Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 4126 |
|---|---|
| ensemblid | ENSG00000109323.11 |
| hgncid | 6831 |
| symbol | MANBA |
| name | mannosidase beta |
| refseq_nuc | NM_005908.4 |
| refseq_prot | NP_005899.3 |
| ensembl_nuc | ENST00000647097.2 |
| ensembl_prot | ENSP00000495247.1 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 102630770 |
| end | 102760968 |
| strand | - |
| ver | v1.2 |
| region | chr4:102630770-102760968 |
| region5000 | chr4:102625770-102765968 |
| regionname0 | MANBA_chr4_102630770_102760968 |
| regionname5000 | MANBA_chr4_102625770_102765968 |
| 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 | 0/0 | 879 | 146 | 46 | 35 | 46 | 5 | 14 | 32 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0002 | 0/1 | 879 | 78 | 11 | 18 | 29 | 5 | 14 | 19 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0003 | 1/0 | 879 | 33 | 18 | 3 | 8 | 1 | 2 | 4 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0004 | 0/0 | 879 | 13 | 0 | 3 | 8 | 1 | 1 | 8 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0005 | 0/0 | 879 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0006 | 0/0 | 879 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0007 | 0/0 | 879 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0008 | 0/0 | 879 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0009 | 0/0 | 879 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0010 | 0/0 | 879 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| 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 | 0/0 | 2640 | 124 | 27 | 34 | 45 | 4 | 14 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| c0002 | 0/1 | 2640 | 72 | 5 | 18 | 29 | 5 | 14 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| c0003 | 1/0 | 2640 | 18 | 4 | 2 | 8 | 1 | 2 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| c0004 | 0/0 | 2640 | 17 | 15 | 1 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| c0005 | 0/0 | 2640 | 13 | 12 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| c0006 | 0/0 | 2640 | 13 | 0 | 3 | 8 | 1 | 1 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| c0007 | 0/0 | 2640 | 6 | 6 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| c0008 | 0/0 | 2640 | 5 | 5 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| c0009 | 0/0 | 2640 | 3 | 3 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| c0010 | 0/0 | 2640 | 2 | 2 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| c0011 | 0/0 | 2640 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| c0012 | 0/0 | 2640 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| c0013 | 0/0 | 2640 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| c0014 | 0/0 | 2640 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| c0015 | 0/0 | 2640 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| c0016 | 0/0 | 2640 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| c0017 | 0/0 | 2640 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| 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 | 0/0 | 1350 | 57 | 3 | 16 | 29 | 2 | 7 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0002 | 1/1 | 1362 | 55 | 4 | 12 | 21 | 6 | 10 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0003 | 0/0 | 1360 | 37 | 17 | 10 | 8 | 1 | 1 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0004 | 0/0 | 1352 | 14 | 0 | 4 | 7 | 1 | 2 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0005 | 0/0 | 1356 | 13 | 8 | 1 | 3 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0006 | 0/0 | 1362 | 11 | 5 | 3 | 1 | 0 | 2 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0007 | 0/0 | 1366 | 11 | 5 | 0 | 5 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0008 | 0/0 | 1352 | 10 | 9 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0009 | 0/0 | 1358 | 7 | 1 | 4 | 0 | 2 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0010 | 0/0 | 1348 | 7 | 3 | 0 | 3 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0011 | 0/0 | 1364 | 6 | 0 | 2 | 2 | 0 | 2 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0012 | 0/0 | 1356 | 5 | 5 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0013 | 0/0 | 1356 | 5 | 0 | 1 | 3 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0014 | 0/0 | 1358 | 5 | 3 | 1 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0015 | 0/0 | 1356 | 5 | 3 | 0 | 2 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0016 | 0/0 | 1358 | 4 | 1 | 1 | 1 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0017 | 0/0 | 1368 | 4 | 1 | 0 | 1 | 0 | 2 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0018 | 0/0 | 1364 | 3 | 1 | 0 | 1 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0019 | 0/0 | 1344 | 3 | 3 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0020 | 0/0 | 1362 | 2 | 2 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0021 | 0/0 | 1362 | 2 | 2 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0022 | 0/0 | 1346 | 2 | 0 | 2 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0023 | 0/0 | 1348 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0024 | 0/0 | 1350 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0025 | 0/0 | 1358 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0026 | 0/0 | 1351 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0027 | 0/0 | 1358 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0028 | 0/0 | 1346 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0029 | 0/0 | 1350 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0030 | 0/0 | 1350 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0031 | 0/0 | 1368 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0032 | 0/0 | 1348 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0033 | 0/0 | 1362 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| t0034 | 0/0 | 1360 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| 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 | 2 | 2 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0121 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0270 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| 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 | 0/0 | 2640 | 124 | 27 | 34 | 45 | 4 | 14 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0004 | 0/0 | 2640 | 17 | 15 | 1 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0009 | 0/0 | 2640 | 3 | 3 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0015 | 0/0 | 2640 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0017 | 0/0 | 2640 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0002c0002 | 0/1 | 2640 | 72 | 5 | 18 | 29 | 5 | 14 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0002c0007 | 0/0 | 2640 | 6 | 6 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0003c0003 | 1/0 | 2640 | 18 | 4 | 2 | 8 | 1 | 2 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0003c0005 | 0/0 | 2640 | 13 | 12 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0003c0010 | 0/0 | 2640 | 2 | 2 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0004c0006 | 0/0 | 2640 | 13 | 0 | 3 | 8 | 1 | 1 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0005c0008 | 0/0 | 2640 | 5 | 5 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0006c0013 | 0/0 | 2640 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0007c0011 | 0/0 | 2640 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0008c0012 | 0/0 | 2640 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0009c0014 | 0/0 | 2640 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0010c0016 | 0/0 | 2640 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3989 | 48 | 1 | 14 | 26 | 1 | 6 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0001t0003 | 0/0 | 3999 | 29 | 12 | 10 | 5 | 1 | 1 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0001t0004 | 0/0 | 3991 | 11 | 0 | 3 | 6 | 0 | 2 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0001t0005 | 0/0 | 3995 | 5 | 1 | 1 | 2 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0001t0006 | 0/0 | 4001 | 10 | 4 | 3 | 1 | 0 | 2 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0001t0009 | 0/0 | 3997 | 5 | 1 | 2 | 0 | 2 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0001t0010 | 0/0 | 3987 | 3 | 0 | 0 | 2 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0001t0012 | 0/0 | 3995 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0001t0018 | 0/0 | 4003 | 3 | 1 | 0 | 1 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0001t0019 | 0/0 | 3983 | 3 | 3 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0001t0020 | 0/0 | 4001 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0001t0025 | 0/0 | 3997 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0001t0026 | 0/0 | 3990 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0001t0027 | 0/0 | 3997 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0001t0028 | 0/0 | 3985 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0001t0033 | 0/0 | 4001 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0004t0001 | 0/0 | 3989 | 2 | 1 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0004t0005 | 0/0 | 3995 | 6 | 6 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0004t0006 | 0/0 | 4001 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0004t0009 | 0/0 | 3997 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0004t0010 | 0/0 | 3987 | 3 | 3 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0004t0012 | 0/0 | 3995 | 2 | 2 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0004t0020 | 0/0 | 4001 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0004t0023 | 0/0 | 3987 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0009t0012 | 0/0 | 3995 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0009t0024 | 0/0 | 3989 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0009t0034 | 0/0 | 3999 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0015t0010 | 0/0 | 3987 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0001c0017t0005 | 0/0 | 3995 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0002c0002t0002 | 0/1 | 4001 | 50 | 4 | 12 | 19 | 5 | 9 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0002c0002t0007 | 0/0 | 4005 | 3 | 0 | 0 | 3 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0002c0002t0011 | 0/0 | 4003 | 6 | 0 | 2 | 2 | 0 | 2 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0002c0002t0013 | 0/0 | 3995 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0002c0002t0014 | 0/0 | 3997 | 2 | 1 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0002c0002t0015 | 0/0 | 3995 | 2 | 0 | 0 | 2 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0002c0002t0016 | 0/0 | 3997 | 2 | 0 | 0 | 1 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0002c0002t0017 | 0/0 | 4007 | 3 | 0 | 0 | 1 | 0 | 2 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0002c0002t0022 | 0/0 | 3985 | 2 | 0 | 2 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0002c0002t0032 | 0/0 | 3987 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0002c0007t0007 | 0/0 | 4005 | 5 | 5 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0002c0007t0017 | 0/0 | 4007 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0003c0003t0002 | 1/0 | 4001 | 3 | 0 | 0 | 1 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0003c0003t0007 | 0/0 | 4005 | 3 | 0 | 0 | 2 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0003c0003t0013 | 0/0 | 3995 | 4 | 0 | 0 | 3 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0003c0003t0014 | 0/0 | 3997 | 3 | 2 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0003c0003t0015 | 0/0 | 3995 | 2 | 2 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0003c0003t0016 | 0/0 | 3997 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0003c0003t0030 | 0/0 | 3989 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0003c0003t0031 | 0/0 | 4007 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0003c0005t0008 | 0/0 | 3991 | 10 | 9 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0003c0005t0012 | 0/0 | 3995 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0003c0005t0021 | 0/0 | 4001 | 2 | 2 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0003c0010t0015 | 0/0 | 3995 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0003c0010t0016 | 0/0 | 3997 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0004c0006t0001 | 0/0 | 3989 | 6 | 0 | 2 | 3 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0004c0006t0003 | 0/0 | 3999 | 3 | 0 | 0 | 3 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0004c0006t0004 | 0/0 | 3991 | 2 | 0 | 0 | 1 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0004c0006t0005 | 0/0 | 3995 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0004c0006t0009 | 0/0 | 3997 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0005c0008t0003 | 0/0 | 3999 | 5 | 5 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0006c0013t0002 | 0/0 | 4001 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0007c0011t0029 | 0/0 | 3989 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0008c0012t0002 | 0/0 | 4001 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0009c0014t0001 | 0/0 | 3989 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| a0010c0016t0004 | 0/0 | 3991 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | copy fasta | chr4 | 102625770 | 102765968 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0005g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0005g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0005g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0006g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0006g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0006g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0006g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0006g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0006g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0006g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0006g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0006g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0006g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0009g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0009g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0009g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0009g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0009g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0010g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0010g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0010g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0012g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0018g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0018g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0018g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0019g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0019g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0019g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0020g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0025g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0026g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0027g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0028g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0001t0033g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0005g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0005g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0005g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0006g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0009g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0010g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0010g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0010g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0012g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0012g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0020g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0004t0023g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0009t0012g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0009t0024g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0009t0034g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0015t0010g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0001c0017t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0270 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0007g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0007g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0007g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0011g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0011g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0011g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0011g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0011g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0011g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0013g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0014g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0014g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0015g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0015g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0016g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0016g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0017g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0017g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0017g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0022g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0022g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0002t0032g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0007t0007g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0007t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0007t0007g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0007t0007g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0007t0007g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0002c0007t0017g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0002g0121 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0007g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0007g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0007g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0013g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0013g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0013g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0013g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0014g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0014g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0014g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0015g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0015g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0016g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0030g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0003t0031g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0005t0008g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0005t0008g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0005t0008g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0005t0008g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0005t0008g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0005t0008g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0005t0008g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0005t0008g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0005t0008g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0005t0012g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0005t0021g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0005t0021g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0010t0015g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0003c0010t0016g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0004c0006t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0004c0006t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0004c0006t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0004c0006t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0004c0006t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0004c0006t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0004c0006t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0004c0006t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0004c0006t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0004c0006t0004g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0004c0006t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0004c0006t0005g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0004c0006t0009g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0005c0008t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0005c0008t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0005c0008t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0005c0008t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0005c0008t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0006c0013t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0007c0011t0029g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0008c0012t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0009c0014t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| a0010c0016t0004g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0004 | t0001 | g0026 | EUR | GBR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0079 | EUR | GBR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0124 | EUR | GBR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0246 | EUR | GBR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0030 | EUR | FIN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00280 | hp2 | a0003 | c0003 | t0002 | g0151 | EUR | FIN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0242 | EUR | FIN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0029 | EUR | FIN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0245 | EAS | CHS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0101 | EAS | CHS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00438 | hp2 | a0003 | c0003 | t0013 | g0257 | EAS | CHS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | CHS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0044 | EAS | CHS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00558 | hp1 | a0001 | c0001 | t0010 | g0176 | EAS | CHS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0066 | EAS | CHS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00609 | hp1 | a0001 | c0001 | t0005 | g0162 | EAS | CHS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00609 | hp2 | a0002 | c0002 | t0032 | g0100 | EAS | CHS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | CHS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00639 | hp1 | a0010 | c0016 | t0004 | g0214 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0086 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00735 | hp1 | a0004 | c0006 | t0001 | g0061 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG00735 | hp2 | a0001 | c0004 | t0009 | g0014 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01070 | hp1 | a0003 | c0003 | t0031 | g0238 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01070 | hp2 | a0002 | c0002 | t0022 | g0239 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01071 | hp1 | a0002 | c0002 | t0022 | g0233 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0200 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01081 | hp1 | a0001 | c0001 | t0009 | g0215 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01081 | hp2 | a0004 | c0006 | t0001 | g0115 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01099 | hp1 | a0002 | c0002 | t0013 | g0064 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0075 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01106 | hp2 | a0001 | c0001 | t0006 | g0077 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0139 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0094 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01167 | hp2 | a0002 | c0002 | t0002 | g0084 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01168 | hp2 | a0002 | c0002 | t0011 | g0122 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0089 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01175 | hp1 | a0001 | c0001 | t0009 | g0216 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0032 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0039 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01192 | hp2 | a0003 | c0005 | t0008 | g0009 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0043 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01243 | hp2 | a0004 | c0006 | t0009 | g0112 | AMR | PUR | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0155 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0028 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0158 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01258 | hp2 | a0002 | c0002 | t0011 | g0078 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01261 | hp2 | a0002 | c0002 | t0002 | g0080 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0082 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0091 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01358 | hp2 | a0001 | c0001 | t0006 | g0081 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0120 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01433 | hp2 | a0002 | c0002 | t0002 | g0126 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0074 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01496 | hp2 | a0003 | c0003 | t0016 | g0211 | AMR | CLM | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01515 | hp1 | a0001 | c0001 | t0009 | g0240 | EUR | IBS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0085 | EUR | IBS | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01884 | hp1 | a0003 | c0005 | t0008 | g0013 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0217 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0273 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01891 | hp2 | a0001 | c0004 | t0005 | g0262 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0090 | AMR | PEL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01978 | hp1 | a0001 | c0001 | t0026 | g0145 | AMR | PEL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01978 | hp2 | a0001 | c0001 | t0006 | g0088 | AMR | PEL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0087 | AMR | PEL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0137 | AMR | PEL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0191 | EAS | KHV | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02015 | hp2 | a0002 | c0002 | t0002 | g0063 | EAS | KHV | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02056 | hp1 | a0003 | c0003 | t0002 | g0228 | EAS | KHV | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0065 | EAS | KHV | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02080 | hp2 | a0002 | c0002 | t0015 | g0058 | EAS | KHV | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02083 | hp1 | a0001 | c0001 | t0005 | g0205 | EAS | KHV | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02083 | hp2 | a0003 | c0003 | t0007 | g0258 | EAS | KHV | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0040 | EAS | KHV | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02135 | hp1 | a0002 | c0002 | t0007 | g0259 | EAS | KHV | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02135 | hp2 | a0003 | c0003 | t0030 | g0117 | EAS | KHV | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02145 | hp1 | a0003 | c0005 | t0008 | g0006 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02145 | hp2 | a0001 | c0004 | t0005 | g0266 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0097 | AMR | PEL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02148 | hp2 | a0002 | c0002 | t0014 | g0116 | AMR | PEL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02257 | hp1 | a0002 | c0007 | t0017 | g0107 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02257 | hp2 | a0009 | c0014 | t0001 | g0031 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02280 | hp1 | a0002 | c0002 | t0014 | g0033 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02280 | hp2 | a0001 | c0001 | t0019 | g0152 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0144 | AMR | PEL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02451 | hp1 | a0002 | c0007 | t0007 | g0106 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0224 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0166 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0231 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0156 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02602 | hp2 | a0003 | c0003 | t0007 | g0130 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02615 | hp1 | a0001 | c0009 | t0034 | g0016 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02615 | hp2 | a0002 | c0002 | t0002 | g0057 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02622 | hp1 | a0002 | c0007 | t0007 | g0109 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02622 | hp2 | a0001 | c0001 | t0027 | g0202 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02630 | hp1 | a0001 | c0004 | t0005 | g0265 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02630 | hp2 | a0003 | c0003 | t0015 | g0198 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02647 | hp1 | a0005 | c0008 | t0003 | g0219 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02647 | hp2 | a0001 | c0004 | t0010 | g0024 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02698 | hp1 | a0006 | c0013 | t0002 | g0272 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0190 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02717 | hp2 | a0003 | c0005 | t0008 | g0012 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02723 | hp1 | a0001 | c0017 | t0005 | g0237 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02723 | hp2 | a0001 | c0001 | t0018 | g0021 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02735 | hp1 | a0001 | c0001 | t0006 | g0136 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0050 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0054 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02738 | hp2 | a0001 | c0001 | t0010 | g0159 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02809 | hp2 | a0005 | c0008 | t0003 | g0138 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0260 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02818 | hp2 | a0001 | c0004 | t0001 | g0243 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02886 | hp1 | a0003 | c0005 | t0012 | g0015 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02886 | hp2 | a0001 | c0004 | t0020 | g0141 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02896 | hp1 | a0001 | c0004 | t0005 | g0263 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02896 | hp2 | a0005 | c0008 | t0003 | g0222 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0172 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02897 | hp2 | a0005 | c0008 | t0003 | g0218 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02922 | hp1 | a0003 | c0003 | t0015 | g0199 | AFR | ESN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02922 | hp2 | a0001 | c0004 | t0010 | g0140 | AFR | ESN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02965 | hp1 | a0007 | c0011 | t0029 | g0018 | AFR | ESN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02965 | hp2 | a0001 | c0009 | t0012 | g0034 | AFR | ESN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02970 | hp1 | a0002 | c0007 | t0007 | g0110 | AFR | ESN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02970 | hp2 | a0003 | c0010 | t0016 | g0271 | AFR | ESN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03041 | hp1 | a0003 | c0005 | t0008 | g0008 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03098 | hp1 | a0002 | c0002 | t0002 | g0114 | AFR | MSL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03098 | hp2 | a0003 | c0003 | t0014 | g0220 | AFR | MSL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0007 | AFR | ESN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03130 | hp2 | a0003 | c0005 | t0008 | g0001 | AFR | ESN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03195 | hp1 | a0003 | c0005 | t0008 | g0017 | AFR | ESN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03195 | hp2 | a0001 | c0001 | t0019 | g0023 | AFR | ESN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03209 | hp1 | a0001 | c0004 | t0005 | g0264 | AFR | MSL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03209 | hp2 | a0001 | c0004 | t0012 | g0275 | AFR | MSL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03225 | hp1 | a0001 | c0001 | t0009 | g0250 | AFR | MSL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03225 | hp2 | a0001 | c0009 | t0024 | g0005 | AFR | MSL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0111 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03486 | hp1 | a0003 | c0005 | t0021 | g0252 | AFR | MSL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0223 | AFR | MSL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03492 | hp1 | a0002 | c0002 | t0017 | g0132 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0069 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03516 | hp1 | a0003 | c0005 | t0021 | g0251 | AFR | ESN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0168 | AFR | ESN | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03540 | hp1 | a0005 | c0008 | t0003 | g0221 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03540 | hp2 | a0001 | c0001 | t0033 | g0174 | AFR | GWD | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03579 | hp1 | a0001 | c0004 | t0010 | g0011 | AFR | MSL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03579 | hp2 | a0001 | c0004 | t0023 | g0004 | AFR | MSL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03654 | hp2 | a0002 | c0002 | t0016 | g0125 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | STU | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03688 | hp2 | a0002 | c0002 | t0011 | g0060 | SAS | STU | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0127 | SAS | PJL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0277 | SAS | BEB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0247 | SAS | BEB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0052 | SAS | BEB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03942 | hp1 | a0002 | c0002 | t0017 | g0119 | SAS | BEB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03942 | hp2 | a0001 | c0001 | t0006 | g0209 | SAS | BEB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0099 | SAS | BEB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG04184 | hp2 | a0003 | c0003 | t0013 | g0160 | SAS | BEB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0059 | SAS | STU | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | STU | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG04204 | hp1 | a0004 | c0006 | t0001 | g0154 | SAS | STU | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG04204 | hp2 | a0002 | c0002 | t0011 | g0073 | SAS | STU | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18522 | hp1 | a0003 | c0005 | t0008 | g0010 | AFR | YRI | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18522 | hp2 | a0001 | c0004 | t0006 | g0268 | AFR | YRI | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18906 | hp1 | a0002 | c0007 | t0007 | g0118 | AFR | YRI | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18906 | hp2 | a0001 | c0001 | t0012 | g0232 | AFR | YRI | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18949 | hp2 | a0004 | c0006 | t0001 | g0045 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18954 | hp2 | a0002 | c0002 | t0015 | g0113 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18957 | hp1 | a0002 | c0002 | t0002 | g0048 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18957 | hp2 | a0003 | c0003 | t0013 | g0255 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18960 | hp1 | a0002 | c0002 | t0011 | g0096 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18960 | hp2 | a0001 | c0001 | t0018 | g0051 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0150 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0183 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18965 | hp1 | a0002 | c0002 | t0007 | g0046 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0171 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18968 | hp1 | a0001 | c0001 | t0028 | g0194 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18969 | hp2 | a0004 | c0006 | t0003 | g0072 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18970 | hp2 | a0002 | c0002 | t0017 | g0049 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18972 | hp2 | a0002 | c0002 | t0002 | g0128 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0180 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0055 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18981 | hp1 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18981 | hp2 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18986 | hp1 | a0002 | c0002 | t0016 | g0249 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18988 | hp2 | a0004 | c0006 | t0003 | g0068 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18990 | hp1 | a0004 | c0006 | t0001 | g0035 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18990 | hp2 | a0001 | c0001 | t0010 | g0184 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18994 | hp2 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18995 | hp2 | a0003 | c0003 | t0007 | g0244 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18999 | hp1 | a0001 | c0001 | t0025 | g0157 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA18999 | hp2 | a0002 | c0002 | t0011 | g0067 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19000 | hp2 | a0004 | c0006 | t0003 | g0053 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19001 | hp1 | a0002 | c0002 | t0002 | g0062 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19030 | hp1 | a0001 | c0004 | t0005 | g0267 | AFR | LWK | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19030 | hp2 | a0003 | c0003 | t0014 | g0256 | AFR | LWK | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0235 | AFR | LWK | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0169 | AFR | LWK | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19054 | hp1 | a0001 | c0001 | t0006 | g0092 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19054 | hp2 | a0003 | c0003 | t0014 | g0143 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19055 | hp1 | a0008 | c0012 | t0002 | g0103 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19055 | hp2 | a0004 | c0006 | t0005 | g0129 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19062 | hp2 | a0002 | c0002 | t0007 | g0056 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19063 | hp1 | a0001 | c0015 | t0010 | g0173 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19063 | hp2 | a0003 | c0003 | t0013 | g0248 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19077 | hp2 | a0004 | c0006 | t0004 | g0042 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0213 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19091 | hp1 | a0004 | c0006 | t0001 | g0204 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19240 | hp1 | a0003 | c0005 | t0008 | g0027 | AFR | YRI | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA19240 | hp2 | a0003 | c0005 | t0008 | g0001 | AFR | YRI | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA20129 | hp1 | a0001 | c0001 | t0020 | g0225 | AFR | ASW | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ASW | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA20752 | hp1 | a0001 | c0001 | t0009 | g0076 | EUR | TSI | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA20752 | hp2 | a0004 | c0006 | t0004 | g0025 | EUR | TSI | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0070 | SAS | GIH | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA20905 | hp2 | a0001 | c0001 | t0018 | g0210 | SAS | GIH | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0230 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02109 | hp2 | a0003 | c0010 | t0015 | g0274 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02486 | hp1 | a0002 | c0007 | t0007 | g0108 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0261 | AFR | ACB | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03471 | hp1 | a0001 | c0004 | t0012 | g0253 | AFR | MSL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | MSL | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0083 | AFR | USA | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| NA20300 | hp2 | a0001 | c0001 | t0019 | g0153 | AFR | USA | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0002 | g0270 | REF | REF | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| homoSapiens_grch38 | hp1 | a0003 | c0003 | t0002 | g0121 | REF | REF | MANBA_chr4_102625770_102765968 | MANBA | chr4 | 102625770 | 102765968 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:102632215
|
C | T | 1 | a0010 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.2482G>A | p.Val828Ile | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 2556/4001 | 2482/2640 | 828/879 | chr4 | 102632215 | ||
| chr4:102634852
|
G | C | 1 | a0005 | 5 | HG02647.hp1 HG02809.hp2 HG02896.hp2 others(2): Show |
missense_variant | MODERATE | c.2351C>G | p.Pro784Arg | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/17 | 2425/4001 | 2351/2640 | 784/879 | chr4 | 102634852 | ||
| chr4:102634957
|
A | T | 1 | a0008 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.2246T>A | p.Leu749His | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/17 | 2320/4001 | 2246/2640 | 749/879 | chr4 | 102634957 | ||
| chr4:102635023
|
G | A | 1 | a0007 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.2180C>T | p.Ser727Phe | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/17 | 2254/4001 | 2180/2640 | 727/879 | chr4 | 102635023 | ||
| chr4:102635920
|
G | A | 6 | a0001a0004a0005others(3): Show | 167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
missense_variant | MODERATE | c.2102C>T | p.Thr701Met | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 15/17 | 2176/4001 | 2102/2640 | 701/879 | chr4 | 102635920 | ||
| chr4:102650568
|
C | A | 1 | a0006 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.1838G>T | p.Arg613Leu | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/17 | 1912/4001 | 1838/2640 | 613/879 | chr4 | 102650568 | ||
| chr4:102664693
|
C | T | 1 | a0009 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.1477G>A | p.Val493Ile | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/17 | 1551/4001 | 1477/2640 | 493/879 | chr4 | 102664693 | ||
| chr4:102690688
|
C | T | 5 | a0002a0004a0006others(2): Show | 94 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(91): Show |
missense_variant | MODERATE | c.757G>A | p.Val253Ile | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 6/17 | 831/4001 | 757/2640 | 253/879 | chr4 | 102690688 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:102634835
|
A | G | 10 | a0001c0001a0001c0004a0001c0009others(7): Show | 167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
synonymous_variant | LOW | c.2368T>C | p.Leu790Leu | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/17 | 2442/4001 | 2368/2640 | 790/879 | chr4 | 102634835 | ||
| chr4:102635907
|
A | G | 1 | a0001c0015 | 1 | NA19063.hp1 | synonymous_variant | LOW | c.2115T>C | p.Tyr705Tyr | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 15/17 | 2189/4001 | 2115/2640 | 705/879 | chr4 | 102635907 | ||
| chr4:102664688
|
C | A | 1 | a0002c0007 | 6 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
synonymous_variant | LOW | c.1482G>T | p.Leu494Leu | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/17 | 1556/4001 | 1482/2640 | 494/879 | chr4 | 102664688 | ||
| chr4:102690614
|
T | C | 3 | a0001c0009a0001c0017a0003c0005 | 17 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
synonymous_variant | LOW | c.831A>G | p.Leu277Leu | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 6/17 | 905/4001 | 831/2640 | 277/879 | chr4 | 102690614 | ||
| chr4:102723925
|
C | T | 5 | a0001c0004a0001c0009a0003c0005others(2): Show | 36 | HG00099.hp1 HG00735.hp2 HG01192.hp2 others(33): Show |
synonymous_variant | LOW | c.315G>A | p.Thr105Thr | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 3/17 | 389/4001 | 315/2640 | 105/879 | chr4 | 102723925 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:102630911
|
T | C | 39 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(36): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*1146A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 1146 | chr4 | 102630911 | |||||
| chr4:102630998
|
C | T | 6 | a0001c0001t0012a0001c0004t0012a0001c0004t0023others(3): Show | 7 | HG02886.hp1 HG02965.hp1 HG02965.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1059G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 1059 | chr4 | 102630998 | |||||
| chr4:102631091
|
C | T | 1 | a0001c0001t0027 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*966G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 966 | chr4 | 102631091 | |||||
| chr4:102631096
|
T | C | 39 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(36): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*961A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 961 | chr4 | 102631096 | |||||
| chr4:102631104
|
C | CTG | 1 | a0001c0001t0018 | 3 | HG02723.hp2 NA18960.hp2 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*952_*953insCA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 952 | chr4 | 102631104 | |||||
