3 | HG01261.hp1 HG02300.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.2797-1378G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036376 | |||||||
chr3:149036378 | TCCTGGGT others(5): Show |
T | 5 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2797-1392_2797-138 others(16): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036378 | |||||||
chr3:149036578 | C | T | 1 | a0001c0002t0021g0365 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2797-1580G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036578 | |||||||
chr3:149036579 | G | C | 1 | a0001c0001t0001g0169 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2797-1581C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036579 | |||||||
chr3:149036581 | G | A | 5 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2797-1583C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036581 | |||||||
chr3:149036619 | T | C | 1 | a0001c0003t0002g0346 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2797-1621A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036619 | |||||||
chr3:149036692 | T | C | 98 | a0001c0002t0003g0002 a0001c0002t0003g0004 a0001c0002t0003g0005 others(95): Show |
113 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.2797-1694A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036692 | |||||||
chr3:149036756 | A | G | 1 | a0001c0002t0003g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2797-1758T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036756 | |||||||
chr3:149036757 | G | A | 1 | a0001c0002t0003g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2797-1759C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036757 | |||||||
chr3:149036767 | T | A | 2 | a0009c0013t0002g0035 a0009c0013t0002g0036 |
2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2797-1769A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036767 | |||||||
chr3:149036829 | G | A | 3 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0248 |
3 | NA18992.hp1 NA19002.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.2797-1831C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036829 | |||||||
chr3:149037134 | A | C | 1 | a0001c0005t0002g0142 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2796+1915T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149037134 | |||||||
chr3:149037171 | A | T | 1 | a0001c0002t0003g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2796+1878T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149037171 | |||||||
chr3:149037327 | C | A | 1 | a0001c0003t0002g0278 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2796+1722G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149037327 | |||||||
chr3:149037372 | G | A | 114 | a0001c0002t0003g0002 a0001c0002t0003g0004 a0001c0002t0003g0005 others(111): Show |
130 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.2796+1677C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149037372 | |||||||
chr3:149037447 | G | A | 2 | a0001c0003t0002g0284 a0001c0003t0002g0333 |
2 | HG03942.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.2796+1602C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149037447 | |||||||
chr3:149037460 | T | C | 9 | a0001c0005t0002g0015 a0001c0005t0002g0137 a0001c0005t0002g0138 others(6): Show |
10 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.2796+1589A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149037460 | |||||||
chr3:149037467 | C | CA | 142 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(139): Show |
159 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.2796+1581dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149037467 | |||||||
chr3:149037477 | A | G | 5 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2796+1572T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149037477 | |||||||
chr3:149037685 | T | C | 2 | a0001c0002t0003g0014 a0001c0002t0003g0114 |
3 | HG03491.hp1 HG03492.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2796+1364A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149037685 | |||||||
chr3:149037784 | G | T | 65 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0017 others(62): Show |
73 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.2796+1265C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149037784 | |||||||
chr3:149037840 | G | C | 1 | a0001c0002t0004g0265 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2796+1209C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149037840 | |||||||
chr3:149038074 | G | A | 128 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(125): Show |
144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.2796+975C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149038074 | |||||||
chr3:149038125 | T | C | 1 | a0001c0003t0002g0307 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2796+924A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149038125 | |||||||
chr3:149038133 | C | T | 1 | a0001c0005t0019g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2796+916G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149038133 | |||||||
chr3:149038147 | C | G | 148 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(145): Show |
165 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.2796+902G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149038147 | |||||||
chr3:149038216 | G | A | 5 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2796+833C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149038216 | |||||||
chr3:149038398 | C | A | 2 | a0003c0006t0005g0043 a0003c0006t0005g0362 |
2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2796+651G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149038398 | |||||||
chr3:149038436 | A | G | 1 | a0003c0006t0005g0054 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2796+613T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149038436 | |||||||
chr3:149038563 | C | T | 6 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG02273.hp2 HG02683.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.2796+486G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149038563 | |||||||
chr3:149038592 | T | C | 1 | a0005c0009t0002g0032 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2796+457A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149038592 | |||||||
chr3:149038664 | A | T | 1 | a0001c0001t0001g0019 | 2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2796+385T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149038664 | |||||||
chr3:149038698 | A | C | 1 | a0001c0005t0002g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2796+351T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149038698 | |||||||
chr3:149038739 | C | G | 12 | a0001c0005t0002g0015 a0001c0005t0002g0135 a0001c0005t0002g0137 others(9): Show |
13 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.2796+310G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149038739 | |||||||
chr3:149038759 | C | T | 1 | a0002c0004t0009g0016 | 2 | HG00323.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.2796+290G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149038759 | |||||||
chr3:149038877 | T | G | 6 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG02273.hp2 HG02683.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.2796+172A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149038877 | |||||||
chr3:149038974 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2796+75A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149038974 | |||||||
chr3:149039015 | C | T | 2 | a0001c0002t0006g0042 a0013c0015t0006g0041 |
2 | HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2796+34G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149039015 | |||||||
chr3:149039038 | G | A | 358 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(355): Show |
393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.2796+11C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149039038 | |||||||
chr3:149039294 | G | A | 1 | a0001c0007t0003g0097 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2616-65C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 22/24 | chr3 | 149039294 | |||||||
chr3:149039381 | T | G | 1 | a0001c0002t0003g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2616-152A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 22/24 | chr3 | 149039381 | |||||||
chr3:149039503 | G | GT | 9 | a0001c0002t0006g0051 a0001c0002t0006g0052 a0003c0006t0005g0012 others(6): Show |
10 | HG02055.hp2 HG02615.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.2615+77dupA | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 22/24 | chr3 | 149039503 | |||||||
chr3:149039940 | T | C | 1 | a0001c0003t0002g0338 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2502+91A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 21/24 | chr3 | 149039940 | |||||||
chr3:149040162 | T | TAAGAAAG others(342): Show |
1 | a0005c0009t0002g0034 | 1 | HG03239.hp1 | splice_region_variant&intron_variant | LOW | c.2377-7_2377-6insTT others(347): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 20/24 | chr3 | 149040162 | |||||||
chr3:149040172 | C | G | 1 | a0001c0003t0002g0309 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2377-16G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 20/24 | chr3 | 149040172 | |||||||
chr3:149040173 | G | A | 1 | a0001c0002t0003g0113 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2377-17C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 20/24 | chr3 | 149040173 | |||||||
chr3:149040348 | C | T | 293 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(290): Show |
326 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.2377-192G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 20/24 | chr3 | 149040348 | |||||||
chr3:149040435 | T | TA | 127 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(124): Show |
143 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.2377-280dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 20/24 | chr3 | 149040435 | |||||||
chr3:149040915 | C | T | 1 | a0001c0003t0002g0313 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2376+575G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 20/24 | chr3 | 149040915 | |||||||
chr3:149041282 | G | A | 3 | a0001c0002t0004g0253 a0001c0002t0004g0261 a0001c0002t0004g0263 |
3 | HG02717.hp2 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2376+208C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 20/24 | chr3 | 149041282 | |||||||
chr3:149041320 | C | T | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2376+170G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 20/24 | chr3 | 149041320 | |||||||
chr3:149041342 | A | T | 1 | a0005c0009t0002g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2376+148T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 20/24 | chr3 | 149041342 | |||||||
chr3:149041472 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2376+18T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 20/24 | chr3 | 149041472 | |||||||
chr3:149041755 | C | T | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0222 |
3 | HG01070.hp1 HG01071.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2198-87G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 19/24 | chr3 | 149041755 | |||||||
chr3:149041773 | A | C | 128 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(125): Show |
144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.2198-105T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 19/24 | chr3 | 149041773 | |||||||
chr3:149042498 | C | G | 161 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(158): Show |
179 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.2073-208G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149042498 | |||||||
chr3:149042559 | C | T | 16 | a0001c0002t0006g0042 a0001c0002t0006g0046 a0001c0002t0006g0050 others(13): Show |
17 | HG00738.hp2 HG02055.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.2073-269G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149042559 | |||||||
chr3:149042592 | G | T | 4 | a0005c0009t0002g0031 a0005c0009t0002g0032 a0005c0009t0002g0033 others(1): Show |
4 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.2073-302C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149042592 | |||||||
chr3:149042640 | T | C | 1 | a0001c0003t0002g0322 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2073-350A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149042640 | |||||||
chr3:149042689 | G | A | 2 | a0001c0001t0001g0231 a0001c0001t0001g0236 |
2 | NA18955.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2073-399C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149042689 | |||||||
chr3:149042881 | T | C | 5 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2073-591A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149042881 | |||||||
chr3:149042901 | A | G | 1 | a0001c0001t0001g0236 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2073-611T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149042901 | |||||||
chr3:149043059 | T | A | 1 | a0001c0001t0001g0165 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2073-769A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043059 | |||||||
chr3:149043272 | A | T | 1 | a0001c0001t0001g0159 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2073-982T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043272 | |||||||
chr3:149043275 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2073-985C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043275 | |||||||
chr3:149043277 | T | A | 1 | a0001c0001t0001g0159 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2073-987A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043277 | |||||||
chr3:149043283 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2073-993G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043283 | |||||||
chr3:149043524 | A | G | 161 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(158): Show |
179 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.2073-1234T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043524 | |||||||
chr3:149043547 | G | GA | 39 | a0001c0001t0001g0162 a0001c0001t0001g0171 a0001c0001t0001g0190 others(36): Show |
40 | HG00621.hp2 HG00738.hp2 HG01358.hp1 others(37): Show |
intron_variant | MODIFIER | c.2073-1258dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043547 | |||||||
chr3:149043547 | GA | G | 16 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0150 others(13): Show |
16 | HG01255.hp2 HG01515.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.2073-1258delT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043547 | |||||||
chr3:149043548 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2073-1258T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043548 | |||||||
chr3:149043558 | A | C | 22 | a0001c0003t0002g0128 a0001c0003t0002g0268 a0001c0003t0002g0269 others(19): Show |
22 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.2073-1268T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043558 | |||||||
