| geneid | 731220 |
|---|---|
| ensemblid | ENSG00000196460.14 |
| hgncid | 37253 |
| symbol | RFX8 |
| name | regulatory factor X8 |
| refseq_nuc | NM_001145664.2 |
| refseq_prot | NP_001139136.2 |
| ensembl_nuc | ENST00000428343.6 |
| ensembl_prot | ENSP00000401536.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 101397359 |
| end | 101475112 |
| strand | - |
| ver | v1.2 |
| region | chr2:101397359-101475112 |
| region5000 | chr2:101392359-101480112 |
| regionname0 | RFX8_chr2_101397359_101475112 |
| regionname5000 | RFX8_chr2_101392359_101480112 |
| 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 | 0/1 | 473 | 151 | 31 | 33 | 64 | 7 | 15 | 48 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0002 | 0/0 | 473 | 116 | 25 | 21 | 52 | 7 | 11 | 39 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0003 | 1/0 | 473 | 43 | 12 | 10 | 20 | 0 | 0 | 18 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0004 | 0/0 | 473 | 6 | 0 | 2 | 4 | 0 | 0 | 2 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0005 | 0/0 | 473 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0006 | 0/0 | 473 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0007 | 0/0 | 473 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0008 | 0/0 | 472 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0009 | 0/0 | 473 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0010 | 0/0 | 473 | 3 | 2 | 0 | 1 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0011 | 0/0 | 473 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0012 | 0/0 | 473 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0013 | 0/0 | 473 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0014 | 0/0 | 473 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0015 | 0/0 | 473 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0016 | 0/0 | 473 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0017 | 0/0 | 473 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0018 | 0/0 | 473 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0019 | 0/0 | 473 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0020 | 0/0 | 473 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0021 | 0/0 | 473 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| 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 | 0/1 | 1422 | 149 | 29 | 33 | 64 | 7 | 15 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| c0002 | 0/0 | 1422 | 111 | 20 | 21 | 52 | 7 | 11 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| c0003 | 1/0 | 1422 | 43 | 12 | 10 | 20 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| c0004 | 0/0 | 1422 | 6 | 0 | 2 | 4 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| c0005 | 0/0 | 1422 | 5 | 5 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| c0006 | 0/0 | 1422 | 3 | 3 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| c0007 | 0/0 | 1422 | 3 | 2 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| c0008 | 0/0 | 1422 | 3 | 3 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| c0009 | 0/0 | 1419 | 3 | 2 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| c0010 | 0/0 | 1422 | 3 | 3 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| c0011 | 0/0 | 1422 | 3 | 3 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| c0012 | 0/0 | 1422 | 2 | 1 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| c0013 | 0/0 | 1422 | 2 | 0 | 0 | 0 | 0 | 2 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| c0014 | 0/0 | 1422 | 2 | 2 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| c0015 | 0/0 | 1422 | 2 | 2 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| c0016 | 0/0 | 1422 | 2 | 0 | 0 | 0 | 0 | 2 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| c0017 | 0/0 | 1422 | 2 | 2 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| c0018 | 0/0 | 1422 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| c0019 | 0/0 | 1422 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| c0020 | 0/0 | 1422 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| c0021 | 0/0 | 1422 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| c0022 | 0/0 | 1422 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| c0023 | 0/0 | 1422 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| c0024 | 0/0 | 1422 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| c0025 | 0/0 | 1422 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| 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 | 1/0 | 719 | 245 | 66 | 34 | 117 | 11 | 16 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| t0002 | 0/1 | 719 | 87 | 10 | 33 | 27 | 3 | 13 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| t0003 | 0/0 | 719 | 13 | 11 | 1 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| t0004 | 0/0 | 707 | 3 | 3 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| t0005 | 0/0 | 719 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| t0006 | 0/0 | 719 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| t0007 | 0/0 | 719 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| t0008 | 0/0 | 719 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| 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 | 6 | 0 | 6 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0004 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0009 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0170 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| 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 | 0/1 | 1422 | 149 | 29 | 33 | 64 | 7 | 15 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0001c0015 | 0/0 | 1422 | 2 | 2 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0002c0002 | 0/0 | 1422 | 111 | 20 | 21 | 52 | 7 | 11 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0002c0008 | 0/0 | 1422 | 3 | 3 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0002c0020 | 0/0 | 1422 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0002c0021 | 0/0 | 1422 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0003c0003 | 1/0 | 1422 | 43 | 12 | 10 | 20 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0004c0004 | 0/0 | 1422 | 6 | 0 | 2 | 4 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0005c0005 | 0/0 | 1422 | 5 | 5 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0006c0011 | 0/0 | 1422 | 3 | 3 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0007c0010 | 0/0 | 1422 | 3 | 3 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0008c0009 | 0/0 | 1419 | 3 | 2 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0009c0006 | 0/0 | 1422 | 3 | 3 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0010c0007 | 0/0 | 1422 | 3 | 2 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0011c0014 | 0/0 | 1422 | 2 | 2 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0012c0013 | 0/0 | 1422 | 2 | 0 | 0 | 0 | 0 | 2 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0013c0016 | 0/0 | 1422 | 2 | 0 | 0 | 0 | 0 | 2 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0014c0017 | 0/0 | 1422 | 2 | 2 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0015c0012 | 0/0 | 1422 | 2 | 1 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0016c0025 | 0/0 | 1422 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0017c0024 | 0/0 | 1422 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0018c0022 | 0/0 | 1422 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0019c0019 | 0/0 | 1422 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0020c0023 | 0/0 | 1422 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0021c0018 | 0/0 | 1422 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2140 | 93 | 21 | 15 | 44 | 5 | 8 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0001c0001t0002 | 0/1 | 2140 | 50 | 4 | 17 | 20 | 2 | 6 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0001c0001t0003 | 0/0 | 2140 | 5 | 3 | 1 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0001c0001t0008 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0001c0015t0001 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0001c0015t0002 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0002c0002t0001 | 0/0 | 2140 | 92 | 16 | 17 | 46 | 6 | 7 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0002c0002t0002 | 0/0 | 2140 | 17 | 2 | 4 | 6 | 1 | 4 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0002c0002t0003 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0002c0002t0005 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0002c0008t0004 | 0/0 | 2128 | 3 | 3 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0002c0020t0001 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0002c0021t0001 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0003c0003t0001 | 1/0 | 2140 | 31 | 11 | 0 | 19 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0003c0003t0002 | 0/0 | 2140 | 12 | 1 | 10 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0004c0004t0001 | 0/0 | 2140 | 4 | 0 | 0 | 4 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0004c0004t0002 | 0/0 | 2140 | 2 | 0 | 2 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0005c0005t0003 | 0/0 | 2140 | 5 | 5 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0006c0011t0001 | 0/0 | 2140 | 3 | 3 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0007c0010t0001 | 0/0 | 2140 | 2 | 2 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0007c0010t0007 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0008c0009t0001 | 0/0 | 2137 | 2 | 1 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0008c0009t0002 | 0/0 | 2137 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0009c0006t0001 | 0/0 | 2140 | 3 | 3 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0010c0007t0001 | 0/0 | 2140 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0010c0007t0003 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0010c0007t0006 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0011c0014t0001 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0011c0014t0003 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0012c0013t0001 | 0/0 | 2140 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0012c0013t0002 | 0/0 | 2140 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0013c0016t0002 | 0/0 | 2140 | 2 | 0 | 0 | 0 | 0 | 2 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0014c0017t0001 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0014c0017t0002 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0015c0012t0001 | 0/0 | 2140 | 2 | 1 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0016c0025t0001 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0017c0024t0001 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0018c0022t0001 | 0/0 | 2140 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0019c0019t0001 | 0/0 | 2140 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0020c0023t0001 | 0/0 | 2140 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| a0021c0018t0001 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | copy fasta | chr2 | 101392359 | 101480112 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0001 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0004 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0009 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0001t0008g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0015t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0001c0015t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0002t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0008t0004g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0008t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0020t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0002c0021t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0001g0170 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0003c0003t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0004c0004t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0004c0004t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0004c0004t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0004c0004t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0004c0004t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0005c0005t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0005c0005t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0005c0005t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0005c0005t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0005c0005t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0006c0011t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0006c0011t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0007c0010t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0007c0010t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0007c0010t0007g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0008c0009t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0008c0009t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0008c0009t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0009c0006t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0009c0006t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0009c0006t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0010c0007t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0010c0007t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0010c0007t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0011c0014t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0011c0014t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0012c0013t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0012c0013t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0013c0016t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0013c0016t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0014c0017t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0014c0017t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0015c0012t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0015c0012t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0016c0025t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0017c0024t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0018c0022t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0019c0019t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0020c0023t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| a0021c0018t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0270 | EUR | GBR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0269 | EUR | GBR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0062 | EUR | GBR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | GBR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0286 | EUR | FIN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0144 | EUR | FIN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG00408 | hp2 | a0020 | c0023 | t0001 | g0142 | EAS | CHS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | CHS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0088 | EAS | CHS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG00544 | hp2 | a0004 | c0004 | t0001 | g0272 | EAS | CHS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG00558 | hp1 | a0004 | c0004 | t0001 | g0206 | EAS | CHS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0232 | EAS | CHS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0223 | EAS | CHS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0283 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG00642 | hp2 | a0003 | c0003 | t0002 | g0055 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG00673 | hp1 | a0003 | c0003 | t0001 | g0126 | EAS | CHS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0079 | EAS | CHS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0302 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0285 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG00741 | hp1 | a0002 | c0002 | t0002 | g0084 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG00741 | hp2 | a0003 | c0003 | t0002 | g0059 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0198 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0254 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0282 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0212 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0289 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01167 | hp1 | a0004 | c0004 | t0002 | g0011 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0094 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01169 | hp1 | a0004 | c0004 | t0002 | g0011 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0199 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0266 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01243 | hp2 | a0015 | c0012 | t0001 | g0175 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0076 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0061 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0108 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01358 | hp2 | a0008 | c0009 | t0001 | g0157 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0207 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01361 | hp2 | a0002 | c0002 | t0002 | g0054 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0263 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01433 | hp2 | a0003 | c0003 | t0002 | g0045 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0010 | EUR | IBS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0290 | EUR | IBS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0304 | EUR | IBS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0307 | EUR | IBS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01884 | hp1 | a0017 | c0024 | t0001 | g0184 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01884 | hp2 | a0001 | c0015 | t0001 | g0185 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01891 | hp1 | a0001 | c0001 | t0008 | g0320 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01928 | hp1 | a0003 | c0003 | t0002 | g0057 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01934 | hp2 | a0003 | c0003 | t0002 | g0042 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0213 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01943 | hp2 | a0003 | c0003 | t0002 | g0053 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01978 | hp1 | a0003 | c0003 | t0002 | g0058 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0146 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0081 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0078 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0246 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0162 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02083 | hp2 | a0003 | c0003 | t0001 | g0278 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0248 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02148 | hp2 | a0003 | c0003 | t0002 | g0038 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | CDX | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CDX | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02257 | hp1 | a0002 | c0002 | t0003 | g0095 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0156 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0256 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02273 | hp2 | a0003 | c0003 | t0002 | g0056 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02280 | hp1 | a0005 | c0005 | t0003 | g0101 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02280 | hp2 | a0007 | c0010 | t0001 | g0234 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02300 | hp1 | a0003 | c0003 | t0002 | g0040 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02451 | hp2 | a0011 | c0014 | t0001 | g0188 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0301 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02572 | hp1 | a0008 | c0009 | t0001 | g0182 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02572 | hp2 | a0005 | c0005 | t0003 | g0102 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0287 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02622 | hp2 | a0003 | c0003 | t0001 | g0317 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02630 | hp1 | a0002 | c0008 | t0004 | g0008 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02630 | hp2 | a0002 | c0002 | t0005 | g0022 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0020 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02683 | hp2 | a0012 | c0013 | t0002 | g0092 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0220 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0294 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02723 | hp1 | a0008 | c0009 | t0002 | g0032 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02723 | hp2 | a0003 | c0003 | t0001 | g0315 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0311 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0098 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0091 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02809 | hp2 | a0009 | c0006 | t0001 | g0158 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0255 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02895 | hp1 | a0005 | c0005 | t0003 | g0100 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02895 | hp2 | a0003 | c0003 | t0001 | g0318 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0019 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02896 | hp2 | a0003 | c0003 | t0001 | g0205 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02897 | hp1 | a0005 | c0005 | t0003 | g0104 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02922 | hp1 | a0002 | c0002 | t0002 | g0034 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0257 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02965 | hp2 | a0014 | c0017 | t0001 | g0186 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02970 | hp1 | a0014 | c0017 | t0002 | g0031 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02970 | hp2 | a0002 | c0008 | t0004 | g0008 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02976 | hp1 | a0003 | c0003 | t0001 | g0235 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02976 | hp2 | a0006 | c0011 | t0001 | g0018 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0071 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03041 | hp1 | a0007 | c0010 | t0007 | g0236 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03041 | hp2 | a0003 | c0003 | t0001 | g0202 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0316 | AFR | MSL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03130 | hp2 | a0002 | c0020 | t0001 | g0244 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03139 | hp1 | a0009 | c0006 | t0001 | g0164 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03195 | hp1 | a0001 | c0015 | t0002 | g0028 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0035 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | MSL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03209 | hp2 | a0003 | c0003 | t0002 | g0030 | AFR | MSL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03225 | hp1 | a0011 | c0014 | t0003 | g0093 | AFR | MSL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03225 | hp2 | a0002 | c0008 | t0004 | g0021 | AFR | MSL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03239 | hp2 | a0012 | c0013 | t0001 | g0319 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03453 | hp1 | a0003 | c0003 | t0001 | g0189 | AFR | MSL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0096 | AFR | MSL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03486 | hp1 | a0021 | c0018 | t0001 | g0187 | AFR | MSL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0103 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03540 | hp2 | a0010 | c0007 | t0003 | g0097 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0105 | AFR | MSL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | STU | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | STU | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0247 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0048 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0073 | SAS | BEB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0259 | SAS | BEB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0313 | SAS | BEB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0063 | SAS | BEB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0191 | SAS | BEB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | BEB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | STU | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG04115 | hp2 | a0013 | c0016 | t0002 | g0065 | SAS | STU | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG04184 | hp1 | a0013 | c0016 | t0002 | g0083 | SAS | BEB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0253 | SAS | BEB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0029 | SAS | STU | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | STU | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18522 | hp1 | a0003 | c0003 | t0001 | g0204 | AFR | YRI | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18522 | hp2 | a0006 | c0011 | t0001 | g0018 | AFR | YRI | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | CHB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0179 | EAS | CHB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0221 | EAS | CHB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0249 | AFR | YRI | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18906 | hp2 | a0003 | c0003 | t0001 | g0180 | AFR | YRI | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0305 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18943 | hp2 | a0003 | c0003 | t0001 | g0169 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18944 | hp2 | a0003 | c0003 | t0001 | g0113 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18950 | hp2 | a0003 | c0003 | t0002 | g0060 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18954 | hp1 | a0003 | c0003 | t0001 | g0292 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0310 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18961 | hp2 | a0019 | c0019 | t0001 | g0245 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18962 | hp1 | a0003 | c0003 | t0001 | g0173 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18966 | hp1 | a0004 | c0004 | t0001 | g0132 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18967 | hp1 | a0003 | c0003 | t0001 | g0161 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18968 | hp2 | a0003 | c0003 | t0001 | g0167 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18969 | hp2 | a0003 | c0003 | t0001 | g0178 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18971 | hp2 | a0003 | c0003 | t0001 | g0114 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18973 | hp1 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18973 | hp2 | a0003 | c0003 | t0001 | g0239 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0295 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18975 | hp2 | a0003 | c0003 | t0001 | g0228 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18977 | hp2 | a0003 | c0003 | t0001 | g0160 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18980 | hp2 | a0003 | c0003 | t0001 | g0172 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18986 | hp1 | a0003 | c0003 | t0001 | g0171 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18990 | hp1 | a0003 | c0003 | t0001 | g0296 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0242 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0288 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0152 | AFR | LWK | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19030 | hp2 | a0010 | c0007 | t0006 | g0106 | AFR | LWK | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19043 | hp2 | a0007 | c0010 | t0001 | g0260 | AFR | LWK | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19056 | hp1 | a0010 | c0007 | t0001 | g0163 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0297 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19057 | hp1 | a0003 | c0003 | t0001 | g0300 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0299 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19064 | hp1 | a0003 | c0003 | t0001 | g0166 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19070 | hp2 | a0004 | c0004 | t0001 | g0127 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0240 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19083 | hp2 | a0003 | c0003 | t0001 | g0168 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | YRI | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA19240 | hp2 | a0003 | c0003 | t0001 | g0203 | AFR | YRI | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0284 | EUR | TSI | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0010 | EUR | TSI | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0280 | EUR | TSI | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0143 | EUR | TSI | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0020 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02109 | hp2 | a0006 | c0011 | t0001 | g0183 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02486 | hp1 | a0005 | c0005 | t0003 | g0099 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0130 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02559 | hp1 | a0003 | c0003 | t0001 | g0153 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG02559 | hp2 | a0002 | c0021 | t0001 | g0241 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03471 | hp1 | a0016 | c0025 | t0001 | g0159 | AFR | MSL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG03471 | hp2 | a0015 | c0012 | t0001 | g0177 | AFR | MSL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | USA | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| HG06807 | hp2 | a0009 | c0006 | t0001 | g0165 | AFR | USA | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18955 | hp1 | a0018 | c0022 | t0001 | g0123 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0211 | AFR | USA | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | USA | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | LWK | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | LWK | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0009 | REF | REF | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| homoSapiens_grch38 | hp1 | a0003 | c0003 | t0001 | g0170 | REF | REF | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:101402446