| chr4:102631104
|
CTT | C | 4 | a0001c0001t0003a0001c0009t0034a0004c0006t0003others(1): Show | 38 | HG00140.hp2 HG00544.hp1 HG00621.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*951_*952delAA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 951 | chr4 | 102631104 | |||||
| chr4:102631104
|
CTTTG | C | 5 | a0001c0001t0009a0001c0001t0025a0001c0001t0027others(2): Show | 9 | HG00735.hp2 HG01081.hp1 HG01175.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*949_*952delCAAA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 949 | chr4 | 102631104 | |||||
| chr4:102631104
|
CTTTGTG | C | 8 | a0001c0001t0005a0001c0001t0012a0001c0004t0005others(5): Show | 18 | HG00609.hp1 HG01346.hp1 HG01884.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*947_*952delCACAAA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 947 | chr4 | 102631104 | |||||
| chr4:102631104
|
CTTTGTGT others(3): Show |
C | 3 | a0001c0001t0004a0004c0006t0004a0010c0016t0004 | 14 | HG00639.hp1 HG01074.hp1 HG01257.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*943_*952delCACACA others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 943 | chr4 | 102631104 | |||||
| chr4:102631104
|
CTTTGTGT others(5): Show |
C | 6 | a0001c0001t0001a0001c0004t0001a0001c0009t0024others(3): Show | 59 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*941_*952delCACACA others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 941 | chr4 | 102631104 | |||||
| chr4:102631104
|
CTTTGTGT others(7): Show |
C | 4 | a0001c0001t0010a0001c0004t0010a0001c0004t0023others(1): Show | 8 | HG00558.hp1 HG02647.hp2 HG02738.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*939_*952delCACACA others(8): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 939 | chr4 | 102631104 | |||||
| chr4:102631104
|
CTTTGTGT others(9): Show |
C | 1 | a0001c0001t0028 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*937_*952delCACACA others(10): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 937 | chr4 | 102631104 | |||||
| chr4:102631104
|
CTTTGTGT others(11): Show |
C | 1 | a0001c0001t0019 | 3 | HG02280.hp2 HG03195.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*935_*952delCACACA others(12): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 935 | chr4 | 102631104 | |||||
| chr4:102631106
|
T | G | 5 | a0001c0001t0006a0001c0001t0018a0001c0001t0026others(2): Show | 16 | HG01106.hp2 HG01358.hp2 HG01978.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*951A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 951 | chr4 | 102631106 | |||||
| chr4:102631106
|
T | TTG | 1 | a0002c0002t0011 | 6 | HG01168.hp2 HG01258.hp2 HG03688.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*949_*950dupCA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 950 | chr4 | 102631106 | |||||
| chr4:102631106
|
T | TTGTG | 3 | a0002c0002t0007a0002c0007t0007a0003c0003t0007 | 11 | HG02083.hp2 HG02135.hp1 HG02451.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*947_*950dupCACA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 950 | chr4 | 102631106 | |||||
| chr4:102631106
|
T | TTGTGTG | 3 | a0002c0002t0017a0002c0007t0017a0003c0003t0031 | 5 | HG01070.hp1 HG02257.hp1 HG03492.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*945_*950dupCACACA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 950 | chr4 | 102631106 | |||||
| chr4:102631106
|
TTGTG | T | 5 | a0002c0002t0014a0002c0002t0016a0003c0003t0014others(2): Show | 9 | HG01496.hp2 HG02148.hp2 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*947_*950delCACA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 947 | chr4 | 102631106 | |||||
| chr4:102631106
|
TTGTGTG | T | 5 | a0002c0002t0013a0002c0002t0015a0003c0003t0013others(2): Show | 10 | HG00438.hp2 HG01099.hp1 HG02080.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*945_*950delCACACA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 945 | chr4 | 102631106 | |||||
| chr4:102631106
|
TTGTGTGT others(3): Show |
T | 1 | a0003c0005t0008 | 10 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*941_*950delCACACA others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 941 | chr4 | 102631106 | |||||
| chr4:102631106
|
TTGTGTGT others(5): Show |
T | 1 | a0003c0003t0030 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*939_*950delCACACA others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 939 | chr4 | 102631106 | |||||
| chr4:102631106
|
TTGTGTGT others(7): Show |
T | 1 | a0002c0002t0032 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*937_*950delCACACA others(8): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 937 | chr4 | 102631106 | |||||
| chr4:102631106
|
TTGTGTGT others(9): Show |
T | 1 | a0002c0002t0022 | 2 | HG01070.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*935_*950delCACACA others(10): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 935 | chr4 | 102631106 | |||||
| chr4:102631141
|
TGTGTGTG others(4): Show |
T | 1 | a0001c0001t0026 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*905_*915delCACACA others(5): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 905 | chr4 | 102631141 | |||||
| chr4:102631273
|
A | G | 39 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(36): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*784T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 784 | chr4 | 102631273 | |||||
| chr4:102631376
|
C | T | 1 | a0003c0005t0021 | 2 | HG03486.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*681G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 681 | chr4 | 102631376 | |||||
| chr4:102631536
|
C | T | 1 | a0007c0011t0029 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*521G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 521 | chr4 | 102631536 | |||||
| chr4:102631541
|
A | G | 1 | a0001c0001t0025 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*516T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 516 | chr4 | 102631541 | |||||
| chr4:102631552
|
C | T | 39 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(36): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*505G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 505 | chr4 | 102631552 | |||||
| chr4:102631611
|
G | A | 1 | a0001c0001t0019 | 3 | HG02280.hp2 HG03195.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*446C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 446 | chr4 | 102631611 | |||||
| chr4:102631656
|
C | T | 39 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(36): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*401G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 401 | chr4 | 102631656 | |||||
| chr4:102631673
|
G | A | 39 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(36): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*384C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 384 | chr4 | 102631673 | |||||
| chr4:102631701
|
C | T | 6 | a0002c0002t0013a0002c0002t0014a0003c0003t0013others(3): Show | 12 | HG00438.hp2 HG01070.hp1 HG01099.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*356G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 356 | chr4 | 102631701 | |||||
| chr4:102631740
|
T | C | 6 | a0001c0001t0012a0001c0004t0012a0001c0004t0023others(3): Show | 7 | HG02886.hp1 HG02965.hp1 HG02965.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*317A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 317 | chr4 | 102631740 | |||||
| chr4:102631896
|
G | A | 39 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(36): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*161C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 161 | chr4 | 102631896 | |||||
| chr4:102631933
|
A | G | 39 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(36): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*124T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 124 | chr4 | 102631933 | |||||
| chr4:102631979
|
T | C | 2 | a0001c0001t0033a0001c0009t0034 | 2 | HG02615.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*78A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 17/17 | 78 | chr4 | 102631979 | |||||
| chr4:102760941
|
C | T | 1 | a0001c0009t0024 | 1 | HG03225.hp2 | 5_prime_UTR_variant | MODIFIER | c.-47G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/17 | 47 | chr4 | 102760941 | |||||
| chr4:102760952
|
C | T | 1 | a0001c0004t0023 | 1 | HG03579.hp2 | 5_prime_UTR_variant | MODIFIER | c.-58G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/17 | 58 | chr4 | 102760952 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:102632290
|
GA | G | 165 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(162): Show | 167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2416-10delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102632290 | ||||||
| chr4:102632346
|
A | C | 1 | a0004c0006t0001g0035 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2416-65T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102632346 | ||||||
| chr4:102632386
|
C | T | 166 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(163): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2416-105G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102632386 | ||||||
| chr4:102632417
|
A | G | 1 | a0007c0011t0029g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2416-136T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102632417 | ||||||
| chr4:102632470
|
C | T | 3 | a0001c0001t0019g0023a0001c0001t0019g0152a0001c0001t0019g0153 | 3 | HG02280.hp2 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2416-189G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102632470 | ||||||
| chr4:102632508
|
G | A | 166 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(163): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2416-227C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102632508 | ||||||
| chr4:102632759
|
A | C | 166 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(163): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2416-478T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102632759 | ||||||
| chr4:102632769
|
C | T | 166 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(163): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2416-488G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102632769 | ||||||
| chr4:102632803
|
T | C | 15 | a0002c0002t0013g0064a0002c0002t0014g0033a0002c0002t0014g0116others(12): Show | 15 | HG00438.hp2 HG01070.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.2416-522A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102632803 | ||||||
| chr4:102632862
|
G | A | 166 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(163): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2416-581C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102632862 | ||||||
| chr4:102632951
|
C | G | 166 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(163): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2416-670G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102632951 | ||||||
| chr4:102632956
|
T | A | 166 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(163): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2416-675A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102632956 | ||||||
| chr4:102633104
|
T | G | 166 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(163): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2416-823A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633104 | ||||||
| chr4:102633116
|
A | G | 4 | a0001c0001t0012g0232a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02886.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2416-835T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633116 | ||||||
| chr4:102633173
|
C | CT | 166 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(163): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2416-893dupA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633173 | ||||||
| chr4:102633178
|
T | A | 166 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(163): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2416-897A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633178 | ||||||
| chr4:102633183
|
C | T | 166 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(163): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2416-902G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633183 | ||||||
| chr4:102633193
|
T | A | 166 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(163): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2416-912A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633193 | ||||||
| chr4:102633196
|
T | C | 3 | a0001c0001t0019g0023a0001c0001t0019g0152a0001c0001t0019g0153 | 3 | HG02280.hp2 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2416-915A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633196 | ||||||
| chr4:102633214
|
CA | C | 5 | a0001c0001t0012g0232a0001c0004t0012g0253a0001c0004t0012g0275others(2): Show | 5 | HG02886.hp1 HG03209.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.2416-934delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633214 | ||||||
| chr4:102633216
|
G | T | 5 | a0001c0001t0012g0232a0001c0004t0012g0253a0001c0004t0012g0275others(2): Show | 5 | HG02886.hp1 HG03209.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.2416-935C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633216 | ||||||
| chr4:102633365
|
C | T | 166 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(163): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2416-1084G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633365 | ||||||
| chr4:102633395
|
T | C | 27 | a0001c0001t0003g0002a0001c0001t0003g0038a0001c0001t0003g0089others(24): Show | 28 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.2416-1114A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633395 | ||||||
| chr4:102633418
|
T | G | 3 | a0001c0001t0019g0023a0001c0001t0019g0152a0001c0001t0019g0153 | 3 | HG02280.hp2 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2416-1137A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633418 | ||||||
| chr4:102633556
|
G | A | 166 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(163): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2415+1232C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633556 | ||||||
| chr4:102633565
|
A | G | 166 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(163): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2415+1223T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633565 | ||||||
| chr4:102633576
|
G | A | 166 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(163): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2415+1212C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633576 | ||||||
| chr4:102633616
|
C | G | 166 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(163): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2415+1172G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633616 | ||||||
| chr4:102633618
|
C | T | 1 | a0002c0002t0002g0059 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2415+1170G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633618 | ||||||
| chr4:102633636
|
A | G | 166 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(163): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2415+1152T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633636 | ||||||
| chr4:102633653
|
C | A | 166 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(163): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2415+1135G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633653 | ||||||
| chr4:102633664
|
T | C | 185 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(182): Show | 187 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.2415+1124A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633664 | ||||||
| chr4:102633665
|
C | T | 16 | a0001c0001t0003g0002a0001c0001t0003g0089a0001c0001t0003g0090others(13): Show | 17 | HG00544.hp1 HG01167.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.2415+1123G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633665 | ||||||
| chr4:102633753
|
A | C | 166 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(163): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2415+1035T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633753 | ||||||
| chr4:102633773
|
TG | T | 166 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(163): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2415+1014delC | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633773 | ||||||
| chr4:102633818
|
A | G | 166 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(163): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2415+970T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633818 | ||||||
| chr4:102633835
|
A | G | 166 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(163): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2415+953T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633835 | ||||||
| chr4:102633904
|
G | GC | 166 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(163): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2415+883dupG | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102633904 | ||||||
| chr4:102634076
|
T | C | 166 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(163): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2415+712A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102634076 | ||||||
| chr4:102634095
|
G | A | 166 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(163): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2415+693C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102634095 | ||||||
| chr4:102634096
|
T | C | 166 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(163): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2415+692A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102634096 | ||||||
| chr4:102634260
|
A | C | 166 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(163): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2415+528T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102634260 | ||||||
| chr4:102634454
|
A | C | 165 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(162): Show | 167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2415+334T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102634454 | ||||||
| chr4:102634455
|
G | A | 165 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(162): Show | 167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2415+333C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102634455 | ||||||
| chr4:102634462
|
C | G | 165 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(162): Show | 167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2415+326G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102634462 | ||||||
| chr4:102634485
|
T | C | 1 | a0002c0002t0016g0249 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2415+303A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102634485 | ||||||
| chr4:102634488
|
TG | T | 165 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(162): Show | 167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2415+299delC | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102634488 | ||||||
| chr4:102634519
|
T | C | 165 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(162): Show | 167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2415+269A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102634519 | ||||||
| chr4:102634646
|
G | C | 165 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(162): Show | 167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2415+142C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102634646 | ||||||
| chr4:102634664
|
G | A | 165 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(162): Show | 167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2415+124C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102634664 | ||||||
| chr4:102634769
|
C | T | 1 | a0001c0001t0025g0157 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2415+19G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102634769 | ||||||
| chr4:102634770
|
G | A | 1 | a0002c0007t0007g0110 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2415+18C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 16/16 | chr4 | 102634770 | ||||||
| chr4:102635159
|
T | C | 163 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(160): Show | 165 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.2158-114A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 15/16 | chr4 | 102635159 | ||||||
| chr4:102635210
|
G | GT | 165 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(162): Show | 167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2158-166dupA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 15/16 | chr4 | 102635210 | ||||||
| chr4:102635305
|
G | C | 160 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(157): Show | 162 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.2158-260C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 15/16 | chr4 | 102635305 | ||||||
| chr4:102635318
|
G | A | 1 | a0003c0005t0008g0006 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2158-273C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 15/16 | chr4 | 102635318 | ||||||
| chr4:102635370
|
C | T | 1 | a0001c0001t0010g0159 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2158-325G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 15/16 | chr4 | 102635370 | ||||||
| chr4:102635653
|
C | T | 1 | a0002c0002t0002g0277 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2157+212G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 15/16 | chr4 | 102635653 | ||||||
| chr4:102635704
|
T | C | 158 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(155): Show | 160 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.2157+161A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 15/16 | chr4 | 102635704 | ||||||
| chr4:102635790
|
A | G | 1 | a0001c0001t0025g0157 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2157+75T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 15/16 | chr4 | 102635790 | ||||||
| chr4:102636035
|
C | T | 165 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(162): Show | 167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2015-28G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636035 | ||||||
| chr4:102636047
|
G | A | 1 | a0001c0004t0010g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2015-40C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636047 | ||||||
| chr4:102636062
|
C | T | 165 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(162): Show | 167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2015-55G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636062 | ||||||
| chr4:102636093
|
C | CA | 3 | a0001c0001t0012g0232a0001c0004t0012g0253a0001c0004t0012g0275 | 3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2015-87_2015-86ins others(1): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636093 | ||||||
| chr4:102636094
|
G | A | 163 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(160): Show | 165 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.2015-87C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636094 | ||||||
| chr4:102636097
|
G | T | 3 | a0001c0001t0012g0232a0001c0004t0012g0253a0001c0004t0012g0275 | 3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2015-90C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636097 | ||||||
| chr4:102636131
|
C | G | 1 | a0001c0001t0001g0164 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2015-124G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636131 | ||||||
| chr4:102636154
|
G | C | 165 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(162): Show | 167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2015-147C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636154 | ||||||
| chr4:102636303
|
G | T | 1 | a0003c0010t0016g0271 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2015-296C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636303 | ||||||
| chr4:102636306
|
A | T | 41 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0022others(38): Show | 41 | HG00735.hp2 HG01081.hp1 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.2015-299T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636306 | ||||||
| chr4:102636372
|
T | G | 165 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(162): Show | 167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2015-365A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636372 | ||||||
| chr4:102636386
|
A | G | 2 | a0001c0001t0020g0225a0001c0009t0012g0034 | 2 | HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2015-379T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636386 | ||||||
| chr4:102636504
|
T | C | 1 | a0001c0004t0005g0262 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2015-497A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636504 | ||||||
| chr4:102636507
|
A | G | 163 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(160): Show | 165 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.2015-500T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636507 | ||||||
| chr4:102636527
|
T | C | 1 | a0001c0001t0001g0178 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2015-520A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636527 | ||||||
| chr4:102636596
|
T | C | 165 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(162): Show | 167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2015-589A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636596 | ||||||
| chr4:102636960
|
G | C | 1 | a0003c0003t0015g0199 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2015-953C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102636960 | ||||||
| chr4:102637001
|
C | A | 1 | a0001c0001t0001g0234 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2015-994G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102637001 | ||||||
| chr4:102637012
|
C | G | 165 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(162): Show | 167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2015-1005G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102637012 | ||||||
| chr4:102637357
|
T | A | 165 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(162): Show | 167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2015-1350A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102637357 | ||||||
| chr4:102637549
|
G | C | 1 | a0002c0002t0007g0046 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2015-1542C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102637549 | ||||||
| chr4:102637574
|
C | T | 39 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0022others(36): Show | 39 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.2015-1567G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102637574 | ||||||
| chr4:102637648
|
T | C | 165 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(162): Show | 167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2015-1641A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102637648 | ||||||
| chr4:102637676
|
C | A | 69 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0020others(66): Show | 70 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.2015-1669G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102637676 | ||||||
| chr4:102637696
|
A | G | 165 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(162): Show | 167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2015-1689T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102637696 | ||||||
| chr4:102637794
|
T | C | 165 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(162): Show | 167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2015-1787A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102637794 | ||||||
| chr4:102637908
|
G | A | 1 | a0003c0003t0007g0258 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2014+1805C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102637908 | ||||||
| chr4:102637972
|
C | A | 1 | a0002c0002t0002g0134 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2014+1741G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102637972 | ||||||
| chr4:102638172
|
C | T | 11 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0022others(8): Show | 11 | HG02572.hp1 HG02615.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.2014+1541G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102638172 | ||||||
| chr4:102638183
|
G | T | 1 | a0004c0006t0001g0035 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2014+1530C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102638183 | ||||||
| chr4:102638193
|
G | C | 4 | a0003c0005t0008g0001a0003c0005t0008g0006a0003c0005t0008g0008others(1): Show | 5 | HG01192.hp2 HG02145.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2014+1520C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102638193 | ||||||
| chr4:102638316
|
C | G | 1 | a0003c0005t0008g0001 | 2 | HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2014+1397G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102638316 | ||||||
| chr4:102638398
|
C | A | 2 | a0001c0004t0010g0011a0001c0004t0010g0024 | 2 | HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2014+1315G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102638398 | ||||||
| chr4:102638471
|
G | GT | 160 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(157): Show | 162 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.2014+1241dupA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102638471 | ||||||
| chr4:102638471
|
G | GTT | 3 | a0001c0001t0004g0156a0001c0001t0010g0159a0004c0006t0003g0053 | 3 | HG02602.hp1 HG02738.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.2014+1241_2014+124 others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102638471 | ||||||
| chr4:102638473
|
C | T | 165 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(162): Show | 167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2014+1240G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102638473 | ||||||
| chr4:102638476
|
G | T | 165 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(162): Show | 167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2014+1237C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102638476 | ||||||
| chr4:102638705
|
C | T | 2 | a0002c0002t0002g0063a0002c0002t0002g0101 | 2 | HG00438.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.2014+1008G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102638705 | ||||||
| chr4:102638719
|
A | G | 153 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(150): Show | 155 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.2014+994T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102638719 | ||||||
| chr4:102639011
|
T | C | 3 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140 | 3 | HG02647.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2014+702A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102639011 | ||||||
| chr4:102639102
|
T | G | 3 | a0001c0001t0019g0023a0001c0001t0019g0152a0001c0001t0019g0153 | 3 | HG02280.hp2 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2014+611A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102639102 | ||||||
| chr4:102639161
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2014+552T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102639161 | ||||||
| chr4:102639544
|
C | T | 3 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140 | 3 | HG02647.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2014+169G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102639544 | ||||||
| chr4:102639588
|
A | T | 69 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0020others(66): Show | 70 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.2014+125T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102639588 | ||||||
| chr4:102639644
|
T | C | 3 | a0001c0001t0003g0246a0001c0001t0005g0082a0001c0001t0005g0247 | 3 | HG00140.hp2 HG01346.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.2014+69A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 14/16 | chr4 | 102639644 | ||||||
| chr4:102639949
|
T | C | 20 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(17): Show | 21 | HG00639.hp1 HG00673.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.1870-92A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102639949 | ||||||
| chr4:102640181
|
A | G | 1 | a0002c0002t0002g0213 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1870-324T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102640181 | ||||||
| chr4:102640323
|
A | T | 3 | a0003c0003t0015g0198a0003c0003t0015g0199a0003c0010t0015g0274 | 3 | HG02109.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1870-466T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102640323 | ||||||
| chr4:102640384
|
T | C | 1 | a0001c0004t0023g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1870-527A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102640384 | ||||||
| chr4:102640552
|
G | A | 94 | a0001c0001t0001g0254a0002c0002t0002g0028a0002c0002t0002g0029others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.1870-695C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102640552 | ||||||
| chr4:102640748
|
G | A | 11 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(8): Show | 11 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1870-891C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102640748 | ||||||
| chr4:102640773
|
A | C | 1 | a0001c0001t0006g0224 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1870-916T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102640773 | ||||||
| chr4:102641091
|
T | A | 5 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(2): Show | 5 | HG01071.hp2 HG01109.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.1870-1234A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102641091 | ||||||
| chr4:102641165
|
A | C | 1 | a0001c0004t0001g0243 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1870-1308T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102641165 | ||||||
| chr4:102641197
|
A | G | 1 | a0001c0001t0020g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1870-1340T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102641197 | ||||||
| chr4:102641841
|
A | G | 1 | a0001c0004t0020g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1870-1984T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102641841 | ||||||
| chr4:102642002
|
C | T | 2 | a0001c0001t0001g0195a0004c0006t0004g0042 | 2 | HG02080.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1870-2145G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102642002 | ||||||
| chr4:102642067
|
C | T | 1 | a0001c0001t0005g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1870-2210G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102642067 | ||||||
| chr4:102642092
|
GGCTATT | G | 25 | a0001c0001t0003g0002a0001c0001t0003g0089a0001c0001t0003g0090others(22): Show | 26 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.1870-2241_1870-223 others(10): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102642092 | ||||||
| chr4:102642408
|
T | C | 3 | a0001c0015t0010g0173a0002c0002t0002g0270a0003c0003t0014g0256 | 3 | NA19030.hp2 NA19063.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1870-2551A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102642408 | ||||||
| chr4:102642534
|
G | A | 2 | a0001c0001t0001g0269a0001c0001t0025g0157 | 2 | HG00408.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1870-2677C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102642534 | ||||||
| chr4:102642535
|
A | G | 2 | a0001c0001t0001g0269a0001c0001t0025g0157 | 2 | HG00408.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1870-2678T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102642535 | ||||||
| chr4:102642536
|
G | T | 2 | a0001c0001t0001g0269a0001c0001t0025g0157 | 2 | HG00408.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1870-2679C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102642536 | ||||||
| chr4:102642540
|
G | GTGAGCCG others(9): Show |
2 | a0001c0001t0001g0269a0001c0001t0025g0157 | 2 | HG00408.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1870-2684_1870-268 others(20): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102642540 | ||||||
| chr4:102642543
|
G | C | 2 | a0001c0001t0001g0269a0001c0001t0025g0157 | 2 | HG00408.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1870-2686C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102642543 | ||||||
| chr4:102642544
|
T | TTGGAG | 2 | a0001c0001t0001g0269a0001c0001t0025g0157 | 2 | HG00408.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1870-2688_1870-268 others(9): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102642544 | ||||||
| chr4:102642593
|
C | CG | 12 | a0001c0001t0003g0223a0001c0001t0003g0231a0001c0001t0006g0261others(9): Show | 12 | HG01070.hp1 HG01175.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1870-2737dupC | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102642593 | ||||||
| chr4:102642756
|
T | C | 3 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140 | 3 | HG02647.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1870-2899A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102642756 | ||||||
| chr4:102642809
|
T | C | 1 | a0001c0017t0005g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1870-2952A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102642809 | ||||||
| chr4:102642868
|
T | C | 13 | a0001c0009t0024g0005a0003c0005t0008g0001a0003c0005t0008g0006others(10): Show | 14 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1870-3011A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102642868 | ||||||
| chr4:102643056
|
T | C | 2 | a0001c0001t0003g0231a0001c0001t0009g0216 | 2 | HG01175.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1870-3199A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102643056 | ||||||
| chr4:102643105
|
G | C | 1 | a0003c0003t0014g0220 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1870-3248C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102643105 | ||||||
| chr4:102643183
|
C | T | 3 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140 | 3 | HG02647.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1870-3326G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102643183 | ||||||
| chr4:102643266
|
A | T | 1 | a0001c0001t0019g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1870-3409T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102643266 | ||||||
| chr4:102643275
|
C | T | 2 | a0003c0003t0015g0198a0003c0003t0015g0199 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1870-3418G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102643275 | ||||||
| chr4:102643310
|
T | G | 1 | a0001c0004t0020g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1870-3453A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102643310 | ||||||
| chr4:102643382
|
T | C | 1 | a0001c0001t0033g0174 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1870-3525A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102643382 | ||||||
| chr4:102643556
|
T | C | 1 | a0004c0006t0004g0025 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1870-3699A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102643556 | ||||||
| chr4:102643655
|
T | C | 2 | a0003c0003t0015g0198a0003c0003t0015g0199 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1870-3798A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102643655 | ||||||
| chr4:102643859
|
T | G | 1 | a0001c0001t0010g0159 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1870-4002A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102643859 | ||||||
| chr4:102643863
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1870-4006C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102643863 | ||||||
| chr4:102643995
|
A | G | 6 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0004t0020g0141others(3): Show | 6 | HG02280.hp2 HG02630.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1870-4138T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102643995 | ||||||
| chr4:102644052
|
C | A | 1 | a0001c0004t0009g0014 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1870-4195G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102644052 | ||||||
| chr4:102644215
|
A | T | 1 | a0001c0017t0005g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1870-4358T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102644215 | ||||||
| chr4:102644352
|
A | T | 3 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140 | 3 | HG02647.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1870-4495T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102644352 | ||||||
| chr4:102644429
|
C | T | 3 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140 | 3 | HG02647.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1870-4572G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102644429 | ||||||
| chr4:102644780
|
A | G | 1 | a0001c0001t0001g0236 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1870-4923T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102644780 | ||||||
| chr4:102644810
|
C | T | 3 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140 | 3 | HG02647.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1870-4953G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102644810 | ||||||
| chr4:102644921
|
A | T | 6 | a0001c0001t0001g0178a0001c0001t0001g0182a0001c0001t0001g0185others(3): Show | 6 | HG00621.hp2 HG02071.hp1 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.1870-5064T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102644921 | ||||||
| chr4:102645206
|
T | C | 7 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1869+5331A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102645206 | ||||||
| chr4:102645297
|
A | G | 1 | a0002c0002t0002g0128 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1869+5240T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102645297 | ||||||
| chr4:102645637
|
T | A | 3 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140 | 3 | HG02647.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1869+4900A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102645637 | ||||||
| chr4:102645805
|
T | C | 7 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1869+4732A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102645805 | ||||||
| chr4:102645908
|
T | C | 1 | a0003c0005t0008g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1869+4629A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102645908 | ||||||
| chr4:102645966
|
T | C | 3 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140 | 3 | HG02647.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1869+4571A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102645966 | ||||||
| chr4:102646191
|
G | T | 123 | a0001c0001t0001g0254a0001c0001t0019g0152a0001c0001t0019g0153others(120): Show | 124 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.1869+4346C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102646191 | ||||||
| chr4:102646325
|
C | A | 1 | a0005c0008t0003g0219 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1869+4212G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102646325 | ||||||
| chr4:102646406
|
C | T | 1 | a0001c0004t0010g0011 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1869+4131G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102646406 | ||||||
| chr4:102646892
|
C | T | 1 | a0001c0001t0003g0231 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1869+3645G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102646892 | ||||||
| chr4:102646919
|
T | G | 1 | a0001c0004t0020g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1869+3618A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102646919 | ||||||
| chr4:102646928
|
G | A | 3 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140 | 3 | HG02647.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1869+3609C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102646928 | ||||||
| chr4:102647327
|
G | A | 1 | a0001c0001t0001g0177 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1869+3210C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102647327 | ||||||
| chr4:102647332
|
T | C | 1 | a0001c0001t0001g0178 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1869+3205A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102647332 | ||||||
| chr4:102647565
|
C | T | 1 | a0003c0003t0007g0130 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1869+2972G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102647565 | ||||||
| chr4:102647638
|
T | C | 1 | a0001c0004t0023g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1869+2899A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102647638 | ||||||
| chr4:102647850
|
A | T | 1 | a0001c0004t0023g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1869+2687T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102647850 | ||||||
| chr4:102647852
|
G | A | 6 | a0001c0001t0001g0254a0003c0003t0013g0248a0003c0003t0013g0255others(3): Show | 6 | HG00438.hp2 HG02056.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.1869+2685C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102647852 | ||||||
| chr4:102648051
|
A | C | 1 | a0001c0001t0001g0196 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1869+2486T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102648051 | ||||||
| chr4:102648059
|
C | A | 4 | a0002c0002t0002g0050a0002c0002t0002g0054a0002c0002t0002g0059others(1): Show | 4 | HG02735.hp2 HG02738.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1869+2478G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102648059 | ||||||