chr3:149043699 | G | T | 2 | a0001c0002t0006g0051 a0001c0002t0006g0052 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2073-1409C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043699 | |||||||
chr3:149043703 | A | G | 2 | a0001c0002t0003g0014 a0001c0002t0003g0114 |
3 | HG03491.hp1 HG03492.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2073-1413T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043703 | |||||||
chr3:149043813 | T | C | 98 | a0001c0002t0003g0002 a0001c0002t0003g0004 a0001c0002t0003g0005 others(95): Show |
113 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.2073-1523A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043813 | |||||||
chr3:149043854 | T | C | 1 | a0001c0002t0006g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2073-1564A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043854 | |||||||
chr3:149043889 | T | C | 4 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(1): Show |
4 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.2073-1599A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043889 | |||||||
chr3:149043891 | C | T | 2 | a0003c0006t0005g0043 a0003c0006t0005g0362 |
2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2073-1601G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043891 | |||||||
chr3:149044021 | A | G | 1 | a0001c0002t0003g0081 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2073-1731T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044021 | |||||||
chr3:149044028 | A | C | 88 | a0001c0002t0003g0002 a0001c0002t0003g0004 a0001c0002t0003g0005 others(85): Show |
103 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.2073-1738T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044028 | |||||||
chr3:149044032 | A | G | 1 | a0001c0003t0002g0335 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2073-1742T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044032 | |||||||
chr3:149044042 | C | A | 2 | a0001c0001t0001g0231 a0001c0001t0001g0236 |
2 | NA18955.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2073-1752G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044042 | |||||||
chr3:149044054 | C | T | 2 | a0001c0005t0002g0015 a0001c0005t0002g0139 |
3 | HG02559.hp2 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2073-1764G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044054 | |||||||
chr3:149044073 | T | C | 6 | a0001c0002t0006g0050 a0004c0008t0002g0029 a0004c0008t0008g0027 others(3): Show |
6 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2073-1783A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044073 | |||||||
chr3:149044486 | C | CT | 3 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0237 |
3 | HG02258.hp2 HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2072+1593dupA | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044486 | |||||||
chr3:149044501 | G | C | 6 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG02273.hp2 HG02683.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.2072+1579C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044501 | |||||||
chr3:149044564 | C | G | 292 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(289): Show |
325 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.2072+1516G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044564 | |||||||
chr3:149044576 | T | G | 1 | a0001c0021t0002g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2072+1504A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044576 | |||||||
chr3:149044640 | T | C | 1 | a0001c0017t0001g0158 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2072+1440A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044640 | |||||||
chr3:149044643 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2072+1437T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044643 | |||||||
chr3:149044727 | G | T | 1 | a0001c0003t0002g0327 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2072+1353C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044727 | |||||||
chr3:149044849 | T | C | 1 | a0001c0003t0002g0330 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2072+1231A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044849 | |||||||
chr3:149044862 | T | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
6 | HG00558.hp1 HG02165.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2072+1218A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044862 | |||||||
chr3:149044927 | G | A | 1 | a0001c0003t0002g0335 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2072+1153C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044927 | |||||||
chr3:149045043 | A | G | 140 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(137): Show |
157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.2072+1037T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149045043 | |||||||
chr3:149045076 | C | T | 5 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2072+1004G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149045076 | |||||||
chr3:149045077 | G | A | 1 | a0001c0002t0006g0042 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2072+1003C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149045077 | |||||||
chr3:149045196 | G | C | 6 | a0006c0010t0007g0037 a0006c0010t0007g0038 a0006c0010t0007g0039 others(3): Show |
6 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2072+884C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149045196 | |||||||
chr3:149045196 | G | T | 54 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0019 others(51): Show |
62 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.2072+884C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149045196 | |||||||
chr3:149045412 | G | C | 6 | a0001c0002t0006g0050 a0004c0008t0002g0029 a0004c0008t0008g0027 others(3): Show |
6 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2072+668C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149045412 | |||||||
chr3:149045618 | G | T | 1 | a0001c0003t0002g0297 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2072+462C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149045618 | |||||||
chr3:149045669 | T | C | 3 | a0001c0003t0002g0308 a0001c0003t0002g0331 a0001c0003t0002g0332 |
3 | HG00099.hp2 HG01070.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.2072+411A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149045669 | |||||||
chr3:149045703 | G | A | 1 | a0001c0002t0003g0107 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2072+377C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149045703 | |||||||
chr3:149045719 | G | A | 128 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(125): Show |
144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.2072+361C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149045719 | |||||||
chr3:149045822 | T | C | 1 | a0006c0010t0007g0040 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2072+258A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149045822 | |||||||
chr3:149046303 | C | T | 171 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(168): Show |
189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.1893-44G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 17/24 | chr3 | 149046303 | |||||||
chr3:149046498 | T | G | 3 | a0001c0001t0011g0129 a0001c0001t0011g0131 a0001c0001t0015g0130 |
3 | HG02258.hp1 HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1893-239A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 17/24 | chr3 | 149046498 | |||||||
chr3:149046515 | T | C | 1 | a0001c0021t0002g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1893-256A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 17/24 | chr3 | 149046515 | |||||||
chr3:149046519 | G | C | 4 | a0005c0009t0002g0031 a0005c0009t0002g0032 a0005c0009t0002g0033 others(1): Show |
4 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.1893-260C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 17/24 | chr3 | 149046519 | |||||||
chr3:149046756 | A | G | 128 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(125): Show |
144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1893-497T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 17/24 | chr3 | 149046756 | |||||||
chr3:149046883 | A | G | 15 | a0001c0002t0006g0042 a0001c0002t0006g0046 a0001c0002t0006g0051 others(12): Show |
16 | HG00738.hp2 HG02055.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1893-624T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 17/24 | chr3 | 149046883 | |||||||
chr3:149047012 | C | T | 1 | a0004c0008t0008g0030 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1893-753G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 17/24 | chr3 | 149047012 | |||||||
chr3:149047149 | C | T | 7 | a0003c0006t0005g0012 a0003c0006t0005g0043 a0003c0006t0005g0044 others(4): Show |
8 | HG02055.hp2 HG02922.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1892+879G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 17/24 | chr3 | 149047149 | |||||||
chr3:149047162 | C | G | 6 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG02273.hp2 HG02683.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1892+866G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 17/24 | chr3 | 149047162 | |||||||
chr3:149047211 | T | TTAGTC | 292 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(289): Show |
325 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.1892+816_1892+817i others(7): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 17/24 | chr3 | 149047211 | |||||||
chr3:149047598 | C | T | 2 | a0009c0013t0002g0035 a0009c0013t0002g0036 |
2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1892+430G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 17/24 | chr3 | 149047598 | |||||||
chr3:149047634 | T | C | 2 | a0001c0003t0002g0342 a0001c0003t0002g0343 |
2 | NA18967.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1892+394A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 17/24 | chr3 | 149047634 | |||||||
chr3:149047659 | A | C | 2 | a0001c0002t0003g0061 a0001c0002t0003g0073 |
2 | NA18970.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1892+369T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 17/24 | chr3 | 149047659 | |||||||
chr3:149048439 | C | T | 2 | a0001c0002t0006g0042 a0013c0015t0006g0041 |
2 | HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1757-276G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 16/24 | chr3 | 149048439 | |||||||
chr3:149048494 | G | A | 1 | a0001c0002t0006g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1757-331C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 16/24 | chr3 | 149048494 | |||||||
chr3:149048636 | G | T | 2 | a0001c0002t0006g0042 a0013c0015t0006g0041 |
2 | HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1756+227C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 16/24 | chr3 | 149048636 | |||||||
chr3:149048675 | A | G | 2 | a0001c0001t0001g0217 a0001c0001t0001g0222 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1756+188T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 16/24 | chr3 | 149048675 | |||||||
chr3:149048698 | C | A | 1 | a0001c0001t0001g0216 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1756+165G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 16/24 | chr3 | 149048698 | |||||||
chr3:149048836 | T | C | 6 | a0001c0002t0006g0042 a0001c0002t0006g0050 a0001c0002t0010g0047 others(3): Show |
6 | HG00738.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1756+27A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 16/24 | chr3 | 149048836 | |||||||
chr3:149049171 | C | T | 2 | a0001c0003t0002g0273 a0001c0003t0016g0285 |
2 | HG04228.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1618-170G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 15/24 | chr3 | 149049171 | |||||||
chr3:149049193 | C | T | 99 | a0001c0002t0003g0002 a0001c0002t0003g0004 a0001c0002t0003g0005 others(96): Show |
114 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.1618-192G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 15/24 | chr3 | 149049193 | |||||||
chr3:149049329 | C | T | 140 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(137): Show |
157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1618-328G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 15/24 | chr3 | 149049329 | |||||||
chr3:149049370 | G | T | 128 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(125): Show |
144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1618-369C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 15/24 | chr3 | 149049370 | |||||||
chr3:149049599 | A | C | 4 | a0006c0010t0007g0037 a0006c0010t0007g0038 a0006c0010t0007g0039 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1618-598T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 15/24 | chr3 | 149049599 | |||||||
chr3:149049993 | G | A | 6 | a0006c0010t0007g0037 a0006c0010t0007g0038 a0006c0010t0007g0039 others(3): Show |
6 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1617+239C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 15/24 | chr3 | 149049993 | |||||||
chr3:149050023 | G | T | 5 | a0001c0003t0002g0301 a0001c0003t0002g0318 a0001c0003t0002g0341 others(2): Show |
5 | HG00438.hp2 HG00558.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.1617+209C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 15/24 | chr3 | 149050023 | |||||||
chr3:149050221 | A | G | 1 | a0001c0021t0002g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1617+11T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 15/24 | chr3 | 149050221 | |||||||
chr3:149050444 | A | C | 1 | a0001c0002t0010g0047 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1474-69T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149050444 | |||||||
chr3:149050526 | A | T | 2 | a0006c0010t0007g0037 a0006c0010t0007g0038 |
2 | HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1474-151T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149050526 | |||||||
chr3:149050634 | T | C | 1 | a0001c0001t0001g0240 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1474-259A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149050634 | |||||||
chr3:149050687 | G | A | 1 | a0001c0002t0006g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1474-312C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149050687 | |||||||
chr3:149050836 | C | T | 3 | a0001c0005t0002g0138 a0001c0005t0002g0140 a0001c0005t0002g0143 |
3 | HG02895.hp2 HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1474-461G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149050836 | |||||||
chr3:149050847 | T | C | 2 | a0001c0001t0001g0172 a0001c0001t0001g0251 |
2 | HG02074.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1474-472A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149050847 | |||||||
chr3:149050955 | A | C | 1 | a0005c0009t0002g0033 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1474-580T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149050955 | |||||||
chr3:149051133 | G | A | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0239 |
