Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 4211 |
|---|---|
| ensemblid | ENSG00000143995.20 |
| hgncid | 7000 |
| symbol | MEIS1 |
| name | Meis homeobox 1 |
| refseq_nuc | NM_002398.3 |
| refseq_prot | NP_002389.1 |
| ensembl_nuc | ENST00000272369.14 |
| ensembl_prot | ENSP00000272369.8 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 66435125 |
| end | 66573869 |
| strand | + |
| ver | v1.2 |
| region | chr2:66435125-66573869 |
| region5000 | chr2:66430125-66578869 |
| regionname0 | MEIS1_chr2_66435125_66573869 |
| regionname5000 | MEIS1_chr2_66430125_66578869 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 390 | 246 | 72 | 42 | 88 | 8 | 34 | 72 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1173 | 242 | 71 | 42 | 86 | 8 | 33 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| c0002 | 0/0 | 1173 | 2 | 0 | 0 | 2 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| c0003 | 0/0 | 1173 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| c0004 | 0/0 | 1173 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 3392 | 78 | 17 | 18 | 24 | 6 | 12 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0002 | 0/0 | 3394 | 50 | 10 | 10 | 28 | 1 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0003 | 0/0 | 3392 | 25 | 7 | 0 | 7 | 0 | 11 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0004 | 0/0 | 3393 | 17 | 3 | 4 | 8 | 0 | 2 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0005 | 1/0 | 3394 | 13 | 4 | 1 | 5 | 1 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0006 | 0/0 | 3395 | 10 | 3 | 0 | 5 | 0 | 2 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0007 | 0/0 | 3393 | 8 | 3 | 0 | 2 | 0 | 3 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0008 | 0/0 | 3394 | 5 | 0 | 4 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0009 | 0/0 | 3393 | 5 | 5 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0010 | 0/0 | 3392 | 4 | 2 | 2 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0011 | 0/0 | 3391 | 3 | 2 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0012 | 0/0 | 3394 | 2 | 2 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0013 | 0/0 | 3395 | 2 | 1 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0014 | 0/0 | 3394 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0015 | 0/0 | 3392 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0016 | 0/0 | 3392 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0017 | 0/0 | 3391 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0018 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0019 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0020 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0021 | 0/0 | 3392 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0022 | 0/0 | 3392 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0023 | 0/0 | 3392 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0024 | 0/0 | 3392 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0025 | 0/0 | 3394 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0026 | 0/0 | 3394 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0027 | 0/0 | 3394 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0028 | 0/0 | 3394 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0029 | 0/0 | 3394 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0030 | 0/0 | 3394 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0031 | 0/0 | 3394 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0032 | 0/0 | 3394 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0033 | 0/0 | 3394 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0034 | 0/0 | 3395 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0035 | 0/0 | 3392 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0036 | 0/0 | 3395 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| t0037 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0054 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0142 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1173 | 242 | 71 | 42 | 86 | 8 | 33 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0002 | 0/0 | 1173 | 2 | 0 | 0 | 2 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0003 | 0/0 | 1173 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0004 | 0/0 | 1173 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4564 | 75 | 16 | 18 | 23 | 6 | 11 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0002 | 0/0 | 4566 | 50 | 10 | 10 | 28 | 1 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0003 | 0/0 | 4564 | 25 | 7 | 0 | 7 | 0 | 11 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0004 | 0/0 | 4565 | 16 | 3 | 4 | 7 | 0 | 2 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0005 | 1/0 | 4566 | 13 | 4 | 1 | 5 | 1 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0006 | 0/0 | 4567 | 10 | 3 | 0 | 5 | 0 | 2 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0007 | 0/0 | 4565 | 8 | 3 | 0 | 2 | 0 | 3 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0008 | 0/0 | 4566 | 5 | 0 | 4 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0009 | 0/0 | 4565 | 5 | 5 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0010 | 0/0 | 4564 | 4 | 2 | 2 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0011 | 0/0 | 4563 | 3 | 2 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0012 | 0/0 | 4566 | 2 | 2 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0013 | 0/0 | 4567 | 2 | 1 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0014 | 0/0 | 4566 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0015 | 0/0 | 4564 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0016 | 0/0 | 4564 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0017 | 0/0 | 4563 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0018 | 0/0 | 4563 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0019 | 0/0 | 4563 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0020 | 0/0 | 4563 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0021 | 0/0 | 4564 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0022 | 0/0 | 4564 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0023 | 0/0 | 4564 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0024 | 0/0 | 4564 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0025 | 0/0 | 4566 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0026 | 0/0 | 4566 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0027 | 0/0 | 4566 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0028 | 0/0 | 4566 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0029 | 0/0 | 4566 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0030 | 0/0 | 4566 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0031 | 0/0 | 4566 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0032 | 0/0 | 4566 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0033 | 0/0 | 4566 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0034 | 0/0 | 4567 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0035 | 0/0 | 4564 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0036 | 0/0 | 4567 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0001t0037 | 0/0 | 4565 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0002t0001 | 0/0 | 4564 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0002t0004 | 0/0 | 4565 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0003t0001 | 0/0 | 4564 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| a0001c0004t0001 | 0/0 | 4564 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | copy fasta | chr2 | 66430125 | 66578869 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0142 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0003g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0004g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0004g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0005g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0005g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0005g0054 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0005g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0005g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0006g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0006g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0006g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0006g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0006g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0006g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0006g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0007g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0007g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0007g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0007g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0007g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0007g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0007g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0008g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0008g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0008g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0008g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0008g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0009g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0009g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0009g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0009g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0009g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0010g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0010g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0010g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0010g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0011g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0011g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0011g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0012g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0012g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0013g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0013g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0014g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0015g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0016g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0017g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0018g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0019g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0020g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0021g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0022g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0023g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0024g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0025g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0026g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0027g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0028g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0029g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0030g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0031g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0032g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0033g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0034g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0035g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0036g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0001t0037g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0002t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| a0001c0004t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0187 | EUR | GBR | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | FIN | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG00280 | hp2 | a0001 | c0001 | t0005 | g0065 | EUR | FIN | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | FIN | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | FIN | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG00408 | hp2 | a0001 | c0001 | t0014 | g0049 | EAS | CHS | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG00544 | hp1 | a0001 | c0001 | t0006 | g0078 | EAS | CHS | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0114 | EAS | CHS | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | CHS | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG00621 | hp2 | a0001 | c0001 | t0008 | g0050 | EAS | CHS | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG00642 | hp2 | a0001 | c0001 | t0008 | g0086 | AMR | PUR | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | CHS | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | CHS | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0195 | AMR | PUR | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG00733 | hp2 | a0001 | c0001 | t0004 | g0097 | AMR | PUR | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG00738 | hp1 | a0001 | c0001 | t0032 | g0016 | AMR | PUR | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG01109 | hp1 | a0001 | c0001 | t0011 | g0005 | AMR | PUR | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG01167 | hp1 | a0001 | c0001 | t0008 | g0072 | AMR | PUR | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG01167 | hp2 | a0001 | c0001 | t0010 | g0092 | AMR | PUR | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG01243 | hp2 | a0001 | c0001 | t0035 | g0199 | AMR | PUR | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG01258 | hp2 | a0001 | c0001 | t0008 | g0051 | AMR | CLM | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | CLM | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0152 | AMR | CLM | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | CLM | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0084 | AMR | CLM | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0208 | AMR | PEL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG01978 | hp2 | a0001 | c0001 | t0008 | g0044 | AMR | PEL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | PEL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0209 | AMR | PEL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02027 | hp1 | a0001 | c0001 | t0013 | g0052 | EAS | KHV | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | ACB | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02055 | hp2 | a0001 | c0001 | t0021 | g0183 | AFR | ACB | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | KHV | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | KHV | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02083 | hp1 | a0001 | c0001 | t0006 | g0056 | EAS | KHV | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0146 | EAS | KHV | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | ACB | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02145 | hp2 | a0001 | c0001 | t0023 | g0002 | AFR | ACB | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | CDX | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CDX | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0139 | AFR | ACB | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0228 | AFR | ACB | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02258 | hp2 | a0001 | c0001 | t0010 | g0118 | AFR | ACB | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02280 | hp2 | a0001 | c0001 | t0009 | g0242 | AFR | ACB | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0151 | AMR | PEL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PEL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | GWD | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | GWD | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02717 | hp1 | a0001 | c0001 | t0009 | g0246 | AFR | GWD | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0202 | AFR | GWD | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0196 | SAS | PJL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0212 | AFR | GWD | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0233 | AFR | GWD | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | GWD | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02818 | hp2 | a0001 | c0001 | t0006 | g0081 | AFR | GWD | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02886 | hp1 | a0001 | c0001 | t0036 | g0245 | AFR | GWD | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02886 | hp2 | a0001 | c0001 | t0027 | g0211 | AFR | GWD | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02895 | hp1 | a0001 | c0001 | t0009 | g0241 | AFR | GWD | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02895 | hp2 | a0001 | c0001 | t0011 | g0219 | AFR | GWD | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02897 | hp1 | a0001 | c0001 | t0006 | g0027 | AFR | GWD | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02897 | hp2 | a0001 | c0001 | t0011 | g0220 | AFR | GWD | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0237 | AFR | ESN | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0029 | AFR | ESN | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02976 | hp1 | a0001 | c0001 | t0024 | g0088 | AFR | ESN | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02976 | hp2 | a0001 | c0001 | t0019 | g0095 | AFR | ESN | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03041 | hp1 | a0001 | c0001 | t0030 | g0014 | AFR | GWD | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0244 | AFR | GWD | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0201 | AFR | MSL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03130 | hp1 | a0001 | c0001 | t0018 | g0177 | AFR | ESN | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | ESN | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03139 | hp1 | a0001 | c0001 | t0009 | g0243 | AFR | ESN | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0227 | AFR | ESN | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03195 | hp1 | a0001 | c0001 | t0010 | g0221 | AFR | ESN | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03195 | hp2 | a0001 | c0001 | t0013 | g0028 | AFR | ESN | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03225 | hp1 | a0001 | c0001 | t0016 | g0122 | AFR | MSL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0026 | AFR | MSL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0042 | SAS | PJL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03453 | hp1 | a0001 | c0001 | t0037 | g0020 | AFR | MSL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0236 | AFR | MSL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0215 | AFR | MSL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0155 | SAS | PJL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03491 | hp1 | a0001 | c0001 | t0007 | g0163 | SAS | PJL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0171 | SAS | PJL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0188 | SAS | PJL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0090 | SAS | PJL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0089 | AFR | ESN | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03540 | hp1 | a0001 | c0001 | t0012 | g0045 | AFR | GWD | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0230 | AFR | GWD | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03579 | hp2 | a0001 | c0001 | t0020 | g0015 | AFR | MSL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0004 | SAS | PJL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | STU | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03688 | hp2 | a0001 | c0001 | t0006 | g0025 | SAS | STU | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0126 | SAS | PJL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0127 | SAS | BEB | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03927 | hp1 | a0001 | c0001 | t0031 | g0057 | SAS | BEB | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | BEB | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0125 | SAS | BEB | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG04184 | hp1 | a0001 | c0001 | t0007 | g0120 | SAS | BEB | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0136 | SAS | BEB | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG04204 | hp2 | a0001 | c0001 | t0006 | g0058 | SAS | STU | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0106 | SAS | STU | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG04228 | hp2 | a0001 | c0001 | t0007 | g0102 | SAS | STU | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | YRI | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | YRI | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | YRI | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18941 | hp1 | a0001 | c0001 | t0005 | g0085 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18945 | hp1 | a0001 | c0001 | t0017 | g0168 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0112 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18959 | hp1 | a0001 | c0001 | t0006 | g0066 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0174 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18975 | hp2 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18985 | hp2 | a0001 | c0001 | t0025 | g0024 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18989 | hp1 | a0001 | c0002 | t0004 | g0131 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18990 | hp2 | a0001 | c0001 | t0005 | g0080 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18995 | hp1 | a0001 | c0001 | t0007 | g0109 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0173 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19006 | hp2 | a0001 | c0001 | t0006 | g0033 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0226 | AFR | LWK | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | LWK | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | LWK | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19043 | hp2 | a0001 | c0001 | t0012 | g0205 | AFR | LWK | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19063 | hp1 | a0001 | c0001 | t0006 | g0204 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0175 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19064 | hp2 | a0001 | c0001 | t0005 | g0055 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19068 | hp2 | a0001 | c0001 | t0005 | g0077 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19077 | hp1 | a0001 | c0001 | t0007 | g0239 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19077 | hp2 | a0001 | c0001 | t0034 | g0087 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19081 | hp1 | a0001 | c0001 | t0033 | g0073 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19084 | hp1 | a0001 | c0001 | t0015 | g0147 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0213 | AFR | YRI | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA19240 | hp2 | a0001 | c0001 | t0029 | g0018 | AFR | YRI | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | ASW | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA20129 | hp2 | a0001 | c0004 | t0001 | g0124 | AFR | ASW | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0046 | EUR | TSI | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0192 | EUR | TSI | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA20905 | hp1 | a0001 | c0003 | t0001 | g0141 | SAS | GIH | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA20905 | hp2 | a0001 | c0001 | t0026 | g0240 | SAS | GIH | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG01123 | hp1 | a0001 | c0001 | t0010 | g0115 | AMR | CLM | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02486 | hp1 | a0001 | c0001 | t0022 | g0186 | AFR | ACB | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0023 | AFR | ACB | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0218 | AFR | MSL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0140 | AFR | MSL | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | USA | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | USA | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18955 | hp1 | a0001 | c0001 | t0028 | g0061 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0142 | REF | REF | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0005 | g0054 | REF | REF | MEIS1_chr2_66430125_66578869 | MEIS1 | chr2 | 66430125 | 66578869 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:66464216
|
G | A | 1 | a0001c0003 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.738G>A | p.Glu246Glu | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/13 | 1470/4566 | 738/1173 | 246/390 | chr2 | 66464216 | ||
| chr2:66567468
|
G | T | 1 | a0001c0002 | 2 | NA18940.hp2 NA18989.hp1 |
synonymous_variant | LOW | c.981G>T | p.Arg327Arg | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 10/13 | 1713/4566 | 981/1173 | 327/390 | chr2 | 66567468 | ||
| chr2:66568725
|
C | T | 1 | a0001c0004 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.1083C>T | p.Asp361Asp | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 11/13 | 1815/4566 | 1083/1173 | 361/390 | chr2 | 66568725 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:66435179
|
G | A | 2 | a0001c0001t0008a0001c0001t0014 | 6 | HG00408.hp2 HG00621.hp2 HG00642.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-678G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 1/13 | 678 | chr2 | 66435179 | |||||
| chr2:66435238
|
T | A | 1 | a0001c0001t0015 | 1 | NA19084.hp1 | 5_prime_UTR_variant | MODIFIER | c.-619T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 1/13 | 619 | chr2 | 66435238 | |||||
| chr2:66435239
|
T | C | 1 | a0001c0001t0016 | 1 | HG03225.hp1 | 5_prime_UTR_variant | MODIFIER | c.-618T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 1/13 | 618 | chr2 | 66435239 | |||||
| chr2:66435601
|
C | CT | 4 | a0001c0001t0009a0001c0001t0035a0001c0001t0036others(1): Show | 8 | HG01243.hp2 HG02280.hp2 HG02717.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-248dupT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 1/13 | 247 | INFO_REALIGN_3_PRIME | chr2 | 66435601 | ||||
| chr2:66435655
|
C | T | 1 | a0001c0001t0037 | 1 | HG03453.hp1 | 5_prime_UTR_variant | MODIFIER | c.-202C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 1/13 | 202 | chr2 | 66435655 | |||||
| chr2:66435743
|
C | CT | 3 | a0001c0001t0006a0001c0001t0013a0001c0001t0034 | 13 | HG00544.hp1 HG02027.hp1 HG02083.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-90dupT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 1/13 | 89 | INFO_REALIGN_3_PRIME | chr2 | 66435743 | ||||
| chr2:66435743
|
CT | C | 3 | a0001c0001t0004a0001c0001t0007a0001c0002t0004 | 25 | HG00544.hp2 HG00733.hp1 HG00733.hp2 others(22): Show |
5_prime_UTR_variant | MODIFIER | c.-90delT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 1/13 | 90 | INFO_REALIGN_3_PRIME | chr2 | 66435743 | ||||
| chr2:66435743
|
CTT | C | 14 | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(11): Show | 119 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(116): Show |
5_prime_UTR_variant | MODIFIER | c.-91_-90delTT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 1/13 | 90 | INFO_REALIGN_3_PRIME | chr2 | 66435743 | ||||
| chr2:66435743
|
CTTT | C | 6 | a0001c0001t0011a0001c0001t0017a0001c0001t0018others(3): Show | 8 | HG01109.hp1 HG01243.hp2 HG02895.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-92_-90delTTT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 1/13 | 90 | INFO_REALIGN_3_PRIME | chr2 | 66435743 | ||||
| chr2:66571522
|
C | T | 3 | a0001c0001t0010a0001c0001t0012a0001c0001t0016 | 7 | HG01123.hp1 HG01167.hp2 HG02258.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*314C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 13/13 | 2414 | chr2 | 66571522 | |||||
| chr2:66571799
|
T | A | 1 | a0001c0001t0025 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*591T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 13/13 | 2691 | chr2 | 66571799 | |||||
| chr2:66571800
|
A | T | 1 | a0001c0001t0024 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*592A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 13/13 | 2692 | chr2 | 66571800 | |||||
| chr2:66571997
|
C | T | 1 | a0001c0001t0033 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*789C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 13/13 | 2889 | chr2 | 66571997 | |||||
| chr2:66572262
|
A | G | 2 | a0001c0001t0023a0001c0001t0032 | 2 | HG00738.hp1 HG02145.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1054A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 13/13 | 3154 | chr2 | 66572262 | |||||
| chr2:66572854
|
C | T | 2 | a0001c0001t0022a0001c0001t0031 | 2 | HG02486.hp1 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1646C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 13/13 | 3746 | chr2 | 66572854 | |||||
| chr2:66572855
|
A | C | 1 | a0001c0001t0030 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1647A>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 13/13 | 3747 | chr2 | 66572855 | |||||
| chr2:66572946
|
G | A | 1 | a0001c0001t0026 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1738G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 13/13 | 3838 | chr2 | 66572946 | |||||
| chr2:66573184
|
T | G | 1 | a0001c0001t0027 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1976T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 13/13 | 4076 | chr2 | 66573184 | |||||
| chr2:66573435
|
C | T | 3 | a0001c0001t0020a0001c0001t0021a0001c0001t0029 | 3 | HG02055.hp2 HG03579.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2227C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 13/13 | 4327 | chr2 | 66573435 | |||||
| chr2:66573568
|
T | C | 3 | a0001c0001t0017a0001c0001t0028a0001c0001t0034 | 3 | NA18945.hp1 NA18955.hp1 NA19077.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2360T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 13/13 | 4460 | chr2 | 66573568 | |||||
| chr2:66573709
|
A | G | 1 | a0001c0001t0011 | 3 | HG01109.hp1 HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2501A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 13/13 | 4601 | chr2 | 66573709 | |||||
| chr2:66573842
|
C | A | 28 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(25): Show | 189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
3_prime_UTR_variant | MODIFIER | c.*2634C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 13/13 | 4734 | chr2 | 66573842 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:66436009
|
A | T | 6 | a0001c0001t0009g0241a0001c0001t0009g0242a0001c0001t0009g0243others(3): Show | 6 | HG02280.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+141A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 1/12 | chr2 | 66436009 | ||||||
| chr2:66436060
|
A | G | 1 | a0001c0001t0026g0240 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.12+192A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 1/12 | chr2 | 66436060 | ||||||
| chr2:66436144
|
T | A | 10 | a0001c0001t0001g0001a0001c0001t0003g0003a0001c0001t0004g0004others(7): Show | 10 | HG02145.hp2 HG02280.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.12+276T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 1/12 | chr2 | 66436144 | ||||||
| chr2:66436145
|
A | T | 1 | a0001c0001t0007g0239 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.12+277A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 1/12 | chr2 | 66436145 | ||||||
| chr2:66436340
|
A | T | 1 | a0001c0001t0001g0238 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.12+472A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 1/12 | chr2 | 66436340 | ||||||
| chr2:66436380
|
A | G | 1 | a0001c0001t0004g0004 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.12+512A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 1/12 | chr2 | 66436380 | ||||||
| chr2:66436765
|
C | T | 7 | a0001c0001t0002g0231a0001c0001t0002g0232a0001c0001t0002g0233others(4): Show | 7 | HG01433.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.12+897C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 1/12 | chr2 | 66436765 | ||||||
| chr2:66436872
|
G | GT | 141 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0098others(138): Show | 141 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.13-849dupT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 66436872 | |||||
| chr2:66436872
|
G | GTT | 5 | a0001c0001t0002g0230a0001c0001t0003g0226a0001c0001t0003g0227others(2): Show | 5 | HG02056.hp1 HG02257.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-850_13-849dupTT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 66436872 | |||||
| chr2:66437282
|
CT | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0094a0001c0001t0001g0096others(9): Show | 12 | HG00280.hp1 HG01070.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.13-439delT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 66437282 | |||||
| chr2:66437619
|
C | T | 21 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0214others(18): Show | 21 | HG01109.hp2 HG01167.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.13-118C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 1/12 | chr2 | 66437619 | ||||||
| chr2:66437678
|
G | A | 1 | a0001c0001t0004g0004 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.13-59G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 1/12 | chr2 | 66437678 | ||||||
| chr2:66437678
|
G | C | 1 | a0001c0001t0002g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.13-59G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 1/12 | chr2 | 66437678 | ||||||
| chr2:66438014
|
T | C | 137 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0091others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.239+51T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 2/12 | chr2 | 66438014 | ||||||
| chr2:66438273
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0002g0230 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.239+310C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 2/12 | chr2 | 66438273 | ||||||
| chr2:66438642
|
T | C | 11 | a0001c0001t0001g0001a0001c0001t0004g0004a0001c0001t0009g0241others(8): Show | 11 | HG01109.hp1 HG01243.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.239+679T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 2/12 | chr2 | 66438642 | ||||||
| chr2:66438798
|
T | A | 1 | a0001c0001t0001g0001 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.239+835T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 2/12 | chr2 | 66438798 | ||||||
| chr2:66438840
|
A | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0197a0001c0001t0001g0198others(2): Show | 5 | HG01258.hp1 HG02738.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.239+877A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 2/12 | chr2 | 66438840 | ||||||
| chr2:66438841
|
AT | A | 5 | a0001c0001t0001g0217a0001c0001t0004g0218a0001c0001t0009g0242others(2): Show | 5 | HG01109.hp2 HG02280.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.239+879delT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 2/12 | chr2 | 66438841 | ||||||
| chr2:66438842
|
T | A | 7 | a0001c0001t0001g0096a0001c0001t0001g0214a0001c0001t0001g0216others(4): Show | 7 | HG01243.hp1 HG02895.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.239+879T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 2/12 | chr2 | 66438842 | ||||||
| chr2:66438965
|
C | G | 5 | a0001c0001t0009g0242a0001c0001t0009g0243a0001c0001t0009g0244others(2): Show | 5 | HG02280.hp2 HG02717.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.240-878C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 2/12 | chr2 | 66438965 | ||||||
| chr2:66439065
|
TTTC | T | 131 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0091others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.240-763_240-761del others(3): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 66439065 | |||||
| chr2:66439080
|
CT | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0096a0001c0001t0002g0017others(9): Show | 12 | HG00738.hp1 HG01243.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.240-747delT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 66439080 | |||||
| chr2:66439096
|
T | C | 2 | a0001c0001t0011g0005a0001c0001t0020g0015 | 2 | HG01109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.240-747T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 2/12 | chr2 | 66439096 | ||||||
| chr2:66439097
|
C | T | 2 | a0001c0001t0011g0005a0001c0001t0020g0015 | 2 | HG01109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.240-746C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 2/12 | chr2 | 66439097 | ||||||
| chr2:66439215
|
G | C | 1 | a0001c0001t0003g0213 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.240-628G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 2/12 | chr2 | 66439215 | ||||||
| chr2:66439456
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0004g0004 | 2 | HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.240-387G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 2/12 | chr2 | 66439456 | ||||||
| chr2:66439730
|
A | G | 2 | a0001c0001t0002g0210a0001c0001t0027g0211 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.240-113A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 2/12 | chr2 | 66439730 | ||||||
| chr2:66440054
|
C | T | 133 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0091others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.381+70C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 3/12 | chr2 | 66440054 | ||||||
| chr2:66440068
|
A | AAC | 8 | a0001c0001t0005g0029a0001c0001t0006g0025a0001c0001t0006g0026others(5): Show | 8 | HG02897.hp1 HG02965.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+107_381+108dup others(2): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 66440068 | |||||
| chr2:66440068
|
A | AACAC | 2 | a0001c0001t0002g0210a0001c0001t0027g0211 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.381+105_381+108dup others(4): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 66440068 | |||||
| chr2:66440068
|
A | AACACACA others(1): Show |
3 | a0001c0001t0001g0194a0001c0001t0003g0196a0001c0001t0004g0195 | 3 | HG00733.hp1 HG01070.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.381+101_381+108dup others(8): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 66440068 | |||||
| chr2:66440068
|
A | AACACACA others(3): Show |
1 | a0001c0001t0001g0193 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.381+99_381+108dupA others(9): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 66440068 | |||||
| chr2:66440068
|
A | AACACACA others(5): Show |
19 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0182others(16): Show | 19 | HG00099.hp1 HG00741.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.381+97_381+108dupA others(11): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 66440068 | |||||
| chr2:66440068
|
A | AACACACA others(7): Show |
56 | a0001c0001t0001g0012a0001c0001t0001g0098a0001c0001t0001g0099others(53): Show | 56 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.381+95_381+108dupA others(13): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 66440068 | |||||
| chr2:66440068
|
A | AACACACA others(9): Show |
41 | a0001c0001t0001g0011a0001c0001t0001g0096a0001c0001t0001g0116others(38): Show | 41 | HG00408.hp1 HG02004.hp1 HG02145.hp2 others(38): Show |