| chr4:102648126
|
A | G | 131 | a0001c0001t0001g0254a0001c0001t0006g0077a0001c0001t0006g0081others(128): Show | 132 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.1869+2411T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102648126 | ||||||
| chr4:102648133
|
A | T | 6 | a0001c0001t0019g0023a0005c0008t0003g0138a0005c0008t0003g0218others(3): Show | 6 | HG02647.hp1 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1869+2404T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102648133 | ||||||
| chr4:102648148
|
C | A | 276 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(273): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.1869+2389G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102648148 | ||||||
| chr4:102648543
|
A | G | 2 | a0002c0002t0002g0043a0002c0002t0002g0057 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1869+1994T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102648543 | ||||||
| chr4:102648895
|
T | A | 8 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0004t0010g0011others(5): Show | 8 | HG02280.hp2 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1869+1642A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102648895 | ||||||
| chr4:102648987
|
A | G | 1 | a0001c0017t0005g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1869+1550T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102648987 | ||||||
| chr4:102649069
|
C | G | 1 | a0002c0002t0002g0128 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1869+1468G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102649069 | ||||||
| chr4:102649118
|
G | A | 1 | a0003c0003t0014g0143 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1869+1419C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102649118 | ||||||
| chr4:102649130
|
T | C | 3 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140 | 3 | HG02647.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1869+1407A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102649130 | ||||||
| chr4:102649526
|
G | T | 8 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0004t0010g0011others(5): Show | 8 | HG02280.hp2 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1869+1011C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102649526 | ||||||
| chr4:102649679
|
T | C | 1 | a0001c0001t0001g0269 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1869+858A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102649679 | ||||||
| chr4:102649698
|
C | G | 1 | a0001c0004t0010g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1869+839G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102649698 | ||||||
| chr4:102649760
|
A | C | 1 | a0002c0007t0007g0118 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1869+777T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102649760 | ||||||
| chr4:102650103
|
C | T | 1 | a0001c0004t0005g0267 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1869+434G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102650103 | ||||||
| chr4:102650356
|
T | C | 5 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(2): Show | 5 | HG01071.hp2 HG01109.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.1869+181A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 13/16 | chr4 | 102650356 | ||||||
| chr4:102650714
|
G | A | 3 | a0001c0001t0012g0232a0001c0004t0012g0253a0001c0004t0012g0275 | 3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1705-13C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102650714 | ||||||
| chr4:102650714
|
G | T | 6 | a0001c0001t0003g0190a0001c0001t0003g0230a0001c0001t0003g0273others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.1705-13C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102650714 | ||||||
| chr4:102650770
|
G | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0179 | 2 | HG01074.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1705-69C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102650770 | ||||||
| chr4:102651163
|
G | A | 124 | a0001c0001t0001g0254a0001c0001t0019g0152a0001c0001t0019g0153others(121): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.1705-462C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102651163 | ||||||
| chr4:102651283
|
G | A | 124 | a0001c0001t0001g0254a0001c0001t0019g0152a0001c0001t0019g0153others(121): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.1705-582C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102651283 | ||||||
| chr4:102651298
|
TA | T | 3 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140 | 3 | HG02647.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1705-598delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102651298 | ||||||
| chr4:102651460
|
A | G | 1 | a0004c0006t0005g0129 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1705-759T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102651460 | ||||||
| chr4:102651537
|
T | C | 3 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140 | 3 | HG02647.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1705-836A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102651537 | ||||||
| chr4:102651594
|
G | T | 110 | a0001c0001t0001g0254a0001c0004t0010g0011a0001c0004t0010g0024others(107): Show | 111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1705-893C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102651594 | ||||||
| chr4:102651789
|
C | T | 116 | a0001c0001t0001g0254a0001c0001t0019g0152a0001c0001t0019g0153others(113): Show | 117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.1705-1088G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102651789 | ||||||
| chr4:102651925
|
C | T | 107 | a0001c0001t0001g0254a0001c0009t0024g0005a0001c0017t0005g0237others(104): Show | 108 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1705-1224G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102651925 | ||||||
| chr4:102651965
|
TTTAA | T | 107 | a0001c0001t0001g0254a0001c0009t0024g0005a0001c0017t0005g0237others(104): Show | 108 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1705-1268_1705-126 others(8): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102651965 | ||||||
| chr4:102651989
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1705-1288G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102651989 | ||||||
| chr4:102652098
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1705-1397C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102652098 | ||||||
| chr4:102652166
|
C | T | 109 | a0001c0001t0001g0254a0001c0001t0006g0077a0001c0001t0006g0081others(106): Show | 110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.1705-1465G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102652166 | ||||||
| chr4:102652220
|
G | C | 108 | a0001c0001t0001g0254a0001c0001t0006g0077a0001c0001t0006g0081others(105): Show | 109 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1705-1519C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102652220 | ||||||
| chr4:102652283
|
T | C | 4 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1705-1582A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102652283 | ||||||
| chr4:102652334
|
C | A | 1 | a0002c0002t0013g0064 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1705-1633G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102652334 | ||||||
| chr4:102652469
|
G | A | 1 | a0001c0004t0001g0243 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1705-1768C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102652469 | ||||||
| chr4:102652568
|
TA | T | 4 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1705-1868delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102652568 | ||||||
| chr4:102652569
|
A | T | 18 | a0001c0001t0012g0232a0001c0001t0019g0152a0001c0001t0019g0153others(15): Show | 18 | HG01891.hp2 HG02145.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.1705-1868T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102652569 | ||||||
| chr4:102652592
|
G | A | 121 | a0001c0001t0001g0254a0001c0001t0006g0077a0001c0001t0006g0081others(118): Show | 122 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.1705-1891C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102652592 | ||||||
| chr4:102652670
|
T | C | 2 | a0001c0001t0033g0174a0001c0009t0034g0016 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1705-1969A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102652670 | ||||||
| chr4:102652706
|
C | T | 87 | a0001c0001t0006g0077a0001c0001t0006g0081a0002c0002t0002g0028others(84): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.1705-2005G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102652706 | ||||||
| chr4:102652718
|
C | T | 1 | a0002c0002t0002g0114 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1705-2017G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102652718 | ||||||
| chr4:102652747
|
C | T | 126 | a0001c0001t0001g0254a0001c0001t0006g0077a0001c0001t0006g0081others(123): Show | 127 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1705-2046G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102652747 | ||||||
| chr4:102652761
|
G | A | 13 | a0001c0009t0024g0005a0003c0005t0008g0001a0003c0005t0008g0006others(10): Show | 14 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1705-2060C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102652761 | ||||||
| chr4:102653046
|
G | T | 1 | a0001c0001t0010g0159 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1705-2345C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653046 | ||||||
| chr4:102653197
|
C | T | 1 | a0001c0004t0023g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1705-2496G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653197 | ||||||
| chr4:102653202
|
G | A | 276 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(273): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.1705-2501C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653202 | ||||||
| chr4:102653220
|
GCA | G | 23 | a0001c0001t0001g0146a0001c0001t0001g0175a0001c0001t0001g0179others(20): Show | 23 | HG00280.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1705-2521_1705-252 others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653220 | ||||||
| chr4:102653220
|
GCACA | G | 48 | a0001c0001t0001g0003a0001c0001t0001g0105a0001c0001t0001g0133others(45): Show | 49 | HG00639.hp1 HG00673.hp1 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.1705-2523_1705-252 others(8): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653220 | ||||||
| chr4:102653220
|
GCACACA | G | 35 | a0001c0001t0001g0269a0001c0001t0003g0002a0001c0001t0003g0038others(32): Show | 36 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.1705-2525_1705-252 others(10): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653220 | ||||||
| chr4:102653220
|
GCACACAC others(1): Show |
G | 10 | a0001c0001t0001g0093a0001c0001t0001g0193a0001c0001t0003g0190others(7): Show | 10 | HG01243.hp2 HG01358.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.1705-2527_1705-252 others(12): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653220 | ||||||
| chr4:102653220
|
GCACACAC others(5): Show |
G | 7 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1705-2531_1705-252 others(16): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653220 | ||||||
| chr4:102653220
|
GCACACAC others(7): Show |
G | 4 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141others(1): Show | 4 | HG02886.hp2 HG02922.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1705-2533_1705-252 others(18): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653220 | ||||||
| chr4:102653220
|
GCACACAC others(9): Show |
G | 3 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0009t0012g0034 | 3 | HG02280.hp2 HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1705-2535_1705-252 others(20): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653220 | ||||||
| chr4:102653220
|
GCACACAC others(11): Show |
G | 2 | a0001c0004t0010g0024a0003c0003t0015g0198 | 2 | HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1705-2537_1705-252 others(22): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653220 | ||||||
| chr4:102653220
|
GCACACAC others(13): Show |
G | 1 | a0001c0004t0023g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1705-2539_1705-252 others(24): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653220 | ||||||
| chr4:102653220
|
GCACACAC others(15): Show |
G | 108 | a0001c0001t0001g0254a0001c0001t0006g0077a0001c0001t0006g0081others(105): Show | 109 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1705-2541_1705-252 others(26): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653220 | ||||||
| chr4:102653220
|
GCACACAC others(17): Show |
G | 1 | a0001c0017t0005g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1705-2543_1705-252 others(28): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653220 | ||||||
| chr4:102653350
|
G | A | 1 | a0001c0004t0023g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1705-2649C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653350 | ||||||
| chr4:102653418
|
G | A | 5 | a0001c0001t0003g0038a0001c0001t0003g0206a0001c0001t0003g0207others(2): Show | 5 | HG00621.hp1 HG02083.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.1705-2717C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653418 | ||||||
| chr4:102653493
|
T | G | 1 | a0001c0004t0023g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1705-2792A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653493 | ||||||
| chr4:102653910
|
C | T | 122 | a0001c0001t0001g0254a0001c0001t0006g0077a0001c0001t0006g0081others(119): Show | 123 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.1705-3209G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653910 | ||||||
| chr4:102653996
|
A | G | 7 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1705-3295T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102653996 | ||||||
| chr4:102654083
|
C | T | 1 | a0001c0017t0005g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1705-3382G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102654083 | ||||||
| chr4:102654123
|
T | C | 117 | a0001c0001t0001g0254a0001c0001t0006g0077a0001c0001t0006g0081others(114): Show | 118 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.1705-3422A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102654123 | ||||||
| chr4:102654129
|
C | T | 2 | a0001c0004t0010g0140a0001c0004t0020g0141 | 2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1705-3428G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102654129 | ||||||
| chr4:102654228
|
C | A | 117 | a0001c0001t0001g0254a0001c0001t0006g0077a0001c0001t0006g0081others(114): Show | 118 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.1704+3454G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102654228 | ||||||
| chr4:102654656
|
A | G | 1 | a0001c0001t0004g0180 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1704+3026T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102654656 | ||||||
| chr4:102654816
|
T | C | 1 | a0001c0001t0001g0234 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1704+2866A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102654816 | ||||||
| chr4:102654853
|
G | A | 5 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0009t0012g0034others(2): Show | 5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1704+2829C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102654853 | ||||||
| chr4:102655011
|
A | G | 4 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1704+2671T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102655011 | ||||||
| chr4:102655328
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1704+2354A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102655328 | ||||||
| chr4:102655603
|
G | C | 1 | a0002c0002t0016g0125 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1704+2079C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102655603 | ||||||
| chr4:102655635
|
T | C | 1 | a0001c0001t0005g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1704+2047A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102655635 | ||||||
| chr4:102655686
|
C | G | 1 | a0001c0017t0005g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1704+1996G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102655686 | ||||||
| chr4:102655710
|
C | T | 3 | a0001c0001t0012g0232a0001c0004t0012g0253a0001c0004t0012g0275 | 3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1704+1972G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102655710 | ||||||
| chr4:102655903
|
T | C | 1 | a0001c0017t0005g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1704+1779A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102655903 | ||||||
| chr4:102656308
|
T | C | 124 | a0001c0001t0001g0254a0001c0001t0019g0152a0001c0001t0019g0153others(121): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.1704+1374A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102656308 | ||||||
| chr4:102656723
|
T | A | 1 | a0002c0002t0002g0075 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1704+959A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102656723 | ||||||
| chr4:102656835
|
T | C | 28 | a0001c0001t0001g0269a0001c0001t0003g0002a0001c0001t0003g0038others(25): Show | 29 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.1704+847A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102656835 | ||||||
| chr4:102656872
|
G | GA | 5 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0009t0012g0034others(2): Show | 5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1704+809dupT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102656872 | ||||||
| chr4:102656898
|
C | T | 2 | a0003c0003t0015g0198a0003c0003t0015g0199 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1704+784G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102656898 | ||||||
| chr4:102657108
|
A | C | 4 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1704+574T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102657108 | ||||||
| chr4:102657118
|
C | A | 5 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0009t0012g0034others(2): Show | 5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1704+564G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102657118 | ||||||
| chr4:102657172
|
A | T | 1 | a0002c0002t0017g0132 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1704+510T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102657172 | ||||||
| chr4:102657221
|
G | GT | 6 | a0001c0001t0001g0254a0001c0004t0010g0024a0003c0003t0013g0248others(3): Show | 6 | HG01496.hp2 HG02056.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1704+460dupA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102657221 | ||||||
| chr4:102657222
|
T | TG | 77 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0104others(74): Show | 78 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.1704+459dupC | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102657222 | ||||||
| chr4:102657222
|
T | TTG | 19 | a0001c0004t0010g0140a0001c0004t0020g0141a0001c0009t0024g0005others(16): Show | 19 | HG00438.hp2 HG01884.hp1 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.1704+459_1704+460i others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102657222 | ||||||
| chr4:102657222
|
T | TTGG | 46 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(43): Show | 47 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.1704+459_1704+460i others(5): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102657222 | ||||||
| chr4:102657222
|
T | TTGGG | 43 | a0001c0004t0023g0004a0002c0002t0002g0032a0002c0002t0002g0039others(40): Show | 43 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1704+459_1704+460i others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102657222 | ||||||
| chr4:102657222
|
T | TTGGGG | 4 | a0002c0002t0002g0114a0002c0002t0002g0235a0002c0002t0022g0233others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1704+459_1704+460i others(7): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102657222 | ||||||
| chr4:102657227
|
G | A | 7 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1704+455C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102657227 | ||||||
| chr4:102657230
|
G | C | 3 | a0001c0001t0012g0232a0001c0004t0012g0253a0001c0004t0012g0275 | 3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1704+452C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102657230 | ||||||
| chr4:102657238
|
G | A | 115 | a0001c0001t0001g0254a0001c0004t0005g0262a0001c0004t0005g0263others(112): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.1704+444C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102657238 | ||||||
| chr4:102657243
|
T | G | 276 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(273): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.1704+439A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102657243 | ||||||
| chr4:102657436
|
A | G | 1 | a0010c0016t0004g0214 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1704+246T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102657436 | ||||||
| chr4:102657480
|
G | A | 128 | a0001c0001t0001g0254a0001c0001t0012g0232a0001c0001t0019g0152others(125): Show | 129 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1704+202C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 12/16 | chr4 | 102657480 | ||||||
| chr4:102658075
|
C | T | 2 | a0003c0003t0014g0220a0003c0003t0031g0238 | 2 | HG01070.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1486-175G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102658075 | ||||||
| chr4:102658303
|
A | C | 5 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0009t0012g0034others(2): Show | 5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1486-403T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102658303 | ||||||
| chr4:102658303
|
A | T | 115 | a0001c0001t0001g0254a0001c0004t0005g0262a0001c0004t0005g0263others(112): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.1486-403T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102658303 | ||||||
| chr4:102658450
|
G | A | 1 | a0001c0004t0005g0265 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1486-550C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102658450 | ||||||
| chr4:102658463
|
G | A | 2 | a0002c0002t0002g0043a0002c0002t0002g0057 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1486-563C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102658463 | ||||||
| chr4:102658534
|
G | A | 124 | a0001c0001t0001g0254a0001c0001t0019g0152a0001c0001t0019g0153others(121): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.1486-634C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102658534 | ||||||
| chr4:102658568
|
T | C | 1 | a0001c0004t0023g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1486-668A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102658568 | ||||||
| chr4:102658569
|
T | C | 1 | a0002c0002t0002g0071 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1486-669A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102658569 | ||||||
| chr4:102658608
|
G | A | 4 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1486-708C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102658608 | ||||||
| chr4:102658737
|
A | T | 1 | a0002c0002t0002g0055 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1486-837T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102658737 | ||||||
| chr4:102658897
|
C | A | 1 | a0001c0004t0023g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1486-997G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102658897 | ||||||
| chr4:102658907
|
T | C | 5 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0009t0012g0034others(2): Show | 5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1486-1007A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102658907 | ||||||
| chr4:102658921
|
A | G | 4 | a0003c0005t0008g0001a0003c0005t0008g0006a0003c0005t0008g0008others(1): Show | 5 | HG01192.hp2 HG02145.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1486-1021T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102658921 | ||||||
| chr4:102658997
|
G | A | 9 | a0001c0009t0024g0005a0003c0005t0008g0010a0003c0005t0008g0012others(6): Show | 9 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1486-1097C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102658997 | ||||||
| chr4:102659139
|
C | T | 5 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0009t0012g0034others(2): Show | 5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1486-1239G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102659139 | ||||||
| chr4:102659160
|
T | C | 1 | a0001c0004t0023g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1486-1260A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102659160 | ||||||
| chr4:102659220
|
G | C | 4 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1486-1320C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102659220 | ||||||
| chr4:102659454
|
C | A | 7 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1486-1554G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102659454 | ||||||
| chr4:102659631
|
T | C | 126 | a0001c0001t0001g0254a0001c0001t0006g0077a0001c0001t0006g0081others(123): Show | 127 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1486-1731A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102659631 | ||||||
| chr4:102660105
|
C | T | 5 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0009t0012g0034others(2): Show | 5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1486-2205G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102660105 | ||||||
| chr4:102660219
|
T | G | 5 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0009t0012g0034others(2): Show | 5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1486-2319A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102660219 | ||||||
| chr4:102660245
|
C | G | 3 | a0002c0002t0002g0124a0002c0002t0002g0126a0002c0002t0016g0125 | 3 | HG00140.hp1 HG01433.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1486-2345G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102660245 | ||||||
| chr4:102660247
|
G | T | 2 | a0001c0001t0003g0169a0001c0001t0006g0168 | 2 | HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1486-2347C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102660247 | ||||||
| chr4:102660259
|
C | T | 1 | a0002c0002t0002g0070 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1486-2359G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102660259 | ||||||
| chr4:102660335
|
T | A | 7 | a0001c0009t0024g0005a0003c0005t0008g0010a0003c0005t0008g0012others(4): Show | 7 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1486-2435A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102660335 | ||||||
| chr4:102660933
|
C | T | 1 | a0004c0006t0001g0061 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1486-3033G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102660933 | ||||||
| chr4:102661055
|
G | A | 1 | a0002c0002t0002g0235 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1486-3155C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102661055 | ||||||
| chr4:102661092
|
T | C | 1 | a0002c0002t0002g0059 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1486-3192A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102661092 | ||||||
| chr4:102661119
|
T | A | 5 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0009t0012g0034others(2): Show | 5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1486-3219A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102661119 | ||||||
| chr4:102661446
|
A | G | 5 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0009t0012g0034others(2): Show | 5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1485+3239T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102661446 | ||||||
| chr4:102661641
|
C | T | 4 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1485+3044G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102661641 | ||||||
| chr4:102661643
|
C | T | 1 | a0002c0002t0002g0213 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1485+3042G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102661643 | ||||||
| chr4:102661689
|
C | T | 7 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1485+2996G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102661689 | ||||||
| chr4:102661776
|
A | G | 1 | a0001c0009t0012g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1485+2909T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102661776 | ||||||
| chr4:102661930
|
T | G | 5 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0009t0012g0034others(2): Show | 5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1485+2755A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102661930 | ||||||
| chr4:102661980
|
G | A | 4 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1485+2705C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102661980 | ||||||
| chr4:102661985
|
T | TAATACTA others(811): Show |
2 | a0001c0001t0003g0038a0001c0001t0003g0207 | 2 | NA18949.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1485+2699_1485+270 others(822): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102661985 | ||||||
| chr4:102661985
|
T | TAATACTA others(810): Show |
1 | a0001c0001t0003g0208 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1485+2699_1485+270 others(821): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102661985 | ||||||
| chr4:102662032
|
A | C | 108 | a0001c0001t0001g0254a0001c0004t0023g0004a0001c0009t0024g0005others(105): Show | 109 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1485+2653T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102662032 | ||||||
| chr4:102662039
|
G | A | 107 | a0001c0001t0001g0254a0001c0009t0024g0005a0001c0017t0005g0237others(104): Show | 108 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1485+2646C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102662039 | ||||||
| chr4:102662051
|
A | G | 107 | a0001c0001t0001g0254a0001c0009t0024g0005a0001c0017t0005g0237others(104): Show | 108 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1485+2634T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102662051 | ||||||
| chr4:102662262
|
C | A | 7 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1485+2423G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102662262 | ||||||
| chr4:102662300
|
C | T | 2 | a0003c0005t0021g0251a0003c0005t0021g0252 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1485+2385G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102662300 | ||||||
| chr4:102662368
|
TG | T | 7 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1485+2316delC | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102662368 | ||||||
| chr4:102662504
|
T | C | 12 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0004t0005g0262others(9): Show | 12 | HG01891.hp2 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1485+2181A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102662504 | ||||||
| chr4:102662538
|
T | C | 1 | a0002c0002t0002g0114 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1485+2147A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102662538 | ||||||
| chr4:102662551
|
CA | C | 113 | a0001c0001t0001g0254a0001c0001t0006g0077a0001c0001t0006g0081others(110): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.1485+2133delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102662551 | ||||||
| chr4:102662551
|
CAA | C | 9 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(6): Show | 9 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1485+2132_1485+213 others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102662551 | ||||||
| chr4:102662612
|
G | A | 7 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1485+2073C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102662612 | ||||||
| chr4:102662619
|
C | T | 3 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0009t0012g0034 | 3 | HG02280.hp2 HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1485+2066G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102662619 | ||||||
| chr4:102663101
|
C | T | 7 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1485+1584G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102663101 | ||||||
| chr4:102663150
|
C | T | 7 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1485+1535G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102663150 | ||||||
| chr4:102663153
|
G | A | 16 | a0001c0001t0003g0002a0001c0001t0003g0089a0001c0001t0003g0090others(13): Show | 17 | HG00544.hp1 HG01167.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.1485+1532C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102663153 | ||||||
| chr4:102663176
|
T | TA | 12 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0004t0005g0262others(9): Show | 12 | HG01891.hp2 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1485+1508dupT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102663176 | ||||||
| chr4:102663294
|
T | C | 4 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1485+1391A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102663294 | ||||||
| chr4:102663380
|
A | G | 7 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1485+1305T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102663380 | ||||||
| chr4:102663438
|
A | C | 1 | a0001c0004t0010g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1485+1247T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102663438 | ||||||
| chr4:102663461
|
G | C | 1 | a0001c0004t0010g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1485+1224C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102663461 | ||||||
| chr4:102663710
|
C | T | 5 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0009t0012g0034others(2): Show | 5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1485+975G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102663710 | ||||||
| chr4:102663770
|
A | C | 4 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1485+915T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102663770 | ||||||
| chr4:102663819
|
A | G | 7 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1485+866T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102663819 | ||||||
| chr4:102663901
|
G | A | 5 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0009t0012g0034others(2): Show | 5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1485+784C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102663901 | ||||||
| chr4:102663922
|
T | A | 1 | a0001c0004t0023g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1485+763A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102663922 | ||||||
| chr4:102664037
|
C | T | 7 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1485+648G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102664037 | ||||||
| chr4:102664041
|
C | T | 7 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1485+644G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102664041 | ||||||
| chr4:102664042
|
G | T | 5 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0009t0012g0034others(2): Show | 5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1485+643C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102664042 | ||||||
| chr4:102664171
|
T | C | 2 | a0001c0001t0019g0152a0001c0001t0019g0153 | 2 | HG02280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1485+514A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102664171 | ||||||
| chr4:102664352
|
C | CT | 113 | a0001c0001t0001g0254a0001c0001t0006g0077a0001c0001t0006g0081others(110): Show | 114 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.1485+332dupA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102664352 | ||||||
| chr4:102664352
|
CT | C | 5 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140others(2): Show | 5 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1485+332delA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102664352 | ||||||
| chr4:102664380
|
G | A | 1 | a0001c0004t0010g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1485+305C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102664380 | ||||||
| chr4:102664400
|
G | C | 1 | a0002c0002t0002g0213 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1485+285C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102664400 | ||||||
| chr4:102664418
|
G | A | 1 | a0002c0002t0013g0064 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1485+267C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102664418 | ||||||
| chr4:102664473
|
C | G | 6 | a0001c0001t0001g0123a0001c0001t0001g0131a0001c0001t0001g0167others(3): Show | 6 | HG01074.hp2 HG02257.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1485+212G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102664473 | ||||||
| chr4:102664515
|
AT | A | 7 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1485+169delA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102664515 | ||||||
| chr4:102664557
|
C | A | 1 | a0003c0003t0014g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1485+128G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102664557 | ||||||
| chr4:102664662
|
C | T | 7 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1485+23G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 11/16 | chr4 | 102664662 | ||||||
| chr4:102664978
|
T | C | 1 | a0002c0002t0002g0270 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1318-126A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102664978 | ||||||
| chr4:102665183
|
C | G | 1 | a0003c0003t0016g0211 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1318-331G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102665183 | ||||||
| chr4:102665491
|
G | A | 1 | a0003c0010t0016g0271 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1318-639C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102665491 | ||||||
| chr4:102665573
|
G | A | 1 | a0002c0002t0002g0037 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1318-721C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102665573 | ||||||
| chr4:102665618
|
T | C | 1 | a0002c0002t0002g0075 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1318-766A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102665618 | ||||||
| chr4:102665628
|
C | CA | 5 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0009t0012g0034others(2): Show | 5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1318-777dupT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102665628 | ||||||
| chr4:102665685
|
C | T | 5 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0009t0012g0034others(2): Show | 5 | HG02280.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1318-833G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102665685 | ||||||
| chr4:102665820
|
C | T | 128 | a0001c0001t0001g0254a0001c0001t0012g0232a0001c0001t0019g0152others(125): Show | 129 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1318-968G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102665820 | ||||||
| chr4:102665850
|
C | T | 4 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1318-998G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102665850 | ||||||
| chr4:102665957
|
A | T | 2 | a0001c0001t0003g0172a0005c0008t0003g0218 | 2 | HG02897.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1318-1105T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102665957 | ||||||
| chr4:102666046
|
T | C | 1 | a0002c0002t0017g0132 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1318-1194A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102666046 | ||||||
| chr4:102666158
|
T | TA | 3 | a0001c0001t0004g0069a0001c0001t0004g0156a0003c0003t0007g0130 | 3 | HG02602.hp1 HG02602.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1318-1307dupT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102666158 | ||||||
| chr4:102666174
|
G | A | 7 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1318-1322C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102666174 | ||||||
| chr4:102666330
|
C | T | 13 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(10): Show | 13 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1318-1478G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102666330 | ||||||
| chr4:102666421
|
T | C | 1 | a0003c0003t0014g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1318-1569A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102666421 | ||||||
| chr4:102666488
|
G | C | 1 | a0001c0004t0005g0262 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1318-1636C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102666488 | ||||||
| chr4:102666610
|
T | C | 9 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(6): Show | 9 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1318-1758A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102666610 | ||||||
| chr4:102666649
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1318-1797C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102666649 | ||||||
| chr4:102666658
|
C | T | 2 | a0003c0003t0015g0198a0003c0003t0015g0199 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1318-1806G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102666658 | ||||||
| chr4:102666659
|
AT | A | 9 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(6): Show | 9 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1318-1808delA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102666659 | ||||||
| chr4:102666738
|
T | C | 1 | a0001c0001t0001g0269 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1318-1886A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102666738 | ||||||
| chr4:102666800
|
C | T | 4 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1318-1948G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102666800 | ||||||
| chr4:102666816
|
A | T | 3 | a0001c0001t0012g0232a0001c0004t0012g0253a0001c0004t0012g0275 | 3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1318-1964T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102666816 | ||||||
| chr4:102666989
|
A | T | 4 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1317+1974T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102666989 | ||||||
| chr4:102667015
|
A | C | 13 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(10): Show | 13 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1317+1948T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102667015 | ||||||
| chr4:102667057
|
T | C | 13 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(10): Show | 13 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1317+1906A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102667057 | ||||||
| chr4:102667115
|
T | C | 2 | a0001c0001t0033g0174a0001c0009t0034g0016 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1317+1848A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102667115 | ||||||
| chr4:102667356
|
A | G | 11 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(8): Show | 11 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1317+1607T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102667356 | ||||||
| chr4:102667367
|
TAACATTG others(8): Show |
T | 6 | a0001c0001t0001g0123a0001c0001t0001g0131a0001c0001t0001g0167others(3): Show | 6 | HG01074.hp2 HG02257.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1317+1581_1317+159 others(19): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102667367 | ||||||
| chr4:102667419
|
G | A | 4 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1317+1544C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102667419 | ||||||
| chr4:102667473
|
C | A | 10 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(7): Show | 10 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1317+1490G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102667473 | ||||||
| chr4:102667510
|
C | T | 1 | a0001c0001t0006g0007 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1317+1453G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102667510 | ||||||
| chr4:102667521
|
C | T | 14 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(11): Show | 14 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1317+1442G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102667521 | ||||||
| chr4:102667766
|
T | C | 1 | a0002c0002t0017g0119 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1317+1197A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102667766 | ||||||
| chr4:102667796
|
T | C | 4 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1317+1167A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102667796 | ||||||
| chr4:102667892
|
C | T | 4 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1317+1071G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102667892 | ||||||
| chr4:102667977
|
G | T | 17 | a0001c0001t0001g0201a0001c0001t0003g0139a0001c0001t0003g0223others(14): Show | 17 | HG01070.hp1 HG01109.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.1317+986C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102667977 | ||||||
| chr4:102668012
|
C | T | 1 | a0001c0004t0001g0243 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1317+951G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102668012 | ||||||
| chr4:102668054
|
A | G | 27 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(24): Show | 28 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1317+909T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102668054 | ||||||
| chr4:102668102
|
G | A | 1 | a0002c0002t0011g0073 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1317+861C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102668102 | ||||||