3 | HG02273.hp2 HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1474-758C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149051133 | |||||||
chr3:149051235 | TA | T | 20 | a0001c0001t0001g0147 a0001c0001t0001g0169 a0001c0001t0001g0233 others(17): Show |
20 | HG00140.hp1 HG00558.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.1474-861delT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149051235 | |||||||
chr3:149051236 | A | T | 95 | a0001c0002t0003g0002 a0001c0002t0003g0004 a0001c0002t0003g0005 others(92): Show |
110 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1474-861T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149051236 | |||||||
chr3:149051237 | A | T | 1 | a0001c0007t0003g0066 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1474-862T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149051237 | |||||||
chr3:149051259 | A | T | 1 | a0001c0021t0002g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1474-884T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149051259 | |||||||
chr3:149051280 | A | G | 1 | a0001c0003t0002g0296 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1474-905T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149051280 | |||||||
chr3:149051364 | T | C | 1 | a0001c0002t0006g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1474-989A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149051364 | |||||||
chr3:149051609 | C | T | 128 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(125): Show |
144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1474-1234G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149051609 | |||||||
chr3:149051695 | T | C | 22 | a0001c0003t0002g0128 a0001c0003t0002g0268 a0001c0003t0002g0269 others(19): Show |
22 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.1474-1320A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149051695 | |||||||
chr3:149051740 | C | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0166 |
2 | NA18965.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1474-1365G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149051740 | |||||||
chr3:149051799 | G | A | 5 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1474-1424C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149051799 | |||||||
chr3:149052077 | C | T | 125 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(122): Show |
141 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1474-1702G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149052077 | |||||||
chr3:149052148 | T | TA | 44 | a0001c0001t0001g0184 a0001c0001t0001g0195 a0001c0001t0001g0211 others(41): Show |
45 | HG00738.hp1 HG00738.hp2 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.1474-1774dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149052148 | |||||||
chr3:149052148 | TA | T | 10 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0168 others(7): Show |
10 | HG01515.hp1 HG01516.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1474-1774delT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149052148 | |||||||
chr3:149052289 | A | C | 171 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(168): Show |
189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.1474-1914T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149052289 | |||||||
chr3:149052642 | A | C | 2 | a0001c0002t0006g0051 a0001c0002t0006g0052 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1474-2267T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149052642 | |||||||
chr3:149052965 | A | G | 1 | a0004c0008t0017g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1473+2338T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149052965 | |||||||
chr3:149053153 | A | AG | 3 | a0001c0001t0011g0129 a0001c0001t0011g0131 a0001c0001t0015g0130 |
3 | HG02258.hp1 HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1473+2149dupC | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149053153 | |||||||
chr3:149053405 | T | A | 1 | a0008c0012t0001g0238 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1473+1898A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149053405 | |||||||
chr3:149053447 | C | T | 6 | a0001c0002t0006g0042 a0001c0002t0006g0050 a0001c0002t0010g0047 others(3): Show |
6 | HG00738.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1473+1856G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149053447 | |||||||
chr3:149053525 | C | T | 88 | a0001c0002t0003g0002 a0001c0002t0003g0004 a0001c0002t0003g0005 others(85): Show |
103 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.1473+1778G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149053525 | |||||||
chr3:149053913 | A | T | 1 | a0001c0002t0003g0071 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1473+1390T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149053913 | |||||||
chr3:149053939 | C | A | 3 | a0001c0001t0001g0184 a0008c0012t0001g0183 a0008c0012t0001g0238 |
3 | HG01891.hp1 HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1473+1364G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149053939 | |||||||
chr3:149054086 | G | A | 1 | a0001c0003t0002g0338 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1473+1217C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149054086 | |||||||
chr3:149054135 | A | G | 270 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(267): Show |
303 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.1473+1168T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149054135 | |||||||
chr3:149054481 | G | A | 128 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(125): Show |
144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1473+822C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149054481 | |||||||
chr3:149054668 | T | C | 140 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(137): Show |
157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1473+635A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149054668 | |||||||
chr3:149054982 | A | T | 1 | a0001c0001t0001g0188 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1473+321T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149054982 | |||||||
chr3:149055075 | G | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0159 a0001c0001t0001g0182 |
4 | HG00597.hp1 NA18941.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1473+228C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149055075 | |||||||
chr3:149055476 | T | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0159 others(3): Show |
8 | HG00597.hp1 HG02293.hp2 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.1376-76A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149055476 | |||||||
chr3:149055793 | C | T | 1 | a0001c0001t0001g0252 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1376-393G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149055793 | |||||||
chr3:149056106 | G | A | 5 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1376-706C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149056106 | |||||||
chr3:149056176 | C | T | 1 | a0001c0005t0019g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1376-776G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149056176 | |||||||
chr3:149056183 | G | A | 8 | a0002c0004t0001g0197 a0002c0004t0001g0199 a0002c0004t0001g0201 others(5): Show |
8 | HG00280.hp2 HG01123.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.1376-783C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149056183 | |||||||
chr3:149056267 | T | C | 5 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1376-867A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149056267 | |||||||
chr3:149056269 | G | T | 1 | a0001c0001t0001g0167 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1376-869C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149056269 | |||||||
chr3:149056491 | A | G | 3 | a0001c0001t0011g0129 a0001c0001t0011g0131 a0001c0001t0015g0130 |
3 | HG02258.hp1 HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1376-1091T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149056491 | |||||||
chr3:149056629 | A | C | 1 | a0001c0002t0013g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1376-1229T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149056629 | |||||||
chr3:149056787 | C | T | 1 | a0004c0008t0002g0029 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1376-1387G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149056787 | |||||||
chr3:149056807 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1376-1407C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149056807 | |||||||
chr3:149056862 | C | A | 1 | a0001c0002t0006g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1376-1462G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149056862 | |||||||
chr3:149056891 | C | T | 6 | a0001c0002t0003g0255 a0001c0002t0004g0256 a0006c0010t0007g0037 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1376-1491G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149056891 | |||||||
chr3:149056950 | A | T | 9 | a0001c0005t0002g0015 a0001c0005t0002g0137 a0001c0005t0002g0138 others(6): Show |
10 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1376-1550T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149056950 | |||||||
chr3:149057012 | G | A | 4 | a0005c0009t0002g0031 a0005c0009t0002g0032 a0005c0009t0002g0033 others(1): Show |
4 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.1376-1612C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057012 | |||||||
chr3:149057026 | G | A | 6 | a0001c0003t0002g0349 a0004c0008t0002g0029 a0004c0008t0008g0027 others(3): Show |
6 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1376-1626C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057026 | |||||||
chr3:149057035 | A | G | 1 | a0001c0003t0002g0349 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1376-1635T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057035 | |||||||
chr3:149057107 | C | CA | 44 | a0001c0002t0003g0058 a0001c0002t0003g0060 a0001c0002t0003g0070 others(41): Show |
44 | HG00597.hp2 HG00621.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.1376-1708dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057107 | |||||||
chr3:149057107 | CA | C | 60 | a0001c0001t0001g0022 a0001c0001t0001g0055 a0001c0001t0001g0134 others(57): Show |
63 | HG00597.hp1 HG00673.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.1376-1708delT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057107 | |||||||
chr3:149057107 | CAA | C | 108 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(105): Show |
123 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1376-1709_1376-170 others(6): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057107 | |||||||
chr3:149057107 | CAAA | C | 6 | a0001c0001t0001g0198 a0004c0008t0002g0029 a0004c0008t0008g0027 others(3): Show |
6 | HG01069.hp1 HG01255.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1376-1710_1376-170 others(7): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057107 | |||||||
chr3:149057107 | CAAAAAAA others(4): Show |
C | 4 | a0005c0009t0002g0034 a0006c0010t0007g0037 a0006c0010t0007g0038 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.1376-1718_1376-170 others(15): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057107 | |||||||
chr3:149057107 | CAAAAAAA others(5): Show |
C | 4 | a0001c0001t0001g0154 a0001c0001t0001g0166 a0001c0002t0003g0072 others(1): Show |
4 | HG01074.hp1 HG02723.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1376-1719_1376-170 others(16): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057107 | |||||||
chr3:149057107 | CAAAAAAA others(8): Show |
C | 1 | a0001c0005t0002g0137 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1376-1722_1376-170 others(19): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057107 | |||||||
chr3:149057191 | A | C | 3 | a0001c0001t0011g0129 a0001c0001t0011g0131 a0001c0001t0015g0130 |
3 | HG02258.hp1 HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1376-1791T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057191 | |||||||
chr3:149057283 | G | A | 1 | a0001c0001t0001g0243 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1376-1883C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057283 | |||||||
chr3:149057315 | A | G | 2 | a0001c0002t0006g0051 a0001c0002t0006g0052 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1376-1915T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057315 | |||||||
chr3:149057413 | G | A | 1 | a0001c0002t0006g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1376-2013C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057413 | |||||||
chr3:149057426 | A | AAAAC | 8 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(5): Show |
8 | HG01109.hp2 HG01257.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.1376-2030_1376-202 others(8): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057426 | |||||||
chr3:149057456 | G | A | 1 | a0001c0003t0002g0313 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1376-2056C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057456 | |||||||
chr3:149057515 | C | A | 1 | a0001c0002t0003g0361 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1376-2115G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057515 | |||||||
chr3:149057593 | A | C | 2 | a0009c0013t0002g0035 a0009c0013t0002g0036 |
2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1375+2125T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057593 | |||||||
chr3:149057602 | G | A | 2 | a0003c0006t0005g0043 a0003c0006t0005g0362 |
2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1375+2116C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057602 | |||||||
chr3:149057700 | G | A | 1 | a0001c0002t0004g0262 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1375+2018C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057700 | |||||||
chr3:149058224 | A | C | 1 | a0001c0003t0002g0283 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1375+1494T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149058224 | |||||||
chr3:149058224 | A | G | 2 | a0001c0002t0006g0042 a0013c0015t0006g0041 |
2 | HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1375+1494T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149058224 | |||||||
chr3:149058310 | G | C | 1 | a0001c0002t0003g0361 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1375+1408C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149058310 | |||||||
chr3:149058348 | ATGCCTGC | A | 4 | a0005c0009t0002g0031 a0005c0009t0002g0032 a0005c0009t0002g0033 others(1): Show |
4 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.1375+1363_1375+136 others(11): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149058348 | |||||||
chr3:149058457 | T | C | 2 | a0009c0013t0002g0035 a0009c0013t0002g0036 |
2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1375+1261A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149058457 | |||||||