intron_variant | MODIFIER | c.381+93_381+108dupA others(15): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 66440068 | |||||
| chr2:66440068
|
A | AACACACA others(11): Show |
28 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0094others(25): Show | 28 | HG00280.hp1 HG00544.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.381+91_381+108dupA others(17): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 66440068 | |||||
| chr2:66440068
|
A | AACACACA others(13): Show |
4 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0003g0010others(1): Show | 4 | HG02683.hp2 HG03239.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+89_381+108dupA others(19): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 66440068 | |||||
| chr2:66440068
|
A | AACACACA others(15): Show |
3 | a0001c0001t0001g0105a0001c0001t0003g0213a0001c0001t0010g0221 | 3 | HG01123.hp2 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.381+87_381+108dupA others(21): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 66440068 | |||||
| chr2:66440068
|
A | AACACACA others(17): Show |
2 | a0001c0001t0001g0104a0001c0001t0035g0199 | 2 | HG01243.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.381+85_381+108dupA others(23): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 66440068 | |||||
| chr2:66440092
|
C | CACACACA others(10): Show |
1 | a0001c0001t0010g0115 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.381+108_381+109ins others(17): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 3/12 | chr2 | 66440092 | ||||||
| chr2:66440166
|
C | T | 11 | a0001c0001t0001g0001a0001c0001t0004g0004a0001c0001t0009g0241others(8): Show | 11 | HG01109.hp1 HG01243.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.381+182C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 3/12 | chr2 | 66440166 | ||||||
| chr2:66440501
|
C | A | 2 | a0001c0001t0011g0005a0001c0001t0020g0015 | 2 | HG01109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.382-61C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 3/12 | chr2 | 66440501 | ||||||
| chr2:66440711
|
C | A | 2 | a0001c0001t0011g0005a0001c0001t0020g0015 | 2 | HG01109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.432+99C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 4/12 | chr2 | 66440711 | ||||||
| chr2:66440755
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0002g0230 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.432+143C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 4/12 | chr2 | 66440755 | ||||||
| chr2:66440766
|
T | G | 6 | a0001c0001t0002g0200a0001c0001t0002g0203a0001c0001t0002g0212others(3): Show | 6 | HG02145.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.432+154T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 4/12 | chr2 | 66440766 | ||||||
| chr2:66440843
|
G | GT | 7 | a0001c0001t0002g0231a0001c0001t0002g0232a0001c0001t0002g0233others(4): Show | 7 | HG01433.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.432+237dupT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 66440843 | |||||
| chr2:66440876
|
T | C | 1 | a0001c0001t0002g0030 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.432+264T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 4/12 | chr2 | 66440876 | ||||||
| chr2:66440884
|
G | A | 1 | a0001c0001t0030g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.432+272G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 4/12 | chr2 | 66440884 | ||||||
| chr2:66440969
|
C | T | 1 | a0001c0001t0007g0102 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.432+357C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 4/12 | chr2 | 66440969 | ||||||
| chr2:66440979
|
C | T | 1 | a0001c0001t0034g0087 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.432+367C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 4/12 | chr2 | 66440979 | ||||||
| chr2:66441177
|
A | G | 132 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0091others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.433-237A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 4/12 | chr2 | 66441177 | ||||||
| chr2:66441268
|
G | A | 2 | a0001c0001t0011g0005a0001c0001t0020g0015 | 2 | HG01109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.433-146G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 4/12 | chr2 | 66441268 | ||||||
| chr2:66441941
|
C | T | 1 | a0001c0001t0008g0086 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.483+477C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 5/12 | chr2 | 66441941 | ||||||
| chr2:66441982
|
C | T | 4 | a0001c0001t0002g0210a0001c0001t0007g0228a0001c0001t0012g0205others(1): Show | 4 | HG02257.hp2 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+518C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 5/12 | chr2 | 66441982 | ||||||
| chr2:66442242
|
T | C | 1 | a0001c0001t0029g0018 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.484-660T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 5/12 | chr2 | 66442242 | ||||||
| chr2:66442245
|
T | A | 1 | a0001c0001t0001g0116 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.484-657T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 5/12 | chr2 | 66442245 | ||||||
| chr2:66442264
|
TTTTTGTA others(7): Show |
T | 12 | a0001c0001t0001g0012a0001c0001t0001g0104a0001c0001t0001g0105others(9): Show | 12 | HG00099.hp2 HG00733.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.484-637_484-624del others(14): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 5/12 | chr2 | 66442264 | ||||||
| chr2:66442270
|
T | TA | 12 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0034others(9): Show | 12 | HG02280.hp2 HG02717.hp1 HG02976.hp1 others(9): Show |
intron_variant | MODIFIER | c.484-608dupA | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 66442270 | |||||
| chr2:66442270
|
TA | T | 93 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0091others(90): Show | 93 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.484-608delA | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 66442270 | |||||
| chr2:66442270
|
TAA | T | 14 | a0001c0001t0001g0138a0001c0001t0001g0176a0001c0001t0001g0178others(11): Show | 14 | HG02257.hp1 HG02280.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.484-609_484-608del others(2): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 66442270 | |||||
| chr2:66442279
|
A | C | 12 | a0001c0001t0001g0012a0001c0001t0001g0104a0001c0001t0001g0105others(9): Show | 12 | HG00099.hp2 HG00733.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.484-623A>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 5/12 | chr2 | 66442279 | ||||||
| chr2:66442837
|
A | C | 3 | a0001c0001t0004g0101a0001c0001t0004g0174a0001c0001t0004g0175 | 3 | NA18959.hp2 NA18975.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.484-65A>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 5/12 | chr2 | 66442837 | ||||||
| chr2:66443067
|
C | A | 1 | a0001c0001t0026g0240 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.630+19C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66443067 | ||||||
| chr2:66443080
|
A | G | 1 | a0001c0001t0005g0084 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.630+32A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66443080 | ||||||
| chr2:66443167
|
A | C | 2 | a0001c0001t0002g0082a0001c0001t0002g0083 | 2 | NA18968.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.630+119A>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66443167 | ||||||
| chr2:66443186
|
T | A | 2 | a0001c0001t0011g0005a0001c0001t0020g0015 | 2 | HG01109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.630+138T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66443186 | ||||||
| chr2:66443360
|
G | A | 2 | a0001c0001t0001g0091a0001c0001t0003g0090 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.630+312G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66443360 | ||||||
| chr2:66443498
|
T | C | 1 | a0001c0001t0019g0095 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.630+450T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66443498 | ||||||
| chr2:66443670
|
G | A | 1 | a0001c0001t0029g0018 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.630+622G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66443670 | ||||||
| chr2:66443797
|
G | A | 1 | a0001c0001t0007g0120 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.630+749G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66443797 | ||||||
| chr2:66443844
|
C | A | 123 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0091others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.630+796C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66443844 | ||||||
| chr2:66444104
|
G | C | 1 | a0001c0001t0001g0111 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.630+1056G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66444104 | ||||||
| chr2:66444187
|
A | T | 1 | a0001c0001t0035g0199 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.630+1139A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66444187 | ||||||
| chr2:66444223
|
C | T | 1 | a0001c0001t0006g0081 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.630+1175C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66444223 | ||||||
| chr2:66444301
|
T | A | 1 | a0001c0001t0001g0180 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.630+1253T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66444301 | ||||||
| chr2:66444702
|
C | T | 3 | a0001c0001t0011g0005a0001c0001t0020g0015a0001c0001t0021g0183 | 3 | HG01109.hp1 HG02055.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.630+1654C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66444702 | ||||||
| chr2:66444720
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0004g0004 | 2 | HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.630+1672G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66444720 | ||||||
| chr2:66444726
|
C | A | 146 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.630+1678C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66444726 | ||||||
| chr2:66445229
|
TGGGCTCG others(16): Show |
T | 1 | a0001c0001t0005g0019 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.630+2188_630+2210d others(25): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 66445229 | |||||
| chr2:66445281
|
G | A | 1 | a0001c0001t0007g0102 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.630+2233G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66445281 | ||||||
| chr2:66445416
|
G | A | 3 | a0001c0001t0002g0203a0001c0001t0005g0201a0001c0001t0005g0202 | 3 | HG02145.hp1 HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.630+2368G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66445416 | ||||||
| chr2:66445564
|
G | A | 1 | a0001c0001t0002g0040 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.630+2516G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66445564 | ||||||
| chr2:66445605
|
T | C | 5 | a0001c0001t0005g0029a0001c0001t0006g0025a0001c0001t0006g0026others(2): Show | 5 | HG02897.hp1 HG02965.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.630+2557T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66445605 | ||||||
| chr2:66445691
|
C | A | 1 | a0001c0001t0006g0025 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.630+2643C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66445691 | ||||||
| chr2:66445841
|
CTATT | C | 3 | a0001c0001t0002g0203a0001c0001t0005g0201a0001c0001t0005g0202 | 3 | HG02145.hp1 HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.630+2807_630+2810d others(6): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 66445841 | |||||
| chr2:66445848
|
T | C | 1 | a0001c0001t0030g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.630+2800T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66445848 | ||||||
| chr2:66445859
|
T | A | 1 | a0001c0001t0001g0107 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.630+2811T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66445859 | ||||||
| chr2:66445949
|
G | C | 1 | a0001c0001t0030g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.630+2901G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66445949 | ||||||
| chr2:66446038
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.630+2990G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66446038 | ||||||
| chr2:66446059
|
C | A | 1 | a0001c0001t0001g0094 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.630+3011C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66446059 | ||||||
| chr2:66446192
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.630+3144A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66446192 | ||||||
| chr2:66446304
|
A | G | 1 | a0001c0001t0005g0080 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.630+3256A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66446304 | ||||||
| chr2:66446730
|
A | C | 130 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0091others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.630+3682A>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66446730 | ||||||
| chr2:66446865
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.630+3817G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66446865 | ||||||
| chr2:66446949
|
T | A | 1 | a0001c0001t0002g0200 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.630+3901T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66446949 | ||||||
| chr2:66446979
|
CT | C | 4 | a0001c0001t0001g0001a0001c0001t0004g0004a0001c0001t0030g0014others(1): Show | 4 | HG01243.hp2 HG03041.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.630+3934delT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 66446979 | |||||
| chr2:66446983
|
G | A | 2 | a0001c0001t0002g0231a0001c0001t0002g0232 | 2 | HG01433.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.630+3935G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66446983 | ||||||
| chr2:66447016
|
A | C | 1 | a0001c0001t0004g0171 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.630+3968A>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66447016 | ||||||
| chr2:66447032
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.630+3984G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66447032 | ||||||
| chr2:66447313
|
G | A | 3 | a0001c0001t0011g0005a0001c0001t0020g0015a0001c0001t0021g0183 | 3 | HG01109.hp1 HG02055.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.630+4265G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66447313 | ||||||
| chr2:66447520
|
A | G | 2 | a0001c0001t0001g0001a0001c0001t0004g0004 | 2 | HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.630+4472A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66447520 | ||||||
| chr2:66447707
|
A | C | 2 | a0001c0001t0011g0005a0001c0001t0020g0015 | 2 | HG01109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.630+4659A>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66447707 | ||||||
| chr2:66447810
|
G | A | 2 | a0001c0001t0030g0014a0001c0001t0035g0199 | 2 | HG01243.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.630+4762G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66447810 | ||||||
| chr2:66448009
|
C | T | 1 | a0001c0001t0004g0004 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.630+4961C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66448009 | ||||||
| chr2:66448474
|
C | T | 1 | a0001c0001t0004g0097 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.630+5426C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66448474 | ||||||
| chr2:66448629
|
A | G | 1 | a0001c0001t0001g0001 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.630+5581A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66448629 | ||||||
| chr2:66448839
|
A | G | 1 | a0001c0001t0021g0183 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.630+5791A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66448839 | ||||||
| chr2:66448965
|
TATG | T | 3 | a0001c0001t0011g0005a0001c0001t0020g0015a0001c0001t0021g0183 | 3 | HG01109.hp1 HG02055.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.630+5920_630+5922d others(5): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 66448965 | |||||
| chr2:66448994
|
A | G | 8 | a0001c0001t0002g0034a0001c0001t0002g0074a0001c0001t0002g0075others(5): Show | 8 | HG00544.hp1 HG02056.hp2 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.630+5946A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66448994 | ||||||
| chr2:66449098
|
C | T | 1 | a0001c0001t0035g0199 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.630+6050C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66449098 | ||||||
| chr2:66449235
|
G | C | 150 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0022others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.630+6187G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66449235 | ||||||
| chr2:66449383
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.630+6335A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66449383 | ||||||
| chr2:66449423
|
G | T | 1 | a0001c0001t0033g0073 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.630+6375G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66449423 | ||||||
| chr2:66449448
|
T | A | 1 | a0001c0001t0005g0029 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.630+6400T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66449448 | ||||||
| chr2:66449676
|
G | A | 2 | a0001c0001t0007g0140a0001c0001t0012g0205 | 2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.630+6628G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66449676 | ||||||
| chr2:66449705
|
A | G | 1 | a0001c0001t0003g0136 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.630+6657A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66449705 | ||||||
| chr2:66449717
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.630+6669G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66449717 | ||||||
| chr2:66449860
|
A | G | 1 | a0001c0001t0006g0081 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.630+6812A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66449860 | ||||||
| chr2:66450399
|
G | C | 131 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0091others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.630+7351G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66450399 | ||||||
| chr2:66450420
|
A | G | 1 | a0001c0001t0035g0199 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.630+7372A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66450420 | ||||||
| chr2:66450508
|
A | G | 2 | a0001c0001t0001g0135a0001c0001t0003g0170 | 2 | NA19068.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.630+7460A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66450508 | ||||||
| chr2:66450564
|
A | G | 1 | a0001c0001t0021g0183 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.630+7516A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66450564 | ||||||
| chr2:66450684
|
G | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.630+7636G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66450684 | ||||||
| chr2:66450749
|
G | T | 148 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0022others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.630+7701G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66450749 | ||||||
| chr2:66451023
|
A | G | 1 | a0001c0001t0001g0001 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.630+7975A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66451023 | ||||||
| chr2:66451033
|
T | A | 1 | a0001c0001t0030g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.630+7985T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66451033 | ||||||
| chr2:66451212
|
T | G | 1 | a0001c0001t0010g0092 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.630+8164T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66451212 | ||||||
| chr2:66451556
|
C | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0238 | 2 | HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.630+8508C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66451556 | ||||||
| chr2:66451714
|
A | G | 1 | a0001c0001t0030g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.630+8666A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66451714 | ||||||
| chr2:66451834
|
C | T | 2 | a0001c0001t0002g0082a0001c0001t0002g0083 | 2 | NA18968.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.630+8786C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66451834 | ||||||
| chr2:66451841
|
G | T | 1 | a0001c0001t0004g0236 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.630+8793G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66451841 | ||||||
| chr2:66451884
|
C | G | 1 | a0001c0001t0008g0072 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.630+8836C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66451884 | ||||||
| chr2:66451929
|
G | A | 1 | a0001c0001t0029g0018 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.630+8881G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66451929 | ||||||
| chr2:66452127
|
T | C | 1 | a0001c0001t0001g0001 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.630+9079T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66452127 | ||||||
| chr2:66452154
|
C | T | 3 | a0001c0001t0002g0203a0001c0001t0005g0201a0001c0001t0005g0202 | 3 | HG02145.hp1 HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.630+9106C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66452154 | ||||||
| chr2:66452266
|
G | A | 1 | a0001c0001t0009g0241 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.630+9218G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66452266 | ||||||
| chr2:66452327
|
A | G | 1 | a0001c0001t0005g0080 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.630+9279A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66452327 | ||||||
| chr2:66452488
|
T | C | 2 | a0001c0001t0002g0210a0001c0001t0027g0211 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.630+9440T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66452488 | ||||||
| chr2:66453111
|
C | T | 3 | a0001c0001t0002g0008a0001c0001t0002g0070a0001c0001t0002g0071 | 3 | HG01070.hp2 HG01071.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.630+10063C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66453111 | ||||||
| chr2:66453142
|
T | C | 4 | a0001c0001t0003g0089a0001c0001t0009g0244a0001c0001t0009g0246others(1): Show | 4 | HG02717.hp1 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.630+10094T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66453142 | ||||||
| chr2:66453342
|
T | A | 3 | a0001c0001t0011g0005a0001c0001t0020g0015a0001c0001t0021g0183 | 3 | HG01109.hp1 HG02055.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.630+10294T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66453342 | ||||||
| chr2:66453467
|
G | A | 1 | a0001c0001t0030g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.630+10419G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66453467 | ||||||
| chr2:66453760
|
G | A | 153 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.631-10349G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66453760 | ||||||
| chr2:66453844
|
T | C | 6 | a0001c0001t0003g0089a0001c0001t0009g0242a0001c0001t0009g0244others(3): Show | 6 | HG02280.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.631-10265T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66453844 | ||||||
| chr2:66454021
|
A | G | 1 | a0001c0001t0030g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.631-10088A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66454021 | ||||||
| chr2:66454172
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0004g0004 | 2 | HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.631-9937C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66454172 | ||||||
| chr2:66454251
|
A | G | 1 | a0001c0001t0001g0169 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.631-9858A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66454251 | ||||||
| chr2:66454395
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.631-9714C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66454395 | ||||||
| chr2:66454496
|
T | C | 2 | a0001c0001t0002g0233a0001c0001t0006g0025 | 2 | HG02809.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.631-9613T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66454496 | ||||||
| chr2:66454538
|
T | C | 5 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0121others(2): Show | 5 | HG02293.hp1 HG02683.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.631-9571T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66454538 | ||||||
| chr2:66454759
|
G | A | 4 | a0001c0001t0002g0041a0001c0001t0005g0006a0001c0001t0005g0085others(1): Show | 4 | HG02165.hp1 NA18941.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.631-9350G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66454759 | ||||||
| chr2:66454760
|
C | A | 4 | a0001c0001t0002g0041a0001c0001t0005g0006a0001c0001t0005g0085others(1): Show | 4 | HG02165.hp1 NA18941.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.631-9349C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66454760 | ||||||
| chr2:66454979
|
C | T | 1 | a0001c0001t0030g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.631-9130C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66454979 | ||||||
| chr2:66455219
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0002g0230 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.631-8890G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66455219 | ||||||
| chr2:66455359
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.631-8750C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66455359 | ||||||
| chr2:66455737
|
C | A | 1 | a0001c0001t0030g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.631-8372C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66455737 | ||||||
| chr2:66456020
|
T | C | 1 | a0001c0001t0002g0070 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.631-8089T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66456020 | ||||||
| chr2:66456233
|
T | TAC | 3 | a0001c0001t0001g0194a0001c0001t0003g0196a0001c0001t0004g0195 | 3 | HG00733.hp1 HG01070.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.631-7875_631-7874i others(4): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 66456233 | |||||
| chr2:66456235
|
T | C | 3 | a0001c0001t0001g0194a0001c0001t0003g0196a0001c0001t0004g0195 | 3 | HG00733.hp1 HG01070.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.631-7874T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66456235 | ||||||
| chr2:66456235
|
T | TAC | 35 | a0001c0001t0001g0011a0001c0001t0001g0100a0001c0001t0001g0108others(32): Show | 35 | HG00621.hp1 HG00741.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.631-7849_631-7848d others(4): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 66456235 | |||||
| chr2:66456235
|
T | TACACACA others(3): Show |
15 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0145others(12): Show | 15 | HG00280.hp1 HG00733.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.631-7857_631-7848d others(12): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 66456235 | |||||
| chr2:66456235
|
T | TACACACA others(5): Show |
8 | a0001c0001t0001g0158a0001c0001t0001g0223a0001c0001t0003g0089others(5): Show | 8 | HG00642.hp1 HG02717.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.631-7859_631-7848d others(14): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 66456235 | |||||
| chr2:66456235
|
T | TACACACA others(7): Show |
62 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0091others(59): Show | 62 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.631-7861_631-7848d others(16): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 66456235 | |||||
| chr2:66456235
|
T | TACACACA others(9): Show |
19 | a0001c0001t0001g0098a0001c0001t0001g0113a0001c0001t0001g0116others(16): Show | 19 | HG01167.hp2 HG02258.hp2 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.631-7863_631-7848d others(18): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 66456235 | |||||
| chr2:66456235
|
T | TACACACA others(11): Show |
3 | a0001c0001t0001g0193a0001c0001t0004g0112a0001c0001t0019g0095 | 3 | HG02630.hp1 HG02976.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.631-7865_631-7848d others(20): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 66456235 | |||||
| chr2:66456235
|
T | TACACACA others(13): Show |
5 | a0001c0001t0001g0185a0001c0001t0002g0210a0001c0001t0007g0228others(2): Show | 5 | HG02165.hp2 HG02257.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.631-7867_631-7848d others(22): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 66456235 | |||||
| chr2:66456235
|
T | TACACACA others(15): Show |
2 | a0001c0001t0003g0184a0001c0001t0012g0205 | 2 | NA18970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.631-7869_631-7848d others(24): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 66456235 | |||||
| chr2:66456235
|
T | TACACACA others(17): Show |
1 | a0001c0001t0001g0138 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.631-7871_631-7848d others(26): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 66456235 | |||||
| chr2:66456262
|
G | T | 4 | a0001c0001t0001g0022a0001c0001t0003g0021a0001c0001t0007g0023others(1): Show | 4 | HG01243.hp2 HG02055.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.631-7847G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66456262 | ||||||
| chr2:66456436
|
A | G | 1 | a0001c0001t0003g0179 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.631-7673A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66456436 | ||||||
| chr2:66456626
|
A | G | 1 | a0001c0001t0001g0098 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.631-7483A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66456626 | ||||||
| chr2:66456660
|
C | T | 5 | a0001c0001t0003g0089a0001c0001t0009g0244a0001c0001t0009g0246others(2): Show | 5 | HG02717.hp1 HG02886.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.631-7449C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66456660 | ||||||
| chr2:66456803
|
T | C | 1 | a0001c0001t0002g0082 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.631-7306T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66456803 | ||||||
| chr2:66456882
|
C | T | 1 | a0001c0001t0037g0020 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.631-7227C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66456882 | ||||||
| chr2:66456921
|
T | C | 1 | a0001c0001t0005g0042 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.631-7188T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66456921 | ||||||
| chr2:66457084
|
GA | G | 25 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0119others(22): Show | 25 | HG01109.hp2 HG01167.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.631-7015delA | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 66457084 | |||||
| chr2:66457161
|
AT | A | 123 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0091others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.631-6930delT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 66457161 | |||||
| chr2:66457271
|
G | C | 3 | a0001c0001t0002g0031a0001c0001t0002g0043a0001c0001t0004g0175 | 3 | NA18973.hp2 NA19064.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.631-6838G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66457271 | ||||||
| chr2:66457551
|
C | T | 1 | a0001c0001t0001g0180 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.631-6558C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66457551 | ||||||
| chr2:66457812
|
G | A | 109 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0091others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.631-6297G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66457812 | ||||||
| chr2:66457849
|
T | G | 2 | a0001c0001t0001g0165a0001c0001t0003g0162 | 2 | NA18968.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.631-6260T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66457849 | ||||||
| chr2:66457850
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0003g0162 | 2 | NA18968.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.631-6259C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66457850 | ||||||
| chr2:66457995
|
G | A | 5 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0038others(2): Show | 5 | NA18945.hp2 NA18983.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.631-6114G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66457995 | ||||||
| chr2:66457998
|
G | A | 1 | a0001c0001t0001g0001 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.631-6111G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66457998 | ||||||
| chr2:66458040
|
A | T | 4 | a0001c0001t0002g0231a0001c0001t0002g0232a0001c0001t0002g0235others(1): Show | 4 | HG01433.hp1 HG02647.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.631-6069A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66458040 | ||||||
| chr2:66458133
|
T | G | 1 | a0001c0001t0001g0107 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.631-5976T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66458133 | ||||||
| chr2:66458202
|
G | T | 1 | a0001c0001t0001g0165 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.631-5907G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66458202 | ||||||
| chr2:66458396
|
A | G | 1 | a0001c0001t0004g0004 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.631-5713A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66458396 | ||||||
| chr2:66458508
|
T | C | 4 | a0001c0001t0010g0115a0001c0001t0010g0118a0001c0001t0016g0122others(1): Show | 4 | HG01123.hp1 HG02258.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.631-5601T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66458508 | ||||||
| chr2:66458663
|
A | T | 1 | a0001c0001t0001g0164 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.631-5446A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66458663 | ||||||
| chr2:66458952
|
G | A | 1 | a0001c0001t0036g0245 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.631-5157G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66458952 | ||||||
| chr2:66458960
|
G | T | 2 | a0001c0001t0002g0082a0001c0001t0002g0083 | 2 | NA18968.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.631-5149G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66458960 | ||||||
| chr2:66459015
|
T | C | 1 | a0001c0001t0008g0044 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.631-5094T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66459015 | ||||||
| chr2:66459083
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.631-5026T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66459083 | ||||||
| chr2:66459194
|
A | T | 1 | a0001c0001t0004g0004 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.631-4915A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66459194 | ||||||
| chr2:66459196
|
C | A | 1 | a0001c0001t0001g0001 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.631-4913C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66459196 | ||||||
| chr2:66459464
|
T | C | 116 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0091others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.631-4645T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66459464 | ||||||
| chr2:66459702
|
T | G | 8 | a0001c0001t0002g0034a0001c0001t0002g0074a0001c0001t0002g0075others(5): Show | 8 | HG00544.hp1 HG02056.hp2 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.631-4407T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66459702 | ||||||
| chr2:66459713
|
C | T | 1 | a0001c0001t0001g0001 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.631-4396C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66459713 | ||||||
| chr2:66459968
|
A | G | 1 | a0001c0001t0036g0245 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.631-4141A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66459968 | ||||||
| chr2:66460205
|
T | C | 8 | a0001c0001t0003g0089a0001c0001t0009g0244a0001c0001t0009g0246others(5): Show | 8 | HG01109.hp1 HG02055.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.631-3904T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66460205 | ||||||
| chr2:66460228
|
T | C | 4 | a0001c0001t0003g0089a0001c0001t0009g0244a0001c0001t0009g0246others(1): Show | 4 | HG02717.hp1 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.631-3881T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66460228 | ||||||
| chr2:66460371
|
G | A | 1 | a0001c0001t0005g0029 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.631-3738G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66460371 | ||||||
| chr2:66460526
|
T | C | 1 | a0001c0001t0001g0121 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.631-3583T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66460526 | ||||||
| chr2:66460694
|
C | A | 1 | a0001c0001t0036g0245 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.631-3415C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66460694 | ||||||
| chr2:66460711
|
C | A | 106 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0091others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.631-3398C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66460711 | ||||||
| chr2:66460834
|
G | C | 1 | a0001c0001t0036g0245 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.631-3275G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66460834 | ||||||
| chr2:66460850
|
A | G | 2 | a0001c0001t0035g0199a0001c0001t0036g0245 | 2 | HG01243.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.631-3259A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66460850 | ||||||
| chr2:66460904
|
A | G | 1 | a0001c0001t0001g0133 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.631-3205A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66460904 | ||||||
| chr2:66460982
|
G | T | 25 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0119others(22): Show | 25 | HG01109.hp2 HG01167.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.631-3127G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66460982 | ||||||
| chr2:66461152
|
G | C | 2 | a0001c0001t0001g0182a0001c0001t0001g0238 | 2 | HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.631-2957G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66461152 | ||||||
| chr2:66461228
|
T | A | 4 | a0001c0001t0003g0089a0001c0001t0009g0244a0001c0001t0009g0246others(1): Show | 4 | HG02717.hp1 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.631-2881T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66461228 | ||||||
| chr2:66461681
|
G | A | 4 | a0001c0001t0001g0022a0001c0001t0003g0021a0001c0001t0007g0023others(1): Show | 4 | HG01243.hp2 HG02055.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.631-2428G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66461681 | ||||||
| chr2:66461882
|
A | G | 1 | a0001c0001t0030g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.631-2227A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66461882 | ||||||
| chr2:66462128
|
