Item | Value |
---|---|
geneid | 4241 |
ensemblid | ENSG00000163975.14 |
hgncid | 7037 |
symbol | MELTF |
name | melanotransferrin |
refseq_nuc | NM_005929.6 |
refseq_prot | NP_005920.2 |
ensembl_nuc | ENST00000296350.10 |
ensembl_prot | ENSP00000296350.5 |
mane_status | MANE Select |
chr | chr3 |
start | 197001740 |
end | 197029817 |
strand | - |
ver | v1.2 |
region | chr3:197001740-197029817 |
region5000 | chr3:196996740-197034817 |
regionname0 | MELTF_chr3_197001740_197029817 |
regionname5000 | MELTF_chr3_196996740_197034817 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 738 | 374 | 76 | 80 | 157 | 14 | 45 | 120 | MELTF_chr3_196996740_197034817 | MELTF | MRGPS others(733): Show |
chr3 | 196996740 | 197034817 |
a0002 | 0/0 | 738 | 17 | 2 | 1 | 13 | 0 | 1 | 12 | MELTF_chr3_196996740_197034817 | MELTF | MRGPS others(733): Show |
chr3 | 196996740 | 197034817 |
a0003 | 0/0 | 738 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | MELTF_chr3_196996740_197034817 | MELTF | MRGPS others(733): Show |
chr3 | 196996740 | 197034817 |
a0004 | 0/0 | 738 | 4 | 2 | 0 | 2 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | MRGPS others(733): Show |
chr3 | 196996740 | 197034817 |
a0005 | 0/0 | 738 | 3 | 0 | 0 | 2 | 0 | 1 | 0 | MELTF_chr3_196996740_197034817 | MELTF | MRGPS others(733): Show |
chr3 | 196996740 | 197034817 |
a0006 | 0/0 | 738 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | MRGPS others(733): Show |
chr3 | 196996740 | 197034817 |
a0007 | 0/0 | 738 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | MRGPS others(733): Show |
chr3 | 196996740 | 197034817 |
a0008 | 0/0 | 738 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | MRGPS others(733): Show |
chr3 | 196996740 | 197034817 |
a0009 | 0/0 | 738 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | MRGPS others(733): Show |
chr3 | 196996740 | 197034817 |
a0010 | 0/0 | 305 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | MRGPS others(300): Show |
chr3 | 196996740 | 197034817 |
a0011 | 0/0 | 738 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | MRGPS others(733): Show |
chr3 | 196996740 | 197034817 |
a0012 | 0/0 | 738 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | MRGPS others(733): Show |
chr3 | 196996740 | 197034817 |
a0013 | 0/0 | 738 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MELTF_chr3_196996740_197034817 | MELTF | MRGPS others(733): Show |
chr3 | 196996740 | 197034817 |
a0014 | 0/0 | 738 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | MRGPS others(733): Show |
chr3 | 196996740 | 197034817 |
a0015 | 0/0 | 738 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | MRGPS others(733): Show |
chr3 | 196996740 | 197034817 |
a0016 | 0/0 | 738 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | MRGPS others(733): Show |
chr3 | 196996740 | 197034817 |
a0017 | 0/0 | 738 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | MRGPS others(733): Show |
chr3 | 196996740 | 197034817 |
a0018 | 0/0 | 738 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | MRGPS others(733): Show |
chr3 | 196996740 | 197034817 |
a0019 | 0/0 | 738 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | MRGPS others(733): Show |
chr3 | 196996740 | 197034817 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2214 | 263 | 46 | 60 | 107 | 11 | 37 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0001c0002 | 0/0 | 2214 | 77 | 12 | 16 | 42 | 3 | 4 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0001c0003 | 0/0 | 2214 | 22 | 14 | 1 | 6 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0001c0005 | 0/0 | 2214 | 3 | 3 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0001c0013 | 0/0 | 2214 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0001c0014 | 0/0 | 2214 | 2 | 1 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0001c0016 | 0/0 | 2214 | 2 | 0 | 0 | 0 | 0 | 2 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0001c0018 | 0/0 | 2214 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0001c0020 | 0/0 | 2214 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0001c0022 | 0/0 | 2214 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0002c0004 | 0/0 | 2214 | 12 | 0 | 0 | 11 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0002c0009 | 0/0 | 2214 | 2 | 2 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0002c0032 | 0/0 | 2214 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0002c0034 | 0/0 | 2214 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0002c0036 | 0/0 | 2214 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0003c0006 | 0/0 | 2214 | 3 | 0 | 0 | 3 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0003c0035 | 0/0 | 2214 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0004c0012 | 0/0 | 2214 | 2 | 2 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0004c0015 | 0/0 | 2214 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0005c0010 | 0/0 | 2214 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0005c0027 | 0/0 | 2214 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0006c0007 | 0/0 | 2214 | 2 | 2 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0006c0017 | 0/0 | 2214 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0007c0011 | 0/0 | 2214 | 2 | 1 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0008c0008 | 0/0 | 2214 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0009c0033 | 0/0 | 2214 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0010c0031 | 0/0 | 2214 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0011c0029 | 0/0 | 2214 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0012c0030 | 0/0 | 2214 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0013c0021 | 0/0 | 2214 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0014c0023 | 0/0 | 2214 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0015c0019 | 0/0 | 2214 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0016c0028 | 0/0 | 2214 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0017c0025 | 0/0 | 2214 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0018c0024 | 0/0 | 2214 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 | ||
a0019c0026 | 0/0 | 2214 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | ATGCG others(2209): Show |
chr3 | 196996740 | 197034817 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3964 | 97 | 1 | 30 | 54 | 4 | 7 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0002 | 0/0 | 3964 | 29 | 0 | 8 | 6 | 3 | 12 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0003 | 1/0 | 3964 | 23 | 4 | 8 | 5 | 2 | 3 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0005 | 0/0 | 3964 | 18 | 6 | 0 | 11 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0006 | 0/0 | 3964 | 17 | 15 | 2 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0007 | 0/0 | 3964 | 3 | 1 | 0 | 0 | 0 | 2 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0008 | 0/0 | 3964 | 10 | 1 | 5 | 0 | 1 | 3 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0010 | 0/0 | 3964 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0011 | 0/0 | 3964 | 6 | 0 | 3 | 2 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0012 | 0/0 | 3964 | 8 | 0 | 1 | 3 | 0 | 4 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0014 | 0/0 | 3964 | 6 | 6 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0015 | 0/0 | 3964 | 3 | 0 | 1 | 0 | 0 | 2 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0016 | 0/0 | 3964 | 6 | 0 | 0 | 6 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0018 | 0/0 | 3964 | 2 | 0 | 0 | 1 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0019 | 0/0 | 3964 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0020 | 0/0 | 3964 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0022 | 0/0 | 3964 | 3 | 3 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0023 | 0/0 | 3964 | 3 | 0 | 0 | 3 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0024 | 0/0 | 3964 | 3 | 0 | 0 | 3 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0025 | 0/0 | 3964 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0029 | 0/0 | 3964 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0030 | 0/0 | 3964 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0032 | 0/0 | 3964 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0033 | 0/0 | 3964 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0034 | 0/0 | 3964 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0035 | 0/0 | 3964 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0036 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3978): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0037 | 0/0 | 3964 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0038 | 0/0 | 3964 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0039 | 0/0 | 3964 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0046 | 0/0 | 3964 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0047 | 0/0 | 3964 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0048 | 0/0 | 3964 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0049 | 0/0 | 3964 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0050 | 0/0 | 3964 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0051 | 0/0 | 3964 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0052 | 0/0 | 3964 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0053 | 0/0 | 3964 | 1 | 0 | 0 | 0 | 1 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0001t0054 | 0/0 | 3964 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0002t0001 | 0/0 | 3964 | 20 | 0 | 1 | 19 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0002t0002 | 0/0 | 3964 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0002t0004 | 0/0 | 3964 | 23 | 4 | 13 | 2 | 3 | 1 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0002t0006 | 0/0 | 3964 | 2 | 2 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0002t0007 | 0/0 | 3964 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0002t0008 | 0/0 | 3964 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0002t0009 | 0/0 | 3960 | 8 | 0 | 0 | 8 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3955): Show |
chr3 | 196996740 | 197034817 |
a0001c0002t0010 | 0/0 | 3964 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0002t0011 | 0/0 | 3964 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0002t0013 | 0/0 | 3960 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3955): Show |
chr3 | 196996740 | 197034817 |
a0001c0002t0015 | 0/0 | 3964 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0002t0017 | 0/0 | 3960 | 4 | 0 | 0 | 4 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3955): Show |
chr3 | 196996740 | 197034817 |
a0001c0002t0018 | 0/0 | 3964 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0002t0026 | 0/0 | 3960 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3955): Show |
chr3 | 196996740 | 197034817 |
a0001c0002t0028 | 0/0 | 3960 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3955): Show |
chr3 | 196996740 | 197034817 |
a0001c0002t0031 | 0/0 | 3964 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0002t0040 | 0/0 | 3964 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0002t0042 | 0/0 | 3960 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3955): Show |
chr3 | 196996740 | 197034817 |
a0001c0002t0043 | 0/0 | 3964 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0002t0044 | 0/0 | 3964 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0002t0055 | 0/0 | 3964 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0002t0056 | 0/0 | 3964 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0003t0001 | 0/0 | 3964 | 6 | 0 | 0 | 5 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0003t0003 | 0/0 | 3964 | 2 | 2 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0003t0005 | 0/0 | 3964 | 2 | 2 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0003t0013 | 0/0 | 3960 | 5 | 5 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3955): Show |
chr3 | 196996740 | 197034817 |
a0001c0003t0014 | 0/0 | 3964 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0003t0015 | 0/0 | 3964 | 2 | 1 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0003t0017 | 0/0 | 3960 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3955): Show |
chr3 | 196996740 | 197034817 |
a0001c0003t0019 | 0/0 | 3964 | 3 | 3 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0005t0010 | 0/0 | 3964 | 3 | 3 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0013t0009 | 0/0 | 3960 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3955): Show |
chr3 | 196996740 | 197034817 |
a0001c0014t0003 | 0/0 | 3964 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0014t0013 | 0/0 | 3960 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3955): Show |
chr3 | 196996740 | 197034817 |
a0001c0016t0011 | 0/0 | 3964 | 2 | 0 | 0 | 0 | 0 | 2 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0018t0001 | 0/0 | 3964 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0020t0001 | 0/0 | 3964 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0001c0022t0003 | 0/0 | 3964 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0002c0004t0001 | 0/0 | 3964 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0002c0004t0002 | 0/0 | 3964 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0002c0004t0007 | 0/0 | 3964 | 9 | 0 | 0 | 9 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0002c0009t0021 | 0/0 | 3964 | 2 | 2 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0002c0032t0005 | 0/0 | 3964 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0002c0034t0009 | 0/0 | 3960 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3955): Show |
chr3 | 196996740 | 197034817 |
a0002c0036t0002 | 0/0 | 3964 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0003c0006t0002 | 0/0 | 3964 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0003c0006t0020 | 0/0 | 3964 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0003c0035t0001 | 0/0 | 3964 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0004c0012t0005 | 0/0 | 3964 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0004c0012t0006 | 0/0 | 3964 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0004c0015t0010 | 0/0 | 3964 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0005c0010t0001 | 0/0 | 3964 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0005c0027t0001 | 0/0 | 3964 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0006c0007t0010 | 0/0 | 3964 | 2 | 2 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0006c0017t0007 | 0/0 | 3964 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0007c0011t0008 | 0/0 | 3964 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0007c0011t0018 | 0/0 | 3964 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0008c0008t0027 | 0/0 | 3964 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0009c0033t0001 | 0/0 | 3964 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0010c0031t0001 | 0/0 | 3964 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0011c0029t0021 | 0/0 | 3964 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0012c0030t0013 | 0/0 | 3960 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3955): Show |
chr3 | 196996740 | 197034817 |
a0013c0021t0045 | 0/0 | 3960 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3955): Show |
chr3 | 196996740 | 197034817 |
a0014c0023t0001 | 0/0 | 3964 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0015c0019t0001 | 0/0 | 3964 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0016c0028t0041 | 0/0 | 3960 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3955): Show |
chr3 | 196996740 | 197034817 |
a0017c0025t0001 | 0/0 | 3964 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0018c0024t0005 | 0/0 | 3964 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
a0019c0026t0012 | 0/0 | 3964 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | GCACT others(3959): Show |
chr3 | 196996740 | 197034817 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 15 | 1 | 5 | 7 | 2 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0054 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0060 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0002g0002 | 0/0 | 7 | 0 | 3 | 1 | 2 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0002g0013 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0002g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0002g0059 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0003g0014 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0003g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0003g0061 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0003g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0005g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0005g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0005g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0005g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0005g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0005g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0005g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0005g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0006g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0006g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0006g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0006g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0006g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0006g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0006g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0006g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0007g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0007g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0007g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0008g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0008g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0008g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0008g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0008g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0008g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0008g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0008g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0008g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0008g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0010g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0011g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0011g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0011g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0011g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0011g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0012g0020 