chr3:149058501 | T | C | 1 | a0001c0002t0004g0261 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1375+1217A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149058501 | |||||||
chr3:149058520 | A | G | 1 | a0001c0003t0002g0269 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1375+1198T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149058520 | |||||||
chr3:149058606 | C | T | 7 | a0003c0006t0005g0012 a0003c0006t0005g0043 a0003c0006t0005g0044 others(4): Show |
8 | HG02055.hp2 HG02922.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1375+1112G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149058606 | |||||||
chr3:149058689 | C | T | 6 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0184 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1375+1029G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149058689 | |||||||
chr3:149058774 | T | C | 5 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0240 others(2): Show |
5 | HG00673.hp2 NA18986.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.1375+944A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149058774 | |||||||
chr3:149058824 | G | A | 98 | a0001c0002t0003g0002 a0001c0002t0003g0004 a0001c0002t0003g0005 others(95): Show |
113 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1375+894C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149058824 | |||||||
chr3:149058899 | G | A | 2 | a0001c0001t0001g0193 a0001c0001t0001g0195 |
2 | NA19012.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1375+819C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149058899 | |||||||
chr3:149058944 | A | C | 1 | a0001c0001t0001g0243 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1375+774T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149058944 | |||||||
chr3:149059130 | A | G | 1 | a0001c0003t0002g0128 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1375+588T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149059130 | |||||||
chr3:149059185 | C | CTAT | 6 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG02273.hp2 HG02683.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1375+532_1375+533i others(5): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149059185 | |||||||
chr3:149059341 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1375+377T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149059341 | |||||||
chr3:149059395 | C | T | 5 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1375+323G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149059395 | |||||||
chr3:149059511 | C | A | 1 | a0001c0001t0001g0148 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1375+207G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149059511 | |||||||
chr3:149059597 | T | G | 1 | a0001c0003t0002g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1375+121A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149059597 | |||||||
chr3:149059677 | G | GA | 9 | a0001c0001t0001g0215 a0001c0001t0001g0230 a0001c0002t0003g0071 others(6): Show |
9 | HG00423.hp1 HG02572.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1375+40dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149059677 | |||||||
chr3:149060025 | TGAG | T | 5 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1286-221_1286-219d others(5): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 12/24 | chr3 | 149060025 | |||||||
chr3:149060303 | A | G | 98 | a0001c0002t0003g0002 a0001c0002t0003g0004 a0001c0002t0003g0005 others(95): Show |
113 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1285+340T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 12/24 | chr3 | 149060303 | |||||||
chr3:149060372 | T | C | 3 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0237 |
3 | HG02258.hp2 HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1285+271A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 12/24 | chr3 | 149060372 | |||||||
chr3:149061130 | C | A | 1 | a0013c0015t0006g0041 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1161-272G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061130 | |||||||
chr3:149061233 | C | T | 1 | a0003c0006t0005g0044 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1161-375G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061233 | |||||||
chr3:149061268 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1161-410C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061268 | |||||||
chr3:149061277 | G | C | 3 | a0001c0001t0011g0129 a0001c0001t0011g0131 a0001c0001t0015g0130 |
3 | HG02258.hp1 HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1161-419C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061277 | |||||||
chr3:149061284 | G | A | 5 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1161-426C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061284 | |||||||
chr3:149061294 | C | G | 16 | a0001c0002t0006g0042 a0001c0002t0006g0046 a0001c0002t0006g0050 others(13): Show |
17 | HG00738.hp2 HG02055.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1161-436G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061294 | |||||||
chr3:149061370 | C | T | 1 | a0001c0001t0001g0245 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1161-512G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061370 | |||||||
chr3:149061413 | A | AAAAAT | 22 | a0001c0002t0006g0050 a0001c0002t0010g0047 a0001c0002t0010g0048 others(19): Show |
23 | HG00738.hp2 HG01243.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.1161-560_1161-556d others(7): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061413 | |||||||
chr3:149061413 | A | AAAAATAA others(3): Show |
1 | a0001c0021t0002g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1161-565_1161-556d others(12): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061413 | |||||||
chr3:149061413 | AAAAATAA others(3): Show |
A | 98 | a0001c0002t0003g0002 a0001c0002t0003g0004 a0001c0002t0003g0005 others(95): Show |
113 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1161-565_1161-556d others(12): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061413 | |||||||
chr3:149061729 | A | T | 1 | a0001c0002t0003g0103 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1161-871T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061729 | |||||||
chr3:149061759 | C | A | 1 | a0001c0002t0003g0111 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1161-901G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061759 | |||||||
chr3:149061785 | G | A | 1 | a0001c0002t0003g0094 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1161-927C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061785 | |||||||
chr3:149061836 | C | CA | 8 | a0001c0003t0002g0311 a0001c0003t0002g0313 a0002c0004t0001g0242 others(5): Show |
8 | HG01255.hp2 HG01433.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1161-979dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061836 | |||||||
chr3:149061837 | A | C | 1 | a0003c0006t0005g0362 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1161-979T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061837 | |||||||
chr3:149061914 | G | A | 16 | a0001c0002t0006g0042 a0001c0002t0006g0046 a0001c0002t0006g0050 others(13): Show |
17 | HG00738.hp2 HG02055.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1161-1056C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061914 | |||||||
chr3:149061959 | A | G | 4 | a0001c0003t0002g0289 a0001c0003t0002g0304 a0001c0003t0002g0315 others(1): Show |
4 | HG01975.hp2 HG02148.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.1161-1101T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061959 | |||||||
chr3:149061983 | C | T | 1 | a0001c0002t0004g0253 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1161-1125G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061983 | |||||||
chr3:149062102 | T | C | 125 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(122): Show |
141 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1161-1244A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149062102 | |||||||
chr3:149062251 | T | G | 1 | a0001c0003t0002g0335 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1160+1180A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149062251 | |||||||
chr3:149062276 | T | C | 2 | a0009c0013t0002g0035 a0009c0013t0002g0036 |
2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1160+1155A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149062276 | |||||||
chr3:149062307 | GT | G | 12 | a0001c0005t0002g0015 a0001c0005t0002g0135 a0001c0005t0002g0137 others(9): Show |
13 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1160+1123delA | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149062307 | |||||||
chr3:149062482 | G | C | 7 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0220 others(4): Show |
7 | HG00408.hp2 HG00673.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.1160+949C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149062482 | |||||||
chr3:149062501 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1160+930G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149062501 | |||||||
chr3:149062581 | T | C | 1 | a0002c0004t0001g0204 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1160+850A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149062581 | |||||||
chr3:149062722 | C | T | 1 | a0001c0002t0010g0049 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1160+709G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149062722 | |||||||
chr3:149062808 | T | C | 1 | a0001c0005t0002g0142 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1160+623A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149062808 | |||||||
chr3:149062817 | A | G | 1 | a0001c0002t0004g0267 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1160+614T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149062817 | |||||||
chr3:149062862 | A | G | 22 | a0001c0003t0002g0128 a0001c0003t0002g0268 a0001c0003t0002g0269 others(19): Show |
22 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.1160+569T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149062862 | |||||||
chr3:149062900 | C | T | 1 | a0001c0005t0019g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1160+531G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149062900 | |||||||
chr3:149063051 | C | T | 4 | a0001c0003t0002g0302 a0001c0003t0002g0303 a0001c0003t0002g0314 others(1): Show |
4 | NA18948.hp1 NA19006.hp1 NA19088.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160+380G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149063051 | |||||||
chr3:149063668 | C | G | 12 | a0001c0005t0002g0015 a0001c0005t0002g0135 a0001c0005t0002g0137 others(9): Show |
13 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1067-144G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 9/24 | chr3 | 149063668 | |||||||
chr3:149063733 | G | C | 1 | a0001c0001t0020g0221 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1067-209C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 9/24 | chr3 | 149063733 | |||||||
chr3:149063752 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1067-228G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 9/24 | chr3 | 149063752 | |||||||
chr3:149063874 | T | C | 22 | a0001c0003t0002g0128 a0001c0003t0002g0268 a0001c0003t0002g0269 others(19): Show |
22 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.1067-350A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 9/24 | chr3 | 149063874 | |||||||
chr3:149064046 | G | A | 4 | a0001c0005t0002g0015 a0001c0005t0002g0139 a0001c0005t0002g0144 others(1): Show |
5 | HG01243.hp2 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1067-522C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 9/24 | chr3 | 149064046 | |||||||
chr3:149064070 | T | C | 1 | a0001c0003t0002g0280 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1067-546A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 9/24 | chr3 | 149064070 | |||||||
chr3:149064160 | G | C | 4 | a0005c0009t0002g0031 a0005c0009t0002g0032 a0005c0009t0002g0033 others(1): Show |
4 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.1066+631C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 9/24 | chr3 | 149064160 | |||||||
chr3:149064162 | T | C | 1 | a0001c0003t0002g0322 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1066+629A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 9/24 | chr3 | 149064162 | |||||||
chr3:149064271 | T | A | 1 | a0001c0003t0002g0353 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1066+520A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 9/24 | chr3 | 149064271 | |||||||
chr3:149064313 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
6 | HG00558.hp1 HG02165.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.1066+478G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 9/24 | chr3 | 149064313 | |||||||
chr3:149064432 | C | T | 1 | a0001c0002t0003g0071 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1066+359G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 9/24 | chr3 | 149064432 | |||||||
chr3:149064459 | A | G | 5 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1066+332T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 9/24 | chr3 | 149064459 | |||||||
chr3:149064713 | C | T | 1 | a0001c0003t0002g0286 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1066+78G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 9/24 | chr3 | 149064713 | |||||||
chr3:149064988 | T | C | 1 | a0001c0002t0004g0267 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.991-122A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149064988 | |||||||
chr3:149065066 | C | CA | 8 | a0001c0003t0002g0312 a0001c0003t0002g0336 a0001c0003t0002g0337 others(5): Show |
8 | HG00323.hp1 HG01255.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.991-201dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065066 | |||||||
chr3:149065076 | A | T | 16 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(13): Show |
16 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.991-210T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065076 | |||||||
chr3:149065109 | C | T | 22 | a0001c0003t0002g0128 a0001c0003t0002g0268 a0001c0003t0002g0269 others(19): Show |
22 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.991-243G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065109 | |||||||
chr3:149065156 | G | A | 99 | a0001c0002t0003g0002 a0001c0002t0003g0004 a0001c0002t0003g0005 others(96): Show |
114 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.991-290C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065156 | |||||||
chr3:149065260 | T | C | 2 | a0001c0003t0002g0321 a0001c0003t0002g0340 |
2 | NA18964.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.991-394A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065260 | |||||||
chr3:149065272 | C | T | 5 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.991-406G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065272 | |||||||
chr3:149065288 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.991-422G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065288 | |||||||