|
A | G | 9 | a0002a0005a0008others(6): Show | 133 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(130): Show |
missense_variant | MODERATE | c.1235T>C | p.Met412Thr | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/12 | 1764/2140 | 1235/1422 | 412/473 | chr2 | 101402446 | ||
| chr2:101402476
|
C | T | 2 | a0006a0011 | 5 | HG02109.hp2 HG02451.hp2 HG02976.hp2 others(2): Show |
missense_variant | MODERATE | c.1205G>A | p.Arg402Lys | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/12 | 1734/2140 | 1205/1422 | 402/473 | chr2 | 101402476 | ||
| chr2:101402546
|
G | T | 1 | a0012 | 2 | HG02683.hp2 HG03239.hp2 |
missense_variant | MODERATE | c.1135C>A | p.Pro379Thr | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/12 | 1664/2140 | 1135/1422 | 379/473 | chr2 | 101402546 | ||
| chr2:101402621
|
C | T | 2 | a0004a0020 | 7 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(4): Show |
missense_variant | MODERATE | c.1060G>A | p.Gly354Ser | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/12 | 1589/2140 | 1060/1422 | 354/473 | chr2 | 101402621 | ||
| chr2:101405989
|
GAGA | G | 1 | a0008 | 3 | HG01358.hp2 HG02572.hp1 HG02723.hp1 |
disruptive_inframe_deletion | MODERATE | c.879_881delTCT | p.Leu294del | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/12 | 1410/2140 | 879/1422 | 293/473 | chr2 | 101405989 | ||
| chr2:101412986
|
G | A | 1 | a0013 | 2 | HG04115.hp2 HG04184.hp1 |
missense_variant | MODERATE | c.647C>T | p.Ala216Val | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/12 | 1176/2140 | 647/1422 | 216/473 | chr2 | 101412986 | ||
| chr2:101414862
|
T | G | 1 | a0007 | 3 | HG02280.hp2 HG03041.hp1 NA19043.hp2 |
missense_variant | MODERATE | c.553A>C | p.Met185Leu | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/12 | 1082/2140 | 553/1422 | 185/473 | chr2 | 101414862 | ||
| chr2:101414889
|
G | C | 1 | a0018 | 1 | NA18955.hp1 | missense_variant | MODERATE | c.526C>G | p.Leu176Val | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/12 | 1055/2140 | 526/1422 | 176/473 | chr2 | 101414889 | ||
| chr2:101417573
|
C | T | 1 | a0019 | 1 | NA18961.hp2 | missense_variant | MODERATE | c.463G>A | p.Glu155Lys | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/12 | 992/2140 | 463/1422 | 155/473 | chr2 | 101417573 | ||
| chr2:101417662
|
T | C | 2 | a0014a0021 | 3 | HG02965.hp2 HG02970.hp1 HG03486.hp1 |
missense_variant | MODERATE | c.374A>G | p.His125Arg | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/12 | 903/2140 | 374/1422 | 125/473 | chr2 | 101417662 | ||
| chr2:101418897
|
G | A | 1 | a0005 | 5 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
missense_variant | MODERATE | c.305C>T | p.Pro102Leu | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 5/12 | 834/2140 | 305/1422 | 102/473 | chr2 | 101418897 | ||
| chr2:101422362
|
C | T | 2 | a0009a0015 | 5 | HG01243.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
missense_variant&splice_region_variant | MODERATE | c.183G>A | p.Met61Ile | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 3/12 | 712/2140 | 183/1422 | 61/473 | chr2 | 101422362 | ||
| chr2:101422385
|
C | A | 1 | a0020 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.160G>T | p.Ala54Ser | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 3/12 | 689/2140 | 160/1422 | 54/473 | chr2 | 101422385 | ||
| chr2:101422387
|
T | A | 16 | a0001a0002a0004others(13): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
missense_variant | MODERATE | c.158A>T | p.Gln53Leu | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 3/12 | 687/2140 | 158/1422 | 53/473 | chr2 | 101422387 | ||
| chr2:101466793
|
G | A | 3 | a0006a0016a0017 | 5 | HG01884.hp1 HG02109.hp2 HG02976.hp2 others(2): Show |
missense_variant | MODERATE | c.56C>T | p.Pro19Leu | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/12 | 585/2140 | 56/1422 | 19/473 | chr2 | 101466793 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:101397683
|
T | C | 1 | a0002c0020 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.1287A>G | p.Ala429Ala | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 12/12 | 1816/2140 | 1287/1422 | 429/473 | chr2 | 101397683 | ||
| chr2:101402448
|
G | A | 1 | a0002c0021 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.1233C>T | p.Ala411Ala | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/12 | 1762/2140 | 1233/1422 | 411/473 | chr2 | 101402448 | ||
| chr2:101402502
|
G | A | 1 | a0001c0015 | 2 | HG01884.hp2 HG03195.hp1 |
synonymous_variant | LOW | c.1179C>T | p.Pro393Pro | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/12 | 1708/2140 | 1179/1422 | 393/473 | chr2 | 101402502 | ||
| chr2:101410670
|
G | T | 1 | a0002c0008 | 3 | HG02630.hp1 HG02970.hp2 HG03225.hp2 |
synonymous_variant | LOW | c.762C>A | p.Leu254Leu | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/12 | 1291/2140 | 762/1422 | 254/473 | chr2 | 101410670 | ||
| chr2:101414902
|
T | C | 1 | a0021c0018 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.513A>G | p.Leu171Leu | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/12 | 1042/2140 | 513/1422 | 171/473 | chr2 | 101414902 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:101466863
|
C | T | 1 | a0007c0010t0007 | 1 | HG03041.hp1 | 5_prime_UTR_variant | MODIFIER | c.-15G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/12 | 15 | chr2 | 101466863 | |||||
| chr2:101474646
|
A | G | 1 | a0010c0007t0006 | 1 | NA19030.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-63T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/12 | chr2 | 101474646 | ||||||
| chr2:101474655
|
C | T | 6 | a0001c0001t0003a0001c0001t0008a0002c0002t0003others(3): Show | 14 | HG01167.hp2 HG01891.hp1 HG02257.hp1 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-72G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/12 | 7807 | chr2 | 101474655 | |||||
| chr2:101474758
|
C | T | 9 | a0001c0001t0002a0001c0015t0002a0002c0002t0002others(6): Show | 87 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(84): Show |
5_prime_UTR_variant | MODIFIER | c.-175G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/12 | 7910 | chr2 | 101474758 | |||||
| chr2:101474839
|
G | A | 1 | a0001c0001t0008 | 1 | HG01891.hp1 | 5_prime_UTR_variant | MODIFIER | c.-256C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/12 | 7991 | chr2 | 101474839 | |||||
| chr2:101474854
|
C | T | 1 | a0002c0002t0005 | 1 | HG02630.hp2 | 5_prime_UTR_variant | MODIFIER | c.-271G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/12 | 8006 | chr2 | 101474854 | |||||
| chr2:101475024
|
G | T | 2 | a0002c0002t0005a0002c0008t0004 | 4 | HG02630.hp1 HG02630.hp2 HG02970.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-441C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/12 | 8176 | chr2 | 101475024 | |||||
| chr2:101475063
|
TTGCTGTG others(3): Show |
T | 1 | a0002c0008t0004 | 3 | HG02630.hp1 HG02970.hp2 HG03225.hp2 |
5_prime_UTR_variant | MODIFIER | c.-490_-481delTCACAC others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/12 | 8216 | chr2 | 101475063 | |||||
| chr2:101475074
|
C | A | 1 | a0002c0008t0004 | 3 | HG02630.hp1 HG02970.hp2 HG03225.hp2 |
5_prime_UTR_variant | MODIFIER | c.-491G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/12 | 8226 | chr2 | 101475074 | |||||
| chr2:101475077
|
GGA | G | 1 | a0002c0008t0004 | 3 | HG02630.hp1 HG02970.hp2 HG03225.hp2 |
5_prime_UTR_variant | MODIFIER | c.-496_-495delTC | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/12 | 8230 | chr2 | 101475077 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:101397740
|
G | A | 1 | a0002c0002t0002g0091 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1246-16C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101397740 | ||||||
| chr2:101397818
|
C | T | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1246-94G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101397818 | ||||||
| chr2:101397900
|
C | T | 4 | a0002c0002t0001g0195a0002c0002t0001g0196a0002c0002t0002g0078others(1): Show | 4 | HG00673.hp2 HG02040.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.1246-176G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101397900 | ||||||
| chr2:101398099
|
C | T | 1 | a0001c0001t0002g0070 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1246-375G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101398099 | ||||||
| chr2:101398292
|
G | A | 99 | a0002c0002t0001g0003a0002c0002t0001g0006a0002c0002t0001g0007others(96): Show | 109 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.1246-568C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101398292 | ||||||
| chr2:101398331
|
T | C | 1 | a0003c0003t0001g0318 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1246-607A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101398331 | ||||||
| chr2:101398557
|
G | GA | 5 | a0002c0002t0001g0288a0005c0005t0003g0099a0005c0005t0003g0100others(2): Show | 5 | HG02486.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1246-834dupT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101398557 | ||||||
| chr2:101398959
|
T | C | 9 | a0001c0001t0001g0250a0001c0015t0001g0185a0001c0015t0002g0028others(6): Show | 9 | HG01884.hp2 HG02622.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1246-1235A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101398959 | ||||||
| chr2:101399290
|
A | G | 11 | a0001c0001t0002g0089a0003c0003t0002g0038a0003c0003t0002g0040others(8): Show | 11 | HG00642.hp2 HG00741.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.1246-1566T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101399290 | ||||||
| chr2:101399446
|
G | T | 3 | a0002c0002t0001g0266a0002c0002t0002g0062a0002c0002t0002g0063 | 3 | HG00140.hp1 HG01175.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1246-1722C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101399446 | ||||||
| chr2:101399486
|
G | T | 285 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(282): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.1246-1762C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101399486 | ||||||
| chr2:101399626
|
G | A | 3 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0263 | 5 | HG01123.hp1 HG01433.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.1246-1902C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101399626 | ||||||
| chr2:101399637
|
G | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0224 | 2 | HG04115.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1246-1913C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101399637 | ||||||
| chr2:101399739
|
C | A | 1 | a0001c0001t0001g0140 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1246-2015G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101399739 | ||||||
| chr2:101399780
|
G | T | 7 | a0001c0001t0001g0250a0003c0003t0001g0180a0003c0003t0001g0235others(4): Show | 7 | HG02622.hp2 HG02723.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1246-2056C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101399780 | ||||||
| chr2:101399781
|
G | A | 7 | a0001c0001t0001g0250a0003c0003t0001g0180a0003c0003t0001g0235others(4): Show | 7 | HG02622.hp2 HG02723.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1246-2057C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101399781 | ||||||
| chr2:101399782
|
G | GATAAGTT others(6): Show |
7 | a0001c0001t0001g0250a0003c0003t0001g0180a0003c0003t0001g0235others(4): Show | 7 | HG02622.hp2 HG02723.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1246-2059_1246-205 others(17): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101399782 | ||||||
| chr2:101400077
|
G | A | 2 | a0009c0006t0001g0164a0009c0006t0001g0165 | 2 | HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1246-2353C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101400077 | ||||||
| chr2:101400136
|
C | T | 1 | a0002c0002t0001g0207 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1245+2300G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101400136 | ||||||
| chr2:101400268
|
C | T | 1 | a0002c0002t0002g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1245+2168G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101400268 | ||||||
| chr2:101400324
|
G | A | 1 | a0001c0001t0003g0098 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1245+2112C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101400324 | ||||||
| chr2:101400499
|
T | C | 224 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0107others(221): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.1245+1937A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101400499 | ||||||
| chr2:101400634
|
C | G | 1 | a0002c0002t0001g0248 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1245+1802G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101400634 | ||||||
| chr2:101400639
|
C | T | 111 | a0002c0002t0001g0003a0002c0002t0001g0006a0002c0002t0001g0007others(108): Show | 121 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1245+1797G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101400639 | ||||||
| chr2:101400655
|
G | A | 3 | a0002c0002t0002g0034a0002c0002t0002g0035a0010c0007t0003g0097 | 3 | HG02922.hp1 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1245+1781C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101400655 | ||||||
| chr2:101400724
|
C | T | 220 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0107others(217): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1245+1712G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101400724 | ||||||
| chr2:101400904
|
C | T | 1 | a0002c0002t0002g0073 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1245+1532G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101400904 | ||||||
| chr2:101401027
|
C | A | 4 | a0006c0011t0001g0018a0006c0011t0001g0183a0011c0014t0001g0188others(1): Show | 5 | HG02109.hp2 HG02451.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1245+1409G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101401027 | ||||||
| chr2:101401134
|
T | C | 2 | a0012c0013t0001g0319a0012c0013t0002g0092 | 2 | HG02683.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1245+1302A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101401134 | ||||||
| chr2:101401253
|
C | T | 6 | a0001c0001t0002g0033a0006c0011t0001g0018a0006c0011t0001g0183others(3): Show | 7 | HG02109.hp2 HG02451.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1245+1183G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101401253 | ||||||
| chr2:101401292
|
C | T | 3 | a0008c0009t0001g0157a0008c0009t0001g0182a0008c0009t0002g0032 | 3 | HG01358.hp2 HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1245+1144G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101401292 | ||||||
| chr2:101401350
|
C | T | 89 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0107others(86): Show | 95 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.1245+1086G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101401350 | ||||||
| chr2:101401387
|
G | A | 1 | a0002c0002t0001g0213 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1245+1049C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101401387 | ||||||
| chr2:101401538
|
T | A | 8 | a0001c0001t0001g0250a0003c0003t0001g0153a0003c0003t0001g0180others(5): Show | 8 | HG02559.hp1 HG02622.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1245+898A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101401538 | ||||||
| chr2:101401580
|
T | C | 285 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(282): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.1245+856A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101401580 | ||||||
| chr2:101401581
|
A | T | 8 | a0001c0001t0001g0013a0001c0001t0001g0115a0001c0001t0001g0116others(5): Show | 9 | NA18944.hp1 NA18945.hp1 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.1245+855T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101401581 | ||||||
| chr2:101401788
|
T | G | 1 | a0002c0002t0001g0139 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1245+648A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101401788 | ||||||
| chr2:101401806
|
G | C | 1 | a0014c0017t0002g0031 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1245+630C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101401806 | ||||||
| chr2:101402158
|
A | T | 114 | a0002c0002t0001g0003a0002c0002t0001g0006a0002c0002t0001g0007others(111): Show | 124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.1245+278T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101402158 | ||||||
| chr2:101402416
|
G | A | 95 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0107others(92): Show | 102 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.1245+20C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101402416 | ||||||
| chr2:101402859
|
C | T | 1 | a0003c0003t0001g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.929-107G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101402859 | ||||||
| chr2:101402914
|
ATCAGTAG others(6): Show |
A | 1 | a0002c0002t0001g0242 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.929-175_929-163del others(13): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101402914 | ||||||
| chr2:101403136
|
C | T | 117 | a0002c0002t0001g0003a0002c0002t0001g0006a0002c0002t0001g0007others(114): Show | 127 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.929-384G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101403136 | ||||||
| chr2:101403184
|
A | G | 1 | a0002c0002t0001g0297 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.929-432T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101403184 | ||||||
| chr2:101403339
|
T | G | 89 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0107others(86): Show | 95 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.929-587A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101403339 | ||||||
| chr2:101403557
|
C | T | 1 | a0001c0001t0001g0017 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.929-805G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101403557 | ||||||
| chr2:101403568
|
C | T | 2 | a0001c0001t0001g0128a0001c0001t0001g0217 | 2 | HG00621.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.929-816G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101403568 | ||||||
| chr2:101403585
|
G | A | 9 | a0001c0001t0001g0149a0001c0001t0001g0181a0001c0001t0001g0197others(6): Show | 10 | HG00140.hp2 HG00642.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.929-833C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101403585 | ||||||
| chr2:101403611
|
C | G | 1 | a0003c0003t0002g0045 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.929-859G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101403611 | ||||||
| chr2:101403693
|
G | A | 285 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(282): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.929-941C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101403693 | ||||||
| chr2:101403741
|
C | T | 6 | a0001c0001t0002g0033a0006c0011t0001g0018a0006c0011t0001g0183others(3): Show | 7 | HG02109.hp2 HG02451.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.929-989G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101403741 | ||||||
| chr2:101403774
|
G | A | 2 | a0009c0006t0001g0164a0009c0006t0001g0165 | 2 | HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.929-1022C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101403774 | ||||||
| chr2:101403924
|
T | C | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | NA18980.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.929-1172A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101403924 | ||||||
| chr2:101404118
|
G | C | 1 | a0002c0002t0001g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.929-1366C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101404118 | ||||||
| chr2:101404230
|
C | T | 3 | a0008c0009t0001g0157a0008c0009t0001g0182a0008c0009t0002g0032 | 3 | HG01358.hp2 HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.929-1478G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101404230 | ||||||
| chr2:101404267
|
A | G | 1 | a0003c0003t0001g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.929-1515T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101404267 | ||||||
| chr2:101404308
|
A | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0016others(61): Show | 79 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.929-1556T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101404308 | ||||||
| chr2:101404444
|
T | G | 1 | a0008c0009t0002g0032 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.928+1499A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101404444 | ||||||
| chr2:101404582
|
C | A | 1 | a0001c0001t0001g0133 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.928+1361G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101404582 | ||||||
| chr2:101404592
|
AT | A | 6 | a0002c0002t0001g0139a0002c0002t0001g0240a0002c0002t0001g0282others(3): Show | 6 | HG01099.hp2 HG02922.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.928+1350delA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101404592 | ||||||
| chr2:101404602
|
T | C | 3 | a0002c0002t0001g0108a0002c0002t0001g0143a0002c0002t0001g0144 | 3 | HG00323.hp2 HG01261.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.928+1341A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101404602 | ||||||
| chr2:101404607
|
C | T | 2 | a0009c0006t0001g0164a0009c0006t0001g0165 | 2 | HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.928+1336G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101404607 | ||||||
| chr2:101404668
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.928+1275G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101404668 | ||||||
| chr2:101404673
|
T | C | 3 | a0008c0009t0001g0157a0008c0009t0001g0182a0008c0009t0002g0032 | 3 | HG01358.hp2 HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.928+1270A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101404673 | ||||||
| chr2:101404836
|
C | A | 20 | a0001c0001t0002g0089a0003c0003t0001g0113a0003c0003t0001g0114others(17): Show | 20 | HG00642.hp2 HG00673.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.928+1107G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101404836 | ||||||
| chr2:101405147
|
C | CT | 9 | a0001c0001t0002g0033a0001c0001t0002g0087a0002c0002t0001g0194others(6): Show | 10 | HG02109.hp2 HG02451.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.928+795dupA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101405147 | ||||||
| chr2:101405161
|
C | T | 116 | a0002c0002t0001g0003a0002c0002t0001g0006a0002c0002t0001g0007others(113): Show | 126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.928+782G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101405161 | ||||||
| chr2:101405172
|
G | A | 89 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0107others(86): Show | 95 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.928+771C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101405172 | ||||||
| chr2:101405205
|
G | T | 3 | a0008c0009t0001g0157a0008c0009t0001g0182a0008c0009t0002g0032 | 3 | HG01358.hp2 HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.928+738C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101405205 | ||||||
| chr2:101405220
|
C | T | 1 | a0002c0002t0001g0207 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.928+723G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101405220 | ||||||
| chr2:101405291
|
C | T | 1 | a0002c0002t0002g0023 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.928+652G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101405291 | ||||||
| chr2:101405299
|
A | T | 1 | a0003c0003t0001g0114 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.928+644T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101405299 | ||||||
| chr2:101405302
|
G | A | 3 | a0008c0009t0001g0157a0008c0009t0001g0182a0008c0009t0002g0032 | 3 | HG01358.hp2 HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.928+641C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101405302 | ||||||
| chr2:101405676
|
G | C | 1 | a0001c0001t0001g0311 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.928+267C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101405676 | ||||||
| chr2:101405759
|
T | C | 3 | a0008c0009t0001g0157a0008c0009t0001g0182a0008c0009t0002g0032 | 3 | HG01358.hp2 HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.928+184A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101405759 | ||||||
| chr2:101405856
|
T | C | 1 | a0002c0002t0001g0108 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.928+87A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101405856 | ||||||
| chr2:101406127
|
T | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0154a0007c0010t0001g0234others(2): Show | 8 | HG02055.hp1 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.814-70A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101406127 | ||||||
| chr2:101406247
|
C | T | 2 | a0001c0001t0002g0033a0014c0017t0002g0031 | 2 | HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.814-190G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101406247 | ||||||
| chr2:101406283
|
G | A | 3 | a0002c0002t0002g0034a0002c0002t0002g0035a0010c0007t0003g0097 | 3 | HG02922.hp1 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.814-226C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101406283 | ||||||
| chr2:101406325
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.814-268A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101406325 | ||||||
| chr2:101406339
|
AT | A | 15 | a0001c0001t0002g0033a0001c0001t0002g0037a0001c0015t0001g0185others(12): Show | 19 | HG00544.hp1 HG01884.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.814-283delA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101406339 | ||||||
| chr2:101406417
|
G | A | 4 | a0002c0002t0001g0152a0002c0002t0001g0304a0002c0008t0004g0008others(1): Show | 5 | HG01516.hp1 HG02630.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.814-360C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101406417 | ||||||
| chr2:101406508
|
G | A | 2 | a0002c0020t0001g0244a0002c0021t0001g0241 | 2 | HG02559.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.814-451C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101406508 | ||||||
| chr2:101406509
|
G | C | 1 | a0002c0002t0001g0221 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.814-452C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101406509 | ||||||
| chr2:101406510
|
G | C | 2 | a0001c0001t0001g0200a0001c0001t0001g0281 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.814-453C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101406510 | ||||||
| chr2:101406542
|
A | G | 1 | a0001c0001t0002g0049 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.814-485T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101406542 | ||||||
| chr2:101406604
|