C | T | 9 | a0001c0001t0003g0089a0001c0001t0009g0244a0001c0001t0009g0246others(6): Show | 9 | HG01109.hp1 HG01243.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.631-1981C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66462128 | ||||||
| chr2:66462197
|
T | G | 1 | a0001c0001t0004g0004 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.631-1912T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66462197 | ||||||
| chr2:66462521
|
C | T | 1 | a0001c0001t0030g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.631-1588C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66462521 | ||||||
| chr2:66462618
|
T | C | 1 | a0001c0001t0005g0080 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.631-1491T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66462618 | ||||||
| chr2:66462659
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0004g0004 | 2 | HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.631-1450C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66462659 | ||||||
| chr2:66462896
|
A | T | 2 | a0001c0001t0011g0005a0001c0001t0020g0015 | 2 | HG01109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.631-1213A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66462896 | ||||||
| chr2:66462967
|
A | G | 1 | a0001c0001t0002g0212 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.631-1142A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66462967 | ||||||
| chr2:66463190
|
A | G | 1 | a0001c0001t0001g0001 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.631-919A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66463190 | ||||||
| chr2:66463755
|
A | G | 1 | a0001c0001t0002g0069 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.631-354A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 6/12 | chr2 | 66463755 | ||||||
| chr2:66464452
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.742+232G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66464452 | ||||||
| chr2:66464532
|
G | T | 1 | a0001c0001t0006g0027 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.742+312G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66464532 | ||||||
| chr2:66464554
|
G | C | 1 | a0001c0001t0006g0027 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.742+334G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66464554 | ||||||
| chr2:66464700
|
T | C | 1 | a0001c0001t0005g0042 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.742+480T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66464700 | ||||||
| chr2:66464820
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.742+600T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66464820 | ||||||
| chr2:66464823
|
G | A | 1 | a0001c0001t0002g0074 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.742+603G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66464823 | ||||||
| chr2:66465347
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.742+1127G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66465347 | ||||||
| chr2:66465376
|
C | T | 30 | a0001c0001t0001g0011a0001c0001t0001g0093a0001c0001t0001g0107others(27): Show | 30 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.742+1156C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66465376 | ||||||
| chr2:66465592
|
A | T | 4 | a0001c0001t0001g0238a0001c0001t0003g0227a0001c0001t0011g0005others(1): Show | 4 | HG01109.hp1 HG02647.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.742+1372A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66465592 | ||||||
| chr2:66465687
|
A | G | 1 | a0001c0001t0005g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.742+1467A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66465687 | ||||||
| chr2:66465694
|
C | T | 3 | a0001c0001t0002g0212a0001c0001t0002g0233a0001c0001t0006g0025 | 3 | HG02809.hp1 HG02809.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.742+1474C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66465694 | ||||||
| chr2:66465779
|
G | A | 4 | a0001c0001t0001g0238a0001c0001t0003g0227a0001c0001t0011g0005others(1): Show | 4 | HG01109.hp1 HG02647.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.742+1559G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66465779 | ||||||
| chr2:66465833
|
C | T | 4 | a0001c0001t0010g0092a0001c0001t0010g0115a0001c0001t0010g0118others(1): Show | 4 | HG01123.hp1 HG01167.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.742+1613C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66465833 | ||||||
| chr2:66465929
|
T | C | 1 | a0001c0001t0003g0010 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.742+1709T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66465929 | ||||||
| chr2:66466196
|
T | C | 100 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0091others(97): Show | 100 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(97): Show |
intron_variant | MODIFIER | c.742+1976T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66466196 | ||||||
| chr2:66466669
|
C | T | 1 | a0001c0001t0005g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.742+2449C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66466669 | ||||||
| chr2:66466908
|
C | G | 1 | a0001c0001t0002g0074 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.742+2688C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66466908 | ||||||
| chr2:66466941
|
T | TA | 44 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0116others(41): Show | 44 | HG01109.hp1 HG01123.hp1 HG01167.hp2 others(41): Show |
intron_variant | MODIFIER | c.742+2735dupA | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66466941 | |||||
| chr2:66466941
|
TA | T | 9 | a0001c0001t0001g0022a0001c0001t0001g0117a0001c0001t0002g0069others(6): Show | 9 | HG02055.hp1 HG02486.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.742+2735delA | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66466941 | |||||
| chr2:66467335
|
G | A | 2 | a0001c0001t0003g0226a0001c0001t0005g0019 | 2 | HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.742+3115G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66467335 | ||||||
| chr2:66467351
|
G | A | 101 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0091others(98): Show | 101 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(98): Show |
intron_variant | MODIFIER | c.742+3131G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66467351 | ||||||
| chr2:66467354
|
T | C | 1 | a0001c0001t0005g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.742+3134T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66467354 | ||||||
| chr2:66467367
|
TA | T | 62 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0093others(59): Show | 62 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(59): Show |
intron_variant | MODIFIER | c.742+3148delA | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66467367 | ||||||
| chr2:66467368
|
A | G | 32 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0116others(29): Show | 32 | HG01123.hp1 HG01167.hp2 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.742+3148A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66467368 | ||||||
| chr2:66467469
|
C | T | 3 | a0001c0001t0003g0226a0001c0001t0005g0019a0001c0001t0006g0026 | 3 | HG02622.hp2 HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.742+3249C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66467469 | ||||||
| chr2:66467527
|
G | A | 4 | a0001c0001t0001g0178a0001c0001t0002g0200a0001c0001t0030g0014others(1): Show | 4 | HG02280.hp1 HG02886.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.742+3307G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66467527 | ||||||
| chr2:66467534
|
T | C | 52 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0093others(49): Show | 52 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.742+3314T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66467534 | ||||||
| chr2:66467604
|
GA | G | 21 | a0001c0001t0001g0022a0001c0001t0001g0119a0001c0001t0001g0138others(18): Show | 21 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.742+3395delA | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66467604 | |||||
| chr2:66467931
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.742+3711A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66467931 | ||||||
| chr2:66468023
|
T | A | 97 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0091others(94): Show | 97 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(94): Show |
intron_variant | MODIFIER | c.742+3803T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66468023 | ||||||
| chr2:66468139
|
A | G | 1 | a0001c0001t0006g0081 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.742+3919A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66468139 | ||||||
| chr2:66468155
|
G | A | 5 | a0001c0001t0001g0238a0001c0001t0003g0227a0001c0001t0004g0004others(2): Show | 5 | HG01109.hp1 HG02647.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.742+3935G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66468155 | ||||||
| chr2:66468189
|
G | A | 101 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0091others(98): Show | 101 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(98): Show |
intron_variant | MODIFIER | c.742+3969G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66468189 | ||||||
| chr2:66468331
|
C | T | 27 | a0001c0001t0001g0011a0001c0001t0001g0093a0001c0001t0001g0111others(24): Show | 27 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.742+4111C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66468331 | ||||||
| chr2:66468356
|
T | G | 2 | a0001c0001t0002g0233a0001c0001t0006g0025 | 2 | HG02809.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.742+4136T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66468356 | ||||||
| chr2:66468403
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.742+4183C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66468403 | ||||||
| chr2:66468469
|
T | C | 1 | a0001c0001t0003g0162 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.742+4249T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66468469 | ||||||
| chr2:66468482
|
G | A | 1 | a0001c0001t0005g0019 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.742+4262G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66468482 | ||||||
| chr2:66468540
|
G | T | 1 | a0001c0001t0002g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.742+4320G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66468540 | ||||||
| chr2:66468631
|
C | T | 2 | a0001c0001t0003g0226a0001c0001t0005g0019 | 2 | HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.742+4411C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66468631 | ||||||
| chr2:66468700
|
G | C | 97 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0091others(94): Show | 97 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(94): Show |
intron_variant | MODIFIER | c.742+4480G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66468700 | ||||||
| chr2:66468744
|
G | C | 31 | a0001c0001t0001g0011a0001c0001t0001g0093a0001c0001t0001g0107others(28): Show | 31 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.742+4524G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66468744 | ||||||
| chr2:66468780
|
A | C | 1 | a0001c0001t0002g0041 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.742+4560A>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66468780 | ||||||
| chr2:66468948
|
C | T | 87 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0091others(84): Show | 87 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(84): Show |
intron_variant | MODIFIER | c.742+4728C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66468948 | ||||||
| chr2:66469156
|
T | C | 1 | a0001c0003t0001g0141 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.742+4936T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66469156 | ||||||
| chr2:66469160
|
A | G | 92 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0091others(89): Show | 92 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(89): Show |
intron_variant | MODIFIER | c.742+4940A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66469160 | ||||||
| chr2:66469191
|
T | TA | 87 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0091others(84): Show | 87 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(84): Show |
intron_variant | MODIFIER | c.742+4983dupA | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66469191 | |||||
| chr2:66469833
|
G | A | 21 | a0001c0001t0001g0022a0001c0001t0001g0119a0001c0001t0001g0138others(18): Show | 21 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.742+5613G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66469833 | ||||||
| chr2:66469883
|
T | G | 21 | a0001c0001t0001g0022a0001c0001t0001g0119a0001c0001t0001g0138others(18): Show | 21 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.742+5663T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66469883 | ||||||
| chr2:66469933
|
T | TAA | 36 | a0001c0001t0001g0022a0001c0001t0001g0119a0001c0001t0001g0121others(33): Show | 36 | HG01109.hp2 HG01123.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.742+5722_742+5723d others(4): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66469933 | |||||
| chr2:66469933
|
T | TAAA | 19 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0116others(16): Show | 19 | HG02055.hp2 HG02965.hp2 HG03490.hp1 others(16): Show |
intron_variant | MODIFIER | c.742+5721_742+5723d others(5): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66469933 | |||||
| chr2:66470035
|
T | C | 21 | a0001c0001t0001g0022a0001c0001t0001g0119a0001c0001t0001g0138others(18): Show | 21 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.742+5815T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66470035 | ||||||
| chr2:66470250
|
T | C | 1 | a0001c0001t0009g0246 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.742+6030T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66470250 | ||||||
| chr2:66470601
|
T | C | 35 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0116others(32): Show | 35 | HG01123.hp1 HG01167.hp2 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.742+6381T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66470601 | ||||||
| chr2:66470740
|
C | T | 2 | a0001c0001t0003g0226a0001c0001t0005g0019 | 2 | HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.742+6520C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66470740 | ||||||
| chr2:66470869
|
G | C | 5 | a0001c0001t0001g0238a0001c0001t0003g0227a0001c0001t0004g0004others(2): Show | 5 | HG01109.hp1 HG02647.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.742+6649G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66470869 | ||||||
| chr2:66470885
|
T | G | 100 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0091others(97): Show | 100 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(97): Show |
intron_variant | MODIFIER | c.742+6665T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66470885 | ||||||
| chr2:66470886
|
G | T | 3 | a0001c0001t0001g0022a0001c0001t0003g0021a0001c0001t0007g0023 | 3 | HG02055.hp1 HG02486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.742+6666G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66470886 | ||||||
| chr2:66471030
|
C | T | 56 | a0001c0001t0001g0022a0001c0001t0001g0091a0001c0001t0001g0096others(53): Show | 56 | HG01109.hp2 HG01123.hp1 HG01167.hp2 others(53): Show |
intron_variant | MODIFIER | c.742+6810C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66471030 | ||||||
| chr2:66471216
|
G | A | 5 | a0001c0001t0001g0178a0001c0001t0001g0222a0001c0001t0002g0200others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.742+6996G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66471216 | ||||||
| chr2:66471371
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.742+7151T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66471371 | ||||||
| chr2:66471403
|
G | T | 3 | a0001c0001t0001g0022a0001c0001t0003g0021a0001c0001t0007g0023 | 3 | HG02055.hp1 HG02486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.742+7183G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66471403 | ||||||
| chr2:66471409
|
T | A | 2 | a0001c0001t0001g0091a0001c0001t0003g0090 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.742+7189T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66471409 | ||||||
| chr2:66471595
|
A | G | 1 | a0001c0001t0027g0211 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.742+7375A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66471595 | ||||||
| chr2:66471664
|
G | A | 56 | a0001c0001t0001g0022a0001c0001t0001g0091a0001c0001t0001g0096others(53): Show | 56 | HG01109.hp2 HG01123.hp1 HG01167.hp2 others(53): Show |
intron_variant | MODIFIER | c.742+7444G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66471664 | ||||||
| chr2:66471816
|
A | G | 10 | a0001c0001t0001g0098a0001c0001t0001g0144a0001c0001t0002g0039others(7): Show | 10 | HG00673.hp1 NA18952.hp2 NA18968.hp1 others(7): Show |
intron_variant | MODIFIER | c.742+7596A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66471816 | ||||||
| chr2:66471849
|
G | T | 4 | a0001c0001t0001g0238a0001c0001t0003g0227a0001c0001t0011g0005others(1): Show | 4 | HG01109.hp1 HG02647.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.742+7629G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66471849 | ||||||
| chr2:66472256
|
T | C | 21 | a0001c0001t0001g0022a0001c0001t0001g0119a0001c0001t0001g0138others(18): Show | 21 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.742+8036T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66472256 | ||||||
| chr2:66472619
|
T | C | 1 | a0001c0001t0004g0114 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.742+8399T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66472619 | ||||||
| chr2:66472629
|
A | T | 12 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0004g0151others(9): Show | 12 | HG01123.hp1 HG01167.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.742+8409A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66472629 | ||||||
| chr2:66472822
|
G | C | 3 | a0001c0001t0001g0130a0001c0001t0001g0167a0001c0001t0001g0190 | 3 | HG00741.hp1 HG01981.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.742+8602G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66472822 | ||||||
| chr2:66472971
|
C | A | 1 | a0001c0001t0004g0004 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.742+8751C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66472971 | ||||||
| chr2:66473128
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.742+8908C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66473128 | ||||||
| chr2:66473145
|
A | G | 100 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0091others(97): Show | 100 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(97): Show |
intron_variant | MODIFIER | c.742+8925A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66473145 | ||||||
| chr2:66473156
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.742+8936A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66473156 | ||||||
| chr2:66473234
|
C | T | 1 | a0001c0001t0006g0026 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.742+9014C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66473234 | ||||||
| chr2:66473293
|
G | A | 35 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0116others(32): Show | 35 | HG01123.hp1 HG01167.hp2 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.742+9073G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66473293 | ||||||
| chr2:66473321
|
T | A | 4 | a0001c0001t0001g0178a0001c0001t0002g0200a0001c0001t0030g0014others(1): Show | 4 | HG02280.hp1 HG02886.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.742+9101T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66473321 | ||||||
| chr2:66473378
|
C | CA | 27 | a0001c0001t0001g0011a0001c0001t0001g0093a0001c0001t0001g0111others(24): Show | 27 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.742+9178dupA | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473378 | |||||
| chr2:66473378
|
C | CAAAAAAA others(3): Show |
3 | a0001c0001t0001g0138a0001c0001t0001g0222a0001c0001t0012g0045 | 3 | HG02630.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.742+9169_742+9178d others(12): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473378 | |||||
| chr2:66473378
|
CA | C | 6 | a0001c0001t0001g0129a0001c0001t0001g0134a0001c0001t0001g0169others(3): Show | 6 | HG00408.hp1 HG02004.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.742+9178delA | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473378 | |||||
| chr2:66473397
|
A | AAAAAAAA others(21): Show |
1 | a0001c0001t0001g0193 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.742+9178_742+9179i others(30): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAA others(31): Show |
1 | a0001c0001t0007g0023 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.742+9178_742+9179i others(40): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAA others(20): Show |
2 | a0001c0001t0001g0216a0001c0001t0004g0151 | 2 | HG01243.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.742+9178_742+9179i others(29): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAA others(22): Show |
1 | a0001c0001t0001g0119 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.742+9178_742+9179i others(31): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAA others(32): Show |
1 | a0001c0001t0003g0021 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.742+9178_742+9179i others(41): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAA others(17): Show |
1 | a0001c0001t0002g0233 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.742+9178_742+9179i others(26): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAA others(19): Show |
1 | a0001c0001t0001g0214 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.742+9178_742+9179i others(28): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAA others(31): Show |
1 | a0001c0001t0001g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.742+9178_742+9179i others(40): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAA others(18): Show |
2 | a0001c0001t0001g0182a0001c0001t0003g0213 | 2 | HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.742+9178_742+9179i others(27): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAA others(17): Show |
3 | a0001c0001t0002g0210a0001c0001t0006g0025a0001c0001t0007g0228 | 3 | HG02257.hp2 HG02818.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.742+9178_742+9179i others(26): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAA others(19): Show |
2 | a0001c0001t0003g0215a0001c0001t0019g0095 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.742+9178_742+9179i others(28): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAA others(20): Show |
1 | a0001c0001t0001g0217 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.742+9178_742+9179i others(29): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAA others(28): Show |
1 | a0001c0001t0016g0122 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.742+9178_742+9179i others(37): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAA others(11): Show |
1 | a0001c0001t0003g0003 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.742+9178_742+9179i others(20): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAA others(19): Show |
1 | a0001c0001t0007g0140 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.742+9178_742+9179i others(28): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAA others(21): Show |
1 | a0001c0001t0004g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.742+9178_742+9179i others(30): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAA others(23): Show |
1 | a0001c0001t0001g0121 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.742+9178_742+9179i others(32): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAA others(25): Show |
1 | a0001c0001t0002g0212 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.742+9178_742+9179i others(34): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAA others(12): Show |
1 | a0001c0001t0004g0013 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.742+9178_742+9179i others(21): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAA others(18): Show |
3 | a0001c0001t0011g0219a0001c0001t0011g0220a0001c0001t0012g0205 | 3 | HG02895.hp2 HG02897.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.742+9178_742+9179i others(27): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAA others(28): Show |
1 | a0001c0001t0010g0118 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.742+9178_742+9179i others(37): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAA others(11): Show |
9 | a0001c0001t0001g0091a0001c0001t0001g0137a0001c0001t0001g0148others(6): Show | 9 | HG03490.hp1 HG03492.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.742+9178_742+9179i others(20): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAA others(23): Show |
2 | a0001c0001t0009g0243a0001c0001t0010g0221 | 2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.742+9178_742+9179i others(32): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAA others(27): Show |
1 | a0001c0001t0010g0092 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.742+9178_742+9179i others(36): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAA others(6): Show |
1 | a0001c0001t0002g0200 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.742+9178_742+9179i others(15): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAA others(8): Show |
2 | a0001c0001t0001g0116a0001c0001t0006g0026 | 2 | HG03225.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.742+9178_742+9179i others(17): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAA others(10): Show |
1 | a0001c0001t0001g0123 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.742+9178_742+9179i others(19): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAA others(14): Show |
1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.742+9178_742+9179i others(23): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAA others(22): Show |
2 | a0001c0001t0010g0115a0001c0001t0013g0028 | 2 | HG01123.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.742+9178_742+9179i others(31): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0021g0183 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.742+9178_742+9179i others(22): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAA others(21): Show |
1 | a0001c0001t0035g0199 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.742+9178_742+9179i others(30): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAT others(14): Show |
1 | a0001c0001t0002g0230 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.742+9178_742+9179i others(23): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAAAT others(18): Show |
1 | a0001c0001t0004g0112 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.742+9178_742+9179i others(27): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAATA others(11): Show |
1 | a0001c0001t0005g0029 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.742+9178_742+9179i others(20): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAATA others(13): Show |
1 | a0001c0001t0001g0096 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.742+9178_742+9179i others(22): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAATA others(19): Show |
1 | a0001c0001t0018g0177 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.742+9178_742+9179i others(28): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAAATA others(21): Show |
1 | a0001c0001t0001g0176 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.742+9178_742+9179i others(30): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAATAT others(6): Show |
2 | a0001c0001t0001g0178a0001c0001t0036g0245 | 2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.742+9178_742+9179i others(15): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAAATAT others(8): Show |
1 | a0001c0001t0030g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.742+9178_742+9179i others(17): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAAT | 5 | a0001c0001t0001g0133a0001c0001t0015g0147a0001c0001t0020g0015others(2): Show | 5 | HG02886.hp2 HG03579.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.742+9178_742+9179i others(5): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AAT | 8 | a0001c0001t0001g0100a0001c0001t0001g0110a0001c0001t0002g0234others(5): Show | 8 | HG00733.hp2 HG01074.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.742+9197_742+9198d others(4): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66473397 | |||||
| chr2:66473397
|
A | AT | 9 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0161others(6): Show | 9 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.742+9177_742+9178i others(3): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66473397 | ||||||
| chr2:66473397
|
A | T | 3 | a0001c0001t0002g0017a0001c0001t0004g0173a0001c0001t0008g0072 | 3 | HG01167.hp1 NA19003.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.742+9177A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66473397 | ||||||
| chr2:66473399
|
T | A | 13 | a0001c0001t0001g0001a0001c0001t0001g0190a0001c0001t0002g0038others(10): Show | 13 | HG00741.hp1 HG01074.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.742+9179T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66473399 | ||||||
| chr2:66473401
|
T | A | 3 | a0001c0001t0001g0001a0001c0001t0003g0226a0001c0001t0005g0019 | 3 | HG02622.hp2 HG03704.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.742+9181T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66473401 | ||||||
| chr2:66473403
|
T | A | 2 | a0001c0001t0003g0226a0001c0001t0005g0019 | 2 | HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.742+9183T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66473403 | ||||||
| chr2:66473412
|
A | G | 2 | a0001c0001t0003g0227a0001c0001t0020g0015 | 2 | HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.742+9192A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66473412 | ||||||
| chr2:66473555
|
A | G | 1 | a0001c0001t0003g0150 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.742+9335A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66473555 | ||||||
| chr2:66473593
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.742+9373A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66473593 | ||||||
| chr2:66473600
|
C | T | 5 | a0001c0001t0001g0178a0001c0001t0001g0222a0001c0001t0002g0200others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.742+9380C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66473600 | ||||||
| chr2:66473652
|
T | C | 21 | a0001c0001t0001g0022a0001c0001t0001g0119a0001c0001t0001g0138others(18): Show | 21 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.742+9432T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66473652 | ||||||
| chr2:66473754
|
C | T | 1 | a0001c0001t0006g0026 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.742+9534C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66473754 | ||||||
| chr2:66473778
|
A | G | 35 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0116others(32): Show | 35 | HG01123.hp1 HG01167.hp2 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.742+9558A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66473778 | ||||||
| chr2:66473779
|
G | T | 35 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0116others(32): Show | 35 | HG01123.hp1 HG01167.hp2 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.742+9559G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66473779 | ||||||
| chr2:66473820
|
T | A | 31 | a0001c0001t0001g0011a0001c0001t0001g0093a0001c0001t0001g0107others(28): Show | 31 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.742+9600T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66473820 | ||||||
| chr2:66473852
|
A | T | 1 | a0001c0001t0004g0004 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.742+9632A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66473852 | ||||||
| chr2:66473871
|
G | A | 5 | a0001c0001t0001g0238a0001c0001t0003g0227a0001c0001t0004g0004others(2): Show | 5 | HG01109.hp1 HG02647.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.742+9651G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66473871 | ||||||
| chr2:66473997
|
T | A | 3 | a0001c0001t0001g0178a0001c0001t0030g0014a0001c0001t0036g0245 | 3 | HG02280.hp1 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.742+9777T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66473997 | ||||||
| chr2:66474051
|
G | T | 21 | a0001c0001t0001g0022a0001c0001t0001g0119a0001c0001t0001g0138others(18): Show | 21 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.742+9831G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66474051 | ||||||
| chr2:66474091
|
AT | A | 56 | a0001c0001t0001g0022a0001c0001t0001g0091a0001c0001t0001g0096others(53): Show | 56 | HG01109.hp2 HG01123.hp1 HG01167.hp2 others(53): Show |
intron_variant | MODIFIER | c.742+9881delT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66474091 | |||||
| chr2:66474204
|
C | T | 2 | a0001c0001t0002g0047a0001c0001t0002g0048 | 2 | HG01074.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.742+9984C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66474204 | ||||||
| chr2:66474376
|
GT | G | 3 | a0001c0001t0001g0022a0001c0001t0003g0021a0001c0001t0007g0023 | 3 | HG02055.hp1 HG02486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.742+10161delT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66474376 | |||||
| chr2:66474441
|
A | G | 21 | a0001c0001t0001g0022a0001c0001t0001g0119a0001c0001t0001g0138others(18): Show | 21 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.742+10221A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66474441 | ||||||
| chr2:66474487
|
A | G | 1 | a0001c0001t0005g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.742+10267A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66474487 | ||||||
| chr2:66474938
|
C | A | 101 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0091others(98): Show | 101 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(98): Show |
intron_variant | MODIFIER | c.742+10718C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66474938 | ||||||
| chr2:66474958
|
T | C | 1 | a0001c0001t0002g0203 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.742+10738T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66474958 | ||||||
| chr2:66474973
|
G | A | 6 | a0001c0001t0008g0044a0001c0001t0008g0050a0001c0001t0008g0051others(3): Show | 6 | HG00408.hp2 HG00621.hp2 HG00642.hp2 others(3): Show |
intron_variant | MODIFIER | c.742+10753G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66474973 | ||||||
| chr2:66475025
|
A | G | 4 | a0001c0001t0001g0178a0001c0001t0002g0200a0001c0001t0030g0014others(1): Show | 4 | HG02280.hp1 HG02886.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.742+10805A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66475025 | ||||||
| chr2:66475137
|
CAT | C | 101 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0091others(98): Show | 101 | HG00323.hp2 HG00733.hp1 HG00741.hp1 others(98): Show |
intron_variant | MODIFIER | c.742+10929_742+1093 others(6): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66475137 | |||||
| chr2:66475139
|
T | C | 1 | a0001c0001t0036g0245 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.742+10919T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66475139 | ||||||
| chr2:66475209
|
A | AATAAATA others(15): Show |
56 | a0001c0001t0001g0022a0001c0001t0001g0091a0001c0001t0001g0096others(53): Show | 56 | HG01109.hp2 HG01123.hp1 HG01167.hp2 others(53): Show |
intron_variant | MODIFIER | c.742+11001_742+1100 others(26): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66475209 | |||||
| chr2:66475263
|
TATATA | T | 5 | a0001c0001t0001g0238a0001c0001t0003g0227a0001c0001t0004g0004others(2): Show | 5 | HG01109.hp1 HG02647.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.742+11049_742+1105 others(9): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66475263 | |||||
| chr2:66475273
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.742+11053A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66475273 | ||||||
| chr2:66475513
|
A | G | 56 | a0001c0001t0001g0022a0001c0001t0001g0091a0001c0001t0001g0096others(53): Show | 56 | HG01109.hp2 HG01123.hp1 HG01167.hp2 others(53): Show |
intron_variant | MODIFIER | c.742+11293A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66475513 | ||||||
| chr2:66475536
|
T | C | 3 | a0001c0001t0001g0022a0001c0001t0003g0021a0001c0001t0007g0023 | 3 | HG02055.hp1 HG02486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.742+11316T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66475536 | ||||||
| chr2:66475673
|
A | G | 1 | a0001c0001t0003g0139 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.742+11453A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66475673 | ||||||
| chr2:66475697
|
C | T | 1 | a0001c0001t0002g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.742+11477C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66475697 | ||||||
| chr2:66475925
|
T | C | 35 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0116others(32): Show | 35 | HG01123.hp1 HG01167.hp2 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.742+11705T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66475925 | ||||||
| chr2:66475965
|
A | G | 1 | a0001c0001t0037g0020 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.742+11745A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66475965 | ||||||
| chr2:66476119
|
A | G | 56 | a0001c0001t0001g0022a0001c0001t0001g0091a0001c0001t0001g0096others(53): Show | 56 | HG01109.hp2 HG01123.hp1 HG01167.hp2 others(53): Show |
intron_variant | MODIFIER | c.742+11899A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66476119 | ||||||
| chr2:66476462
|
G | A | 5 | a0001c0001t0001g0178a0001c0001t0001g0222a0001c0001t0002g0200others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.742+12242G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66476462 | ||||||
| chr2:66476572
|
C | A | 2 | a0001c0001t0001g0012a0001c0001t0026g0240 | 2 | HG00099.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.742+12352C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66476572 | ||||||
| chr2:66476625
|
C | T | 2 | a0001c0001t0002g0067a0001c0001t0003g0179 | 2 | NA18995.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.742+12405C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66476625 | ||||||
| chr2:66476756
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0003g0021a0001c0001t0007g0023 | 3 | HG02055.hp1 HG02486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.742+12536C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66476756 | ||||||
| chr2:66476782
|
G | A | 35 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0116others(32): Show | 35 | HG01123.hp1 HG01167.hp2 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.742+12562G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66476782 | ||||||