chr3:149065428 | T | G | 1 | a0001c0001t0001g0148 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.991-562A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065428 | |||||||
chr3:149065565 | G | A | 2 | a0001c0002t0006g0051 a0001c0002t0006g0052 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.991-699C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065565 | |||||||
chr3:149065599 | G | A | 2 | a0001c0002t0006g0042 a0013c0015t0006g0041 |
2 | HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.991-733C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065599 | |||||||
chr3:149065605 | G | A | 1 | a0001c0002t0004g0355 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.991-739C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065605 | |||||||
chr3:149065666 | C | T | 1 | a0001c0002t0004g0355 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.991-800G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065666 | |||||||
chr3:149065685 | C | G | 22 | a0001c0003t0002g0128 a0001c0003t0002g0268 a0001c0003t0002g0269 others(19): Show |
22 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.991-819G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065685 | |||||||
chr3:149065698 | C | T | 87 | a0001c0002t0003g0002 a0001c0002t0003g0004 a0001c0002t0003g0005 others(84): Show |
102 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.991-832G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065698 | |||||||
chr3:149065779 | A | G | 1 | a0002c0004t0001g0199 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.991-913T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065779 | |||||||
chr3:149065787 | G | A | 1 | a0003c0006t0005g0054 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.991-921C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065787 | |||||||
chr3:149066023 | T | G | 1 | a0001c0002t0003g0065 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.991-1157A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066023 | |||||||
chr3:149066099 | T | G | 1 | a0001c0001t0001g0149 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.991-1233A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066099 | |||||||
chr3:149066104 | C | T | 3 | a0001c0003t0002g0349 a0001c0003t0002g0350 a0001c0003t0002g0351 |
3 | NA18985.hp1 NA18992.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.991-1238G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066104 | |||||||
chr3:149066105 | G | A | 6 | a0001c0003t0002g0313 a0004c0008t0002g0029 a0004c0008t0008g0027 others(3): Show |
6 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.991-1239C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066105 | |||||||
chr3:149066116 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.991-1250C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066116 | |||||||
chr3:149066129 | C | T | 2 | a0001c0001t0001g0160 a0001c0001t0001g0181 |
2 | HG00733.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.991-1263G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066129 | |||||||
chr3:149066195 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.991-1329G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066195 | |||||||
chr3:149066204 | A | G | 270 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(267): Show |
303 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.991-1338T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066204 | |||||||
chr3:149066293 | G | A | 26 | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0188 others(23): Show |
29 | HG00408.hp2 HG00558.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.991-1427C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066293 | |||||||
chr3:149066529 | AT | A | 18 | a0001c0001t0001g0147 a0001c0001t0001g0181 a0001c0001t0001g0222 others(15): Show |
18 | HG01069.hp1 HG01070.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.991-1664delA | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066529 | |||||||
chr3:149066553 | C | T | 6 | a0001c0002t0006g0042 a0001c0002t0006g0050 a0001c0002t0010g0047 others(3): Show |
6 | HG00738.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.990+1687G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066553 | |||||||
chr3:149066678 | T | A | 1 | a0005c0009t0002g0032 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.990+1562A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066678 | |||||||
chr3:149066775 | G | A | 1 | a0001c0007t0003g0095 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.990+1465C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066775 | |||||||
chr3:149066822 | G | T | 87 | a0001c0002t0003g0002 a0001c0002t0003g0004 a0001c0002t0003g0005 others(84): Show |
102 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.990+1418C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066822 | |||||||
chr3:149066953 | C | A | 1 | a0001c0021t0002g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.990+1287G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066953 | |||||||
chr3:149066986 | T | A | 1 | a0001c0003t0002g0128 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.990+1254A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066986 | |||||||
chr3:149067145 | C | T | 1 | a0001c0005t0002g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.990+1095G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149067145 | |||||||
chr3:149067186 | G | A | 4 | a0006c0010t0007g0037 a0006c0010t0007g0038 a0006c0010t0007g0039 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.990+1054C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149067186 | |||||||
chr3:149067197 | C | T | 4 | a0005c0009t0002g0031 a0005c0009t0002g0032 a0005c0009t0002g0033 others(1): Show |
4 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.990+1043G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149067197 | |||||||
chr3:149067200 | A | G | 5 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.990+1040T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149067200 | |||||||
chr3:149067286 | A | G | 1 | a0001c0005t0019g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.990+954T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149067286 | |||||||
chr3:149067384 | A | G | 6 | a0001c0001t0001g0055 a0001c0001t0001g0245 a0001c0001t0001g0246 others(3): Show |
6 | HG00423.hp2 NA18992.hp1 NA19002.hp2 others(3): Show |
intron_variant | MODIFIER | c.990+856T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149067384 | |||||||
chr3:149067388 | T | C | 1 | a0001c0001t0001g0182 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.990+852A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149067388 | |||||||
chr3:149067462 | G | T | 1 | a0001c0001t0015g0130 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.990+778C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149067462 | |||||||
chr3:149067540 | T | G | 1 | a0001c0002t0003g0102 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.990+700A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149067540 | |||||||
chr3:149067547 | A | G | 171 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(168): Show |
189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.990+693T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149067547 | |||||||
chr3:149067693 | A | T | 2 | a0001c0001t0001g0148 a0001c0005t0002g0142 |
2 | HG02647.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.990+547T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149067693 | |||||||
chr3:149067708 | A | T | 2 | a0001c0002t0006g0051 a0001c0002t0006g0052 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.990+532T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149067708 | |||||||
chr3:149067744 | CTGGTAAC others(70): Show |
C | 2 | a0001c0002t0003g0096 a0001c0002t0003g0098 |
2 | NA18941.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.990+419_990+495del others(77): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149067744 | |||||||
chr3:149067887 | T | C | 5 | a0001c0001t0001g0359 a0005c0009t0002g0031 a0005c0009t0002g0032 others(2): Show |
5 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.990+353A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149067887 | |||||||
chr3:149068109 | A | G | 2 | a0001c0002t0006g0051 a0001c0002t0006g0052 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.990+131T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149068109 | |||||||
chr3:149068981 | A | G | 293 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(290): Show |
326 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.895-646T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149068981 | |||||||
chr3:149069002 | A | C | 2 | a0009c0013t0002g0035 a0009c0013t0002g0036 |
2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.895-667T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149069002 | |||||||
chr3:149069158 | T | TA | 129 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(126): Show |
145 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.895-824dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149069158 | |||||||
chr3:149069292 | T | A | 3 | a0001c0001t0001g0184 a0008c0012t0001g0183 a0008c0012t0001g0238 |
3 | HG01891.hp1 HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.895-957A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149069292 | |||||||
chr3:149069403 | G | A | 6 | a0006c0010t0007g0037 a0006c0010t0007g0038 a0006c0010t0007g0039 others(3): Show |
6 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.895-1068C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149069403 | |||||||
chr3:149069472 | G | GA | 45 | a0001c0001t0001g0231 a0001c0002t0006g0042 a0001c0002t0006g0046 others(42): Show |
47 | HG00738.hp2 HG01167.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.895-1138dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149069472 | |||||||
chr3:149069472 | G | GAA | 127 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(124): Show |
143 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.895-1139_895-1138d others(4): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149069472 | |||||||
chr3:149069494 | G | A | 2 | a0001c0002t0003g0255 a0001c0002t0004g0256 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.895-1159C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149069494 | |||||||
chr3:149069556 | T | A | 1 | a0001c0002t0003g0112 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.895-1221A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149069556 | |||||||
chr3:149069858 | T | G | 119 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(116): Show |
135 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.894+1394A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149069858 | |||||||
chr3:149069976 | T | C | 1 | a0001c0003t0002g0339 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.894+1276A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149069976 | |||||||
chr3:149070092 | CAG | C | 13 | a0001c0002t0006g0042 a0001c0002t0006g0046 a0001c0002t0006g0050 others(10): Show |
13 | HG00738.hp2 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.894+1158_894+1159d others(4): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149070092 | |||||||
chr3:149070249 | C | T | 1 | a0001c0003t0002g0360 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.894+1003G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149070249 | |||||||
chr3:149070642 | A | C | 4 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(1): Show |
4 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.894+610T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149070642 | |||||||
chr3:149070711 | A | G | 4 | a0005c0009t0002g0031 a0005c0009t0002g0032 a0005c0009t0002g0033 others(1): Show |
4 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.894+541T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149070711 | |||||||
chr3:149070816 | G | A | 2 | a0001c0001t0011g0129 a0001c0001t0011g0131 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.894+436C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149070816 | |||||||
chr3:149070841 | T | A | 4 | a0006c0010t0007g0037 a0006c0010t0007g0038 a0006c0010t0007g0039 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.894+411A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149070841 | |||||||
chr3:149071017 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.894+235G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149071017 | |||||||
chr3:149071044 | CA | C | 8 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(5): Show |
8 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.894+207delT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149071044 | |||||||
chr3:149071052 | A | AT | 4 | a0005c0009t0002g0031 a0005c0009t0002g0032 a0005c0009t0002g0033 others(1): Show |
4 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.894+199_894+200ins others(1): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149071052 | |||||||
chr3:149071106 | C | T | 293 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(290): Show |
326 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.894+146G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149071106 | |||||||
chr3:149071154 | G | C | 128 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(125): Show |
144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.894+98C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149071154 | |||||||
chr3:149071467 | G | A | 2 | a0001c0002t0003g0255 a0001c0002t0004g0256 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.703-24C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 6/24 | chr3 | 149071467 | |||||||
chr3:149071502 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.703-59A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 6/24 | chr3 | 149071502 | |||||||
chr3:149071751 | G | A | 5 | a0001c0002t0003g0113 a0005c0009t0002g0031 a0005c0009t0002g0032 others(2): Show |
5 | HG01167.hp2 HG01261.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.628-94C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 5/24 | chr3 | 149071751 | |||||||
chr3:149071838 | G | A | 1 | a0001c0005t0002g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.628-181C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 5/24 | chr3 | 149071838 | |||||||
chr3:149071875 | C | T | 1 | a0002c0004t0009g0153 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.628-218G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 5/24 | chr3 | 149071875 | |||||||
chr3:149072136 | A | G | 293 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(290): Show |
326 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.628-479T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 5/24 | chr3 | 149072136 | |||||||
chr3:149072172 | C | G | 5 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.628-515G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 5/24 | chr3 | 149072172 | |||||||