G | A | 7 | a0001c0001t0001g0250a0003c0003t0001g0180a0003c0003t0001g0235others(4): Show | 7 | HG02622.hp2 HG02723.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.814-547C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101406604 | ||||||
| chr2:101406633
|
T | A | 1 | a0003c0003t0002g0042 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.814-576A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101406633 | ||||||
| chr2:101406861
|
G | C | 6 | a0002c0002t0001g0152a0002c0002t0001g0304a0002c0008t0004g0008others(3): Show | 7 | HG01516.hp1 HG02630.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.814-804C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101406861 | ||||||
| chr2:101406878
|
C | A | 4 | a0001c0001t0001g0298a0008c0009t0001g0157a0008c0009t0001g0182others(1): Show | 4 | HG01358.hp2 HG02572.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.814-821G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101406878 | ||||||
| chr2:101407418
|
A | G | 283 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(280): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.814-1361T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101407418 | ||||||
| chr2:101407460
|
C | A | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.814-1403G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101407460 | ||||||
| chr2:101407521
|
G | A | 1 | a0001c0001t0002g0080 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.814-1464C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101407521 | ||||||
| chr2:101407586
|
G | A | 2 | a0002c0002t0001g0212a0002c0002t0001g0259 | 2 | HG01106.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.814-1529C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101407586 | ||||||
| chr2:101407607
|
G | A | 2 | a0001c0015t0001g0185a0001c0015t0002g0028 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.814-1550C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101407607 | ||||||
| chr2:101407651
|
C | T | 1 | a0001c0001t0001g0125 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.814-1594G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101407651 | ||||||
| chr2:101407652
|
G | A | 6 | a0001c0001t0002g0033a0006c0011t0001g0018a0006c0011t0001g0183others(3): Show | 7 | HG02109.hp2 HG02451.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.814-1595C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101407652 | ||||||
| chr2:101407674
|
A | G | 1 | a0003c0003t0001g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.814-1617T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101407674 | ||||||
| chr2:101407688
|
T | C | 10 | a0002c0002t0001g0111a0002c0002t0001g0112a0002c0002t0001g0119others(7): Show | 10 | HG00558.hp2 NA18747.hp1 NA18941.hp1 others(7): Show |
intron_variant | MODIFIER | c.814-1631A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101407688 | ||||||
| chr2:101407695
|
T | TA | 7 | a0001c0001t0001g0298a0002c0002t0001g0208a0002c0020t0001g0244others(4): Show | 7 | HG01358.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.814-1639dupT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101407695 | ||||||
| chr2:101407696
|
A | T | 4 | a0002c0002t0001g0191a0002c0002t0001g0285a0002c0002t0001g0286others(1): Show | 4 | HG00323.hp1 HG00738.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.814-1639T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101407696 | ||||||
| chr2:101407707
|
C | A | 6 | a0001c0001t0001g0298a0002c0020t0001g0244a0002c0021t0001g0241others(3): Show | 6 | HG01358.hp2 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.814-1650G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101407707 | ||||||
| chr2:101407772
|
G | A | 3 | a0002c0002t0002g0034a0002c0002t0002g0035a0010c0007t0003g0097 | 3 | HG02922.hp1 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.814-1715C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101407772 | ||||||
| chr2:101407831
|
A | G | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0151others(2): Show | 7 | HG01257.hp1 HG01258.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.814-1774T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101407831 | ||||||
| chr2:101408212
|
G | A | 1 | a0001c0001t0002g0039 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.814-2155C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408212 | ||||||
| chr2:101408248
|
G | A | 1 | a0011c0014t0003g0093 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.814-2191C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408248 | ||||||
| chr2:101408267
|
C | T | 1 | a0002c0002t0001g0246 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.814-2210G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408267 | ||||||
| chr2:101408281
|
G | C | 285 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(282): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.814-2224C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408281 | ||||||
| chr2:101408295
|
C | T | 1 | a0002c0002t0001g0207 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.814-2238G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408295 | ||||||
| chr2:101408470
|
G | T | 1 | a0002c0002t0001g0263 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.813+2149C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408470 | ||||||
| chr2:101408482
|
CA | C | 106 | a0002c0002t0001g0003a0002c0002t0001g0006a0002c0002t0001g0007others(103): Show | 116 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.813+2136delT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408482 | ||||||
| chr2:101408494
|
A | C | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.813+2125T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408494 | ||||||
| chr2:101408495
|
C | A | 2 | a0002c0002t0002g0035a0010c0007t0006g0106 | 2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.813+2124G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408495 | ||||||
| chr2:101408495
|
C | CA | 5 | a0001c0001t0001g0131a0002c0002t0002g0034a0003c0003t0001g0168others(2): Show | 5 | HG01978.hp1 HG02922.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.813+2123dupT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408495 | ||||||
| chr2:101408551
|
A | G | 6 | a0001c0001t0003g0103a0003c0003t0001g0202a0003c0003t0001g0203others(3): Show | 6 | HG02809.hp2 HG02896.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.813+2068T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408551 | ||||||
| chr2:101408682
|
A | G | 1 | a0020c0023t0001g0142 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.813+1937T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408682 | ||||||
| chr2:101408821
|
C | T | 4 | a0006c0011t0001g0018a0006c0011t0001g0183a0011c0014t0001g0188others(1): Show | 5 | HG02109.hp2 HG02451.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.813+1798G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408821 | ||||||
| chr2:101408874
|
G | A | 6 | a0001c0001t0002g0033a0006c0011t0001g0018a0006c0011t0001g0183others(3): Show | 7 | HG02109.hp2 HG02451.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.813+1745C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408874 | ||||||
| chr2:101408962
|
C | T | 1 | a0002c0002t0001g0257 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.813+1657G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408962 | ||||||
| chr2:101408980
|
C | T | 2 | a0001c0015t0001g0185a0001c0015t0002g0028 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.813+1639G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408980 | ||||||
| chr2:101408984
|
G | A | 1 | a0002c0002t0001g0276 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.813+1635C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408984 | ||||||
| chr2:101409187
|
C | T | 1 | a0002c0002t0001g0254 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.813+1432G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101409187 | ||||||
| chr2:101409424
|
C | A | 67 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(64): Show | 83 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.813+1195G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101409424 | ||||||
| chr2:101409459
|
C | G | 7 | a0001c0001t0001g0250a0003c0003t0001g0180a0003c0003t0001g0235others(4): Show | 7 | HG02622.hp2 HG02723.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.813+1160G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101409459 | ||||||
| chr2:101409647
|
G | A | 1 | a0003c0003t0001g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.813+972C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101409647 | ||||||
| chr2:101410071
|
C | T | 285 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(282): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.813+548G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101410071 | ||||||
| chr2:101410085
|
T | C | 285 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(282): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.813+534A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101410085 | ||||||
| chr2:101410305
|
C | T | 2 | a0001c0001t0001g0269a0001c0001t0001g0307 | 2 | HG00099.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.813+314G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101410305 | ||||||
| chr2:101410351
|
C | T | 1 | a0002c0002t0001g0223 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.813+268G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101410351 | ||||||
| chr2:101410391
|
T | A | 1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.813+228A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101410391 | ||||||
| chr2:101410391
|
T | TCA | 8 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0136others(5): Show | 12 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.813+226_813+227dup others(2): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101410391 | ||||||
| chr2:101410391
|
T | TCACA | 78 | a0001c0001t0001g0013a0001c0001t0001g0107a0001c0001t0001g0109others(75): Show | 83 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.813+224_813+227dup others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101410391 | ||||||
| chr2:101410391
|
TCA | T | 70 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(67): Show | 83 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.813+226_813+227del others(2): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101410391 | ||||||
| chr2:101410394
|
C | CAT | 3 | a0002c0002t0002g0034a0002c0002t0002g0035a0010c0007t0003g0097 | 3 | HG02922.hp1 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.813+224_813+225ins others(2): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101410394 | ||||||
| chr2:101410417
|
A | ACACACAC others(3): Show |
1 | a0002c0002t0001g0282 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.813+201_813+202ins others(10): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101410417 | ||||||
| chr2:101410417
|
A | ACACACAC others(1): Show |
3 | a0002c0002t0001g0257a0002c0002t0001g0286a0002c0002t0002g0078 | 3 | HG00323.hp1 HG02040.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.813+201_813+202ins others(8): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101410417 | ||||||
| chr2:101410417
|
A | ACACACT | 7 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0144others(4): Show | 9 | HG00323.hp2 HG01123.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.813+201_813+202ins others(6): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101410417 | ||||||
| chr2:101410417
|
A | ACACT | 96 | a0002c0002t0001g0003a0002c0002t0001g0006a0002c0002t0001g0007others(93): Show | 104 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.813+201_813+202ins others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101410417 | ||||||
| chr2:101410417
|
A | ACT | 3 | a0002c0002t0001g0220a0015c0012t0001g0175a0015c0012t0001g0177 | 3 | HG01243.hp2 HG02698.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.813+200_813+201dup others(2): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101410417 | ||||||
| chr2:101410588
|
CT | C | 16 | a0001c0001t0001g0250a0001c0001t0001g0265a0001c0015t0001g0185others(13): Show | 16 | HG00323.hp1 HG00323.hp2 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.813+30delA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101410588 | ||||||
| chr2:101410714
|
C | G | 1 | a0001c0001t0003g0103 | 1 | HG03516.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.719-1G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101410714 | ||||||
| chr2:101410747
|
G | T | 1 | a0003c0003t0001g0113 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.719-34C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101410747 | ||||||
| chr2:101411051
|
C | G | 2 | a0002c0002t0001g0019a0002c0002t0001g0263 | 3 | HG01433.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.719-338G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101411051 | ||||||
| chr2:101411334
|
G | A | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | NA18980.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.719-621C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101411334 | ||||||
| chr2:101411437
|
G | A | 1 | a0002c0002t0001g0199 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.719-724C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101411437 | ||||||
| chr2:101411498
|
G | A | 7 | a0001c0001t0001g0250a0003c0003t0001g0180a0003c0003t0001g0235others(4): Show | 7 | HG02622.hp2 HG02723.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.719-785C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101411498 | ||||||
| chr2:101411503
|
A | AG | 272 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(269): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.719-791dupC | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101411503 | ||||||
| chr2:101411508
|
G | GT | 4 | a0006c0011t0001g0018a0006c0011t0001g0183a0011c0014t0001g0188others(1): Show | 5 | HG02109.hp2 HG02451.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.719-796dupA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101411508 | ||||||
| chr2:101411601
|
T | A | 1 | a0003c0003t0001g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.719-888A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101411601 | ||||||
| chr2:101411670
|
A | G | 7 | a0001c0001t0001g0298a0002c0020t0001g0244a0002c0021t0001g0241others(4): Show | 7 | HG01358.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.719-957T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101411670 | ||||||
| chr2:101411772
|
G | A | 6 | a0001c0001t0002g0033a0006c0011t0001g0018a0006c0011t0001g0183others(3): Show | 7 | HG02109.hp2 HG02451.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.719-1059C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101411772 | ||||||
| chr2:101411946
|
G | A | 1 | a0001c0001t0002g0064 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.718+969C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101411946 | ||||||
| chr2:101412006
|
A | G | 2 | a0001c0015t0001g0185a0001c0015t0002g0028 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.718+909T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101412006 | ||||||
| chr2:101412050
|
T | A | 2 | a0002c0002t0001g0019a0002c0002t0001g0263 | 3 | HG01433.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.718+865A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101412050 | ||||||
| chr2:101412084
|
T | C | 1 | a0001c0001t0001g0201 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.718+831A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101412084 | ||||||
| chr2:101412125
|
T | C | 1 | a0002c0002t0003g0095 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.718+790A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101412125 | ||||||
| chr2:101412168
|
C | T | 3 | a0002c0002t0002g0034a0002c0002t0002g0035a0010c0007t0003g0097 | 3 | HG02922.hp1 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.718+747G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101412168 | ||||||
| chr2:101412196
|
C | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0150a0016c0025t0001g0159 | 5 | HG02809.hp1 HG03098.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.718+719G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101412196 | ||||||
| chr2:101412241
|
C | T | 4 | a0006c0011t0001g0018a0006c0011t0001g0183a0011c0014t0001g0188others(1): Show | 5 | HG02109.hp2 HG02451.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.718+674G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101412241 | ||||||
| chr2:101412466
|
A | G | 84 | a0001c0001t0001g0013a0001c0001t0001g0107a0001c0001t0001g0109others(81): Show | 89 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.718+449T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101412466 | ||||||
| chr2:101412811
|
T | C | 91 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0015others(88): Show | 100 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.718+104A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101412811 | ||||||
| chr2:101412812
|
A | G | 6 | a0001c0001t0001g0015a0001c0001t0001g0136a0002c0002t0001g0152others(3): Show | 8 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.718+103T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101412812 | ||||||
| chr2:101413081
|
A | G | 3 | a0002c0002t0002g0034a0002c0002t0002g0035a0010c0007t0003g0097 | 3 | HG02922.hp1 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.562-10T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101413081 | ||||||
| chr2:101413086
|
G | A | 55 | a0001c0001t0001g0107a0001c0001t0001g0134a0001c0001t0001g0135others(52): Show | 59 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.562-15C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101413086 | ||||||
| chr2:101413184
|
T | C | 61 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(58): Show | 68 | HG00140.hp2 HG00621.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.562-113A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101413184 | ||||||
| chr2:101413277
|
G | A | 165 | a0001c0001t0001g0107a0001c0001t0001g0134a0001c0001t0001g0135others(162): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.562-206C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101413277 | ||||||
| chr2:101413367
|
G | A | 5 | a0003c0003t0001g0180a0003c0003t0001g0235a0003c0003t0001g0317others(2): Show | 5 | HG02622.hp2 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.562-296C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101413367 | ||||||
| chr2:101413532
|
G | C | 3 | a0002c0002t0002g0034a0002c0002t0002g0035a0010c0007t0003g0097 | 3 | HG02922.hp1 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.562-461C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101413532 | ||||||
| chr2:101413562
|
GCCTGGGA others(4): Show |
G | 1 | a0011c0014t0003g0093 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.562-502_562-492del others(11): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101413562 | ||||||
| chr2:101413623
|
CT | C | 2 | a0002c0008t0004g0008a0002c0008t0004g0021 | 3 | HG02630.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.562-553delA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101413623 | ||||||
| chr2:101413763
|
C | T | 1 | a0003c0003t0001g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.562-692G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101413763 | ||||||
| chr2:101413864
|
T | G | 282 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(279): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.562-793A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101413864 | ||||||
| chr2:101413909
|
T | C | 1 | a0002c0002t0002g0088 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.562-838A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101413909 | ||||||
| chr2:101414028
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0154 | 5 | HG02055.hp1 HG02258.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.561+826G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101414028 | ||||||
| chr2:101414440
|
A | AT | 207 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0107others(204): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.561+413dupA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101414440 | ||||||
| chr2:101414440
|
A | ATT | 69 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(66): Show | 80 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.561+412_561+413dup others(2): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101414440 | ||||||
| chr2:101414543
|
C | T | 7 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0151others(4): Show | 9 | HG01257.hp1 HG01258.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.561+311G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101414543 | ||||||
| chr2:101414616
|
C | T | 1 | a0011c0014t0003g0093 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.561+238G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101414616 | ||||||
| chr2:101414714
|
A | G | 280 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(277): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.561+140T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101414714 | ||||||
| chr2:101415027
|
C | G | 165 | a0001c0001t0001g0107a0001c0001t0001g0134a0001c0001t0001g0135others(162): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.503-115G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415027 | ||||||
| chr2:101415088
|
G | A | 1 | a0021c0018t0001g0187 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.503-176C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415088 | ||||||
| chr2:101415147
|
G | A | 2 | a0001c0001t0002g0049a0002c0002t0002g0029 | 2 | HG03239.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.503-235C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415147 | ||||||
| chr2:101415218
|
G | A | 164 | a0001c0001t0001g0107a0001c0001t0001g0134a0001c0001t0001g0135others(161): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.503-306C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415218 | ||||||
| chr2:101415275
|
G | A | 2 | a0002c0008t0004g0008a0002c0008t0004g0021 | 3 | HG02630.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.503-363C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415275 | ||||||
| chr2:101415353
|
T | C | 279 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(276): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.503-441A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415353 | ||||||
| chr2:101415365
|
C | A | 3 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0046 | 3 | HG01243.hp1 HG01975.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.503-453G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415365 | ||||||
| chr2:101415515
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0154 | 5 | HG02055.hp1 HG02258.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.503-603C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415515 | ||||||
| chr2:101415563
|
C | G | 1 | a0007c0010t0001g0234 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.503-651G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415563 | ||||||
| chr2:101415620
|
CGCAT | C | 40 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(37): Show | 45 | HG00140.hp2 HG00642.hp1 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.503-712_503-709del others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415620 | ||||||
| chr2:101415621
|
GCATT | G | 228 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0015others(225): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.503-713_503-710del others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415621 | ||||||
| chr2:101415625
|
T | A | 40 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(37): Show | 45 | HG00140.hp2 HG00642.hp1 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.503-713A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415625 | ||||||
| chr2:101415709
|
C | T | 158 | a0001c0001t0001g0107a0001c0001t0001g0134a0001c0001t0001g0135others(155): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.503-797G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415709 | ||||||
| chr2:101415771
|
C | G | 3 | a0002c0002t0001g0152a0006c0011t0001g0018a0006c0011t0001g0183 | 4 | HG02109.hp2 HG02976.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.503-859G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415771 | ||||||
| chr2:101415833
|
G | C | 2 | a0001c0001t0001g0002a0001c0001t0001g0154 | 5 | HG02055.hp1 HG02258.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.503-921C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415833 | ||||||
| chr2:101415973
|
C | A | 1 | a0002c0002t0001g0209 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.503-1061G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415973 | ||||||
| chr2:101415980
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.503-1068A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415980 | ||||||
| chr2:101415994
|
C | T | 25 | a0001c0001t0001g0013a0001c0001t0001g0109a0001c0001t0001g0115others(22): Show | 26 | HG00621.hp1 HG02040.hp2 HG02056.hp2 others(23): Show |
intron_variant | MODIFIER | c.503-1082G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415994 | ||||||
| chr2:101416065
|
G | A | 1 | a0010c0007t0003g0097 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.503-1153C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101416065 | ||||||
| chr2:101416074
|
T | C | 7 | a0001c0001t0001g0250a0003c0003t0001g0180a0003c0003t0001g0235others(4): Show | 7 | HG02622.hp2 HG02723.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.503-1162A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101416074 | ||||||
| chr2:101416149
|
T | C | 29 | a0001c0001t0001g0015a0001c0001t0001g0118a0001c0001t0001g0121others(26): Show | 38 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.503-1237A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101416149 | ||||||
| chr2:101416198
|
G | C | 1 | a0002c0002t0001g0302 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.503-1286C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101416198 | ||||||
| chr2:101416199
|
G | C | 25 | a0001c0001t0001g0131a0001c0001t0001g0149a0001c0001t0001g0181others(22): Show | 26 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.503-1287C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101416199 | ||||||
| chr2:101416270
|
T | G | 3 | a0007c0010t0001g0234a0007c0010t0001g0260a0007c0010t0007g0236 | 3 | HG02280.hp2 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.502+1264A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101416270 | ||||||
| chr2:101416329
|
T | C | 65 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0015others(62): Show | 71 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.502+1205A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101416329 | ||||||
| chr2:101416441
|
C | T | 1 | a0002c0002t0001g0199 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.502+1093G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101416441 | ||||||
| chr2:101416523
|
G | A | 266 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(263): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.502+1011C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101416523 | ||||||
| chr2:101416528
|
T | C | 8 | a0001c0001t0001g0005a0001c0001t0001g0150a0001c0001t0001g0298others(5): Show | 10 | HG01358.hp2 HG02572.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.502+1006A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101416528 | ||||||
| chr2:101416604
|
G | C | 1 | a0002c0002t0001g0156 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.502+930C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101416604 | ||||||
| chr2:101416816
|
G | A | 2 | a0014c0017t0001g0186a0014c0017t0002g0031 | 2 | HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.502+718C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101416816 | ||||||
| chr2:101416817
|
C | T | 2 | a0002c0020t0001g0244a0002c0021t0001g0241 | 2 | HG02559.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.502+717G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101416817 | ||||||
| chr2:101416958
|
G | A | 269 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(266): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.502+576C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101416958 | ||||||
| chr2:101417311
|
C | T | 7 | a0001c0001t0001g0125a0001c0001t0002g0001a0001c0001t0002g0039others(4): Show | 12 | HG00639.hp2 HG00735.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.502+223G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101417311 | ||||||
| chr2:101417389
|