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0012g0055 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0012g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0012g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0012g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0014g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0014g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0014g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0015g0058 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0015g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0016g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0016g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0016g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0016g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0016g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0018g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0018g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0019g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0020g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0022g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0022g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0023g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0023g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0024g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0024g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0024g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0025g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0029g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0030g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0032g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0033g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0034g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0035g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0036g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0037g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0038g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0039g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0046g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0047g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0048g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0049g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0050g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0051g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0052g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0053g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0001t0054g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0004g0009 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0004g0010 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0004g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0004g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0004g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0004g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0004g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0004g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0006g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0007g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0008g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0009g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0009g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0009g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0009g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0009g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0010g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0011g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0013g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0015g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0017g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0017g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0017g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0017g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0018g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0026g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0026g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0028g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0028g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0031g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0040g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0042g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0043g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0044g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0055g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0002t0056g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0003t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0003t0003g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0003t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0003t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0003t0013g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0003t0013g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0003t0013g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0003t0014g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0003t0015g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0003t0015g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0003t0017g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0003t0019g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0005t0010g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0005t0010g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0013t0009g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0013t0009g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0014t0003g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0014t0013g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0016t0011g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0016t0011g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0018t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0020t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0001c0022t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0002c0004t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0002c0004t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0002c0004t0007g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0002c0004t0007g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0002c0004t0007g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0002c0004t0007g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0002c0004t0007g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0002c0009t0021g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0002c0009t0021g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0002c0032t0005g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0002c0034t0009g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0002c0036t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0003c0006t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0003c0006t0020g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0003c0006t0020g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0003c0035t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0004c0012t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0004c0012t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0004c0015t0010g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0004c0015t0010g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0005c0010t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0005c0010t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0005c0027t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0006c0007t0010g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0006c0017t0007g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0007c0011t0008g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0007c0011t0018g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0008c0008t0027g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0009c0033t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0010c0031t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0011c0029t0021g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0012c0030t0013g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0013c0021t0045g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0014c0023t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0015c0019t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0016c0028t0041g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0017c0025t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0018c0024t0005g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
a0019c0026t0012g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00099 | hp2 | a0001 | c0001 | t0008 | g0276 | EUR | GBR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00140 | hp1 | a0001 | c0002 | t0004 | g0009 | EUR | GBR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0292 | EUR | GBR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0235 | EUR | FIN | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0250 | EUR | FIN | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0291 | EUR | FIN | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0286 | EAS | CHS | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | CHS | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00438 | hp2 | a0001 | c0002 | t0017 | g0139 | EAS | CHS | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00544 | hp2 | a0001 | c0002 | t0042 | g0157 | EAS | CHS | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | CHS | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00609 | hp2 | a0009 | c0033 | t0001 | g0113 | EAS | CHS | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00621 | hp1 | a0001 | c0013 | t0009 | g0225 | EAS | CHS | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00639 | hp1 | a0001 | c0002 | t0004 | g0200 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0061 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00642 | hp1 | a0001 | c0001 | t0008 | g0216 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00642 | hp2 | a0001 | c0001 | t0011 | g0280 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | CHS | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00673 | hp2 | a0005 | c0010 | t0001 | g0183 | EAS | CHS | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0163 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00738 | hp2 | a0001 | c0001 | t0012 | g0294 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00741 | hp1 | a0001 | c0002 | t0004 | g0153 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG00741 | hp2 | a0001 | c0001 | t0032 | g0176 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01070 | hp1 | a0001 | c0018 | t0001 | g0219 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0037 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0037 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01074 | hp2 | a0001 | c0001 | t0020 | g0256 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01081 | hp2 | a0007 | c0011 | t0018 | g0245 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01099 | hp2 | a0001 | c0001 | t0006 | g0070 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01109 | hp1 | a0001 | c0001 | t0015 | g0270 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01167 | hp1 | a0001 | c0002 | t0004 | g0147 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01167 | hp2 | a0001 | c0001 | t0008 | g0223 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01169 | hp1 | a0001 | c0001 | t0008 | g0137 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01175 | hp1 | a0001 | c0003 | t0015 | g0079 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01175 | hp2 | a0010 | c0031 | t0001 | g0232 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01192 | hp1 | a0001 | c0001 | t0008 | g0196 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01243 | hp2 | a0001 | c0002 | t0004 | g0051 | AMR | PUR | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01255 | hp1 | a0001 | c0002 | t0015 | g0170 | AMR | CLM | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01255 | hp2 | a0011 | c0029 | t0021 | g0067 | AMR | CLM | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01256 | hp2 | a0001 | c0001 | t0011 | g0045 | AMR | CLM | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01257 | hp2 | a0001 | c0002 | t0004 | g0010 | AMR | CLM | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01258 | hp1 | a0001 | c0001 | t0011 | g0045 | AMR | CLM | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01258 | hp2 | a0001 | c0002 | t0004 | g0010 | AMR | CLM | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0288 | AMR | CLM | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01261 | hp2 | a0001 | c0001 | t0008 | g0190 | AMR | CLM | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01346 | hp1 | a0001 | c0002 | t0004 | g0151 | AMR | CLM | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01346 | hp2 | a0001 | c0002 | t0004 | g0009 | AMR | CLM | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0202 | AMR | CLM | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01361 | hp2 | a0001 | c0002 | t0007 | g0062 | AMR | CLM | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01433 | hp1 | a0001 | c0002 | t0004 | g0161 | AMR | CLM | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01515 | hp1 | a0001 | c0001 | t0053 | g0192 | EUR | IBS | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01515 | hp2 | a0001 | c0002 | t0004 | g0010 | EUR | IBS | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0014 | EUR | IBS | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01517 | hp2 | a0001 | c0002 | t0004 | g0010 | EUR | IBS | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01884 | hp1 | a0002 | c0009 | t0021 | g0088 | AFR | ACB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01884 | hp2 | a0001 | c0001 | t0047 | g0297 | AFR | ACB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01891 | hp1 | a0001 | c0001 | t0054 | g0279 | AFR | ACB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01891 | hp2 | a0001 | c0001 | t0006 | g0077 | AFR | ACB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0255 | AMR | PEL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01934 | hp2 | a0001 | c0022 | t0003 | g0091 | AMR | PEL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PEL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01975 | hp1 | a0001 | c0001 | t0006 | g0019 | AMR | PEL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01978 | hp1 | a0001 | c0020 | t0001 | g0220 | AMR | PEL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | PEL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0254 | AMR | PEL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02004 | hp2 | a0001 | c0002 | t0004 | g0009 | AMR | PEL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | KHV | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02015 | hp2 | a0008 | c0008 | t0027 | g0028 | EAS | KHV | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | KHV | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02027 | hp2 | a0001 | c0013 | t0009 | g0121 | EAS | KHV | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02055 | hp1 | a0001 | c0005 | t0010 | g0026 | AFR | ACB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02055 | hp2 | a0006 | c0007 | t0010 | g0022 | AFR | ACB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0126 | EAS | KHV | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02056 | hp2 | a0001 | c0001 | t0011 | g0165 | EAS | KHV | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02071 | hp2 | a0001 | c0001 | t0039 | g0277 | EAS | KHV | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02074 | hp2 | a0002 | c0004 | t0007 | g0164 | EAS | KHV | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02080 | hp1 | a0001 | c0001 | t0033 | g0173 | EAS | KHV | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | KHV | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02129 | hp1 | a0003 | c0035 | t0001 | g0275 | EAS | KHV | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02132 | hp1 | a0008 | c0008 | t0027 | g0028 | EAS | KHV | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | KHV | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02135 | hp1 | a0001 | c0001 | t0030 | g0046 | EAS | KHV | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02135 | hp2 | a0001 | c0002 | t0004 | g0287 | EAS | KHV | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02145 | hp2 | a0001 | c0001 | t0036 | g0130 | AFR | ACB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02148 | hp2 | a0001 | c0002 | t0004 | g0051 | AMR | PEL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02155 | hp1 | a0001 | c0001 | t0034 | g0189 | EAS | CDX | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02155 | hp2 | a0004 | c0015 | t0010 | g0218 | EAS | CDX | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02257 | hp1 | a0007 | c0011 | t0008 | g0127 | AFR | ACB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02257 | hp2 | a0001 | c0001 | t0014 | g0129 | AFR | ACB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02273 | hp1 | a0002 | c0036 | t0002 | g0118 | AMR | PEL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02280 | hp1 | a0001 | c0001 | t0005 | g0072 | AFR | ACB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0092 | AFR | ACB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02300 | hp2 | a0001 | c0002 | t0004 | g0162 | AMR | PEL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02451 | hp1 | a0001 | c0001 | t0007 | g0074 | AFR | ACB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02451 | hp2 | a0001 | c0002 | t0056 | g0247 | AFR | ACB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02523 | hp2 | a0005 | c0010 | t0001 | g0184 | EAS | KHV | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02572 | hp1 | a0012 | c0030 | t0013 | g0301 | AFR | GWD | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0078 | AFR | GWD | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02602 | hp1 | a0001 | c0001 | t0008 | g0172 | SAS | PJL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02615 | hp1 | a0001 | c0001 | t0005 | g0117 | AFR | GWD | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02615 | hp2 | a0001 | c0003 | t0005 | g0246 | AFR | GWD | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02622 | hp1 | a0001 | c0003 | t0019 | g0018 | AFR | GWD | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02622 