chr3:149072247 | A | T | 6 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG02273.hp2 HG02683.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.628-590T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 5/24 | chr3 | 149072247 | |||||||
chr3:149072471 | C | T | 5 | a0001c0003t0002g0301 a0001c0003t0002g0318 a0001c0003t0002g0341 others(2): Show |
5 | HG00438.hp2 HG00558.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.627+754G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 5/24 | chr3 | 149072471 | |||||||
chr3:149072516 | T | C | 15 | a0001c0005t0002g0015 a0001c0005t0002g0135 a0001c0005t0002g0137 others(12): Show |
17 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.627+709A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 5/24 | chr3 | 149072516 | |||||||
chr3:149072626 | G | A | 1 | a0001c0002t0003g0119 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.627+599C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 5/24 | chr3 | 149072626 | |||||||
chr3:149072744 | T | C | 1 | a0002c0004t0001g0205 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.627+481A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 5/24 | chr3 | 149072744 | |||||||
chr3:149072971 | C | A | 1 | a0001c0003t0002g0354 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.627+254G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 5/24 | chr3 | 149072971 | |||||||
chr3:149072972 | G | A | 1 | a0005c0009t0002g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.627+253C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 5/24 | chr3 | 149072972 | |||||||
chr3:149073072 | T | C | 2 | a0001c0002t0003g0057 a0001c0002t0003g0058 |
2 | HG00597.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.627+153A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 5/24 | chr3 | 149073072 | |||||||
chr3:149073333 | C | G | 15 | a0001c0005t0002g0015 a0001c0005t0002g0135 a0001c0005t0002g0137 others(12): Show |
17 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.530-11G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 4/24 | chr3 | 149073333 | |||||||
chr3:149073454 | G | T | 1 | a0006c0010t0007g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.530-132C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 4/24 | chr3 | 149073454 | |||||||
chr3:149073515 | G | A | 5 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.530-193C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 4/24 | chr3 | 149073515 | |||||||
chr3:149073559 | T | C | 3 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 |
3 | HG03490.hp1 HG03492.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.530-237A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 4/24 | chr3 | 149073559 | |||||||
chr3:149073564 | T | G | 2 | a0001c0002t0003g0121 a0001c0002t0003g0125 |
2 | NA18947.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.530-242A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 4/24 | chr3 | 149073564 | |||||||
chr3:149073669 | C | T | 4 | a0005c0009t0002g0031 a0005c0009t0002g0032 a0005c0009t0002g0033 others(1): Show |
4 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-347G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 4/24 | chr3 | 149073669 | |||||||
chr3:149073844 | C | G | 4 | a0006c0010t0007g0037 a0006c0010t0007g0038 a0006c0010t0007g0039 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.529+371G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 4/24 | chr3 | 149073844 | |||||||
chr3:149073854 | G | A | 2 | a0001c0003t0002g0273 a0001c0003t0016g0285 |
2 | HG04228.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.529+361C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 4/24 | chr3 | 149073854 | |||||||
chr3:149073917 | A | G | 1 | a0001c0001t0011g0131 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.529+298T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 4/24 | chr3 | 149073917 | |||||||
chr3:149073953 | T | C | 1 | a0001c0003t0002g0298 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.529+262A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 4/24 | chr3 | 149073953 | |||||||
chr3:149074013 | C | T | 6 | a0001c0003t0002g0293 a0001c0003t0002g0299 a0001c0003t0002g0323 others(3): Show |
6 | HG02074.hp1 HG02135.hp2 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.529+202G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 4/24 | chr3 | 149074013 | |||||||
chr3:149074155 | G | A | 1 | a0001c0002t0003g0122 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.529+60C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 4/24 | chr3 | 149074155 | |||||||
chr3:149074514 | C | A | 8 | a0001c0002t0004g0253 a0001c0002t0004g0260 a0001c0002t0004g0261 others(5): Show |
8 | HG02630.hp1 HG02717.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.396-166G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149074514 | |||||||
chr3:149074666 | C | T | 1 | a0001c0002t0021g0365 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.396-318G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149074666 | |||||||
chr3:149074684 | T | C | 4 | a0005c0009t0002g0031 a0005c0009t0002g0032 a0005c0009t0002g0033 others(1): Show |
4 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.396-336A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149074684 | |||||||
chr3:149074723 | G | A | 1 | a0001c0007t0003g0097 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.396-375C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149074723 | |||||||
chr3:149074737 | T | C | 5 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.396-389A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149074737 | |||||||
chr3:149074797 | T | C | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0239 |
3 | HG02273.hp2 HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.396-449A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149074797 | |||||||
chr3:149074819 | A | G | 1 | a0001c0002t0004g0264 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.396-471T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149074819 | |||||||
chr3:149074943 | T | C | 1 | a0001c0005t0002g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.396-595A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149074943 | |||||||
chr3:149075072 | T | A | 1 | a0001c0001t0001g0188 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.396-724A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075072 | |||||||
chr3:149075092 | A | G | 4 | a0003c0006t0005g0043 a0003c0006t0005g0044 a0003c0006t0005g0045 others(1): Show |
4 | HG02055.hp2 HG02965.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.396-744T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075092 | |||||||
chr3:149075097 | T | A | 15 | a0001c0005t0002g0015 a0001c0005t0002g0135 a0001c0005t0002g0137 others(12): Show |
17 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.396-749A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075097 | |||||||
chr3:149075195 | G | A | 1 | a0001c0021t0002g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.395+686C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075195 | |||||||
chr3:149075247 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.395+634C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075247 | |||||||
chr3:149075291 | G | A | 5 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.395+590C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075291 | |||||||
chr3:149075315 | G | A | 1 | a0001c0003t0002g0277 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.395+566C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075315 | |||||||
chr3:149075426 | G | A | 1 | a0001c0001t0011g0129 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.395+455C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075426 | |||||||
chr3:149075500 | C | T | 6 | a0006c0010t0007g0037 a0006c0010t0007g0038 a0006c0010t0007g0039 others(3): Show |
6 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.395+381G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075500 | |||||||
chr3:149075544 | AAAAT | A | 15 | a0001c0005t0002g0015 a0001c0005t0002g0135 a0001c0005t0002g0137 others(12): Show |
17 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.395+333_395+336del others(4): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075544 | |||||||
chr3:149075544 | AAAATAAA others(1): Show |
A | 5 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.395+329_395+336del others(8): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075544 | |||||||
chr3:149075613 | G | A | 1 | a0005c0009t0002g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.395+268C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075613 | |||||||
chr3:149075648 | A | C | 5 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.395+233T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075648 | |||||||
chr3:149075712 | GGTA | G | 15 | a0001c0001t0001g0198 a0002c0004t0001g0196 a0002c0004t0001g0197 others(12): Show |
16 | HG00280.hp2 HG00323.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.395+166_395+168del others(3): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075712 | |||||||
chr3:149075809 | C | G | 1 | a0001c0001t0001g0190 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.395+72G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075809 | |||||||
chr3:149075869 | A | C | 1 | a0002c0004t0001g0241 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.395+12T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075869 | |||||||
chr3:149076067 | G | A | 22 | a0001c0003t0002g0128 a0001c0003t0002g0268 a0001c0003t0002g0269 others(19): Show |
22 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.229-20C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149076067 | |||||||
chr3:149076183 | C | G | 1 | a0002c0004t0001g0196 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.229-136G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149076183 | |||||||
chr3:149076294 | T | C | 4 | a0006c0010t0007g0037 a0006c0010t0007g0038 a0006c0010t0007g0039 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.229-247A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149076294 | |||||||
chr3:149076304 | C | A | 1 | a0001c0002t0003g0098 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.229-257G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149076304 | |||||||
chr3:149076412 | T | C | 4 | a0006c0010t0007g0037 a0006c0010t0007g0038 a0006c0010t0007g0039 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.229-365A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149076412 | |||||||
chr3:149076444 | G | A | 1 | a0001c0003t0002g0278 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.229-397C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149076444 | |||||||
chr3:149076642 | T | C | 1 | a0001c0001t0001g0195 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.229-595A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149076642 | |||||||
chr3:149076679 | T | C | 1 | a0001c0002t0006g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.229-632A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149076679 | |||||||
chr3:149076914 | T | C | 1 | a0001c0002t0003g0098 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.229-867A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149076914 | |||||||
chr3:149077031 | G | A | 2 | a0001c0002t0006g0051 a0001c0002t0006g0052 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.229-984C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077031 | |||||||
chr3:149077112 | G | T | 1 | a0001c0003t0002g0322 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.229-1065C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077112 | |||||||
chr3:149077121 | G | A | 1 | a0003c0006t0005g0362 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.229-1074C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077121 | |||||||
chr3:149077204 | T | C | 269 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(266): Show |
302 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.229-1157A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077204 | |||||||
chr3:149077204 | T | G | 1 | a0001c0002t0003g0126 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.229-1157A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077204 | |||||||
chr3:149077233 | C | T | 3 | a0001c0002t0004g0253 a0001c0002t0004g0261 a0001c0002t0004g0263 |
3 | HG02717.hp2 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.229-1186G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077233 | |||||||
chr3:149077247 | A | AAAAT | 25 | a0001c0001t0011g0129 a0001c0001t0011g0131 a0001c0001t0015g0130 others(22): Show |
25 | HG00621.hp1 HG01167.hp2 HG01346.hp2 others(22): Show |
intron_variant | MODIFIER | c.229-1204_229-1201d others(6): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077247 | |||||||
chr3:149077247 | AAAAT | A | 53 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0190 others(50): Show |
55 | HG00140.hp2 HG00738.hp2 HG01167.hp1 others(52): Show |
intron_variant | MODIFIER | c.229-1204_229-1201d others(6): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077247 | |||||||
chr3:149077247 | AAAATAAA others(1): Show |
A | 117 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(114): Show |
133 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.229-1208_229-1201d others(10): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077247 | |||||||
chr3:149077247 | AAAATAAA others(5): Show |
A | 2 | a0001c0002t0006g0042 a0013c0015t0006g0041 |
2 | HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.229-1212_229-1201d others(14): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077247 | |||||||
chr3:149077251 | T | C | 3 | a0006c0010t0007g0037 a0006c0010t0007g0038 a0006c0010t0007g0040 |
3 | HG02109.hp1 HG02572.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.229-1204A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077251 | |||||||
chr3:149077255 | T | C | 1 | a0006c0010t0007g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.229-1208A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077255 | |||||||
chr3:149077260 | A | T | 2 | a0001c0002t0003g0069 a0001c0002t0003g0070 |
2 | HG00738.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.229-1213T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077260 | |||||||
chr3:149077264 | A | T | 19 | a0001c0002t0003g0013 a0001c0002t0003g0061 a0001c0002t0003g0067 others(16): Show |
20 | HG00621.hp2 HG00738.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.229-1217T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077264 | |||||||
chr3:149077268 | A | T | 70 | a0001c0002t0003g0002 a0001c0002t0003g0004 a0001c0002t0003g0005 others(67): Show |
81 | HG00099.hp1 HG00597.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.229-1221T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077268 | |||||||
chr3:149077270 | A | T | 1 | a0001c0007t0003g0066 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.229-1223T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077270 | |||||||
chr3:149077272 | A | T | 85 | a0001c0002t0003g0002 a0001c0002t0003g0004 a0001c0002t0003g0005 others(82): Show |