T | TA | 289 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(286): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.502+144_502+145ins others(1): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101417389 | ||||||
| chr2:101417400
|
C | A | 1 | a0001c0001t0003g0103 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.502+134G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101417400 | ||||||
| chr2:101417405
|
T | C | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(268): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.502+129A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101417405 | ||||||
| chr2:101417759
|
G | T | 7 | a0001c0001t0001g0125a0001c0001t0002g0001a0001c0001t0002g0039others(4): Show | 12 | HG00639.hp2 HG00735.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.352-75C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 5/11 | chr2 | 101417759 | ||||||
| chr2:101417804
|
T | C | 1 | a0001c0001t0002g0033 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.352-120A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 5/11 | chr2 | 101417804 | ||||||
| chr2:101417914
|
G | A | 1 | a0011c0014t0003g0093 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.352-230C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 5/11 | chr2 | 101417914 | ||||||
| chr2:101417956
|
T | C | 7 | a0001c0001t0001g0125a0001c0001t0002g0001a0001c0001t0002g0039others(4): Show | 12 | HG00639.hp2 HG00735.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.352-272A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 5/11 | chr2 | 101417956 | ||||||
| chr2:101417972
|
C | T | 8 | a0001c0001t0001g0250a0003c0003t0001g0180a0003c0003t0001g0189others(5): Show | 8 | HG02622.hp2 HG02723.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.352-288G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 5/11 | chr2 | 101417972 | ||||||
| chr2:101417983
|
C | T | 265 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(262): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.352-299G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 5/11 | chr2 | 101417983 | ||||||
| chr2:101418032
|
G | T | 3 | a0014c0017t0001g0186a0014c0017t0002g0031a0021c0018t0001g0187 | 3 | HG02965.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.352-348C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 5/11 | chr2 | 101418032 | ||||||
| chr2:101418061
|
T | C | 6 | a0001c0001t0001g0013a0001c0001t0001g0115a0001c0001t0001g0120others(3): Show | 7 | NA18944.hp1 NA18961.hp1 NA18988.hp1 others(4): Show |
intron_variant | MODIFIER | c.352-377A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 5/11 | chr2 | 101418061 | ||||||
| chr2:101418098
|
G | C | 1 | a0011c0014t0003g0093 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.352-414C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 5/11 | chr2 | 101418098 | ||||||
| chr2:101418234
|
A | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0136a0001c0001t0001g0251others(3): Show | 8 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.352-550T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 5/11 | chr2 | 101418234 | ||||||
| chr2:101418714
|
T | G | 1 | a0003c0003t0002g0040 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.351+137A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 5/11 | chr2 | 101418714 | ||||||
| chr2:101418730
|
C | T | 212 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0107others(209): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.351+121G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 5/11 | chr2 | 101418730 | ||||||
| chr2:101418735
|
A | C | 6 | a0003c0003t0001g0202a0003c0003t0001g0203a0003c0003t0001g0204others(3): Show | 6 | HG02896.hp2 HG03041.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.351+116T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 5/11 | chr2 | 101418735 | ||||||
| chr2:101419060
|
G | A | 3 | a0003c0003t0001g0160a0003c0003t0001g0172a0003c0003t0002g0060 | 3 | NA18950.hp2 NA18977.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.238-96C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101419060 | ||||||
| chr2:101419298
|
G | T | 169 | a0001c0001t0001g0107a0001c0001t0001g0131a0001c0001t0001g0134others(166): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.238-334C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101419298 | ||||||
| chr2:101419610
|
G | A | 1 | a0002c0002t0001g0139 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.238-646C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101419610 | ||||||
| chr2:101419750
|
G | A | 1 | a0001c0001t0002g0075 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.238-786C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101419750 | ||||||
| chr2:101419801
|
T | C | 1 | a0003c0003t0001g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.238-837A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101419801 | ||||||
| chr2:101419887
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.238-923C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101419887 | ||||||
| chr2:101419922
|
C | T | 1 | a0011c0014t0001g0188 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.238-958G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101419922 | ||||||
| chr2:101419993
|
C | T | 59 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0140others(56): Show | 63 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.238-1029G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101419993 | ||||||
| chr2:101420168
|
G | C | 263 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(260): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.238-1204C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101420168 | ||||||
| chr2:101420437
|
G | T | 1 | a0002c0002t0001g0257 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.237+1287C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101420437 | ||||||
| chr2:101420474
|
G | C | 1 | a0001c0001t0001g0298 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.237+1250C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101420474 | ||||||
| chr2:101420552
|
C | A | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.237+1172G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101420552 | ||||||
| chr2:101420554
|
C | A | 253 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(250): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.237+1170G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101420554 | ||||||
| chr2:101420554
|
C | CA | 13 | a0001c0001t0001g0015a0001c0001t0001g0125a0001c0001t0001g0136others(10): Show | 20 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.237+1169dupT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101420554 | ||||||
| chr2:101420681
|
T | C | 1 | a0002c0002t0001g0259 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.237+1043A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101420681 | ||||||
| chr2:101421117
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0154 | 5 | HG02055.hp1 HG02258.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.237+607G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101421117 | ||||||
| chr2:101421316
|
C | T | 1 | a0007c0010t0007g0236 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.237+408G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101421316 | ||||||
| chr2:101421385
|
C | T | 3 | a0003c0003t0001g0169a0003c0003t0001g0171a0003c0003t0001g0173 | 3 | NA18943.hp2 NA18962.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.237+339G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101421385 | ||||||
| chr2:101421392
|
A | G | 7 | a0001c0001t0001g0125a0001c0001t0002g0001a0001c0001t0002g0039others(4): Show | 12 | HG00639.hp2 HG00735.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.237+332T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101421392 | ||||||
| chr2:101421393
|
T | C | 64 | a0001c0001t0001g0107a0001c0001t0001g0134a0001c0001t0001g0135others(61): Show | 68 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.237+331A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101421393 | ||||||
| chr2:101421508
|
T | C | 3 | a0003c0003t0002g0042a0003c0003t0002g0045a0003c0003t0002g0053 | 3 | HG01433.hp2 HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.237+216A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101421508 | ||||||
| chr2:101421866
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.184-89G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 3/11 | chr2 | 101421866 | ||||||
| chr2:101422048
|
C | T | 1 | a0003c0003t0001g0228 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.184-271G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 3/11 | chr2 | 101422048 | ||||||
| chr2:101422109
|
C | G | 10 | a0003c0003t0002g0038a0003c0003t0002g0040a0003c0003t0002g0042others(7): Show | 10 | HG00642.hp2 HG00741.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.183+253G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 3/11 | chr2 | 101422109 | ||||||
| chr2:101422474
|
T | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0109others(36): Show | 45 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(42): Show |
splice_acceptor_variant&intron_variant | HIGH | c.73-2A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101422474 | ||||||
| chr2:101422669
|
A | G | 268 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(265): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.73-197T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101422669 | ||||||
| chr2:101422670
|
T | C | 1 | a0010c0007t0003g0097 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.73-198A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101422670 | ||||||
| chr2:101423007
|
C | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | NA18945.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.73-535G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423007 | ||||||
| chr2:101423028
|
C | A | 1 | a0002c0002t0001g0223 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.73-556G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423028 | ||||||
| chr2:101423028
|
C | T | 2 | a0001c0001t0001g0281a0002c0002t0001g0198 | 2 | HG01070.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.73-556G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423028 | ||||||
| chr2:101423046
|
T | C | 39 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0109others(36): Show | 45 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.73-574A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423046 | ||||||
| chr2:101423115
|
G | A | 1 | a0001c0001t0003g0103 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.73-643C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423115 | ||||||
| chr2:101423195
|
T | C | 1 | a0001c0001t0002g0033 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.73-723A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423195 | ||||||
| chr2:101423214
|
C | T | 7 | a0003c0003t0001g0189a0003c0003t0001g0202a0003c0003t0001g0203others(4): Show | 7 | HG02896.hp2 HG03041.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.73-742G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423214 | ||||||
| chr2:101423259
|
C | CA | 7 | a0001c0001t0001g0224a0001c0001t0002g0050a0001c0001t0002g0052others(4): Show | 7 | HG01358.hp2 HG01884.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.73-788dupT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423259 | ||||||
| chr2:101423259
|
C | CAA | 71 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0125others(68): Show | 82 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.73-789_73-788dupTT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423259 | ||||||
| chr2:101423283
|
A | G | 41 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(38): Show | 46 | HG00140.hp2 HG00642.hp1 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.73-811T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423283 | ||||||
| chr2:101423317
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.73-845C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423317 | ||||||
| chr2:101423483
|
C | T | 1 | a0001c0001t0002g0070 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.73-1011G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423483 | ||||||
| chr2:101423491
|
A | G | 1 | a0001c0001t0001g0271 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.73-1019T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423491 | ||||||
| chr2:101423540
|
C | T | 1 | a0003c0003t0001g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-1068G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423540 | ||||||
| chr2:101423571
|
C | T | 1 | a0001c0001t0001g0313 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.73-1099G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423571 | ||||||
| chr2:101423589
|
C | T | 3 | a0006c0011t0001g0018a0006c0011t0001g0183a0017c0024t0001g0184 | 4 | HG01884.hp1 HG02109.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.73-1117G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423589 | ||||||
| chr2:101423590
|
G | A | 1 | a0003c0003t0001g0204 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.73-1118C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423590 | ||||||
| chr2:101423821
|
A | G | 111 | a0001c0001t0001g0013a0001c0001t0001g0115a0001c0001t0001g0120others(108): Show | 122 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.73-1349T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423821 | ||||||
| chr2:101423849
|
C | T | 1 | a0021c0018t0001g0187 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.73-1377G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423849 | ||||||
| chr2:101423881
|
G | A | 1 | a0002c0002t0002g0029 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.73-1409C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423881 | ||||||
| chr2:101423888
|
A | G | 269 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(266): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.73-1416T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423888 | ||||||
| chr2:101424001
|
C | G | 5 | a0002c0002t0001g0195a0002c0002t0001g0196a0002c0002t0001g0270others(2): Show | 5 | HG00099.hp1 HG00673.hp2 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-1529G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101424001 | ||||||
| chr2:101424134
|
C | T | 1 | a0002c0002t0001g0302 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.73-1662G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101424134 | ||||||
| chr2:101424197
|
T | C | 1 | a0003c0003t0002g0030 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.73-1725A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101424197 | ||||||
| chr2:101424324
|
T | C | 1 | a0003c0003t0001g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-1852A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101424324 | ||||||
| chr2:101424405
|
T | C | 13 | a0001c0001t0001g0015a0001c0001t0001g0125a0001c0001t0001g0136others(10): Show | 20 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.73-1933A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101424405 | ||||||
| chr2:101424533
|
C | T | 287 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(284): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.73-2061G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101424533 | ||||||
| chr2:101424644
|
A | G | 8 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0124others(5): Show | 8 | HG00621.hp1 HG02083.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.73-2172T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101424644 | ||||||
| chr2:101424709
|
C | T | 1 | a0002c0002t0001g0240 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.73-2237G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101424709 | ||||||
| chr2:101424755
|
C | T | 1 | a0001c0001t0002g0052 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.73-2283G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101424755 | ||||||
| chr2:101424794
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.73-2322G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101424794 | ||||||
| chr2:101424808
|
T | C | 13 | a0001c0001t0001g0015a0001c0001t0001g0125a0001c0001t0001g0136others(10): Show | 20 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.73-2336A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101424808 | ||||||
| chr2:101424873
|
G | A | 3 | a0001c0001t0002g0075a0002c0002t0002g0076a0002c0002t0002g0084 | 3 | HG00741.hp1 HG01255.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.73-2401C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101424873 | ||||||
| chr2:101424955
|
T | C | 1 | a0002c0002t0001g0253 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.73-2483A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101424955 | ||||||
| chr2:101424989
|
C | T | 1 | a0001c0015t0002g0028 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.73-2517G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101424989 | ||||||
| chr2:101425019
|
A | C | 41 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(38): Show | 46 | HG00140.hp2 HG00642.hp1 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.73-2547T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101425019 | ||||||
| chr2:101425039
|
G | GA | 260 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(257): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.73-2568dupT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101425039 | ||||||
| chr2:101425060
|
T | G | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.73-2588A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101425060 | ||||||
| chr2:101425638
|
A | AT | 288 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(285): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.73-3167dupA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101425638 | ||||||
| chr2:101425762
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.73-3290G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101425762 | ||||||
| chr2:101425829
|
G | A | 1 | a0001c0001t0002g0089 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.73-3357C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101425829 | ||||||
| chr2:101425836
|
G | A | 42 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(39): Show | 47 | HG00140.hp2 HG00642.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.73-3364C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101425836 | ||||||
| chr2:101425990
|
C | T | 6 | a0003c0003t0001g0180a0003c0003t0001g0235a0003c0003t0001g0315others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.73-3518G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101425990 | ||||||
| chr2:101426093
|
C | T | 3 | a0007c0010t0001g0234a0007c0010t0001g0260a0007c0010t0007g0236 | 3 | HG02280.hp2 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.73-3621G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101426093 | ||||||
| chr2:101426146
|
G | A | 2 | a0014c0017t0001g0186a0014c0017t0002g0031 | 2 | HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.73-3674C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101426146 | ||||||
| chr2:101426175
|
T | C | 4 | a0001c0001t0002g0068a0002c0002t0001g0110a0002c0002t0001g0138others(1): Show | 4 | NA18939.hp1 NA18973.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-3703A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101426175 | ||||||
| chr2:101426251
|
G | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0136a0001c0001t0001g0251others(3): Show | 8 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.73-3779C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101426251 | ||||||
| chr2:101426253
|
AC | A | 6 | a0003c0003t0001g0180a0003c0003t0001g0235a0003c0003t0001g0315others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.73-3782delG | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101426253 | ||||||
| chr2:101426319
|
G | C | 1 | a0016c0025t0001g0159 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.73-3847C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101426319 | ||||||
| chr2:101426367
|
A | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0150 | 4 | HG02809.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.73-3895T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101426367 | ||||||
| chr2:101426496
|
G | A | 2 | a0014c0017t0001g0186a0014c0017t0002g0031 | 2 | HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.73-4024C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101426496 | ||||||
| chr2:101426566
|
T | C | 1 | a0002c0002t0001g0221 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.73-4094A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101426566 | ||||||
| chr2:101426647
|
T | C | 49 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0109others(46): Show | 60 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.73-4175A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101426647 | ||||||
| chr2:101426750
|
C | A | 269 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(266): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.73-4278G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101426750 | ||||||
| chr2:101426841
|
A | C | 265 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(262): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.73-4369T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101426841 | ||||||
| chr2:101426964
|
T | C | 2 | a0003c0003t0001g0169a0003c0003t0001g0171 | 2 | NA18943.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.73-4492A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101426964 | ||||||
| chr2:101427039
|
G | A | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | NA18980.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.73-4567C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101427039 | ||||||
| chr2:101427134
|
T | C | 265 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(262): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.73-4662A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101427134 | ||||||
| chr2:101427179
|
C | T | 1 | a0001c0001t0003g0103 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.73-4707G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101427179 | ||||||
| chr2:101427220
|
T | C | 6 | a0003c0003t0001g0189a0009c0006t0001g0158a0009c0006t0001g0164others(3): Show | 6 | HG01243.hp2 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.73-4748A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101427220 | ||||||
| chr2:101427316
|
C | T | 2 | a0001c0001t0001g0149a0001c0001t0002g0049 | 2 | HG00140.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.73-4844G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101427316 | ||||||
| chr2:101427363
|
A | G | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.73-4891T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101427363 | ||||||
| chr2:101427421
|
G | A | 1 | a0002c0002t0001g0192 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.73-4949C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101427421 | ||||||
| chr2:101427499
|
G | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0154a0016c0025t0001g0159 | 6 | HG02055.hp1 HG02258.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.73-5027C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101427499 | ||||||
| chr2:101427581
|
G | A | 2 | a0001c0015t0001g0185a0001c0015t0002g0028 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.73-5109C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101427581 | ||||||
| chr2:101427651
|
C | T | 37 | a0001c0001t0001g0109a0001c0001t0001g0118a0001c0001t0001g0121others(34): Show | 39 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.73-5179G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101427651 | ||||||
| chr2:101427680
|
A | C | 1 | a0005c0005t0003g0099 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.73-5208T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101427680 | ||||||
| chr2:101427796
|
C | T | 4 | a0002c0002t0001g0152a0006c0011t0001g0018a0006c0011t0001g0183others(1): Show | 5 | HG01884.hp1 HG02109.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.73-5324G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101427796 | ||||||
| chr2:101427889
|
C | T | 1 | a0001c0001t0001g0237 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.73-5417G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101427889 | ||||||
| chr2:101428061
|
A | AG | 203 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(200): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.73-5590dupC | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101428061 | ||||||
| chr2:101428062
|
G | GGC | 7 | a0003c0003t0001g0189a0009c0006t0001g0158a0009c0006t0001g0164others(4): Show | 7 | HG01243.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.73-5591_73-5590ins others(2): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101428062 | ||||||
| chr2:101428065
|
G | A | 1 | a0003c0003t0002g0030 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.73-5593C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101428065 | ||||||
| chr2:101428185
|
T | A | 3 | a0007c0010t0001g0234a0007c0010t0001g0260a0007c0010t0007g0236 | 3 | HG02280.hp2 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.73-5713A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101428185 | ||||||
| chr2:101428393
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.73-5921C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101428393 | ||||||
| chr2:101428495
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.73-6023T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101428495 | ||||||
| chr2:101428677
|
C | T | 1 | a0003c0003t0001g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-6205G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101428677 | ||||||
| chr2:101428768
|
A | T | 3 | a0002c0002t0001g0270a0002c0002t0002g0076a0002c0002t0002g0084 | 3 | HG00099.hp1 HG00741.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.73-6296T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101428768 | ||||||
| chr2:101428866
|
C | T | 115 | a0001c0001t0001g0015a0001c0001t0001g0136a0001c0001t0001g0190others(112): Show | 122 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.73-6394G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101428866 | ||||||
| chr2:101428884
|
G | A | 5 | a0009c0006t0001g0158a0009c0006t0001g0164a0009c0006t0001g0165others(2): Show | 5 | HG01243.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-6412C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101428884 | ||||||
| chr2:101428888
|
G | A | 2 | a0003c0003t0001g0315a0014c0017t0002g0031 | 2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.73-6416C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101428888 | ||||||
| chr2:101429053
|
A | G | 1 | a0002c0002t0001g0266 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.73-6581T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101429053 | ||||||
| chr2:101429057
|
A | G | 1 | a0002c0002t0002g0081 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.73-6585T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101429057 | ||||||
| chr2:101429145
|
C | T | 43 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(40): Show | 49 | HG00140.hp2 HG00642.hp1 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.73-6673G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101429145 | ||||||
| chr2:101429247
|
C | T | 310 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(307): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.73-6775G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101429247 | ||||||
| chr2:101429319
|
G | A | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.73-6847C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101429319 | ||||||
| chr2:101429920
|
C | T | 183 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(180): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-7448G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101429920 | ||||||
| chr2:101430039
|
T | C | 1 | a0001c0001t0003g0105 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.73-7567A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101430039 | ||||||
| chr2:101430049
|
T | C | 1 | a0004c0004t0001g0132 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.73-7577A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101430049 | ||||||
| chr2:101430203
|
A | G | 12 | a0001c0001t0001g0015a0001c0001t0001g0136a0001c0001t0001g0251others(9): Show | 13 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.73-7731T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101430203 | ||||||