| chr2:66476849
|
G | C | 21 | a0001c0001t0001g0022a0001c0001t0001g0119a0001c0001t0001g0138others(18): Show | 21 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.742+12629G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66476849 | ||||||
| chr2:66476869
|
C | A | 4 | a0001c0001t0001g0238a0001c0001t0003g0227a0001c0001t0011g0005others(1): Show | 4 | HG01109.hp1 HG02647.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.742+12649C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66476869 | ||||||
| chr2:66477020
|
G | A | 4 | a0001c0001t0001g0238a0001c0001t0003g0227a0001c0001t0011g0005others(1): Show | 4 | HG01109.hp1 HG02647.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.742+12800G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66477020 | ||||||
| chr2:66477028
|
A | G | 1 | a0001c0001t0012g0045 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.742+12808A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66477028 | ||||||
| chr2:66477110
|
G | A | 5 | a0001c0001t0001g0238a0001c0001t0003g0227a0001c0001t0004g0004others(2): Show | 5 | HG01109.hp1 HG02647.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.742+12890G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66477110 | ||||||
| chr2:66477140
|
G | A | 2 | a0001c0001t0003g0226a0001c0001t0005g0019 | 2 | HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.742+12920G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66477140 | ||||||
| chr2:66477583
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.742+13363C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66477583 | ||||||
| chr2:66477659
|
C | A | 3 | a0001c0001t0002g0212a0001c0001t0002g0233a0001c0001t0006g0025 | 3 | HG02809.hp1 HG02809.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.742+13439C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66477659 | ||||||
| chr2:66477662
|
C | T | 5 | a0001c0001t0001g0178a0001c0001t0001g0222a0001c0001t0002g0200others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.742+13442C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66477662 | ||||||
| chr2:66477685
|
G | T | 2 | a0001c0001t0003g0226a0001c0001t0005g0019 | 2 | HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.742+13465G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66477685 | ||||||
| chr2:66477688
|
A | T | 1 | a0001c0001t0001g0182 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.742+13468A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66477688 | ||||||
| chr2:66477859
|
C | CA | 5 | a0001c0001t0001g0238a0001c0001t0003g0227a0001c0001t0004g0004others(2): Show | 5 | HG01109.hp1 HG02647.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.742+13640dupA | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66477859 | |||||
| chr2:66477886
|
A | C | 5 | a0001c0001t0001g0238a0001c0001t0003g0227a0001c0001t0004g0004others(2): Show | 5 | HG01109.hp1 HG02647.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.742+13666A>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66477886 | ||||||
| chr2:66478305
|
G | C | 5 | a0001c0001t0001g0238a0001c0001t0003g0227a0001c0001t0004g0004others(2): Show | 5 | HG01109.hp1 HG02647.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.742+14085G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66478305 | ||||||
| chr2:66478321
|
T | C | 1 | a0001c0001t0002g0034 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.742+14101T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66478321 | ||||||
| chr2:66478653
|
C | A | 73 | a0001c0001t0001g0022a0001c0001t0001g0091a0001c0001t0001g0096others(70): Show | 73 | HG01109.hp1 HG01109.hp2 HG01123.hp1 others(70): Show |
intron_variant | MODIFIER | c.742+14433C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66478653 | ||||||
| chr2:66478730
|
A | C | 5 | a0001c0001t0001g0178a0001c0001t0001g0222a0001c0001t0002g0200others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.742+14510A>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66478730 | ||||||
| chr2:66478831
|
C | A | 34 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0116others(31): Show | 34 | HG01123.hp1 HG01167.hp2 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.742+14611C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66478831 | ||||||
| chr2:66479343
|
A | G | 11 | a0001c0001t0001g0022a0001c0001t0001g0178a0001c0001t0001g0217others(8): Show | 11 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.742+15123A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66479343 | ||||||
| chr2:66479418
|
T | G | 1 | a0001c0001t0001g0117 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.742+15198T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66479418 | ||||||
| chr2:66479701
|
A | C | 1 | a0001c0001t0003g0179 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.742+15481A>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66479701 | ||||||
| chr2:66479767
|
G | GTCTTAAG others(5): Show |
1 | a0001c0001t0004g0004 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.742+15547_742+1554 others(16): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66479767 | ||||||
| chr2:66479832
|
T | A | 19 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0116others(16): Show | 19 | HG02055.hp2 HG02965.hp2 HG03490.hp1 others(16): Show |
intron_variant | MODIFIER | c.742+15612T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66479832 | ||||||
| chr2:66479867
|
T | C | 1 | a0001c0001t0004g0004 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.742+15647T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66479867 | ||||||
| chr2:66479924
|
GC | G | 5 | a0001c0001t0001g0238a0001c0001t0003g0227a0001c0001t0004g0004others(2): Show | 5 | HG01109.hp1 HG02647.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.742+15706delC | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66479924 | |||||
| chr2:66479954
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.742+15734G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66479954 | ||||||
| chr2:66480000
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.742+15780A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66480000 | ||||||
| chr2:66480310
|
G | T | 2 | a0001c0001t0003g0226a0001c0001t0005g0019 | 2 | HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.742+16090G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66480310 | ||||||
| chr2:66480359
|
G | C | 1 | a0001c0001t0001g0182 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.742+16139G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66480359 | ||||||
| chr2:66480372
|
A | G | 11 | a0001c0001t0001g0022a0001c0001t0001g0178a0001c0001t0001g0217others(8): Show | 11 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.742+16152A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66480372 | ||||||
| chr2:66480430
|
G | A | 1 | a0001c0001t0029g0018 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.742+16210G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66480430 | ||||||
| chr2:66480436
|
T | C | 2 | a0001c0001t0001g0096a0001c0001t0002g0230 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.742+16216T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66480436 | ||||||
| chr2:66480465
|
A | G | 2 | a0001c0001t0009g0243a0001c0001t0035g0199 | 2 | HG01243.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.742+16245A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66480465 | ||||||
| chr2:66480562
|
G | A | 1 | a0001c0001t0002g0046 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.742+16342G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66480562 | ||||||
| chr2:66480611
|
C | G | 1 | a0001c0001t0006g0078 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.742+16391C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66480611 | ||||||
| chr2:66480629
|
TG | T | 34 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0116others(31): Show | 34 | HG01123.hp1 HG01167.hp2 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.742+16412delG | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66480629 | |||||
| chr2:66481010
|
A | C | 2 | a0001c0001t0002g0233a0001c0001t0006g0025 | 2 | HG02809.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.742+16790A>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66481010 | ||||||
| chr2:66481011
|
C | A | 2 | a0001c0001t0003g0226a0001c0001t0005g0019 | 2 | HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.742+16791C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66481011 | ||||||
| chr2:66481209
|
A | G | 2 | a0001c0001t0003g0226a0001c0001t0005g0019 | 2 | HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.742+16989A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66481209 | ||||||
| chr2:66481289
|
T | G | 2 | a0001c0001t0003g0226a0001c0001t0005g0019 | 2 | HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.742+17069T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66481289 | ||||||
| chr2:66481374
|
G | T | 1 | a0001c0001t0005g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.742+17154G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66481374 | ||||||
| chr2:66481509
|
G | A | 1 | a0001c0001t0002g0200 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.742+17289G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66481509 | ||||||
| chr2:66481850
|
C | CT | 12 | a0001c0001t0001g0148a0001c0001t0001g0216a0001c0001t0002g0034others(9): Show | 12 | HG01243.hp1 HG01243.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.742+17653dupT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66481850 | |||||
| chr2:66481850
|
CT | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0094others(52): Show | 55 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.742+17653delT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66481850 | |||||
| chr2:66481938
|
T | C | 1 | a0001c0001t0005g0042 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.742+17718T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66481938 | ||||||
| chr2:66481940
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.742+17720C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66481940 | ||||||
| chr2:66482005
|
CCACCACA | C | 53 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0116others(50): Show | 53 | HG01109.hp1 HG01123.hp1 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.742+17794_742+1780 others(11): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66482005 | |||||
| chr2:66482088
|
T | A | 34 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0116others(31): Show | 34 | HG01123.hp1 HG01167.hp2 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.742+17868T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66482088 | ||||||
| chr2:66482098
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.742+17878G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66482098 | ||||||
| chr2:66482288
|
G | A | 1 | a0001c0001t0005g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.742+18068G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66482288 | ||||||
| chr2:66482336
|
G | T | 160 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.742+18116G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66482336 | ||||||
| chr2:66482345
|
A | G | 5 | a0001c0001t0001g0238a0001c0001t0003g0227a0001c0001t0004g0004others(2): Show | 5 | HG01109.hp1 HG02647.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.742+18125A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66482345 | ||||||
| chr2:66482398
|
C | A | 5 | a0001c0001t0001g0238a0001c0001t0003g0227a0001c0001t0004g0004others(2): Show | 5 | HG01109.hp1 HG02647.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.742+18178C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66482398 | ||||||
| chr2:66482404
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.742+18184C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66482404 | ||||||
| chr2:66482534
|
G | C | 1 | a0001c0001t0004g0004 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.742+18314G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66482534 | ||||||
| chr2:66482652
|
A | G | 1 | a0001c0001t0006g0026 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.742+18432A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66482652 | ||||||
| chr2:66482690
|
G | C | 3 | a0001c0001t0002g0009a0001c0001t0004g0152a0001c0003t0001g0141 | 3 | HG01361.hp2 HG02258.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.742+18470G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66482690 | ||||||
| chr2:66482837
|
T | A | 5 | a0001c0001t0001g0238a0001c0001t0003g0227a0001c0001t0004g0004others(2): Show | 5 | HG01109.hp1 HG02647.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.742+18617T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66482837 | ||||||
| chr2:66482950
|
C | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0145 | 2 | HG00280.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.742+18730C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66482950 | ||||||
| chr2:66482958
|
G | A | 34 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0116others(31): Show | 34 | HG01123.hp1 HG01167.hp2 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.742+18738G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66482958 | ||||||
| chr2:66483216
|
A | AT | 29 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0098others(26): Show | 29 | HG00673.hp1 HG02055.hp2 HG02735.hp2 others(26): Show |
intron_variant | MODIFIER | c.742+19009dupT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66483216 | |||||
| chr2:66483216
|
A | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0180 | 2 | NA18944.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.742+18996A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66483216 | ||||||
| chr2:66483216
|
AT | A | 8 | a0001c0001t0001g0178a0001c0001t0001g0238a0001c0001t0002g0200others(5): Show | 8 | HG01109.hp1 HG02280.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.742+19009delT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66483216 | |||||
| chr2:66483216
|
ATT | A | 14 | a0001c0001t0001g0119a0001c0001t0001g0182a0001c0001t0001g0193others(11): Show | 14 | HG01243.hp1 HG01243.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.742+19008_742+1900 others(6): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66483216 | |||||
| chr2:66483218
|
TTTTTTTT others(7): Show |
T | 11 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0004g0151others(8): Show | 11 | HG01123.hp1 HG01167.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.742+19010_742+1902 others(18): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66483218 | |||||
| chr2:66483228
|
T | G | 1 | a0001c0001t0013g0028 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.742+19008T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66483228 | ||||||
| chr2:66483230
|
G | C | 1 | a0001c0001t0013g0028 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.742+19010G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66483230 | ||||||
| chr2:66483230
|
G | T | 1 | a0001c0001t0001g0148 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.742+19010G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66483230 | ||||||
| chr2:66483232
|
C | G | 1 | a0001c0001t0001g0148 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.742+19012C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66483232 | ||||||
| chr2:66483232
|
CT | C | 23 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0116others(20): Show | 23 | HG02055.hp2 HG02809.hp1 HG02809.hp2 others(20): Show |
intron_variant | MODIFIER | c.742+19024delT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66483232 | |||||
| chr2:66483262
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.742+19042G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66483262 | ||||||
| chr2:66483269
|
C | T | 14 | a0001c0001t0001g0119a0001c0001t0001g0182a0001c0001t0001g0193others(11): Show | 14 | HG01243.hp1 HG01243.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.742+19049C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66483269 | ||||||
| chr2:66483302
|
A | G | 64 | a0001c0001t0001g0022a0001c0001t0001g0091a0001c0001t0001g0096others(61): Show | 64 | HG01109.hp1 HG01109.hp2 HG01123.hp1 others(61): Show |
intron_variant | MODIFIER | c.742+19082A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66483302 | ||||||
| chr2:66483365
|
C | T | 2 | a0001c0001t0003g0226a0001c0001t0005g0019 | 2 | HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.742+19145C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66483365 | ||||||
| chr2:66483369
|
C | T | 3 | a0001c0001t0002g0212a0001c0001t0002g0233a0001c0001t0006g0025 | 3 | HG02809.hp1 HG02809.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.742+19149C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66483369 | ||||||
| chr2:66483446
|
A | G | 99 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0091others(96): Show | 99 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(96): Show |
intron_variant | MODIFIER | c.742+19226A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66483446 | ||||||
| chr2:66483672
|
G | C | 1 | a0001c0001t0002g0053 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.742+19452G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66483672 | ||||||
| chr2:66484012
|
A | G | 1 | a0001c0001t0006g0026 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.742+19792A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66484012 | ||||||
| chr2:66484116
|
T | C | 98 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0091others(95): Show | 98 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(95): Show |
intron_variant | MODIFIER | c.742+19896T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66484116 | ||||||
| chr2:66484173
|
G | A | 1 | a0001c0001t0037g0020 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.742+19953G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66484173 | ||||||
| chr2:66484199
|
G | C | 1 | a0001c0001t0001g0193 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.742+19979G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66484199 | ||||||
| chr2:66484567
|
A | AT | 4 | a0001c0001t0002g0008a0001c0001t0002g0070a0001c0001t0002g0071others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.742+20355dupT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66484567 | |||||
| chr2:66484574
|
T | C | 1 | a0001c0001t0002g0053 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.742+20354T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66484574 | ||||||
| chr2:66484647
|
C | T | 11 | a0001c0001t0001g0022a0001c0001t0001g0178a0001c0001t0001g0217others(8): Show | 11 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.742+20427C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66484647 | ||||||
| chr2:66484710
|
C | A | 11 | a0001c0001t0001g0022a0001c0001t0001g0178a0001c0001t0001g0217others(8): Show | 11 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.742+20490C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66484710 | ||||||
| chr2:66484725
|
A | AT | 34 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0116others(31): Show | 34 | HG01123.hp1 HG01167.hp2 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.742+20513dupT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66484725 | |||||
| chr2:66484733
|
T | A | 1 | a0001c0001t0006g0026 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.742+20513T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66484733 | ||||||
| chr2:66484811
|
T | C | 98 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0091others(95): Show | 98 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(95): Show |
intron_variant | MODIFIER | c.742+20591T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66484811 | ||||||
| chr2:66484817
|
G | C | 99 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0091others(96): Show | 99 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(96): Show |
intron_variant | MODIFIER | c.742+20597G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66484817 | ||||||
| chr2:66484819
|
C | G | 1 | a0001c0001t0006g0026 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.742+20599C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66484819 | ||||||
| chr2:66485081
|
T | TTA | 17 | a0001c0001t0001g0119a0001c0001t0001g0182a0001c0001t0001g0193others(14): Show | 17 | HG01243.hp1 HG01243.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.742+20872_742+2087 others(6): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66485081 | |||||
| chr2:66485081
|
TTA | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0111 | 2 | HG03942.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.742+20872_742+2087 others(6): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66485081 | |||||
| chr2:66485096
|
C | T | 1 | a0001c0001t0002g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.742+20876C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66485096 | ||||||
| chr2:66485242
|
A | G | 56 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0116others(53): Show | 56 | HG01109.hp1 HG01123.hp1 HG01167.hp2 others(53): Show |
intron_variant | MODIFIER | c.742+21022A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66485242 | ||||||
| chr2:66485251
|
C | T | 1 | a0001c0001t0002g0037 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.742+21031C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66485251 | ||||||
| chr2:66485420
|
C | T | 1 | a0001c0001t0004g0152 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.742+21200C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66485420 | ||||||
| chr2:66485583
|
A | G | 56 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0116others(53): Show | 56 | HG01109.hp1 HG01123.hp1 HG01167.hp2 others(53): Show |
intron_variant | MODIFIER | c.742+21363A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66485583 | ||||||
| chr2:66485823
|
T | C | 1 | a0001c0001t0009g0243 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.742+21603T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66485823 | ||||||
| chr2:66485882
|
C | G | 1 | a0001c0001t0001g0222 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.742+21662C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66485882 | ||||||
| chr2:66485964
|
T | A | 28 | a0001c0001t0001g0011a0001c0001t0001g0093a0001c0001t0001g0107others(25): Show | 28 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.742+21744T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66485964 | ||||||
| chr2:66486020
|
G | A | 1 | a0001c0001t0006g0026 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.742+21800G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66486020 | ||||||
| chr2:66486196
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.742+21976G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66486196 | ||||||
| chr2:66486230
|
G | A | 1 | a0001c0001t0001g0123 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.742+22010G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66486230 | ||||||
| chr2:66486335
|
C | T | 1 | a0001c0001t0006g0026 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.742+22115C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66486335 | ||||||
| chr2:66486727
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.742+22507G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66486727 | ||||||
| chr2:66486851
|
T | C | 98 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0091others(95): Show | 98 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(95): Show |
intron_variant | MODIFIER | c.742+22631T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66486851 | ||||||
| chr2:66486901
|
A | G | 7 | a0001c0001t0001g0119a0001c0001t0001g0214a0001c0001t0001g0216others(4): Show | 7 | HG01243.hp1 HG03195.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.742+22681A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66486901 | ||||||
| chr2:66486925
|
T | A | 4 | a0001c0001t0001g0238a0001c0001t0003g0227a0001c0001t0011g0005others(1): Show | 4 | HG01109.hp1 HG02647.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.742+22705T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66486925 | ||||||
| chr2:66486925
|
T | C | 3 | a0001c0001t0003g0226a0001c0001t0004g0004a0001c0001t0005g0019 | 3 | HG02622.hp2 HG03669.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.742+22705T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66486925 | ||||||
| chr2:66487029
|
G | C | 2 | a0001c0001t0003g0226a0001c0001t0005g0019 | 2 | HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.742+22809G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66487029 | ||||||
| chr2:66487155
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.742+22935G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66487155 | ||||||
| chr2:66487465
|
A | G | 34 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0116others(31): Show | 34 | HG01123.hp1 HG01167.hp2 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.742+23245A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66487465 | ||||||
| chr2:66487957
|
G | A | 7 | a0001c0001t0001g0238a0001c0001t0003g0226a0001c0001t0003g0227others(4): Show | 7 | HG01109.hp1 HG02622.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.742+23737G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66487957 | ||||||
| chr2:66488140
|
T | G | 32 | a0001c0001t0001g0011a0001c0001t0001g0093a0001c0001t0001g0107others(29): Show | 32 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.742+23920T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66488140 | ||||||
| chr2:66488166
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.742+23946T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66488166 | ||||||
| chr2:66488232
|
T | G | 100 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0091others(97): Show | 100 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(97): Show |
intron_variant | MODIFIER | c.743-23917T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66488232 | ||||||
| chr2:66488308
|
A | G | 1 | a0001c0001t0002g0038 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.743-23841A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66488308 | ||||||
| chr2:66488602
|
C | T | 1 | a0001c0001t0005g0042 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.743-23547C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66488602 | ||||||
| chr2:66488603
|
G | A | 34 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0116others(31): Show | 34 | HG01123.hp1 HG01167.hp2 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.743-23546G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66488603 | ||||||
| chr2:66488656
|
C | A | 11 | a0001c0001t0001g0022a0001c0001t0001g0178a0001c0001t0001g0217others(8): Show | 11 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.743-23493C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66488656 | ||||||
| chr2:66488691
|
A | T | 1 | a0001c0001t0001g0164 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.743-23458A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66488691 | ||||||
| chr2:66488884
|
G | C | 1 | a0001c0001t0002g0075 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.743-23265G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66488884 | ||||||
| chr2:66489460
|
C | T | 52 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0116others(49): Show | 52 | HG01123.hp1 HG01167.hp2 HG01243.hp1 others(49): Show |
intron_variant | MODIFIER | c.743-22689C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66489460 | ||||||
| chr2:66489754
|
T | C | 1 | a0001c0001t0005g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.743-22395T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66489754 | ||||||
| chr2:66489757
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.743-22392A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66489757 | ||||||
| chr2:66490029
|
T | C | 1 | a0001c0001t0006g0066 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.743-22120T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66490029 | ||||||
| chr2:66490081
|
A | G | 3 | a0001c0001t0001g0108a0001c0001t0003g0188a0001c0001t0007g0163 | 3 | HG02683.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.743-22068A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66490081 | ||||||
| chr2:66490126
|
A | G | 1 | a0001c0001t0005g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.743-22023A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66490126 | ||||||
| chr2:66490199
|
C | T | 1 | a0001c0001t0002g0232 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.743-21950C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66490199 | ||||||
| chr2:66490285
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.743-21864T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66490285 | ||||||
| chr2:66490461
|
A | G | 15 | a0001c0001t0001g0119a0001c0001t0001g0182a0001c0001t0001g0193others(12): Show | 15 | HG01243.hp1 HG01243.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.743-21688A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66490461 | ||||||
| chr2:66490474
|
CT | C | 49 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0116others(46): Show | 49 | HG01123.hp1 HG01167.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.743-21670delT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66490474 | |||||
| chr2:66490505
|
T | A | 15 | a0001c0001t0001g0119a0001c0001t0001g0182a0001c0001t0001g0193others(12): Show | 15 | HG01243.hp1 HG01243.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.743-21644T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66490505 | ||||||
| chr2:66491042
|
G | GA | 11 | a0001c0001t0001g0022a0001c0001t0001g0178a0001c0001t0001g0217others(8): Show | 11 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.743-21097dupA | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66491042 | |||||
| chr2:66491093
|
A | AAG | 99 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0091others(96): Show | 99 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(96): Show |
intron_variant | MODIFIER | c.743-21052_743-2105 others(6): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66491093 | |||||
| chr2:66491291
|
G | A | 16 | a0001c0001t0001g0119a0001c0001t0001g0182a0001c0001t0001g0193others(13): Show | 16 | HG01243.hp1 HG01243.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.743-20858G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66491291 | ||||||
| chr2:66491424
|
A | G | 16 | a0001c0001t0001g0119a0001c0001t0001g0182a0001c0001t0001g0193others(13): Show | 16 | HG01243.hp1 HG01243.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.743-20725A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66491424 | ||||||
| chr2:66491567
|
C | T | 1 | a0001c0001t0002g0200 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.743-20582C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66491567 | ||||||
| chr2:66491644
|
G | C | 1 | a0001c0001t0003g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.743-20505G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66491644 | ||||||
| chr2:66491982
|
G | A | 1 | a0001c0001t0006g0026 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.743-20167G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66491982 | ||||||
| chr2:66492069
|
T | TTG | 31 | a0001c0001t0001g0011a0001c0001t0001g0093a0001c0001t0001g0108others(28): Show | 31 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.743-20060_743-2005 others(6): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66492069 | |||||
| chr2:66492069
|
TTG | T | 3 | a0001c0001t0002g0053a0001c0001t0003g0150a0001c0001t0006g0204 | 3 | HG00621.hp1 HG00673.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.743-20060_743-2005 others(6): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66492069 | |||||
| chr2:66492069
|
TTGTG | T | 2 | a0001c0001t0001g0182a0001c0001t0002g0200 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.743-20062_743-2005 others(8): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66492069 | |||||
| chr2:66492095
|
T | A | 99 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0091others(96): Show | 99 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(96): Show |
intron_variant | MODIFIER | c.743-20054T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66492095 | ||||||
| chr2:66492291
|
T | C | 1 | a0001c0001t0013g0028 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.743-19858T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66492291 | ||||||
| chr2:66492371
|
A | G | 41 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0116others(38): Show | 41 | HG01109.hp1 HG01123.hp1 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.743-19778A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66492371 | ||||||
| chr2:66492684
|
T | G | 2 | a0001c0001t0001g0182a0001c0001t0005g0201 | 2 | HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.743-19465T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66492684 | ||||||
| chr2:66492848
|
C | G | 1 | a0001c0001t0018g0177 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.743-19301C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66492848 | ||||||
| chr2:66492901
|
G | A | 1 | a0001c0001t0006g0027 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.743-19248G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66492901 | ||||||
| chr2:66492958
|
A | G | 11 | a0001c0001t0001g0022a0001c0001t0001g0178a0001c0001t0001g0217others(8): Show | 11 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.743-19191A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66492958 | ||||||
| chr2:66492967
|
A | C | 31 | a0001c0001t0001g0011a0001c0001t0001g0093a0001c0001t0001g0107others(28): Show | 31 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.743-19182A>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66492967 | ||||||
| chr2:66493079
|
C | G | 3 | a0001c0001t0001g0217a0001c0001t0011g0219a0001c0001t0011g0220 | 3 | HG01109.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.743-19070C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66493079 | ||||||
| chr2:66493491
|
C | G | 3 | a0001c0001t0001g0096a0001c0001t0002g0230a0001c0001t0021g0183 | 3 | HG02055.hp2 HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.743-18658C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66493491 | ||||||
| chr2:66493702
|
C | A | 34 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0116others(31): Show | 34 | HG01123.hp1 HG01167.hp2 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.743-18447C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66493702 | ||||||
| chr2:66493706
|
C | A | 36 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0116others(33): Show | 36 | HG01123.hp1 HG01167.hp2 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.743-18443C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66493706 | ||||||
| chr2:66493763
|
C | A | 1 | a0001c0001t0018g0177 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.743-18386C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66493763 | ||||||
| chr2:66493947
|
T | C | 1 | a0001c0001t0004g0004 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.743-18202T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66493947 | ||||||
| chr2:66493952
|
G | A | 1 | a0001c0001t0013g0028 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.743-18197G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66493952 | ||||||
| chr2:66494117
|
CAA | C | 34 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0116others(31): Show | 34 | HG01123.hp1 HG01167.hp2 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.743-18026_743-1802 others(6): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66494117 | |||||
| chr2:66494127
|
G | C | 1 | a0001c0001t0004g0004 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.743-18022G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66494127 | ||||||
| chr2:66494216
|
T | C | 1 | a0001c0001t0004g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.743-17933T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66494216 | ||||||
| chr2:66494222
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.743-17927C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66494222 | ||||||
| chr2:66494270
|
C | A | 11 | a0001c0001t0001g0022a0001c0001t0001g0178a0001c0001t0001g0217others(8): Show | 11 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.743-17879C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66494270 | ||||||
| chr2:66494423
|
A | G | 1 | a0001c0001t0037g0020 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.743-17726A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66494423 | ||||||
| chr2:66494457
|
C | A | 4 | a0001c0001t0001g0238a0001c0001t0003g0227a0001c0001t0011g0005others(1): Show | 4 | HG01109.hp1 HG02647.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.743-17692C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66494457 | ||||||
| chr2:66494507
|
A | G | 1 | a0001c0001t0009g0244 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743-17642A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66494507 | ||||||
| chr2:66494728
|
G | A | 55 | a0001c0001t0001g0022a0001c0001t0001g0091a0001c0001t0001g0096others(52): Show | 55 | HG01109.hp1 HG01109.hp2 HG01123.hp1 others(52): Show |
intron_variant | MODIFIER | c.743-17421G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66494728 | ||||||
| chr2:66495078
|
A | AT | 4 | a0001c0001t0001g0104a0001c0001t0001g0198a0001c0001t0002g0034others(1): Show | 4 | HG01258.hp1 HG01978.hp2 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.743-17071_743-1707 others(5): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66495078 | ||||||
| chr2:66495078
|
ACC | A | 5 | a0001c0001t0001g0099a0001c0001t0001g0117a0001c0001t0002g0067others(2): Show | 5 | HG00323.hp1 HG02897.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.743-17070_743-1706 others(6): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66495078 | ||||||
| chr2:66495079
|
C | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0094others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.743-17070C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66495079 | ||||||
| chr2:66495080
|
C | CT | 32 | a0001c0001t0001g0011a0001c0001t0001g0093a0001c0001t0001g0111others(29): Show | 32 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.743-17041dupT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66495080 | |||||
| chr2:66495080
|
C | T | 4 | a0001c0001t0001g0104a0001c0001t0001g0198a0001c0001t0002g0034others(1): Show | 4 | HG01258.hp1 HG01978.hp2 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.743-17069C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66495080 | ||||||
| chr2:66495080
|
CT | C | 72 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0094others(69): Show | 72 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.743-17041delT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66495080 | |||||