| chr4:102668148
|
T | C | 1 | a0001c0009t0034g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1317+815A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102668148 | ||||||
| chr4:102668323
|
T | G | 27 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(24): Show | 28 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1317+640A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102668323 | ||||||
| chr4:102668356
|
TAAG | T | 93 | a0001c0001t0001g0254a0002c0002t0002g0028a0002c0002t0002g0029others(90): Show | 93 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.1317+604_1317+606d others(5): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102668356 | ||||||
| chr4:102668453
|
G | A | 1 | a0001c0001t0010g0159 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1317+510C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102668453 | ||||||
| chr4:102668564
|
C | T | 1 | a0001c0004t0006g0268 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1317+399G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102668564 | ||||||
| chr4:102668628
|
T | C | 3 | a0001c0001t0006g0136a0001c0001t0006g0209a0001c0001t0018g0210 | 3 | HG02735.hp1 HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1317+335A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102668628 | ||||||
| chr4:102668642
|
C | A | 4 | a0003c0005t0008g0001a0003c0005t0008g0006a0003c0005t0008g0008others(1): Show | 5 | HG01192.hp2 HG02145.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1317+321G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102668642 | ||||||
| chr4:102668768
|
C | G | 2 | a0002c0002t0014g0033a0002c0002t0014g0116 | 2 | HG02148.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1317+195G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102668768 | ||||||
| chr4:102668856
|
C | A | 23 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(20): Show | 24 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1317+107G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102668856 | ||||||
| chr4:102668857
|
A | T | 23 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(20): Show | 24 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1317+106T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102668857 | ||||||
| chr4:102668892
|
C | G | 27 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(24): Show | 28 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1317+71G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 10/16 | chr4 | 102668892 | ||||||
| chr4:102669107
|
A | G | 4 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-58T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102669107 | ||||||
| chr4:102669188
|
G | A | 1 | a0001c0001t0001g0201 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1231-139C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102669188 | ||||||
| chr4:102669313
|
A | G | 1 | a0001c0004t0006g0268 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1231-264T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102669313 | ||||||
| chr4:102669333
|
G | A | 4 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-284C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102669333 | ||||||
| chr4:102669343
|
A | G | 1 | a0001c0004t0010g0011 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1231-294T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102669343 | ||||||
| chr4:102669705
|
G | T | 10 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(7): Show | 10 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1231-656C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102669705 | ||||||
| chr4:102669707
|
A | G | 182 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(179): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1231-658T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102669707 | ||||||
| chr4:102669775
|
T | C | 1 | a0007c0011t0029g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1231-726A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102669775 | ||||||
| chr4:102669781
|
C | A | 1 | a0003c0005t0021g0251 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1231-732G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102669781 | ||||||
| chr4:102669821
|
G | A | 1 | a0004c0006t0001g0061 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1231-772C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102669821 | ||||||
| chr4:102669896
|
C | T | 2 | a0001c0004t0001g0243a0001c0004t0023g0004 | 2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1231-847G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102669896 | ||||||
| chr4:102669897
|
G | A | 10 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(7): Show | 10 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1231-848C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102669897 | ||||||
| chr4:102669905
|
A | G | 5 | a0001c0001t0003g0038a0001c0001t0003g0206a0001c0001t0003g0207others(2): Show | 5 | HG00621.hp1 HG02083.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.1231-856T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102669905 | ||||||
| chr4:102669936
|
T | C | 27 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(24): Show | 28 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1231-887A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102669936 | ||||||
| chr4:102670016
|
G | A | 1 | a0002c0002t0002g0270 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1231-967C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102670016 | ||||||
| chr4:102670070
|
G | A | 4 | a0002c0002t0002g0050a0002c0002t0002g0054a0002c0002t0002g0059others(1): Show | 4 | HG02735.hp2 HG02738.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-1021C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102670070 | ||||||
| chr4:102670127
|
C | T | 2 | a0002c0002t0002g0048a0002c0002t0002g0055 | 2 | NA18957.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1231-1078G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102670127 | ||||||
| chr4:102670154
|
C | CA | 10 | a0001c0001t0001g0182a0001c0001t0001g0226a0001c0001t0001g0276others(7): Show | 10 | HG00621.hp2 HG01175.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1231-1106dupT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102670154 | ||||||
| chr4:102670154
|
C | CAAAA | 9 | a0001c0009t0024g0005a0003c0005t0008g0001a0003c0005t0008g0006others(6): Show | 10 | HG01192.hp2 HG02145.hp1 HG03130.hp2 others(7): Show |
intron_variant | MODIFIER | c.1231-1109_1231-110 others(8): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102670154 | ||||||
| chr4:102670154
|
C | CAAAAAA | 8 | a0001c0001t0012g0232a0001c0004t0005g0263a0001c0004t0005g0264others(5): Show | 8 | HG02145.hp2 HG02630.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1231-1111_1231-110 others(10): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102670154 | ||||||
| chr4:102670154
|
CA | C | 13 | a0001c0001t0001g0234a0001c0001t0003g0038a0001c0001t0003g0094others(10): Show | 13 | HG00621.hp1 HG01070.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.1231-1106delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102670154 | ||||||
| chr4:102670154
|
CAAAAAAA others(3): Show |
C | 1 | a0004c0006t0001g0035 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1231-1115_1231-110 others(14): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102670154 | ||||||
| chr4:102670154
|
CAAAAAAA others(4): Show |
C | 92 | a0001c0001t0001g0254a0002c0002t0002g0028a0002c0002t0002g0029others(89): Show | 92 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.1230+1116_1231-110 others(15): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102670154 | ||||||
| chr4:102670169
|
A | T | 2 | a0001c0004t0001g0243a0001c0004t0023g0004 | 2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1230+1112T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102670169 | ||||||
| chr4:102670481
|
A | T | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1230+800T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102670481 | ||||||
| chr4:102670609
|
A | C | 26 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(23): Show | 27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1230+672T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102670609 | ||||||
| chr4:102670949
|
C | G | 2 | a0003c0003t0015g0198a0003c0003t0015g0199 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1230+332G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102670949 | ||||||
| chr4:102671116
|
G | GCT | 26 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(23): Show | 27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1230+164_1230+165i others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102671116 | ||||||
| chr4:102671128
|
C | T | 5 | a0002c0002t0002g0120a0002c0002t0002g0124a0002c0002t0002g0126others(2): Show | 5 | HG00140.hp1 HG01168.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.1230+153G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102671128 | ||||||
| chr4:102671137
|
T | A | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1230+144A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 9/16 | chr4 | 102671137 | ||||||
| chr4:102671473
|
A | ATC | 26 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(23): Show | 27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1113-77_1113-76dup others(2): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102671473 | ||||||
| chr4:102671495
|
A | G | 26 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(23): Show | 27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1113-97T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102671495 | ||||||
| chr4:102671513
|
T | C | 1 | a0001c0001t0006g0224 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1113-115A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102671513 | ||||||
| chr4:102671712
|
C | A | 4 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0009t0012g0034others(1): Show | 4 | HG02280.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113-314G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102671712 | ||||||
| chr4:102671889
|
T | C | 3 | a0001c0001t0012g0232a0001c0004t0012g0253a0001c0004t0012g0275 | 3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1113-491A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102671889 | ||||||
| chr4:102671923
|
A | C | 1 | a0001c0001t0001g0123 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1113-525T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102671923 | ||||||
| chr4:102671933
|
C | G | 2 | a0001c0004t0010g0140a0001c0004t0020g0141 | 2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1113-535G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102671933 | ||||||
| chr4:102672021
|
T | C | 26 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(23): Show | 27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1113-623A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102672021 | ||||||
| chr4:102672185
|
C | T | 26 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(23): Show | 27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1113-787G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102672185 | ||||||
| chr4:102672289
|
A | C | 26 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(23): Show | 27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1113-891T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102672289 | ||||||
| chr4:102672323
|
A | G | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1113-925T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102672323 | ||||||
| chr4:102672438
|
A | G | 1 | a0001c0001t0001g0269 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1113-1040T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102672438 | ||||||
| chr4:102672639
|
G | C | 1 | a0001c0001t0001g0192 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1113-1241C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102672639 | ||||||
| chr4:102672672
|
T | C | 23 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(20): Show | 24 | HG00639.hp1 HG00673.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.1112+1247A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102672672 | ||||||
| chr4:102672699
|
A | G | 26 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(23): Show | 27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1112+1220T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102672699 | ||||||
| chr4:102672709
|
C | T | 1 | a0001c0001t0003g0172 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1112+1210G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102672709 | ||||||
| chr4:102672710
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1112+1209C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102672710 | ||||||
| chr4:102672741
|
A | C | 134 | a0001c0001t0001g0254a0001c0001t0006g0077a0001c0001t0006g0081others(131): Show | 135 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1112+1178T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102672741 | ||||||
| chr4:102672930
|
G | A | 26 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(23): Show | 27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1112+989C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102672930 | ||||||
| chr4:102672931
|
T | G | 26 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(23): Show | 27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1112+988A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102672931 | ||||||
| chr4:102673014
|
A | AT | 26 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(23): Show | 27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1112+904dupA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102673014 | ||||||
| chr4:102673131
|
C | T | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1112+788G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102673131 | ||||||
| chr4:102673132
|
G | A | 26 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(23): Show | 27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1112+787C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102673132 | ||||||
| chr4:102673149
|
G | A | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1112+770C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102673149 | ||||||
| chr4:102673168
|
T | C | 23 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(20): Show | 24 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1112+751A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102673168 | ||||||
| chr4:102673435
|
G | A | 1 | a0003c0005t0008g0013 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1112+484C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102673435 | ||||||
| chr4:102673439
|
C | T | 23 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(20): Show | 24 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1112+480G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102673439 | ||||||
| chr4:102673466
|
C | G | 26 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(23): Show | 27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1112+453G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102673466 | ||||||
| chr4:102673761
|
T | C | 99 | a0001c0001t0001g0254a0001c0001t0006g0077a0001c0001t0006g0081others(96): Show | 99 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1112+158A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102673761 | ||||||
| chr4:102673781
|
G | A | 127 | a0001c0001t0001g0254a0001c0001t0006g0077a0001c0001t0006g0081others(124): Show | 128 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.1112+138C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102673781 | ||||||
| chr4:102673793
|
G | A | 26 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(23): Show | 27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1112+126C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102673793 | ||||||
| chr4:102673805
|
A | G | 3 | a0001c0001t0012g0232a0001c0004t0012g0253a0001c0004t0012g0275 | 3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1112+114T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 8/16 | chr4 | 102673805 | ||||||
| chr4:102674120
|
A | G | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.961-50T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102674120 | ||||||
| chr4:102674132
|
A | T | 27 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(24): Show | 28 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.961-62T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102674132 | ||||||
| chr4:102674226
|
A | G | 2 | a0001c0004t0001g0243a0001c0004t0023g0004 | 2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.961-156T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102674226 | ||||||
| chr4:102674241
|
T | C | 2 | a0003c0003t0015g0198a0003c0003t0015g0199 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.961-171A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102674241 | ||||||
| chr4:102674326
|
T | C | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.961-256A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102674326 | ||||||
| chr4:102674371
|
C | T | 26 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(23): Show | 27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.961-301G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102674371 | ||||||
| chr4:102674449
|
G | A | 26 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(23): Show | 27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.961-379C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102674449 | ||||||
| chr4:102674464
|
A | T | 1 | a0001c0001t0001g0269 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.961-394T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102674464 | ||||||
| chr4:102674494
|
A | G | 101 | a0001c0001t0001g0254a0001c0001t0006g0077a0001c0001t0006g0081others(98): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.961-424T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102674494 | ||||||
| chr4:102674557
|
A | G | 26 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(23): Show | 27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.961-487T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102674557 | ||||||
| chr4:102674585
|
A | G | 23 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(20): Show | 24 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.961-515T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102674585 | ||||||
| chr4:102674923
|
T | A | 1 | a0001c0001t0001g0229 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.961-853A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102674923 | ||||||
| chr4:102674992
|
C | T | 26 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(23): Show | 27 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.961-922G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102674992 | ||||||
| chr4:102675052
|
C | T | 10 | a0001c0001t0012g0232a0001c0004t0005g0262a0001c0004t0005g0263others(7): Show | 10 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.961-982G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102675052 | ||||||
| chr4:102675250
|
C | G | 2 | a0001c0004t0001g0243a0001c0004t0023g0004 | 2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.961-1180G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102675250 | ||||||
| chr4:102675726
|
C | T | 19 | a0001c0001t0012g0232a0001c0004t0010g0011a0001c0004t0010g0140others(16): Show | 20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-1656G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102675726 | ||||||
| chr4:102675768
|
C | G | 16 | a0001c0001t0012g0232a0001c0004t0012g0253a0001c0004t0012g0275others(13): Show | 17 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.961-1698G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102675768 | ||||||
| chr4:102675802
|
A | C | 1 | a0005c0008t0003g0138 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.961-1732T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102675802 | ||||||
| chr4:102675823
|
T | C | 16 | a0001c0001t0012g0232a0001c0004t0012g0253a0001c0004t0012g0275others(13): Show | 17 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.961-1753A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102675823 | ||||||
| chr4:102675875
|
A | G | 131 | a0001c0001t0001g0254a0001c0001t0006g0077a0001c0001t0006g0081others(128): Show | 132 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.961-1805T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102675875 | ||||||
| chr4:102675905
|
AG | A | 19 | a0001c0001t0012g0232a0001c0004t0010g0011a0001c0004t0010g0140others(16): Show | 20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-1836delC | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102675905 | ||||||
| chr4:102675907
|
T | A | 19 | a0001c0001t0012g0232a0001c0004t0010g0011a0001c0004t0010g0140others(16): Show | 20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-1837A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102675907 | ||||||
| chr4:102675934
|
G | T | 19 | a0001c0001t0012g0232a0001c0004t0010g0011a0001c0004t0010g0140others(16): Show | 20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-1864C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102675934 | ||||||
| chr4:102676195
|
G | A | 19 | a0001c0001t0012g0232a0001c0004t0010g0011a0001c0004t0010g0140others(16): Show | 20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-2125C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102676195 | ||||||
| chr4:102676273
|
A | G | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.961-2203T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102676273 | ||||||
| chr4:102676369
|
A | G | 1 | a0002c0002t0002g0213 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.961-2299T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102676369 | ||||||
| chr4:102676423
|
C | T | 16 | a0001c0001t0012g0232a0001c0004t0012g0253a0001c0004t0012g0275others(13): Show | 17 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.961-2353G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102676423 | ||||||
| chr4:102676491
|
C | T | 19 | a0001c0001t0012g0232a0001c0004t0010g0011a0001c0004t0010g0140others(16): Show | 20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-2421G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102676491 | ||||||
| chr4:102676632
|
T | C | 2 | a0003c0003t0015g0198a0003c0003t0015g0199 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.961-2562A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102676632 | ||||||
| chr4:102676692
|
ACTT | A | 19 | a0001c0001t0012g0232a0001c0004t0010g0011a0001c0004t0010g0140others(16): Show | 20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-2625_961-2623d others(5): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102676692 | ||||||
| chr4:102676711
|
T | C | 19 | a0001c0001t0012g0232a0001c0004t0010g0011a0001c0004t0010g0140others(16): Show | 20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-2641A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102676711 | ||||||
| chr4:102676878
|
G | C | 7 | a0001c0001t0019g0023a0003c0003t0013g0160a0005c0008t0003g0138others(4): Show | 7 | HG02647.hp1 HG02809.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.961-2808C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102676878 | ||||||
| chr4:102676923
|
GA | G | 131 | a0001c0001t0001g0254a0001c0001t0006g0077a0001c0001t0006g0081others(128): Show | 132 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.961-2854delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102676923 | ||||||
| chr4:102677150
|
TAGAA | T | 19 | a0001c0001t0012g0232a0001c0004t0010g0011a0001c0004t0010g0140others(16): Show | 20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-3084_961-3081d others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102677150 | ||||||
| chr4:102677188
|
A | C | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.961-3118T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102677188 | ||||||
| chr4:102677191
|
T | C | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.961-3121A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102677191 | ||||||
| chr4:102677207
|
A | G | 20 | a0002c0002t0002g0036a0002c0002t0002g0037a0002c0002t0002g0040others(17): Show | 20 | HG00408.hp1 HG00609.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-3137T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102677207 | ||||||
| chr4:102677228
|
G | A | 6 | a0001c0001t0001g0123a0001c0001t0001g0131a0001c0001t0001g0167others(3): Show | 6 | HG01074.hp2 HG02257.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.961-3158C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102677228 | ||||||
| chr4:102677261
|
G | A | 19 | a0001c0001t0012g0232a0001c0004t0010g0011a0001c0004t0010g0140others(16): Show | 20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-3191C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102677261 | ||||||
| chr4:102677510
|
G | T | 2 | a0003c0003t0015g0198a0003c0003t0015g0199 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.961-3440C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102677510 | ||||||
| chr4:102677566
|
C | T | 1 | a0002c0002t0002g0086 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.961-3496G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102677566 | ||||||
| chr4:102677637
|
T | G | 1 | a0001c0001t0001g0269 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.961-3567A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102677637 | ||||||
| chr4:102677682
|
C | T | 1 | a0004c0006t0001g0061 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.961-3612G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102677682 | ||||||
| chr4:102677820
|
C | T | 16 | a0001c0001t0012g0232a0001c0004t0012g0253a0001c0004t0012g0275others(13): Show | 17 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.961-3750G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102677820 | ||||||
| chr4:102677897
|
G | T | 2 | a0001c0001t0003g0166a0001c0001t0003g0172 | 2 | HG02572.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.961-3827C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102677897 | ||||||
| chr4:102678026
|
G | A | 1 | a0002c0002t0002g0070 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.961-3956C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102678026 | ||||||
| chr4:102678107
|
AT | A | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.961-4038delA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102678107 | ||||||
| chr4:102678113
|
T | C | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.961-4043A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102678113 | ||||||
| chr4:102678364
|
G | A | 4 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0009t0012g0034others(1): Show | 4 | HG02280.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.961-4294C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102678364 | ||||||
| chr4:102678439
|
A | G | 2 | a0003c0005t0021g0251a0003c0005t0021g0252 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.961-4369T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102678439 | ||||||
| chr4:102678447
|
T | TGAAAAGA others(2068): Show |
1 | a0001c0004t0010g0011 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.961-4378_961-4377i others(2077): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102678447 | ||||||
| chr4:102678447
|
T | TGAAAAGA others(2068): Show |
2 | a0001c0004t0010g0140a0001c0004t0020g0141 | 2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.961-4378_961-4377i others(2077): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102678447 | ||||||
| chr4:102678469
|
A | G | 7 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.961-4399T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102678469 | ||||||
| chr4:102678805
|
G | A | 16 | a0001c0001t0012g0232a0001c0004t0012g0253a0001c0004t0012g0275others(13): Show | 17 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.961-4735C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102678805 | ||||||
| chr4:102678948
|
C | G | 19 | a0001c0001t0012g0232a0001c0004t0010g0011a0001c0004t0010g0140others(16): Show | 20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-4878G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102678948 | ||||||
| chr4:102679265
|
G | A | 2 | a0001c0001t0001g0182a0001c0001t0004g0183 | 2 | HG00621.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.961-5195C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102679265 | ||||||
| chr4:102679318
|
A | T | 2 | a0001c0001t0001g0195a0001c0001t0028g0194 | 2 | HG02080.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.961-5248T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102679318 | ||||||
| chr4:102679440
|
C | T | 19 | a0001c0001t0012g0232a0001c0004t0010g0011a0001c0004t0010g0140others(16): Show | 20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-5370G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102679440 | ||||||
| chr4:102679905
|
T | C | 19 | a0001c0001t0012g0232a0001c0004t0010g0011a0001c0004t0010g0140others(16): Show | 20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-5835A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102679905 | ||||||
| chr4:102679926
|
TA | T | 10 | a0001c0001t0001g0178a0001c0001t0001g0182a0001c0001t0001g0185others(7): Show | 10 | HG00621.hp2 HG02071.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.961-5857delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102679926 | ||||||
| chr4:102680057
|
T | C | 16 | a0001c0001t0012g0232a0001c0004t0012g0253a0001c0004t0012g0275others(13): Show | 17 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.961-5987A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102680057 | ||||||
| chr4:102680097
|
T | C | 17 | a0001c0001t0001g0201a0001c0001t0003g0139a0001c0001t0003g0223others(14): Show | 17 | HG01070.hp1 HG01109.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.961-6027A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102680097 | ||||||
| chr4:102680184
|
A | G | 19 | a0001c0001t0012g0232a0001c0004t0010g0011a0001c0004t0010g0140others(16): Show | 20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-6114T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102680184 | ||||||
| chr4:102680189
|
G | T | 19 | a0001c0001t0012g0232a0001c0004t0010g0011a0001c0004t0010g0140others(16): Show | 20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.961-6119C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102680189 | ||||||
| chr4:102680273
|
C | T | 1 | a0002c0002t0013g0064 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.961-6203G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102680273 | ||||||
| chr4:102680582
|
T | TA | 20 | a0001c0001t0012g0232a0001c0004t0010g0011a0001c0004t0010g0140others(17): Show | 21 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.961-6513dupT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102680582 | ||||||
| chr4:102680696
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.961-6626A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102680696 | ||||||
| chr4:102680739
|
C | T | 2 | a0003c0003t0015g0198a0003c0003t0015g0199 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.961-6669G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102680739 | ||||||
| chr4:102680886
|
C | T | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.961-6816G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102680886 | ||||||
| chr4:102680943
|
C | T | 3 | a0001c0004t0010g0024a0003c0003t0015g0198a0003c0003t0015g0199 | 3 | HG02630.hp2 HG02647.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.961-6873G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102680943 | ||||||
| chr4:102680949
|
T | C | 1 | a0001c0001t0020g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.961-6879A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102680949 | ||||||
| chr4:102680970
|
C | T | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.961-6900G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102680970 | ||||||
| chr4:102681072
|
C | T | 1 | a0001c0001t0009g0076 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.961-7002G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102681072 | ||||||
| chr4:102681080
|
T | C | 97 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0104others(94): Show | 99 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.961-7010A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102681080 | ||||||
| chr4:102681392
|
A | G | 2 | a0003c0003t0015g0198a0003c0003t0015g0199 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.961-7322T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102681392 | ||||||
| chr4:102681443
|
C | T | 21 | a0001c0001t0012g0232a0001c0004t0010g0011a0001c0004t0010g0140others(18): Show | 22 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.961-7373G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102681443 | ||||||
| chr4:102681462
|
A | G | 21 | a0001c0001t0012g0232a0001c0004t0010g0011a0001c0004t0010g0140others(18): Show | 22 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.961-7392T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102681462 | ||||||
| chr4:102681538
|
C | T | 4 | a0001c0004t0010g0024a0003c0003t0015g0198a0003c0003t0015g0199others(1): Show | 4 | HG02630.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.961-7468G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102681538 | ||||||
| chr4:102681740
|
A | G | 18 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141others(15): Show | 19 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.961-7670T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102681740 | ||||||
| chr4:102681880
|
T | C | 1 | a0003c0005t0021g0252 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.960+7694A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102681880 | ||||||
| chr4:102681927
|
C | T | 1 | a0001c0009t0012g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.960+7647G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102681927 | ||||||
| chr4:102682039
|
C | T | 2 | a0001c0001t0020g0225a0003c0005t0021g0251 | 2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.960+7535G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102682039 | ||||||
| chr4:102682096
|
G | GAGATCAC others(26): Show |
1 | a0002c0002t0002g0040 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.960+7445_960+7477d others(35): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102682096 | ||||||
| chr4:102682125
|
T | C | 1 | a0003c0005t0008g0012 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.960+7449A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102682125 | ||||||
| chr4:102682146
|
C | CA | 23 | a0001c0001t0001g0201a0001c0001t0001g0227a0001c0001t0003g0169others(20): Show | 24 | HG00438.hp2 HG01192.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.960+7427dupT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102682146 | ||||||
| chr4:102682186
|
T | G | 15 | a0001c0009t0012g0034a0001c0009t0024g0005a0001c0009t0034g0016others(12): Show | 16 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.960+7388A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102682186 | ||||||
| chr4:102682322
|
G | A | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.960+7252C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102682322 | ||||||
| chr4:102682468
|
T | C | 18 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141others(15): Show | 19 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.960+7106A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102682468 | ||||||
| chr4:102682676
|
G | C | 2 | a0002c0002t0002g0039a0002c0002t0002g0270 | 2 | HG01192.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.960+6898C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102682676 | ||||||
| chr4:102682792
|
A | G | 183 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(180): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.960+6782T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102682792 | ||||||
| chr4:102682831
|
G | A | 1 | a0001c0001t0009g0216 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.960+6743C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102682831 | ||||||
| chr4:102682904
|
G | C | 1 | a0002c0002t0002g0075 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.960+6670C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102682904 | ||||||
| chr4:102682952
|
CAGA | C | 3 | a0001c0001t0012g0232a0001c0004t0012g0253a0001c0004t0012g0275 | 3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.960+6619_960+6621d others(5): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102682952 | ||||||
| chr4:102683176
|
GA | G | 13 | a0001c0001t0001g0161a0001c0001t0001g0234a0001c0001t0003g0038others(10): Show | 13 | HG00609.hp1 HG01257.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.960+6397delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102683176 | ||||||
| chr4:102683276
|
C | T | 18 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141others(15): Show | 19 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.960+6298G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102683276 | ||||||
| chr4:102683426
|
A | G | 18 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141others(15): Show | 19 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.960+6148T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102683426 | ||||||
| chr4:102683550
|
T | C | 18 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141others(15): Show | 19 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.960+6024A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102683550 | ||||||
| chr4:102683554
|
C | A | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.960+6020G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102683554 | ||||||
| chr4:102683568
|
C | T | 1 | a0001c0001t0003g0273 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.960+6006G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102683568 | ||||||
| chr4:102683747
|
C | T | 12 | a0001c0009t0024g0005a0001c0009t0034g0016a0003c0005t0008g0001others(9): Show | 13 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.960+5827G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102683747 | ||||||
| chr4:102683794
|
T | C | 1 | a0007c0011t0029g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.960+5780A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102683794 | ||||||
| chr4:102683877
|
C | G | 2 | a0001c0001t0004g0163a0001c0001t0004g0180 | 2 | NA18979.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.960+5697G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102683877 | ||||||
| chr4:102683966
|
C | T | 1 | a0001c0001t0003g0172 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.960+5608G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102683966 | ||||||
| chr4:102684099
|
A | G | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.960+5475T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102684099 | ||||||
| chr4:102684108
|
T | TA | 18 | a0001c0004t0010g0024a0001c0009t0012g0034a0001c0009t0034g0016others(15): Show | 19 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.960+5465dupT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102684108 | ||||||
| chr4:102684133
|
G | A | 7 | a0002c0002t0002g0050a0002c0002t0002g0052a0002c0002t0002g0054others(4): Show | 7 | HG02735.hp2 HG02738.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.960+5441C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102684133 | ||||||
| chr4:102684586
|
T | A | 35 | a0002c0002t0002g0036a0002c0002t0002g0037a0002c0002t0002g0039others(32): Show | 35 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.960+4988A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102684586 | ||||||
| chr4:102684660
|
C | T | 15 | a0001c0009t0012g0034a0001c0009t0024g0005a0001c0009t0034g0016others(12): Show | 16 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.960+4914G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102684660 | ||||||
| chr4:102684756
|
A | G | 1 | a0001c0001t0001g0234 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.960+4818T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102684756 | ||||||
| chr4:102684759
|
G | A | 159 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(156): Show | 160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.960+4815C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102684759 | ||||||
| chr4:102684988
|
A | G | 18 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141others(15): Show | 19 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.960+4586T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102684988 | ||||||
| chr4:102685116
|
C | T | 18 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141others(15): Show | 19 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.960+4458G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102685116 | ||||||
| chr4:102685237
|
A | G | 1 | a0002c0002t0002g0086 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.960+4337T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102685237 | ||||||
| chr4:102685279
|
A | G | 3 | a0001c0001t0012g0232a0001c0004t0012g0253a0001c0004t0012g0275 | 3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.960+4295T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102685279 | ||||||
| chr4:102685292
|
T | C | 18 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141others(15): Show | 19 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.960+4282A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102685292 | ||||||
| chr4:102685499
|
T | A | 3 | a0001c0001t0012g0232a0001c0004t0012g0253a0001c0004t0012g0275 | 3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.960+4075A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102685499 | ||||||
| chr4:102685501
|
C | T | 3 | a0001c0001t0012g0232a0001c0004t0012g0253a0001c0004t0012g0275 | 3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.960+4073G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102685501 | ||||||
| chr4:102685503
|
C | CTATGAAA others(5): Show |
3 | a0001c0001t0012g0232a0001c0004t0012g0253a0001c0004t0012g0275 | 3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.960+4070_960+4071i others(14): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102685503 | ||||||
| chr4:102685511
|
A | T | 3 | a0001c0001t0012g0232a0001c0004t0012g0253a0001c0004t0012g0275 | 3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.960+4063T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102685511 | ||||||
| chr4:102685515
|
C | T | 165 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(162): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.960+4059G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102685515 | ||||||
| chr4:102685697
|
T | A | 1 | a0001c0001t0003g0142 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.960+3877A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102685697 | ||||||
| chr4:102685715
|
C | T | 165 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(162): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.960+3859G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102685715 | ||||||
| chr4:102685729
|
C | A | 183 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(180): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.960+3845G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102685729 | ||||||
| chr4:102685921
|
TTGAAGAC | T | 276 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(273): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.960+3646_960+3652d others(9): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102685921 | ||||||
| chr4:102685974
|
A | G | 1 | a0001c0004t0001g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.960+3600T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102685974 | ||||||
| chr4:102686096
|
C | G | 184 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(181): Show | 186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.960+3478G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102686096 | ||||||
| chr4:102686190
|
A | ATG | 151 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(148): Show | 152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.960+3382_960+3383d others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102686190 | ||||||
| chr4:102686190
|
A | ATGTG | 14 | a0001c0001t0012g0232a0001c0004t0010g0011a0001c0004t0010g0140others(11): Show | 14 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.960+3380_960+3383d others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102686190 | ||||||
| chr4:102686190
|
A | ATGTGTG | 17 | a0001c0009t0024g0005a0001c0009t0034g0016a0002c0002t0002g0048others(14): Show | 18 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.960+3378_960+3383d others(8): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102686190 | ||||||
| chr4:102686190
|
A | ATGTGTGT others(5): Show |
1 | a0001c0017t0005g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.960+3372_960+3383d others(14): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102686190 | ||||||
| chr4:102686249
|
T | C | 16 | a0001c0009t0012g0034a0001c0009t0024g0005a0001c0009t0034g0016others(13): Show | 17 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.960+3325A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102686249 | ||||||
| chr4:102686267
|
C | T | 2 | a0002c0002t0002g0040a0002c0002t0002g0041 | 2 | HG02129.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.960+3307G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102686267 | ||||||