100 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.229-1225T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077272 | |||||||
chr3:149077274 | A | T | 1 | a0001c0007t0003g0066 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.229-1227T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077274 | |||||||
chr3:149077276 | A | T | 97 | a0001c0002t0003g0002 a0001c0002t0003g0004 a0001c0002t0003g0005 others(94): Show |
112 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.229-1229T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077276 | |||||||
chr3:149077278 | A | T | 1 | a0001c0007t0003g0066 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.229-1231T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077278 | |||||||
chr3:149077280 | A | C | 1 | a0001c0007t0003g0066 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.229-1233T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077280 | |||||||
chr3:149077280 | A | T | 97 | a0001c0002t0003g0002 a0001c0002t0003g0004 a0001c0002t0003g0005 others(94): Show |
112 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.229-1233T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077280 | |||||||
chr3:149077284 | A | T | 98 | a0001c0002t0003g0002 a0001c0002t0003g0004 a0001c0002t0003g0005 others(95): Show |
113 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.229-1237T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077284 | |||||||
chr3:149077288 | A | T | 18 | a0001c0002t0003g0006 a0001c0002t0003g0068 a0001c0002t0003g0099 others(15): Show |
21 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.229-1241T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077288 | |||||||
chr3:149077429 | A | C | 1 | a0001c0002t0003g0126 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.229-1382T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077429 | |||||||
chr3:149077488 | A | G | 1 | a0001c0001t0015g0130 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.229-1441T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077488 | |||||||
chr3:149077496 | C | G | 1 | a0001c0005t0019g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.229-1449G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077496 | |||||||
chr3:149077505 | T | G | 1 | a0001c0001t0001g0186 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.229-1458A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077505 | |||||||
chr3:149077592 | C | T | 1 | a0001c0003t0002g0317 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.229-1545G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077592 | |||||||
chr3:149077738 | C | A | 4 | a0006c0010t0007g0037 a0006c0010t0007g0038 a0006c0010t0007g0039 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.229-1691G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077738 | |||||||
chr3:149077739 | C | T | 2 | a0001c0003t0002g0296 a0001c0003t0002g0316 |
2 | HG01175.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.229-1692G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077739 | |||||||
chr3:149077930 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.229-1883C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077930 | |||||||
chr3:149078071 | T | C | 16 | a0001c0002t0006g0042 a0001c0002t0006g0046 a0001c0002t0006g0050 others(13): Show |
17 | HG00738.hp2 HG02055.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.229-2024A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078071 | |||||||
chr3:149078102 | A | G | 3 | a0001c0002t0003g0060 a0001c0002t0003g0112 a0001c0002t0003g0113 |
3 | HG01261.hp1 HG02300.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.229-2055T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078102 | |||||||
chr3:149078167 | A | G | 1 | a0001c0002t0003g0098 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.229-2120T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078167 | |||||||
chr3:149078205 | T | C | 4 | a0006c0010t0007g0037 a0006c0010t0007g0038 a0006c0010t0007g0039 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.229-2158A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078205 | |||||||
chr3:149078210 | G | A | 4 | a0006c0010t0007g0037 a0006c0010t0007g0038 a0006c0010t0007g0039 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.229-2163C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078210 | |||||||
chr3:149078285 | C | T | 1 | a0001c0003t0002g0315 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.229-2238G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078285 | |||||||
chr3:149078323 | A | T | 99 | a0001c0002t0003g0002 a0001c0002t0003g0004 a0001c0002t0003g0005 others(96): Show |
114 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.229-2276T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078323 | |||||||
chr3:149078363 | T | C | 1 | a0001c0001t0001g0252 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.229-2316A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078363 | |||||||
chr3:149078497 | C | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0240 |
2 | HG00673.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.229-2450G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078497 | |||||||
chr3:149078507 | G | A | 1 | a0001c0003t0002g0314 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.229-2460C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078507 | |||||||
chr3:149078615 | T | C | 54 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0019 others(51): Show |
62 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.229-2568A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078615 | |||||||
chr3:149078726 | G | A | 1 | a0001c0002t0003g0098 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.229-2679C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078726 | |||||||
chr3:149078741 | C | T | 128 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(125): Show |
144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.229-2694G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078741 | |||||||
chr3:149078763 | A | G | 1 | a0001c0003t0002g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.229-2716T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078763 | |||||||
chr3:149078851 | C | T | 1 | a0001c0002t0003g0067 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.229-2804G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078851 | |||||||
chr3:149078856 | CA | C | 141 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(138): Show |
158 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.229-2810delT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078856 | |||||||
chr3:149078916 | C | A | 5 | a0001c0002t0003g0255 a0001c0002t0004g0023 a0001c0002t0004g0256 others(2): Show |
6 | HG01167.hp1 HG01169.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.229-2869G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078916 | |||||||
chr3:149078936 | G | A | 5 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.229-2889C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078936 | |||||||
chr3:149078938 | C | T | 6 | a0001c0001t0001g0152 a0004c0008t0002g0029 a0004c0008t0008g0027 others(3): Show |
6 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.229-2891G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078938 | |||||||
chr3:149078985 | G | T | 16 | a0001c0002t0006g0042 a0001c0002t0006g0046 a0001c0002t0006g0050 others(13): Show |
17 | HG00738.hp2 HG02055.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.229-2938C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078985 | |||||||
chr3:149079028 | G | A | 4 | a0005c0009t0002g0031 a0005c0009t0002g0032 a0005c0009t0002g0033 others(1): Show |
4 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.229-2981C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079028 | |||||||
chr3:149079102 | A | C | 2 | a0001c0002t0006g0051 a0001c0002t0006g0052 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.229-3055T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079102 | |||||||
chr3:149079107 | A | G | 1 | a0001c0021t0002g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.229-3060T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079107 | |||||||
chr3:149079162 | A | G | 5 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.229-3115T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079162 | |||||||
chr3:149079248 | C | T | 4 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(1): Show |
4 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.229-3201G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079248 | |||||||
chr3:149079373 | T | C | 1 | a0001c0002t0003g0126 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.229-3326A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | |||||||
chr3:149079373 | T | TA | 35 | a0001c0002t0010g0047 a0001c0002t0010g0048 a0001c0003t0002g0024 others(32): Show |
36 | HG00323.hp1 HG00738.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.229-3327dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | |||||||
chr3:149079373 | T | TAA | 14 | a0001c0002t0010g0049 a0001c0003t0002g0025 a0001c0003t0002g0288 others(11): Show |
15 | HG00558.hp2 HG02723.hp1 HG02738.hp2 others(12): Show |
intron_variant | MODIFIER | c.229-3328_229-3327d others(4): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | |||||||
chr3:149079373 | T | TAAAA | 5 | a0001c0003t0002g0348 a0001c0003t0002g0352 a0001c0005t0002g0015 others(2): Show |
6 | HG00438.hp2 HG01243.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.229-3330_229-3327d others(6): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | |||||||
chr3:149079373 | T | TAAAAAAA others(3): Show |
1 | a0001c0001t0015g0130 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.229-3336_229-3327d others(12): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | |||||||
chr3:149079373 | T | TAAAAAAA others(6): Show |
1 | a0001c0001t0011g0131 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.229-3339_229-3327d others(15): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | |||||||
chr3:149079373 | TA | T | 16 | a0001c0002t0003g0119 a0001c0002t0003g0120 a0001c0002t0003g0121 others(13): Show |
16 | HG01167.hp2 HG01346.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.229-3327delT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | |||||||
chr3:149079373 | TAA | T | 14 | a0001c0002t0003g0118 a0001c0002t0003g0125 a0001c0002t0004g0023 others(11): Show |
15 | HG01256.hp1 HG02486.hp1 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.229-3328_229-3327d others(4): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | |||||||
chr3:149079373 | TAAA | T | 23 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0003g0014 others(20): Show |
28 | HG01243.hp1 HG01261.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.229-3329_229-3327d others(5): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | |||||||
chr3:149079373 | TAAAAAAA others(2): Show |
T | 15 | a0001c0002t0003g0099 a0001c0002t0003g0100 a0001c0002t0003g0101 others(12): Show |
15 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.229-3335_229-3327d others(11): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | |||||||
chr3:149079373 | TAAAAAAA others(3): Show |
T | 53 | a0001c0001t0001g0055 a0001c0001t0001g0134 a0001c0001t0001g0245 others(50): Show |
62 | HG00423.hp2 HG00597.hp2 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.229-3336_229-3327d others(12): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | |||||||
chr3:149079373 | TAAAAAAA others(4): Show |
T | 26 | a0001c0001t0001g0022 a0001c0001t0001g0146 a0001c0001t0001g0230 others(23): Show |
27 | HG00099.hp1 HG00735.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.229-3337_229-3327d others(13): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | |||||||
chr3:149079373 | TAAAAAAA others(5): Show |
T | 95 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(92): Show |
110 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.229-3338_229-3327d others(14): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | |||||||
chr3:149079373 | TAAAAAAA others(6): Show |
T | 1 | a0001c0001t0001g0154 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.229-3339_229-3327d others(15): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | |||||||
chr3:149079373 | TAAAAAAA others(8): Show |
T | 1 | a0001c0003t0002g0290 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.229-3341_229-3327d others(17): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | |||||||
chr3:149079373 | TAAAAAAA others(9): Show |
T | 1 | a0001c0003t0002g0289 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.229-3342_229-3327d others(18): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | |||||||
chr3:149079373 | TAAAAAAA others(10): Show |
T | 2 | a0001c0021t0002g0254 a0003c0006t0005g0054 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.229-3343_229-3327d others(19): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | |||||||
chr3:149079373 | TAAAAAAA others(11): Show |
T | 6 | a0003c0006t0005g0012 a0003c0006t0005g0043 a0003c0006t0005g0044 others(3): Show |
7 | HG02055.hp2 HG02922.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.229-3344_229-3327d others(20): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | |||||||
chr3:149079373 | TAAAAAAA others(12): Show |
T | 1 | a0001c0002t0006g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.229-3345_229-3327d others(21): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | |||||||
chr3:149079373 | TAAAAAAA others(15): Show |
T | 3 | a0001c0002t0004g0256 a0009c0013t0002g0035 a0009c0013t0002g0036 |
3 | HG01167.hp1 HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.229-3348_229-3327d others(24): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | |||||||
chr3:149079373 | TAAAAAAA others(16): Show |
T | 1 | a0001c0002t0003g0255 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.229-3349_229-3327d others(25): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | |||||||
chr3:149079374 | A | T | 1 | a0001c0002t0003g0126 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.229-3327T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079374 | |||||||
chr3:149079401 | AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0001g0251 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.229-3366_229-3355d others(14): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079401 | |||||||
chr3:149079426 | T | A | 1 | a0001c0002t0006g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.229-3379A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079426 | |||||||
chr3:149079463 | CTATCTCA others(47): Show |
C | 128 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(125): Show |
144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.229-3470_229-3417d others(56): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079463 | |||||||
chr3:149079468 | T | C | 4 | a0006c0010t0007g0037 a0006c0010t0007g0038 a0006c0010t0007g0039 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.229-3421A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079468 | |||||||