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | GWD | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02630 | hp1 | a0001 | c0001 | t0006 | g0085 | AFR | GWD | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02630 | hp2 | a0001 | c0001 | t0006 | g0019 | AFR | GWD | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02647 | hp1 | a0001 | c0014 | t0013 | g0066 | AFR | GWD | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02647 | hp2 | a0001 | c0002 | t0013 | g0089 | AFR | GWD | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0059 | SAS | PJL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02683 | hp2 | a0001 | c0001 | t0018 | g0306 | SAS | PJL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0272 | SAS | PJL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02698 | hp2 | a0001 | c0002 | t0008 | g0159 | SAS | PJL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0032 | AFR | GWD | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02717 | hp2 | a0001 | c0001 | t0006 | g0076 | AFR | GWD | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02738 | hp1 | a0001 | c0001 | t0012 | g0264 | SAS | PJL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0258 | SAS | PJL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0299 | AFR | GWD | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02809 | hp2 | a0001 | c0002 | t0004 | g0149 | AFR | GWD | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02818 | hp1 | a0001 | c0001 | t0006 | g0115 | AFR | GWD | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02818 | hp2 | a0002 | c0009 | t0021 | g0087 | AFR | GWD | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0093 | AFR | GWD | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02886 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | GWD | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02895 | hp1 | a0001 | c0001 | t0005 | g0116 | AFR | GWD | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02895 | hp2 | a0001 | c0002 | t0006 | g0053 | AFR | GWD | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02897 | hp1 | a0001 | c0002 | t0006 | g0053 | AFR | GWD | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02897 | hp2 | a0001 | c0003 | t0013 | g0094 | AFR | GWD | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02922 | hp1 | a0001 | c0003 | t0003 | g0023 | AFR | ESN | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02922 | hp2 | a0001 | c0001 | t0022 | g0071 | AFR | ESN | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02965 | hp1 | a0001 | c0001 | t0006 | g0027 | AFR | ESN | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02965 | hp2 | a0001 | c0003 | t0015 | g0128 | AFR | ESN | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02970 | hp1 | a0006 | c0017 | t0007 | g0063 | AFR | ESN | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02970 | hp2 | a0001 | c0003 | t0013 | g0030 | AFR | ESN | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02976 | hp1 | a0001 | c0002 | t0055 | g0248 | AFR | ESN | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02976 | hp2 | a0001 | c0001 | t0014 | g0007 | AFR | ESN | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03017 | hp1 | a0001 | c0002 | t0011 | g0207 | SAS | PJL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03017 | hp2 | a0005 | c0027 | t0001 | g0136 | SAS | PJL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03041 | hp1 | a0001 | c0001 | t0014 | g0007 | AFR | GWD | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03041 | hp2 | a0001 | c0003 | t0013 | g0030 | AFR | GWD | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03098 | hp1 | a0001 | c0001 | t0022 | g0038 | AFR | MSL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03098 | hp2 | a0001 | c0001 | t0050 | g0298 | AFR | MSL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0081 | AFR | ESN | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03130 | hp2 | a0001 | c0003 | t0013 | g0029 | AFR | ESN | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03139 | hp1 | a0001 | c0001 | t0014 | g0300 | AFR | ESN | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03139 | hp2 | a0001 | c0001 | t0051 | g0075 | AFR | ESN | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03195 | hp1 | a0001 | c0003 | t0013 | g0029 | AFR | ESN | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03195 | hp2 | a0001 | c0002 | t0004 | g0148 | AFR | ESN | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03225 | hp1 | a0001 | c0002 | t0004 | g0150 | AFR | MSL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03225 | hp2 | a0001 | c0001 | t0006 | g0303 | AFR | MSL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0273 | SAS | PJL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03486 | hp1 | a0006 | c0007 | t0010 | g0022 | AFR | MSL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03486 | hp2 | a0001 | c0001 | t0006 | g0073 | AFR | MSL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03490 | hp1 | a0001 | c0002 | t0004 | g0009 | SAS | PJL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03490 | hp2 | a0001 | c0001 | t0015 | g0058 | SAS | PJL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03491 | hp1 | a0001 | c0001 | t0012 | g0055 | SAS | PJL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03492 | hp1 | a0001 | c0001 | t0015 | g0058 | SAS | PJL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03492 | hp2 | a0001 | c0001 | t0012 | g0055 | SAS | PJL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03516 | hp1 | a0001 | c0001 | t0019 | g0240 | AFR | ESN | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03516 | hp2 | a0001 | c0003 | t0005 | g0095 | AFR | ESN | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03579 | hp1 | a0001 | c0001 | t0022 | g0038 | AFR | MSL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03579 | hp2 | a0001 | c0003 | t0019 | g0018 | AFR | MSL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03654 | hp2 | a0001 | c0001 | t0008 | g0103 | SAS | PJL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03669 | hp1 | a0001 | c0001 | t0011 | g0252 | SAS | PJL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03669 | hp2 | a0013 | c0021 | t0045 | g0122 | SAS | PJL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03710 | hp1 | a0001 | c0001 | t0007 | g0083 | SAS | PJL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0271 | SAS | PJL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03831 | hp1 | a0001 | c0014 | t0003 | g0304 | SAS | BEB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03831 | hp2 | a0001 | c0001 | t0008 | g0131 | SAS | BEB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0281 | SAS | BEB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03927 | hp1 | a0001 | c0001 | t0012 | g0020 | SAS | BEB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0014 | SAS | BEB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03942 | hp2 | a0001 | c0016 | t0011 | g0305 | SAS | BEB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG04115 | hp1 | a0001 | c0002 | t0044 | g0158 | SAS | STU | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG04115 | hp2 | a0002 | c0004 | t0001 | g0109 | SAS | STU | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0269 | SAS | BEB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | BEB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0059 | SAS | STU | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG04199 | hp2 | a0001 | c0001 | t0007 | g0090 | SAS | STU | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG04204 | hp1 | a0001 | c0016 | t0011 | g0086 | SAS | STU | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG04204 | hp2 | a0001 | c0001 | t0038 | g0203 | SAS | STU | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0105 | SAS | STU | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG04228 | hp2 | a0001 | c0003 | t0001 | g0102 | SAS | STU | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18522 | hp1 | a0001 | c0001 | t0006 | g0025 | AFR | YRI | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18522 | hp2 | a0001 | c0002 | t0043 | g0097 | AFR | YRI | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18612 | hp2 | a0001 | c0002 | t0004 | g0251 | EAS | CHB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18747 | hp1 | a0001 | c0002 | t0040 | g0156 | EAS | CHB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18747 | hp2 | a0014 | c0023 | t0001 | g0187 | EAS | CHB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18906 | hp1 | a0001 | c0005 | t0010 | g0080 | AFR | YRI | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18906 | hp2 | a0001 | c0001 | t0049 | g0082 | AFR | YRI | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18939 | hp1 | a0002 | c0032 | t0005 | g0101 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18940 | hp1 | a0001 | c0001 | t0011 | g0238 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18940 | hp2 | a0002 | c0004 | t0007 | g0004 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18942 | hp1 | a0001 | c0002 | t0026 | g0160 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18943 | hp1 | a0003 | c0006 | t0020 | g0302 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18943 | hp2 | a0001 | c0003 | t0001 | g0015 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18944 | hp1 | a0001 | c0001 | t0023 | g0267 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18944 | hp2 | a0002 | c0004 | t0007 | g0004 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18945 | hp1 | a0001 | c0001 | t0023 | g0056 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18945 | hp2 | a0001 | c0001 | t0037 | g0204 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18947 | hp1 | a0001 | c0001 | t0005 | g0036 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18948 | hp1 | a0001 | c0002 | t0017 | g0133 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18948 | hp2 | a0001 | c0001 | t0016 | g0283 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18949 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18950 | hp1 | a0015 | c0019 | t0001 | g0167 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18950 | hp2 | a0001 | c0001 | t0005 | g0263 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18952 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18953 | hp2 | a0016 | c0028 | t0041 | g0233 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18954 | hp1 | a0001 | c0002 | t0009 | g0143 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18962 | hp1 | a0002 | c0004 | t0002 | g0031 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18962 | hp2 | a0001 | c0002 | t0017 | g0141 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18964 | hp2 | a0001 | c0002 | t0009 | g0035 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18965 | hp1 | a0001 | c0001 | t0029 | g0057 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18966 | hp1 | a0001 | c0001 | t0023 | g0056 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18966 | hp2 | a0001 | c0001 | t0018 | g0243 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18967 | hp2 | a0001 | c0002 | t0009 | g0034 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18970 | hp1 | a0001 | c0001 | t0012 | g0020 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18970 | hp2 | a0001 | c0002 | t0009 | g0033 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18971 | hp2 | a0001 | c0003 | t0017 | g0222 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18972 | hp1 | a0001 | c0001 | t0030 | g0046 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18972 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18975 | hp1 | a0001 | c0003 | t0001 | g0015 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18977 | hp1 | a0001 | c0001 | t0024 | g0266 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18977 | hp2 | a0001 | c0001 | t0005 | g0229 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18979 | hp1 | a0002 | c0004 | t0007 | g0177 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18979 | hp2 | a0002 | c0004 | t0007 | g0236 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18980 | hp1 | a0001 | c0001 | t0024 | g0144 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18983 | hp1 | a0004 | c0015 | t0010 | g0217 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18984 | hp2 | a0001 | c0002 | t0009 | g0035 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18986 | hp1 | a0001 | c0001 | t0052 | g0284 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18989 | hp1 | a0001 | c0001 | t0016 | g0039 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18989 | hp2 | a0001 | c0002 | t0018 | g0041 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18990 | hp2 | a0001 | c0001 | t0029 | g0057 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18995 | hp1 | a0001 | c0001 | t0005 | g0262 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18995 | hp2 | a0003 | c0006 | t0020 | g0211 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18997 | hp1 | a0017 | c0025 | t0001 | g0206 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18997 | hp2 | a0001 | c0001 | t0012 | g0020 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18998 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18999 | hp2 | a0001 | c0001 | t0025 | g0021 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19000 | hp2 | a0001 | c0003 | t0001 | g0198 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19002 | hp2 | a0001 | c0001 | t0024 | g0228 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19004 | hp2 | a0002 | c0004 | t0002 | g0031 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19006 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19009 | hp1 | a0018 | c0024 | t0005 | g0268 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19009 | hp2 | a0002 | c0004 | t0007 | g0004 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19010 | hp2 | a0001 | c0002 | t0026 | g0123 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19030 | hp1 | a0004 | c0012 | t0006 | g0107 | AFR | LWK | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19030 | hp2 | a0001 | c0001 | t0006 | g0027 | AFR | LWK | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19055 | hp1 | a0001 | c0001 | t0016 | g0039 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19055 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19056 | hp1 | a0003 | c0006 | t0002 | g0112 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19057 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19060 | hp2 | a0001 | c0002 | t0017 | g0140 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19063 | hp2 | a0001 | c0003 | t0001 | g0015 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19064 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19066 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19067 | hp1 | a0001 | c0001 | t0012 | g0104 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19068 | hp2 | a0001 | c0002 | t0009 | g0033 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19070 | hp1 | a0001 | c0002 | t0018 | g0041 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19072 | hp2 | a0001 | c0002 | t0031 | g0234 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19074 | hp1 | a0001 | c0003 | t0001 | g0199 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19074 | hp2 | a0001 | c0002 | t0009 | g0034 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19077 | hp1 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0293 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19078 | hp1 | a0001 | c0001 | t0035 | g0120 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19078 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19079 | hp1 | a0001 | c0001 | t0025 | g0021 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19079 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19080 | hp2 | a0002 | c0004 | t0007 | g0004 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19081 | hp1 | a0002 | c0034 | t0009 | g0114 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19083 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19084 | hp1 | a0001 | c0001 | t0016 | g0285 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19084 | hp2 | a0002 | c0004 | t0007 | g0111 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19085 | hp1 | a0001 | c0002 | t0028 | g0124 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19087 | hp1 | a0001 | c0001 | t0010 | g0191 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19087 | hp2 | a0001 | c0001 | t0005 | g0036 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19088 | hp1 | a0001 | c0002 | t0009 | g0224 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19088 | hp2 | a0002 | c0004 | t0007 | g0004 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19090 | hp1 | a0001 | c0002 | t0028 | g0154 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19091 | hp1 | a0001 | c0001 | t0016 | g0227 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19240 | hp1 | a0001 | c0003 | t0014 | g0259 | AFR | YRI | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA19240 | hp2 | a0001 | c0001 | t0014 | g0007 | AFR | YRI | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0295 | AFR | ASW | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA20129 | hp2 | a0004 | c0012 | t0005 | g0108 | AFR | ASW | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA20905 | hp1 | a0001 | c0001 | t0005 | g0257 | SAS | GIH | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | GIH | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01123 | hp1 | a0001 | c0002 | t0004 | g0134 | AMR | CLM | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02109 | hp1 | a0001 | c0002 | t0002 | g0249 | AFR | ACB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02109 | hp2 | a0001 | c0001 | t0005 | g0032 | AFR | ACB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02486 | hp1 | a0001 | c0005 | t0010 | g0026 | AFR | ACB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02486 | hp2 | a0001 | c0001 | t0014 | g0007 | AFR | ACB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02559 | hp1 | a0001 | c0002 | t0010 | g0064 | AFR | ACB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG02559 | hp2 | a0001 | c0001 | t0006 | g0019 | AFR | ACB | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03471 | hp1 | a0001 | c0003 | t0019 | g0018 | AFR | MSL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG03471 | hp2 | a0001 | c0001 | t0006 | g0025 | AFR | MSL | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG06807 | hp1 | a0001 | c0003 | t0003 | g0023 | AFR | USA | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