| chr2:101430341
|
A | G | 189 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(186): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.73-7869T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101430341 | ||||||
| chr2:101430343
|
A | G | 189 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(186): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.73-7871T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101430343 | ||||||
| chr2:101430363
|
T | C | 108 | a0001c0001t0001g0190a0001c0001t0001g0200a0001c0001t0001g0214others(105): Show | 114 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.73-7891A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101430363 | ||||||
| chr2:101430369
|
A | T | 183 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(180): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-7897T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101430369 | ||||||
| chr2:101430535
|
C | T | 1 | a0002c0002t0001g0263 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.73-8063G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101430535 | ||||||
| chr2:101430786
|
T | C | 183 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(180): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-8314A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101430786 | ||||||
| chr2:101430988
|
G | C | 103 | a0001c0001t0001g0190a0001c0001t0001g0200a0001c0001t0001g0214others(100): Show | 109 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.73-8516C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101430988 | ||||||
| chr2:101431019
|
T | C | 67 | a0001c0001t0001g0107a0001c0001t0001g0134a0001c0001t0001g0135others(64): Show | 72 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.73-8547A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101431019 | ||||||
| chr2:101431117
|
TCCATCCA others(9): Show |
T | 183 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(180): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-8661_73-8646del others(16): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101431117 | ||||||
| chr2:101431149
|
A | T | 183 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(180): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-8677T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101431149 | ||||||
| chr2:101431157
|
C | T | 3 | a0002c0002t0001g0194a0002c0002t0001g0288a0004c0004t0001g0272 | 3 | HG00544.hp2 NA18992.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.73-8685G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101431157 | ||||||
| chr2:101431158
|
A | G | 183 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(180): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-8686T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101431158 | ||||||
| chr2:101431350
|
C | T | 183 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(180): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-8878G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101431350 | ||||||
| chr2:101431464
|
GT | G | 183 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(180): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-8993delA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101431464 | ||||||
| chr2:101431524
|
T | A | 2 | a0001c0001t0002g0025a0001c0001t0002g0026 | 2 | NA18955.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.73-9052A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101431524 | ||||||
| chr2:101431867
|
A | G | 2 | a0001c0001t0002g0070a0001c0001t0002g0074 | 2 | HG02738.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.73-9395T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101431867 | ||||||
| chr2:101432093
|
G | T | 183 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(180): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-9621C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101432093 | ||||||
| chr2:101432129
|
C | T | 183 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(180): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-9657G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101432129 | ||||||
| chr2:101432196
|
C | T | 183 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(180): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-9724G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101432196 | ||||||
| chr2:101432208
|
T | C | 183 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(180): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-9736A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101432208 | ||||||
| chr2:101432251
|
A | G | 52 | a0001c0001t0001g0013a0001c0001t0001g0109a0001c0001t0001g0115others(49): Show | 60 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.73-9779T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101432251 | ||||||
| chr2:101432382
|
G | A | 183 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(180): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-9910C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101432382 | ||||||
| chr2:101432383
|
T | G | 183 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(180): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-9911A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101432383 | ||||||
| chr2:101432520
|
T | C | 292 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(289): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.73-10048A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101432520 | ||||||
| chr2:101432601
|
C | T | 67 | a0001c0001t0001g0107a0001c0001t0001g0134a0001c0001t0001g0135others(64): Show | 72 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.73-10129G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101432601 | ||||||
| chr2:101432653
|
G | A | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0151others(2): Show | 7 | HG01257.hp1 HG01258.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.73-10181C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101432653 | ||||||
| chr2:101432794
|
G | A | 1 | a0002c0002t0001g0297 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.73-10322C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101432794 | ||||||
| chr2:101432909
|
G | T | 1 | a0002c0002t0001g0257 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.73-10437C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101432909 | ||||||
| chr2:101432912
|
C | T | 5 | a0009c0006t0001g0158a0009c0006t0001g0164a0009c0006t0001g0165others(2): Show | 5 | HG01243.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-10440G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101432912 | ||||||
| chr2:101432968
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.73-10496C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101432968 | ||||||
| chr2:101432969
|
G | A | 1 | a0009c0006t0001g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.73-10497C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101432969 | ||||||
| chr2:101433027
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.73-10555C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101433027 | ||||||
| chr2:101433035
|
C | G | 1 | a0001c0001t0003g0105 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.73-10563G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101433035 | ||||||
| chr2:101433042
|
T | C | 1 | a0001c0001t0001g0298 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.73-10570A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101433042 | ||||||
| chr2:101433088
|
C | T | 101 | a0001c0001t0001g0190a0001c0001t0001g0200a0001c0001t0001g0214others(98): Show | 107 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.73-10616G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101433088 | ||||||
| chr2:101433099
|
C | T | 292 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(289): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.73-10627G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101433099 | ||||||
| chr2:101433184
|
C | A | 12 | a0001c0001t0001g0015a0001c0001t0001g0136a0001c0001t0001g0251others(9): Show | 13 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.73-10712G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101433184 | ||||||
| chr2:101433189
|
A | G | 5 | a0009c0006t0001g0158a0009c0006t0001g0164a0009c0006t0001g0165others(2): Show | 5 | HG01243.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-10717T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101433189 | ||||||
| chr2:101433280
|
C | T | 1 | a0016c0025t0001g0159 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.73-10808G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101433280 | ||||||
| chr2:101433471
|
G | A | 183 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(180): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-10999C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101433471 | ||||||
| chr2:101433649
|
T | C | 1 | a0001c0001t0001g0219 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.73-11177A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101433649 | ||||||
| chr2:101433681
|
G | A | 4 | a0001c0015t0001g0185a0001c0015t0002g0028a0002c0008t0004g0008others(1): Show | 5 | HG01884.hp2 HG02630.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.73-11209C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101433681 | ||||||
| chr2:101433713
|
G | C | 2 | a0001c0001t0001g0154a0001c0001t0001g0298 | 2 | HG02055.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.73-11241C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101433713 | ||||||
| chr2:101433736
|
A | C | 1 | a0016c0025t0001g0159 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.73-11264T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101433736 | ||||||
| chr2:101433795
|
C | T | 1 | a0001c0001t0002g0070 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.73-11323G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101433795 | ||||||
| chr2:101433802
|
A | G | 183 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(180): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-11330T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101433802 | ||||||
| chr2:101434065
|
C | T | 1 | a0007c0010t0001g0234 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.73-11593G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101434065 | ||||||
| chr2:101434089
|
TA | T | 12 | a0001c0001t0001g0015a0001c0001t0001g0136a0001c0001t0001g0251others(9): Show | 13 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.73-11618delT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101434089 | ||||||
| chr2:101434122
|
T | C | 1 | a0002c0002t0001g0247 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.73-11650A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101434122 | ||||||
| chr2:101434266
|
A | G | 183 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(180): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-11794T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101434266 | ||||||
| chr2:101434341
|
C | T | 183 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(180): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-11869G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101434341 | ||||||
| chr2:101434364
|
A | C | 11 | a0001c0001t0001g0015a0001c0001t0001g0136a0001c0001t0001g0251others(8): Show | 12 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.73-11892T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101434364 | ||||||
| chr2:101434437
|
G | A | 1 | a0001c0001t0003g0105 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.73-11965C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101434437 | ||||||
| chr2:101434541
|
CAATGCAA others(3): Show |
C | 183 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(180): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-12079_73-12070d others(12): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101434541 | ||||||
| chr2:101434598
|
C | T | 1 | a0002c0002t0002g0081 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.73-12126G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101434598 | ||||||
| chr2:101434733
|
CA | C | 183 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(180): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-12262delT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101434733 | ||||||
| chr2:101434745
|
T | C | 184 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(181): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.73-12273A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101434745 | ||||||
| chr2:101434752
|
T | C | 184 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(181): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.73-12280A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101434752 | ||||||
| chr2:101434829
|
T | C | 12 | a0001c0001t0001g0279a0001c0001t0001g0280a0002c0002t0001g0207others(9): Show | 12 | HG00673.hp1 HG01074.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.73-12357A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101434829 | ||||||
| chr2:101434891
|
C | T | 35 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0149others(32): Show | 38 | HG00140.hp2 HG00642.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.73-12419G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101434891 | ||||||
| chr2:101435040
|
C | T | 1 | a0002c0002t0001g0304 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.73-12568G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101435040 | ||||||
| chr2:101435283
|
C | T | 184 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(181): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.73-12811G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101435283 | ||||||
| chr2:101435330
|
G | A | 184 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(181): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.73-12858C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101435330 | ||||||
| chr2:101435450
|
T | C | 11 | a0001c0001t0001g0015a0001c0001t0001g0136a0001c0001t0001g0251others(8): Show | 12 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.73-12978A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101435450 | ||||||
| chr2:101435472
|
G | C | 1 | a0001c0001t0002g0050 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.73-13000C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101435472 | ||||||
| chr2:101435543
|
C | T | 1 | a0003c0003t0001g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.73-13071G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101435543 | ||||||
| chr2:101435645
|
C | A | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-13173G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101435645 | ||||||
| chr2:101435698
|
A | C | 1 | a0001c0001t0001g0154 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.73-13226T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101435698 | ||||||
| chr2:101435791
|
G | A | 1 | a0002c0002t0001g0240 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.73-13319C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101435791 | ||||||
| chr2:101435806
|
A | G | 1 | a0002c0002t0002g0063 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.73-13334T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101435806 | ||||||
| chr2:101435832
|
T | TA | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-13361dupT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101435832 | ||||||
| chr2:101435899
|
G | A | 6 | a0001c0001t0001g0002a0002c0002t0001g0152a0003c0003t0001g0153others(3): Show | 10 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.73-13427C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101435899 | ||||||
| chr2:101435940
|
C | T | 71 | a0001c0001t0001g0107a0001c0001t0001g0134a0001c0001t0001g0135others(68): Show | 76 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.73-13468G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101435940 | ||||||
| chr2:101436097
|
G | A | 38 | a0001c0001t0001g0109a0001c0001t0001g0116a0001c0001t0001g0117others(35): Show | 40 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.73-13625C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436097 | ||||||
| chr2:101436106
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.73-13634C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436106 | ||||||
| chr2:101436113
|
G | A | 39 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0149others(36): Show | 43 | HG00140.hp2 HG00642.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.73-13641C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436113 | ||||||
| chr2:101436202
|
G | A | 69 | a0001c0001t0001g0107a0001c0001t0001g0134a0001c0001t0001g0135others(66): Show | 74 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.73-13730C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436202 | ||||||
| chr2:101436320
|
G | C | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-13848C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436320 | ||||||
| chr2:101436389
|
T | C | 2 | a0001c0001t0001g0218a0001c0001t0001g0219 | 2 | HG01261.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.73-13917A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436389 | ||||||
| chr2:101436485
|
C | T | 1 | a0003c0003t0002g0040 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.73-14013G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436485 | ||||||
| chr2:101436538
|
C | T | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-14066G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436538 | ||||||
| chr2:101436552
|
T | C | 1 | a0001c0001t0001g0252 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.73-14080A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436552 | ||||||
| chr2:101436558
|
G | C | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-14086C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436558 | ||||||
| chr2:101436622
|
A | AT | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-14151dupA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436622 | ||||||
| chr2:101436650
|
T | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0136a0001c0001t0001g0251others(2): Show | 6 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.73-14178A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436650 | ||||||
| chr2:101436655
|
A | G | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-14183T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436655 | ||||||
| chr2:101436703
|
G | C | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-14231C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436703 | ||||||
| chr2:101436812
|
G | A | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.73-14340C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436812 | ||||||
| chr2:101436822
|
T | C | 2 | a0001c0001t0001g0190a0002c0002t0001g0232 | 2 | HG00558.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.73-14350A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436822 | ||||||
| chr2:101436901
|
G | A | 71 | a0001c0001t0001g0107a0001c0001t0001g0134a0001c0001t0001g0135others(68): Show | 76 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.73-14429C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436901 | ||||||
| chr2:101436977
|
G | A | 71 | a0001c0001t0001g0107a0001c0001t0001g0134a0001c0001t0001g0135others(68): Show | 76 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.73-14505C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436977 | ||||||
| chr2:101436996
|
C | T | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-14524G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436996 | ||||||
| chr2:101437046
|
C | A | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-14574G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437046 | ||||||
| chr2:101437049
|
G | A | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-14577C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437049 | ||||||
| chr2:101437059
|
C | A | 184 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(181): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.73-14587G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437059 | ||||||
| chr2:101437200
|
G | A | 1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.73-14728C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437200 | ||||||
| chr2:101437204
|
C | T | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-14732G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437204 | ||||||
| chr2:101437230
|
A | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0136a0001c0001t0001g0251others(8): Show | 12 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.73-14758T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437230 | ||||||
| chr2:101437256
|
A | G | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-14784T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437256 | ||||||
| chr2:101437260
|
G | C | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-14788C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437260 | ||||||
| chr2:101437264
|
C | T | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-14792G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437264 | ||||||
| chr2:101437388
|
C | T | 113 | a0001c0001t0001g0015a0001c0001t0001g0136a0001c0001t0001g0190others(110): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.73-14916G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437388 | ||||||
| chr2:101437484
|
G | A | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15012C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437484 | ||||||
| chr2:101437555
|
C | A | 1 | a0001c0001t0002g0070 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.73-15083G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437555 | ||||||
| chr2:101437573
|
C | CA | 9 | a0001c0001t0001g0217a0002c0002t0001g0112a0002c0002t0001g0137others(6): Show | 9 | HG00621.hp1 HG02074.hp1 NA18974.hp1 others(6): Show |
intron_variant | MODIFIER | c.73-15102dupT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437573 | ||||||
| chr2:101437642
|
G | T | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15170C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437642 | ||||||
| chr2:101437674
|
A | T | 1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.73-15202T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437674 | ||||||
| chr2:101437744
|
A | C | 1 | a0008c0009t0001g0157 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.73-15272T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437744 | ||||||
| chr2:101437746
|
G | A | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15274C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437746 | ||||||
| chr2:101437759
|
G | A | 1 | a0016c0025t0001g0159 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.73-15287C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437759 | ||||||
| chr2:101437762
|
G | GT | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15291_73-15290i others(3): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437762 | ||||||
| chr2:101437773
|
TCCCAAGT others(13): Show |
T | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15321_73-15302d others(22): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437773 | ||||||
| chr2:101437811
|
T | C | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15339A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437811 | ||||||
| chr2:101437822
|
G | A | 4 | a0001c0001t0001g0121a0001c0001t0001g0148a0002c0002t0001g0110others(1): Show | 4 | NA18941.hp2 NA18949.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-15350C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437822 | ||||||
| chr2:101437843
|
C | T | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15371G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437843 | ||||||
| chr2:101437867
|
A | G | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15395T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437867 | ||||||
| chr2:101437869
|
CCACCACC others(3): Show |
C | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15407_73-15398d others(12): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437869 | ||||||
| chr2:101437910
|
T | C | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15438A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437910 | ||||||
| chr2:101437916
|
C | T | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15444G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437916 | ||||||
| chr2:101438037
|
CTCT | C | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15568_73-15566d others(5): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438037 | ||||||
| chr2:101438155
|
G | T | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15683C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438155 | ||||||
| chr2:101438157
|
C | T | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15685G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438157 | ||||||
| chr2:101438207
|
AT | A | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15736delA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438207 | ||||||
| chr2:101438266
|
A | G | 1 | a0002c0002t0001g0306 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.73-15794T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438266 | ||||||
| chr2:101438339
|
C | T | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15867G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438339 | ||||||
| chr2:101438347
|
A | C | 2 | a0001c0001t0001g0271a0002c0002t0001g0179 | 2 | NA18747.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.73-15875T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438347 | ||||||
| chr2:101438375
|
A | G | 2 | a0002c0002t0002g0076a0002c0002t0002g0084 | 2 | HG00741.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.73-15903T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438375 | ||||||
| chr2:101438385
|
A | G | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15913T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438385 | ||||||
| chr2:101438524
|
T | A | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-16052A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438524 | ||||||
| chr2:101438547
|
G | A | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-16075C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438547 | ||||||
| chr2:101438601
|
G | T | 1 | a0021c0018t0001g0187 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.73-16129C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438601 | ||||||
| chr2:101438608
|
T | C | 1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.73-16136A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438608 | ||||||
| chr2:101438622
|
G | A | 1 | a0001c0001t0002g0086 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.73-16150C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438622 | ||||||
| chr2:101438631
|
A | G | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-16159T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438631 | ||||||
| chr2:101438727
|
T | C | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-16255A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438727 | ||||||
| chr2:101438735
|
T | C | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-16263A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438735 | ||||||
| chr2:101438815
|
A | C | 3 | a0001c0001t0002g0010a0001c0001t0002g0064a0001c0001t0002g0090 | 4 | HG01358.hp1 HG01515.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-16343T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438815 | ||||||
| chr2:101438833
|
C | T | 1 | a0002c0002t0001g0242 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.73-16361G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438833 | ||||||
| chr2:101438834
|
G | A | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-16362C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438834 | ||||||
| chr2:101438848
|
G | T | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-16376C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438848 | ||||||
| chr2:101438897
|
T | C | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-16425A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438897 | ||||||
| chr2:101438965
|
C | T | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-16493G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438965 | ||||||
| chr2:101439056
|
A | G | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-16584T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439056 | ||||||
| chr2:101439104
|
C | G | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-16632G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439104 | ||||||