| chr4:102686478
|
G | A | 165 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(162): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.960+3096C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102686478 | ||||||
| chr4:102686649
|
C | T | 166 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(163): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.960+2925G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102686649 | ||||||
| chr4:102687039
|
T | C | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.960+2535A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102687039 | ||||||
| chr4:102687151
|
C | T | 166 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(163): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.960+2423G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102687151 | ||||||
| chr4:102687182
|
A | T | 1 | a0001c0001t0001g0170 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.960+2392T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102687182 | ||||||
| chr4:102687241
|
G | A | 1 | a0001c0001t0006g0168 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.960+2333C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102687241 | ||||||
| chr4:102687470
|
A | G | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.960+2104T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102687470 | ||||||
| chr4:102687573
|
C | T | 3 | a0002c0002t0007g0056a0002c0002t0011g0096a0002c0002t0017g0049 | 3 | NA18960.hp1 NA18970.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.960+2001G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102687573 | ||||||
| chr4:102688096
|
C | T | 2 | a0001c0004t0010g0024a0003c0010t0016g0271 | 2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.960+1478G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688096 | ||||||
| chr4:102688138
|
T | C | 7 | a0001c0001t0001g0104a0001c0001t0001g0179a0001c0001t0001g0186others(4): Show | 7 | HG01071.hp2 HG01074.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.960+1436A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688138 | ||||||
| chr4:102688173
|
T | C | 2 | a0001c0004t0001g0243a0001c0004t0023g0004 | 2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.960+1401A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688173 | ||||||
| chr4:102688212
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.960+1362G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688212 | ||||||
| chr4:102688290
|
C | T | 1 | a0005c0008t0003g0221 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.960+1284G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688290 | ||||||
| chr4:102688292
|
C | T | 1 | a0001c0017t0005g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.960+1282G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688292 | ||||||
| chr4:102688293
|
G | A | 1 | a0001c0004t0001g0243 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.960+1281C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688293 | ||||||
| chr4:102688295
|
G | GCA | 6 | a0001c0001t0003g0139a0001c0001t0033g0174a0001c0004t0010g0011others(3): Show | 6 | HG01109.hp2 HG02886.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.960+1277_960+1278d others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688295 | ||||||
| chr4:102688295
|
GCA | G | 3 | a0001c0001t0012g0232a0001c0004t0012g0253a0001c0004t0012g0275 | 3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.960+1277_960+1278d others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688295 | ||||||
| chr4:102688295
|
GCACA | G | 6 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(3): Show | 6 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.960+1275_960+1278d others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688295 | ||||||
| chr4:102688297
|
A | G | 5 | a0005c0008t0003g0138a0005c0008t0003g0218a0005c0008t0003g0219others(2): Show | 5 | HG02647.hp1 HG02809.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.960+1277T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688297 | ||||||
| chr4:102688322
|
CACAT | C | 6 | a0002c0007t0007g0106a0002c0007t0007g0108a0002c0007t0007g0109others(3): Show | 6 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.960+1248_960+1251d others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688322 | ||||||
| chr4:102688353
|
A | G | 1 | a0001c0001t0004g0183 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.960+1221T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688353 | ||||||
| chr4:102688364
|
TTC | T | 5 | a0001c0001t0003g0230a0001c0001t0003g0273a0001c0001t0006g0136others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.960+1208_960+1209d others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688364 | ||||||
| chr4:102688386
|
T | TAC | 5 | a0001c0001t0001g0201a0001c0001t0003g0206a0001c0001t0004g0183others(2): Show | 5 | HG00621.hp1 HG02738.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.960+1186_960+1187d others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688386 | ||||||
| chr4:102688386
|
T | TACAC | 14 | a0001c0001t0001g0161a0001c0001t0004g0069a0001c0001t0012g0232others(11): Show | 14 | HG01496.hp2 HG02145.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.960+1184_960+1187d others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688386 | ||||||
| chr4:102688386
|
T | TACACAC | 20 | a0001c0001t0001g0093a0001c0001t0001g0105a0001c0001t0001g0133others(17): Show | 20 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.960+1182_960+1187d others(8): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688386 | ||||||
| chr4:102688386
|
T | TACACACA others(1): Show |
84 | a0001c0001t0001g0003a0001c0001t0001g0146a0001c0001t0001g0148others(81): Show | 85 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.960+1180_960+1187d others(10): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688386 | ||||||
| chr4:102688386
|
T | TACACACA others(3): Show |
29 | a0001c0001t0003g0095a0001c0001t0003g0246a0001c0001t0004g0155others(26): Show | 29 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.960+1178_960+1187d others(12): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688386 | ||||||
| chr4:102688386
|
T | TACACACA others(5): Show |
14 | a0001c0001t0003g0089a0001c0001t0003g0090a0001c0001t0003g0091others(11): Show | 14 | HG00438.hp1 HG00609.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.960+1176_960+1187d others(14): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688386 | ||||||
| chr4:102688386
|
T | TACACACA others(7): Show |
2 | a0002c0002t0002g0098a0002c0002t0002g0102 | 2 | NA18968.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.960+1174_960+1187d others(16): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688386 | ||||||
| chr4:102688386
|
TAC | T | 46 | a0001c0001t0001g0104a0001c0001t0001g0179a0001c0001t0001g0186others(43): Show | 47 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.960+1186_960+1187d others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688386 | ||||||
| chr4:102688386
|
TACACACA others(5): Show |
T | 1 | a0001c0001t0018g0210 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.960+1176_960+1187d others(14): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688386 | ||||||
| chr4:102688636
|
T | A | 166 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(163): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.960+938A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688636 | ||||||
| chr4:102688672
|
G | A | 1 | a0002c0002t0002g0050 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.960+902C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102688672 | ||||||
| chr4:102689075
|
C | T | 1 | a0003c0003t0031g0238 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.960+499G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689075 | ||||||
| chr4:102689091
|
C | T | 165 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(162): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.960+483G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689091 | ||||||
| chr4:102689104
|
C | T | 1 | a0001c0004t0010g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.960+470G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689104 | ||||||
| chr4:102689153
|
T | A | 184 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(181): Show | 186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.960+421A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689153 | ||||||
| chr4:102689348
|
CA | C | 108 | a0001c0001t0001g0254a0001c0001t0003g0089a0001c0001t0003g0090others(105): Show | 108 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.960+225delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689348 | ||||||
| chr4:102689348
|
CAAA | C | 6 | a0001c0004t0020g0141a0003c0005t0008g0001a0003c0005t0008g0006others(3): Show | 7 | HG01192.hp2 HG02145.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.960+223_960+225del others(3): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689348 | ||||||
| chr4:102689352
|
A | G | 9 | a0001c0009t0024g0005a0001c0009t0034g0016a0003c0005t0008g0010others(6): Show | 9 | HG01884.hp1 HG02615.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.960+222T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689352 | ||||||
| chr4:102689353
|
A | G | 1 | a0003c0005t0008g0012 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.960+221T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689353 | ||||||
| chr4:102689355
|
A | G | 4 | a0003c0005t0008g0001a0003c0005t0008g0006a0003c0005t0008g0008others(1): Show | 5 | HG01192.hp2 HG02145.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.960+219T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689355 | ||||||
| chr4:102689358
|
AAAT | A | 18 | a0001c0001t0020g0225a0001c0004t0005g0263a0001c0004t0010g0140others(15): Show | 18 | HG01496.hp2 HG01884.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.960+213_960+215del others(3): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689358 | ||||||
| chr4:102689359
|
A | T | 2 | a0001c0001t0001g0175a0001c0017t0005g0237 | 2 | HG01993.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.960+215T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689359 | ||||||
| chr4:102689360
|
AT | A | 37 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(34): Show | 38 | HG00323.hp2 HG00408.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.960+213delA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689360 | ||||||
| chr4:102689361
|
T | A | 6 | a0001c0001t0001g0276a0001c0001t0003g0169a0001c0001t0006g0168others(3): Show | 6 | HG00639.hp1 HG02970.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.960+213A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689361 | ||||||
| chr4:102689363
|
T | A | 2 | a0001c0001t0001g0148a0003c0010t0016g0271 | 2 | HG02970.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.960+211A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689363 | ||||||
| chr4:102689365
|
T | A | 2 | a0001c0001t0012g0232a0001c0004t0012g0275 | 2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.960+209A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689365 | ||||||
| chr4:102689378
|
ATGTG | A | 149 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(146): Show | 150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.960+192_960+195del others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689378 | ||||||
| chr4:102689380
|
G | A | 31 | a0001c0001t0012g0232a0001c0001t0020g0225a0001c0004t0005g0266others(28): Show | 32 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.960+194C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689380 | ||||||
| chr4:102689382
|
G | A | 15 | a0001c0001t0012g0232a0001c0004t0005g0266a0001c0004t0010g0024others(12): Show | 15 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.960+192C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689382 | ||||||
| chr4:102689439
|
C | A | 3 | a0001c0001t0003g0095a0001c0001t0006g0092a0001c0001t0018g0051 | 3 | HG00544.hp1 NA18960.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.960+135G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689439 | ||||||
| chr4:102689466
|
T | A | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.960+108A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 7/16 | chr4 | 102689466 | ||||||
| chr4:102689715
|
A | G | 166 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(163): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.850-31T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 6/16 | chr4 | 102689715 | ||||||
| chr4:102689823
|
G | T | 1 | a0001c0004t0010g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.850-139C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 6/16 | chr4 | 102689823 | ||||||
| chr4:102690006
|
T | A | 1 | a0003c0003t0013g0248 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.850-322A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 6/16 | chr4 | 102690006 | ||||||
| chr4:102690067
|
A | T | 1 | a0003c0003t0014g0220 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.850-383T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 6/16 | chr4 | 102690067 | ||||||
| chr4:102690207
|
G | A | 165 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(162): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.849+389C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 6/16 | chr4 | 102690207 | ||||||
| chr4:102690376
|
A | T | 158 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(155): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.849+220T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 6/16 | chr4 | 102690376 | ||||||
| chr4:102690583
|
T | G | 3 | a0002c0002t0007g0056a0002c0002t0011g0096a0002c0002t0017g0049 | 3 | NA18960.hp1 NA18970.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.849+13A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 6/16 | chr4 | 102690583 | ||||||
| chr4:102690794
|
A | AAT | 4 | a0001c0001t0009g0250a0001c0004t0009g0014a0001c0004t0010g0011others(1): Show | 4 | HG00735.hp2 HG02280.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.674-25_674-24dupAT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102690794 | ||||||
| chr4:102690794
|
AATATAT | A | 16 | a0001c0009t0012g0034a0001c0009t0024g0005a0001c0009t0034g0016others(13): Show | 17 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.674-29_674-24delAT others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102690794 | ||||||
| chr4:102690861
|
G | T | 166 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(163): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.674-90C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102690861 | ||||||
| chr4:102690886
|
T | C | 185 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(182): Show | 187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.674-115A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102690886 | ||||||
| chr4:102690924
|
A | G | 2 | a0001c0001t0012g0232a0001c0004t0012g0275 | 2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.674-153T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102690924 | ||||||
| chr4:102690980
|
G | A | 166 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(163): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.674-209C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102690980 | ||||||
| chr4:102690999
|
C | T | 1 | a0004c0006t0004g0025 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.674-228G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102690999 | ||||||
| chr4:102691014
|
T | A | 1 | a0002c0002t0002g0071 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.674-243A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102691014 | ||||||
| chr4:102691059
|
G | A | 1 | a0010c0016t0004g0214 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.674-288C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102691059 | ||||||
| chr4:102691382
|
T | C | 1 | a0001c0017t0005g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.674-611A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102691382 | ||||||
| chr4:102691493
|
G | C | 1 | a0001c0017t0005g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.674-722C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102691493 | ||||||
| chr4:102691514
|
CT | C | 6 | a0001c0001t0012g0232a0001c0001t0027g0202a0001c0004t0012g0253others(3): Show | 6 | HG01070.hp1 HG02622.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.674-744delA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102691514 | ||||||
| chr4:102691557
|
C | T | 1 | a0001c0009t0012g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.674-786G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102691557 | ||||||
| chr4:102691634
|
C | A | 16 | a0001c0009t0012g0034a0001c0009t0024g0005a0001c0009t0034g0016others(13): Show | 17 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.674-863G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102691634 | ||||||
| chr4:102691635
|
A | G | 16 | a0001c0009t0012g0034a0001c0009t0024g0005a0001c0009t0034g0016others(13): Show | 17 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.674-864T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102691635 | ||||||
| chr4:102691760
|
T | C | 182 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(179): Show | 184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.674-989A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102691760 | ||||||
| chr4:102691785
|
G | A | 2 | a0001c0001t0003g0169a0001c0001t0006g0168 | 2 | HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.674-1014C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102691785 | ||||||
| chr4:102692109
|
A | G | 185 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(182): Show | 187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.674-1338T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102692109 | ||||||
| chr4:102692142
|
A | G | 166 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(163): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.674-1371T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102692142 | ||||||
| chr4:102692242
|
G | C | 1 | a0001c0001t0001g0093 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.674-1471C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102692242 | ||||||
| chr4:102692409
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.674-1638C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102692409 | ||||||
| chr4:102692410
|
C | T | 5 | a0001c0001t0012g0232a0001c0004t0010g0024a0001c0004t0012g0253others(2): Show | 5 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.674-1639G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102692410 | ||||||
| chr4:102692421
|
T | C | 1 | a0001c0017t0005g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.674-1650A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102692421 | ||||||
| chr4:102692448
|
T | C | 5 | a0001c0001t0012g0232a0001c0004t0010g0024a0001c0004t0012g0253others(2): Show | 5 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.674-1677A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102692448 | ||||||
| chr4:102692468
|
C | T | 5 | a0001c0001t0012g0232a0001c0004t0010g0024a0001c0004t0012g0253others(2): Show | 5 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.674-1697G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102692468 | ||||||
| chr4:102692615
|
CA | C | 3 | a0001c0001t0012g0232a0001c0004t0012g0253a0001c0004t0012g0275 | 3 | HG03209.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.674-1845delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102692615 | ||||||
| chr4:102692746
|
G | A | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-1975C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102692746 | ||||||
| chr4:102692747
|
T | G | 14 | a0001c0009t0024g0005a0001c0009t0034g0016a0003c0005t0008g0001others(11): Show | 15 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.674-1976A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102692747 | ||||||
| chr4:102692793
|
C | T | 1 | a0002c0002t0017g0132 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.674-2022G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102692793 | ||||||
| chr4:102692850
|
G | A | 16 | a0001c0001t0003g0139a0001c0001t0003g0223a0001c0001t0003g0231others(13): Show | 16 | HG01070.hp1 HG01109.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.674-2079C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102692850 | ||||||
| chr4:102692881
|
G | A | 2 | a0001c0009t0012g0034a0001c0017t0005g0237 | 2 | HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.674-2110C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102692881 | ||||||
| chr4:102693201
|
G | A | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-2430C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102693201 | ||||||
| chr4:102693302
|
T | C | 2 | a0002c0002t0002g0052a0002c0002t0002g0111 | 2 | HG03239.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.674-2531A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102693302 | ||||||
| chr4:102693454
|
G | A | 1 | a0003c0010t0016g0271 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.674-2683C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102693454 | ||||||
| chr4:102693659
|
A | C | 1 | a0001c0001t0001g0192 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.674-2888T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102693659 | ||||||
| chr4:102693717
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.674-2946C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102693717 | ||||||
| chr4:102693844
|
CA | C | 20 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(17): Show | 21 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.674-3074delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102693844 | ||||||
| chr4:102694001
|
C | T | 1 | a0001c0009t0034g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.674-3230G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102694001 | ||||||
| chr4:102694101
|
G | A | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-3330C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102694101 | ||||||
| chr4:102694145
|
C | T | 1 | a0003c0003t0014g0143 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.674-3374G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102694145 | ||||||
| chr4:102694267
|
A | G | 2 | a0001c0004t0010g0140a0001c0004t0020g0141 | 2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.674-3496T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102694267 | ||||||
| chr4:102694352
|
G | C | 1 | a0001c0004t0010g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.674-3581C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102694352 | ||||||
| chr4:102694521
|
C | T | 1 | a0005c0008t0003g0219 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.674-3750G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102694521 | ||||||
| chr4:102694577
|
T | C | 1 | a0001c0001t0001g0227 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.674-3806A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102694577 | ||||||
| chr4:102694803
|
C | T | 1 | a0001c0009t0012g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.674-4032G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102694803 | ||||||
| chr4:102694827
|
CT | C | 5 | a0002c0002t0002g0098a0002c0002t0002g0099a0002c0002t0002g0101others(2): Show | 5 | HG00438.hp1 HG00609.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.674-4057delA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102694827 | ||||||
| chr4:102694847
|
G | T | 1 | a0003c0005t0008g0008 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.674-4076C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102694847 | ||||||
| chr4:102694866
|
C | T | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-4095G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102694866 | ||||||
| chr4:102695017
|
C | A | 2 | a0001c0001t0005g0162a0001c0001t0025g0157 | 2 | HG00609.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.674-4246G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102695017 | ||||||
| chr4:102695237
|
A | G | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-4466T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102695237 | ||||||
| chr4:102695369
|
C | T | 1 | a0001c0001t0006g0224 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.674-4598G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102695369 | ||||||
| chr4:102695421
|
C | T | 1 | a0001c0017t0005g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.674-4650G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102695421 | ||||||
| chr4:102695659
|
G | A | 5 | a0001c0001t0001g0254a0003c0003t0013g0248a0003c0003t0013g0255others(2): Show | 5 | HG00438.hp2 HG02056.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.674-4888C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102695659 | ||||||
| chr4:102695818
|
C | T | 13 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(10): Show | 14 | HG00673.hp1 HG01081.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.674-5047G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102695818 | ||||||
| chr4:102696019
|
G | A | 1 | a0001c0017t0005g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.674-5248C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102696019 | ||||||
| chr4:102696064
|
A | G | 4 | a0003c0005t0008g0001a0003c0005t0008g0006a0003c0005t0008g0008others(1): Show | 5 | HG01192.hp2 HG02145.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.674-5293T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102696064 | ||||||
| chr4:102696334
|
C | G | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-5563G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102696334 | ||||||
| chr4:102696364
|
G | GA | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-5594_674-5593i others(3): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102696364 | ||||||
| chr4:102696447
|
G | A | 2 | a0001c0004t0001g0243a0001c0004t0023g0004 | 2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.674-5676C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102696447 | ||||||
| chr4:102696459
|
A | G | 2 | a0001c0004t0001g0243a0001c0004t0023g0004 | 2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.674-5688T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102696459 | ||||||
| chr4:102696493
|
T | C | 1 | a0001c0001t0009g0076 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.674-5722A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102696493 | ||||||
| chr4:102696530
|
C | A | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.674-5759G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102696530 | ||||||
| chr4:102696545
|
A | G | 2 | a0003c0003t0015g0198a0003c0003t0015g0199 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.674-5774T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102696545 | ||||||
| chr4:102696546
|
G | A | 1 | a0001c0001t0004g0156 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.674-5775C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102696546 | ||||||
| chr4:102696563
|
A | G | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-5792T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102696563 | ||||||
| chr4:102696688
|
T | C | 2 | a0001c0004t0012g0253a0001c0004t0012g0275 | 2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.674-5917A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102696688 | ||||||
| chr4:102696762
|
T | C | 1 | a0001c0001t0018g0210 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.674-5991A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102696762 | ||||||
| chr4:102696866
|
T | C | 97 | a0001c0001t0005g0082a0001c0001t0006g0077a0001c0001t0006g0081others(94): Show | 97 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.674-6095A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102696866 | ||||||
| chr4:102696967
|
G | A | 1 | a0005c0008t0003g0138 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.674-6196C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102696967 | ||||||
| chr4:102697119
|
T | C | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-6348A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102697119 | ||||||
| chr4:102697341
|
CTTTAT | C | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-6575_674-6571d others(7): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102697341 | ||||||
| chr4:102697442
|
G | C | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-6671C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102697442 | ||||||
| chr4:102697463
|
T | C | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-6692A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102697463 | ||||||
| chr4:102697502
|
C | G | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-6731G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102697502 | ||||||
| chr4:102697523
|
A | G | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-6752T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102697523 | ||||||
| chr4:102697551
|
C | T | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-6780G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102697551 | ||||||
| chr4:102697603
|
C | T | 1 | a0001c0001t0001g0227 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.674-6832G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102697603 | ||||||
| chr4:102697665
|
T | C | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-6894A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102697665 | ||||||
| chr4:102697776
|
G | A | 1 | a0003c0003t0013g0255 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.674-7005C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102697776 | ||||||
| chr4:102697776
|
G | C | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-7005C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102697776 | ||||||
| chr4:102697820
|
C | G | 1 | a0003c0010t0016g0271 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.674-7049G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102697820 | ||||||
| chr4:102697904
|
C | A | 184 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(181): Show | 186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.674-7133G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102697904 | ||||||
| chr4:102698075
|
T | C | 1 | a0003c0003t0002g0228 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.674-7304A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698075 | ||||||
| chr4:102698114
|
A | C | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-7343T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698114 | ||||||
| chr4:102698128
|
A | ATG | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-7359_674-7358d others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698128 | ||||||
| chr4:102698179
|
C | T | 159 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(156): Show | 160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.674-7408G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698179 | ||||||
| chr4:102698208
|
T | A | 2 | a0003c0005t0021g0251a0003c0005t0021g0252 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.674-7437A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698208 | ||||||
| chr4:102698209
|
C | T | 2 | a0003c0005t0021g0251a0003c0005t0021g0252 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.674-7438G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698209 | ||||||
| chr4:102698389
|
T | G | 1 | a0001c0001t0001g0170 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.674-7618A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698389 | ||||||
| chr4:102698450
|
G | C | 2 | a0001c0004t0010g0024a0003c0010t0016g0271 | 2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.674-7679C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698450 | ||||||
| chr4:102698494
|
A | C | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-7723T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698494 | ||||||
| chr4:102698497
|
G | A | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-7726C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698497 | ||||||
| chr4:102698572
|
T | C | 2 | a0003c0005t0021g0251a0003c0005t0021g0252 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.674-7801A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698572 | ||||||
| chr4:102698596
|
C | T | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-7825G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698596 | ||||||
| chr4:102698605
|
G | A | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-7834C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698605 | ||||||
| chr4:102698606
|
A | T | 1 | a0001c0004t0010g0011 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.674-7835T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698606 | ||||||
| chr4:102698615
|
T | A | 1 | a0001c0009t0012g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.674-7844A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698615 | ||||||
| chr4:102698628
|
G | T | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-7857C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698628 | ||||||
| chr4:102698638
|
C | G | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-7867G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698638 | ||||||
| chr4:102698657
|
A | C | 2 | a0001c0004t0010g0024a0003c0010t0016g0271 | 2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.674-7886T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698657 | ||||||
| chr4:102698678
|
G | A | 1 | a0001c0001t0003g0169 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.674-7907C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698678 | ||||||
| chr4:102698706
|
C | A | 20 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(17): Show | 21 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.674-7935G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698706 | ||||||
| chr4:102698758
|
A | T | 1 | a0001c0001t0003g0095 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.674-7987T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698758 | ||||||
| chr4:102698765
|
T | C | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-7994A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698765 | ||||||
| chr4:102698767
|
G | T | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-7996C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698767 | ||||||
| chr4:102698783
|
G | A | 1 | a0007c0011t0029g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.674-8012C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698783 | ||||||
| chr4:102698804
|
T | C | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-8033A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102698804 | ||||||
| chr4:102699097
|
G | C | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-8326C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699097 | ||||||
| chr4:102699102
|
T | G | 1 | a0001c0009t0012g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.674-8331A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699102 | ||||||
| chr4:102699170
|
G | T | 16 | a0001c0009t0012g0034a0001c0009t0024g0005a0001c0009t0034g0016others(13): Show | 17 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.674-8399C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699170 | ||||||
| chr4:102699183
|
C | T | 1 | a0001c0001t0026g0145 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.674-8412G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699183 | ||||||
| chr4:102699193
|
A | T | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-8422T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699193 | ||||||
| chr4:102699228
|
C | A | 186 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(183): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.674-8457G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699228 | ||||||
| chr4:102699243
|
T | G | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-8472A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699243 | ||||||
| chr4:102699295
|
G | A | 14 | a0001c0009t0024g0005a0001c0009t0034g0016a0003c0005t0008g0001others(11): Show | 15 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.674-8524C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699295 | ||||||
| chr4:102699338
|
A | G | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-8567T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699338 | ||||||
| chr4:102699399
|
A | C | 1 | a0001c0001t0018g0021 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.674-8628T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699399 | ||||||
| chr4:102699477
|
T | A | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-8706A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699477 | ||||||
| chr4:102699526
|
C | T | 7 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.674-8755G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699526 | ||||||
| chr4:102699607
|
A | T | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-8836T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699607 | ||||||
| chr4:102699608
|
G | A | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.674-8837C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699608 | ||||||
| chr4:102699636
|
T | C | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-8865A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699636 | ||||||
| chr4:102699652
|
T | G | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-8881A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699652 | ||||||
| chr4:102699661
|
G | T | 185 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(182): Show | 187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.674-8890C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699661 | ||||||
| chr4:102699672
|
A | G | 180 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(177): Show | 182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.674-8901T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699672 | ||||||
| chr4:102699702
|
T | C | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-8931A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699702 | ||||||
| chr4:102699749
|
A | T | 1 | a0001c0009t0012g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.674-8978T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699749 | ||||||
| chr4:102699751
|
C | A | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-8980G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699751 | ||||||
| chr4:102699752
|
C | T | 5 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(2): Show | 5 | HG02647.hp2 HG02723.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.674-8981G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699752 | ||||||
| chr4:102699796
|
G | C | 161 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(158): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.674-9025C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699796 | ||||||
| chr4:102699867
|
C | A | 1 | a0001c0004t0010g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.674-9096G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102699867 | ||||||
| chr4:102700092
|
T | C | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.674-9321A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700092 | ||||||
| chr4:102700101
|
C | T | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-9330G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700101 | ||||||
| chr4:102700102
|
G | C | 7 | a0001c0004t0010g0011a0001c0004t0010g0024a0001c0004t0010g0140others(4): Show | 7 | HG02647.hp2 HG02886.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.674-9331C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700102 | ||||||
| chr4:102700144
|
G | A | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-9373C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700144 | ||||||
| chr4:102700161
|
A | T | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-9390T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700161 | ||||||
| chr4:102700284
|
T | G | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-9513A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700284 | ||||||
| chr4:102700303
|
A | C | 1 | a0002c0002t0002g0059 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.674-9532T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700303 | ||||||
| chr4:102700559
|
T | C | 1 | a0001c0017t0005g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.674-9788A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700559 | ||||||
| chr4:102700665
|
G | A | 1 | a0003c0005t0008g0006 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.674-9894C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700665 | ||||||
| chr4:102700708
|
G | A | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-9937C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700708 | ||||||
| chr4:102700740
|
A | C | 2 | a0001c0004t0001g0243a0001c0004t0023g0004 | 2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.674-9969T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700740 | ||||||
| chr4:102700748
|
C | T | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-9977G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700748 | ||||||
| chr4:102700790
|
A | C | 1 | a0003c0003t0015g0199 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.674-10019T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700790 | ||||||
| chr4:102700807
|
A | G | 6 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(3): Show | 6 | HG02630.hp2 HG02647.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.674-10036T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700807 | ||||||
| chr4:102700847
|
T | A | 2 | a0001c0004t0012g0253a0001c0004t0012g0275 | 2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.674-10076A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700847 | ||||||
| chr4:102700936
|
T | C | 1 | a0001c0001t0025g0157 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.674-10165A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102700936 | ||||||
| chr4:102701017
|
G | A | 161 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(158): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.674-10246C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701017 | ||||||
| chr4:102701065
|
T | G | 1 | a0001c0017t0005g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.674-10294A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701065 | ||||||
| chr4:102701178
|
C | G | 1 | a0001c0001t0001g0187 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.674-10407G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701178 | ||||||
| chr4:102701293
|
T | C | 13 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0022others(10): Show | 13 | HG02572.hp1 HG02622.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.674-10522A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701293 | ||||||
| chr4:102701306
|
T | G | 1 | a0002c0002t0002g0057 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.674-10535A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701306 | ||||||
| chr4:102701400
|
T | C | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-10629A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701400 | ||||||
| chr4:102701411
|
G | A | 95 | a0001c0001t0003g0038a0002c0002t0002g0028a0002c0002t0002g0029others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.674-10640C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701411 | ||||||
| chr4:102701412
|
C | T | 95 | a0001c0001t0003g0038a0002c0002t0002g0028a0002c0002t0002g0029others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.674-10641G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701412 | ||||||
| chr4:102701456
|
C | G | 1 | a0003c0003t0015g0198 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.674-10685G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701456 | ||||||
| chr4:102701468
|
A | G | 1 | a0001c0009t0012g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.674-10697T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701468 | ||||||
| chr4:102701518
|
G | T | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-10747C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701518 | ||||||
| chr4:102701541
|
T | G | 1 | a0003c0003t0031g0238 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.674-10770A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701541 | ||||||
| chr4:102701544
|
G | A | 1 | a0003c0003t0031g0238 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.674-10773C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701544 | ||||||
| chr4:102701551
|
C | T | 2 | a0001c0004t0010g0024a0003c0010t0016g0271 | 2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.674-10780G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701551 | ||||||
| chr4:102701594
|
G | T | 184 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(181): Show | 186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.674-10823C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701594 | ||||||
| chr4:102701644
|
T | C | 4 | a0002c0002t0014g0033a0002c0002t0014g0116a0004c0006t0001g0115others(1): Show | 4 | HG01081.hp2 HG01243.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-10873A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701644 | ||||||
| chr4:102701663
|