HG06807 | hp2 | a0001 | c0001 | t0046 | g0145 | AFR | USA | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA18955 | hp2 | a0001 | c0001 | t0016 | g0282 | EAS | JPT | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA20300 | hp1 | a0001 | c0001 | t0008 | g0260 | AFR | USA | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA20300 | hp2 | a0001 | c0002 | t0004 | g0152 | AFR | USA | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA21309 | hp1 | a0019 | c0026 | t0012 | g0068 | AFR | LWK | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
NA21309 | hp2 | a0001 | c0001 | t0048 | g0069 | AFR | LWK | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0065 | REF | REF | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0061 | REF | REF | MELTF_chr3_196996740_197034817 | MELTF | chr3 | 196996740 | 197034817 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:197003395 | G | A | 1 | a0012 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.2194C>T | p.Arg732Cys | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 16/16 | 2309/3964 | 2194/2217 | 732/738 | chr3 | 197003395 | |||
chr3:197003946 | C | G | 1 | a0011 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.2092G>C | p.Val698Leu | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 15/16 | 2207/3964 | 2092/2217 | 698/738 | chr3 | 197003946 | |||
chr3:197006656 | C | A | 1 | a0009 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.1831G>T | p.Val611Leu | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/16 | 1946/3964 | 1831/2217 | 611/738 | chr3 | 197006656 | |||
chr3:197006725 | C | T | 1 | a0019 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1762G>A | p.Glu588Lys | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/16 | 1877/3964 | 1762/2217 | 588/738 | chr3 | 197006725 | |||
chr3:197008816 | C | T | 3 | a0003 a0004 a0009 |
9 | HG00609.hp2 HG02129.hp1 HG02155.hp2 others(6): Show |
missense_variant | MODERATE | c.1675G>A | p.Ala559Thr | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 12/16 | 1790/3964 | 1675/2217 | 559/738 | chr3 | 197008816 | |||
chr3:197008876 | C | T | 1 | a0017 | 1 | NA18997.hp1 | missense_variant | MODERATE | c.1615G>A | p.Glu539Lys | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 12/16 | 1730/3964 | 1615/2217 | 539/738 | chr3 | 197008876 | |||
chr3:197008885 | C | T | 1 | a0018 | 1 | NA19009.hp1 | missense_variant | MODERATE | c.1606G>A | p.Val536Met | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 12/16 | 1721/3964 | 1606/2217 | 536/738 | chr3 | 197008885 | |||
chr3:197009675 | C | T | 1 | a0014 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.1468G>A | p.Val490Met | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 11/16 | 1583/3964 | 1468/2217 | 490/738 | chr3 | 197009675 | |||
chr3:197009704 | A | G | 1 | a0007 | 2 | HG01081.hp2 HG02257.hp1 |
missense_variant | MODERATE | c.1439T>C | p.Phe480Ser | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 11/16 | 1554/3964 | 1439/2217 | 480/738 | chr3 | 197009704 | |||
chr3:197009785 | A | T | 1 | a0016 | 1 | NA18953.hp2 | missense_variant | MODERATE | c.1358T>A | p.Val453Glu | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 11/16 | 1473/3964 | 1358/2217 | 453/738 | chr3 | 197009785 | |||
chr3:197015373 | G | A | 1 | a0008 | 2 | HG02015.hp2 HG02132.hp1 |
missense_variant | MODERATE | c.1225C>T | p.Arg409Trp | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/16 | 1340/3964 | 1225/2217 | 409/738 | chr3 | 197015373 | |||
chr3:197015406 | C | T | 1 | a0005 | 3 | HG00673.hp2 HG02523.hp2 HG03017.hp2 |
missense_variant | MODERATE | c.1192G>A | p.Val398Met | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/16 | 1307/3964 | 1192/2217 | 398/738 | chr3 | 197015406 | |||
chr3:197016354 | C | A | 1 | a0010 | 1 | HG01175.hp2 | stop_gained | HIGH | c.916G>T | p.Glu306* | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 8/16 | 1031/3964 | 916/2217 | 306/738 | chr3 | 197016354 | |||
chr3:197017122 | C | T | 1 | a0002 | 2 | HG01884.hp1 HG02818.hp2 |
missense_variant | MODERATE | c.881G>A | p.Arg294Gln | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 7/16 | 996/3964 | 881/2217 | 294/738 | chr3 | 197017122 | |||
chr3:197017123 | G | A | 3 | a0002 a0003 a0009 |
20 | HG00609.hp2 HG02074.hp2 HG02129.hp1 others(17): Show |
missense_variant | MODERATE | c.880C>T | p.Arg294Trp | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 7/16 | 995/3964 | 880/2217 | 294/738 | chr3 | 197017123 | |||
chr3:197022967 | C | T | 1 | a0013 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.634G>A | p.Gly212Arg | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 5/16 | 749/3964 | 634/2217 | 212/738 | chr3 | 197022967 | |||
chr3:197024410 | A | C | 1 | a0008 | 2 | HG02015.hp2 HG02132.hp1 |
missense_variant | MODERATE | c.380T>G | p.Val127Gly | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 4/16 | 495/3964 | 380/2217 | 127/738 | chr3 | 197024410 | |||
chr3:197024428 | A | G | 1 | a0015 | 1 | NA18950.hp1 | missense_variant | MODERATE | c.362T>C | p.Ile121Thr | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 4/16 | 477/3964 | 362/2217 | 121/738 | chr3 | 197024428 | |||
chr3:197027797 | C | T | 1 | a0006 | 3 | HG02055.hp2 HG02970.hp1 HG03486.hp1 |
missense_variant | MODERATE | c.163G>A | p.Val55Ile | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 2/16 | 278/3964 | 163/2217 | 55/738 | chr3 | 197027797 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:197004055 | G | A | 2 | a0001c0013 a0002c0034 |
3 | HG00621.hp1 HG02027.hp2 NA19081.hp1 |
synonymous_variant | LOW | c.1983C>T | p.Phe661Phe | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 15/16 | 2098/3964 | 1983/2217 | 661/738 | chr3 | 197004055 | |||
chr3:197008937 | G | A | 1 | a0007c0011 | 2 | HG01081.hp2 HG02257.hp1 |
synonymous_variant | LOW | c.1554C>T | p.Cys518Cys | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 12/16 | 1669/3964 | 1554/2217 | 518/738 | chr3 | 197008937 | |||
chr3:197009727 | G | C | 1 | a0008c0008 | 2 | HG02015.hp2 HG02132.hp1 |
synonymous_variant | LOW | c.1416C>G | p.Gly472Gly | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 11/16 | 1531/3964 | 1416/2217 | 472/738 | chr3 | 197009727 | |||
chr3:197015419 | T | C | 18 | a0001c0002 a0001c0005 a0001c0013 others(15): Show |
116 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(113): Show |
synonymous_variant | LOW | c.1179A>G | p.Pro393Pro | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/16 | 1294/3964 | 1179/2217 | 393/738 | chr3 | 197015419 | |||
chr3:197016238 | C | T | 1 | a0001c0005 | 3 | HG02055.hp1 HG02486.hp1 NA18906.hp1 |
synonymous_variant | LOW | c.1032G>A | p.Leu344Leu | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 8/16 | 1147/3964 | 1032/2217 | 344/738 | chr3 | 197016238 | |||
chr3:197016259 | T | C | 23 | a0001c0002 a0001c0003 a0001c0005 others(20): Show |
143 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(140): Show |
synonymous_variant | LOW | c.1011A>G | p.Thr337Thr | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 8/16 | 1126/3964 | 1011/2217 | 337/738 | chr3 | 197016259 | |||
chr3:197017166 | G | A | 1 | a0003c0035 | 1 | HG02129.hp1 | synonymous_variant | LOW | c.837C>T | p.His279His | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 7/16 | 952/3964 | 837/2217 | 279/738 | chr3 | 197017166 | |||
chr3:197021423 | C | T | 1 | a0001c0022 | 1 | HG01934.hp2 | synonymous_variant | LOW | c.693G>A | p.Thr231Thr | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/16 | 808/3964 | 693/2217 | 231/738 | chr3 | 197021423 | |||
chr3:197024316 | G | A | 3 | a0001c0014 a0001c0016 a0004c0015 |
6 | HG02155.hp2 HG02647.hp1 HG03831.hp1 others(3): Show |
synonymous_variant | LOW | c.474C>T | p.Cys158Cys | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 4/16 | 589/3964 | 474/2217 | 158/738 | chr3 | 197024316 | |||
chr3:197024328 | C | G | 1 | a0001c0020 | 1 | HG01978.hp1 | synonymous_variant | LOW | c.462G>C | p.Ser154Ser | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 4/16 | 577/3964 | 462/2217 | 154/738 | chr3 | 197024328 | |||
chr3:197024436 | A | G | 1 | a0001c0018 | 1 | HG01070.hp1 | synonymous_variant | LOW | c.354T>C | p.His118His | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 4/16 | 469/3964 | 354/2217 | 118/738 | chr3 | 197024436 | |||
chr3:197026667 | G | A | 1 | a0002c0036 | 1 | HG02273.hp1 | synonymous_variant | LOW | c.297C>T | p.Tyr99Tyr | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/16 | 412/3964 | 297/2217 | 99/738 | chr3 | 197026667 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:197001762 | T | G | 61 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0008 others(58): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
3_prime_UTR_variant | MODIFIER | c.*1610A>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 16/16 | 1610 | chr3 | 197001762 | ||||||
chr3:197001807 | T | A | 1 | a0001c0001t0035 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1565A>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 16/16 | 1565 | chr3 | 197001807 | ||||||
chr3:197001835 | T | C | 78 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(75): Show |
320 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(317): Show |
3_prime_UTR_variant | MODIFIER | c.*1537A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 16/16 | 1537 | chr3 | 197001835 | ||||||
chr3:197001875 | C | CACCCACG others(12): Show |
1 | a0001c0001t0036 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1478_*1496dupAGGT others(15): Show |
MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 16/16 | 1496 | chr3 | 197001875 | ||||||
chr3:197001942 | C | T | 5 | a0001c0001t0014 a0001c0001t0046 a0001c0001t0049 others(2): Show |
10 | HG02257.hp2 HG02486.hp2 HG02976.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1430G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 16/16 | 1430 | chr3 | 197001942 | ||||||
chr3:197002108 | T | C | 3 | a0001c0001t0047 a0002c0009t0021 a0011c0029t0021 |
4 | HG01255.hp2 HG01884.hp1 HG01884.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1264A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 16/16 | 1264 | chr3 | 197002108 | ||||||
chr3:197002141 | T | C | 1 | a0001c0001t0048 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1231A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 16/16 | 1231 | chr3 | 197002141 | ||||||
chr3:197002145 | G | T | 1 | a0008c0008t0027 | 2 | HG02015.hp2 HG02132.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1227C>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 16/16 | 1227 | chr3 | 197002145 | ||||||
chr3:197002147 | TGAGA | T | 14 | a0001c0002t0009 a0001c0002t0013 a0001c0002t0017 others(11): Show |
31 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1221_*1224delTCTC | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 16/16 | 1221 | chr3 | 197002147 | ||||||
chr3:197002210 | T | C | 30 | a0001c0001t0014 a0001c0001t0015 a0001c0001t0018 others(27): Show |
80 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1162A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 16/16 | 1162 | chr3 | 197002210 | ||||||
chr3:197002252 | G | A | 1 | a0001c0001t0051 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1120C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 16/16 | 1120 | chr3 | 197002252 | ||||||
chr3:197002392 | G | A | 2 | a0001c0001t0023 a0001c0001t0029 |
5 | NA18944.hp1 NA18945.hp1 NA18965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*980C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 16/16 | 980 | chr3 | 197002392 | ||||||
chr3:197002409 | G | A | 1 | a0001c0001t0037 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*963C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 16/16 | 963 | chr3 | 197002409 | ||||||
chr3:197002452 | G | C | 1 | a0001c0001t0038 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*920C>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 16/16 | 920 | chr3 | 197002452 | ||||||
chr3:197002456 | T | G | 1 | a0001c0001t0035 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*916A>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 16/16 | 916 | chr3 | 197002456 | ||||||
chr3:197002457 | C | T | 1 | a0001c0001t0035 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*915G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 16/16 | 915 | chr3 | 197002457 | ||||||
chr3:197002459 | C | T | 1 | a0001c0001t0034 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*913G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 16/16 | 913 | chr3 | 197002459 | ||||||
chr3:197002556 | C | T | 4 | a0001c0002t0013 a0001c0003t0013 a0001c0014t0013 others(1): Show |
8 | HG02572.hp1 HG02647.hp1 HG02647.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*816G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 16/16 | 816 | chr3 | 197002556 | ||||||
chr3:197002599 | C | T | 1 | a0001c0001t0033 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*773G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 16/16 | 773 | chr3 | 197002599 | ||||||
chr3:197002638 | G | A | 20 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0012 others(17): Show |
67 | HG00738.hp2 HG01099.hp2 HG01884.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*734C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 16/16 | 734 | chr3 | 197002638 | ||||||
chr3:197002668 | G | A | 3 | a0001c0001t0016 a0001c0001t0024 a0001c0001t0052 |
10 | NA18948.hp2 NA18955.hp2 NA18977.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*704C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 16/16 | 704 | chr3 | 197002668 | ||||||
chr3:197002698 | C | T | 7 | a0001c0001t0032 a0001c0002t0004 a0001c0002t0040 others(4): Show |
29 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*674G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 16/16 | 674 | chr3 | 197002698 | ||||||
chr3:197002749 | C | T | 1 | a0001c0001t0039 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*623G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 16/16 | 623 | chr3 | 197002749 | ||||||
chr3:197002937 | G | A | 1 | a0001c0001t0053 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*435C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 16/16 | 435 | chr3 | 197002937 | ||||||
chr3:197003002 | C | T | 1 | a0001c0002t0031 | 1 | NA19072.hp2 | 3_prime_UTR_variant | MODIFIER | c.*370G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 16/16 | 370 | chr3 | 197003002 | ||||||
chr3:197003068 | C | T | 46 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0010 others(43): Show |
199 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*304G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 16/16 | 304 | chr3 | 197003068 | ||||||
chr3:197003069 | G | C | 1 | a0001c0001t0054 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*303C>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 16/16 | 303 | chr3 | 197003069 | ||||||
chr3:197003191 | G | A | 1 | a0001c0001t0030 | 2 | HG02135.hp1 NA18972.hp1 |
3_prime_UTR_variant | MODIFIER | c.*181C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 16/16 | 181 | chr3 | 197003191 | ||||||
chr3:197003324 | G | A | 2 | a0001c0002t0055 a0001c0002t0056 |
2 | HG02451.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*48C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 16/16 | 48 | chr3 | 197003324 | ||||||
chr3:197029727 | C | T | 1 | a0001c0001t0025 | 2 | NA18999.hp2 NA19079.hp1 |
5_prime_UTR_variant | MODIFIER | c.-25G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 1/16 | 25 | chr3 | 197029727 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:197003480 | CG | C | 6 | a0001c0001t0002g0059 a0001c0001t0002g0258 a0001c0001t0002g0269 others(3): Show |
7 | HG01109.hp1 HG01891.hp1 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.2138-30delC | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 15/15 | chr3 | 197003480 | |||||||
chr3:197003519 | T | TGGGGTG | 195 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(192): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.2138-74_2138-69dup others(6): Show |
MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 15/15 | chr3 | 197003519 | |||||||
chr3:197003541 | T | C | 23 | a0001c0001t0005g0036 a0001c0001t0016g0282 a0001c0002t0001g0099 others(20): Show |
30 | HG00438.hp2 HG00621.hp1 HG02027.hp2 others(27): Show |
intron_variant | MODIFIER | c.2138-90A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 15/15 | chr3 | 197003541 | |||||||
chr3:197003622 | C | T | 7 | a0001c0002t0006g0053 a0001c0002t0013g0089 a0001c0003t0013g0029 others(4): Show |
10 | HG02572.hp1 HG02647.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2138-171G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 15/15 | chr3 | 197003622 | |||||||
chr3:197003676 | A | G | 20 | a0001c0002t0001g0099 a0001c0002t0009g0033 a0001c0002t0009g0034 others(17): Show |
26 | HG00438.hp2 HG00621.hp1 HG02027.hp2 others(23): Show |
intron_variant | MODIFIER | c.2137+225T>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 15/15 | chr3 | 197003676 | |||||||
chr3:197003733 | C | T | 1 | a0005c0010t0001g0183 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2137+168G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 15/15 | chr3 | 197003733 | |||||||
chr3:197003888 | G | A | 4 | a0001c0001t0003g0202 a0001c0001t0003g0254 a0001c0001t0003g0255 others(1): Show |
4 | HG01261.hp1 HG01361.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.2137+13C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 15/15 | chr3 | 197003888 | |||||||
chr3:197003896 | C | A | 1 | a0001c0001t0001g0106 | 1 | HG00558.hp2 | splice_region_variant&intron_variant | LOW | c.2137+5G>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 15/15 | chr3 | 197003896 | |||||||
chr3:197004172 | T | A | 1 | a0001c0001t0001g0193 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1939-73A>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/15 | chr3 | 197004172 | |||||||
chr3:197004336 | C | T | 10 | a0001c0001t0005g0032 a0001c0001t0005g0116 a0001c0001t0005g0117 others(7): Show |
11 | HG01884.hp2 HG02109.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1939-237G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/15 | chr3 | 197004336 | |||||||
chr3:197004440 | C | T | 1 | a0001c0003t0019g0018 | 3 | HG02622.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1939-341G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/15 | chr3 | 197004440 | |||||||
chr3:197004592 | C | T | 20 | a0001c0002t0001g0099 a0001c0002t0009g0033 a0001c0002t0009g0034 others(17): Show |
26 | HG00438.hp2 HG00621.hp1 HG02027.hp2 others(23): Show |