| chr2:66495080
|
CTT | C | 26 | a0001c0001t0001g0096a0001c0001t0001g0116a0001c0001t0001g0121others(23): Show | 26 | HG01123.hp1 HG01167.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.743-17042_743-1704 others(6): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66495080 | |||||
| chr2:66495082
|
T | C | 5 | a0001c0001t0001g0099a0001c0001t0001g0117a0001c0001t0002g0067others(2): Show | 5 | HG00323.hp1 HG02897.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.743-17067T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66495082 | ||||||
| chr2:66495109
|
A | T | 1 | a0001c0001t0005g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.743-17040A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66495109 | ||||||
| chr2:66495155
|
T | C | 34 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0116others(31): Show | 34 | HG01123.hp1 HG01167.hp2 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.743-16994T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66495155 | ||||||
| chr2:66495228
|
C | G | 1 | a0001c0001t0003g0196 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.743-16921C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66495228 | ||||||
| chr2:66495370
|
C | A | 4 | a0001c0001t0001g0238a0001c0001t0003g0227a0001c0001t0011g0005others(1): Show | 4 | HG01109.hp1 HG02647.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.743-16779C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66495370 | ||||||
| chr2:66495480
|
T | C | 1 | a0001c0001t0002g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.743-16669T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66495480 | ||||||
| chr2:66495679
|
C | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0094others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.743-16470C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66495679 | ||||||
| chr2:66496002
|
A | G | 2 | a0001c0001t0002g0232a0001c0001t0004g0004 | 2 | HG01433.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.743-16147A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66496002 | ||||||
| chr2:66496080
|
A | T | 1 | a0001c0001t0002g0200 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.743-16069A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66496080 | ||||||
| chr2:66496131
|
G | A | 7 | a0001c0001t0001g0022a0001c0001t0001g0217a0001c0001t0001g0222others(4): Show | 7 | HG01109.hp2 HG02055.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.743-16018G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66496131 | ||||||
| chr2:66496176
|
C | G | 1 | a0001c0001t0002g0083 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.743-15973C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66496176 | ||||||
| chr2:66496475
|
A | G | 1 | a0001c0001t0025g0024 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.743-15674A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66496475 | ||||||
| chr2:66496509
|
C | G | 1 | a0001c0001t0001g0105 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.743-15640C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66496509 | ||||||
| chr2:66496546
|
G | A | 3 | a0001c0001t0001g0156a0001c0001t0001g0187a0001c0001t0022g0186 | 3 | HG00099.hp1 HG00741.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.743-15603G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66496546 | ||||||
| chr2:66496559
|
A | T | 3 | a0001c0001t0005g0019a0001c0001t0005g0201a0001c0001t0006g0026 | 3 | HG02622.hp2 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.743-15590A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66496559 | ||||||
| chr2:66496567
|
C | T | 189 | a0001c0001t0001g0012a0001c0001t0001g0091a0001c0001t0001g0093others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.743-15582C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66496567 | ||||||
| chr2:66496813
|
T | G | 1 | a0001c0001t0005g0019 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.743-15336T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66496813 | ||||||
| chr2:66496931
|
C | T | 120 | a0001c0001t0001g0012a0001c0001t0001g0091a0001c0001t0001g0093others(117): Show | 120 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.743-15218C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66496931 | ||||||
| chr2:66497010
|
C | T | 124 | a0001c0001t0001g0012a0001c0001t0001g0091a0001c0001t0001g0093others(121): Show | 124 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.743-15139C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66497010 | ||||||
| chr2:66497011
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.743-15138G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66497011 | ||||||
| chr2:66497126
|
G | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0193 | 2 | HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.743-15023G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66497126 | ||||||
| chr2:66497381
|
G | A | 129 | a0001c0001t0001g0012a0001c0001t0001g0091a0001c0001t0001g0093others(126): Show | 129 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.743-14768G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66497381 | ||||||
| chr2:66497448
|
T | C | 3 | a0001c0001t0001g0138a0001c0001t0006g0027a0001c0001t0036g0245 | 3 | HG02886.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.743-14701T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66497448 | ||||||
| chr2:66497630
|
C | T | 1 | a0001c0001t0008g0072 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.743-14519C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66497630 | ||||||
| chr2:66497644
|
C | T | 1 | a0001c0001t0006g0025 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.743-14505C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66497644 | ||||||
| chr2:66497731
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.743-14418A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66497731 | ||||||
| chr2:66497930
|
T | C | 66 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0103others(63): Show | 66 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.743-14219T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66497930 | ||||||
| chr2:66497934
|
T | TA | 6 | a0001c0001t0001g0022a0001c0001t0001g0193a0001c0001t0001g0238others(3): Show | 6 | HG02630.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.743-14214dupA | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66497934 | |||||
| chr2:66497938
|
C | G | 163 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.743-14211C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66497938 | ||||||
| chr2:66498018
|
GA | G | 20 | a0001c0001t0001g0116a0001c0001t0001g0128a0001c0001t0001g0154others(17): Show | 20 | HG00099.hp1 HG00741.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.743-14123delA | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66498018 | |||||
| chr2:66498029
|
G | GTA | 3 | a0001c0001t0001g0093a0001c0001t0032g0016a0001c0003t0001g0141 | 3 | HG00738.hp1 HG02683.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.743-14118_743-1411 others(6): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66498029 | |||||
| chr2:66498156
|
T | C | 1 | a0001c0001t0007g0228 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.743-13993T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66498156 | ||||||
| chr2:66498445
|
T | C | 74 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0104others(71): Show | 74 | HG00621.hp1 HG00673.hp1 HG00673.hp2 others(71): Show |
intron_variant | MODIFIER | c.743-13704T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66498445 | ||||||
| chr2:66498506
|
T | C | 18 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(15): Show | 18 | HG01081.hp2 HG02280.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.743-13643T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66498506 | ||||||
| chr2:66498519
|
G | C | 6 | a0001c0001t0001g0182a0001c0001t0001g0222a0001c0001t0011g0005others(3): Show | 6 | HG01109.hp1 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.743-13630G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66498519 | ||||||
| chr2:66498521
|
C | T | 1 | a0001c0001t0007g0109 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.743-13628C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66498521 | ||||||
| chr2:66498580
|
G | C | 1 | a0001c0001t0006g0026 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.743-13569G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66498580 | ||||||
| chr2:66498693
|
T | C | 2 | a0001c0001t0001g0130a0001c0001t0001g0172 | 2 | HG01255.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.743-13456T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66498693 | ||||||
| chr2:66498697
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.743-13452C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66498697 | ||||||
| chr2:66498702
|
G | A | 3 | a0001c0001t0002g0041a0001c0001t0002g0060a0001c0001t0004g0101 | 3 | HG02165.hp1 NA18959.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.743-13447G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66498702 | ||||||
| chr2:66498713
|
G | T | 3 | a0001c0001t0001g0178a0001c0001t0009g0246a0001c0001t0035g0199 | 3 | HG01243.hp2 HG02280.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.743-13436G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66498713 | ||||||
| chr2:66498735
|
G | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0022others(141): Show | 144 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.743-13414G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66498735 | ||||||
| chr2:66498745
|
T | C | 1 | a0001c0001t0001g0001 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.743-13404T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66498745 | ||||||
| chr2:66498804
|
T | C | 5 | a0001c0001t0001g0096a0001c0001t0001g0176a0001c0001t0001g0214others(2): Show | 5 | HG02257.hp1 HG03098.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.743-13345T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66498804 | ||||||
| chr2:66498808
|
T | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0093others(125): Show | 128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.743-13341T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66498808 | ||||||
| chr2:66499011
|
T | A | 1 | a0001c0001t0002g0233 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.743-13138T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66499011 | ||||||
| chr2:66499085
|
C | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0022others(107): Show | 110 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.743-13064C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66499085 | ||||||
| chr2:66499299
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.743-12850T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66499299 | ||||||
| chr2:66499321
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0022others(105): Show | 108 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.743-12828C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66499321 | ||||||
| chr2:66499378
|
CT | C | 6 | a0001c0001t0001g0138a0001c0001t0001g0193a0001c0001t0005g0019others(3): Show | 6 | HG02622.hp2 HG02630.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.743-12770delT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66499378 | ||||||
| chr2:66499397
|
C | T | 7 | a0001c0001t0001g0143a0001c0001t0001g0189a0001c0001t0002g0035others(4): Show | 7 | HG00621.hp2 HG01358.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.743-12752C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66499397 | ||||||
| chr2:66499436
|
C | T | 47 | a0001c0001t0001g0011a0001c0001t0001g0105a0001c0001t0001g0108others(44): Show | 47 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.743-12713C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66499436 | ||||||
| chr2:66499508
|
G | C | 3 | a0001c0001t0021g0183a0001c0001t0029g0018a0001c0001t0037g0020 | 3 | HG02055.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.743-12641G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66499508 | ||||||
| chr2:66499696
|
T | TA | 109 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0022others(106): Show | 109 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.743-12436dupA | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66499696 | |||||
| chr2:66499696
|
TA | T | 5 | a0001c0001t0001g0098a0001c0001t0001g0123a0001c0001t0001g0169others(2): Show | 5 | HG02717.hp1 NA18990.hp1 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.743-12436delA | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66499696 | |||||
| chr2:66499770
|
C | T | 21 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(18): Show | 21 | HG02280.hp2 HG02622.hp1 HG02717.hp1 others(18): Show |
intron_variant | MODIFIER | c.743-12379C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66499770 | ||||||
| chr2:66499990
|
C | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0093a0001c0001t0001g0103others(51): Show | 54 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.743-12159C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66499990 | ||||||
| chr2:66500394
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.743-11755G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66500394 | ||||||
| chr2:66500691
|
C | T | 14 | a0001c0001t0001g0192a0001c0001t0002g0030a0001c0001t0002g0053others(11): Show | 14 | HG00642.hp2 HG00673.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.743-11458C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66500691 | ||||||
| chr2:66500715
|
G | A | 12 | a0001c0001t0001g0169a0001c0001t0001g0181a0001c0001t0001g0185others(9): Show | 12 | HG02165.hp1 HG02165.hp2 NA18942.hp1 others(9): Show |
intron_variant | MODIFIER | c.743-11434G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66500715 | ||||||
| chr2:66500801
|
A | G | 3 | a0001c0001t0003g0215a0001c0001t0003g0227a0001c0001t0020g0015 | 3 | HG03139.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.743-11348A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66500801 | ||||||
| chr2:66500839
|
T | TACAC | 5 | a0001c0001t0001g0096a0001c0001t0001g0176a0001c0001t0001g0214others(2): Show | 5 | HG02257.hp1 HG03098.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.743-11306_743-1130 others(8): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66500839 | |||||
| chr2:66500846
|
A | G | 2 | a0001c0001t0001g0193a0001c0001t0009g0244 | 2 | HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.743-11303A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66500846 | ||||||
| chr2:66500971
|
G | C | 1 | a0001c0001t0018g0177 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.743-11178G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66500971 | ||||||
| chr2:66501034
|
T | C | 2 | a0001c0001t0001g0144a0001c0001t0002g0064 | 2 | NA18952.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.743-11115T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501034 | ||||||
| chr2:66501427
|
G | A | 2 | a0001c0001t0003g0021a0001c0001t0007g0023 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.743-10722G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501427 | ||||||
| chr2:66501495
|
G | GT | 11 | a0001c0001t0001g0094a0001c0001t0001g0138a0001c0001t0001g0153others(8): Show | 11 | HG00280.hp1 HG00733.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.743-10644dupT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66501495 | |||||
| chr2:66501564
|
T | C | 1 | a0001c0001t0001g0192 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.743-10585T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501564 | ||||||
| chr2:66501588
|
A | G | 56 | a0001c0001t0001g0091a0001c0001t0001g0104a0001c0001t0001g0128others(53): Show | 56 | HG00544.hp2 HG00642.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.743-10561A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501588 | ||||||
| chr2:66501661
|
A | G | 6 | a0001c0001t0001g0222a0001c0001t0001g0238a0001c0001t0002g0200others(3): Show | 6 | HG02630.hp2 HG02647.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.743-10488A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501661 | ||||||
| chr2:66501829
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.743-10320C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501829 | ||||||
| chr2:66501833
|
C | G | 1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.743-10316C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501833 | ||||||
| chr2:66501836
|
T | G | 1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.743-10313T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501836 | ||||||
| chr2:66501840
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.743-10309C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501840 | ||||||
| chr2:66501842
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.743-10307C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501842 | ||||||
| chr2:66501849
|
T | A | 1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.743-10300T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501849 | ||||||
| chr2:66501851
|
C | A | 1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.743-10298C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501851 | ||||||
| chr2:66501853
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.743-10296C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501853 | ||||||
| chr2:66501855
|
T | A | 1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.743-10294T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501855 | ||||||
| chr2:66501857
|
C | A | 1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.743-10292C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501857 | ||||||
| chr2:66501859
|
C | A | 1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.743-10290C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501859 | ||||||
| chr2:66501870
|
T | A | 1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.743-10279T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501870 | ||||||
| chr2:66501872
|
T | C | 1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.743-10277T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501872 | ||||||
| chr2:66501880
|
T | A | 1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.743-10269T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501880 | ||||||
| chr2:66501881
|
C | A | 1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.743-10268C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501881 | ||||||
| chr2:66501884
|
T | G | 1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.743-10265T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501884 | ||||||
| chr2:66501887
|
A | T | 1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.743-10262A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501887 | ||||||
| chr2:66501889
|
G | T | 1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.743-10260G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501889 | ||||||
| chr2:66501890
|
A | T | 1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.743-10259A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501890 | ||||||
| chr2:66501895
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.743-10254C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501895 | ||||||
| chr2:66501897
|
A | T | 1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.743-10252A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501897 | ||||||
| chr2:66501898
|
G | T | 1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.743-10251G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501898 | ||||||
| chr2:66501903
|
T | G | 1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.743-10246T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501903 | ||||||
| chr2:66501905
|
TTTTCATT others(5): Show |
T | 1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.743-10242_743-1023 others(16): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66501905 | |||||
| chr2:66501921
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.743-10228C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501921 | ||||||
| chr2:66501923
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.743-10226G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501923 | ||||||
| chr2:66501924
|
T | G | 1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.743-10225T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501924 | ||||||
| chr2:66501925
|
T | A | 1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.743-10224T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501925 | ||||||
| chr2:66501929
|
T | C | 1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.743-10220T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501929 | ||||||
| chr2:66501930
|
G | T | 1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.743-10219G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501930 | ||||||
| chr2:66501932
|
T | A | 1 | a0001c0001t0001g0149 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.743-10217T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501932 | ||||||
| chr2:66501976
|
A | G | 2 | a0001c0001t0001g0193a0001c0001t0009g0244 | 2 | HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.743-10173A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66501976 | ||||||
| chr2:66502028
|
G | A | 1 | a0001c0001t0005g0065 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.743-10121G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66502028 | ||||||
| chr2:66502065
|
C | T | 1 | a0001c0001t0004g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.743-10084C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66502065 | ||||||
| chr2:66502195
|
T | C | 3 | a0001c0001t0005g0019a0001c0001t0005g0201a0001c0004t0001g0124 | 3 | HG02622.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.743-9954T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66502195 | ||||||
| chr2:66502288
|
A | G | 148 | a0001c0001t0001g0001a0001c0001t0001g0091a0001c0001t0001g0093others(145): Show | 148 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.743-9861A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66502288 | ||||||
| chr2:66502337
|
T | C | 1 | a0001c0001t0037g0020 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.743-9812T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66502337 | ||||||
| chr2:66502375
|
C | T | 3 | a0001c0001t0001g0138a0001c0001t0001g0193a0001c0001t0009g0244 | 3 | HG02630.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.743-9774C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66502375 | ||||||
| chr2:66502992
|
A | G | 2 | a0001c0001t0005g0201a0001c0004t0001g0124 | 2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.743-9157A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66502992 | ||||||
| chr2:66503174
|
A | T | 1 | a0001c0001t0001g0197 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.743-8975A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66503174 | ||||||
| chr2:66503269
|
C | T | 5 | a0001c0001t0001g0096a0001c0001t0001g0176a0001c0001t0001g0214others(2): Show | 5 | HG02257.hp1 HG03098.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.743-8880C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66503269 | ||||||
| chr2:66503440
|
T | C | 3 | a0001c0001t0001g0138a0001c0001t0001g0193a0001c0001t0009g0244 | 3 | HG02630.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.743-8709T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66503440 | ||||||
| chr2:66503478
|
T | G | 55 | a0001c0001t0001g0091a0001c0001t0001g0104a0001c0001t0001g0128others(52): Show | 55 | HG00544.hp2 HG00642.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.743-8671T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66503478 | ||||||
| chr2:66503651
|
A | G | 9 | a0001c0001t0001g0094a0001c0001t0001g0153a0001c0001t0001g0160others(6): Show | 9 | HG00280.hp1 HG00733.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.743-8498A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66503651 | ||||||
| chr2:66503671
|
G | GCTT | 174 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0022others(171): Show | 174 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.743-8478_743-8477i others(5): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66503671 | ||||||
| chr2:66503736
|
A | AT | 17 | a0001c0001t0001g0011a0001c0001t0001g0111a0001c0001t0001g0113others(14): Show | 17 | HG00733.hp1 HG00741.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.743-8387dupT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66503736 | |||||
| chr2:66503736
|
AT | A | 29 | a0001c0001t0001g0107a0001c0001t0001g0149a0001c0001t0001g0167others(26): Show | 29 | HG00544.hp2 HG00642.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.743-8387delT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66503736 | |||||
| chr2:66503736
|
ATT | A | 132 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0022others(129): Show | 132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.743-8388_743-8387d others(4): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66503736 | |||||
| chr2:66503736
|
ATTT | A | 10 | a0001c0001t0001g0096a0001c0001t0001g0159a0001c0001t0001g0169others(7): Show | 10 | HG01109.hp1 HG02165.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.743-8389_743-8387d others(5): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66503736 | |||||
| chr2:66503997
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.743-8152G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66503997 | ||||||
| chr2:66504089
|
G | A | 4 | a0001c0001t0005g0019a0001c0001t0005g0201a0001c0001t0009g0246others(1): Show | 4 | HG02622.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.743-8060G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66504089 | ||||||
| chr2:66504110
|
T | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0022others(161): Show | 164 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.743-8039T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66504110 | ||||||
| chr2:66504315
|
C | A | 3 | a0001c0001t0001g0138a0001c0001t0001g0193a0001c0001t0009g0244 | 3 | HG02630.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.743-7834C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66504315 | ||||||
| chr2:66504337
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.743-7812G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66504337 | ||||||
| chr2:66504729
|
G | A | 1 | a0001c0001t0011g0005 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.743-7420G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66504729 | ||||||
| chr2:66504954
|
C | G | 9 | a0001c0001t0001g0116a0001c0001t0001g0137a0001c0001t0001g0149others(6): Show | 9 | NA18941.hp2 NA18944.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.743-7195C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66504954 | ||||||
| chr2:66505043
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.743-7106A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66505043 | ||||||
| chr2:66505312
|
C | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0022others(132): Show | 135 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.743-6837C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66505312 | ||||||
| chr2:66505428
|
A | T | 1 | a0001c0001t0001g0165 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.743-6721A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66505428 | ||||||
| chr2:66505468
|
C | T | 4 | a0001c0001t0001g0096a0001c0001t0001g0214a0001c0001t0003g0139others(1): Show | 4 | HG02257.hp1 HG03139.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.743-6681C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66505468 | ||||||
| chr2:66506321
|
G | T | 1 | a0001c0003t0001g0141 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.743-5828G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66506321 | ||||||
| chr2:66506416
|
C | T | 4 | a0001c0001t0001g0012a0001c0001t0005g0029a0001c0001t0007g0140others(1): Show | 4 | HG00099.hp2 HG02965.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.743-5733C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66506416 | ||||||
| chr2:66506702
|
A | T | 4 | a0001c0001t0001g0012a0001c0001t0005g0029a0001c0001t0007g0140others(1): Show | 4 | HG00099.hp2 HG02965.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.743-5447A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66506702 | ||||||
| chr2:66506936
|
G | T | 5 | a0001c0001t0001g0096a0001c0001t0001g0176a0001c0001t0001g0214others(2): Show | 5 | HG02257.hp1 HG03098.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.743-5213G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66506936 | ||||||
| chr2:66507055
|
C | T | 2 | a0001c0001t0005g0201a0001c0004t0001g0124 | 2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.743-5094C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66507055 | ||||||
| chr2:66507091
|
C | G | 1 | a0001c0001t0001g0224 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.743-5058C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66507091 | ||||||
| chr2:66507313
|
T | TA | 3 | a0001c0001t0001g0111a0001c0001t0001g0145a0001c0001t0006g0058 | 3 | HG02735.hp2 HG03942.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.743-4833dupA | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66507313 | |||||
| chr2:66507328
|
G | A | 2 | a0001c0001t0003g0021a0001c0001t0007g0023 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.743-4821G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66507328 | ||||||
| chr2:66507988
|
G | A | 63 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0104others(60): Show | 63 | HG00544.hp2 HG00642.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.743-4161G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66507988 | ||||||
| chr2:66508336
|
G | A | 3 | a0001c0001t0021g0183a0001c0001t0029g0018a0001c0001t0037g0020 | 3 | HG02055.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.743-3813G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66508336 | ||||||
| chr2:66508367
|
C | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(206): Show | 209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.743-3782C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66508367 | ||||||
| chr2:66508375
|
G | T | 5 | a0001c0001t0001g0096a0001c0001t0001g0176a0001c0001t0001g0214others(2): Show | 5 | HG02257.hp1 HG03098.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.743-3774G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66508375 | ||||||
| chr2:66508441
|
G | C | 2 | a0001c0001t0001g0193a0001c0001t0009g0244 | 2 | HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.743-3708G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66508441 | ||||||
| chr2:66508526
|
G | C | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG02280.hp2 HG02622.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.743-3623G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66508526 | ||||||
| chr2:66508748
|
A | G | 1 | a0001c0001t0001g0001 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.743-3401A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66508748 | ||||||
| chr2:66509014
|
C | T | 5 | a0001c0001t0001g0096a0001c0001t0001g0176a0001c0001t0001g0214others(2): Show | 5 | HG02257.hp1 HG03098.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.743-3135C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66509014 | ||||||
| chr2:66509226
|
A | G | 6 | a0001c0001t0009g0241a0001c0001t0010g0092a0001c0001t0010g0115others(3): Show | 6 | HG01123.hp1 HG01167.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.743-2923A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66509226 | ||||||
| chr2:66509342
|
C | A | 1 | a0001c0001t0003g0125 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.743-2807C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66509342 | ||||||
| chr2:66509468
|
G | A | 1 | a0001c0001t0034g0087 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.743-2681G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66509468 | ||||||
| chr2:66509571
|
G | C | 3 | a0001c0001t0001g0111a0001c0001t0001g0145a0001c0001t0006g0058 | 3 | HG02735.hp2 HG03942.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.743-2578G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66509571 | ||||||
| chr2:66509584
|
T | C | 3 | a0001c0001t0001g0094a0001c0001t0001g0160a0001c0001t0002g0048 | 3 | HG00280.hp1 HG01074.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.743-2565T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66509584 | ||||||
| chr2:66509932
|
T | A | 4 | a0001c0001t0002g0032a0001c0001t0002g0034a0001c0001t0005g0077others(1): Show | 4 | NA18940.hp1 NA18944.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.743-2217T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66509932 | ||||||
| chr2:66510101
|
G | A | 4 | a0001c0001t0001g0012a0001c0001t0005g0029a0001c0001t0007g0140others(1): Show | 4 | HG00099.hp2 HG02965.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.743-2048G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66510101 | ||||||
| chr2:66510241
|
T | G | 6 | a0001c0001t0001g0096a0001c0001t0001g0176a0001c0001t0001g0214others(3): Show | 6 | HG02257.hp1 HG03098.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.743-1908T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66510241 | ||||||
| chr2:66510365
|
T | A | 1 | a0001c0001t0004g0101 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.743-1784T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66510365 | ||||||
| chr2:66510577
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.743-1572C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66510577 | ||||||
| chr2:66510624
|
T | G | 7 | a0001c0001t0001g0222a0001c0001t0001g0238a0001c0001t0002g0200others(4): Show | 7 | HG02622.hp2 HG02630.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.743-1525T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66510624 | ||||||
| chr2:66510644
|
C | T | 1 | a0001c0001t0009g0244 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743-1505C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66510644 | ||||||
| chr2:66511036
|
G | A | 3 | a0001c0001t0005g0201a0001c0001t0009g0246a0001c0004t0001g0124 | 3 | HG02717.hp1 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.743-1113G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66511036 | ||||||
| chr2:66511069
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.743-1080G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66511069 | ||||||
| chr2:66511081
|
G | A | 16 | a0001c0001t0001g0099a0001c0001t0001g0133a0001c0001t0001g0143others(13): Show | 16 | HG00323.hp1 HG00621.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.743-1068G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66511081 | ||||||
| chr2:66511196
|
T | C | 1 | a0001c0001t0005g0065 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.743-953T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66511196 | ||||||
| chr2:66511235
|
A | T | 68 | a0001c0001t0001g0001a0001c0001t0001g0093a0001c0001t0001g0103others(65): Show | 68 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.743-914A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66511235 | ||||||
| chr2:66511363
|
A | C | 1 | a0001c0001t0001g0110 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.743-786A>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66511363 | ||||||
| chr2:66511500
|
A | G | 3 | a0001c0001t0001g0138a0001c0001t0001g0193a0001c0001t0009g0244 | 3 | HG02630.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.743-649A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66511500 | ||||||
| chr2:66511829
|
TTACACTT others(10): Show |
T | 16 | a0001c0001t0001g0099a0001c0001t0001g0133a0001c0001t0001g0143others(13): Show | 16 | HG00323.hp1 HG00621.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.743-319_743-303del others(17): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66511829 | ||||||
| chr2:66511924
|
T | G | 30 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0099others(27): Show | 30 | HG00099.hp2 HG00323.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.743-225T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66511924 | ||||||
| chr2:66511992
|
C | CTT | 3 | a0001c0001t0001g0138a0001c0001t0001g0193a0001c0001t0009g0244 | 3 | HG02630.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.743-156_743-155ins others(2): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 66511992 | |||||
| chr2:66512030
|
A | G | 3 | a0001c0001t0001g0138a0001c0001t0001g0193a0001c0001t0009g0244 | 3 | HG02630.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.743-119A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 7/12 | chr2 | 66512030 | ||||||
| chr2:66512496
|
C | T | 1 | a0001c0001t0002g0035 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.888+202C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66512496 | ||||||
| chr2:66512946
|
C | T | 3 | a0001c0001t0001g0138a0001c0001t0001g0193a0001c0001t0009g0244 | 3 | HG02630.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.888+652C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66512946 | ||||||
| chr2:66513092
|
A | C | 1 | a0001c0001t0001g0159 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.888+798A>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66513092 | ||||||
| chr2:66513197
|
A | G | 1 | a0001c0001t0001g0135 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.888+903A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66513197 | ||||||
| chr2:66513408
|
C | T | 18 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(15): Show | 18 | HG02280.hp2 HG02622.hp1 HG02717.hp2 others(15): Show |
intron_variant | MODIFIER | c.888+1114C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66513408 | ||||||
| chr2:66513596
|
T | TA | 8 | a0001c0001t0001g0096a0001c0001t0001g0138a0001c0001t0001g0176others(5): Show | 8 | HG02257.hp1 HG02630.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.888+1316dupA | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66513596 | |||||
| chr2:66513819
|
A | C | 5 | a0001c0001t0001g0096a0001c0001t0001g0176a0001c0001t0001g0214others(2): Show | 5 | HG02257.hp1 HG03098.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.888+1525A>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66513819 | ||||||
| chr2:66513854
|
G | A | 30 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0099others(27): Show | 30 | HG00099.hp2 HG00323.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.888+1560G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66513854 | ||||||
| chr2:66513879
|
A | G | 3 | a0001c0001t0001g0138a0001c0001t0001g0193a0001c0001t0009g0244 | 3 | HG02630.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.888+1585A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66513879 | ||||||
| chr2:66513972
|
C | T | 1 | a0001c0001t0003g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.888+1678C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66513972 | ||||||