T | C | 1 | a0001c0004t0012g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.674-10892A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701663 | ||||||
| chr4:102701728
|
C | T | 1 | a0001c0001t0005g0162 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.674-10957G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701728 | ||||||
| chr4:102701746
|
C | T | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-10975G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701746 | ||||||
| chr4:102701843
|
G | A | 1 | a0002c0002t0002g0030 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.674-11072C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701843 | ||||||
| chr4:102701922
|
C | T | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-11151G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701922 | ||||||
| chr4:102701923
|
A | G | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-11152T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102701923 | ||||||
| chr4:102702005
|
C | T | 1 | a0001c0001t0010g0159 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.674-11234G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702005 | ||||||
| chr4:102702042
|
G | A | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0003c0003t0002g0151 | 3 | HG00280.hp2 HG00323.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.674-11271C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702042 | ||||||
| chr4:102702063
|
T | G | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-11292A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702063 | ||||||
| chr4:102702093
|
G | A | 16 | a0001c0001t0003g0139a0001c0001t0003g0223a0001c0001t0003g0231others(13): Show | 16 | HG01070.hp1 HG01109.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.674-11322C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702093 | ||||||
| chr4:102702107
|
A | G | 1 | a0002c0007t0007g0118 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.674-11336T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702107 | ||||||
| chr4:102702198
|
T | C | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-11427A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702198 | ||||||
| chr4:102702259
|
G | A | 2 | a0001c0001t0003g0231a0001c0001t0009g0216 | 2 | HG01175.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.674-11488C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702259 | ||||||
| chr4:102702268
|
C | T | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-11497G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702268 | ||||||
| chr4:102702334
|
C | T | 184 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(181): Show | 186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.674-11563G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702334 | ||||||
| chr4:102702341
|
C | A | 2 | a0001c0001t0001g0192a0001c0015t0010g0173 | 2 | NA18953.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.674-11570G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702341 | ||||||
| chr4:102702357
|
T | C | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-11586A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702357 | ||||||
| chr4:102702360
|
C | G | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-11589G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702360 | ||||||
| chr4:102702407
|
C | T | 3 | a0002c0002t0002g0070a0002c0002t0002g0075a0002c0002t0013g0064 | 3 | HG01099.hp1 HG01106.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.674-11636G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702407 | ||||||
| chr4:102702476
|
A | G | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-11705T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702476 | ||||||
| chr4:102702483
|
C | T | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-11712G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702483 | ||||||
| chr4:102702484
|
G | A | 2 | a0003c0005t0021g0251a0003c0005t0021g0252 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.674-11713C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702484 | ||||||
| chr4:102702499
|
T | G | 2 | a0001c0004t0010g0140a0001c0004t0020g0141 | 2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.674-11728A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702499 | ||||||
| chr4:102702564
|
T | G | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.674-11793A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702564 | ||||||
| chr4:102702670
|
A | G | 1 | a0002c0002t0016g0249 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.673+11768T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702670 | ||||||
| chr4:102702690
|
T | C | 1 | a0002c0002t0017g0119 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.673+11748A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702690 | ||||||
| chr4:102702765
|
C | CAATT | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+11672_673+1167 others(8): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702765 | ||||||
| chr4:102702808
|
A | C | 1 | a0004c0006t0001g0154 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.673+11630T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702808 | ||||||
| chr4:102702951
|
G | A | 1 | a0003c0005t0008g0001 | 2 | HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.673+11487C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102702951 | ||||||
| chr4:102703022
|
T | C | 20 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(17): Show | 21 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.673+11416A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102703022 | ||||||
| chr4:102703023
|
G | A | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+11415C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102703023 | ||||||
| chr4:102703081
|
T | G | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+11357A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102703081 | ||||||
| chr4:102703112
|
C | T | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.673+11326G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102703112 | ||||||
| chr4:102703132
|
C | CTTGT | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+11302_673+1130 others(8): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102703132 | ||||||
| chr4:102703197
|
C | A | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+11241G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102703197 | ||||||
| chr4:102703278
|
A | G | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+11160T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102703278 | ||||||
| chr4:102703356
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.673+11082A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102703356 | ||||||
| chr4:102703430
|
C | T | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+11008G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102703430 | ||||||
| chr4:102703622
|
G | A | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+10816C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102703622 | ||||||
| chr4:102703628
|
G | C | 6 | a0002c0002t0002g0036a0002c0002t0002g0037a0002c0002t0002g0040others(3): Show | 6 | HG01496.hp1 HG02129.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.673+10810C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102703628 | ||||||
| chr4:102703713
|
C | T | 2 | a0001c0004t0012g0253a0001c0004t0012g0275 | 2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.673+10725G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102703713 | ||||||
| chr4:102703814
|
C | T | 1 | a0001c0004t0010g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.673+10624G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102703814 | ||||||
| chr4:102703867
|
G | A | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+10571C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102703867 | ||||||
| chr4:102704005
|
G | A | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+10433C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704005 | ||||||
| chr4:102704026
|
T | C | 111 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0123others(108): Show | 113 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.673+10412A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704026 | ||||||
| chr4:102704073
|
T | C | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+10365A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704073 | ||||||
| chr4:102704090
|
A | G | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+10348T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704090 | ||||||
| chr4:102704107
|
C | A | 20 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(17): Show | 21 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.673+10331G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704107 | ||||||
| chr4:102704108
|
C | A | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+10330G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704108 | ||||||
| chr4:102704134
|
C | T | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+10304G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704134 | ||||||
| chr4:102704191
|
C | G | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+10247G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704191 | ||||||
| chr4:102704258
|
G | A | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+10180C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704258 | ||||||
| chr4:102704276
|
G | C | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+10162C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704276 | ||||||
| chr4:102704303
|
G | C | 1 | a0001c0017t0005g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.673+10135C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704303 | ||||||
| chr4:102704374
|
T | A | 58 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(55): Show | 59 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.673+10064A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704374 | ||||||
| chr4:102704433
|
C | T | 114 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0123others(111): Show | 116 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.673+10005G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704433 | ||||||
| chr4:102704445
|
C | G | 1 | a0001c0004t0010g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.673+9993G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704445 | ||||||
| chr4:102704469
|
C | T | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+9969G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704469 | ||||||
| chr4:102704552
|
CT | C | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+9885delA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704552 | ||||||
| chr4:102704579
|
T | A | 20 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(17): Show | 21 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.673+9859A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704579 | ||||||
| chr4:102704610
|
C | T | 1 | a0001c0001t0001g0178 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.673+9828G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704610 | ||||||
| chr4:102704760
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.673+9678G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704760 | ||||||
| chr4:102704778
|
T | G | 1 | a0001c0001t0003g0097 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.673+9660A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102704778 | ||||||
| chr4:102705112
|
G | C | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+9326C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102705112 | ||||||
| chr4:102705356
|
C | A | 1 | a0003c0010t0015g0274 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.673+9082G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102705356 | ||||||
| chr4:102705366
|
A | C | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+9072T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102705366 | ||||||
| chr4:102705567
|
G | A | 1 | a0001c0009t0012g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.673+8871C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102705567 | ||||||
| chr4:102705570
|
C | T | 2 | a0001c0004t0010g0140a0001c0004t0020g0141 | 2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.673+8868G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102705570 | ||||||
| chr4:102705637
|
C | T | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+8801G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102705637 | ||||||
| chr4:102705676
|
T | C | 2 | a0001c0004t0012g0253a0001c0004t0012g0275 | 2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.673+8762A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102705676 | ||||||
| chr4:102705702
|
T | C | 117 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0123others(114): Show | 119 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.673+8736A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102705702 | ||||||
| chr4:102705833
|
C | A | 1 | a0001c0017t0005g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.673+8605G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102705833 | ||||||
| chr4:102706040
|
C | T | 16 | a0001c0009t0012g0034a0001c0009t0024g0005a0001c0009t0034g0016others(13): Show | 17 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.673+8398G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102706040 | ||||||
| chr4:102706060
|
G | A | 1 | a0001c0004t0010g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.673+8378C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102706060 | ||||||
| chr4:102706062
|
G | T | 2 | a0001c0004t0010g0024a0003c0010t0016g0271 | 2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.673+8376C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102706062 | ||||||
| chr4:102706331
|
T | C | 1 | a0001c0004t0010g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.673+8107A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102706331 | ||||||
| chr4:102706408
|
G | C | 4 | a0003c0005t0008g0001a0003c0005t0008g0006a0003c0005t0008g0008others(1): Show | 5 | HG01192.hp2 HG02145.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.673+8030C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102706408 | ||||||
| chr4:102706517
|
G | A | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+7921C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102706517 | ||||||
| chr4:102706530
|
T | C | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+7908A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102706530 | ||||||
| chr4:102706538
|
C | G | 1 | a0002c0002t0002g0235 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.673+7900G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102706538 | ||||||
| chr4:102706717
|
A | G | 117 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0123others(114): Show | 119 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.673+7721T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102706717 | ||||||
| chr4:102706803
|
A | C | 1 | a0001c0001t0001g0135 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.673+7635T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102706803 | ||||||
| chr4:102706811
|
T | C | 115 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0123others(112): Show | 117 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.673+7627A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102706811 | ||||||
| chr4:102707128
|
A | T | 8 | a0001c0001t0001g0175a0001c0001t0001g0177a0001c0001t0001g0197others(5): Show | 8 | HG00558.hp1 HG01993.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.673+7310T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102707128 | ||||||
| chr4:102707417
|
C | G | 1 | a0001c0001t0001g0175 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.673+7021G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102707417 | ||||||
| chr4:102707525
|
T | C | 14 | a0001c0009t0024g0005a0001c0009t0034g0016a0003c0005t0008g0001others(11): Show | 15 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.673+6913A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102707525 | ||||||
| chr4:102707883
|
G | A | 1 | a0001c0004t0020g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.673+6555C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102707883 | ||||||
| chr4:102707978
|
T | C | 1 | a0002c0002t0013g0064 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.673+6460A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102707978 | ||||||
| chr4:102708186
|
A | G | 1 | a0001c0001t0003g0190 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.673+6252T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102708186 | ||||||
| chr4:102708319
|
G | A | 16 | a0001c0009t0012g0034a0001c0009t0024g0005a0001c0009t0034g0016others(13): Show | 17 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.673+6119C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102708319 | ||||||
| chr4:102708608
|
A | G | 2 | a0002c0002t0002g0059a0002c0002t0011g0060 | 2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.673+5830T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102708608 | ||||||
| chr4:102708646
|
T | A | 2 | a0001c0001t0019g0152a0001c0001t0019g0153 | 2 | HG02280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.673+5792A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102708646 | ||||||
| chr4:102708648
|
A | G | 2 | a0001c0001t0019g0152a0001c0001t0019g0153 | 2 | HG02280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.673+5790T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102708648 | ||||||
| chr4:102708939
|
A | G | 2 | a0001c0004t0010g0024a0003c0010t0016g0271 | 2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.673+5499T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102708939 | ||||||
| chr4:102708980
|
A | G | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+5458T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102708980 | ||||||
| chr4:102708983
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.673+5455T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102708983 | ||||||
| chr4:102709145
|
C | T | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+5293G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709145 | ||||||
| chr4:102709234
|
A | C | 1 | a0001c0009t0012g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.673+5204T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709234 | ||||||
| chr4:102709278
|
GAAAGAAA others(41): Show |
G | 2 | a0001c0004t0012g0253a0001c0004t0012g0275 | 2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.673+5112_673+5159d others(50): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709278 | ||||||
| chr4:102709283
|
AAAGG | A | 147 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(144): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.673+5151_673+5154d others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709283 | ||||||
| chr4:102709283
|
AAAGGAAG others(1): Show |
A | 15 | a0001c0001t0001g0123a0001c0001t0001g0131a0001c0001t0001g0182others(12): Show | 15 | HG00621.hp2 HG01192.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.673+5147_673+5154d others(10): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709283 | ||||||
| chr4:102709283
|
AAAGGAAG others(5): Show |
A | 14 | a0001c0009t0024g0005a0001c0009t0034g0016a0003c0005t0008g0001others(11): Show | 15 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.673+5143_673+5154d others(14): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709283 | ||||||
| chr4:102709291
|
GAAGGAAG others(33): Show |
G | 2 | a0001c0004t0010g0024a0003c0010t0016g0271 | 2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.673+5107_673+5146d others(42): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709291 | ||||||
| chr4:102709303
|
G | A | 4 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141others(1): Show | 4 | HG02886.hp2 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+5135C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709303 | ||||||
| chr4:102709304
|
AAGGAAGG | A | 4 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141others(1): Show | 4 | HG02886.hp2 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+5127_673+5133d others(9): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709304 | ||||||
| chr4:102709307
|
G | A | 87 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0135others(84): Show | 88 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.673+5131C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709307 | ||||||
| chr4:102709308
|
AAGG | A | 87 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0135others(84): Show | 88 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.673+5127_673+5129d others(5): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709308 | ||||||
| chr4:102709323
|
AG | A | 91 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0135others(88): Show | 92 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.673+5114delC | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709323 | ||||||
| chr4:102709326
|
A | G | 91 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0135others(88): Show | 92 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.673+5112T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709326 | ||||||
| chr4:102709331
|
A | G | 91 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0135others(88): Show | 92 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.673+5107T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709331 | ||||||
| chr4:102709383
|
GAAGAAAG others(14): Show |
G | 1 | a0001c0009t0012g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.673+5034_673+5054d others(23): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709383 | ||||||
| chr4:102709390
|
GAAAGAAA others(6): Show |
G | 14 | a0002c0002t0002g0028a0002c0002t0002g0029a0002c0002t0002g0030others(11): Show | 14 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(11): Show |
intron_variant | MODIFIER | c.673+5035_673+5047d others(15): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709390 | ||||||
| chr4:102709398
|
GA | G | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG00544.hp2 HG02647.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+5039delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709398 | ||||||
| chr4:102709433
|
G | A | 1 | a0001c0009t0012g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.673+5005C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709433 | ||||||
| chr4:102709436
|
A | AAAGG | 110 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0123others(107): Show | 112 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.673+4998_673+5001d others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709436 | ||||||
| chr4:102709436
|
A | G | 1 | a0001c0009t0012g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.673+5002T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709436 | ||||||
| chr4:102709643
|
C | T | 271 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(268): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.673+4795G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709643 | ||||||
| chr4:102709969
|
T | C | 14 | a0001c0009t0024g0005a0001c0009t0034g0016a0003c0005t0008g0001others(11): Show | 15 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.673+4469A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102709969 | ||||||
| chr4:102710117
|
C | T | 1 | a0001c0017t0005g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.673+4321G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102710117 | ||||||
| chr4:102710159
|
A | G | 1 | a0001c0004t0010g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.673+4279T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102710159 | ||||||
| chr4:102710282
|
T | C | 1 | a0001c0009t0012g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.673+4156A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102710282 | ||||||
| chr4:102710549
|
T | G | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+3889A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102710549 | ||||||
| chr4:102710594
|
C | T | 14 | a0001c0009t0024g0005a0001c0009t0034g0016a0003c0005t0008g0001others(11): Show | 15 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.673+3844G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102710594 | ||||||
| chr4:102710645
|
C | T | 1 | a0001c0001t0003g0002 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.673+3793G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102710645 | ||||||
| chr4:102710653
|
G | A | 2 | a0003c0005t0021g0251a0003c0005t0021g0252 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.673+3785C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102710653 | ||||||
| chr4:102711002
|
C | T | 1 | a0001c0004t0010g0011 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.673+3436G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102711002 | ||||||
| chr4:102711003
|
G | A | 4 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG02647.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+3435C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102711003 | ||||||
| chr4:102711029
|
G | T | 1 | a0003c0003t0013g0257 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.673+3409C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102711029 | ||||||
| chr4:102711063
|
T | G | 1 | a0002c0002t0015g0113 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.673+3375A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102711063 | ||||||
| chr4:102711391
|
C | A | 5 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(2): Show | 5 | HG02647.hp2 HG02965.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.673+3047G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102711391 | ||||||
| chr4:102711573
|
T | C | 5 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(2): Show | 5 | HG02647.hp2 HG02965.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.673+2865A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102711573 | ||||||
| chr4:102711709
|
G | A | 1 | a0001c0009t0012g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.673+2729C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102711709 | ||||||
| chr4:102711714
|
C | T | 8 | a0001c0009t0024g0005a0001c0009t0034g0016a0003c0005t0008g0010others(5): Show | 8 | HG01884.hp1 HG02615.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.673+2724G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102711714 | ||||||
| chr4:102711738
|
A | C | 1 | a0007c0011t0029g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.673+2700T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102711738 | ||||||
| chr4:102711806
|
C | T | 73 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0123others(70): Show | 74 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.673+2632G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102711806 | ||||||
| chr4:102711852
|
A | G | 20 | a0001c0004t0010g0024a0001c0004t0012g0253a0001c0004t0012g0275others(17): Show | 21 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.673+2586T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102711852 | ||||||
| chr4:102712118
|
G | A | 2 | a0002c0002t0002g0120a0002c0002t0011g0122 | 2 | HG01168.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.673+2320C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102712118 | ||||||
| chr4:102712235
|
T | A | 2 | a0001c0004t0001g0243a0001c0004t0023g0004 | 2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.673+2203A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102712235 | ||||||
| chr4:102712402
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.673+2036G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102712402 | ||||||
| chr4:102712403
|
A | T | 1 | a0001c0001t0001g0165 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.673+2035T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102712403 | ||||||
| chr4:102712524
|
C | CT | 7 | a0001c0001t0006g0224a0001c0004t0010g0011a0001c0004t0010g0140others(4): Show | 7 | HG02451.hp2 HG02886.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.673+1913dupA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102712524 | ||||||
| chr4:102712524
|
C | CTT | 89 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0123others(86): Show | 90 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.673+1912_673+1913d others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102712524 | ||||||
| chr4:102712539
|
A | T | 98 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0123others(95): Show | 99 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.673+1899T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102712539 | ||||||
| chr4:102712658
|
G | A | 94 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0123others(91): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.673+1780C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102712658 | ||||||
| chr4:102712680
|
G | A | 14 | a0001c0009t0024g0005a0001c0009t0034g0016a0003c0005t0008g0001others(11): Show | 15 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.673+1758C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102712680 | ||||||
| chr4:102712737
|
T | C | 114 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0123others(111): Show | 116 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.673+1701A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102712737 | ||||||
| chr4:102712887
|
G | A | 1 | a0001c0017t0005g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.673+1551C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102712887 | ||||||
| chr4:102712890
|
T | G | 1 | a0001c0017t0005g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.673+1548A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102712890 | ||||||
| chr4:102712923
|
T | C | 1 | a0001c0004t0005g0267 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.673+1515A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102712923 | ||||||
| chr4:102713043
|
C | T | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.673+1395G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102713043 | ||||||
| chr4:102713063
|
C | T | 90 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0123others(87): Show | 91 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.673+1375G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102713063 | ||||||
| chr4:102713084
|
C | A | 2 | a0001c0004t0010g0024a0003c0010t0016g0271 | 2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.673+1354G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102713084 | ||||||
| chr4:102713174
|
G | A | 2 | a0003c0005t0021g0251a0003c0005t0021g0252 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.673+1264C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102713174 | ||||||
| chr4:102713271
|
C | T | 1 | a0002c0002t0002g0036 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.673+1167G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102713271 | ||||||
| chr4:102713277
|
C | T | 2 | a0003c0005t0021g0251a0003c0005t0021g0252 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.673+1161G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102713277 | ||||||
| chr4:102713468
|
G | A | 1 | a0001c0001t0010g0184 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.673+970C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102713468 | ||||||
| chr4:102713571
|
T | C | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.673+867A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102713571 | ||||||
| chr4:102713694
|
G | A | 4 | a0002c0002t0014g0033a0002c0002t0014g0116a0004c0006t0001g0115others(1): Show | 4 | HG01081.hp2 HG01243.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+744C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102713694 | ||||||
| chr4:102713815
|
G | A | 4 | a0001c0001t0001g0105a0001c0001t0001g0133a0001c0001t0001g0147others(1): Show | 4 | HG00673.hp1 HG02129.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+623C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102713815 | ||||||
| chr4:102713835
|
G | A | 1 | a0001c0009t0034g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.673+603C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102713835 | ||||||
| chr4:102713865
|
C | T | 1 | a0001c0009t0012g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.673+573G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102713865 | ||||||
| chr4:102713896
|
CA | C | 22 | a0001c0001t0001g0135a0001c0001t0001g0226a0001c0001t0001g0242others(19): Show | 23 | HG00323.hp1 HG00544.hp2 HG00558.hp2 others(20): Show |
intron_variant | MODIFIER | c.673+541delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102713896 | ||||||
| chr4:102713896
|
CAA | C | 14 | a0001c0009t0012g0034a0001c0009t0024g0005a0001c0009t0034g0016others(11): Show | 14 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.673+540_673+541del others(2): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102713896 | ||||||
| chr4:102713912
|
A | G | 1 | a0001c0015t0010g0173 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.673+526T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102713912 | ||||||
| chr4:102714026
|
T | C | 114 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0123others(111): Show | 116 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.673+412A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102714026 | ||||||
| chr4:102714183
|
C | A | 19 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141others(16): Show | 20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.673+255G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102714183 | ||||||
| chr4:102714263
|
C | T | 1 | a0001c0009t0012g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.673+175G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 5/16 | chr4 | 102714263 | ||||||
| chr4:102714713
|
T | C | 1 | a0003c0003t0013g0160 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.550-152A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102714713 | ||||||
| chr4:102714743
|
A | G | 1 | a0001c0001t0004g0171 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.550-182T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102714743 | ||||||
| chr4:102714771
|
T | A | 1 | a0003c0010t0016g0271 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.550-210A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102714771 | ||||||
| chr4:102714850
|
C | T | 1 | a0002c0002t0002g0052 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.550-289G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102714850 | ||||||
| chr4:102715135
|
A | G | 33 | a0001c0004t0001g0243a0001c0004t0005g0262a0001c0004t0005g0263others(30): Show | 34 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.550-574T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102715135 | ||||||
| chr4:102715279
|
G | T | 14 | a0001c0001t0003g0139a0001c0001t0003g0223a0001c0001t0003g0231others(11): Show | 14 | HG01070.hp1 HG01109.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.550-718C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102715279 | ||||||
| chr4:102715432
|
T | C | 20 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0004t0010g0140others(17): Show | 21 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.550-871A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102715432 | ||||||
| chr4:102715503
|
T | G | 6 | a0001c0009t0012g0034a0003c0005t0008g0001a0003c0005t0008g0006others(3): Show | 7 | HG01192.hp2 HG02145.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.550-942A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102715503 | ||||||
| chr4:102715655
|
C | T | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.550-1094G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102715655 | ||||||
| chr4:102716060
|
A | C | 4 | a0002c0002t0002g0065a0002c0002t0002g0066a0002c0002t0002g0128others(1): Show | 4 | HG00558.hp2 HG02071.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.550-1499T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102716060 | ||||||
| chr4:102716075
|
C | T | 1 | a0003c0005t0008g0010 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.550-1514G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102716075 | ||||||
| chr4:102716080
|
C | T | 1 | a0001c0009t0012g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.550-1519G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102716080 | ||||||
| chr4:102716155
|
C | T | 5 | a0001c0009t0012g0034a0003c0005t0008g0001a0003c0005t0008g0006others(2): Show | 6 | HG01192.hp2 HG02145.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.550-1594G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102716155 | ||||||
| chr4:102716177
|
T | C | 34 | a0001c0004t0001g0026a0001c0004t0001g0243a0001c0004t0005g0262others(31): Show | 35 | HG00099.hp1 HG00735.hp2 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.550-1616A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102716177 | ||||||
| chr4:102716178
|
A | G | 21 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0004t0010g0140others(18): Show | 22 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.550-1617T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102716178 | ||||||
| chr4:102716309
|
C | CA | 39 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(36): Show | 40 | HG00621.hp1 HG00639.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.550-1749dupT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102716309 | ||||||
| chr4:102716309
|
CA | C | 99 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0123others(96): Show | 101 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.550-1749delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102716309 | ||||||
| chr4:102716309
|
CAA | C | 6 | a0001c0001t0001g0241a0001c0001t0003g0019a0003c0003t0015g0198others(3): Show | 6 | HG01099.hp2 HG02630.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.550-1750_550-1749d others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102716309 | ||||||
| chr4:102716649
|
T | C | 4 | a0001c0004t0001g0026a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG00099.hp1 HG02109.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.550-2088A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102716649 | ||||||
| chr4:102716753
|
G | A | 21 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0004t0010g0140others(18): Show | 22 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.550-2192C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102716753 | ||||||
| chr4:102716979
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.550-2418C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102716979 | ||||||
| chr4:102717046
|
A | AT | 3 | a0001c0001t0003g0246a0001c0001t0005g0247a0002c0002t0002g0277 | 3 | HG00140.hp2 HG03831.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.550-2486dupA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102717046 | ||||||
| chr4:102717112
|
T | C | 1 | a0001c0001t0001g0185 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.550-2551A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102717112 | ||||||
| chr4:102717263
|
T | C | 3 | a0001c0001t0005g0082a0001c0001t0006g0077a0001c0001t0006g0081 | 3 | HG01106.hp2 HG01346.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.550-2702A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102717263 | ||||||
| chr4:102717382
|
C | T | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.550-2821G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102717382 | ||||||
| chr4:102717424
|
C | CT | 7 | a0001c0001t0001g0165a0002c0007t0007g0106a0002c0007t0007g0108others(4): Show | 7 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.550-2864dupA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102717424 | ||||||
| chr4:102717424
|
CT | C | 7 | a0001c0009t0012g0034a0002c0002t0002g0120a0002c0002t0011g0122others(4): Show | 8 | HG01168.hp2 HG01192.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.550-2864delA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102717424 | ||||||
| chr4:102717444
|
G | A | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.550-2883C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102717444 | ||||||
| chr4:102718113
|
A | C | 7 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.550-3552T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102718113 | ||||||
| chr4:102718167
|
C | A | 1 | a0001c0001t0009g0250 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.550-3606G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102718167 | ||||||
| chr4:102718246
|
C | T | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.550-3685G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102718246 | ||||||
| chr4:102718281
|
A | G | 2 | a0001c0001t0004g0155a0001c0001t0004g0158 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.550-3720T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102718281 | ||||||
| chr4:102718490
|
T | G | 3 | a0002c0002t0002g0044a0002c0002t0015g0058a0002c0002t0015g0113 | 3 | HG00544.hp2 HG02080.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.550-3929A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102718490 | ||||||
| chr4:102718515
|
C | T | 5 | a0001c0004t0001g0026a0001c0004t0010g0024a0001c0004t0012g0253others(2): Show | 5 | HG00099.hp1 HG02109.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.550-3954G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102718515 | ||||||
| chr4:102718527
|
T | A | 1 | a0001c0001t0001g0193 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.550-3966A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102718527 | ||||||
| chr4:102718614
|
G | T | 2 | a0001c0004t0001g0243a0001c0004t0023g0004 | 2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.550-4053C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102718614 | ||||||
| chr4:102718683
|
A | G | 21 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0004t0010g0140others(18): Show | 22 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.550-4122T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102718683 | ||||||
| chr4:102718703
|
C | G | 4 | a0001c0004t0001g0026a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG00099.hp1 HG02109.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.550-4142G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102718703 | ||||||
| chr4:102718715
|
A | G | 12 | a0001c0004t0009g0014a0001c0009t0024g0005a0001c0009t0034g0016others(9): Show | 12 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.550-4154T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102718715 | ||||||
| chr4:102718780
|
A | G | 1 | a0002c0002t0002g0120 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.549+4091T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102718780 | ||||||
| chr4:102718833
|
G | A | 18 | a0001c0004t0009g0014a0001c0009t0012g0034a0001c0009t0024g0005others(15): Show | 19 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.549+4038C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102718833 | ||||||
| chr4:102718978
|
C | T | 1 | a0002c0002t0002g0235 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.549+3893G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102718978 | ||||||
| chr4:102718986
|
A | G | 118 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0123others(115): Show | 120 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.549+3885T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102718986 | ||||||
| chr4:102719016
|
T | C | 18 | a0001c0004t0009g0014a0001c0009t0012g0034a0001c0009t0024g0005others(15): Show | 19 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.549+3855A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719016 | ||||||
| chr4:102719156
|
G | A | 1 | a0001c0004t0001g0243 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.549+3715C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719156 | ||||||
| chr4:102719158
|
A | C | 1 | a0001c0009t0012g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.549+3713T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719158 | ||||||
| chr4:102719183
|
C | T | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.549+3688G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719183 | ||||||
| chr4:102719184
|
G | A | 1 | a0003c0010t0016g0271 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.549+3687C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719184 | ||||||
| chr4:102719253
|
G | A | 2 | a0001c0001t0006g0224a0001c0001t0006g0261 | 2 | HG02451.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.549+3618C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719253 | ||||||
| chr4:102719276
|
C | T | 2 | a0003c0005t0021g0251a0003c0005t0021g0252 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.549+3595G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719276 | ||||||
| chr4:102719379
|
G | A | 1 | a0002c0002t0011g0067 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.549+3492C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719379 | ||||||
| chr4:102719403
|
C | T | 4 | a0001c0004t0001g0026a0001c0004t0012g0253a0001c0004t0012g0275others(1): Show | 4 | HG00099.hp1 HG02109.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.549+3468G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719403 | ||||||
| chr4:102719574
|
C | T | 1 | a0004c0006t0001g0035 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.549+3297G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719574 | ||||||
| chr4:102719601
|