| chr2:101439120
|
G | A | 1 | a0016c0025t0001g0159 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.73-16648C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439120 | ||||||
| chr2:101439253
|
TTTTGAGC others(4): Show |
T | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-16792_73-16782d others(13): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439253 | ||||||
| chr2:101439300
|
T | C | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-16828A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439300 | ||||||
| chr2:101439490
|
A | C | 1 | a0001c0015t0002g0028 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.73-17018T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439490 | ||||||
| chr2:101439596
|
C | CT | 56 | a0001c0001t0001g0200a0001c0001t0001g0218a0001c0001t0001g0219others(53): Show | 60 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.73-17125_73-17124i others(3): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439596 | ||||||
| chr2:101439596
|
C | CTT | 74 | a0001c0001t0001g0002a0001c0001t0001g0107a0001c0001t0001g0134others(71): Show | 83 | HG00099.hp2 HG00544.hp1 HG01123.hp2 others(80): Show |
intron_variant | MODIFIER | c.73-17125_73-17124i others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439596 | ||||||
| chr2:101439596
|
C | CTTT | 13 | a0001c0001t0001g0015a0001c0001t0001g0136a0001c0001t0001g0251others(10): Show | 14 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.73-17125_73-17124i others(5): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439596 | ||||||
| chr2:101439597
|
A | T | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-17125T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439597 | ||||||
| chr2:101439641
|
G | T | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-17169C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439641 | ||||||
| chr2:101439669
|
A | G | 1 | a0001c0001t0002g0077 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.73-17197T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439669 | ||||||
| chr2:101439716
|
A | AT | 6 | a0001c0001t0001g0015a0001c0001t0001g0136a0001c0001t0001g0251others(3): Show | 7 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.73-17245dupA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439716 | ||||||
| chr2:101439716
|
AT | A | 102 | a0001c0001t0001g0190a0001c0001t0001g0200a0001c0001t0001g0214others(99): Show | 109 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.73-17245delA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439716 | ||||||
| chr2:101439769
|
A | G | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-17297T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439769 | ||||||
| chr2:101439805
|
T | C | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-17333A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439805 | ||||||
| chr2:101439815
|
C | T | 1 | a0008c0009t0001g0157 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.73-17343G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439815 | ||||||
| chr2:101439836
|
G | A | 1 | a0002c0002t0001g0287 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.73-17364C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439836 | ||||||
| chr2:101439939
|
G | A | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-17467C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439939 | ||||||
| chr2:101439971
|
A | G | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-17499T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439971 | ||||||
| chr2:101440005
|
C | T | 25 | a0001c0001t0001g0149a0001c0001t0001g0181a0001c0001t0001g0261others(22): Show | 26 | HG00140.hp2 HG00642.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.73-17533G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440005 | ||||||
| chr2:101440107
|
T | TAA | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-17636_73-17635i others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440107 | ||||||
| chr2:101440108
|
T | A | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-17636A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440108 | ||||||
| chr2:101440143
|
A | G | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-17671T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440143 | ||||||
| chr2:101440188
|
A | G | 12 | a0001c0001t0001g0015a0001c0001t0001g0136a0001c0001t0001g0251others(9): Show | 13 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.73-17716T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440188 | ||||||
| chr2:101440209
|
A | G | 1 | a0002c0002t0001g0287 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.73-17737T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440209 | ||||||
| chr2:101440305
|
G | A | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-17833C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440305 | ||||||
| chr2:101440394
|
C | A | 1 | a0002c0002t0001g0111 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.73-17922G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440394 | ||||||
| chr2:101440425
|
C | T | 2 | a0001c0015t0001g0185a0011c0014t0001g0188 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.73-17953G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440425 | ||||||
| chr2:101440481
|
C | T | 1 | a0001c0001t0001g0215 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.73-18009G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440481 | ||||||
| chr2:101440542
|
T | C | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-18070A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440542 | ||||||
| chr2:101440543
|
G | A | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-18071C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440543 | ||||||
| chr2:101440545
|
G | A | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-18073C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440545 | ||||||
| chr2:101440659
|
CTG | C | 6 | a0002c0002t0001g0119a0002c0002t0001g0227a0002c0002t0001g0229others(3): Show | 6 | NA18941.hp1 NA18945.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.73-18189_73-18188d others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440659 | ||||||
| chr2:101440702
|
C | T | 1 | a0003c0003t0002g0053 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.73-18230G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440702 | ||||||
| chr2:101440738
|
G | C | 1 | a0002c0002t0001g0287 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.73-18266C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440738 | ||||||
| chr2:101440764
|
C | T | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-18292G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440764 | ||||||
| chr2:101440862
|
T | C | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-18390A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440862 | ||||||
| chr2:101440874
|
G | A | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-18402C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440874 | ||||||
| chr2:101440921
|
C | T | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-18449G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440921 | ||||||
| chr2:101440966
|
A | ATTTT | 6 | a0001c0001t0001g0002a0001c0001t0001g0218a0001c0001t0001g0219others(3): Show | 9 | HG01261.hp2 HG02258.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.73-18498_73-18495d others(6): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440966 | ||||||
| chr2:101440966
|
A | ATTTTT | 106 | a0001c0001t0001g0015a0001c0001t0001g0136a0001c0001t0001g0190others(103): Show | 114 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.73-18499_73-18495d others(7): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440966 | ||||||
| chr2:101440966
|
A | ATTTTTT | 11 | a0001c0001t0002g0037a0001c0001t0003g0098a0002c0002t0001g0162others(8): Show | 11 | HG01516.hp1 HG02074.hp1 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.73-18500_73-18495d others(8): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440966 | ||||||
| chr2:101440966
|
A | ATTTTTTT | 60 | a0001c0001t0001g0107a0001c0001t0001g0134a0001c0001t0001g0135others(57): Show | 65 | HG00099.hp2 HG00544.hp1 HG01123.hp2 others(62): Show |
intron_variant | MODIFIER | c.73-18501_73-18495d others(9): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440966 | ||||||
| chr2:101440966
|
AT | A | 86 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0109others(83): Show | 97 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.73-18495delA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440966 | ||||||
| chr2:101441104
|
C | A | 1 | a0001c0001t0001g0307 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.73-18632G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101441104 | ||||||
| chr2:101441108
|
A | G | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-18636T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101441108 | ||||||
| chr2:101441109
|
G | A | 1 | a0002c0002t0002g0054 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.73-18637C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101441109 | ||||||
| chr2:101441111
|
C | T | 2 | a0002c0002t0001g0195a0002c0002t0001g0196 | 2 | NA19080.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.73-18639G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101441111 | ||||||
| chr2:101441212
|
C | T | 1 | a0002c0002t0001g0216 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.73-18740G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101441212 | ||||||
| chr2:101441330
|
G | A | 1 | a0014c0017t0002g0031 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.73-18858C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101441330 | ||||||
| chr2:101441461
|
A | G | 1 | a0002c0002t0001g0302 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.73-18989T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101441461 | ||||||
| chr2:101441524
|
T | C | 191 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(188): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.73-19052A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101441524 | ||||||
| chr2:101441741
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.73-19269T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101441741 | ||||||
| chr2:101441766
|
C | G | 191 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(188): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.73-19294G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101441766 | ||||||
| chr2:101441852
|
T | C | 1 | a0003c0003t0001g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-19380A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101441852 | ||||||
| chr2:101441866
|
C | A | 71 | a0001c0001t0001g0107a0001c0001t0001g0134a0001c0001t0001g0135others(68): Show | 76 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.73-19394G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101441866 | ||||||
| chr2:101441878
|
T | C | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | NA18980.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.73-19406A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101441878 | ||||||
| chr2:101441999
|
T | A | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-19527A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101441999 | ||||||
| chr2:101442016
|
A | G | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-19544T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101442016 | ||||||
| chr2:101442149
|
T | C | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-19677A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101442149 | ||||||
| chr2:101442248
|
T | C | 1 | a0004c0004t0001g0132 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.73-19776A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101442248 | ||||||
| chr2:101442397
|
C | A | 2 | a0001c0015t0001g0185a0011c0014t0001g0188 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.73-19925G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101442397 | ||||||
| chr2:101442399
|
T | G | 4 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0151others(1): Show | 6 | HG01257.hp1 HG01258.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.73-19927A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101442399 | ||||||
| chr2:101442416
|
G | A | 1 | a0003c0003t0001g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.73-19944C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101442416 | ||||||
| chr2:101442432
|
C | CA | 3 | a0001c0015t0002g0028a0002c0008t0004g0008a0002c0008t0004g0021 | 4 | HG02630.hp1 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-19961dupT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101442432 | ||||||
| chr2:101442478
|
T | G | 1 | a0001c0001t0002g0077 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.73-20006A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101442478 | ||||||
| chr2:101442535
|
C | G | 1 | a0001c0001t0001g0002 | 4 | HG02258.hp2 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.73-20063G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101442535 | ||||||
| chr2:101443040
|
C | T | 184 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(181): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.73-20568G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101443040 | ||||||
| chr2:101443165
|
G | A | 4 | a0003c0003t0001g0202a0003c0003t0001g0203a0003c0003t0001g0204others(1): Show | 4 | HG02896.hp2 HG03041.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-20693C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101443165 | ||||||
| chr2:101443208
|
T | A | 1 | a0007c0010t0001g0260 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.73-20736A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101443208 | ||||||
| chr2:101443335
|
G | A | 102 | a0001c0001t0001g0190a0001c0001t0001g0200a0001c0001t0001g0214others(99): Show | 108 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.73-20863C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101443335 | ||||||
| chr2:101443358
|
T | C | 1 | a0001c0001t0001g0290 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.73-20886A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101443358 | ||||||
| chr2:101443360
|
G | A | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-20888C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101443360 | ||||||
| chr2:101443392
|
G | A | 101 | a0001c0001t0001g0190a0001c0001t0001g0200a0001c0001t0001g0214others(98): Show | 107 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.73-20920C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101443392 | ||||||
| chr2:101443434
|
G | A | 1 | a0002c0002t0001g0007 | 3 | HG01891.hp2 HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.73-20962C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101443434 | ||||||
| chr2:101443737
|
G | A | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-21265C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101443737 | ||||||
| chr2:101443814
|
G | A | 6 | a0001c0001t0001g0002a0002c0002t0001g0152a0003c0003t0001g0153others(3): Show | 10 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.73-21342C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101443814 | ||||||
| chr2:101443911
|
C | A | 11 | a0001c0001t0001g0015a0001c0001t0001g0136a0001c0001t0001g0251others(8): Show | 12 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.73-21439G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101443911 | ||||||
| chr2:101443970
|
C | A | 188 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(185): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.73-21498G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101443970 | ||||||
| chr2:101444005
|
G | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0298 | 2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.73-21533C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101444005 | ||||||
| chr2:101444404
|
A | G | 28 | a0001c0001t0001g0190a0001c0001t0001g0214a0001c0001t0001g0231others(25): Show | 28 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.73-21932T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101444404 | ||||||
| chr2:101444462
|
A | G | 1 | a0003c0003t0001g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.73-21990T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101444462 | ||||||
| chr2:101444937
|
A | AAGACCTG others(7): Show |
1 | a0001c0001t0001g0225 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.72+21839_72+21840i others(16): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101444937 | ||||||
| chr2:101444944
|
G | C | 1 | a0001c0001t0001g0225 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.72+21833C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101444944 | ||||||
| chr2:101444978
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.72+21799T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101444978 | ||||||
| chr2:101444982
|
G | C | 1 | a0001c0001t0001g0225 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.72+21795C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101444982 | ||||||
| chr2:101444995
|
G | C | 1 | a0001c0001t0001g0225 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.72+21782C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101444995 | ||||||
| chr2:101445062
|
G | T | 64 | a0001c0001t0001g0107a0001c0001t0001g0134a0001c0001t0001g0135others(61): Show | 69 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.72+21715C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101445062 | ||||||
| chr2:101445111
|
G | A | 1 | a0002c0002t0002g0091 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.72+21666C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101445111 | ||||||
| chr2:101445308
|
CCTT | C | 9 | a0001c0001t0001g0005a0001c0001t0001g0150a0001c0001t0001g0193others(6): Show | 11 | HG02257.hp2 HG02559.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+21466_72+21468d others(5): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101445308 | ||||||
| chr2:101445345
|
G | A | 1 | a0001c0001t0001g0298 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.72+21432C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101445345 | ||||||
| chr2:101445486
|
G | A | 1 | a0002c0002t0002g0073 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.72+21291C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101445486 | ||||||
| chr2:101445488
|
G | A | 5 | a0001c0001t0001g0280a0002c0002t0001g0212a0002c0002t0001g0247others(2): Show | 5 | HG01081.hp2 HG01106.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+21289C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101445488 | ||||||
| chr2:101445531
|
C | T | 1 | a0003c0003t0002g0057 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.72+21246G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101445531 | ||||||
| chr2:101446053
|
A | C | 2 | a0001c0001t0002g0025a0001c0001t0002g0026 | 2 | NA18955.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.72+20724T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446053 | ||||||
| chr2:101446058
|
T | TA | 191 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(188): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.72+20718_72+20719i others(3): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446058 | ||||||
| chr2:101446071
|
C | T | 1 | a0003c0003t0001g0172 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.72+20706G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446071 | ||||||
| chr2:101446112
|
TA | T | 186 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(183): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.72+20664delT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446112 | ||||||
| chr2:101446112
|
TAA | T | 6 | a0001c0001t0001g0002a0002c0002t0001g0152a0003c0003t0001g0153others(3): Show | 10 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.72+20663_72+20664d others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446112 | ||||||
| chr2:101446124
|
T | G | 39 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0149others(36): Show | 43 | HG00140.hp2 HG00642.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.72+20653A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446124 | ||||||
| chr2:101446238
|
T | C | 191 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(188): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.72+20539A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446238 | ||||||
| chr2:101446395
|
C | T | 2 | a0001c0015t0001g0185a0011c0014t0001g0188 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.72+20382G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446395 | ||||||
| chr2:101446425
|
TG | T | 101 | a0001c0001t0001g0190a0001c0001t0001g0200a0001c0001t0001g0214others(98): Show | 107 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.72+20351delC | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446425 | ||||||
| chr2:101446480
|
ATCAATTA others(12): Show |
A | 191 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(188): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.72+20278_72+20296d others(21): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446480 | ||||||
| chr2:101446503
|
G | A | 191 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(188): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.72+20274C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446503 | ||||||
| chr2:101446505
|
ATAG | A | 191 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(188): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.72+20269_72+20271d others(5): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446505 | ||||||
| chr2:101446604
|
A | G | 1 | a0002c0002t0001g0256 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.72+20173T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446604 | ||||||
| chr2:101446607
|
G | A | 6 | a0001c0001t0001g0002a0002c0002t0001g0152a0003c0003t0001g0153others(3): Show | 10 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.72+20170C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446607 | ||||||
| chr2:101446670
|
G | A | 2 | a0001c0015t0001g0185a0011c0014t0001g0188 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.72+20107C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446670 | ||||||
| chr2:101446693
|
C | T | 43 | a0001c0001t0001g0013a0001c0001t0001g0109a0001c0001t0001g0115others(40): Show | 46 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.72+20084G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446693 | ||||||
| chr2:101446694
|
G | A | 2 | a0002c0008t0004g0008a0002c0008t0004g0021 | 3 | HG02630.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.72+20083C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446694 | ||||||
| chr2:101446698
|
A | G | 1 | a0002c0002t0002g0029 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.72+20079T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446698 | ||||||
| chr2:101446723
|
G | A | 1 | a0016c0025t0001g0159 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.72+20054C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446723 | ||||||
| chr2:101446850
|
A | G | 144 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(141): Show | 156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.72+19927T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446850 | ||||||
| chr2:101447009
|
T | A | 1 | a0001c0001t0001g0174 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.72+19768A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101447009 | ||||||
| chr2:101447028
|
A | G | 2 | a0001c0015t0001g0185a0011c0014t0001g0188 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.72+19749T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101447028 | ||||||
| chr2:101447037
|
G | T | 1 | a0002c0002t0002g0091 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.72+19740C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101447037 | ||||||
| chr2:101447039
|
C | T | 1 | a0002c0002t0001g0143 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.72+19738G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101447039 | ||||||
| chr2:101447150
|
C | T | 1 | a0001c0001t0001g0313 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.72+19627G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101447150 | ||||||
| chr2:101447211
|
C | G | 190 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(187): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.72+19566G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101447211 | ||||||
| chr2:101447272
|
A | ATTC | 191 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(188): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.72+19502_72+19504d others(5): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101447272 | ||||||
| chr2:101447422
|
A | G | 192 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(189): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.72+19355T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101447422 | ||||||
| chr2:101447423
|
A | C | 192 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(189): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.72+19354T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101447423 | ||||||
| chr2:101447759
|
T | G | 1 | a0002c0002t0002g0091 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.72+19018A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101447759 | ||||||
| chr2:101447792
|
C | T | 191 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(188): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.72+18985G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101447792 | ||||||
| chr2:101447798
|
T | C | 2 | a0001c0001t0001g0312a0003c0003t0001g0235 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.72+18979A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101447798 | ||||||
| chr2:101447856
|
C | T | 2 | a0001c0015t0001g0185a0011c0014t0001g0188 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.72+18921G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101447856 | ||||||
| chr2:101447872
|
C | T | 5 | a0002c0002t0001g0137a0002c0002t0001g0138a0002c0002t0001g0139others(2): Show | 5 | HG02074.hp1 NA18974.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.72+18905G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101447872 | ||||||
| chr2:101447983
|
G | A | 191 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(188): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.72+18794C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101447983 | ||||||
| chr2:101448003
|
A | G | 4 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0046others(1): Show | 4 | HG01243.hp1 HG01433.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+18774T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101448003 | ||||||
| chr2:101448018
|
A | G | 5 | a0009c0006t0001g0158a0009c0006t0001g0164a0009c0006t0001g0165others(2): Show | 5 | HG01243.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+18759T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101448018 | ||||||
| chr2:101448089
|
T | C | 1 | a0001c0001t0002g0036 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.72+18688A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101448089 | ||||||
| chr2:101448133
|
A | G | 191 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(188): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.72+18644T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101448133 | ||||||
| chr2:101448267
|
G | A | 80 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(77): Show | 86 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.72+18510C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101448267 | ||||||
| chr2:101448565
|
A | G | 1 | a0003c0003t0001g0203 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.72+18212T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101448565 | ||||||
| chr2:101448594
|
G | A | 2 | a0001c0015t0001g0185a0011c0014t0001g0188 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.72+18183C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101448594 | ||||||
| chr2:101448749
|
C | G | 2 | a0002c0002t0001g0006a0002c0002t0001g0233 | 4 | NA18612.hp1 NA18951.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+18028G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101448749 | ||||||
| chr2:101448788
|
C | G | 100 | a0001c0001t0001g0190a0001c0001t0001g0200a0001c0001t0001g0214others(97): Show | 106 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+17989G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101448788 | ||||||
| chr2:101448857
|