| chr2:66513980
|
C | G | 30 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0099others(27): Show | 30 | HG00099.hp2 HG00323.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.888+1686C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66513980 | ||||||
| chr2:66514074
|
T | G | 3 | a0001c0001t0001g0138a0001c0001t0001g0193a0001c0001t0009g0244 | 3 | HG02630.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.888+1780T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66514074 | ||||||
| chr2:66514217
|
G | A | 5 | a0001c0001t0001g0096a0001c0001t0001g0176a0001c0001t0001g0214others(2): Show | 5 | HG02257.hp1 HG03098.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.888+1923G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66514217 | ||||||
| chr2:66514323
|
T | G | 4 | a0001c0001t0001g0012a0001c0001t0005g0029a0001c0001t0007g0140others(1): Show | 4 | HG00099.hp2 HG02965.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.888+2029T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66514323 | ||||||
| chr2:66514445
|
C | T | 1 | a0001c0001t0002g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.888+2151C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66514445 | ||||||
| chr2:66514446
|
G | A | 1 | a0001c0001t0002g0039 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.888+2152G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66514446 | ||||||
| chr2:66514666
|
T | G | 3 | a0001c0001t0001g0138a0001c0001t0001g0193a0001c0001t0009g0244 | 3 | HG02630.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.888+2372T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66514666 | ||||||
| chr2:66514798
|
A | C | 1 | a0001c0001t0008g0051 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.888+2504A>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66514798 | ||||||
| chr2:66515106
|
T | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0022others(125): Show | 128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.888+2812T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66515106 | ||||||
| chr2:66515175
|
T | C | 1 | a0001c0001t0001g0148 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.888+2881T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66515175 | ||||||
| chr2:66515208
|
C | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0022others(132): Show | 135 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.888+2914C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66515208 | ||||||
| chr2:66515221
|
T | G | 1 | a0001c0001t0002g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.888+2927T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66515221 | ||||||
| chr2:66515255
|
T | C | 3 | a0001c0001t0005g0019a0001c0001t0005g0201a0001c0004t0001g0124 | 3 | HG02622.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.888+2961T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66515255 | ||||||
| chr2:66515391
|
C | G | 5 | a0001c0001t0001g0096a0001c0001t0001g0176a0001c0001t0001g0214others(2): Show | 5 | HG02257.hp1 HG03098.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.888+3097C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66515391 | ||||||
| chr2:66515409
|
A | C | 2 | a0001c0001t0011g0219a0001c0001t0011g0220 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.888+3115A>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66515409 | ||||||
| chr2:66515817
|
A | C | 1 | a0001c0001t0007g0140 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.888+3523A>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66515817 | ||||||
| chr2:66516148
|
A | G | 3 | a0001c0001t0013g0028a0001c0001t0027g0211a0001c0001t0030g0014 | 3 | HG02886.hp2 HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.888+3854A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66516148 | ||||||
| chr2:66516168
|
A | G | 2 | a0001c0001t0005g0201a0001c0004t0001g0124 | 2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.888+3874A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66516168 | ||||||
| chr2:66516191
|
C | T | 16 | a0001c0001t0002g0210a0001c0001t0003g0215a0001c0001t0003g0227others(13): Show | 16 | HG01123.hp1 HG01167.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.888+3897C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66516191 | ||||||
| chr2:66516248
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.888+3954C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66516248 | ||||||
| chr2:66516333
|
C | T | 3 | a0001c0001t0003g0215a0001c0001t0003g0227a0001c0001t0020g0015 | 3 | HG03139.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.888+4039C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66516333 | ||||||
| chr2:66516334
|
G | A | 5 | a0001c0001t0001g0096a0001c0001t0001g0176a0001c0001t0001g0214others(2): Show | 5 | HG02257.hp1 HG03098.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.888+4040G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66516334 | ||||||
| chr2:66516424
|
C | T | 1 | a0001c0001t0003g0155 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.888+4130C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66516424 | ||||||
| chr2:66516459
|
C | T | 183 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(180): Show | 183 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.888+4165C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66516459 | ||||||
| chr2:66516577
|
T | G | 1 | a0001c0001t0006g0027 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.888+4283T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66516577 | ||||||
| chr2:66516577
|
TTG | T | 70 | a0001c0001t0001g0022a0001c0001t0001g0096a0001c0001t0001g0098others(67): Show | 70 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.888+4310_888+4311d others(4): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66516577 | |||||
| chr2:66516577
|
TTGTG | T | 6 | a0001c0001t0002g0209a0001c0001t0005g0202a0001c0001t0011g0005others(3): Show | 6 | HG01109.hp1 HG02004.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.888+4308_888+4311d others(6): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66516577 | |||||
| chr2:66517401
|
A | G | 2 | a0001c0001t0021g0183a0001c0001t0029g0018 | 2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.888+5107A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66517401 | ||||||
| chr2:66517414
|
AT | A | 5 | a0001c0001t0001g0096a0001c0001t0001g0176a0001c0001t0001g0214others(2): Show | 5 | HG02976.hp2 HG03098.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.888+5129delT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66517414 | |||||
| chr2:66517442
|
A | T | 1 | a0001c0001t0005g0065 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.888+5148A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66517442 | ||||||
| chr2:66517471
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0091others(105): Show | 108 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.888+5177C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66517471 | ||||||
| chr2:66517607
|
A | G | 2 | a0001c0001t0003g0139a0001c0001t0005g0029 | 2 | HG02257.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.888+5313A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66517607 | ||||||
| chr2:66517682
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.888+5388G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66517682 | ||||||
| chr2:66517765
|
T | G | 1 | a0001c0001t0001g0108 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.888+5471T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66517765 | ||||||
| chr2:66517835
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.888+5541C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66517835 | ||||||
| chr2:66517909
|
C | T | 2 | a0001c0001t0003g0188a0001c0001t0007g0163 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.888+5615C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66517909 | ||||||
| chr2:66518014
|
C | G | 1 | a0001c0001t0001g0138 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.888+5720C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66518014 | ||||||
| chr2:66518053
|
C | T | 1 | a0001c0001t0010g0221 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.888+5759C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66518053 | ||||||
| chr2:66518165
|
C | T | 1 | a0001c0001t0003g0227 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.888+5871C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66518165 | ||||||
| chr2:66518318
|
C | G | 30 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0116others(27): Show | 30 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.888+6024C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66518318 | ||||||
| chr2:66518369
|
G | C | 5 | a0001c0001t0001g0182a0001c0001t0001g0216a0001c0001t0011g0005others(2): Show | 5 | HG01109.hp1 HG01243.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.888+6075G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66518369 | ||||||
| chr2:66518531
|
A | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0091others(198): Show | 201 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.888+6237A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66518531 | ||||||
| chr2:66518534
|
C | A | 1 | a0001c0001t0006g0081 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.888+6240C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66518534 | ||||||
| chr2:66518562
|
A | C | 30 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0099others(27): Show | 30 | HG00099.hp2 HG00323.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.888+6268A>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66518562 | ||||||
| chr2:66518639
|
A | C | 28 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0001g0107others(25): Show | 28 | HG00408.hp1 HG00544.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.888+6345A>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66518639 | ||||||
| chr2:66518677
|
G | A | 10 | a0001c0001t0001g0224a0001c0001t0003g0003a0001c0001t0003g0010others(7): Show | 10 | HG02622.hp1 HG02735.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.888+6383G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66518677 | ||||||
| chr2:66518732
|
G | A | 9 | a0001c0001t0001g0094a0001c0001t0001g0153a0001c0001t0001g0160others(6): Show | 9 | HG00280.hp1 HG00733.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.888+6438G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66518732 | ||||||
| chr2:66518814
|
G | T | 27 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0099others(24): Show | 27 | HG00099.hp2 HG00323.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.888+6520G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66518814 | ||||||
| chr2:66518926
|
G | A | 1 | a0001c0001t0007g0120 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.888+6632G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66518926 | ||||||
| chr2:66518941
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0091others(199): Show | 202 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.888+6647G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66518941 | ||||||
| chr2:66518964
|
G | A | 1 | a0001c0001t0012g0205 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.888+6670G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66518964 | ||||||
| chr2:66519204
|
C | T | 27 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0099others(24): Show | 27 | HG00099.hp2 HG00323.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.888+6910C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66519204 | ||||||
| chr2:66519400
|
C | A | 28 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0116others(25): Show | 28 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.888+7106C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66519400 | ||||||
| chr2:66519401
|
C | A | 1 | a0001c0001t0001g0182 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.888+7107C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66519401 | ||||||
| chr2:66519419
|
C | T | 28 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0116others(25): Show | 28 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.888+7125C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66519419 | ||||||
| chr2:66519476
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.888+7182A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66519476 | ||||||
| chr2:66519624
|
G | A | 1 | a0001c0001t0019g0095 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.888+7330G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66519624 | ||||||
| chr2:66519880
|
G | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.888+7586G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66519880 | ||||||
| chr2:66520012
|
G | A | 2 | a0001c0001t0003g0021a0001c0001t0007g0023 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.888+7718G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66520012 | ||||||
| chr2:66520200
|
C | T | 27 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0099others(24): Show | 27 | HG00099.hp2 HG00323.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.888+7906C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66520200 | ||||||
| chr2:66520316
|
TA | T | 32 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0116others(29): Show | 32 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.888+8037delA | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66520316 | |||||
| chr2:66520316
|
TAA | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0091others(164): Show | 167 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.888+8036_888+8037d others(4): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66520316 | |||||
| chr2:66520348
|
G | A | 9 | a0001c0001t0001g0094a0001c0001t0001g0153a0001c0001t0001g0160others(6): Show | 9 | HG00280.hp1 HG00733.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.888+8054G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66520348 | ||||||
| chr2:66520351
|
G | A | 1 | a0001c0001t0002g0039 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.888+8057G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66520351 | ||||||
| chr2:66520374
|
A | AGGAGGC | 56 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0001g0107others(53): Show | 56 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.888+8081_888+8086d others(8): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66520374 | |||||
| chr2:66520531
|
C | T | 2 | a0001c0001t0003g0010a0001c0001t0003g0127 | 2 | HG03239.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.888+8237C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66520531 | ||||||
| chr2:66520532
|
A | T | 2 | a0001c0001t0003g0010a0001c0001t0003g0127 | 2 | HG03239.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.888+8238A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66520532 | ||||||
| chr2:66520681
|
A | G | 26 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0099others(23): Show | 26 | HG00099.hp2 HG00323.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.888+8387A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66520681 | ||||||
| chr2:66520931
|
C | T | 11 | a0001c0001t0001g0224a0001c0001t0003g0003a0001c0001t0003g0010others(8): Show | 11 | HG02622.hp1 HG02735.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.888+8637C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66520931 | ||||||
| chr2:66520951
|
A | G | 1 | a0001c0001t0023g0002 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.888+8657A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66520951 | ||||||
| chr2:66521070
|
T | C | 1 | a0001c0001t0005g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.888+8776T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66521070 | ||||||
| chr2:66521144
|
T | G | 199 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0091others(196): Show | 199 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.888+8850T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66521144 | ||||||
| chr2:66521223
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.888+8929C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66521223 | ||||||
| chr2:66521277
|
G | C | 1 | a0001c0001t0001g0238 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.888+8983G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66521277 | ||||||
| chr2:66521360
|
A | AT | 138 | a0001c0001t0001g0091a0001c0001t0001g0094a0001c0001t0001g0098others(135): Show | 138 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.888+9078dupT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66521360 | |||||
| chr2:66521360
|
A | ATT | 29 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0093others(26): Show | 29 | HG00323.hp2 HG00642.hp2 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.888+9077_888+9078d others(4): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66521360 | |||||
| chr2:66521453
|
C | T | 2 | a0001c0001t0003g0188a0001c0001t0007g0163 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.888+9159C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66521453 | ||||||
| chr2:66521928
|
T | C | 1 | a0001c0001t0012g0045 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.888+9634T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66521928 | ||||||
| chr2:66521976
|
G | A | 164 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0091others(161): Show | 164 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.888+9682G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66521976 | ||||||
| chr2:66522093
|
A | G | 1 | a0001c0001t0017g0168 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.888+9799A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66522093 | ||||||
| chr2:66522122
|
A | G | 234 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.888+9828A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66522122 | ||||||
| chr2:66522140
|
A | G | 2 | a0001c0001t0008g0072a0001c0001t0023g0002 | 2 | HG01167.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.888+9846A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66522140 | ||||||
| chr2:66522178
|
A | C | 31 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0116others(28): Show | 31 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.888+9884A>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66522178 | ||||||
| chr2:66522455
|
G | T | 1 | a0001c0001t0003g0155 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.888+10161G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66522455 | ||||||
| chr2:66522478
|
A | G | 164 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0091others(161): Show | 164 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.888+10184A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66522478 | ||||||
| chr2:66522561
|
T | A | 4 | a0001c0001t0001g0182a0001c0001t0011g0005a0001c0001t0011g0219others(1): Show | 4 | HG01109.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.888+10267T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66522561 | ||||||
| chr2:66522696
|
G | A | 28 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0116others(25): Show | 28 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.888+10402G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66522696 | ||||||
| chr2:66522699
|
A | G | 2 | a0001c0001t0011g0219a0001c0001t0011g0220 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.888+10405A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66522699 | ||||||
| chr2:66522885
|
T | A | 1 | a0001c0001t0001g0169 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.888+10591T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66522885 | ||||||
| chr2:66522885
|
T | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0091others(137): Show | 140 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.888+10591T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66522885 | ||||||
| chr2:66522906
|
T | G | 2 | a0001c0001t0003g0021a0001c0001t0007g0023 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.888+10612T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66522906 | ||||||
| chr2:66523020
|
T | C | 32 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0116others(29): Show | 32 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.888+10726T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66523020 | ||||||
| chr2:66523060
|
A | T | 1 | a0001c0001t0002g0039 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.888+10766A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66523060 | ||||||
| chr2:66523133
|
C | T | 28 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0116others(25): Show | 28 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.888+10839C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66523133 | ||||||
| chr2:66523152
|
C | A | 15 | a0001c0001t0001g0224a0001c0001t0003g0003a0001c0001t0003g0010others(12): Show | 15 | HG02257.hp1 HG02622.hp1 HG02735.hp1 others(12): Show |
intron_variant | MODIFIER | c.888+10858C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66523152 | ||||||
| chr2:66523171
|
C | T | 20 | a0001c0001t0001g0182a0001c0001t0001g0216a0001c0001t0001g0224others(17): Show | 20 | HG01109.hp1 HG01243.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.888+10877C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66523171 | ||||||
| chr2:66523179
|
G | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(230): Show | 233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.888+10885G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66523179 | ||||||
| chr2:66523432
|
G | T | 5 | a0001c0001t0001g0153a0001c0001t0001g0194a0001c0001t0004g0195others(2): Show | 5 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.888+11138G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66523432 | ||||||
| chr2:66523472
|
A | G | 30 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0001g0107others(27): Show | 30 | HG00408.hp1 HG00544.hp1 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.888+11178A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66523472 | ||||||
| chr2:66523491
|
T | C | 4 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0009g0242others(1): Show | 4 | HG02280.hp2 HG02886.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.888+11197T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66523491 | ||||||
| chr2:66523626
|
C | T | 1 | a0001c0001t0002g0209 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.888+11332C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66523626 | ||||||
| chr2:66523789
|
T | C | 1 | a0001c0001t0015g0147 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.888+11495T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66523789 | ||||||
| chr2:66523901
|
CGTT | C | 6 | a0001c0001t0009g0241a0001c0001t0010g0092a0001c0001t0010g0115others(3): Show | 6 | HG01123.hp1 HG01167.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.888+11611_888+1161 others(7): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66523901 | |||||
| chr2:66524132
|
T | C | 2 | a0001c0001t0002g0035a0001c0001t0004g0173 | 2 | NA18988.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.888+11838T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66524132 | ||||||
| chr2:66524698
|
A | AT | 199 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0091others(196): Show | 199 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.888+12412dupT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66524698 | |||||
| chr2:66524714
|
G | A | 233 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(230): Show | 233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.888+12420G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66524714 | ||||||
| chr2:66524765
|
G | C | 8 | a0001c0001t0001g0138a0001c0001t0001g0182a0001c0001t0001g0193others(5): Show | 8 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.888+12471G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66524765 | ||||||
| chr2:66524944
|
A | T | 1 | a0001c0001t0002g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.888+12650A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66524944 | ||||||
| chr2:66524978
|
C | T | 2 | a0001c0001t0003g0021a0001c0001t0007g0023 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.888+12684C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66524978 | ||||||
| chr2:66525072
|
G | A | 12 | a0001c0001t0002g0210a0001c0001t0003g0215a0001c0001t0003g0227others(9): Show | 12 | HG01123.hp1 HG01167.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.888+12778G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66525072 | ||||||
| chr2:66525106
|
A | G | 1 | a0001c0001t0005g0019 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.888+12812A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66525106 | ||||||
| chr2:66525118
|
C | T | 12 | a0001c0001t0002g0210a0001c0001t0003g0215a0001c0001t0003g0227others(9): Show | 12 | HG01123.hp1 HG01167.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.888+12824C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66525118 | ||||||
| chr2:66525119
|
A | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0091others(167): Show | 170 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.888+12825A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66525119 | ||||||
| chr2:66525128
|
G | A | 1 | a0001c0001t0006g0033 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.888+12834G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66525128 | ||||||
| chr2:66525214
|
AAAAC | A | 29 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0116others(26): Show | 29 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.888+12932_888+1293 others(8): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66525214 | |||||
| chr2:66525424
|
C | G | 29 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0116others(26): Show | 29 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.888+13130C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66525424 | ||||||
| chr2:66525651
|
T | G | 1 | a0001c0001t0001g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.888+13357T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66525651 | ||||||
| chr2:66525665
|
G | C | 3 | a0001c0001t0001g0111a0001c0001t0001g0145a0001c0001t0006g0058 | 3 | HG02735.hp2 HG03942.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.888+13371G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66525665 | ||||||
| chr2:66525863
|
T | C | 1 | a0001c0001t0005g0019 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.888+13569T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66525863 | ||||||
| chr2:66525962
|
C | G | 4 | a0001c0001t0003g0179a0001c0001t0017g0168a0001c0001t0028g0061others(1): Show | 4 | NA18945.hp1 NA18955.hp1 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.888+13668C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66525962 | ||||||
| chr2:66526020
|
T | C | 1 | a0001c0001t0005g0019 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.888+13726T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66526020 | ||||||
| chr2:66526101
|
A | G | 1 | a0001c0001t0002g0047 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.888+13807A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66526101 | ||||||
| chr2:66526307
|
G | A | 1 | a0001c0001t0003g0229 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.888+14013G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66526307 | ||||||
| chr2:66526745
|
G | A | 2 | a0001c0001t0001g0156a0001c0001t0001g0187 | 2 | HG00099.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.888+14451G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66526745 | ||||||
| chr2:66526823
|
C | T | 8 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0225others(5): Show | 8 | HG02280.hp2 HG02630.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.888+14529C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66526823 | ||||||
| chr2:66526921
|
C | A | 29 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0093others(26): Show | 29 | HG00323.hp2 HG00642.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.888+14627C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66526921 | ||||||
| chr2:66527008
|
C | T | 1 | a0001c0001t0002g0075 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.888+14714C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66527008 | ||||||
| chr2:66527189
|
G | A | 1 | a0001c0001t0003g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.888+14895G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66527189 | ||||||
| chr2:66527234
|
C | T | 1 | a0001c0001t0001g0001 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.888+14940C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66527234 | ||||||
| chr2:66527249
|
T | G | 1 | a0001c0001t0001g0167 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.888+14955T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66527249 | ||||||
| chr2:66527514
|
G | A | 226 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(223): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.888+15220G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66527514 | ||||||
| chr2:66527591
|
A | AGT | 12 | a0001c0001t0001g0104a0001c0001t0001g0165a0001c0001t0002g0043others(9): Show | 12 | HG01433.hp2 HG02257.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.888+15346_888+1534 others(6): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66527591 | |||||
| chr2:66527591
|
A | AGTGT | 7 | a0001c0001t0001g0110a0001c0001t0002g0233a0001c0001t0003g0125others(4): Show | 7 | HG02055.hp2 HG02809.hp2 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.888+15344_888+1534 others(8): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66527591 | |||||
| chr2:66527591
|
A | AGTGTGT | 4 | a0001c0001t0001g0111a0001c0001t0001g0224a0001c0001t0003g0010others(1): Show | 4 | HG02622.hp1 HG02965.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.888+15342_888+1534 others(10): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66527591 | |||||
| chr2:66527591
|
A | AGTGTGTG others(1): Show |
3 | a0001c0001t0002g0030a0001c0001t0003g0003a0001c0001t0003g0127 | 3 | HG01361.hp1 HG03669.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.888+15340_888+1534 others(12): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66527591 | |||||
| chr2:66527591
|
A | AGTGTGTG others(3): Show |
2 | a0001c0001t0004g0237a0001c0001t0027g0211 | 2 | HG02886.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.888+15338_888+1534 others(14): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66527591 | |||||
| chr2:66527591
|
AGT | A | 72 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0099others(69): Show | 72 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.888+15346_888+1534 others(6): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66527591 | |||||
| chr2:66527591
|
AGTGT | A | 67 | a0001c0001t0001g0091a0001c0001t0001g0094a0001c0001t0001g0096others(64): Show | 67 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.888+15344_888+1534 others(8): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66527591 | |||||
| chr2:66527591
|
AGTGTGT | A | 26 | a0001c0001t0001g0105a0001c0001t0001g0116a0001c0001t0001g0129others(23): Show | 26 | HG00099.hp1 HG00741.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.888+15342_888+1534 others(10): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66527591 | |||||
| chr2:66527591
|
AGTGTGTG others(1): Show |
A | 7 | a0001c0001t0001g0154a0001c0001t0001g0190a0001c0001t0002g0063others(4): Show | 7 | HG00544.hp1 HG00741.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.888+15340_888+1534 others(12): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66527591 | |||||
| chr2:66527591
|
AGTGTGTG others(3): Show |
A | 1 | a0001c0001t0005g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.888+15338_888+1534 others(14): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66527591 | |||||
| chr2:66527591
|
AGTGTGTG others(5): Show |
A | 3 | a0001c0001t0003g0188a0001c0001t0005g0042a0001c0001t0007g0163 | 3 | HG03239.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.888+15336_888+1534 others(16): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66527591 | |||||
| chr2:66527591
|
AGTGTGTG others(7): Show |
A | 2 | a0001c0001t0001g0133a0001c0001t0005g0019 | 2 | HG02622.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.888+15334_888+1534 others(18): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66527591 | |||||
| chr2:66527591
|
AGTGTGTG others(17): Show |
A | 6 | a0001c0001t0001g0143a0001c0001t0001g0189a0001c0001t0002g0035others(3): Show | 6 | HG01358.hp2 HG02293.hp2 NA18988.hp2 others(3): Show |
intron_variant | MODIFIER | c.888+15324_888+1534 others(28): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66527591 | |||||
| chr2:66527821
|
A | G | 52 | a0001c0001t0001g0091a0001c0001t0001g0128a0001c0001t0001g0154others(49): Show | 52 | HG00544.hp2 HG00642.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.888+15527A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66527821 | ||||||
| chr2:66527859
|
A | G | 1 | a0001c0001t0005g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.888+15565A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66527859 | ||||||
| chr2:66527944
|
G | A | 1 | a0001c0001t0005g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.888+15650G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66527944 | ||||||
| chr2:66528242
|
T | C | 29 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0116others(26): Show | 29 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.888+15948T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66528242 | ||||||
| chr2:66528470
|
C | T | 25 | a0001c0001t0001g0110a0001c0001t0001g0117a0001c0001t0001g0121others(22): Show | 25 | HG00280.hp2 HG00408.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.888+16176C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66528470 | ||||||
| chr2:66528813
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.888+16519A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66528813 | ||||||
| chr2:66528817
|
G | A | 29 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0116others(26): Show | 29 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.888+16523G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66528817 | ||||||
| chr2:66529022
|
C | T | 1 | a0001c0001t0003g0196 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.888+16728C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66529022 | ||||||
| chr2:66529116
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.888+16822T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66529116 | ||||||
| chr2:66529138
|
G | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0091others(167): Show | 170 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.888+16844G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66529138 | ||||||
| chr2:66529281
|
A | G | 171 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0091others(168): Show | 171 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.888+16987A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66529281 | ||||||
| chr2:66529418
|
C | T | 29 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0116others(26): Show | 29 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.888+17124C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66529418 | ||||||
| chr2:66529473
|
G | T | 1 | a0001c0001t0036g0245 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.888+17179G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66529473 | ||||||
| chr2:66529504
|
T | A | 29 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0116others(26): Show | 29 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.888+17210T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66529504 | ||||||
| chr2:66529844
|
A | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0091others(171): Show | 174 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.888+17550A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66529844 | ||||||
| chr2:66529935
|
G | A | 29 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0116others(26): Show | 29 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.888+17641G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66529935 | ||||||
| chr2:66530196
|
C | CA | 52 | a0001c0001t0001g0091a0001c0001t0001g0094a0001c0001t0001g0144others(49): Show | 52 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.889-17734dupA | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66530196 | |||||
| chr2:66530196
|
C | CAA | 31 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0116others(28): Show | 31 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.889-17735_889-1773 others(6): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66530196 | |||||
| chr2:66530196
|
CA | C | 9 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0002g0063others(6): Show | 9 | NA18940.hp2 NA18949.hp2 NA18968.hp2 others(6): Show |
intron_variant | MODIFIER | c.889-17734delA | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66530196 | |||||
| chr2:66530318
|
C | T | 29 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0116others(26): Show | 29 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.889-17625C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66530318 | ||||||
| chr2:66530544
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.889-17399C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66530544 | ||||||
| chr2:66530577
|
G | T | 1 | a0001c0001t0022g0186 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.889-17366G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66530577 | ||||||
| chr2:66530620
|
G | A | 4 | a0001c0001t0001g0096a0001c0001t0001g0176a0001c0001t0001g0214others(1): Show | 4 | HG03098.hp2 HG03139.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-17323G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66530620 | ||||||
| chr2:66530666
|
C | T | 3 | a0001c0001t0001g0128a0001c0001t0003g0106a0001c0001t0003g0136 | 3 | HG03831.hp2 HG04184.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.889-17277C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66530666 | ||||||
| chr2:66530715
|
CA | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0091others(171): Show | 174 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.889-17216delA | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66530715 | |||||
| chr2:66530723
|
A | C | 1 | a0001c0001t0002g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.889-17220A>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66530723 | ||||||
| chr2:66530846
|
T | C | 2 | a0001c0001t0003g0021a0001c0001t0007g0023 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.889-17097T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66530846 | ||||||
| chr2:66530993
|
A | G | 1 | a0001c0001t0010g0221 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.889-16950A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66530993 | ||||||