chr3:149079522 | A | C | 1 | a0001c0003t0002g0288 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.229-3475T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079522 | |||||||
chr3:149079602 | T | C | 1 | a0003c0006t0005g0362 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.229-3555A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079602 | |||||||
chr3:149079634 | C | T | 1 | a0001c0002t0006g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.229-3587G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079634 | |||||||
chr3:149079836 | T | C | 171 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(168): Show |
189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.229-3789A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079836 | |||||||
chr3:149079975 | C | G | 1 | a0001c0005t0019g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.229-3928G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079975 | |||||||
chr3:149080118 | C | T | 7 | a0003c0006t0005g0012 a0003c0006t0005g0043 a0003c0006t0005g0044 others(4): Show |
8 | HG02055.hp2 HG02922.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.229-4071G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149080118 | |||||||
chr3:149080134 | G | A | 3 | a0001c0001t0011g0129 a0001c0001t0011g0131 a0001c0001t0015g0130 |
3 | HG02258.hp1 HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.229-4087C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149080134 | |||||||
chr3:149080240 | G | A | 21 | a0001c0002t0006g0042 a0001c0002t0006g0046 a0001c0002t0006g0050 others(18): Show |
22 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.229-4193C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149080240 | |||||||
chr3:149080398 | AACCT | A | 5 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.228+4280_228+4283d others(6): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149080398 | |||||||
chr3:149080407 | C | T | 1 | a0001c0021t0002g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.228+4275G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149080407 | |||||||
chr3:149080411 | A | ATC | 171 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(168): Show |
189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.228+4270_228+4271i others(4): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149080411 | |||||||
chr3:149080585 | G | C | 2 | a0001c0002t0003g0123 a0001c0002t0003g0124 |
2 | HG00733.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.228+4097C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149080585 | |||||||
chr3:149080711 | C | T | 1 | a0001c0002t0006g0042 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.228+3971G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149080711 | |||||||
chr3:149080769 | G | C | 1 | a0001c0002t0006g0050 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.228+3913C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149080769 | |||||||
chr3:149080805 | G | GA | 4 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(1): Show |
4 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.228+3876dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149080805 | |||||||
chr3:149080893 | C | T | 43 | a0001c0002t0006g0042 a0001c0002t0006g0046 a0001c0002t0006g0050 others(40): Show |
45 | HG00738.hp2 HG01167.hp2 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.228+3789G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149080893 | |||||||
chr3:149080928 | C | T | 270 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(267): Show |
303 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.228+3754G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149080928 | |||||||
chr3:149081214 | C | T | 1 | a0003c0006t0005g0043 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.228+3468G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149081214 | |||||||
chr3:149081260 | C | T | 2 | a0002c0004t0009g0016 a0002c0004t0009g0153 |
3 | HG00323.hp2 HG01081.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.228+3422G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149081260 | |||||||
chr3:149081265 | TA | T | 133 | a0001c0002t0003g0002 a0001c0002t0003g0004 a0001c0002t0003g0005 others(130): Show |
148 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.228+3416delT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149081265 | |||||||
chr3:149081274 | A | T | 1 | a0001c0005t0002g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.228+3408T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149081274 | |||||||
chr3:149081279 | C | A | 1 | a0001c0001t0001g0252 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.228+3403G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149081279 | |||||||
chr3:149081502 | A | C | 1 | a0001c0002t0003g0060 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.228+3180T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149081502 | |||||||
chr3:149081527 | C | T | 2 | a0009c0013t0002g0035 a0009c0013t0002g0036 |
2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.228+3155G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149081527 | |||||||
chr3:149081833 | G | A | 4 | a0001c0003t0002g0349 a0001c0003t0002g0350 a0001c0003t0002g0351 others(1): Show |
4 | HG02083.hp1 NA18985.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.228+2849C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149081833 | |||||||
chr3:149082180 | C | T | 5 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.228+2502G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149082180 | |||||||
chr3:149082184 | C | T | 1 | a0001c0002t0003g0059 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.228+2498G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149082184 | |||||||
chr3:149082233 | C | T | 1 | a0001c0003t0002g0268 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.228+2449G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149082233 | |||||||
chr3:149082408 | G | A | 1 | a0001c0002t0006g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.228+2274C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149082408 | |||||||
chr3:149082414 | C | G | 293 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(290): Show |
326 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.228+2268G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149082414 | |||||||
chr3:149082454 | G | A | 12 | a0001c0005t0002g0015 a0001c0005t0002g0135 a0001c0005t0002g0137 others(9): Show |
13 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.228+2228C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149082454 | |||||||
chr3:149082494 | G | A | 10 | a0001c0002t0004g0253 a0001c0002t0004g0259 a0001c0002t0004g0260 others(7): Show |
10 | HG01256.hp1 HG01516.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.228+2188C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149082494 | |||||||
chr3:149082571 | G | C | 1 | a0001c0003t0002g0353 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.228+2111C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149082571 | |||||||
chr3:149082665 | C | A | 1 | a0001c0003t0002g0354 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.228+2017G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149082665 | |||||||
chr3:149082673 | A | G | 1 | a0001c0002t0004g0253 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.228+2009T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149082673 | |||||||
chr3:149082690 | A | G | 21 | a0001c0002t0006g0042 a0001c0002t0006g0046 a0001c0002t0006g0050 others(18): Show |
22 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.228+1992T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149082690 | |||||||
chr3:149082722 | CA | C | 5 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.228+1959delT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149082722 | |||||||
chr3:149082894 | GAAGAT | G | 5 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.228+1783_228+1787d others(7): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149082894 | |||||||
chr3:149083108 | G | A | 1 | a0005c0009t0002g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.228+1574C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149083108 | |||||||
chr3:149083165 | C | G | 6 | a0006c0010t0007g0037 a0006c0010t0007g0038 a0006c0010t0007g0039 others(3): Show |
6 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.228+1517G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149083165 | |||||||
chr3:149083232 | T | C | 2 | a0001c0002t0006g0051 a0001c0002t0006g0052 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.228+1450A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149083232 | |||||||
chr3:149083253 | A | G | 2 | a0001c0002t0003g0057 a0001c0002t0003g0058 |
2 | HG00597.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.228+1429T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149083253 | |||||||
chr3:149083285 | A | G | 270 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(267): Show |
303 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.228+1397T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149083285 | |||||||
chr3:149083411 | G | A | 1 | a0001c0002t0006g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.228+1271C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149083411 | |||||||
chr3:149083507 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.228+1175G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149083507 | |||||||
chr3:149083680 | C | T | 13 | a0001c0002t0006g0042 a0001c0002t0006g0046 a0001c0002t0006g0050 others(10): Show |
13 | HG00738.hp2 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.228+1002G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149083680 | |||||||
chr3:149083749 | C | CA | 16 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(13): Show |
16 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.228+932dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149083749 | |||||||
chr3:149083749 | C | CAA | 135 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(132): Show |
153 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.228+931_228+932dup others(2): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149083749 | |||||||
chr3:149083758 | A | AC | 4 | a0005c0009t0002g0031 a0005c0009t0002g0032 a0005c0009t0002g0033 others(1): Show |
4 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.228+923_228+924ins others(1): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149083758 | |||||||
chr3:149083830 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.228+852T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149083830 | |||||||
chr3:149083842 | C | G | 1 | a0001c0002t0006g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.228+840G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149083842 | |||||||
chr3:149083928 | G | GA | 122 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(119): Show |
138 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.228+753dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149083928 | |||||||
chr3:149084128 | G | T | 171 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(168): Show |
189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.228+554C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149084128 | |||||||
chr3:149084356 | A | G | 4 | a0003c0006t0005g0043 a0003c0006t0005g0044 a0003c0006t0005g0045 others(1): Show |
4 | HG02055.hp2 HG02965.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.228+326T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149084356 | |||||||
chr3:149084457 | A | G | 2 | a0001c0002t0006g0042 a0013c0015t0006g0041 |
2 | HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.228+225T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149084457 | |||||||
chr3:149084661 | A | ATTTAG | 21 | a0001c0002t0006g0042 a0001c0002t0006g0046 a0001c0002t0006g0050 others(18): Show |
22 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.228+20_228+21insCT others(3): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149084661 | |||||||
chr3:149085422 | T | C | 16 | a0001c0002t0006g0042 a0001c0002t0006g0046 a0001c0002t0006g0050 others(13): Show |
17 | HG00738.hp2 HG02055.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.21-533A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/24 | chr3 | 149085422 | |||||||
chr3:149085518 | T | C | 1 | a0001c0003t0002g0358 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.21-629A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/24 | chr3 | 149085518 | |||||||
chr3:149085721 | G | A | 1 | a0001c0001t0001g0359 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.20+596C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/24 | chr3 | 149085721 | |||||||
chr3:149085795 | T | C | 1 | a0001c0003t0002g0360 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.20+522A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/24 | chr3 | 149085795 | |||||||
chr3:149085818 | G | T | 1 | a0001c0003t0002g0128 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.20+499C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/24 | chr3 | 149085818 | |||||||
chr3:149085892 | A | G | 82 | a0001c0002t0003g0002 a0001c0002t0003g0004 a0001c0002t0003g0005 others(79): Show |
96 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.20+425T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/24 | chr3 | 149085892 | |||||||
chr3:149085892 | A | T | 1 | a0001c0001t0001g0055 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.20+425T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/24 | chr3 | 149085892 | |||||||
chr3:149085972 | A | G | 21 | a0001c0002t0006g0042 a0001c0002t0006g0046 a0001c0002t0006g0050 others(18): Show |
22 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.20+345T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/24 | chr3 | 149085972 | |||||||
chr3:149086034 | T | C | 1 | a0001c0002t0003g0361 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.20+283A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/24 | chr3 | 149086034 | |||||||
chr3:149086048 | G | A | 1 | a0003c0006t0005g0362 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.20+269C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/24 | chr3 | 149086048 | |||||||
chr3:149086068 | A | G | 1 | a0001c0002t0003g0011 | 2 | NA18968.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.20+249T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/24 | chr3 | 149086068 | |||||||
chr3:149086082 | C | T | 10 | a0005c0009t0002g0031 a0005c0009t0002g0032 a0005c0009t0002g0033 others(7): Show |
10 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.20+235G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/24 | chr3 | 149086082 | |||||||
chr3:149086226 | G | T | 5 | a0004c0008t0002g0029 a0004c0008t0008g0027 a0004c0008t0008g0028 others(2): Show |
5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.20+91C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/24 | chr3 | 149086226 |