T | C | 1 | a0003c0003t0001g0202 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.72+17920A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101448857 | ||||||
| chr2:101448859
|
T | C | 294 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(291): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.72+17918A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101448859 | ||||||
| chr2:101448917
|
T | C | 80 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(77): Show | 86 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.72+17860A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101448917 | ||||||
| chr2:101448981
|
T | A | 1 | a0001c0001t0001g0271 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.72+17796A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101448981 | ||||||
| chr2:101449039
|
T | G | 231 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(228): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.72+17738A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101449039 | ||||||
| chr2:101449185
|
AAC | A | 191 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(188): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.72+17590_72+17591d others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101449185 | ||||||
| chr2:101449482
|
A | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(190): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.72+17295T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101449482 | ||||||
| chr2:101449543
|
C | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(190): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.72+17234G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101449543 | ||||||
| chr2:101449550
|
T | C | 1 | a0003c0003t0002g0053 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.72+17227A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101449550 | ||||||
| chr2:101449894
|
G | A | 5 | a0009c0006t0001g0158a0009c0006t0001g0164a0009c0006t0001g0165others(2): Show | 5 | HG01243.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+16883C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101449894 | ||||||
| chr2:101450047
|
T | C | 193 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(190): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.72+16730A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101450047 | ||||||
| chr2:101450127
|
G | C | 1 | a0003c0003t0001g0126 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.72+16650C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101450127 | ||||||
| chr2:101450282
|
G | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(190): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.72+16495C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101450282 | ||||||
| chr2:101450346
|
C | T | 1 | a0002c0002t0001g0302 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.72+16431G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101450346 | ||||||
| chr2:101450416
|
A | T | 193 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(190): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.72+16361T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101450416 | ||||||
| chr2:101450466
|
G | T | 1 | a0001c0001t0001g0226 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.72+16311C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101450466 | ||||||
| chr2:101450519
|
C | T | 61 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0109others(58): Show | 71 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.72+16258G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101450519 | ||||||
| chr2:101450603
|
C | T | 1 | a0001c0001t0001g0280 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.72+16174G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101450603 | ||||||
| chr2:101450621
|
T | C | 193 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(190): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.72+16156A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101450621 | ||||||
| chr2:101450877
|
A | G | 1 | a0002c0002t0001g0282 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.72+15900T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101450877 | ||||||
| chr2:101450930
|
C | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+15847G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101450930 | ||||||
| chr2:101450985
|
G | C | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+15792C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101450985 | ||||||
| chr2:101451067
|
C | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+15710G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451067 | ||||||
| chr2:101451073
|
T | C | 60 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0109others(57): Show | 70 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.72+15704A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451073 | ||||||
| chr2:101451088
|
GA | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+15688delT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451088 | ||||||
| chr2:101451119
|
C | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+15658G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451119 | ||||||
| chr2:101451162
|
G | A | 95 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(92): Show | 107 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(104): Show |
intron_variant | MODIFIER | c.72+15615C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451162 | ||||||
| chr2:101451237
|
C | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+15540G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451237 | ||||||
| chr2:101451284
|
T | C | 2 | a0001c0001t0001g0217a0002c0002t0001g0216 | 2 | HG00621.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.72+15493A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451284 | ||||||
| chr2:101451364
|
A | G | 1 | a0001c0001t0002g0050 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.72+15413T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451364 | ||||||
| chr2:101451414
|
G | A | 2 | a0001c0015t0001g0185a0011c0014t0001g0188 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.72+15363C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451414 | ||||||
| chr2:101451415
|
C | T | 100 | a0001c0001t0001g0190a0001c0001t0001g0200a0001c0001t0001g0214others(97): Show | 106 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+15362G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451415 | ||||||
| chr2:101451420
|
G | C | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+15357C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451420 | ||||||
| chr2:101451447
|
G | A | 3 | a0002c0002t0001g0285a0002c0002t0001g0286a0002c0002t0001g0287 | 3 | HG00323.hp1 HG00738.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.72+15330C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451447 | ||||||
| chr2:101451469
|
T | C | 294 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(291): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.72+15308A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451469 | ||||||
| chr2:101451495
|
C | T | 11 | a0001c0001t0001g0002a0001c0001t0001g0210a0002c0002t0001g0006others(8): Show | 17 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.72+15282G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451495 | ||||||
| chr2:101451559
|
G | A | 1 | a0002c0002t0001g0246 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.72+15218C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451559 | ||||||
| chr2:101451646
|
G | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+15131C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451646 | ||||||
| chr2:101451688
|
T | A | 1 | a0001c0001t0001g0174 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.72+15089A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451688 | ||||||
| chr2:101451689
|
C | CA | 86 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(83): Show | 98 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.72+15087dupT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451689 | ||||||
| chr2:101451689
|
CA | C | 197 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0016others(194): Show | 217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.72+15087delT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451689 | ||||||
| chr2:101451708
|
A | T | 1 | a0001c0001t0001g0271 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.72+15069T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451708 | ||||||
| chr2:101451765
|
T | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+15012A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451765 | ||||||
| chr2:101451820
|
G | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+14957C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451820 | ||||||
| chr2:101451842
|
C | T | 15 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0136others(12): Show | 16 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.72+14935G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451842 | ||||||
| chr2:101451843
|
C | T | 6 | a0001c0001t0001g0200a0001c0001t0001g0225a0002c0002t0001g0198others(3): Show | 6 | HG00140.hp1 HG01069.hp2 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.72+14934G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451843 | ||||||
| chr2:101451856
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.72+14921C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451856 | ||||||
| chr2:101452023
|
C | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+14754G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452023 | ||||||
| chr2:101452026
|
C | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+14751G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452026 | ||||||
| chr2:101452072
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+14705T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452072 | ||||||
| chr2:101452108
|
A | G | 57 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0141others(54): Show | 62 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.72+14669T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452108 | ||||||
| chr2:101452126
|
A | C | 2 | a0001c0015t0001g0185a0011c0014t0001g0188 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.72+14651T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452126 | ||||||
| chr2:101452220
|
CA | C | 3 | a0001c0001t0001g0243a0002c0002t0001g0242a0019c0019t0001g0245 | 3 | NA18944.hp1 NA18961.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.72+14556delT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452220 | ||||||
| chr2:101452253
|
C | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+14524G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452253 | ||||||
| chr2:101452281
|
T | G | 3 | a0001c0015t0002g0028a0002c0008t0004g0008a0002c0008t0004g0021 | 4 | HG02630.hp1 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+14496A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452281 | ||||||
| chr2:101452287
|
T | C | 1 | a0001c0001t0002g0071 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.72+14490A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452287 | ||||||
| chr2:101452410
|
T | A | 91 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(88): Show | 103 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.72+14367A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452410 | ||||||
| chr2:101452413
|
G | A | 1 | a0002c0002t0001g0255 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.72+14364C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452413 | ||||||
| chr2:101452540
|
T | C | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+14237A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452540 | ||||||
| chr2:101452559
|
A | C | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.72+14218T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452559 | ||||||
| chr2:101452607
|
A | C | 4 | a0001c0001t0001g0181a0001c0001t0001g0261a0001c0001t0001g0262others(1): Show | 4 | HG01175.hp1 HG02015.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+14170T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452607 | ||||||
| chr2:101452613
|
T | C | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+14164A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452613 | ||||||
| chr2:101452722
|
G | A | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.72+14055C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452722 | ||||||
| chr2:101452732
|
C | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+14045G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452732 | ||||||
| chr2:101452739
|
A | G | 1 | a0002c0002t0001g0246 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.72+14038T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452739 | ||||||
| chr2:101452765
|
C | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0150a0002c0002t0001g0156 | 5 | HG02257.hp2 HG02809.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.72+14012G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452765 | ||||||
| chr2:101452776
|
A | G | 2 | a0007c0010t0001g0234a0007c0010t0001g0260 | 2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.72+14001T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452776 | ||||||
| chr2:101452887
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+13890T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452887 | ||||||
| chr2:101452933
|
C | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+13844G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452933 | ||||||
| chr2:101452964
|
G | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+13813C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452964 | ||||||
| chr2:101452978
|
GCCTGTAG others(165): Show |
G | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+13627_72+13798d others(2): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452978 | ||||||
| chr2:101453106
|
A | G | 1 | a0003c0003t0002g0056 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.72+13671T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453106 | ||||||
| chr2:101453111
|
AAAAC | A | 7 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0151others(4): Show | 9 | HG01257.hp1 HG01258.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.72+13662_72+13665d others(6): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453111 | ||||||
| chr2:101453187
|
G | A | 1 | a0001c0001t0001g0298 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.72+13590C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453187 | ||||||
| chr2:101453208
|
T | C | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+13569A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453208 | ||||||
| chr2:101453282
|
AAAATAAA others(1): Show |
A | 70 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0141others(67): Show | 77 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.72+13487_72+13494d others(10): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453282 | ||||||
| chr2:101453283
|
AAATAAAT | A | 17 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0136others(14): Show | 18 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.72+13487_72+13493d others(9): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453283 | ||||||
| chr2:101453285
|
ATAAATAA others(2): Show |
A | 6 | a0001c0001t0001g0002a0002c0002t0001g0152a0003c0003t0001g0153others(3): Show | 10 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.72+13483_72+13491d others(11): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453285 | ||||||
| chr2:101453286
|
T | A | 98 | a0001c0001t0001g0190a0001c0001t0001g0200a0001c0001t0001g0214others(95): Show | 104 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.72+13491A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453286 | ||||||
| chr2:101453294
|
T | A | 88 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(85): Show | 96 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(93): Show |
intron_variant | MODIFIER | c.72+13483A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453294 | ||||||
| chr2:101453300
|
G | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+13477C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453300 | ||||||
| chr2:101453349
|
C | T | 10 | a0001c0001t0001g0107a0001c0001t0001g0250a0002c0002t0001g0211others(7): Show | 10 | HG02055.hp2 HG02145.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.72+13428G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453349 | ||||||
| chr2:101453745
|
C | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+13032G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453745 | ||||||
| chr2:101453764
|
T | A | 1 | a0001c0001t0003g0098 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.72+13013A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453764 | ||||||
| chr2:101453785
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+12992T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453785 | ||||||
| chr2:101453904
|
A | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+12873T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453904 | ||||||
| chr2:101453942
|
A | G | 1 | a0002c0008t0004g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.72+12835T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453942 | ||||||
| chr2:101453962
|
G | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+12815C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453962 | ||||||
| chr2:101454071
|
C | T | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.72+12706G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454071 | ||||||
| chr2:101454076
|
T | C | 1 | a0008c0009t0002g0032 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.72+12701A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454076 | ||||||
| chr2:101454112
|
T | G | 3 | a0002c0002t0001g0285a0002c0002t0001g0286a0002c0002t0001g0287 | 3 | HG00323.hp1 HG00738.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.72+12665A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454112 | ||||||
| chr2:101454134
|
G | A | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.72+12643C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454134 | ||||||
| chr2:101454170
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+12607T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454170 | ||||||
| chr2:101454209
|
C | T | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.72+12568G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454209 | ||||||
| chr2:101454270
|
T | C | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+12507A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454270 | ||||||
| chr2:101454343
|
G | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+12434C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454343 | ||||||
| chr2:101454423
|
C | T | 4 | a0001c0001t0001g0210a0002c0002t0001g0006a0002c0002t0001g0209others(1): Show | 6 | NA18612.hp1 NA18951.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.72+12354G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454423 | ||||||
| chr2:101454454
|
A | C | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+12323T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454454 | ||||||
| chr2:101454493
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+12284T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454493 | ||||||
| chr2:101454510
|
C | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+12267G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454510 | ||||||
| chr2:101454597
|
C | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+12180G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454597 | ||||||
| chr2:101454606
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+12171T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454606 | ||||||
| chr2:101454639
|
G | C | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.72+12138C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454639 | ||||||
| chr2:101454642
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+12135T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454642 | ||||||
| chr2:101454932
|
T | C | 1 | a0008c0009t0001g0182 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.72+11845A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454932 | ||||||
| chr2:101454941
|
C | T | 7 | a0001c0001t0001g0002a0002c0002t0001g0152a0003c0003t0001g0153others(4): Show | 11 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.72+11836G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454941 | ||||||
| chr2:101455020
|
C | CTTTTT | 84 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(81): Show | 95 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(92): Show |
intron_variant | MODIFIER | c.72+11752_72+11756d others(7): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455020 | ||||||
| chr2:101455020
|
C | CTTTTTT | 8 | a0002c0002t0001g0152a0002c0002t0001g0191a0003c0003t0001g0153others(5): Show | 9 | HG01884.hp1 HG02109.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.72+11751_72+11756d others(8): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455020 | ||||||
| chr2:101455065
|
C | T | 1 | a0003c0003t0001g0166 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.72+11712G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455065 | ||||||
| chr2:101455072
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+11705T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455072 | ||||||
| chr2:101455082
|
C | G | 1 | a0003c0003t0001g0126 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.72+11695G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455082 | ||||||
| chr2:101455096
|
C | T | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.72+11681G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455096 | ||||||
| chr2:101455113
|
C | T | 2 | a0002c0002t0003g0095a0021c0018t0001g0187 | 2 | HG02257.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.72+11664G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455113 | ||||||
| chr2:101455125
|
C | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+11652G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455125 | ||||||
| chr2:101455177
|
A | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+11600T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455177 | ||||||
| chr2:101455201
|
C | T | 1 | a0010c0007t0001g0163 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.72+11576G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455201 | ||||||
| chr2:101455317
|
T | C | 1 | a0001c0001t0001g0252 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.72+11460A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455317 | ||||||
| chr2:101455331
|
T | C | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+11446A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455331 | ||||||
| chr2:101455393
|
T | C | 4 | a0001c0001t0001g0210a0002c0002t0001g0006a0002c0002t0001g0209others(1): Show | 6 | NA18612.hp1 NA18951.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.72+11384A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455393 | ||||||
| chr2:101455428
|
A | T | 4 | a0001c0001t0001g0201a0001c0001t0001g0222a0001c0001t0002g0082others(1): Show | 4 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+11349T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455428 | ||||||
| chr2:101455455
|
A | G | 1 | a0003c0003t0002g0055 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.72+11322T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455455 | ||||||
| chr2:101455530
|
G | C | 3 | a0006c0011t0001g0018a0006c0011t0001g0183a0017c0024t0001g0184 | 4 | HG01884.hp1 HG02109.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+11247C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455530 | ||||||
| chr2:101455589
|
A | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+11188T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455589 | ||||||
| chr2:101455591
|
C | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+11186G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455591 | ||||||
| chr2:101455613
|
C | T | 5 | a0001c0001t0003g0103a0005c0005t0003g0099a0005c0005t0003g0100others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+11164G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455613 | ||||||
| chr2:101455792
|
T | A | 1 | a0001c0001t0002g0072 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.72+10985A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455792 | ||||||
| chr2:101455832
|
T | G | 2 | a0001c0015t0001g0185a0011c0014t0001g0188 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.72+10945A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455832 | ||||||
| chr2:101455877
|
C | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+10900G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455877 | ||||||
| chr2:101456022
|
T | C | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.72+10755A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101456022 | ||||||
| chr2:101456043
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+10734T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101456043 | ||||||
| chr2:101456051
|
T | C | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+10726A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101456051 | ||||||
| chr2:101456191
|
G | A | 23 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0136others(20): Show | 24 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.72+10586C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101456191 | ||||||
| chr2:101456257
|
G | T | 9 | a0001c0001t0001g0005a0001c0001t0001g0150a0001c0001t0001g0193others(6): Show | 11 | HG02257.hp2 HG02559.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+10520C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101456257 | ||||||
| chr2:101456261
|
T | C | 9 | a0001c0001t0001g0005a0001c0001t0001g0150a0001c0001t0001g0193others(6): Show | 11 | HG02257.hp2 HG02559.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+10516A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101456261 | ||||||
| chr2:101456410
|
T | G | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.72+10367A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101456410 | ||||||
| chr2:101456526
|
G | A | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.72+10251C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101456526 | ||||||
| chr2:101456636
|
G | A | 2 | a0001c0001t0001g0218a0001c0001t0001g0219 | 2 | HG01261.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.72+10141C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101456636 | ||||||
| chr2:101456787
|
G | A | 11 | a0001c0001t0001g0002a0001c0001t0001g0210a0002c0002t0001g0006others(8): Show | 17 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.72+9990C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101456787 | ||||||
| chr2:101456896
|
T | G | 1 | a0003c0003t0001g0172 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.72+9881A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101456896 | ||||||
| chr2:101457018
|
G | A | 1 | a0002c0002t0002g0088 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.72+9759C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101457018 | ||||||
| chr2:101457121
|
G | T | 1 | a0001c0001t0001g0116 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.72+9656C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101457121 | ||||||
| chr2:101457306
|
C | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+9471G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101457306 | ||||||
| chr2:101457347
|
G | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+9430C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101457347 | ||||||
| chr2:101457445
|
C | T | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.72+9332G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101457445 | ||||||
| chr2:101457558
|
C | T | 93 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(90): Show | 105 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(102): Show |
intron_variant | MODIFIER | c.72+9219G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101457558 | ||||||
| chr2:101457621
|
C | T | 1 | a0014c0017t0001g0186 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.72+9156G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101457621 | ||||||
| chr2:101457635
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+9142T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101457635 | ||||||
| chr2:101457657
|