| chr2:66531290
|
A | G | 54 | a0001c0001t0001g0091a0001c0001t0001g0128a0001c0001t0001g0144others(51): Show | 54 | HG00544.hp2 HG00642.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.889-16653A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66531290 | ||||||
| chr2:66531780
|
C | G | 28 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0093others(25): Show | 28 | HG00323.hp2 HG00642.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.889-16163C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66531780 | ||||||
| chr2:66531826
|
T | A | 1 | a0001c0001t0002g0030 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.889-16117T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66531826 | ||||||
| chr2:66532050
|
G | C | 1 | a0001c0001t0001g0216 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.889-15893G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66532050 | ||||||
| chr2:66532396
|
AT | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0091others(166): Show | 169 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.889-15546delT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66532396 | ||||||
| chr2:66532417
|
A | C | 1 | a0001c0001t0001g0159 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.889-15526A>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66532417 | ||||||
| chr2:66532711
|
G | A | 29 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0116others(26): Show | 29 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.889-15232G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66532711 | ||||||
| chr2:66532755
|
T | A | 4 | a0001c0001t0003g0021a0001c0001t0007g0023a0001c0001t0010g0221others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-15188T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66532755 | ||||||
| chr2:66532947
|
T | A | 30 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0116others(27): Show | 30 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.889-14996T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66532947 | ||||||
| chr2:66533093
|
G | A | 1 | a0001c0001t0002g0037 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.889-14850G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66533093 | ||||||
| chr2:66533179
|
A | G | 171 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0091others(168): Show | 171 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.889-14764A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66533179 | ||||||
| chr2:66533324
|
AT | A | 5 | a0001c0001t0001g0142a0001c0001t0001g0161a0001c0001t0002g0009others(2): Show | 5 | HG00738.hp2 HG01433.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.889-14614delT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66533324 | |||||
| chr2:66533529
|
T | A | 1 | a0001c0001t0002g0063 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.889-14414T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66533529 | ||||||
| chr2:66533533
|
C | A | 1 | a0001c0001t0002g0063 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.889-14410C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66533533 | ||||||
| chr2:66533539
|
T | G | 1 | a0001c0001t0002g0063 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.889-14404T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66533539 | ||||||
| chr2:66533540
|
T | A | 1 | a0001c0001t0002g0063 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.889-14403T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66533540 | ||||||
| chr2:66533541
|
A | T | 1 | a0001c0001t0002g0063 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.889-14402A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66533541 | ||||||
| chr2:66533773
|
G | T | 28 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0093others(25): Show | 28 | HG00323.hp2 HG00642.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.889-14170G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66533773 | ||||||
| chr2:66534168
|
C | CAT | 29 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0116others(26): Show | 29 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.889-13773_889-1377 others(6): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66534168 | |||||
| chr2:66534257
|
C | T | 1 | a0001c0001t0005g0065 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.889-13686C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66534257 | ||||||
| chr2:66534306
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.889-13637C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66534306 | ||||||
| chr2:66534312
|
G | A | 1 | a0001c0001t0005g0006 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.889-13631G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66534312 | ||||||
| chr2:66534326
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.889-13617G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66534326 | ||||||
| chr2:66534523
|
G | C | 173 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0091others(170): Show | 173 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.889-13420G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66534523 | ||||||
| chr2:66534559
|
GT | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0091others(169): Show | 172 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.889-13380delT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66534559 | |||||
| chr2:66534918
|
T | C | 3 | a0001c0001t0021g0183a0001c0001t0029g0018a0001c0001t0037g0020 | 3 | HG02055.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.889-13025T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66534918 | ||||||
| chr2:66535016
|
A | T | 29 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0116others(26): Show | 29 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.889-12927A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66535016 | ||||||
| chr2:66535194
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.889-12749G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66535194 | ||||||
| chr2:66535244
|
G | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0091others(199): Show | 202 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.889-12699G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66535244 | ||||||
| chr2:66535279
|
C | T | 173 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0091others(170): Show | 173 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.889-12664C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66535279 | ||||||
| chr2:66535341
|
C | CTATA | 25 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0099others(22): Show | 25 | HG00099.hp2 HG00323.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.889-12599_889-1259 others(8): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66535341 | |||||
| chr2:66535348
|
C | T | 25 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0099others(22): Show | 25 | HG00099.hp2 HG00323.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.889-12595C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66535348 | ||||||
| chr2:66535383
|
A | G | 2 | a0001c0001t0001g0130a0001c0001t0001g0172 | 2 | HG01255.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.889-12560A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66535383 | ||||||
| chr2:66535478
|
C | T | 4 | a0001c0001t0001g0091a0001c0001t0001g0158a0001c0001t0002g0047others(1): Show | 4 | HG00642.hp1 HG02738.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-12465C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66535478 | ||||||
| chr2:66535663
|
T | C | 237 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.889-12280T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66535663 | ||||||
| chr2:66535783
|
AT | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(228): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.889-12150delT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66535783 | |||||
| chr2:66535785
|
T | A | 4 | a0001c0001t0003g0021a0001c0001t0007g0023a0001c0001t0010g0221others(1): Show | 4 | HG02055.hp1 HG02486.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-12158T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66535785 | ||||||
| chr2:66535897
|
G | A | 1 | a0001c0001t0032g0016 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.889-12046G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66535897 | ||||||
| chr2:66535938
|
A | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(228): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.889-12005A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66535938 | ||||||
| chr2:66536128
|
C | G | 1 | a0001c0001t0001g0238 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.889-11815C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66536128 | ||||||
| chr2:66536300
|
A | G | 2 | a0001c0001t0004g0218a0001c0001t0006g0027 | 2 | HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.889-11643A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66536300 | ||||||
| chr2:66537001
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.889-10942A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66537001 | ||||||
| chr2:66537086
|
G | T | 1 | a0001c0001t0003g0089 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.889-10857G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66537086 | ||||||
| chr2:66537176
|
A | G | 44 | a0001c0001t0001g0091a0001c0001t0001g0094a0001c0001t0001g0128others(41): Show | 44 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.889-10767A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66537176 | ||||||
| chr2:66537333
|
C | T | 2 | a0001c0001t0002g0074a0001c0001t0004g0174 | 2 | NA18971.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.889-10610C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66537333 | ||||||
| chr2:66537334
|
G | A | 1 | a0001c0001t0004g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.889-10609G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66537334 | ||||||
| chr2:66537512
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0024g0088 | 2 | HG00099.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.889-10431G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66537512 | ||||||
| chr2:66537536
|
C | T | 4 | a0001c0001t0001g0096a0001c0001t0001g0176a0001c0001t0001g0214others(1): Show | 4 | HG03098.hp2 HG03139.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-10407C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66537536 | ||||||
| chr2:66537568
|
A | G | 29 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0116others(26): Show | 29 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.889-10375A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66537568 | ||||||
| chr2:66537809
|
G | C | 1 | a0001c0001t0001g0108 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.889-10134G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66537809 | ||||||
| chr2:66537865
|
A | G | 175 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0091others(172): Show | 175 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.889-10078A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66537865 | ||||||
| chr2:66538446
|
A | G | 81 | a0001c0001t0001g0091a0001c0001t0001g0094a0001c0001t0001g0105others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.889-9497A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66538446 | ||||||
| chr2:66538755
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.889-9188T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66538755 | ||||||
| chr2:66538877
|
GT | G | 5 | a0001c0001t0001g0096a0001c0001t0001g0176a0001c0001t0001g0214others(2): Show | 5 | HG02976.hp2 HG03098.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.889-9050delT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66538877 | |||||
| chr2:66538882
|
T | G | 1 | a0001c0001t0001g0103 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.889-9061T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66538882 | ||||||
| chr2:66538886
|
T | G | 207 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0091others(204): Show | 207 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.889-9057T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66538886 | ||||||
| chr2:66538887
|
T | G | 1 | a0001c0001t0001g0166 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.889-9056T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66538887 | ||||||
| chr2:66538890
|
T | G | 237 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.889-9053T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66538890 | ||||||
| chr2:66538974
|
G | A | 1 | a0001c0001t0005g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.889-8969G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66538974 | ||||||
| chr2:66539044
|
C | T | 9 | a0001c0001t0001g0138a0001c0001t0001g0182a0001c0001t0001g0193others(6): Show | 9 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.889-8899C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66539044 | ||||||
| chr2:66539122
|
T | C | 237 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.889-8821T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66539122 | ||||||
| chr2:66539174
|
A | T | 6 | a0001c0001t0003g0021a0001c0001t0004g0237a0001c0001t0005g0019others(3): Show | 6 | HG02055.hp1 HG02486.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.889-8769A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66539174 | ||||||
| chr2:66539272
|
A | G | 1 | a0001c0001t0005g0019 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.889-8671A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66539272 | ||||||
| chr2:66539651
|
G | A | 24 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0099others(21): Show | 24 | HG00099.hp2 HG00323.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.889-8292G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66539651 | ||||||
| chr2:66539826
|
C | T | 2 | a0001c0001t0001g0189a0001c0001t0002g0075 | 2 | HG01358.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.889-8117C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66539826 | ||||||
| chr2:66539830
|
C | T | 1 | a0001c0001t0003g0215 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.889-8113C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66539830 | ||||||
| chr2:66539832
|
C | T | 52 | a0001c0001t0001g0091a0001c0001t0001g0094a0001c0001t0001g0128others(49): Show | 52 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.889-8111C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66539832 | ||||||
| chr2:66539885
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.889-8058G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66539885 | ||||||
| chr2:66540415
|
T | A | 19 | a0001c0001t0001g0022a0001c0001t0001g0099a0001c0001t0001g0143others(16): Show | 19 | HG00323.hp1 HG00738.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.889-7528T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66540415 | ||||||
| chr2:66540467
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.889-7476G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66540467 | ||||||
| chr2:66540663
|
A | G | 6 | a0001c0001t0003g0021a0001c0001t0004g0237a0001c0001t0005g0019others(3): Show | 6 | HG02055.hp1 HG02486.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.889-7280A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66540663 | ||||||
| chr2:66540729
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.889-7214T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66540729 | ||||||
| chr2:66541098
|
C | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0093others(78): Show | 81 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.889-6845C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66541098 | ||||||
| chr2:66541099
|
G | A | 24 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0099others(21): Show | 24 | HG00099.hp2 HG00323.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.889-6844G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66541099 | ||||||
| chr2:66541130
|
C | T | 53 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0099others(50): Show | 53 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.889-6813C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66541130 | ||||||
| chr2:66541339
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.889-6604C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66541339 | ||||||
| chr2:66541451
|
A | G | 54 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0099others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.889-6492A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66541451 | ||||||
| chr2:66541843
|
G | A | 29 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0116others(26): Show | 29 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.889-6100G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66541843 | ||||||
| chr2:66541989
|
G | T | 1 | a0001c0001t0001g0110 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.889-5954G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66541989 | ||||||
| chr2:66542022
|
C | T | 29 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0116others(26): Show | 29 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.889-5921C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66542022 | ||||||
| chr2:66542319
|
A | T | 11 | a0001c0001t0001g0116a0001c0001t0001g0137a0001c0001t0001g0148others(8): Show | 11 | NA18941.hp2 NA18944.hp2 NA18945.hp2 others(8): Show |
intron_variant | MODIFIER | c.889-5624A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66542319 | ||||||
| chr2:66542474
|
AT | A | 34 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0096others(31): Show | 34 | HG00099.hp2 HG00323.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.889-5468delT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66542474 | ||||||
| chr2:66542546
|
A | G | 1 | a0001c0001t0002g0230 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.889-5397A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66542546 | ||||||
| chr2:66542903
|
G | A | 29 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0116others(26): Show | 29 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.889-5040G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66542903 | ||||||
| chr2:66542955
|
A | G | 1 | a0001c0001t0032g0016 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.889-4988A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66542955 | ||||||
| chr2:66543141
|
A | G | 1 | a0001c0001t0003g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.889-4802A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66543141 | ||||||
| chr2:66543420
|
A | G | 1 | a0001c0001t0002g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.889-4523A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66543420 | ||||||
| chr2:66543421
|
T | A | 28 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0093others(25): Show | 28 | HG00323.hp2 HG00642.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.889-4522T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66543421 | ||||||
| chr2:66543861
|
G | C | 1 | a0001c0001t0035g0199 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.889-4082G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66543861 | ||||||
| chr2:66543862
|
C | A | 1 | a0001c0001t0035g0199 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.889-4081C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66543862 | ||||||
| chr2:66543915
|
G | A | 63 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0096others(60): Show | 63 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.889-4028G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66543915 | ||||||
| chr2:66543957
|
T | A | 3 | a0001c0001t0001g0094a0001c0001t0001g0160a0001c0001t0002g0048 | 3 | HG00280.hp1 HG01074.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.889-3986T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66543957 | ||||||
| chr2:66543961
|
G | T | 239 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(236): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.889-3982G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66543961 | ||||||
| chr2:66544185
|
T | G | 1 | a0001c0001t0015g0147 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.889-3758T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66544185 | ||||||
| chr2:66544424
|
C | T | 1 | a0001c0001t0002g0074 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.889-3519C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66544424 | ||||||
| chr2:66544454
|
C | CT | 4 | a0001c0001t0001g0022a0001c0001t0001g0178a0001c0001t0002g0212others(1): Show | 4 | HG01243.hp2 HG02280.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-3483dupT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66544454 | |||||
| chr2:66544639
|
A | T | 2 | a0001c0001t0005g0029a0001c0001t0033g0073 | 2 | HG02965.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.889-3304A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66544639 | ||||||
| chr2:66544731
|
T | C | 63 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0096others(60): Show | 63 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.889-3212T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66544731 | ||||||
| chr2:66544741
|
T | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(235): Show | 238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.889-3202T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66544741 | ||||||
| chr2:66544841
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.889-3102A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66544841 | ||||||
| chr2:66544868
|
T | C | 63 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0096others(60): Show | 63 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.889-3075T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66544868 | ||||||
| chr2:66545551
|
A | G | 12 | a0001c0001t0001g0169a0001c0001t0001g0181a0001c0001t0001g0185others(9): Show | 12 | HG02004.hp2 HG02056.hp2 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.889-2392A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66545551 | ||||||
| chr2:66545633
|
A | T | 2 | a0001c0001t0003g0021a0001c0001t0007g0023 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.889-2310A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66545633 | ||||||
| chr2:66545749
|
C | A | 5 | a0001c0001t0003g0215a0001c0001t0003g0227a0001c0001t0013g0028others(2): Show | 5 | HG03041.hp1 HG03139.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.889-2194C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66545749 | ||||||
| chr2:66545830
|
C | T | 62 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0096others(59): Show | 62 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.889-2113C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66545830 | ||||||
| chr2:66546178
|
C | T | 2 | a0001c0001t0003g0021a0001c0001t0007g0023 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.889-1765C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66546178 | ||||||
| chr2:66546187
|
G | A | 25 | a0001c0001t0001g0110a0001c0001t0001g0117a0001c0001t0001g0121others(22): Show | 25 | HG00280.hp2 HG00408.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.889-1756G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66546187 | ||||||
| chr2:66546337
|
C | T | 62 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0096others(59): Show | 62 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.889-1606C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66546337 | ||||||
| chr2:66546338
|
G | A | 1 | a0001c0001t0004g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.889-1605G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66546338 | ||||||
| chr2:66546613
|
A | G | 3 | a0001c0001t0021g0183a0001c0001t0029g0018a0001c0001t0037g0020 | 3 | HG02055.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.889-1330A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66546613 | ||||||
| chr2:66546915
|
G | C | 1 | a0001c0001t0003g0089 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.889-1028G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | chr2 | 66546915 | ||||||
| chr2:66547396
|
G | GT | 4 | a0001c0001t0001g0148a0001c0001t0001g0217a0001c0001t0002g0038others(1): Show | 4 | HG01109.hp2 NA18949.hp2 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-539dupT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 66547396 | |||||
| chr2:66548051
|
T | G | 3 | a0001c0001t0003g0215a0001c0001t0003g0227a0001c0001t0020g0015 | 3 | HG03139.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.965+32T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66548051 | ||||||
| chr2:66548103
|
A | G | 1 | a0001c0001t0006g0026 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.965+84A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66548103 | ||||||
| chr2:66548296
|
ATC | A | 3 | a0001c0001t0003g0139a0001c0001t0005g0029a0001c0001t0007g0140 | 3 | HG02257.hp1 HG02965.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.965+285_965+286del others(2): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66548296 | |||||
| chr2:66548598
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.965+579G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66548598 | ||||||
| chr2:66548691
|
A | G | 1 | a0001c0001t0002g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.965+672A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66548691 | ||||||
| chr2:66549079
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.965+1060T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66549079 | ||||||
| chr2:66549162
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.965+1143A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66549162 | ||||||
| chr2:66549374
|
T | C | 24 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0099others(21): Show | 24 | HG00099.hp2 HG00323.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.965+1355T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66549374 | ||||||
| chr2:66549383
|
G | A | 1 | a0001c0001t0002g0209 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.965+1364G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66549383 | ||||||
| chr2:66549392
|
G | A | 28 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0093others(25): Show | 28 | HG00323.hp2 HG00642.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.965+1373G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66549392 | ||||||
| chr2:66549567
|
C | T | 1 | a0001c0001t0002g0030 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.965+1548C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66549567 | ||||||
| chr2:66549597
|
A | G | 53 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0093others(50): Show | 53 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.965+1578A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66549597 | ||||||
| chr2:66549695
|
C | T | 1 | a0001c0001t0004g0152 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.965+1676C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66549695 | ||||||
| chr2:66549988
|
A | G | 1 | a0001c0001t0005g0065 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.965+1969A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66549988 | ||||||
| chr2:66550389
|
A | G | 128 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0091others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.965+2370A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66550389 | ||||||
| chr2:66550464
|
CTGTTT | C | 58 | a0001c0001t0001g0094a0001c0001t0001g0110a0001c0001t0001g0116others(55): Show | 58 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.965+2493_965+2497d others(7): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66550464 | |||||
| chr2:66550464
|
CTGTTTTG others(3): Show |
C | 154 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.965+2488_965+2497d others(12): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66550464 | |||||
| chr2:66550464
|
CTGTTTTG others(8): Show |
C | 18 | a0001c0001t0001g0096a0001c0001t0001g0165a0001c0001t0001g0176others(15): Show | 18 | HG00642.hp2 HG01109.hp1 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.965+2483_965+2497d others(17): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66550464 | |||||
| chr2:66550464
|
CTGTTTTG others(13): Show |
C | 2 | a0001c0001t0001g0192a0001c0001t0005g0019 | 2 | HG02622.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.965+2478_965+2497d others(22): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66550464 | |||||
| chr2:66550521
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.965+2502C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66550521 | ||||||
| chr2:66550609
|
G | A | 5 | a0001c0001t0001g0096a0001c0001t0001g0176a0001c0001t0001g0214others(2): Show | 5 | HG02976.hp2 HG03098.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.965+2590G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66550609 | ||||||
| chr2:66550901
|
A | G | 8 | a0001c0001t0001g0138a0001c0001t0001g0182a0001c0001t0001g0193others(5): Show | 8 | HG01109.hp1 HG01243.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.965+2882A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66550901 | ||||||
| chr2:66550931
|
C | T | 29 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0116others(26): Show | 29 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.965+2912C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66550931 | ||||||
| chr2:66551128
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.965+3109A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66551128 | ||||||
| chr2:66551752
|
C | T | 5 | a0001c0001t0001g0096a0001c0001t0001g0176a0001c0001t0001g0214others(2): Show | 5 | HG02976.hp2 HG03098.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.965+3733C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66551752 | ||||||
| chr2:66551984
|
A | G | 5 | a0001c0001t0001g0096a0001c0001t0001g0176a0001c0001t0001g0214others(2): Show | 5 | HG02976.hp2 HG03098.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.965+3965A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66551984 | ||||||
| chr2:66552028
|
G | GAC | 63 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0099others(60): Show | 63 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.965+4037_965+4038d others(4): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66552028 | |||||
| chr2:66552028
|
G | GACAC | 7 | a0001c0001t0001g0138a0001c0001t0001g0143a0001c0001t0001g0216others(4): Show | 7 | HG01243.hp1 HG02055.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.965+4035_965+4038d others(6): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66552028 | |||||
| chr2:66552149
|
T | C | 14 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(11): Show | 14 | HG01361.hp1 HG02280.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.965+4130T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66552149 | ||||||
| chr2:66552174
|
G | A | 2 | a0001c0001t0008g0072a0001c0001t0023g0002 | 2 | HG01167.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.965+4155G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66552174 | ||||||
| chr2:66552208
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.965+4189C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66552208 | ||||||
| chr2:66552232
|
G | A | 1 | a0001c0001t0005g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.965+4213G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66552232 | ||||||
| chr2:66552734
|
G | A | 63 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0096others(60): Show | 63 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.965+4715G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66552734 | ||||||
| chr2:66553160
|
A | G | 1 | a0001c0001t0003g0213 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.965+5141A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66553160 | ||||||
| chr2:66553242
|
A | G | 26 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0099others(23): Show | 26 | HG00099.hp2 HG00323.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.965+5223A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66553242 | ||||||
| chr2:66553562
|
G | A | 4 | a0001c0001t0001g0091a0001c0001t0001g0158a0001c0001t0002g0047others(1): Show | 4 | HG00642.hp1 HG02738.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965+5543G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66553562 | ||||||
| chr2:66553770
|
G | A | 1 | a0001c0004t0001g0124 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.965+5751G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66553770 | ||||||
| chr2:66553844
|
C | T | 4 | a0001c0001t0001g0222a0001c0001t0002g0200a0001c0001t0002g0230others(1): Show | 4 | HG02630.hp2 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.965+5825C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66553844 | ||||||
| chr2:66553902
|
C | T | 2 | a0001c0001t0001g0193a0001c0001t0009g0244 | 2 | HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.965+5883C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66553902 | ||||||
| chr2:66554116
|
C | G | 2 | a0001c0001t0003g0021a0001c0001t0007g0023 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.965+6097C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66554116 | ||||||
| chr2:66554185
|
C | A | 2 | a0001c0001t0002g0008a0001c0001t0002g0071 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.965+6166C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66554185 | ||||||
| chr2:66554206
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.965+6187T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66554206 | ||||||
| chr2:66554294
|
A | T | 1 | a0001c0001t0001g0166 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.965+6275A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66554294 | ||||||
| chr2:66554321
|
T | G | 50 | a0001c0001t0001g0091a0001c0001t0001g0094a0001c0001t0001g0128others(47): Show | 50 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.965+6302T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66554321 | ||||||
| chr2:66554529
|
A | C | 9 | a0001c0001t0001g0116a0001c0001t0001g0137a0001c0001t0001g0149others(6): Show | 9 | NA18941.hp2 NA18944.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.965+6510A>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66554529 | ||||||
| chr2:66554576
|
T | C | 28 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0093others(25): Show | 28 | HG00323.hp2 HG00642.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.965+6557T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66554576 | ||||||
| chr2:66554624
|
G | A | 1 | a0001c0001t0007g0140 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.965+6605G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66554624 | ||||||
| chr2:66555067
|
C | G | 5 | a0001c0001t0001g0096a0001c0001t0001g0176a0001c0001t0001g0214others(2): Show | 5 | HG02976.hp2 HG03098.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.965+7048C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66555067 | ||||||
| chr2:66555241
|
T | C | 2 | a0001c0001t0010g0221a0001c0001t0012g0205 | 2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.965+7222T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66555241 | ||||||
| chr2:66555280
|
C | CTCT | 30 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0116others(27): Show | 30 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.965+7261_965+7262i others(5): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66555280 | ||||||
| chr2:66555280
|
C | CTCTCT | 6 | a0001c0001t0001g0096a0001c0001t0001g0176a0001c0001t0001g0214others(3): Show | 6 | HG02976.hp2 HG03098.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.965+7261_965+7262i others(7): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66555280 | ||||||
| chr2:66555280
|
C | CTCTCTCT | 8 | a0001c0001t0001g0182a0001c0001t0001g0193a0001c0001t0009g0244others(5): Show | 8 | HG01109.hp1 HG02055.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.965+7261_965+7262i others(9): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66555280 | ||||||
| chr2:66555280
|
C | CTCTCTCT others(2): Show |
26 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0099others(23): Show | 26 | HG00099.hp2 HG00323.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.965+7261_965+7262i others(11): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66555280 | ||||||
| chr2:66555280
|
C | CTCTCTCT others(4): Show |
78 | a0001c0001t0001g0001a0001c0001t0001g0091a0001c0001t0001g0093others(75): Show | 78 | HG00323.hp2 HG00544.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.965+7261_965+7262i others(13): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66555280 | ||||||
| chr2:66555280
|
C | CTCTCTCT others(7): Show |
1 | a0001c0001t0002g0083 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.965+7261_965+7262i others(16): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66555280 | ||||||
| chr2:66555280
|
C | CTCTCTCT others(6): Show |
40 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0001g0107others(37): Show | 40 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.965+7261_965+7262i others(15): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66555280 | ||||||
| chr2:66555280
|
C | CTCTCTCT others(8): Show |
27 | a0001c0001t0001g0011a0001c0001t0001g0110a0001c0001t0001g0117others(24): Show | 27 | HG00280.hp2 HG00621.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.965+7261_965+7262i others(17): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66555280 | ||||||
| chr2:66555280
|
C | CTCTCTCT others(10): Show |
6 | a0001c0001t0002g0007a0001c0001t0003g0150a0001c0001t0003g0184others(3): Show | 6 | HG00621.hp1 HG01361.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.965+7261_965+7262i others(19): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66555280 | ||||||
| chr2:66555280
|
C | CTCTCTCT others(12): Show |
1 | a0001c0001t0001g0181 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.965+7261_965+7262i others(21): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66555280 | ||||||
| chr2:66555335
|
C | T | 63 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0096others(60): Show | 63 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.965+7316C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66555335 | ||||||
| chr2:66555539
|
T | G | 28 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0093others(25): Show | 28 | HG00323.hp2 HG00642.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.965+7520T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66555539 | ||||||
| chr2:66555614
|
C | T | 1 | a0001c0001t0002g0059 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.965+7595C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66555614 | ||||||
| chr2:66555996
|
G | A | 5 | a0001c0001t0001g0096a0001c0001t0001g0176a0001c0001t0001g0214others(2): Show | 5 | HG02976.hp2 HG03098.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.965+7977G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66555996 | ||||||