intron_variant | MODIFIER | c.1939-493G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/15 | chr3 | 197004592 | |||||||
chr3:197004668 | G | A | 23 | a0001c0001t0002g0105 a0001c0001t0005g0003 a0001c0001t0005g0036 others(20): Show |
35 | HG01891.hp2 HG02630.hp1 HG02717.hp2 others(32): Show |
intron_variant | MODIFIER | c.1939-569C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/15 | chr3 | 197004668 | |||||||
chr3:197004814 | T | C | 39 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0040 others(36): Show |
52 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.1939-715A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/15 | chr3 | 197004814 | |||||||
chr3:197004926 | C | T | 20 | a0001c0002t0001g0099 a0001c0002t0009g0033 a0001c0002t0009g0034 others(17): Show |
26 | HG00438.hp2 HG00621.hp1 HG02027.hp2 others(23): Show |
intron_variant | MODIFIER | c.1939-827G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/15 | chr3 | 197004926 | |||||||
chr3:197004933 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1939-834G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/15 | chr3 | 197004933 | |||||||
chr3:197005050 | C | T | 63 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0040 others(60): Show |
84 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1939-951G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/15 | chr3 | 197005050 | |||||||
chr3:197005051 | G | A | 1 | a0001c0001t0001g0052 | 2 | NA18964.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1939-952C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/15 | chr3 | 197005051 | |||||||
chr3:197005052 | A | G | 1 | a0001c0001t0024g0228 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1939-953T>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/15 | chr3 | 197005052 | |||||||
chr3:197005180 | G | C | 1 | a0001c0002t0004g0151 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1939-1081C>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/15 | chr3 | 197005180 | |||||||
chr3:197005246 | C | T | 4 | a0001c0001t0002g0105 a0001c0001t0007g0090 a0001c0002t0002g0249 others(1): Show |
4 | HG01361.hp2 HG02109.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1939-1147G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/15 | chr3 | 197005246 | |||||||
chr3:197005613 | A | G | 1 | a0001c0001t0007g0090 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1938+936T>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/15 | chr3 | 197005613 | |||||||
chr3:197005645 | G | A | 1 | a0001c0001t0002g0250 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1938+904C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/15 | chr3 | 197005645 | |||||||
chr3:197005657 | A | C | 2 | a0001c0002t0055g0248 a0001c0002t0056g0247 |
2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1938+892T>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/15 | chr3 | 197005657 | |||||||
chr3:197005778 | T | C | 2 | a0001c0001t0016g0283 a0001c0001t0052g0284 |
2 | NA18948.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1938+771A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/15 | chr3 | 197005778 | |||||||
chr3:197005798 | T | TAGTCTCC others(83): Show |
3 | a0002c0009t0021g0087 a0002c0009t0021g0088 a0011c0029t0021g0067 |
3 | HG01255.hp2 HG01884.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1938+750_1938+751i others(92): Show |
MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/15 | chr3 | 197005798 | |||||||
chr3:197005817 | GGGCCAGA others(38): Show |
G | 2 | a0001c0002t0055g0248 a0001c0002t0056g0247 |
2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1938+687_1938+731d others(47): Show |
MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/15 | chr3 | 197005817 | |||||||
chr3:197005837 | C | CTAACTCA others(38): Show |
59 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0040 others(56): Show |
78 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1938+711_1938+712i others(47): Show |
MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/15 | chr3 | 197005837 | |||||||
chr3:197005837 | C | CTAACTCA others(38): Show |
9 | a0003c0006t0002g0112 a0003c0006t0020g0211 a0003c0006t0020g0302 others(6): Show |
9 | HG00609.hp2 HG02129.hp1 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.1938+667_1938+711d others(47): Show |
MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/15 | chr3 | 197005837 | |||||||
chr3:197005837 | C | CTAACTCA others(83): Show |
10 | a0001c0002t0002g0249 a0001c0002t0007g0062 a0001c0002t0010g0064 others(7): Show |
14 | HG01255.hp1 HG01361.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1938+711_1938+712i others(92): Show |
MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/15 | chr3 | 197005837 | |||||||
chr3:197005837 | C | T | 8 | a0001c0002t0011g0207 a0002c0004t0002g0031 a0002c0004t0007g0004 others(5): Show |
13 | HG02074.hp2 HG02273.hp1 HG03017.hp1 others(10): Show |
intron_variant | MODIFIER | c.1938+712G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/15 | chr3 | 197005837 | |||||||
chr3:197005995 | C | T | 1 | a0001c0003t0013g0030 | 2 | HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1938+554G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/15 | chr3 | 197005995 | |||||||
chr3:197006146 | G | A | 2 | a0001c0001t0002g0175 a0008c0008t0027g0028 |
3 | HG02015.hp2 HG02132.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1938+403C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/15 | chr3 | 197006146 | |||||||
chr3:197006177 | T | C | 20 | a0001c0002t0010g0064 a0001c0002t0015g0170 a0001c0002t0055g0248 others(17): Show |
25 | HG00609.hp2 HG01255.hp1 HG02015.hp2 others(22): Show |
intron_variant | MODIFIER | c.1938+372A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/15 | chr3 | 197006177 | |||||||
chr3:197006201 | G | A | 20 | a0001c0002t0001g0099 a0001c0002t0009g0033 a0001c0002t0009g0034 others(17): Show |
26 | HG00438.hp2 HG00621.hp1 HG02027.hp2 others(23): Show |
intron_variant | MODIFIER | c.1938+348C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/15 | chr3 | 197006201 | |||||||
chr3:197006288 | AGTTT | A | 8 | a0001c0002t0011g0207 a0002c0004t0002g0031 a0002c0004t0007g0004 others(5): Show |
13 | HG02074.hp2 HG02273.hp1 HG03017.hp1 others(10): Show |
intron_variant | MODIFIER | c.1938+257_1938+260d others(6): Show |
MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/15 | chr3 | 197006288 | |||||||
chr3:197006482 | G | A | 4 | a0001c0002t0010g0064 a0001c0005t0010g0026 a0001c0005t0010g0080 others(1): Show |
6 | HG02055.hp1 HG02055.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1938+67C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/15 | chr3 | 197006482 | |||||||
chr3:197006497 | C | G | 20 | a0001c0002t0001g0099 a0001c0002t0009g0033 a0001c0002t0009g0034 others(17): Show |
26 | HG00438.hp2 HG00621.hp1 HG02027.hp2 others(23): Show |
intron_variant | MODIFIER | c.1938+52G>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 14/15 | chr3 | 197006497 | |||||||
chr3:197006767 | C | T | 1 | a0001c0002t0002g0249 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1751-31G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 13/15 | chr3 | 197006767 | |||||||
chr3:197006899 | G | A | 1 | a0001c0001t0023g0267 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1751-163C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 13/15 | chr3 | 197006899 | |||||||
chr3:197006923 | C | A | 71 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0040 others(68): Show |
96 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.1751-187G>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 13/15 | chr3 | 197006923 | |||||||
chr3:197006995 | C | T | 2 | a0001c0016t0011g0086 a0001c0016t0011g0305 |
2 | HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1751-259G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 13/15 | chr3 | 197006995 | |||||||
chr3:197007270 | G | A | 2 | a0001c0002t0004g0010 a0001c0002t0004g0147 |
5 | HG01167.hp1 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1751-534C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 13/15 | chr3 | 197007270 | |||||||
chr3:197007414 | T | G | 1 | a0001c0014t0003g0304 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1751-678A>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 13/15 | chr3 | 197007414 | |||||||
chr3:197007459 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1751-723C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 13/15 | chr3 | 197007459 | |||||||
chr3:197007755 | T | C | 8 | a0001c0002t0011g0207 a0002c0004t0002g0031 a0002c0004t0007g0004 others(5): Show |
13 | HG02074.hp2 HG02273.hp1 HG03017.hp1 others(10): Show |
intron_variant | MODIFIER | c.1750+902A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 13/15 | chr3 | 197007755 | |||||||
chr3:197007781 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1750+876G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 13/15 | chr3 | 197007781 | |||||||
chr3:197008018 | C | T | 1 | a0001c0002t0001g0125 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1750+639G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 13/15 | chr3 | 197008018 | |||||||
chr3:197008053 | G | A | 1 | a0001c0001t0006g0076 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1750+604C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 13/15 | chr3 | 197008053 | |||||||
chr3:197008102 | G | A | 40 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0040 others(37): Show |
53 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.1750+555C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 13/15 | chr3 | 197008102 | |||||||
chr3:197008202 | G | C | 1 | a0001c0001t0006g0073 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1750+455C>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 13/15 | chr3 | 197008202 | |||||||
chr3:197008219 | G | C | 2 | a0001c0001t0001g0060 a0001c0001t0018g0306 |
3 | HG01069.hp2 HG01071.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1750+438C>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 13/15 | chr3 | 197008219 | |||||||
chr3:197008402 | C | T | 43 | a0001c0002t0001g0099 a0001c0002t0009g0033 a0001c0002t0009g0034 others(40): Show |
54 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.1750+255G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 13/15 | chr3 | 197008402 | |||||||
chr3:197008454 | T | A | 1 | a0001c0001t0007g0083 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1750+203A>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 13/15 | chr3 | 197008454 | |||||||
chr3:197008753 | G | A | 40 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(37): Show |
59 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.1683-29C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 12/15 | chr3 | 197008753 | |||||||
chr3:197009028 | C | T | 1 | a0001c0002t0026g0160 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1526-63G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 11/15 | chr3 | 197009028 | |||||||
chr3:197009058 | C | A | 43 | a0001c0002t0001g0099 a0001c0002t0009g0033 a0001c0002t0009g0034 others(40): Show |
54 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.1526-93G>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 11/15 | chr3 | 197009058 | |||||||
chr3:197009144 | A | G | 1 | a0001c0001t0001g0044 | 2 | HG00597.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1526-179T>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 11/15 | chr3 | 197009144 | |||||||
chr3:197009179 | C | T | 20 | a0001c0002t0001g0099 a0001c0002t0009g0033 a0001c0002t0009g0034 others(17): Show |
26 | HG00438.hp2 HG00621.hp1 HG02027.hp2 others(23): Show |
intron_variant | MODIFIER | c.1526-214G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 11/15 | chr3 | 197009179 | |||||||
chr3:197009524 | C | T | 2 | a0001c0002t0002g0249 a0001c0002t0007g0062 |
2 | HG01361.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1525+94G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 11/15 | chr3 | 197009524 | |||||||
chr3:197009608 | G | C | 3 | a0002c0009t0021g0087 a0002c0009t0021g0088 a0011c0029t0021g0067 |
3 | HG01255.hp2 HG01884.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1525+10C>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 11/15 | chr3 | 197009608 | |||||||
chr3:197009833 | G | C | 1 | a0001c0001t0001g0106 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1331-21C>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 10/15 | chr3 | 197009833 | |||||||
chr3:197009863 | A | G | 1 | a0008c0008t0027g0028 | 2 | HG02015.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.1331-51T>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 10/15 | chr3 | 197009863 | |||||||
chr3:197009978 | G | A | 20 | a0001c0002t0001g0099 a0001c0002t0009g0033 a0001c0002t0009g0034 others(17): Show |
26 | HG00438.hp2 HG00621.hp1 HG02027.hp2 others(23): Show |
intron_variant | MODIFIER | c.1331-166C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 10/15 | chr3 | 197009978 | |||||||
chr3:197010135 | G | A | 1 | a0001c0002t0001g0155 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1331-323C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 10/15 | chr3 | 197010135 | |||||||
chr3:197010186 | C | A | 2 | a0001c0002t0001g0125 a0001c0002t0001g0155 |
2 | NA18942.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1331-374G>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 10/15 | chr3 | 197010186 | |||||||
chr3:197010245 | A | G | 21 | a0001c0002t0001g0099 a0001c0002t0009g0033 a0001c0002t0009g0034 others(18): Show |
28 | HG00438.hp2 HG00621.hp1 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.1331-433T>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 10/15 | chr3 | 197010245 | |||||||
chr3:197010377 | T | C | 20 | a0001c0002t0001g0099 a0001c0002t0009g0033 a0001c0002t0009g0034 others(17): Show |
26 | HG00438.hp2 HG00621.hp1 HG02027.hp2 others(23): Show |
intron_variant | MODIFIER | c.1330+321A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 10/15 | chr3 | 197010377 | |||||||
chr3:197010424 | A | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(205): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.1330+274T>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 10/15 | chr3 | 197010424 | |||||||
chr3:197010425 | G | A | 1 | a0003c0035t0001g0275 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1330+273C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 10/15 | chr3 | 197010425 | |||||||
chr3:197010646 | T | C | 1 | a0001c0001t0002g0241 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1330+52A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 10/15 | chr3 | 197010646 | |||||||
chr3:197011081 | A | T | 1 | a0016c0028t0041g0233 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1234-287T>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197011081 | |||||||
chr3:197011090 | G | A | 3 | a0002c0009t0021g0087 a0002c0009t0021g0088 a0011c0029t0021g0067 |
3 | HG01255.hp2 HG01884.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1234-296C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197011090 | |||||||
chr3:197011112 | G | A | 2 | a0001c0003t0014g0259 a0001c0003t0015g0128 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1234-318C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197011112 | |||||||
chr3:197011149 | G | A | 3 | a0001c0001t0005g0116 a0001c0002t0010g0064 a0006c0007t0010g0022 |
4 | HG02055.hp2 HG02559.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1234-355C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197011149 | |||||||
chr3:197011190 | G | A | 21 | a0001c0002t0001g0099 a0001c0002t0009g0033 a0001c0002t0009g0034 others(18): Show |
28 | HG00438.hp2 HG00621.hp1 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.1234-396C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197011190 | |||||||
chr3:197011396 | G | A | 1 | a0001c0001t0012g0294 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1234-602C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197011396 | |||||||
chr3:197011404 | A | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(205): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.1234-610T>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197011404 | |||||||
chr3:197011488 | G | C | 1 | a0001c0001t0001g0194 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1234-694C>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197011488 | |||||||
chr3:197011513 | C | G | 303 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(300): Show |
416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.1234-719G>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197011513 | |||||||
chr3:197011544 | G | A | 1 | a0001c0001t0039g0277 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1234-750C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197011544 | |||||||
chr3:197011546 | C | A | 1 | a0001c0002t0010g0064 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1234-752G>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197011546 | |||||||
chr3:197011630 | G | T | 20 | a0001c0002t0001g0099 a0001c0002t0009g0033 a0001c0002t0009g0034 others(17): Show |
26 | HG00438.hp2 HG00621.hp1 HG02027.hp2 others(23): Show |
intron_variant | MODIFIER | c.1234-836C>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197011630 | |||||||
chr3:197011656 | C | T | 19 | a0001c0002t0010g0064 a0001c0002t0015g0170 a0001c0002t0055g0248 others(16): Show |
23 | HG00609.hp2 HG01255.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1234-862G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197011656 | |||||||
chr3:197011657 | C | G | 3 | a0002c0009t0021g0087 a0002c0009t0021g0088 a0011c0029t0021g0067 |
3 | HG01255.hp2 HG01884.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1234-863G>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197011657 | |||||||
chr3:197011887 | C | T | 2 | a0001c0016t0011g0086 a0001c0016t0011g0305 |
2 | HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1234-1093G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197011887 | |||||||
chr3:197011905 | C | G | 20 | a0001c0002t0001g0099 a0001c0002t0009g0033 a0001c0002t0009g0034 others(17): Show |
26 | HG00438.hp2 HG00621.hp1 HG02027.hp2 others(23): Show |
intron_variant | MODIFIER | c.1234-1111G>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197011905 | |||||||
chr3:197011906 | A | C | 2 | a0002c0004t0002g0031 a0002c0004t0007g0236 |
3 | NA18962.hp1 NA18979.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1234-1112T>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197011906 | |||||||