T | C | 86 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0123others(83): Show | 87 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.549+3270A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719601 | ||||||
| chr4:102719745
|
C | T | 21 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0004t0010g0140others(18): Show | 22 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.549+3126G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719745 | ||||||
| chr4:102719746
|
G | A | 1 | a0001c0004t0001g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.549+3125C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719746 | ||||||
| chr4:102719763
|
T | C | 8 | a0001c0001t0001g0104a0001c0001t0001g0186a0001c0001t0001g0187others(5): Show | 8 | HG01071.hp2 HG01074.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.549+3108A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719763 | ||||||
| chr4:102719816
|
A | G | 1 | a0004c0006t0004g0042 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.549+3055T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719816 | ||||||
| chr4:102719865
|
G | A | 1 | a0001c0001t0001g0234 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.549+3006C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719865 | ||||||
| chr4:102719935
|
T | C | 1 | a0001c0001t0004g0171 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.549+2936A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102719935 | ||||||
| chr4:102720028
|
G | A | 1 | a0001c0009t0012g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.549+2843C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102720028 | ||||||
| chr4:102720029
|
A | G | 1 | a0001c0009t0012g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.549+2842T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102720029 | ||||||
| chr4:102720043
|
T | C | 1 | a0003c0003t0031g0238 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.549+2828A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102720043 | ||||||
| chr4:102720263
|
C | T | 1 | a0001c0017t0005g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.549+2608G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102720263 | ||||||
| chr4:102720292
|
G | A | 2 | a0001c0004t0010g0140a0001c0004t0020g0141 | 2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.549+2579C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102720292 | ||||||
| chr4:102720307
|
C | T | 1 | a0002c0002t0002g0071 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.549+2564G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102720307 | ||||||
| chr4:102720434
|
C | CA | 9 | a0001c0001t0001g0104a0001c0001t0001g0186a0001c0001t0001g0187others(6): Show | 9 | HG01071.hp2 HG01074.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.549+2436dupT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102720434 | ||||||
| chr4:102720434
|
CA | C | 11 | a0001c0004t0001g0026a0001c0004t0001g0243a0001c0004t0005g0262others(8): Show | 11 | HG00099.hp1 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.549+2436delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102720434 | ||||||
| chr4:102720447
|
A | C | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.549+2424T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102720447 | ||||||
| chr4:102720498
|
G | A | 1 | a0004c0006t0004g0025 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.549+2373C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102720498 | ||||||
| chr4:102720530
|
G | A | 21 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0004t0010g0140others(18): Show | 22 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.549+2341C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102720530 | ||||||
| chr4:102720668
|
T | C | 2 | a0001c0001t0019g0152a0001c0001t0019g0153 | 2 | HG02280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.549+2203A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102720668 | ||||||
| chr4:102720680
|
G | A | 1 | a0001c0001t0003g0190 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.549+2191C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102720680 | ||||||
| chr4:102720933
|
T | C | 21 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0004t0010g0140others(18): Show | 22 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.549+1938A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102720933 | ||||||
| chr4:102720948
|
A | G | 3 | a0001c0004t0012g0253a0001c0004t0012g0275a0003c0010t0015g0274 | 3 | HG02109.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.549+1923T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102720948 | ||||||
| chr4:102721061
|
C | T | 1 | a0001c0001t0005g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.549+1810G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721061 | ||||||
| chr4:102721062
|
G | C | 1 | a0003c0003t0013g0248 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.549+1809C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721062 | ||||||
| chr4:102721090
|
G | A | 21 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0004t0010g0140others(18): Show | 22 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.549+1781C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721090 | ||||||
| chr4:102721145
|
G | A | 12 | a0001c0004t0009g0014a0001c0009t0024g0005a0001c0009t0034g0016others(9): Show | 12 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.549+1726C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721145 | ||||||
| chr4:102721198
|
C | T | 1 | a0002c0002t0017g0119 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.549+1673G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721198 | ||||||
| chr4:102721199
|
G | A | 2 | a0001c0004t0001g0243a0001c0004t0023g0004 | 2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.549+1672C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721199 | ||||||
| chr4:102721222
|
G | A | 18 | a0001c0004t0009g0014a0001c0009t0012g0034a0001c0009t0024g0005others(15): Show | 19 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.549+1649C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721222 | ||||||
| chr4:102721255
|
C | T | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.549+1616G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721255 | ||||||
| chr4:102721309
|
G | C | 2 | a0001c0004t0001g0243a0001c0004t0023g0004 | 2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.549+1562C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721309 | ||||||
| chr4:102721329
|
C | CATAA | 17 | a0001c0001t0001g0105a0001c0001t0001g0161a0001c0001t0003g0137others(14): Show | 17 | HG01891.hp2 HG01993.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.549+1538_549+1541d others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721329 | ||||||
| chr4:102721329
|
C | CATAAATA others(5): Show |
8 | a0001c0004t0010g0140a0001c0004t0020g0141a0001c0009t0012g0034others(5): Show | 9 | HG01192.hp2 HG02145.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.549+1530_549+1541d others(14): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721329 | ||||||
| chr4:102721329
|
CATAA | C | 3 | a0002c0002t0002g0127a0002c0002t0002g0277a0006c0013t0002g0272 | 3 | HG02698.hp1 HG03710.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.549+1538_549+1541d others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721329 | ||||||
| chr4:102721382
|
A | G | 21 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0004t0010g0140others(18): Show | 22 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.549+1489T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721382 | ||||||
| chr4:102721508
|
T | C | 1 | a0001c0001t0003g0095 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.549+1363A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721508 | ||||||
| chr4:102721532
|
A | T | 1 | a0001c0004t0010g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.549+1339T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721532 | ||||||
| chr4:102721647
|
T | C | 1 | a0002c0002t0014g0033 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.549+1224A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721647 | ||||||
| chr4:102721806
|
T | C | 1 | a0002c0002t0002g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.549+1065A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721806 | ||||||
| chr4:102721864
|
C | T | 2 | a0001c0001t0003g0246a0001c0001t0005g0247 | 2 | HG00140.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.549+1007G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721864 | ||||||
| chr4:102721960
|
G | T | 21 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0004t0010g0140others(18): Show | 22 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.549+911C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721960 | ||||||
| chr4:102721971
|
G | A | 82 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0123others(79): Show | 83 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.549+900C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721971 | ||||||
| chr4:102721972
|
G | A | 12 | a0001c0004t0009g0014a0001c0009t0024g0005a0001c0009t0034g0016others(9): Show | 12 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.549+899C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102721972 | ||||||
| chr4:102722029
|
CA | C | 126 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0105others(123): Show | 127 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.549+841delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102722029 | ||||||
| chr4:102722029
|
CAA | C | 115 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0001g0123others(112): Show | 117 | HG00323.hp1 HG00558.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.549+840_549+841del others(2): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102722029 | ||||||
| chr4:102722094
|
G | A | 18 | a0001c0004t0009g0014a0001c0009t0012g0034a0001c0009t0024g0005others(15): Show | 19 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.549+777C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102722094 | ||||||
| chr4:102722179
|
A | C | 5 | a0001c0009t0012g0034a0003c0005t0008g0001a0003c0005t0008g0006others(2): Show | 6 | HG01192.hp2 HG02145.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.549+692T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102722179 | ||||||
| chr4:102722211
|
A | G | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.549+660T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102722211 | ||||||
| chr4:102722271
|
C | T | 1 | a0002c0002t0002g0126 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.549+600G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102722271 | ||||||
| chr4:102722278
|
T | G | 1 | a0002c0002t0002g0083 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.549+593A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102722278 | ||||||
| chr4:102722429
|
C | T | 2 | a0001c0001t0003g0166a0001c0001t0003g0172 | 2 | HG02572.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.549+442G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102722429 | ||||||
| chr4:102722526
|
C | T | 1 | a0001c0017t0005g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.549+345G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102722526 | ||||||
| chr4:102722631
|
C | T | 3 | a0001c0004t0010g0011a0001c0004t0010g0140a0001c0004t0020g0141 | 3 | HG02886.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.549+240G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102722631 | ||||||
| chr4:102722687
|
A | G | 1 | a0001c0001t0006g0077 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.549+184T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4/16 | chr4 | 102722687 | ||||||
| chr4:102723420
|
C | T | 9 | a0001c0004t0001g0243a0001c0004t0005g0262a0001c0004t0005g0263others(6): Show | 9 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.379-379G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 3/16 | chr4 | 102723420 | ||||||
| chr4:102723492
|
A | C | 1 | a0002c0002t0002g0037 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.378+370T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 3/16 | chr4 | 102723492 | ||||||
| chr4:102723656
|
T | C | 1 | a0001c0001t0001g0234 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.378+206A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 3/16 | chr4 | 102723656 | ||||||
| chr4:102723829
|
AT | A | 9 | a0001c0001t0001g0003a0001c0001t0001g0105a0001c0001t0001g0133others(6): Show | 10 | HG00673.hp1 HG01978.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.378+32delA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 3/16 | chr4 | 102723829 | ||||||
| chr4:102724029
|
T | C | 1 | a0001c0004t0010g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.273-62A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102724029 | ||||||
| chr4:102724403
|
C | T | 1 | a0001c0001t0020g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.273-436G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102724403 | ||||||
| chr4:102724525
|
C | T | 1 | a0001c0004t0010g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.273-558G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102724525 | ||||||
| chr4:102724542
|
C | CA | 8 | a0002c0002t0002g0032a0002c0002t0002g0065a0002c0002t0002g0066others(5): Show | 8 | HG00558.hp2 HG01106.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.273-576dupT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102724542 | ||||||
| chr4:102724542
|
CA | C | 169 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(166): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.273-576delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102724542 | ||||||
| chr4:102724542
|
CAA | C | 10 | a0001c0001t0001g0269a0001c0004t0005g0262a0001c0004t0005g0263others(7): Show | 10 | HG00408.hp1 HG00408.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.273-577_273-576del others(2): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102724542 | ||||||
| chr4:102724721
|
G | A | 1 | a0004c0006t0003g0068 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.273-754C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102724721 | ||||||
| chr4:102724748
|
G | A | 2 | a0003c0005t0021g0251a0003c0005t0021g0252 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.273-781C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102724748 | ||||||
| chr4:102724787
|
C | CA | 7 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.273-821dupT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102724787 | ||||||
| chr4:102725070
|
G | A | 3 | a0001c0004t0012g0253a0001c0004t0012g0275a0003c0010t0015g0274 | 3 | HG02109.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.273-1103C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102725070 | ||||||
| chr4:102725072
|
GT | G | 3 | a0001c0004t0012g0253a0001c0004t0012g0275a0003c0010t0015g0274 | 3 | HG02109.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.273-1106delA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102725072 | ||||||
| chr4:102725277
|
A | T | 10 | a0001c0001t0006g0007a0001c0004t0001g0026a0001c0004t0012g0253others(7): Show | 11 | HG00099.hp1 HG01192.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.273-1310T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102725277 | ||||||
| chr4:102725295
|
C | G | 9 | a0001c0004t0009g0014a0001c0009t0024g0005a0001c0009t0034g0016others(6): Show | 9 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.272+1294G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102725295 | ||||||
| chr4:102725408
|
G | T | 1 | a0001c0009t0012g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.272+1181C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102725408 | ||||||
| chr4:102725414
|
C | T | 7 | a0001c0004t0010g0140a0001c0004t0012g0253a0001c0004t0012g0275others(4): Show | 7 | HG02109.hp2 HG02886.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.272+1175G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102725414 | ||||||
| chr4:102725487
|
C | T | 1 | a0001c0004t0001g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.272+1102G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102725487 | ||||||
| chr4:102725657
|
T | C | 3 | a0001c0004t0010g0140a0001c0004t0020g0141a0003c0005t0008g0027 | 3 | HG02886.hp2 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.272+932A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102725657 | ||||||
| chr4:102725751
|
G | A | 1 | a0003c0005t0008g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.272+838C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102725751 | ||||||
| chr4:102725784
|
C | A | 13 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0004t0012g0253others(10): Show | 13 | HG00735.hp2 HG01884.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.272+805G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102725784 | ||||||
| chr4:102725890
|
C | T | 115 | a0001c0001t0001g0131a0001c0001t0001g0135a0001c0001t0001g0164others(112): Show | 117 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.272+699G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102725890 | ||||||
| chr4:102725985
|
A | G | 10 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0009t0024g0005others(7): Show | 10 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.272+604T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102725985 | ||||||
| chr4:102726074
|
C | G | 1 | a0001c0004t0005g0263 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.272+515G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102726074 | ||||||
| chr4:102726100
|
C | CA | 10 | a0001c0001t0004g0069a0001c0001t0004g0191a0001c0001t0009g0076others(7): Show | 10 | HG00099.hp1 HG02015.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.272+488dupT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102726100 | ||||||
| chr4:102726101
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.272+488T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102726101 | ||||||
| chr4:102726178
|
A | G | 81 | a0001c0001t0001g0131a0001c0001t0001g0135a0001c0001t0001g0164others(78): Show | 82 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.272+411T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102726178 | ||||||
| chr4:102726242
|
T | C | 1 | a0001c0004t0010g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.272+347A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102726242 | ||||||
| chr4:102726398
|
T | C | 1 | a0001c0001t0005g0162 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.272+191A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102726398 | ||||||
| chr4:102726404
|
A | G | 15 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0004t0012g0253others(12): Show | 15 | HG00735.hp2 HG01884.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.272+185T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102726404 | ||||||
| chr4:102726466
|
C | CAAACA | 25 | a0001c0004t0001g0243a0001c0004t0005g0262a0001c0004t0005g0263others(22): Show | 25 | HG00735.hp2 HG01884.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.272+118_272+122dup others(5): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102726466 | ||||||
| chr4:102726528
|
C | A | 10 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0009t0024g0005others(7): Show | 10 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.272+61G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 2/16 | chr4 | 102726528 | ||||||
| chr4:102726795
|
C | T | 1 | a0001c0001t0009g0216 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.178-112G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102726795 | ||||||
| chr4:102726890
|
C | T | 3 | a0001c0004t0010g0024a0003c0005t0021g0251a0003c0005t0021g0252 | 3 | HG02647.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-207G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102726890 | ||||||
| chr4:102727072
|
C | T | 1 | a0001c0001t0020g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.178-389G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102727072 | ||||||
| chr4:102727131
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.178-448C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102727131 | ||||||
| chr4:102727143
|
G | A | 1 | a0001c0004t0001g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.178-460C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102727143 | ||||||
| chr4:102727221
|
C | G | 3 | a0001c0004t0010g0024a0003c0005t0021g0251a0003c0005t0021g0252 | 3 | HG02647.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-538G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102727221 | ||||||
| chr4:102727507
|
T | C | 1 | a0003c0010t0016g0271 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.178-824A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102727507 | ||||||
| chr4:102727569
|
C | T | 1 | a0001c0001t0004g0200 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.178-886G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102727569 | ||||||
| chr4:102727645
|
TCACAGTC others(3): Show |
T | 3 | a0001c0004t0010g0024a0003c0005t0021g0251a0003c0005t0021g0252 | 3 | HG02647.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-972_178-963del others(10): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102727645 | ||||||
| chr4:102727672
|
T | C | 3 | a0001c0004t0010g0024a0003c0005t0021g0251a0003c0005t0021g0252 | 3 | HG02647.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-989A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102727672 | ||||||
| chr4:102727706
|
G | C | 1 | a0001c0004t0006g0268 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.178-1023C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102727706 | ||||||
| chr4:102727782
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.178-1099C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102727782 | ||||||
| chr4:102727828
|
A | G | 1 | a0001c0001t0009g0240 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.178-1145T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102727828 | ||||||
| chr4:102727860
|
A | T | 1 | a0002c0002t0011g0073 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.178-1177T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102727860 | ||||||
| chr4:102727886
|
T | C | 10 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0009t0024g0005others(7): Show | 10 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.178-1203A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102727886 | ||||||
| chr4:102727977
|
T | A | 2 | a0001c0001t0001g0241a0001c0001t0001g0242 | 2 | HG00323.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.178-1294A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102727977 | ||||||
| chr4:102728057
|
G | C | 5 | a0001c0001t0006g0007a0003c0005t0008g0001a0003c0005t0008g0006others(2): Show | 6 | HG01192.hp2 HG02145.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.178-1374C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102728057 | ||||||
| chr4:102728367
|
C | T | 5 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0170others(2): Show | 6 | HG01168.hp1 HG01169.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.178-1684G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102728367 | ||||||
| chr4:102728499
|
A | AG | 3 | a0001c0004t0010g0024a0003c0005t0021g0251a0003c0005t0021g0252 | 3 | HG02647.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-1817_178-1816i others(3): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102728499 | ||||||
| chr4:102728708
|
C | T | 16 | a0001c0001t0003g0139a0001c0001t0003g0223a0001c0001t0003g0231others(13): Show | 16 | HG01070.hp1 HG01109.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.178-2025G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102728708 | ||||||
| chr4:102728709
|
G | A | 7 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-2026C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102728709 | ||||||
| chr4:102728792
|
T | C | 3 | a0001c0004t0010g0024a0003c0005t0021g0251a0003c0005t0021g0252 | 3 | HG02647.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-2109A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102728792 | ||||||
| chr4:102729099
|
C | T | 7 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-2416G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729099 | ||||||
| chr4:102729100
|
G | A | 1 | a0001c0001t0020g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.178-2417C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729100 | ||||||
| chr4:102729124
|
G | A | 1 | a0002c0002t0002g0070 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.178-2441C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729124 | ||||||
| chr4:102729145
|
C | T | 2 | a0001c0004t0010g0140a0001c0004t0020g0141 | 2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.178-2462G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729145 | ||||||
| chr4:102729173
|
T | C | 3 | a0001c0004t0010g0024a0003c0005t0021g0251a0003c0005t0021g0252 | 3 | HG02647.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-2490A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729173 | ||||||
| chr4:102729175
|
C | G | 3 | a0001c0004t0010g0024a0003c0005t0021g0251a0003c0005t0021g0252 | 3 | HG02647.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-2492G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729175 | ||||||
| chr4:102729410
|
C | T | 3 | a0001c0004t0010g0024a0003c0005t0021g0251a0003c0005t0021g0252 | 3 | HG02647.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-2727G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729410 | ||||||
| chr4:102729418
|
C | T | 1 | a0001c0004t0001g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.178-2735G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729418 | ||||||
| chr4:102729497
|
G | C | 1 | a0003c0003t0007g0130 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.178-2814C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729497 | ||||||
| chr4:102729642
|
T | C | 1 | a0001c0004t0001g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.178-2959A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729642 | ||||||
| chr4:102729664
|
C | T | 1 | a0001c0017t0005g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.178-2981G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729664 | ||||||
| chr4:102729829
|
A | G | 34 | a0001c0001t0006g0007a0001c0004t0001g0026a0001c0004t0005g0262others(31): Show | 35 | HG00099.hp1 HG00735.hp2 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.178-3146T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729829 | ||||||
| chr4:102729835
|
C | G | 1 | a0001c0001t0001g0201 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.178-3152G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729835 | ||||||
| chr4:102729852
|
T | C | 1 | a0001c0004t0023g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.178-3169A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729852 | ||||||
| chr4:102729910
|
G | A | 1 | a0002c0002t0002g0087 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.178-3227C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729910 | ||||||
| chr4:102729942
|
T | G | 1 | a0002c0002t0002g0126 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.178-3259A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729942 | ||||||
| chr4:102729997
|
T | C | 3 | a0001c0004t0010g0024a0003c0005t0021g0251a0003c0005t0021g0252 | 3 | HG02647.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-3314A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102729997 | ||||||
| chr4:102730011
|
T | C | 1 | a0001c0004t0023g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.178-3328A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730011 | ||||||
| chr4:102730019
|
G | A | 2 | a0001c0001t0001g0193a0002c0002t0011g0122 | 2 | HG01168.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.178-3336C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730019 | ||||||
| chr4:102730094
|
T | C | 3 | a0001c0004t0010g0024a0003c0005t0021g0251a0003c0005t0021g0252 | 3 | HG02647.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-3411A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730094 | ||||||
| chr4:102730298
|
A | G | 1 | a0001c0001t0001g0201 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.178-3615T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730298 | ||||||
| chr4:102730389
|
C | T | 7 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-3706G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730389 | ||||||
| chr4:102730468
|
C | T | 4 | a0001c0004t0012g0253a0001c0004t0012g0275a0001c0004t0023g0004others(1): Show | 4 | HG02109.hp2 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-3785G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730468 | ||||||
| chr4:102730475
|
G | A | 3 | a0001c0004t0010g0140a0001c0004t0020g0141a0003c0005t0008g0027 | 3 | HG02886.hp2 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.178-3792C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730475 | ||||||
| chr4:102730569
|
G | A | 2 | a0003c0005t0021g0251a0003c0005t0021g0252 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-3886C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730569 | ||||||
| chr4:102730592
|
T | G | 1 | a0002c0002t0002g0213 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.178-3909A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730592 | ||||||
| chr4:102730593
|
C | T | 1 | a0002c0002t0002g0213 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.178-3910G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730593 | ||||||
| chr4:102730611
|
G | C | 2 | a0003c0005t0021g0251a0003c0005t0021g0252 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-3928C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730611 | ||||||
| chr4:102730622
|
T | C | 1 | a0001c0001t0003g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.178-3939A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730622 | ||||||
| chr4:102730689
|
C | T | 3 | a0001c0004t0012g0253a0001c0004t0012g0275a0003c0010t0015g0274 | 3 | HG02109.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.178-4006G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730689 | ||||||
| chr4:102730720
|
G | C | 7 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-4037C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730720 | ||||||
| chr4:102730754
|
A | G | 10 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0009t0024g0005others(7): Show | 10 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.178-4071T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730754 | ||||||
| chr4:102730761
|
T | C | 1 | a0001c0004t0010g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.178-4078A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730761 | ||||||
| chr4:102730778
|
T | C | 1 | a0006c0013t0002g0272 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.178-4095A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730778 | ||||||
| chr4:102730805
|
A | C | 182 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0104others(179): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.178-4122T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730805 | ||||||
| chr4:102730944
|
A | T | 1 | a0001c0001t0001g0226 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.178-4261T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730944 | ||||||
| chr4:102730987
|
T | A | 14 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0004t0012g0253others(11): Show | 14 | HG00735.hp2 HG01884.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.178-4304A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102730987 | ||||||
| chr4:102731011
|
A | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(1): Show | 5 | NA18953.hp1 NA18964.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.178-4328T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102731011 | ||||||
| chr4:102731389
|
T | C | 1 | a0001c0004t0001g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.178-4706A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102731389 | ||||||
| chr4:102731656
|
T | G | 2 | a0003c0005t0021g0251a0003c0005t0021g0252 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-4973A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102731656 | ||||||
| chr4:102731691
|
T | C | 4 | a0001c0001t0001g0135a0001c0001t0001g0195a0001c0001t0001g0196others(1): Show | 4 | HG02080.hp1 NA18968.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-5008A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102731691 | ||||||
| chr4:102731773
|
G | T | 14 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0004t0012g0253others(11): Show | 14 | HG00735.hp2 HG01884.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.178-5090C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102731773 | ||||||
| chr4:102731789
|
G | T | 1 | a0002c0002t0002g0037 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.178-5106C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102731789 | ||||||
| chr4:102731894
|
C | A | 1 | a0001c0004t0023g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.178-5211G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102731894 | ||||||
| chr4:102731898
|
TC | T | 19 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(16): Show | 19 | HG00735.hp2 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.178-5216delG | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102731898 | ||||||
| chr4:102732221
|
C | G | 4 | a0001c0004t0012g0253a0001c0004t0012g0275a0001c0004t0023g0004others(1): Show | 4 | HG02109.hp2 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-5538G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102732221 | ||||||
| chr4:102732433
|
A | T | 4 | a0001c0004t0012g0253a0001c0004t0012g0275a0001c0004t0023g0004others(1): Show | 4 | HG02109.hp2 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-5750T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102732433 | ||||||
| chr4:102732450
|
G | A | 1 | a0002c0002t0002g0071 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.178-5767C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102732450 | ||||||
| chr4:102732761
|
A | G | 1 | a0001c0004t0010g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.178-6078T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102732761 | ||||||
| chr4:102732819
|
T | C | 168 | a0001c0001t0001g0003a0001c0001t0001g0131a0001c0001t0001g0133others(165): Show | 171 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.178-6136A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102732819 | ||||||
| chr4:102733219
|
A | C | 1 | a0002c0002t0011g0122 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.178-6536T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102733219 | ||||||
| chr4:102733282
|
A | G | 114 | a0001c0001t0001g0131a0001c0001t0001g0135a0001c0001t0001g0164others(111): Show | 116 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.178-6599T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102733282 | ||||||
| chr4:102733349
|
A | AT | 31 | a0001c0001t0003g0169a0001c0001t0006g0007a0001c0001t0006g0168others(28): Show | 32 | HG00099.hp1 HG00735.hp2 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.178-6667dupA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102733349 | ||||||
| chr4:102733349
|
AT | A | 19 | a0001c0001t0001g0212a0001c0001t0001g0254a0001c0001t0001g0276others(16): Show | 19 | HG00438.hp2 HG00639.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.178-6667delA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102733349 | ||||||
| chr4:102733413
|
G | A | 6 | a0001c0001t0006g0007a0001c0004t0001g0026a0003c0005t0008g0001others(3): Show | 7 | HG00099.hp1 HG01192.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-6730C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102733413 | ||||||
| chr4:102733446
|
G | A | 2 | a0003c0005t0021g0251a0003c0005t0021g0252 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-6763C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102733446 | ||||||
| chr4:102733567
|
C | T | 2 | a0001c0001t0001g0254a0003c0003t0013g0255 | 2 | HG02056.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.178-6884G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102733567 | ||||||
| chr4:102734105
|
T | C | 1 | a0003c0005t0008g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.178-7422A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102734105 | ||||||
| chr4:102734276
|
G | A | 4 | a0001c0004t0012g0253a0001c0004t0012g0275a0001c0004t0023g0004others(1): Show | 4 | HG02109.hp2 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-7593C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102734276 | ||||||
| chr4:102734318
|
G | A | 25 | a0001c0001t0006g0007a0001c0004t0001g0026a0001c0004t0005g0262others(22): Show | 26 | HG00099.hp1 HG00735.hp2 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.178-7635C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102734318 | ||||||
| chr4:102734400
|
C | T | 1 | a0004c0006t0001g0045 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.178-7717G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102734400 | ||||||
| chr4:102734465
|
T | C | 1 | a0001c0004t0020g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.178-7782A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102734465 | ||||||
| chr4:102734966
|
A | G | 3 | a0001c0004t0010g0140a0001c0004t0020g0141a0003c0005t0008g0027 | 3 | HG02886.hp2 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.178-8283T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102734966 | ||||||
| chr4:102735220
|
A | G | 80 | a0001c0001t0001g0131a0001c0001t0001g0135a0001c0001t0001g0164others(77): Show | 81 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.178-8537T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102735220 | ||||||
| chr4:102735324
|
AC | A | 7 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-8642delG | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102735324 | ||||||
| chr4:102735350
|
A | G | 1 | a0004c0006t0004g0025 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.178-8667T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102735350 | ||||||
| chr4:102735457
|
G | A | 5 | a0001c0004t0001g0026a0001c0004t0012g0253a0001c0004t0012g0275others(2): Show | 5 | HG00099.hp1 HG02109.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.178-8774C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102735457 | ||||||
| chr4:102735470
|
A | G | 1 | a0001c0004t0023g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.178-8787T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102735470 | ||||||
| chr4:102735471
|
A | G | 1 | a0001c0001t0009g0240 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.178-8788T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102735471 | ||||||
| chr4:102735521
|
CA | C | 101 | a0001c0001t0001g0131a0001c0001t0001g0135a0001c0001t0001g0164others(98): Show | 102 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.178-8839delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102735521 | ||||||
| chr4:102735521
|
CAA | C | 6 | a0001c0004t0005g0263a0001c0004t0005g0264a0001c0004t0005g0265others(3): Show | 6 | HG02145.hp2 HG02630.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.178-8840_178-8839d others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102735521 | ||||||
| chr4:102735847
|
T | C | 1 | a0001c0009t0034g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.178-9164A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102735847 | ||||||
| chr4:102736347
|
C | T | 1 | a0001c0004t0001g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.178-9664G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102736347 | ||||||
| chr4:102736383
|
A | G | 1 | a0002c0002t0002g0114 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.178-9700T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102736383 | ||||||
| chr4:102736436
|
C | A | 1 | a0001c0001t0001g0197 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.178-9753G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102736436 | ||||||
| chr4:102737287
|
G | A | 1 | a0001c0004t0010g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.178-10604C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102737287 | ||||||
| chr4:102737385
|
A | G | 10 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0009t0024g0005others(7): Show | 10 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.178-10702T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102737385 | ||||||
| chr4:102737478
|
T | G | 1 | a0002c0002t0011g0073 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.178-10795A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102737478 | ||||||
| chr4:102737494
|
T | G | 90 | a0001c0001t0001g0003a0001c0001t0001g0133a0001c0001t0001g0146others(87): Show | 92 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.178-10811A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102737494 | ||||||
| chr4:102737605
|
C | A | 1 | a0004c0006t0004g0025 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.178-10922G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102737605 | ||||||
| chr4:102737695
|
G | A | 1 | a0001c0001t0004g0200 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.178-11012C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102737695 | ||||||
| chr4:102737848
|
C | A | 3 | a0003c0005t0008g0012a0003c0005t0008g0013a0003c0005t0012g0015 | 3 | HG01884.hp1 HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.178-11165G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102737848 | ||||||
| chr4:102737967
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.178-11284T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102737967 | ||||||
| chr4:102738016
|
T | C | 33 | a0001c0001t0006g0007a0001c0004t0001g0026a0001c0004t0005g0262others(30): Show | 34 | HG00099.hp1 HG00735.hp2 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.178-11333A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102738016 | ||||||
| chr4:102738077
|
C | G | 2 | a0001c0001t0019g0152a0001c0001t0019g0153 | 2 | HG02280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.178-11394G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102738077 | ||||||
| chr4:102738158
|
G | A | 1 | a0008c0012t0002g0103 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.178-11475C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102738158 | ||||||
| chr4:102738211
|
A | C | 10 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0009t0024g0005others(7): Show | 10 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.178-11528T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102738211 | ||||||
| chr4:102738553
|
A | G | 1 | a0002c0002t0007g0046 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.178-11870T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102738553 | ||||||
| chr4:102738726
|
C | T | 1 | a0004c0006t0001g0045 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.178-12043G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102738726 | ||||||
| chr4:102739449
|
T | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0148a0001c0001t0001g0149others(1): Show | 5 | NA18953.hp1 NA18964.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.178-12766A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102739449 | ||||||
| chr4:102739866
|
C | A | 15 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0004t0012g0253others(12): Show | 15 | HG00735.hp2 HG01884.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.178-13183G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102739866 | ||||||
| chr4:102739868
|
C | T | 1 | a0001c0009t0012g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.178-13185G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102739868 | ||||||
| chr4:102739924
|
G | A | 1 | a0001c0001t0003g0208 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.178-13241C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102739924 | ||||||
| chr4:102740114
|
G | A | 3 | a0001c0001t0027g0202a0001c0017t0005g0237a0002c0002t0002g0235 | 3 | HG02622.hp2 HG02723.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.178-13431C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102740114 | ||||||
| chr4:102740228
|
T | C | 1 | a0001c0004t0010g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.178-13545A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102740228 | ||||||
| chr4:102740309
|
T | C | 1 | a0001c0004t0010g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.178-13626A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102740309 | ||||||
| chr4:102740383
|
C | T | 14 | a0001c0001t0003g0139a0001c0001t0003g0223a0001c0001t0003g0231others(11): Show | 14 | HG01070.hp1 HG01109.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.178-13700G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102740383 | ||||||
| chr4:102740404
|
C | T | 1 | a0002c0002t0002g0111 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.178-13721G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102740404 | ||||||
| chr4:102740530
|
A | C | 4 | a0002c0002t0002g0028a0002c0002t0002g0029a0002c0002t0002g0030others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-13847T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102740530 | ||||||
| chr4:102740601
|
T | C | 1 | a0001c0001t0001g0201 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.178-13918A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102740601 | ||||||
| chr4:102740705
|
C | T | 1 | a0001c0001t0003g0166 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.178-14022G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102740705 | ||||||