| chr2:66556060
|
C | CA | 31 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0001g0107others(28): Show | 31 | HG00408.hp1 HG00544.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.965+8050dupA | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66556060 | |||||
| chr2:66556173
|
T | TA | 8 | a0001c0001t0001g0096a0001c0001t0001g0176a0001c0001t0001g0214others(5): Show | 8 | HG02055.hp2 HG02976.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.965+8155dupA | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66556173 | |||||
| chr2:66556439
|
A | G | 2 | a0001c0001t0001g0130a0001c0001t0001g0172 | 2 | HG01255.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.965+8420A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66556439 | ||||||
| chr2:66556491
|
C | CT | 223 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.965+8486dupT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66556491 | |||||
| chr2:66556548
|
A | G | 178 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0091others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.965+8529A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66556548 | ||||||
| chr2:66556808
|
A | G | 27 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0099others(24): Show | 27 | HG00099.hp2 HG00323.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.965+8789A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66556808 | ||||||
| chr2:66556914
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.965+8895C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66556914 | ||||||
| chr2:66556917
|
G | A | 1 | a0001c0001t0002g0040 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.965+8898G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66556917 | ||||||
| chr2:66557087
|
A | G | 36 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0116others(33): Show | 36 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.965+9068A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66557087 | ||||||
| chr2:66557278
|
T | C | 1 | a0001c0001t0003g0010 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.965+9259T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66557278 | ||||||
| chr2:66557517
|
A | C | 110 | a0001c0001t0001g0091a0001c0001t0001g0094a0001c0001t0001g0098others(107): Show | 110 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.965+9498A>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66557517 | ||||||
| chr2:66557523
|
T | A | 1 | a0001c0001t0002g0079 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.965+9504T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66557523 | ||||||
| chr2:66557706
|
C | T | 2 | a0001c0001t0001g0222a0001c0001t0018g0177 | 2 | HG02630.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.965+9687C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66557706 | ||||||
| chr2:66557811
|
G | A | 52 | a0001c0001t0001g0096a0001c0001t0001g0105a0001c0001t0001g0116others(49): Show | 52 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.966-9642G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66557811 | ||||||
| chr2:66557831
|
C | T | 1 | a0001c0001t0036g0245 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.966-9622C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66557831 | ||||||
| chr2:66557871
|
C | G | 1 | a0001c0003t0001g0141 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.966-9582C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66557871 | ||||||
| chr2:66558017
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.966-9436C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66558017 | ||||||
| chr2:66558048
|
G | A | 2 | a0001c0001t0022g0186a0001c0001t0031g0057 | 2 | HG02486.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.966-9405G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66558048 | ||||||
| chr2:66558090
|
A | G | 2 | a0001c0001t0001g0098a0001c0001t0001g0123 | 2 | NA18990.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.966-9363A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66558090 | ||||||
| chr2:66558220
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.966-9233T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66558220 | ||||||
| chr2:66558279
|
C | CA | 62 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0091others(59): Show | 62 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.966-9149dupA | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66558279 | |||||
| chr2:66558279
|
CA | C | 85 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0093others(82): Show | 85 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.966-9149delA | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66558279 | |||||
| chr2:66558279
|
CAA | C | 5 | a0001c0001t0001g0159a0001c0001t0002g0041a0001c0001t0002g0053others(2): Show | 5 | HG00673.hp2 HG02165.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.966-9150_966-9149d others(4): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66558279 | |||||
| chr2:66558279
|
CAAAAAAA | C | 15 | a0001c0001t0001g0099a0001c0001t0001g0117a0001c0001t0001g0143others(12): Show | 15 | HG00323.hp1 HG00738.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.966-9155_966-9149d others(9): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66558279 | |||||
| chr2:66558306
|
A | G | 1 | a0001c0001t0004g0237 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.966-9147A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66558306 | ||||||
| chr2:66558325
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.966-9128A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66558325 | ||||||
| chr2:66558332
|
A | G | 1 | a0001c0001t0001g0142 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.966-9121A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66558332 | ||||||
| chr2:66558339
|
C | G | 2 | a0001c0001t0002g0041a0001c0001t0007g0239 | 2 | HG02165.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.966-9114C>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66558339 | ||||||
| chr2:66558430
|
C | T | 1 | a0001c0001t0004g0237 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.966-9023C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66558430 | ||||||
| chr2:66558962
|
C | T | 2 | a0001c0001t0001g0176a0001c0001t0019g0095 | 2 | HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.966-8491C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66558962 | ||||||
| chr2:66559012
|
G | A | 29 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0099others(26): Show | 29 | HG00099.hp2 HG00323.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.966-8441G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66559012 | ||||||
| chr2:66559123
|
C | CAG | 10 | a0001c0001t0001g0238a0001c0001t0002g0210a0001c0001t0003g0215others(7): Show | 10 | HG00280.hp2 HG01109.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.966-8302_966-8301d others(4): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66559123 | |||||
| chr2:66559123
|
C | CAGAGAG | 47 | a0001c0001t0001g0091a0001c0001t0001g0094a0001c0001t0001g0128others(44): Show | 47 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.966-8306_966-8301d others(8): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66559123 | |||||
| chr2:66559123
|
C | CAGAGAGA others(1): Show |
4 | a0001c0001t0001g0222a0001c0001t0002g0017a0001c0001t0002g0230others(1): Show | 4 | HG02630.hp2 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.966-8308_966-8301d others(10): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66559123 | |||||
| chr2:66559123
|
C | CAGAGAGA others(5): Show |
1 | a0001c0001t0002g0200 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.966-8312_966-8301d others(14): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66559123 | |||||
| chr2:66559123
|
CAG | C | 12 | a0001c0001t0001g0119a0001c0001t0002g0203a0001c0001t0002g0231others(9): Show | 12 | HG00408.hp2 HG00738.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.966-8302_966-8301d others(4): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66559123 | |||||
| chr2:66559123
|
CAGAG | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.966-8304_966-8301d others(6): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66559123 | |||||
| chr2:66559175
|
C | A | 1 | a0001c0001t0001g0108 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.966-8278C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66559175 | ||||||
| chr2:66559273
|
A | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0093others(94): Show | 97 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.966-8180A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66559273 | ||||||
| chr2:66559554
|
A | T | 2 | a0001c0001t0001g0176a0001c0001t0019g0095 | 2 | HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.966-7899A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66559554 | ||||||
| chr2:66559594
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.966-7859T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66559594 | ||||||
| chr2:66559608
|
A | G | 1 | a0001c0001t0002g0030 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.966-7845A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66559608 | ||||||
| chr2:66559637
|
G | A | 9 | a0001c0001t0003g0021a0001c0001t0007g0023a0001c0001t0010g0092others(6): Show | 9 | HG01123.hp1 HG01167.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.966-7816G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66559637 | ||||||
| chr2:66559796
|
G | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.966-7657G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66559796 | ||||||
| chr2:66559853
|
A | G | 243 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.966-7600A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66559853 | ||||||
| chr2:66560040
|
C | T | 5 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(2): Show | 5 | HG02280.hp2 HG02622.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.966-7413C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66560040 | ||||||
| chr2:66560100
|
C | CT | 12 | a0001c0001t0001g0119a0001c0001t0001g0154a0001c0001t0002g0034others(9): Show | 12 | HG00673.hp1 HG02027.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.966-7330dupT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66560100 | |||||
| chr2:66560100
|
CT | C | 37 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0091others(34): Show | 37 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.966-7330delT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66560100 | |||||
| chr2:66560100
|
CTT | C | 13 | a0001c0001t0001g0178a0001c0001t0003g0021a0001c0001t0004g0237others(10): Show | 13 | HG01123.hp1 HG01167.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.966-7331_966-7330d others(4): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66560100 | |||||
| chr2:66560100
|
CTTT | C | 57 | a0001c0001t0001g0096a0001c0001t0001g0105a0001c0001t0001g0116others(54): Show | 57 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.966-7332_966-7330d others(5): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66560100 | |||||
| chr2:66560100
|
CTTTT | C | 30 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0093others(27): Show | 30 | HG00323.hp2 HG00642.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.966-7333_966-7330d others(6): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66560100 | |||||
| chr2:66560114
|
T | C | 1 | a0001c0001t0002g0037 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.966-7339T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66560114 | ||||||
| chr2:66560275
|
G | C | 2 | a0001c0001t0002g0007a0001c0001t0003g0150 | 2 | HG00621.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.966-7178G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66560275 | ||||||
| chr2:66560429
|
A | G | 1 | a0001c0001t0032g0016 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.966-7024A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66560429 | ||||||
| chr2:66560583
|
C | CA | 29 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0099others(26): Show | 29 | HG00099.hp2 HG00323.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.966-6856dupA | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66560583 | |||||
| chr2:66560583
|
CA | C | 55 | a0001c0001t0001g0096a0001c0001t0001g0105a0001c0001t0001g0116others(52): Show | 55 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.966-6856delA | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66560583 | |||||
| chr2:66560657
|
T | C | 1 | a0001c0001t0006g0078 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.966-6796T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66560657 | ||||||
| chr2:66561129
|
A | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0093others(86): Show | 89 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.966-6324A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66561129 | ||||||
| chr2:66561182
|
C | T | 55 | a0001c0001t0001g0096a0001c0001t0001g0105a0001c0001t0001g0116others(52): Show | 55 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.966-6271C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66561182 | ||||||
| chr2:66561338
|
A | G | 1 | a0001c0001t0009g0241 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.966-6115A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66561338 | ||||||
| chr2:66561371
|
C | T | 1 | a0001c0001t0018g0177 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.966-6082C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66561371 | ||||||
| chr2:66561372
|
A | T | 1 | a0001c0001t0018g0177 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.966-6081A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66561372 | ||||||
| chr2:66561376
|
A | C | 1 | a0001c0001t0009g0246 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.966-6077A>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66561376 | ||||||
| chr2:66561410
|
T | C | 1 | a0001c0001t0019g0095 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.966-6043T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66561410 | ||||||
| chr2:66561416
|
C | T | 3 | a0001c0001t0001g0111a0001c0001t0001g0145a0001c0001t0006g0058 | 3 | HG02735.hp2 HG03942.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.966-6037C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66561416 | ||||||
| chr2:66561459
|
A | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.966-5994A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66561459 | ||||||
| chr2:66561640
|
G | A | 62 | a0001c0001t0001g0096a0001c0001t0001g0105a0001c0001t0001g0108others(59): Show | 62 | HG00099.hp1 HG00738.hp2 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.966-5813G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66561640 | ||||||
| chr2:66561691
|
T | C | 29 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0099others(26): Show | 29 | HG00099.hp2 HG00323.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.966-5762T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66561691 | ||||||
| chr2:66561843
|
G | A | 1 | a0001c0001t0005g0065 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.966-5610G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66561843 | ||||||
| chr2:66561932
|
A | G | 1 | a0001c0001t0009g0246 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.966-5521A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66561932 | ||||||
| chr2:66562017
|
A | G | 2 | a0001c0001t0001g0194a0001c0001t0004g0195 | 2 | HG00733.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.966-5436A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66562017 | ||||||
| chr2:66562038
|
A | AT | 6 | a0001c0001t0001g0107a0001c0001t0001g0222a0001c0001t0002g0230others(3): Show | 6 | HG01109.hp1 HG02630.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.966-5383dupT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66562038 | |||||
| chr2:66562038
|
A | ATT | 10 | a0001c0001t0001g0091a0001c0001t0001g0105a0001c0001t0001g0123others(7): Show | 10 | HG01109.hp2 HG01123.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.966-5384_966-5383d others(4): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66562038 | |||||
| chr2:66562038
|
A | ATTT | 42 | a0001c0001t0001g0121a0001c0001t0001g0149a0001c0001t0001g0158others(39): Show | 42 | HG00099.hp1 HG00642.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.966-5385_966-5383d others(5): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66562038 | |||||
| chr2:66562038
|
A | ATTTT | 33 | a0001c0001t0001g0116a0001c0001t0001g0128a0001c0001t0001g0137others(30): Show | 33 | HG00280.hp2 HG00544.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.966-5386_966-5383d others(6): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66562038 | |||||
| chr2:66562038
|
A | ATTTTT | 11 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0002g0037others(8): Show | 11 | HG01258.hp1 HG02145.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.966-5387_966-5383d others(7): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66562038 | |||||
| chr2:66562038
|
A | ATTTTTT | 5 | a0001c0001t0001g0096a0001c0001t0001g0214a0001c0001t0007g0120others(2): Show | 5 | HG03139.hp1 HG03471.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.966-5388_966-5383d others(8): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66562038 | |||||
| chr2:66562038
|
A | ATTTTTTT others(1): Show |
12 | a0001c0001t0001g0001a0001c0001t0001g0093a0001c0001t0001g0157others(9): Show | 12 | HG01255.hp1 HG01258.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.966-5390_966-5383d others(10): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66562038 | |||||
| chr2:66562038
|
A | ATTTTTTT others(2): Show |
7 | a0001c0001t0001g0011a0001c0001t0001g0103a0001c0001t0001g0133others(4): Show | 7 | HG00323.hp2 HG01358.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.966-5391_966-5383d others(11): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66562038 | |||||
| chr2:66562038
|
A | ATTTTTTT others(3): Show |
3 | a0001c0001t0004g0097a0001c0001t0008g0044a0001c0001t0008g0086 | 3 | HG00642.hp2 HG00733.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.966-5392_966-5383d others(12): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66562038 | |||||
| chr2:66562038
|
A | ATTTTTTT others(4): Show |
2 | a0001c0001t0003g0150a0001c0001t0003g0184 | 2 | HG00621.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.966-5393_966-5383d others(13): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66562038 | |||||
| chr2:66562038
|
A | ATTTTTTT others(5): Show |
1 | a0001c0001t0010g0092 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.966-5394_966-5383d others(14): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66562038 | |||||
| chr2:66562038
|
A | ATTTTTTT others(6): Show |
7 | a0001c0001t0002g0041a0001c0001t0002g0231a0001c0001t0002g0234others(4): Show | 7 | HG02165.hp1 HG02258.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.966-5395_966-5383d others(15): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66562038 | |||||
| chr2:66562038
|
A | ATTTTTTT others(7): Show |
8 | a0001c0001t0001g0119a0001c0001t0002g0235a0001c0001t0007g0228others(5): Show | 8 | HG01123.hp1 HG02257.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.966-5396_966-5383d others(16): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66562038 | |||||
| chr2:66562038
|
A | ATTTTTTT others(8): Show |
1 | a0001c0001t0002g0203 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.966-5397_966-5383d others(17): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66562038 | |||||
| chr2:66562038
|
A | ATTTTTTT others(10): Show |
4 | a0001c0001t0001g0129a0001c0001t0002g0008a0001c0001t0002g0071others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.966-5399_966-5383d others(19): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66562038 | |||||
| chr2:66562038
|
A | ATTTTTTT others(11): Show |
3 | a0001c0001t0002g0208a0001c0001t0004g0151a0001c0001t0006g0058 | 3 | HG01978.hp1 HG02293.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.966-5400_966-5383d others(20): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66562038 | |||||
| chr2:66562038
|
A | ATTTTTTT others(12): Show |
4 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0003g0170others(1): Show | 4 | HG01074.hp2 HG03669.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.966-5401_966-5383d others(21): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66562038 | |||||
| chr2:66562038
|
A | ATTTTTTT others(13): Show |
2 | a0001c0001t0001g0111a0001c0001t0004g0152 | 2 | HG01361.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.966-5402_966-5383d others(22): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66562038 | |||||
| chr2:66562038
|
A | ATTTTTTT others(14): Show |
1 | a0001c0001t0006g0078 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.966-5403_966-5383d others(23): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66562038 | |||||
| chr2:66562038
|
A | ATTTTTTT others(15): Show |
1 | a0001c0001t0001g0145 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.966-5404_966-5383d others(24): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66562038 | |||||
| chr2:66562038
|
A | ATTTTTTT others(16): Show |
1 | a0001c0001t0002g0031 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.966-5405_966-5383d others(25): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66562038 | |||||
| chr2:66562038
|
A | ATTTTTTT others(18): Show |
2 | a0001c0001t0003g0146a0001c0001t0008g0050 | 2 | HG00621.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.966-5407_966-5383d others(27): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66562038 | |||||
| chr2:66562038
|
A | ATTTTTTT others(21): Show |
2 | a0001c0001t0003g0229a0001c0001t0013g0028 | 2 | HG02056.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.966-5410_966-5383d others(30): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66562038 | |||||
| chr2:66562038
|
AT | A | 6 | a0001c0001t0001g0094a0001c0001t0001g0160a0001c0001t0001g0194others(3): Show | 6 | HG00280.hp1 HG01070.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.966-5383delT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66562038 | |||||
| chr2:66562038
|
ATTTT | A | 20 | a0001c0001t0001g0104a0001c0001t0001g0113a0001c0001t0001g0134others(17): Show | 20 | HG00408.hp1 HG00408.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.966-5386_966-5383d others(6): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66562038 | |||||
| chr2:66562038
|
ATTTTT | A | 6 | a0001c0001t0001g0117a0001c0001t0002g0035a0001c0001t0002g0038others(3): Show | 6 | HG02717.hp1 NA18945.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.966-5387_966-5383d others(7): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66562038 | |||||
| chr2:66562038
|
ATTTTTT | A | 23 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0099others(20): Show | 23 | HG00099.hp2 HG00323.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.966-5388_966-5383d others(8): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66562038 | |||||
| chr2:66562038
|
ATTTTTTT others(3): Show |
A | 2 | a0001c0001t0001g0154a0001c0001t0002g0030 | 2 | HG01361.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.966-5392_966-5383d others(12): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66562038 | |||||
| chr2:66562038
|
ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0002g0053 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.966-5395_966-5383d others(15): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66562038 | |||||
| chr2:66562209
|
G | C | 91 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0105others(88): Show | 91 | HG00099.hp1 HG00544.hp2 HG00642.hp1 others(88): Show |
intron_variant | MODIFIER | c.966-5244G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66562209 | ||||||
| chr2:66562462
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.966-4991C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66562462 | ||||||
| chr2:66562611
|
T | A | 7 | a0001c0001t0003g0215a0001c0001t0003g0227a0001c0001t0011g0005others(4): Show | 7 | HG01109.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.966-4842T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66562611 | ||||||
| chr2:66562647
|
A | G | 91 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0105others(88): Show | 91 | HG00099.hp1 HG00544.hp2 HG00642.hp1 others(88): Show |
intron_variant | MODIFIER | c.966-4806A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66562647 | ||||||
| chr2:66562767
|
T | G | 3 | a0001c0001t0021g0183a0001c0001t0029g0018a0001c0001t0037g0020 | 3 | HG02055.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.966-4686T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66562767 | ||||||
| chr2:66562921
|
A | T | 4 | a0001c0001t0010g0092a0001c0001t0010g0115a0001c0001t0010g0118others(1): Show | 4 | HG01123.hp1 HG01167.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.966-4532A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66562921 | ||||||
| chr2:66563182
|
A | G | 30 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0093others(27): Show | 30 | HG00323.hp2 HG00642.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.966-4271A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66563182 | ||||||
| chr2:66563574
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.966-3879T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66563574 | ||||||
| chr2:66563685
|
A | C | 1 | a0001c0001t0001g0238 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.966-3768A>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66563685 | ||||||
| chr2:66563858
|
A | G | 1 | a0001c0001t0010g0221 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.966-3595A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66563858 | ||||||
| chr2:66563921
|
C | T | 1 | a0001c0001t0004g0236 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.966-3532C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66563921 | ||||||
| chr2:66564272
|
G | T | 31 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0093others(28): Show | 31 | HG00323.hp2 HG00642.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.966-3181G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66564272 | ||||||
| chr2:66564305
|
T | C | 3 | a0001c0001t0001g0022a0001c0001t0001g0178a0001c0001t0002g0212 | 3 | HG02280.hp1 HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.966-3148T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66564305 | ||||||
| chr2:66564348
|
G | C | 34 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0093others(31): Show | 34 | HG00323.hp2 HG00642.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.966-3105G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66564348 | ||||||
| chr2:66564447
|
G | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0108 | 2 | HG02683.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.966-3006G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66564447 | ||||||
| chr2:66564720
|
G | GT | 11 | a0001c0001t0001g0119a0001c0001t0002g0203a0001c0001t0002g0210others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.966-2719dupT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66564720 | |||||
| chr2:66564720
|
GT | G | 12 | a0001c0001t0001g0121a0001c0001t0001g0165a0001c0001t0001g0238others(9): Show | 12 | HG00280.hp2 HG01123.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.966-2719delT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66564720 | |||||
| chr2:66564750
|
T | C | 125 | a0001c0001t0001g0011a0001c0001t0001g0091a0001c0001t0001g0093others(122): Show | 125 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.966-2703T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66564750 | ||||||
| chr2:66564759
|
C | T | 1 | a0001c0001t0019g0095 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.966-2694C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66564759 | ||||||
| chr2:66564776
|
G | A | 7 | a0001c0001t0001g0119a0001c0001t0002g0203a0001c0001t0002g0231others(4): Show | 7 | HG02145.hp1 HG02257.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.966-2677G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66564776 | ||||||
| chr2:66564867
|
T | C | 20 | a0001c0001t0001g0116a0001c0001t0001g0121a0001c0001t0001g0135others(17): Show | 20 | HG00280.hp2 HG00408.hp2 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.966-2586T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66564867 | ||||||
| chr2:66564918
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.966-2535C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66564918 | ||||||
| chr2:66564977
|
A | G | 54 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0128others(51): Show | 54 | HG00642.hp1 HG00673.hp1 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.966-2476A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66564977 | ||||||
| chr2:66565023
|
C | T | 1 | a0001c0001t0006g0204 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.966-2430C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66565023 | ||||||
| chr2:66565156
|
T | C | 1 | a0001c0001t0004g0004 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.966-2297T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66565156 | ||||||
| chr2:66565159
|
C | T | 166 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.966-2294C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66565159 | ||||||
| chr2:66565281
|
ACTCT | A | 29 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0001g0154others(26): Show | 29 | HG00673.hp1 HG01074.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.966-2159_966-2156d others(6): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66565281 | |||||
| chr2:66565528
|
G | A | 28 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0001g0154others(25): Show | 28 | HG00673.hp1 HG01074.hp1 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.966-1925G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66565528 | ||||||
| chr2:66565551
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0004g0097 | 2 | HG00323.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.966-1902G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66565551 | ||||||
| chr2:66565634
|
C | T | 2 | a0001c0002t0001g0132a0001c0002t0004g0131 | 2 | NA18940.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.966-1819C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66565634 | ||||||
| chr2:66566016
|
G | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.966-1437G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66566016 | ||||||
| chr2:66566121
|
A | T | 5 | a0001c0001t0001g0119a0001c0001t0002g0231a0001c0001t0002g0234others(2): Show | 5 | HG02647.hp1 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.966-1332A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66566121 | ||||||
| chr2:66566180
|
A | G | 2 | a0001c0001t0003g0170a0001c0001t0007g0109 | 2 | NA18995.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.966-1273A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66566180 | ||||||
| chr2:66566222
|
T | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0214 | 2 | NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.966-1231T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66566222 | ||||||
| chr2:66566593
|
G | C | 2 | a0001c0001t0022g0186a0001c0001t0031g0057 | 2 | HG02486.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.966-860G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66566593 | ||||||
| chr2:66566603
|
A | AC | 198 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.966-850_966-849ins others(1): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66566603 | ||||||
| chr2:66566680
|
C | A | 198 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.966-773C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66566680 | ||||||
| chr2:66566810
|
C | CA | 126 | a0001c0001t0001g0011a0001c0001t0001g0091a0001c0001t0001g0093others(123): Show | 126 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.966-629dupA | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66566810 | |||||
| chr2:66566810
|
C | CAA | 51 | a0001c0001t0001g0012a0001c0001t0001g0099a0001c0001t0001g0105others(48): Show | 51 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.966-630_966-629dup others(2): Show |
MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 66566810 | |||||
| chr2:66566963
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.966-490C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66566963 | ||||||
| chr2:66567048
|
A | G | 2 | a0001c0001t0001g0216a0001c0001t0002g0230 | 2 | HG01243.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.966-405A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66567048 | ||||||
| chr2:66567084
|
G | C | 1 | a0001c0001t0001g0182 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.966-369G>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66567084 | ||||||
| chr2:66567287
|
A | T | 2 | a0001c0001t0002g0038a0001c0001t0002g0075 | 2 | HG02293.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.966-166A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66567287 | ||||||
| chr2:66567405
|
C | A | 1 | a0001c0001t0006g0033 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.966-48C>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66567405 | ||||||
| chr2:66567427
|
G | A | 7 | a0001c0001t0002g0210a0001c0001t0003g0215a0001c0001t0003g0227others(4): Show | 7 | HG01109.hp1 HG02818.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.966-26G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 9/12 | chr2 | 66567427 | ||||||
| chr2:66567702
|
G | A | 53 | a0001c0001t0001g0012a0001c0001t0001g0096a0001c0001t0001g0099others(50): Show | 53 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.1024+191G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 10/12 | chr2 | 66567702 | ||||||
| chr2:66567751
|
A | G | 1 | a0001c0001t0019g0095 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1024+240A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 10/12 | chr2 | 66567751 | ||||||
| chr2:66567791
|
A | AT | 203 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(200): Show | 203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.1024+288dupT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 66567791 | |||||
| chr2:66568105
|
C | CT | 16 | a0001c0001t0001g0012a0001c0001t0001g0099a0001c0001t0001g0117others(13): Show | 16 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(13): Show |
intron_variant | MODIFIER | c.1025-549dupT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 66568105 | |||||
| chr2:66568105
|
CT | C | 24 | a0001c0001t0001g0022a0001c0001t0001g0094a0001c0001t0001g0153others(21): Show | 24 | HG00280.hp1 HG00733.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.1025-549delT | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 66568105 | |||||
| chr2:66568333
|
A | C | 1 | a0001c0001t0002g0210 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1025-334A>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 10/12 | chr2 | 66568333 | ||||||
| chr2:66568438
|
A | G | 1 | a0001c0001t0006g0026 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1025-229A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 10/12 | chr2 | 66568438 | ||||||
| chr2:66568826
|
T | A | 1 | a0001c0001t0028g0061 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1114+70T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 11/12 | chr2 | 66568826 | ||||||
| chr2:66568847
|
T | A | 2 | a0001c0001t0001g0216a0001c0001t0002g0230 | 2 | HG01243.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1114+91T>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 11/12 | chr2 | 66568847 | ||||||
| chr2:66569330
|
A | G | 1 | a0001c0001t0032g0016 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.*37+185A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 12/12 | chr2 | 66569330 | ||||||
| chr2:66569392
|
G | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.*37+247G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 12/12 | chr2 | 66569392 | ||||||
| chr2:66569476
|
G | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.*37+331G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 12/12 | chr2 | 66569476 | ||||||
| chr2:66569568
|
T | C | 2 | a0001c0001t0001g0176a0001c0001t0009g0243 | 2 | HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.*37+423T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 12/12 | chr2 | 66569568 | ||||||
| chr2:66569612
|
A | G | 1 | a0001c0001t0001g0133 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.*37+467A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 12/12 | chr2 | 66569612 | ||||||
| chr2:66569873
|
A | T | 242 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.*37+728A>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 12/12 | chr2 | 66569873 | ||||||
| chr2:66570006
|
G | A | 20 | a0001c0001t0001g0098a0001c0001t0001g0107a0001c0001t0001g0110others(17): Show | 20 | HG00408.hp1 HG00544.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.*37+861G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 12/12 | chr2 | 66570006 | ||||||
| chr2:66570145
|
G | A | 1 | a0001c0001t0019g0095 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.*37+1000G>A | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 12/12 | chr2 | 66570145 | ||||||
| chr2:66570184
|
T | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0108 | 2 | HG02683.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.*37+1039T>C | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 12/12 | chr2 | 66570184 | ||||||
| chr2:66570319
|
T | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.*38-927T>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 12/12 | chr2 | 66570319 | ||||||
| chr2:66570357
|
CA | C | 73 | a0001c0001t0001g0022a0001c0001t0001g0094a0001c0001t0001g0098others(70): Show | 73 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.*38-881delA | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 66570357 | |||||
| chr2:66570514
|
A | G | 1 | a0001c0001t0002g0041 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.*38-732A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 12/12 | chr2 | 66570514 | ||||||
| chr2:66570907
|
C | T | 5 | a0001c0001t0001g0119a0001c0001t0002g0231a0001c0001t0002g0234others(2): Show | 5 | HG02647.hp1 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.*38-339C>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 12/12 | chr2 | 66570907 | ||||||
| chr2:66571150
|
G | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.*38-96G>T | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 12/12 | chr2 | 66571150 | ||||||
| chr2:66571235
|
A | G | 1 | a0001c0001t0002g0039 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.*38-11A>G | MEIS1 | ENSG00000143995.20 | transcript | ENST00000272369.14 | protein_coding | 12/12 | chr2 | 66571235 |