chr3:197012040 | C | T | 1 | a0001c0002t0006g0053 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1234-1246G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197012040 | |||||||
chr3:197012048 | C | T | 11 | a0001c0002t0011g0207 a0002c0004t0002g0031 a0002c0004t0007g0004 others(8): Show |
16 | HG01255.hp2 HG01884.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.1234-1254G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197012048 | |||||||
chr3:197012069 | C | T | 1 | a0001c0001t0002g0250 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1234-1275G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197012069 | |||||||
chr3:197012082 | C | T | 41 | a0001c0001t0006g0073 a0001c0002t0001g0008 a0001c0002t0001g0017 others(38): Show |
54 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1234-1288G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197012082 | |||||||
chr3:197012116 | G | A | 3 | a0002c0009t0021g0087 a0002c0009t0021g0088 a0011c0029t0021g0067 |
3 | HG01255.hp2 HG01884.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1234-1322C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197012116 | |||||||
chr3:197012225 | G | A | 8 | a0001c0002t0011g0207 a0002c0004t0002g0031 a0002c0004t0007g0004 others(5): Show |
13 | HG02074.hp2 HG02273.hp1 HG03017.hp1 others(10): Show |
intron_variant | MODIFIER | c.1234-1431C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197012225 | |||||||
chr3:197012317 | C | T | 1 | a0001c0002t0001g0155 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1234-1523G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197012317 | |||||||
chr3:197012440 | G | A | 20 | a0001c0002t0001g0099 a0001c0002t0009g0033 a0001c0002t0009g0034 others(17): Show |
26 | HG00438.hp2 HG00621.hp1 HG02027.hp2 others(23): Show |
intron_variant | MODIFIER | c.1234-1646C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197012440 | |||||||
chr3:197012620 | A | G | 38 | a0001c0002t0001g0099 a0001c0002t0009g0033 a0001c0002t0009g0034 others(35): Show |
47 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1234-1826T>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197012620 | |||||||
chr3:197012667 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(109): Show |
163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.1234-1873G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197012667 | |||||||
chr3:197012710 | C | T | 16 | a0001c0002t0007g0062 a0001c0002t0010g0064 a0001c0002t0011g0207 others(13): Show |
20 | HG01255.hp2 HG01361.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1234-1916G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197012710 | |||||||
chr3:197012877 | T | A | 1 | a0008c0008t0027g0028 | 2 | HG02015.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.1234-2083A>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197012877 | |||||||
chr3:197013010 | G | A | 1 | a0001c0001t0003g0078 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1234-2216C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197013010 | |||||||
chr3:197013173 | T | C | 1 | a0001c0002t0001g0110 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1233+2192A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197013173 | |||||||
chr3:197013285 | A | T | 1 | a0004c0015t0010g0217 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1233+2080T>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197013285 | |||||||
chr3:197013440 | C | T | 2 | a0001c0001t0012g0055 a0001c0001t0012g0264 |
3 | HG02738.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1233+1925G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197013440 | |||||||
chr3:197013519 | G | T | 33 | a0001c0002t0001g0099 a0001c0002t0002g0249 a0001c0002t0007g0062 others(30): Show |
45 | HG00438.hp2 HG00621.hp1 HG01361.hp2 others(42): Show |
intron_variant | MODIFIER | c.1233+1846C>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197013519 | |||||||
chr3:197013678 | A | G | 1 | a0001c0002t0015g0170 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1233+1687T>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197013678 | |||||||
chr3:197013996 | C | G | 2 | a0007c0011t0008g0127 a0007c0011t0018g0245 |
2 | HG01081.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1233+1369G>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197013996 | |||||||
chr3:197014033 | G | A | 1 | a0001c0001t0005g0299 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1233+1332C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197014033 | |||||||
chr3:197014149 | C | T | 2 | a0001c0002t0002g0249 a0001c0002t0007g0062 |
2 | HG01361.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1233+1216G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197014149 | |||||||
chr3:197014240 | T | C | 1 | a0002c0004t0001g0109 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1233+1125A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197014240 | |||||||
chr3:197014285 | A | G | 2 | a0001c0001t0003g0142 a0001c0001t0003g0278 |
2 | NA18954.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1233+1080T>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197014285 | |||||||
chr3:197014287 | A | T | 1 | a0008c0008t0027g0028 | 2 | HG02015.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.1233+1078T>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197014287 | |||||||
chr3:197014315 | C | T | 9 | a0001c0002t0011g0207 a0002c0004t0002g0031 a0002c0004t0007g0004 others(6): Show |
14 | HG02074.hp2 HG02273.hp1 HG03017.hp1 others(11): Show |
intron_variant | MODIFIER | c.1233+1050G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197014315 | |||||||
chr3:197014383 | G | GT | 19 | a0001c0001t0001g0171 a0001c0001t0001g0180 a0001c0001t0001g0201 others(16): Show |
19 | HG00140.hp2 HG01099.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.1233+981dupA | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197014383 | |||||||
chr3:197014383 | G | GTTT | 58 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0040 others(55): Show |
76 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1233+979_1233+981d others(5): Show |
MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197014383 | |||||||
chr3:197014383 | G | GTTTT | 16 | a0001c0002t0001g0242 a0001c0002t0004g0134 a0001c0002t0004g0148 others(13): Show |
18 | HG00438.hp1 HG00741.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.1233+978_1233+981d others(6): Show |
MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197014383 | |||||||
chr3:197014383 | G | GTTTTT | 7 | a0001c0002t0011g0207 a0001c0002t0017g0139 a0002c0004t0002g0031 others(4): Show |
12 | HG00438.hp2 HG02273.hp1 HG03017.hp1 others(9): Show |
intron_variant | MODIFIER | c.1233+977_1233+981d others(7): Show |
MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197014383 | |||||||
chr3:197014383 | G | GTTTTTTT others(3): Show |
1 | a0001c0002t0007g0062 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1233+972_1233+981d others(12): Show |
MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197014383 | |||||||
chr3:197014383 | G | GTTTTTTT others(11): Show |
1 | a0008c0008t0027g0028 | 2 | HG02015.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.1233+964_1233+981d others(20): Show |
MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197014383 | |||||||
chr3:197014383 | GT | G | 7 | a0001c0001t0001g0047 a0001c0001t0001g0205 a0001c0001t0001g0244 others(4): Show |
8 | HG02083.hp1 HG02897.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1233+981delA | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197014383 | |||||||
chr3:197014480 | C | T | 1 | a0001c0002t0017g0133 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1233+885G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197014480 | |||||||
chr3:197014490 | C | A | 1 | a0008c0008t0027g0028 | 2 | HG02015.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.1233+875G>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197014490 | |||||||
chr3:197014491 | G | A | 1 | a0001c0001t0008g0196 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1233+874C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197014491 | |||||||
chr3:197014681 | C | T | 5 | a0001c0003t0013g0029 a0001c0003t0013g0030 a0001c0003t0013g0094 others(2): Show |
9 | HG02622.hp1 HG02647.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.1233+684G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197014681 | |||||||
chr3:197014720 | T | C | 3 | a0001c0001t0001g0197 a0001c0001t0008g0131 a0001c0001t0008g0172 |
3 | HG02602.hp1 HG03831.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1233+645A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197014720 | |||||||
chr3:197014799 | C | T | 15 | a0001c0002t0001g0099 a0001c0002t0009g0033 a0001c0002t0009g0034 others(12): Show |
19 | HG00438.hp2 HG00621.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.1233+566G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197014799 | |||||||
chr3:197014943 | A | G | 1 | a0018c0024t0005g0268 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1233+422T>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197014943 | |||||||
chr3:197014944 | G | A | 1 | a0018c0024t0005g0268 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1233+421C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197014944 | |||||||
chr3:197015042 | G | A | 1 | a0001c0002t0010g0064 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1233+323C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197015042 | |||||||
chr3:197015103 | C | G | 2 | a0001c0002t0004g0161 a0001c0002t0004g0162 |
2 | HG01433.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1233+262G>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197015103 | |||||||
chr3:197015135 | CCTGTCCC others(45): Show |
C | 1 | a0001c0001t0001g0182 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1233+178_1233+229d others(54): Show |
MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197015135 | |||||||
chr3:197015170 | G | C | 1 | a0001c0001t0001g0210 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1233+195C>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197015170 | |||||||
chr3:197015195 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1233+170G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197015195 | |||||||
chr3:197015342 | C | T | 9 | a0001c0002t0011g0207 a0002c0004t0002g0031 a0002c0004t0007g0004 others(6): Show |
14 | HG02074.hp2 HG02273.hp1 HG03017.hp1 others(11): Show |
intron_variant | MODIFIER | c.1233+23G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 9/15 | chr3 | 197015342 | |||||||
chr3:197015524 | G | A | 75 | a0001c0002t0001g0008 a0001c0002t0001g0017 a0001c0002t0001g0040 others(72): Show |
95 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(92): Show |
splice_region_variant&intron_variant | LOW | c.1082-8C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 8/15 | chr3 | 197015524 | |||||||
chr3:197015548 | G | A | 6 | a0001c0003t0013g0029 a0001c0003t0013g0030 a0001c0003t0013g0094 others(3): Show |
11 | HG02015.hp2 HG02132.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1082-32C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 8/15 | chr3 | 197015548 | |||||||
chr3:197015568 | A | G | 1 | a0001c0001t0018g0306 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1082-52T>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 8/15 | chr3 | 197015568 | |||||||
chr3:197015664 | C | T | 14 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0052 others(11): Show |
20 | HG00408.hp1 HG00408.hp2 HG02523.hp1 others(17): Show |
intron_variant | MODIFIER | c.1082-148G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 8/15 | chr3 | 197015664 | |||||||
chr3:197015970 | C | T | 1 | a0001c0002t0015g0170 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1081+219G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 8/15 | chr3 | 197015970 | |||||||
chr3:197015996 | C | T | 1 | a0001c0001t0005g0263 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1081+193G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 8/15 | chr3 | 197015996 | |||||||
chr3:197016130 | C | T | 1 | a0001c0002t0001g0040 | 2 | HG00609.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.1081+59G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 8/15 | chr3 | 197016130 | |||||||
chr3:197016143 | G | T | 9 | a0001c0002t0011g0207 a0002c0004t0002g0031 a0002c0004t0007g0004 others(6): Show |
14 | HG02074.hp2 HG02273.hp1 HG03017.hp1 others(11): Show |
intron_variant | MODIFIER | c.1081+46C>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 8/15 | chr3 | 197016143 | |||||||
chr3:197016179 | G | A | 1 | a0001c0013t0009g0225 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1081+10C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 8/15 | chr3 | 197016179 | |||||||
chr3:197016430 | C | A | 1 | a0001c0001t0008g0131 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.901-61G>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 7/15 | chr3 | 197016430 | |||||||
chr3:197016481 | C | G | 1 | a0001c0001t0002g0179 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.901-112G>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 7/15 | chr3 | 197016481 | |||||||
chr3:197016515 | C | T | 1 | a0001c0001t0022g0071 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.901-146G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 7/15 | chr3 | 197016515 | |||||||
chr3:197016586 | C | T | 1 | a0008c0008t0027g0028 | 2 | HG02015.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.901-217G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 7/15 | chr3 | 197016586 | |||||||
chr3:197016737 | G | A | 4 | a0001c0003t0013g0029 a0001c0003t0013g0030 a0001c0003t0013g0094 others(1): Show |
6 | HG02647.hp1 HG02897.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.900+366C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 7/15 | chr3 | 197016737 | |||||||
chr3:197016739 | C | T | 2 | a0001c0003t0014g0259 a0001c0003t0015g0128 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.900+364G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 7/15 | chr3 | 197016739 | |||||||
chr3:197016794 | G | A | 1 | a0001c0002t0004g0251 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.900+309C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 7/15 | chr3 | 197016794 | |||||||
chr3:197016810 | GGTTT | G | 85 | a0001c0001t0019g0240 a0001c0002t0001g0008 a0001c0002t0001g0017 others(82): Show |
110 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.900+289_900+292del others(4): Show |
MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 7/15 | chr3 | 197016810 | |||||||
chr3:197016954 | G | A | 1 | a0008c0008t0027g0028 | 2 | HG02015.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.900+149C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 7/15 | chr3 | 197016954 | |||||||
chr3:197016969 | C | T | 2 | a0001c0005t0010g0026 a0001c0005t0010g0080 |
3 | HG02055.hp1 HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.900+134G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 7/15 | chr3 | 197016969 | |||||||
chr3:197017054 | C | T | 2 | a0002c0009t0021g0087 a0002c0009t0021g0088 |
2 | HG01884.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.900+49G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 7/15 | chr3 | 197017054 | |||||||
chr3:197017055 | G | A | 3 | a0001c0001t0001g0048 a0001c0001t0001g0169 a0001c0001t0001g0201 |
4 | HG01256.hp1 HG03491.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.900+48C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 7/15 | chr3 | 197017055 | |||||||
chr3:197017463 | ACT | A | 1 | a0001c0003t0019g0018 | 3 | HG02622.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.713-175_713-174del others(2): Show |
MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197017463 | |||||||
chr3:197017591 | A | C | 9 | a0001c0001t0005g0032 a0001c0001t0005g0116 a0001c0001t0005g0117 others(6): Show |
10 | HG01884.hp2 HG02109.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.713-301T>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197017591 | |||||||
chr3:197017604 | G | A | 2 | a0001c0001t0003g0092 a0001c0022t0003g0091 |
2 | HG01934.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.713-314C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197017604 | |||||||
chr3:197017605 | T | C | 2 | a0001c0001t0006g0076 a0001c0001t0006g0303 |
2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.713-315A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197017605 | |||||||
chr3:197017610 | G | T | 1 | a0001c0002t0011g0207 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.713-320C>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197017610 | |||||||
chr3:197017615 | C | A | 1 | a0001c0001t0001g0146 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.713-325G>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197017615 | |||||||
chr3:197017648 | T | C | 10 | a0001c0001t0001g0011 a0001c0001t0001g0049 a0001c0001t0001g0138 others(7): Show |
16 | HG00423.hp2 HG01081.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.713-358A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197017648 | |||||||
chr3:197017652 | C | T | 2 | a0001c0001t0006g0081 a0001c0001t0006g0085 |
2 | HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.713-362G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197017652 | |||||||
chr3:197017654 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0008g0137 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.713-364C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197017654 | |||||||
chr3:197017658 | A | G | 2 | a0001c0001t0001g0138 a0001c0001t0008g0137 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.713-368T>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197017658 | |||||||
chr3:197017674 | A | C | 1 | a0001c0002t0017g0133 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.713-384T>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197017674 | |||||||
chr3:197017674 | A | G | 9 | a0001c0001t0001g0138 a0001c0001t0001g0168 a0001c0001t0001g0174 others(6): Show |
12 | HG01168.hp2 HG01169.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.713-384T>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197017674 | |||||||
chr3:197017702 | C | T | 20 | a0001c0001t0001g0043 a0001c0001t0001g0239 a0001c0002t0006g0053 others(17): Show |
27 | HG00609.hp2 HG02074.hp2 HG02129.hp1 others(24): Show |
intron_variant | MODIFIER | c.713-412G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197017702 | |||||||
chr3:197017705 | A | G | 4 | a0001c0002t0010g0064 a0001c0002t0015g0170 a0006c0007t0010g0022 others(1): Show |