| chr4:102740885
|
G | A | 12 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0009t0024g0005others(9): Show | 12 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.178-14202C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102740885 | ||||||
| chr4:102740933
|
C | A | 1 | a0001c0004t0023g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.178-14250G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102740933 | ||||||
| chr4:102740934
|
G | A | 1 | a0001c0001t0009g0240 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.178-14251C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102740934 | ||||||
| chr4:102741400
|
C | G | 2 | a0001c0004t0010g0140a0001c0004t0020g0141 | 2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.178-14717G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102741400 | ||||||
| chr4:102741619
|
G | A | 15 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0004t0012g0253others(12): Show | 15 | HG00735.hp2 HG01884.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.178-14936C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102741619 | ||||||
| chr4:102741674
|
T | A | 1 | a0002c0002t0002g0127 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.178-14991A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102741674 | ||||||
| chr4:102741867
|
C | T | 3 | a0001c0004t0012g0253a0001c0004t0012g0275a0003c0010t0015g0274 | 3 | HG02109.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.178-15184G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102741867 | ||||||
| chr4:102742165
|
A | G | 33 | a0001c0001t0006g0007a0001c0004t0001g0026a0001c0004t0005g0262others(30): Show | 34 | HG00099.hp1 HG00735.hp2 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.178-15482T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102742165 | ||||||
| chr4:102742176
|
C | T | 1 | a0005c0008t0003g0138 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.178-15493G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102742176 | ||||||
| chr4:102742184
|
G | A | 1 | a0002c0002t0002g0213 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.178-15501C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102742184 | ||||||
| chr4:102742189
|
C | T | 1 | a0003c0010t0016g0271 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.178-15506G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102742189 | ||||||
| chr4:102742307
|
A | G | 1 | a0003c0003t0007g0244 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.178-15624T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102742307 | ||||||
| chr4:102742338
|
C | T | 15 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0004t0012g0253others(12): Show | 15 | HG00735.hp2 HG01884.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.178-15655G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102742338 | ||||||
| chr4:102742352
|
GAGTGGTA others(14): Show |
G | 1 | a0001c0004t0010g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.178-15690_178-1567 others(25): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102742352 | ||||||
| chr4:102742394
|
A | G | 1 | a0002c0002t0014g0033 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.178-15711T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102742394 | ||||||
| chr4:102742605
|
C | T | 3 | a0001c0004t0010g0140a0001c0004t0020g0141a0003c0005t0008g0027 | 3 | HG02886.hp2 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.178-15922G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102742605 | ||||||
| chr4:102742919
|
C | T | 2 | a0001c0001t0019g0152a0001c0001t0019g0153 | 2 | HG02280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.178-16236G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102742919 | ||||||
| chr4:102742927
|
T | TG | 276 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(273): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.178-16245dupC | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102742927 | ||||||
| chr4:102742964
|
T | C | 15 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0004t0012g0253others(12): Show | 15 | HG00735.hp2 HG01884.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.178-16281A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102742964 | ||||||
| chr4:102743000
|
C | T | 3 | a0001c0004t0012g0253a0001c0004t0012g0275a0003c0010t0015g0274 | 3 | HG02109.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.178-16317G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102743000 | ||||||
| chr4:102743334
|
A | T | 1 | a0003c0003t0031g0238 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.178-16651T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102743334 | ||||||
| chr4:102743450
|
G | A | 1 | a0001c0004t0005g0266 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.178-16767C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102743450 | ||||||
| chr4:102743483
|
T | C | 3 | a0001c0004t0010g0140a0001c0004t0020g0141a0003c0005t0008g0027 | 3 | HG02886.hp2 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.178-16800A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102743483 | ||||||
| chr4:102743576
|
T | C | 1 | a0002c0002t0002g0075 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.178-16893A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102743576 | ||||||
| chr4:102743724
|
G | A | 1 | a0001c0004t0001g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.177+16994C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102743724 | ||||||
| chr4:102743747
|
T | C | 3 | a0001c0004t0010g0140a0001c0004t0020g0141a0003c0005t0008g0027 | 3 | HG02886.hp2 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.177+16971A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102743747 | ||||||
| chr4:102743783
|
T | C | 1 | a0002c0002t0002g0041 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.177+16935A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102743783 | ||||||
| chr4:102743896
|
C | T | 1 | a0001c0004t0010g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.177+16822G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102743896 | ||||||
| chr4:102744006
|
C | A | 1 | a0001c0004t0012g0253 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.177+16712G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102744006 | ||||||
| chr4:102744138
|
C | T | 3 | a0001c0004t0010g0140a0001c0004t0020g0141a0003c0005t0008g0027 | 3 | HG02886.hp2 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.177+16580G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102744138 | ||||||
| chr4:102744167
|
G | A | 3 | a0001c0004t0010g0140a0001c0004t0020g0141a0003c0005t0008g0027 | 3 | HG02886.hp2 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.177+16551C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102744167 | ||||||
| chr4:102744260
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.177+16458G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102744260 | ||||||
| chr4:102744315
|
T | A | 1 | a0003c0003t0016g0211 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.177+16403A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102744315 | ||||||
| chr4:102744500
|
T | C | 14 | a0001c0001t0006g0007a0001c0004t0001g0026a0001c0004t0005g0262others(11): Show | 15 | HG00099.hp1 HG01192.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.177+16218A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102744500 | ||||||
| chr4:102744529
|
G | T | 1 | a0001c0004t0001g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.177+16189C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102744529 | ||||||
| chr4:102744869
|
T | C | 30 | a0001c0001t0006g0007a0001c0004t0001g0026a0001c0004t0005g0262others(27): Show | 31 | HG00099.hp1 HG00735.hp2 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.177+15849A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102744869 | ||||||
| chr4:102745267
|
T | C | 1 | a0003c0003t0031g0238 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.177+15451A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745267 | ||||||
| chr4:102745369
|
G | T | 1 | a0001c0001t0001g0131 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.177+15349C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745369 | ||||||
| chr4:102745441
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.177+15277G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745441 | ||||||
| chr4:102745577
|
C | A | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15141G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745577 | ||||||
| chr4:102745584
|
C | A | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15134G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745584 | ||||||
| chr4:102745586
|
G | A | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15132C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745586 | ||||||
| chr4:102745588
|
G | A | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15130C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745588 | ||||||
| chr4:102745592
|
G | A | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15126C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745592 | ||||||
| chr4:102745593
|
ATCAGGCA others(50): Show |
A | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15068_177+1512 others(61): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745593 | ||||||
| chr4:102745653
|
G | A | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15065C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745653 | ||||||
| chr4:102745654
|
C | A | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15064G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745654 | ||||||
| chr4:102745658
|
T | A | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15060A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745658 | ||||||
| chr4:102745662
|
C | A | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15056G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745662 | ||||||
| chr4:102745663
|
T | A | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15055A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745663 | ||||||
| chr4:102745665
|
T | A | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15053A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745665 | ||||||
| chr4:102745668
|
G | GAAAAAAA others(54): Show |
1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15049_177+1505 others(65): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745668 | ||||||
| chr4:102745671
|
C | A | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15047G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745671 | ||||||
| chr4:102745672
|
C | A | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15046G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745672 | ||||||
| chr4:102745674
|
T | A | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15044A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745674 | ||||||
| chr4:102745689
|
A | C | 1 | a0001c0001t0004g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+15029T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745689 | ||||||
| chr4:102745808
|
C | T | 60 | a0001c0001t0001g0131a0001c0001t0001g0135a0001c0001t0001g0164others(57): Show | 61 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.177+14910G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745808 | ||||||
| chr4:102745982
|
G | A | 4 | a0002c0007t0007g0106a0002c0007t0007g0108a0002c0007t0007g0109others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+14736C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102745982 | ||||||
| chr4:102746044
|
C | T | 2 | a0002c0002t0002g0044a0002c0002t0015g0113 | 2 | HG00544.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.177+14674G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102746044 | ||||||
| chr4:102746136
|
C | T | 1 | a0003c0005t0008g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.177+14582G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102746136 | ||||||
| chr4:102746423
|
A | C | 1 | a0001c0004t0001g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.177+14295T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102746423 | ||||||
| chr4:102746483
|
C | T | 5 | a0001c0001t0006g0007a0003c0005t0008g0001a0003c0005t0008g0006others(2): Show | 6 | HG01192.hp2 HG02145.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+14235G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102746483 | ||||||
| chr4:102746555
|
T | C | 1 | a0007c0011t0029g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.177+14163A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102746555 | ||||||
| chr4:102746624
|
T | G | 1 | a0003c0005t0008g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.177+14094A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102746624 | ||||||
| chr4:102746658
|
G | C | 12 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0004t0012g0253others(9): Show | 12 | HG00735.hp2 HG01884.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.177+14060C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102746658 | ||||||
| chr4:102746710
|
C | T | 1 | a0002c0002t0002g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.177+14008G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102746710 | ||||||
| chr4:102746712
|
A | T | 1 | a0001c0004t0010g0140 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.177+14006T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102746712 | ||||||
| chr4:102746840
|
C | T | 1 | a0001c0001t0006g0261 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.177+13878G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102746840 | ||||||
| chr4:102746966
|
C | T | 2 | a0001c0004t0005g0262a0001c0004t0005g0266 | 2 | HG01891.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.177+13752G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102746966 | ||||||
| chr4:102746971
|
C | CAA | 9 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0009t0034g0016others(6): Show | 9 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+13745_177+1374 others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102746971 | ||||||
| chr4:102747001
|
C | T | 12 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0004t0012g0253others(9): Show | 12 | HG00735.hp2 HG01884.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.177+13717G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102747001 | ||||||
| chr4:102747158
|
G | GAT | 10 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(7): Show | 10 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.177+13558_177+1355 others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102747158 | ||||||
| chr4:102747158
|
G | GATAT | 5 | a0001c0001t0006g0007a0003c0005t0008g0001a0003c0005t0008g0006others(2): Show | 6 | HG01192.hp2 HG02145.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+13556_177+1355 others(8): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102747158 | ||||||
| chr4:102747158
|
G | GATATATA others(23): Show |
3 | a0001c0004t0012g0253a0001c0009t0034g0016a0007c0011t0029g0018 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.177+13559_177+1356 others(34): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102747158 | ||||||
| chr4:102747158
|
G | GATATATA others(25): Show |
2 | a0001c0004t0009g0014a0003c0005t0012g0015 | 2 | HG00735.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.177+13559_177+1356 others(36): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102747158 | ||||||
| chr4:102747158
|
G | GATATATA others(29): Show |
5 | a0001c0004t0010g0011a0003c0005t0008g0010a0003c0005t0008g0012others(2): Show | 5 | HG01884.hp1 HG02109.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.177+13559_177+1356 others(40): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102747158 | ||||||
| chr4:102747158
|
G | GATATATA others(37): Show |
1 | a0001c0004t0012g0275 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.177+13559_177+1356 others(48): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102747158 | ||||||
| chr4:102747187
|
T | G | 80 | a0001c0001t0001g0131a0001c0001t0001g0135a0001c0001t0001g0164others(77): Show | 81 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.177+13531A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102747187 | ||||||
| chr4:102747240
|
C | G | 1 | a0004c0006t0004g0025 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.177+13478G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102747240 | ||||||
| chr4:102747313
|
T | A | 1 | a0001c0001t0001g0203 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.177+13405A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102747313 | ||||||
| chr4:102747479
|
C | T | 1 | a0003c0003t0002g0151 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.177+13239G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102747479 | ||||||
| chr4:102747742
|
G | A | 6 | a0001c0001t0003g0230a0001c0001t0003g0273a0001c0001t0006g0136others(3): Show | 6 | HG01496.hp2 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+12976C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102747742 | ||||||
| chr4:102747749
|
T | C | 1 | a0001c0001t0006g0261 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.177+12969A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102747749 | ||||||
| chr4:102747816
|
C | T | 1 | a0003c0010t0016g0271 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.177+12902G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102747816 | ||||||
| chr4:102748330
|
T | C | 2 | a0001c0001t0006g0224a0001c0001t0006g0261 | 2 | HG02451.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.177+12388A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102748330 | ||||||
| chr4:102748333
|
T | A | 2 | a0001c0004t0010g0024a0001c0009t0024g0005 | 2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.177+12385A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102748333 | ||||||
| chr4:102748430
|
C | CTA | 9 | a0001c0001t0003g0038a0001c0001t0003g0206a0001c0001t0003g0207others(6): Show | 9 | HG00099.hp1 HG00621.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+12286_177+1228 others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102748430 | ||||||
| chr4:102748447
|
A | C | 1 | a0001c0009t0012g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.177+12271T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102748447 | ||||||
| chr4:102748806
|
G | A | 16 | a0001c0001t0006g0007a0001c0004t0005g0262a0001c0004t0005g0263others(13): Show | 17 | HG01192.hp2 HG01891.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.177+11912C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102748806 | ||||||
| chr4:102748842
|
A | G | 9 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0009t0034g0016others(6): Show | 9 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+11876T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102748842 | ||||||
| chr4:102748877
|
C | T | 12 | a0001c0001t0001g0003a0001c0001t0001g0133a0001c0001t0001g0146others(9): Show | 13 | HG00673.hp1 HG01081.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.177+11841G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102748877 | ||||||
| chr4:102748885
|
C | A | 1 | a0003c0005t0008g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.177+11833G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102748885 | ||||||
| chr4:102748994
|
T | A | 9 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(6): Show | 9 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+11724A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102748994 | ||||||
| chr4:102749027
|
C | T | 9 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0009t0034g0016others(6): Show | 9 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+11691G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102749027 | ||||||
| chr4:102749387
|
G | A | 19 | a0001c0001t0005g0082a0001c0001t0006g0077a0001c0001t0006g0081others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.177+11331C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102749387 | ||||||
| chr4:102749590
|
G | A | 1 | a0002c0007t0007g0110 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.177+11128C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102749590 | ||||||
| chr4:102749615
|
G | T | 17 | a0001c0001t0006g0007a0001c0004t0001g0026a0001c0004t0005g0262others(14): Show | 18 | HG00099.hp1 HG01192.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.177+11103C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102749615 | ||||||
| chr4:102749673
|
A | G | 1 | a0001c0001t0009g0216 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.177+11045T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102749673 | ||||||
| chr4:102749842
|
C | T | 1 | a0001c0009t0024g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.177+10876G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102749842 | ||||||
| chr4:102750122
|
G | T | 1 | a0004c0006t0004g0042 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.177+10596C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102750122 | ||||||
| chr4:102750184
|
A | G | 2 | a0001c0004t0010g0140a0001c0004t0020g0141 | 2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.177+10534T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102750184 | ||||||
| chr4:102750522
|
T | A | 26 | a0001c0001t0006g0007a0001c0004t0001g0026a0001c0004t0005g0262others(23): Show | 27 | HG00099.hp1 HG00735.hp2 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.177+10196A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102750522 | ||||||
| chr4:102750553
|
C | T | 2 | a0001c0004t0010g0140a0001c0004t0020g0141 | 2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.177+10165G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102750553 | ||||||
| chr4:102750661
|
C | A | 1 | a0001c0001t0009g0250 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.177+10057G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102750661 | ||||||
| chr4:102750692
|
C | T | 1 | a0001c0004t0010g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.177+10026G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102750692 | ||||||
| chr4:102750806
|
G | C | 2 | a0002c0002t0007g0259a0003c0003t0013g0257 | 2 | HG00438.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.177+9912C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102750806 | ||||||
| chr4:102751023
|
A | G | 1 | a0001c0001t0003g0231 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.177+9695T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102751023 | ||||||
| chr4:102751212
|
G | A | 6 | a0001c0001t0003g0230a0001c0001t0003g0273a0001c0001t0006g0136others(3): Show | 6 | HG01496.hp2 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+9506C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102751212 | ||||||
| chr4:102751479
|
G | A | 9 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0009t0034g0016others(6): Show | 9 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+9239C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102751479 | ||||||
| chr4:102751527
|
G | A | 20 | a0001c0001t0001g0093a0001c0001t0001g0104a0001c0001t0003g0089others(17): Show | 20 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.177+9191C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102751527 | ||||||
| chr4:102751552
|
T | C | 1 | a0001c0001t0001g0212 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.177+9166A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102751552 | ||||||
| chr4:102751567
|
T | C | 2 | a0002c0002t0002g0039a0002c0002t0002g0270 | 2 | HG01192.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.177+9151A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102751567 | ||||||
| chr4:102752155
|
A | T | 1 | a0003c0003t0014g0143 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.177+8563T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102752155 | ||||||
| chr4:102752224
|
G | A | 1 | a0002c0002t0002g0213 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.177+8494C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102752224 | ||||||
| chr4:102752272
|
A | G | 1 | a0003c0005t0008g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.177+8446T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102752272 | ||||||
| chr4:102752347
|
C | T | 2 | a0002c0002t0002g0040a0002c0002t0002g0041 | 2 | HG02129.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.177+8371G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102752347 | ||||||
| chr4:102752449
|
CA | C | 5 | a0001c0001t0006g0007a0003c0005t0008g0001a0003c0005t0008g0006others(2): Show | 6 | HG01192.hp2 HG02145.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+8268delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102752449 | ||||||
| chr4:102752462
|
G | T | 1 | a0001c0001t0020g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.177+8256C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102752462 | ||||||
| chr4:102752577
|
G | T | 1 | a0001c0004t0010g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.177+8141C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102752577 | ||||||
| chr4:102752676
|
T | C | 1 | a0001c0001t0001g0104 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.177+8042A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102752676 | ||||||
| chr4:102752750
|
A | C | 2 | a0002c0002t0002g0039a0002c0002t0002g0270 | 2 | HG01192.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.177+7968T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102752750 | ||||||
| chr4:102753172
|
T | C | 1 | a0010c0016t0004g0214 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.177+7546A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102753172 | ||||||
| chr4:102753278
|
T | TAGTA | 9 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0009t0034g0016others(6): Show | 9 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+7439_177+7440i others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102753278 | ||||||
| chr4:102753279
|
T | A | 9 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0009t0034g0016others(6): Show | 9 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+7439A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102753279 | ||||||
| chr4:102753375
|
C | T | 15 | a0001c0001t0006g0007a0001c0004t0005g0262a0001c0004t0005g0263others(12): Show | 16 | HG01192.hp2 HG01891.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.177+7343G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102753375 | ||||||
| chr4:102753381
|
T | C | 17 | a0001c0001t0006g0007a0001c0004t0001g0026a0001c0004t0005g0262others(14): Show | 18 | HG00099.hp1 HG01192.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.177+7337A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102753381 | ||||||
| chr4:102753397
|
A | G | 7 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.177+7321T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102753397 | ||||||
| chr4:102753898
|
C | T | 9 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0009t0034g0016others(6): Show | 9 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+6820G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102753898 | ||||||
| chr4:102753901
|
G | T | 1 | a0004c0006t0004g0025 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.177+6817C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102753901 | ||||||
| chr4:102753951
|
G | C | 122 | a0001c0001t0001g0003a0001c0001t0001g0131a0001c0001t0001g0133others(119): Show | 124 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.177+6767C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102753951 | ||||||
| chr4:102754002
|
CA | C | 148 | a0001c0001t0001g0003a0001c0001t0001g0131a0001c0001t0001g0133others(145): Show | 151 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.177+6715delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754002 | ||||||
| chr4:102754018
|
G | A | 1 | a0003c0005t0008g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.177+6700C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754018 | ||||||
| chr4:102754019
|
A | G | 1 | a0003c0005t0008g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.177+6699T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754019 | ||||||
| chr4:102754286
|
C | T | 1 | a0003c0005t0008g0008 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.177+6432G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754286 | ||||||
| chr4:102754338
|
A | T | 1 | a0003c0005t0008g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.177+6380T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754338 | ||||||
| chr4:102754429
|
C | G | 28 | a0001c0001t0006g0007a0001c0004t0001g0026a0001c0004t0005g0262others(25): Show | 29 | HG00099.hp1 HG00735.hp2 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.177+6289G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754429 | ||||||
| chr4:102754474
|
A | G | 9 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(6): Show | 9 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+6244T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754474 | ||||||
| chr4:102754479
|
T | C | 2 | a0001c0004t0010g0024a0001c0009t0024g0005 | 2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.177+6239A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754479 | ||||||
| chr4:102754563
|
A | T | 5 | a0001c0001t0003g0142a0001c0001t0009g0216a0002c0002t0002g0120others(2): Show | 5 | HG01175.hp1 HG01361.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.177+6155T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754563 | ||||||
| chr4:102754566
|
T | C | 1 | a0001c0001t0009g0215 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.177+6152A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754566 | ||||||
| chr4:102754567
|
T | A | 1 | a0001c0004t0005g0266 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.177+6151A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754567 | ||||||
| chr4:102754650
|
G | A | 3 | a0003c0005t0008g0006a0003c0005t0008g0008a0003c0005t0008g0009 | 3 | HG01192.hp2 HG02145.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.177+6068C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754650 | ||||||
| chr4:102754714
|
G | T | 1 | a0001c0001t0003g0002 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.177+6004C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754714 | ||||||
| chr4:102754758
|
G | A | 2 | a0003c0003t0007g0130a0003c0005t0008g0027 | 2 | HG02602.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.177+5960C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754758 | ||||||
| chr4:102754801
|
C | T | 7 | a0001c0001t0006g0007a0001c0004t0010g0024a0001c0009t0024g0005others(4): Show | 8 | HG01192.hp2 HG02145.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.177+5917G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754801 | ||||||
| chr4:102754910
|
T | G | 6 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0022others(3): Show | 6 | HG02723.hp2 HG02809.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+5808A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102754910 | ||||||
| chr4:102755000
|
G | C | 2 | a0001c0004t0012g0275a0003c0010t0015g0274 | 2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.177+5718C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102755000 | ||||||
| chr4:102755068
|
G | C | 1 | a0001c0004t0010g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.177+5650C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102755068 | ||||||
| chr4:102755077
|
A | C | 9 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0009t0034g0016others(6): Show | 9 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+5641T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102755077 | ||||||
| chr4:102755098
|
T | C | 1 | a0001c0004t0005g0267 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.177+5620A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102755098 | ||||||
| chr4:102755192
|
G | A | 1 | a0003c0003t0007g0258 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.177+5526C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102755192 | ||||||
| chr4:102755513
|
A | C | 1 | a0004c0006t0005g0129 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.177+5205T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102755513 | ||||||
| chr4:102755696
|
A | G | 26 | a0001c0001t0006g0007a0001c0004t0001g0026a0001c0004t0005g0262others(23): Show | 27 | HG00099.hp1 HG00735.hp2 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.177+5022T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102755696 | ||||||
| chr4:102755738
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.177+4980A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102755738 | ||||||
| chr4:102755904
|
C | A | 6 | a0002c0007t0007g0106a0002c0007t0007g0108a0002c0007t0007g0109others(3): Show | 6 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+4814G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102755904 | ||||||
| chr4:102755968
|
T | G | 1 | a0002c0002t0002g0111 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.177+4750A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102755968 | ||||||
| chr4:102756129
|
T | C | 16 | a0001c0001t0003g0139a0001c0001t0003g0223a0001c0001t0003g0231others(13): Show | 16 | HG01070.hp1 HG01109.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.177+4589A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102756129 | ||||||
| chr4:102756207
|
A | G | 1 | a0001c0001t0001g0234 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.177+4511T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102756207 | ||||||
| chr4:102756215
|
T | G | 1 | a0001c0004t0023g0004 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.177+4503A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102756215 | ||||||
| chr4:102756286
|
T | A | 9 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0009t0034g0016others(6): Show | 9 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+4432A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102756286 | ||||||
| chr4:102756288
|
G | A | 17 | a0001c0001t0006g0007a0001c0004t0001g0026a0001c0004t0005g0262others(14): Show | 18 | HG00099.hp1 HG01192.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.177+4430C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102756288 | ||||||
| chr4:102756302
|
G | T | 9 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0009t0034g0016others(6): Show | 9 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+4416C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102756302 | ||||||
| chr4:102756358
|
G | A | 17 | a0001c0001t0006g0007a0001c0004t0001g0026a0001c0004t0005g0262others(14): Show | 18 | HG00099.hp1 HG01192.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.177+4360C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102756358 | ||||||
| chr4:102756542
|
C | T | 1 | a0004c0006t0009g0112 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.177+4176G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102756542 | ||||||
| chr4:102756657
|
A | G | 2 | a0003c0005t0021g0251a0003c0005t0021g0252 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.177+4061T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102756657 | ||||||
| chr4:102756797
|
T | TA | 119 | a0001c0001t0001g0003a0001c0001t0001g0131a0001c0001t0001g0146others(116): Show | 121 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.177+3920dupT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102756797 | ||||||
| chr4:102756797
|
T | TAA | 14 | a0001c0001t0001g0133a0001c0001t0001g0226a0001c0001t0001g0227others(11): Show | 15 | HG00673.hp1 HG00673.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.177+3919_177+3920d others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102756797 | ||||||
| chr4:102756797
|
TA | T | 13 | a0001c0001t0001g0269a0001c0001t0003g0246a0001c0001t0005g0247others(10): Show | 13 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(10): Show |
intron_variant | MODIFIER | c.177+3920delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102756797 | ||||||
| chr4:102756797
|
TAAA | T | 8 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0009t0034g0016others(5): Show | 8 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.177+3918_177+3920d others(5): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102756797 | ||||||
| chr4:102756830
|
TGCTTCAA others(48): Show |
T | 1 | a0001c0001t0001g0133 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.177+3833_177+3887d others(57): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102756830 | ||||||
| chr4:102756891
|
G | GTCCTTTT others(49): Show |
1 | a0001c0001t0001g0133 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.177+3826_177+3827i others(58): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102756891 | ||||||
| chr4:102757110
|
G | A | 9 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0009t0034g0016others(6): Show | 9 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+3608C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102757110 | ||||||
| chr4:102757150
|
A | T | 7 | a0001c0004t0005g0262a0001c0004t0005g0263a0001c0004t0005g0264others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.177+3568T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102757150 | ||||||
| chr4:102757181
|
T | C | 26 | a0001c0001t0006g0007a0001c0004t0001g0026a0001c0004t0005g0262others(23): Show | 27 | HG00099.hp1 HG00735.hp2 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.177+3537A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102757181 | ||||||
| chr4:102757270
|
G | A | 2 | a0001c0004t0010g0024a0001c0009t0024g0005 | 2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.177+3448C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102757270 | ||||||
| chr4:102757289
|
A | G | 1 | a0002c0002t0017g0132 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.177+3429T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102757289 | ||||||
| chr4:102757383
|
G | A | 1 | a0002c0002t0017g0119 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.177+3335C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102757383 | ||||||
| chr4:102757403
|
G | A | 9 | a0001c0004t0009g0014a0001c0004t0010g0011a0001c0009t0034g0016others(6): Show | 9 | HG00735.hp2 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+3315C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102757403 | ||||||
| chr4:102757537
|
C | G | 2 | a0001c0001t0001g0241a0001c0001t0001g0242 | 2 | HG00323.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.177+3181G>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102757537 | ||||||
| chr4:102757601
|
C | T | 270 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0093others(267): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.177+3117G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102757601 | ||||||
| chr4:102757888
|
C | A | 1 | a0001c0001t0019g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.177+2830G>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102757888 | ||||||
| chr4:102757960
|
G | T | 154 | a0001c0001t0001g0003a0001c0001t0001g0131a0001c0001t0001g0133others(151): Show | 157 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.177+2758C>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102757960 | ||||||
| chr4:102758142
|
T | C | 1 | a0002c0002t0002g0127 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.177+2576A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102758142 | ||||||
| chr4:102758204
|
GTA | G | 15 | a0001c0001t0006g0007a0001c0004t0009g0014a0001c0004t0010g0011others(12): Show | 16 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.177+2512_177+2513d others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102758204 | ||||||
| chr4:102758301
|
A | T | 1 | a0001c0001t0001g0131 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.177+2417T>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102758301 | ||||||
| chr4:102758302
|
T | A | 1 | a0001c0001t0009g0240 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.177+2416A>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102758302 | ||||||
| chr4:102758311
|
C | T | 6 | a0001c0001t0006g0007a0001c0004t0023g0004a0003c0005t0008g0001others(3): Show | 7 | HG01192.hp2 HG02145.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.177+2407G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102758311 | ||||||
| chr4:102758347
|
T | G | 1 | a0001c0001t0001g0234 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.177+2371A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102758347 | ||||||
| chr4:102758510
|
G | A | 2 | a0001c0001t0001g0241a0001c0001t0001g0242 | 2 | HG00323.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.177+2208C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102758510 | ||||||
| chr4:102758549
|
T | C | 1 | a0002c0002t0002g0235 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.177+2169A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102758549 | ||||||
| chr4:102758686
|
G | A | 1 | a0002c0002t0002g0128 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.177+2032C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102758686 | ||||||
| chr4:102758692
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.177+2026C>T | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102758692 | ||||||
| chr4:102758693
|
C | T | 1 | a0001c0009t0024g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.177+2025G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102758693 | ||||||
| chr4:102758863
|
C | T | 1 | a0003c0005t0008g0001 | 2 | HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.177+1855G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102758863 | ||||||
| chr4:102758917
|
T | C | 1 | a0003c0005t0008g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.177+1801A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102758917 | ||||||
| chr4:102759031
|
T | G | 1 | a0003c0003t0007g0130 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.177+1687A>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102759031 | ||||||
| chr4:102759118
|
T | C | 1 | a0001c0017t0005g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.177+1600A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102759118 | ||||||
| chr4:102759126
|
ATTCT | A | 2 | a0001c0004t0001g0026a0004c0006t0004g0025 | 2 | HG00099.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.177+1588_177+1591d others(6): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102759126 | ||||||
| chr4:102759137
|
C | CT | 124 | a0001c0001t0001g0003a0001c0001t0001g0131a0001c0001t0001g0133others(121): Show | 126 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.177+1580dupA | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102759137 | ||||||
| chr4:102759137
|
C | CTT | 20 | a0001c0001t0001g0254a0001c0001t0003g0246a0001c0001t0005g0247others(17): Show | 20 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(17): Show |
intron_variant | MODIFIER | c.177+1579_177+1580d others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102759137 | ||||||
| chr4:102759141
|
T | C | 1 | a0003c0005t0008g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.177+1577A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102759141 | ||||||
| chr4:102759342
|
G | C | 1 | a0004c0006t0005g0129 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.177+1376C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102759342 | ||||||
| chr4:102759442
|
A | C | 5 | a0002c0002t0002g0028a0002c0002t0002g0029a0002c0002t0002g0030others(2): Show | 5 | HG00280.hp1 HG00323.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.177+1276T>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102759442 | ||||||
| chr4:102759566
|
GA | G | 169 | a0001c0001t0001g0003a0001c0001t0001g0131a0001c0001t0001g0133others(166): Show | 172 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.177+1151delT | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102759566 | ||||||
| chr4:102759784
|
C | T | 2 | a0001c0001t0003g0019a0001c0001t0003g0020 | 2 | HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.177+934G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102759784 | ||||||
| chr4:102759827
|
A | G | 122 | a0001c0001t0001g0003a0001c0001t0001g0131a0001c0001t0001g0133others(119): Show | 124 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.177+891T>C | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102759827 | ||||||
| chr4:102760089
|
T | TAC | 146 | a0001c0001t0001g0003a0001c0001t0001g0131a0001c0001t0001g0133others(143): Show | 148 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.177+627_177+628dup others(2): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102760089 | ||||||
| chr4:102760089
|
T | TACAC | 3 | a0001c0001t0003g0273a0001c0004t0012g0275a0003c0010t0015g0274 | 3 | HG01891.hp1 HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.177+625_177+628dup others(4): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102760089 | ||||||
| chr4:102760215
|
T | C | 1 | a0001c0001t0001g0276 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.177+503A>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102760215 | ||||||
| chr4:102760244
|
G | C | 1 | a0002c0002t0002g0277 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.177+474C>G | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102760244 | ||||||
| chr4:102760535
|
C | T | 15 | a0001c0001t0006g0007a0001c0004t0009g0014a0001c0004t0010g0011others(12): Show | 16 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.177+183G>A | MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | 102760535 |