5 | HG01255.hp1 HG01255.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.713-415T>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197017705 | |||||||
chr3:197017733 | T | C | 1 | a0001c0001t0001g0205 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.713-443A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197017733 | |||||||
chr3:197017745 | C | T | 2 | a0001c0001t0001g0178 a0001c0001t0001g0296 |
2 | HG00733.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.713-455G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197017745 | |||||||
chr3:197017769 | G | C | 90 | a0001c0001t0005g0262 a0001c0001t0016g0039 a0001c0001t0016g0285 others(87): Show |
116 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.713-479C>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197017769 | |||||||
chr3:197017770 | G | T | 90 | a0001c0001t0005g0262 a0001c0001t0016g0039 a0001c0001t0016g0285 others(87): Show |
116 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.713-480C>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197017770 | |||||||
chr3:197017783 | A | T | 1 | a0001c0002t0002g0249 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.713-493T>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197017783 | |||||||
chr3:197017793 | T | C | 3 | a0001c0001t0002g0258 a0001c0001t0002g0271 a0001c0001t0003g0092 |
3 | HG02280.hp2 HG02738.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.713-503A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197017793 | |||||||
chr3:197017801 | T | C | 1 | a0001c0001t0003g0092 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.713-511A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197017801 | |||||||
chr3:197017815 | T | C | 1 | a0001c0001t0001g0213 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.713-525A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197017815 | |||||||
chr3:197017825 | C | T | 91 | a0001c0001t0003g0092 a0001c0001t0016g0039 a0001c0001t0016g0285 others(88): Show |
117 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.713-535G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197017825 | |||||||
chr3:197017834 | G | A | 2 | a0001c0001t0011g0252 a0017c0025t0001g0206 |
2 | HG03669.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.713-544C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197017834 | |||||||
chr3:197017866 | A | G | 4 | a0001c0013t0009g0121 a0001c0013t0009g0225 a0002c0009t0021g0087 others(1): Show |
4 | HG00621.hp1 HG01884.hp1 HG02027.hp2 others(1): Show |
intron_variant | MODIFIER | c.713-576T>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197017866 | |||||||
chr3:197018023 | C | T | 72 | a0001c0001t0016g0039 a0001c0001t0016g0285 a0001c0001t0019g0240 others(69): Show |
92 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.713-733G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197018023 | |||||||
chr3:197018153 | C | G | 86 | a0001c0001t0016g0039 a0001c0001t0016g0285 a0001c0001t0019g0240 others(83): Show |
111 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.713-863G>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197018153 | |||||||
chr3:197018191 | A | G | 3 | a0001c0002t0010g0064 a0006c0007t0010g0022 a0011c0029t0021g0067 |
4 | HG01255.hp2 HG02055.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.713-901T>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197018191 | |||||||
chr3:197018217 | G | T | 27 | a0001c0001t0019g0240 a0001c0002t0006g0053 a0001c0002t0015g0170 others(24): Show |
34 | HG00609.hp2 HG01255.hp1 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.713-927C>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197018217 | |||||||
chr3:197018301 | C | A | 8 | a0001c0001t0001g0060 a0001c0001t0002g0059 a0001c0001t0002g0258 others(5): Show |
11 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.713-1011G>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197018301 | |||||||
chr3:197018323 | AT | A | 88 | a0001c0001t0016g0039 a0001c0001t0016g0285 a0001c0001t0019g0240 others(85): Show |
114 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.713-1034delA | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197018323 | |||||||
chr3:197018332 | T | A | 15 | a0001c0002t0001g0099 a0001c0002t0009g0033 a0001c0002t0009g0034 others(12): Show |
19 | HG00438.hp2 HG00621.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.713-1042A>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197018332 | |||||||
chr3:197018402 | C | G | 1 | a0003c0006t0020g0302 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.713-1112G>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197018402 | |||||||
chr3:197018441 | A | G | 88 | a0001c0001t0002g0084 a0001c0001t0002g0272 a0001c0001t0016g0039 others(85): Show |
113 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.713-1151T>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197018441 | |||||||
chr3:197018469 | T | C | 88 | a0001c0001t0002g0084 a0001c0001t0002g0272 a0001c0001t0016g0039 others(85): Show |
113 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.713-1179A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197018469 | |||||||
chr3:197018579 | T | A | 3 | a0001c0002t0010g0064 a0006c0007t0010g0022 a0011c0029t0021g0067 |
4 | HG01255.hp2 HG02055.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.713-1289A>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197018579 | |||||||
chr3:197018807 | G | T | 3 | a0001c0002t0001g0126 a0001c0002t0001g0230 a0001c0002t0001g0242 |
3 | HG00438.hp1 HG02056.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.713-1517C>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197018807 | |||||||
chr3:197018846 | G | A | 43 | a0001c0002t0001g0099 a0001c0002t0006g0053 a0001c0002t0009g0033 others(40): Show |
54 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.713-1556C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197018846 | |||||||
chr3:197018906 | G | A | 1 | a0001c0001t0006g0076 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.713-1616C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197018906 | |||||||
chr3:197018997 | A | G | 1 | a0001c0002t0002g0249 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.713-1707T>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197018997 | |||||||
chr3:197019057 | T | C | 1 | a0005c0027t0001g0136 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.713-1767A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197019057 | |||||||
chr3:197019088 | C | A | 62 | a0001c0001t0001g0006 a0001c0001t0001g0135 a0001c0001t0002g0042 others(59): Show |
85 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.713-1798G>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197019088 | |||||||
chr3:197019188 | C | T | 2 | a0001c0001t0001g0261 a0001c0001t0008g0260 |
2 | HG01168.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.713-1898G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197019188 | |||||||
chr3:197019211 | C | T | 43 | a0001c0002t0001g0099 a0001c0002t0004g0148 a0001c0002t0004g0149 others(40): Show |
54 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.713-1921G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197019211 | |||||||
chr3:197019510 | C | G | 1 | a0001c0001t0019g0240 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.712+1894G>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197019510 | |||||||
chr3:197019724 | T | C | 2 | a0001c0003t0013g0030 a0001c0003t0019g0018 |
5 | HG02622.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.712+1680A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197019724 | |||||||
chr3:197019758 | T | C | 92 | a0001c0001t0001g0006 a0001c0001t0001g0135 a0001c0001t0002g0231 others(89): Show |
122 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.712+1646A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197019758 | |||||||
chr3:197019885 | C | T | 2 | a0001c0001t0001g0208 a0001c0001t0032g0176 |
2 | HG00741.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.712+1519G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197019885 | |||||||
chr3:197020211 | A | C | 1 | a0001c0001t0002g0175 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.712+1193T>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197020211 | |||||||
chr3:197020381 | G | T | 89 | a0001c0001t0001g0006 a0001c0001t0001g0135 a0001c0001t0002g0231 others(86): Show |
118 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.712+1023C>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197020381 | |||||||
chr3:197020429 | C | T | 192 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(189): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.712+975G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197020429 | |||||||
chr3:197020489 | G | GCA | 73 | a0001c0001t0001g0006 a0001c0001t0001g0135 a0001c0001t0002g0231 others(70): Show |
97 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.712+913_712+914dup others(2): Show |
MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197020489 | |||||||
chr3:197020666 | T | G | 3 | a0001c0001t0003g0273 a0001c0001t0005g0257 a0001c0001t0012g0294 |
3 | HG00738.hp2 HG03239.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.712+738A>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197020666 | |||||||
chr3:197020673 | T | G | 1 | a0001c0001t0006g0085 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.712+731A>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197020673 | |||||||
chr3:197020702 | C | A | 66 | a0001c0001t0001g0006 a0001c0001t0001g0135 a0001c0001t0002g0231 others(63): Show |
88 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.712+702G>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197020702 | |||||||
chr3:197020754 | T | C | 90 | a0001c0001t0001g0006 a0001c0001t0001g0135 a0001c0001t0002g0231 others(87): Show |
120 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.712+650A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197020754 | |||||||
chr3:197020946 | A | G | 1 | a0001c0001t0003g0273 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.712+458T>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197020946 | |||||||
chr3:197020957 | T | C | 1 | a0001c0001t0003g0273 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.712+447A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197020957 | |||||||
chr3:197020962 | A | G | 1 | a0001c0001t0003g0273 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.712+442T>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197020962 | |||||||
chr3:197020970 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0174 |
2 | NA18984.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.712+434G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197020970 | |||||||
chr3:197020977 | C | A | 91 | a0001c0001t0001g0006 a0001c0001t0001g0135 a0001c0001t0001g0146 others(88): Show |
119 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.712+427G>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197020977 | |||||||
chr3:197021204 | C | G | 1 | a0001c0001t0033g0173 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.712+200G>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197021204 | |||||||
chr3:197021214 | C | T | 91 | a0001c0001t0001g0006 a0001c0001t0001g0135 a0001c0001t0001g0146 others(88): Show |
119 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.712+190G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197021214 | |||||||
chr3:197021262 | G | A | 1 | a0008c0008t0027g0028 | 2 | HG02015.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.712+142C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197021262 | |||||||
chr3:197021383 | C | T | 1 | a0008c0008t0027g0028 | 2 | HG02015.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.712+21G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197021383 | |||||||
chr3:197021385 | G | A | 1 | a0001c0001t0019g0240 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.712+19C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 6/15 | chr3 | 197021385 | |||||||
chr3:197021476 | G | A | 2 | a0001c0002t0011g0207 a0001c0020t0001g0220 |
2 | HG01978.hp1 HG03017.hp1 |
splice_region_variant&intron_variant | LOW | c.645-5C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 5/15 | chr3 | 197021476 | |||||||
chr3:197022007 | C | T | 1 | a0008c0008t0027g0028 | 2 | HG02015.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.645-536G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 5/15 | chr3 | 197022007 | |||||||
chr3:197022061 | G | C | 3 | a0001c0001t0001g0106 a0001c0001t0001g0208 a0001c0001t0001g0214 |
3 | HG00558.hp2 NA18955.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.645-590C>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 5/15 | chr3 | 197022061 | |||||||
chr3:197022073 | A | G | 5 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0237 others(2): Show |
6 | NA18989.hp2 NA19066.hp1 NA19067.hp2 others(3): Show |
intron_variant | MODIFIER | c.645-602T>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 5/15 | chr3 | 197022073 | |||||||
chr3:197022074 | A | C | 5 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0237 others(2): Show |
6 | NA18989.hp2 NA19066.hp1 NA19067.hp2 others(3): Show |
intron_variant | MODIFIER | c.645-603T>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 5/15 | chr3 | 197022074 | |||||||
chr3:197022093 | C | T | 2 | a0007c0011t0008g0127 a0007c0011t0018g0245 |
2 | HG01081.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.645-622G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 5/15 | chr3 | 197022093 | |||||||
chr3:197022225 | AT | A | 5 | a0001c0001t0005g0032 a0001c0001t0005g0116 a0001c0001t0005g0117 others(2): Show |
6 | HG02109.hp2 HG02615.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.644+731delA | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 5/15 | chr3 | 197022225 | |||||||
chr3:197022281 | C | T | 1 | a0008c0008t0027g0028 | 2 | HG02015.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.644+676G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 5/15 | chr3 | 197022281 | |||||||
chr3:197022422 | A | G | 1 | a0001c0001t0008g0172 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.644+535T>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 5/15 | chr3 | 197022422 | |||||||
chr3:197022447 | G | A | 4 | a0001c0001t0001g0171 a0001c0001t0001g0209 a0001c0001t0001g0210 others(1): Show |
4 | HG04184.hp2 NA18950.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.644+510C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 5/15 | chr3 | 197022447 | |||||||
chr3:197022537 | C | A | 42 | a0001c0001t0001g0060 a0001c0001t0001g0261 a0001c0001t0001g0265 others(39): Show |
67 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(64): Show |
intron_variant | MODIFIER | c.644+420G>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 5/15 | chr3 | 197022537 | |||||||
chr3:197022607 | C | T | 3 | a0001c0002t0010g0064 a0006c0007t0010g0022 a0011c0029t0021g0067 |
4 | HG01255.hp2 HG02055.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.644+350G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 5/15 | chr3 | 197022607 | |||||||
chr3:197022637 | A | T | 1 | a0001c0001t0006g0024 | 2 | HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.644+320T>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 5/15 | chr3 | 197022637 | |||||||
chr3:197022716 | C | G | 3 | a0001c0002t0002g0249 a0001c0002t0055g0248 a0001c0002t0056g0247 |
3 | HG02109.hp1 HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.644+241G>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 5/15 | chr3 | 197022716 | |||||||
chr3:197022742 | C | T | 1 | a0008c0008t0027g0028 | 2 | HG02015.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.644+215G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 5/15 | chr3 | 197022742 | |||||||
chr3:197022838 | C | T | 2 | a0001c0001t0001g0171 a0015c0019t0001g0167 |
2 | HG04184.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.644+119G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 5/15 | chr3 | 197022838 | |||||||
chr3:197022868 | G | T | 1 | a0008c0008t0027g0028 | 2 | HG02015.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.644+89C>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 5/15 | chr3 | 197022868 | |||||||
chr3:197022902 | T | C | 10 | a0001c0001t0006g0070 a0001c0001t0022g0038 a0001c0001t0046g0145 others(7): Show |
14 | HG01099.hp2 HG01255.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.644+55A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 5/15 | chr3 | 197022902 | |||||||
chr3:197022927 | T | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(242): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.644+30A>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 5/15 | chr3 | 197022927 | |||||||
chr3:197022950 | C | T | 11 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0003g0273 others(8): Show |
12 | HG00738.hp2 HG01099.hp2 HG01934.hp2 others(9): Show |
splice_region_variant&intron_variant | LOW | c.644+7G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 5/15 | chr3 | 197022950 | |||||||
chr3:197023145 | A | G | 235 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(232): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.488-32T>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 4/15 | chr3 | 197023145 | |||||||
chr3:197023190 | G | A | 1 | a0008c0008t0027g0028 | 2 | HG02015.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.488-77C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 4/15 | chr3 | 197023190 | |||||||
chr3:197023259 | G | A | 1 | a0001c0001t0005g0117 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.488-146C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 4/15 | chr3 | 197023259 | |||||||
chr3:197023336 | A | G | 233 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(230): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.488-223T>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 4/15 | chr3 | 197023336 | |||||||
chr3:197023493 | A | C | 4 | a0001c0002t0010g0064 a0006c0007t0010g0022 a0006c0017t0007g0063 others(1): Show |
5 | HG01255.hp2 HG02055.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.488-380T>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 4/15 | chr3 | 197023493 | |||||||
chr3:197023588 | C | T | 1 | a0001c0002t0015g0170 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.488-475G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 4/15 | chr3 | 197023588 | |||||||
chr3:197023799 | G | C | 4 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(1): Show |
4 | NA18990.hp1 NA19066.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+504C>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 4/15 | chr3 | 197023799 | |||||||
chr3:197023894 | G | A | 1 | a0008c0008t0027g0028 | 2 | HG02015.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.487+409C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 4/15 | chr3 | 197023894 | |||||||
chr3:197023962 | A | G | 4 | a0001c0002t0013g0089 a0002c0009t0021g0087 a0002c0009t0021g0088 others(1): Show |
5 | HG01884.hp1 HG02015.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+341T>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 4/15 | chr3 | 197023962 | |||||||
chr3:197023970 | C | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(146): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.487+333G>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 4/15 | chr3 | 197023970 | |||||||
chr3:197023973 | C | A | 2 | a0002c0009t0021g0087 a0002c0009t0021g0088 |
2 | HG01884.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.487+330G>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 4/15 | chr3 | 197023973 | |||||||
chr3:197023976 | C | T | 8 | a0001c0001t0001g0132 a0001c0001t0001g0221 a0001c0001t0002g0250 others(5): Show |
8 | HG00280.hp2 HG01074.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.487+327G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 4/15 | chr3 | 197023976 | |||||||
chr3:197023977 | C | G | 1 | a0008c0008t0027g0028 | 2 | HG02015.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.487+326G>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 4/15 | chr3 | 197023977 | |||||||
chr3:197024095 | C | A | 1 | a0001c0001t0001g0215 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.487+208G>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 4/15 | chr3 | 197024095 | |||||||
chr3:197024123 | G | A | 1 | a0001c0001t0011g0238 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.487+180C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 4/15 | chr3 | 197024123 | |||||||
chr3:197024134 | C | T | 1 | a0001c0003t0019g0018 | 3 | HG02622.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.487+169G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 4/15 | chr3 | 197024134 | |||||||
chr3:197024145 | AGGCGGGG others(13): Show |
A | 2 | a0007c0011t0008g0127 a0007c0011t0018g0245 |
2 | HG01081.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.487+138_487+157del others(20): Show |
MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 4/15 | chr3 | 197024145 | |||||||
chr3:197024159 | C | T | 1 | a0001c0001t0011g0252 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.487+144G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 4/15 | chr3 | 197024159 | |||||||
chr3:197024181 | G | A | 3 | a0001c0001t0001g0296 a0001c0001t0008g0216 a0001c0001t0008g0276 |
3 | HG00099.hp2 HG00642.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.487+122C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 4/15 | chr3 | 197024181 | |||||||
chr3:197024544 | C | T | 1 | a0001c0002t0001g0098 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.305-59G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197024544 | |||||||
chr3:197024603 | C | T | 187 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(184): Show |
261 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.305-118G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197024603 | |||||||
chr3:197024891 | G | T | 1 | a0001c0001t0001g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.305-406C>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197024891 | |||||||
chr3:197024896 | G | C | 3 | a0001c0001t0001g0132 a0001c0001t0001g0239 a0001c0001t0036g0130 |
3 | HG01109.hp2 HG02145.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.305-411C>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197024896 | |||||||
chr3:197024897 | G | T | 1 | a0001c0001t0001g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.305-412C>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197024897 | |||||||
chr3:197024898 | G | A | 1 | a0001c0001t0001g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.305-413C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197024898 | |||||||
chr3:197024899 | A | T | 1 | a0001c0001t0001g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.305-414T>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197024899 | |||||||
chr3:197024900 | A | C | 1 | a0001c0001t0001g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.305-415T>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197024900 | |||||||
chr3:197024901 | G | T | 1 | a0001c0001t0001g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.305-416C>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197024901 | |||||||
chr3:197024902 | A | C | 1 | a0001c0001t0001g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.305-417T>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197024902 | |||||||
chr3:197024903 | A | C | 1 | a0001c0001t0001g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.305-418T>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197024903 | |||||||
chr3:197024904 | G | T | 1 | a0001c0001t0001g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.305-419C>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197024904 | |||||||
chr3:197024905 | G | C | 1 | a0001c0001t0001g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.305-420C>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197024905 | |||||||
chr3:197024906 | G | T | 1 | a0001c0001t0001g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.305-421C>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197024906 | |||||||
chr3:197024908 | G | C | 1 | a0001c0001t0001g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.305-423C>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197024908 | |||||||
chr3:197024916 | G | C | 1 | a0001c0001t0001g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.305-431C>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197024916 | |||||||
chr3:197024917 | G | C | 1 | a0001c0001t0001g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.305-432C>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197024917 | |||||||
chr3:197024918 | A | T | 1 | a0001c0001t0001g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.305-433T>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197024918 | |||||||
chr3:197024919 | G | C | 1 | a0001c0001t0001g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.305-434C>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197024919 | |||||||
chr3:197024920 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.305-435G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197024920 | |||||||
chr3:197024921 | A | C | 1 | a0001c0001t0001g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.305-436T>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197024921 | |||||||
chr3:197024929 | C | T | 4 | a0001c0002t0010g0064 a0006c0007t0010g0022 a0006c0017t0007g0063 others(1): Show |
5 | HG01255.hp2 HG02055.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.305-444G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197024929 | |||||||
chr3:197024955 | G | C | 1 | a0001c0001t0001g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.305-470C>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197024955 | |||||||
chr3:197024957 | G | C | 1 | a0001c0001t0001g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.305-472C>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197024957 | |||||||
chr3:197024960 | G | T | 1 | a0001c0001t0001g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.305-475C>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197024960 | |||||||
chr3:197024962 | T | C | 1 | a0001c0001t0001g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.305-477A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197024962 | |||||||
chr3:197025070 | T | A | 1 | a0001c0001t0001g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.305-585A>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197025070 | |||||||
chr3:197025071 | G | C | 1 | a0001c0001t0001g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.305-586C>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197025071 | |||||||
chr3:197025072 | G | T | 1 | a0001c0001t0001g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.305-587C>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197025072 | |||||||
chr3:197025090 | A | ACCAACAA others(6): Show |
1 | a0001c0001t0001g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.305-606_305-605ins others(13): Show |
MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197025090 | |||||||
chr3:197025091 | G | C | 1 | a0001c0001t0001g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.305-606C>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197025091 | |||||||
chr3:197025220 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.305-735G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197025220 | |||||||
chr3:197025443 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.305-958G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197025443 | |||||||
chr3:197025508 | T | C | 1 | a0001c0001t0019g0240 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.305-1023A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197025508 | |||||||
chr3:197025576 | TG | T | 5 | a0001c0001t0001g0054 a0001c0001t0001g0253 a0001c0001t0003g0254 others(2): Show |
6 | HG01261.hp1 HG01928.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.304+1083delC | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197025576 | |||||||
chr3:197025577 | G | T | 1 | a0001c0002t0015g0170 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.304+1083C>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197025577 | |||||||
chr3:197025734 | C | T | 1 | a0001c0002t0004g0134 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.304+926G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197025734 | |||||||
chr3:197025993 | G | A | 1 | a0013c0021t0045g0122 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.304+667C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197025993 | |||||||
chr3:197026067 | T | C | 4 | a0001c0001t0007g0090 a0001c0001t0008g0103 a0001c0002t0004g0251 others(1): Show |
4 | HG03654.hp2 HG04199.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.304+593A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197026067 | |||||||
chr3:197026109 | G | T | 2 | a0001c0001t0008g0103 a0001c0003t0001g0102 |
2 | HG03654.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.304+551C>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197026109 | |||||||
chr3:197026249 | G | A | 1 | a0001c0001t0003g0288 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.304+411C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197026249 | |||||||
chr3:197026353 | C | A | 2 | a0002c0009t0021g0087 a0002c0009t0021g0088 |
2 | HG01884.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.304+307G>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197026353 | |||||||
chr3:197026374 | C | T | 1 | a0001c0001t0011g0165 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.304+286G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197026374 | |||||||
chr3:197026389 | G | A | 2 | a0001c0001t0002g0241 a0001c0002t0001g0242 |
2 | HG00438.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.304+271C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197026389 | |||||||
chr3:197026396 | C | T | 22 | a0001c0001t0001g0106 a0001c0001t0002g0105 a0001c0001t0005g0032 others(19): Show |
26 | HG00558.hp2 HG00609.hp2 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.304+264G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197026396 | |||||||
chr3:197026484 | T | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
172 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.304+176A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197026484 | |||||||
chr3:197026496 | C | G | 37 | a0001c0001t0001g0106 a0001c0001t0001g0132 a0001c0001t0002g0105 others(34): Show |
45 | HG00558.hp2 HG00609.hp2 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.304+164G>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197026496 | |||||||
chr3:197026571 | G | A | 37 | a0001c0001t0001g0106 a0001c0001t0001g0132 a0001c0001t0002g0105 others(34): Show |
43 | HG00558.hp2 HG00609.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.304+89C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 3/15 | chr3 | 197026571 | |||||||
chr3:197027035 | G | A | 81 | a0001c0001t0001g0100 a0001c0001t0001g0135 a0001c0001t0001g0138 others(78): Show |
107 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.205-276C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 2/15 | chr3 | 197027035 | |||||||
chr3:197027062 | C | T | 6 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0003t0005g0095 others(3): Show |
7 | HG01934.hp2 HG02280.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.205-303G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 2/15 | chr3 | 197027062 | |||||||
chr3:197027089 | C | T | 1 | a0001c0001t0036g0130 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.205-330G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 2/15 | chr3 | 197027089 | |||||||
chr3:197027104 | G | A | 3 | a0001c0002t0010g0064 a0006c0007t0010g0022 a0006c0017t0007g0063 |
4 | HG02055.hp2 HG02559.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.205-345C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 2/15 | chr3 | 197027104 | |||||||
chr3:197027209 | G | C | 1 | a0001c0001t0001g0100 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.205-450C>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 2/15 | chr3 | 197027209 | |||||||
chr3:197027585 | C | A | 3 | a0001c0001t0007g0090 a0001c0002t0004g0251 a0008c0008t0027g0028 |
4 | HG02015.hp2 HG02132.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+171G>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 2/15 | chr3 | 197027585 | |||||||
chr3:197027619 | C | G | 1 | a0001c0001t0011g0252 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.204+137G>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 2/15 | chr3 | 197027619 | |||||||
chr3:197027648 | G | A | 83 | a0001c0001t0001g0100 a0001c0001t0001g0135 a0001c0001t0001g0138 others(80): Show |
109 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.204+108C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 2/15 | chr3 | 197027648 | |||||||
chr3:197027948 | C | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(113): Show |
169 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.50-38G>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 1/15 | chr3 | 197027948 | |||||||
chr3:197027985 | C | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(103): Show |
157 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.50-75G>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 1/15 | chr3 | 197027985 | |||||||
chr3:197028071 | G | C | 25 | a0001c0001t0001g0106 a0001c0001t0002g0105 a0001c0001t0005g0032 others(22): Show |
29 | HG00558.hp2 HG00609.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.50-161C>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 1/15 | chr3 | 197028071 | |||||||
chr3:197028115 | A | G | 2 | a0001c0001t0014g0129 a0001c0003t0015g0128 |
2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.50-205T>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 1/15 | chr3 | 197028115 | |||||||
chr3:197028277 | C | T | 1 | a0001c0002t0013g0089 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.50-367G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 1/15 | chr3 | 197028277 | |||||||
chr3:197028466 | A | G | 2 | a0001c0001t0002g0250 a0007c0011t0008g0127 |
2 | HG00280.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.50-556T>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 1/15 | chr3 | 197028466 | |||||||
chr3:197028667 | C | T | 1 | a0001c0002t0001g0126 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.50-757G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 1/15 | chr3 | 197028667 | |||||||
chr3:197028812 | G | A | 7 | a0001c0001t0035g0120 a0001c0002t0001g0119 a0001c0002t0009g0033 others(4): Show |
10 | HG02027.hp2 HG03669.hp2 NA18964.hp2 others(7): Show |
intron_variant | MODIFIER | c.49+842C>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 1/15 | chr3 | 197028812 | |||||||
chr3:197028865 | C | G | 3 | a0001c0002t0002g0249 a0001c0002t0055g0248 a0001c0002t0056g0247 |
3 | HG02109.hp1 HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.49+789G>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 1/15 | chr3 | 197028865 | |||||||
chr3:197028866 | C | G | 3 | a0001c0002t0001g0125 a0001c0002t0026g0123 a0001c0002t0028g0124 |
3 | NA18942.hp2 NA19010.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.49+788G>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 1/15 | chr3 | 197028866 | |||||||
chr3:197028882 | G | T | 47 | a0001c0001t0001g0100 a0001c0001t0001g0106 a0001c0001t0002g0105 others(44): Show |
57 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.49+772C>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 1/15 | chr3 | 197028882 | |||||||
chr3:197028933 | C | A | 5 | a0001c0001t0005g0299 a0001c0001t0014g0300 a0001c0001t0047g0297 others(2): Show |
5 | HG01884.hp2 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+721G>T | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 1/15 | chr3 | 197028933 | |||||||
chr3:197029245 | G | C | 1 | a0001c0001t0006g0303 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.49+409C>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 1/15 | chr3 | 197029245 | |||||||
chr3:197029269 | T | C | 200 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(197): Show |
279 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.49+385A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 1/15 | chr3 | 197029269 | |||||||
chr3:197029300 | C | T | 231 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(228): Show |
319 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.49+354G>A | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 1/15 | chr3 | 197029300 | |||||||
chr3:197029405 | T | C | 2 | a0001c0014t0003g0304 a0001c0016t0011g0305 |
2 | HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.49+249A>G | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 1/15 | chr3 | 197029405 | |||||||
chr3:197029447 | T | G | 1 | a0001c0001t0018g0306 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.49+207A>C | MELTF | ENSG00000163975.14 | transcript | ENST00000296350.10 | protein_coding | 1/15 | chr3 | 197029447 |