T | C | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.72+9120A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101457657 | ||||||
| chr2:101457687
|
G | T | 6 | a0001c0001t0001g0002a0002c0002t0001g0152a0003c0003t0001g0153others(3): Show | 10 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.72+9090C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101457687 | ||||||
| chr2:101457726
|
G | A | 6 | a0001c0001t0001g0002a0002c0002t0001g0152a0003c0003t0001g0153others(3): Show | 10 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.72+9051C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101457726 | ||||||
| chr2:101457765
|
T | C | 1 | a0003c0003t0001g0173 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.72+9012A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101457765 | ||||||
| chr2:101457831
|
T | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0136 | 3 | HG01069.hp1 HG01071.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.72+8946A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101457831 | ||||||
| chr2:101457843
|
T | C | 1 | a0006c0011t0001g0183 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.72+8934A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101457843 | ||||||
| chr2:101458047
|
G | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+8730C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101458047 | ||||||
| chr2:101458200
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.72+8577C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101458200 | ||||||
| chr2:101458206
|
T | C | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.72+8571A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101458206 | ||||||
| chr2:101458225
|
T | A | 4 | a0001c0001t0001g0210a0002c0002t0001g0006a0002c0002t0001g0209others(1): Show | 6 | NA18612.hp1 NA18951.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.72+8552A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101458225 | ||||||
| chr2:101458348
|
T | C | 93 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(90): Show | 105 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(102): Show |
intron_variant | MODIFIER | c.72+8429A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101458348 | ||||||
| chr2:101458349
|
C | T | 93 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(90): Show | 105 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(102): Show |
intron_variant | MODIFIER | c.72+8428G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101458349 | ||||||
| chr2:101458567
|
C | G | 234 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(231): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.72+8210G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101458567 | ||||||
| chr2:101458616
|
G | A | 7 | a0001c0001t0001g0002a0002c0002t0001g0152a0003c0003t0001g0153others(4): Show | 11 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.72+8161C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101458616 | ||||||
| chr2:101458676
|
C | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+8101G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101458676 | ||||||
| chr2:101458865
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+7912T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101458865 | ||||||
| chr2:101458894
|
C | T | 2 | a0002c0002t0001g0297a0015c0012t0001g0175 | 2 | HG01243.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.72+7883G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101458894 | ||||||
| chr2:101458895
|
G | A | 1 | a0002c0002t0001g0220 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.72+7882C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101458895 | ||||||
| chr2:101459250
|
C | T | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.72+7527G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101459250 | ||||||
| chr2:101459258
|
G | T | 1 | a0002c0021t0001g0241 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.72+7519C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101459258 | ||||||
| chr2:101459536
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.72+7241G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101459536 | ||||||
| chr2:101459565
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+7212T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101459565 | ||||||
| chr2:101459589
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+7188T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101459589 | ||||||
| chr2:101459661
|
G | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+7116C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101459661 | ||||||
| chr2:101459817
|
G | C | 5 | a0009c0006t0001g0158a0009c0006t0001g0164a0009c0006t0001g0165others(2): Show | 5 | HG01243.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+6960C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101459817 | ||||||
| chr2:101459851
|
A | G | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.72+6926T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101459851 | ||||||
| chr2:101459874
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+6903T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101459874 | ||||||
| chr2:101459879
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+6898T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101459879 | ||||||
| chr2:101459945
|
G | A | 25 | a0001c0001t0001g0200a0001c0001t0001g0225a0001c0001t0001g0290others(22): Show | 29 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.72+6832C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101459945 | ||||||
| chr2:101459984
|
G | A | 101 | a0001c0001t0001g0190a0001c0001t0001g0200a0001c0001t0001g0214others(98): Show | 107 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.72+6793C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101459984 | ||||||
| chr2:101460092
|
C | T | 6 | a0002c0002t0001g0119a0002c0002t0001g0227a0002c0002t0001g0229others(3): Show | 6 | NA18941.hp1 NA18945.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.72+6685G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460092 | ||||||
| chr2:101460197
|
T | TC | 14 | a0001c0001t0001g0002a0001c0001t0001g0210a0001c0015t0001g0185others(11): Show | 20 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.72+6579dupG | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460197 | ||||||
| chr2:101460200
|
T | G | 14 | a0001c0001t0001g0002a0001c0001t0001g0210a0001c0015t0001g0185others(11): Show | 20 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.72+6577A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460200 | ||||||
| chr2:101460200
|
T | TG | 80 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(77): Show | 86 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.72+6576dupC | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460200 | ||||||
| chr2:101460316
|
CT | C | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+6460delA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460316 | ||||||
| chr2:101460365
|
C | T | 80 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(77): Show | 86 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.72+6412G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460365 | ||||||
| chr2:101460366
|
G | A | 1 | a0021c0018t0001g0187 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.72+6411C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460366 | ||||||
| chr2:101460400
|
T | C | 1 | a0001c0001t0001g0117 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.72+6377A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460400 | ||||||
| chr2:101460436
|
T | C | 59 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0109others(56): Show | 69 | HG00323.hp2 HG00408.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.72+6341A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460436 | ||||||
| chr2:101460438
|
TG | T | 59 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0109others(56): Show | 69 | HG00323.hp2 HG00408.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.72+6338delC | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460438 | ||||||
| chr2:101460444
|
T | C | 6 | a0001c0001t0001g0002a0002c0002t0001g0152a0003c0003t0001g0153others(3): Show | 10 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.72+6333A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460444 | ||||||
| chr2:101460538
|
C | T | 1 | a0002c0002t0002g0062 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.72+6239G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460538 | ||||||
| chr2:101460576
|
A | G | 93 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(90): Show | 105 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(102): Show |
intron_variant | MODIFIER | c.72+6201T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460576 | ||||||
| chr2:101460593
|
C | T | 1 | a0021c0018t0001g0187 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.72+6184G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460593 | ||||||
| chr2:101460631
|
A | T | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.72+6146T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460631 | ||||||
| chr2:101460636
|
C | T | 6 | a0001c0001t0001g0002a0002c0002t0001g0152a0003c0003t0001g0153others(3): Show | 10 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.72+6141G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460636 | ||||||
| chr2:101460637
|
G | A | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0141 | 3 | NA18971.hp1 NA18975.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.72+6140C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460637 | ||||||
| chr2:101460638
|
G | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+6139C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460638 | ||||||
| chr2:101460705
|
T | C | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+6072A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460705 | ||||||
| chr2:101460743
|
CT | C | 5 | a0002c0002t0001g0288a0002c0002t0001g0310a0002c0008t0004g0008others(2): Show | 6 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.72+6033delA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460743 | ||||||
| chr2:101460821
|
G | A | 2 | a0002c0008t0004g0008a0002c0008t0004g0021 | 3 | HG02630.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.72+5956C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460821 | ||||||
| chr2:101460845
|
T | C | 1 | a0001c0001t0001g0313 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.72+5932A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460845 | ||||||
| chr2:101460916
|
T | C | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+5861A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460916 | ||||||
| chr2:101461007
|
G | A | 1 | a0008c0009t0002g0032 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.72+5770C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461007 | ||||||
| chr2:101461050
|
C | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+5727G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461050 | ||||||
| chr2:101461059
|
G | A | 9 | a0001c0001t0001g0005a0001c0001t0001g0150a0001c0001t0001g0193others(6): Show | 11 | HG02257.hp2 HG02559.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+5718C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461059 | ||||||
| chr2:101461065
|
G | A | 8 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0311others(5): Show | 11 | HG00438.hp2 HG01106.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.72+5712C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461065 | ||||||
| chr2:101461075
|
T | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+5702A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461075 | ||||||
| chr2:101461120
|
A | G | 5 | a0009c0006t0001g0158a0009c0006t0001g0164a0009c0006t0001g0165others(2): Show | 5 | HG01243.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+5657T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461120 | ||||||
| chr2:101461125
|
C | T | 2 | a0001c0001t0001g0312a0003c0003t0001g0235 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.72+5652G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461125 | ||||||
| chr2:101461126
|
G | A | 8 | a0001c0001t0001g0314a0002c0002t0001g0294a0002c0002t0001g0316others(5): Show | 8 | HG02145.hp1 HG02622.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.72+5651C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461126 | ||||||
| chr2:101461179
|
C | T | 133 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(130): Show | 149 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.72+5598G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461179 | ||||||
| chr2:101461180
|
G | A | 1 | a0004c0004t0001g0127 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.72+5597C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461180 | ||||||
| chr2:101461211
|
C | T | 59 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0109others(56): Show | 69 | HG00323.hp2 HG00408.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.72+5566G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461211 | ||||||
| chr2:101461241
|
C | T | 1 | a0002c0002t0002g0054 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.72+5536G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461241 | ||||||
| chr2:101461262
|
C | CAA | 46 | a0001c0001t0001g0013a0001c0001t0001g0109a0001c0001t0001g0115others(43): Show | 54 | HG00323.hp2 HG00408.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.72+5513_72+5514dup others(2): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461262 | ||||||
| chr2:101461262
|
CA | C | 131 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0149others(128): Show | 141 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.72+5514delT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461262 | ||||||
| chr2:101461279
|
A | AAAG | 13 | a0001c0001t0001g0002a0001c0001t0001g0250a0001c0001t0002g0074others(10): Show | 17 | HG02109.hp2 HG02258.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.72+5497_72+5498ins others(3): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461279 | ||||||
| chr2:101461279
|
A | AAG | 74 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(71): Show | 80 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.72+5497_72+5498ins others(2): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461279 | ||||||
| chr2:101461279
|
A | G | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.72+5498T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461279 | ||||||
| chr2:101461384
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.72+5393G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461384 | ||||||
| chr2:101461485
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.72+5292G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461485 | ||||||
| chr2:101461667
|
G | C | 1 | a0003c0003t0001g0317 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.72+5110C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461667 | ||||||
| chr2:101461773
|
C | G | 1 | a0003c0003t0002g0053 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.72+5004G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461773 | ||||||
| chr2:101461785
|
C | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+4992G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461785 | ||||||
| chr2:101461789
|
G | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+4988C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461789 | ||||||
| chr2:101462041
|
G | C | 1 | a0002c0002t0001g0207 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.72+4736C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462041 | ||||||
| chr2:101462073
|
A | T | 1 | a0002c0002t0001g0213 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.72+4704T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462073 | ||||||
| chr2:101462191
|
G | C | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+4586C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462191 | ||||||
| chr2:101462192
|
G | A | 2 | a0001c0015t0001g0185a0011c0014t0001g0188 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.72+4585C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462192 | ||||||
| chr2:101462260
|
T | G | 5 | a0001c0001t0002g0080a0002c0002t0001g0195a0002c0002t0001g0196others(2): Show | 5 | HG00673.hp2 HG02040.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+4517A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462260 | ||||||
| chr2:101462284
|
T | C | 1 | a0008c0009t0001g0182 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.72+4493A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462284 | ||||||
| chr2:101462286
|
A | G | 294 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(291): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.72+4491T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462286 | ||||||
| chr2:101462301
|
A | G | 90 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(87): Show | 102 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(99): Show |
intron_variant | MODIFIER | c.72+4476T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462301 | ||||||
| chr2:101462403
|
C | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+4374G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462403 | ||||||
| chr2:101462421
|
C | T | 5 | a0002c0002t0001g0152a0003c0003t0001g0153a0006c0011t0001g0018others(2): Show | 6 | HG01884.hp1 HG02109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.72+4356G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462421 | ||||||
| chr2:101462527
|
A | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0136 | 3 | HG01069.hp1 HG01071.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.72+4250T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462527 | ||||||
| chr2:101462535
|
T | C | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+4242A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462535 | ||||||
| chr2:101462656
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+4121T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462656 | ||||||
| chr2:101462660
|
GTACTATT others(8): Show |
G | 80 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0134others(77): Show | 86 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.72+4102_72+4116del others(15): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462660 | ||||||
| chr2:101462809
|
A | C | 57 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0141others(54): Show | 62 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.72+3968T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462809 | ||||||
| chr2:101462829
|
G | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+3948C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462829 | ||||||
| chr2:101462984
|
T | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(91): Show | 106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+3793A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462984 | ||||||
| chr2:101463000
|
C | T | 1 | a0003c0003t0001g0235 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.72+3777G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463000 | ||||||
| chr2:101463045
|
G | C | 1 | a0001c0001t0001g0107 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.72+3732C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463045 | ||||||
| chr2:101463063
|
C | T | 100 | a0001c0001t0001g0190a0001c0001t0001g0200a0001c0001t0001g0214others(97): Show | 106 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+3714G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463063 | ||||||
| chr2:101463100
|
T | C | 2 | a0001c0015t0001g0185a0011c0014t0001g0188 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.72+3677A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463100 | ||||||
| chr2:101463113
|
C | T | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.72+3664G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463113 | ||||||
| chr2:101463162
|
A | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(93): Show | 108 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.72+3615T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463162 | ||||||
| chr2:101463294
|
G | C | 6 | a0001c0001t0001g0002a0002c0002t0001g0152a0003c0003t0001g0153others(3): Show | 10 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.72+3483C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463294 | ||||||
| chr2:101463302
|
A | G | 96 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(93): Show | 108 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.72+3475T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463302 | ||||||
| chr2:101463307
|
T | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(93): Show | 108 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.72+3470A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463307 | ||||||
| chr2:101463351
|
C | T | 1 | a0002c0002t0001g0270 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.72+3426G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463351 | ||||||
| chr2:101463457
|
T | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(93): Show | 108 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.72+3320A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463457 | ||||||
| chr2:101463468
|
C | T | 2 | a0002c0002t0001g0152a0003c0003t0001g0153 | 2 | HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.72+3309G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463468 | ||||||
| chr2:101463548
|
C | T | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.72+3229G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463548 | ||||||
| chr2:101463575
|
C | T | 1 | a0016c0025t0001g0159 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.72+3202G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463575 | ||||||
| chr2:101463585
|
C | T | 96 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(93): Show | 108 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.72+3192G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463585 | ||||||
| chr2:101463613
|
A | G | 96 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(93): Show | 108 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.72+3164T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463613 | ||||||
| chr2:101463616
|
G | A | 96 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(93): Show | 108 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.72+3161C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463616 | ||||||
| chr2:101463620
|
A | G | 4 | a0001c0001t0001g0210a0002c0002t0001g0006a0002c0002t0001g0209others(1): Show | 6 | NA18612.hp1 NA18951.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.72+3157T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463620 | ||||||
| chr2:101463657
|
A | G | 96 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(93): Show | 108 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.72+3120T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463657 | ||||||
| chr2:101463687
|
G | A | 1 | a0003c0003t0001g0292 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.72+3090C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463687 | ||||||
| chr2:101463845
|
G | T | 96 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(93): Show | 108 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.72+2932C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463845 | ||||||
| chr2:101463846
|
C | T | 96 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(93): Show | 108 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.72+2931G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463846 | ||||||
| chr2:101463919
|
G | A | 3 | a0001c0001t0001g0269a0001c0001t0001g0307a0002c0002t0001g0019 | 4 | HG00099.hp2 HG01516.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+2858C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463919 | ||||||
| chr2:101463935
|
C | T | 1 | a0002c0002t0001g0213 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.72+2842G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463935 | ||||||
| chr2:101464066
|
C | A | 96 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(93): Show | 108 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.72+2711G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101464066 | ||||||
| chr2:101464284
|
T | A | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.72+2493A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101464284 | ||||||
| chr2:101464288
|
A | C | 1 | a0002c0002t0001g0270 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.72+2489T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101464288 | ||||||
| chr2:101464371
|
G | A | 1 | a0019c0019t0001g0245 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.72+2406C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101464371 | ||||||
| chr2:101464444
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.72+2333G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101464444 | ||||||
| chr2:101464464
|
G | A | 92 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0107others(89): Show | 104 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.72+2313C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101464464 | ||||||
| chr2:101464533
|
G | T | 1 | a0002c0002t0002g0029 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.72+2244C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101464533 | ||||||
| chr2:101464633
|
G | A | 1 | a0001c0001t0003g0098 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.72+2144C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101464633 | ||||||
| chr2:101464657
|
G | A | 98 | a0001c0001t0001g0190a0001c0001t0001g0200a0001c0001t0001g0214others(95): Show | 104 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.72+2120C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101464657 | ||||||
| chr2:101464769
|
T | A | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.72+2008A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101464769 | ||||||
| chr2:101464845
|
A | AAAGAACT others(14): Show |
4 | a0001c0001t0001g0210a0002c0002t0001g0006a0002c0002t0001g0209others(1): Show | 6 | NA18612.hp1 NA18951.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.72+1931_72+1932ins others(21): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101464845 | ||||||
| chr2:101464944
|
T | C | 1 | a0002c0002t0001g0257 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.72+1833A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101464944 | ||||||
| chr2:101465019
|
T | C | 1 | a0002c0002t0002g0081 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.72+1758A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101465019 | ||||||
| chr2:101465370
|
C | T | 1 | a0002c0002t0001g0302 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.72+1407G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101465370 | ||||||
| chr2:101465441
|
C | T | 11 | a0001c0001t0001g0002a0001c0001t0001g0251a0001c0001t0001g0252others(8): Show | 15 | HG01516.hp1 HG01884.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.72+1336G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101465441 | ||||||
| chr2:101465474
|
C | T | 6 | a0001c0001t0001g0002a0002c0002t0001g0152a0003c0003t0001g0153others(3): Show | 10 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.72+1303G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101465474 | ||||||
| chr2:101465544
|
A | C | 37 | a0001c0001t0001g0013a0001c0001t0001g0109a0001c0001t0001g0115others(34): Show | 40 | HG00323.hp2 HG00408.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.72+1233T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101465544 | ||||||
| chr2:101465588
|
T | C | 1 | a0009c0006t0001g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.72+1189A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101465588 | ||||||
| chr2:101465633
|
TAAC | T | 4 | a0001c0001t0001g0250a0002c0002t0001g0211a0002c0002t0001g0248others(1): Show | 4 | HG02145.hp2 HG03579.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+1141_72+1143del others(3): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101465633 | ||||||
| chr2:101465696
|
G | A | 1 | a0003c0003t0001g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.72+1081C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101465696 | ||||||
| chr2:101465730
|
A | T | 2 | a0003c0003t0001g0189a0011c0014t0001g0188 | 2 | HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.72+1047T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101465730 | ||||||
| chr2:101465816
|
C | T | 11 | a0001c0001t0001g0013a0001c0001t0001g0115a0001c0001t0001g0116others(8): Show | 12 | HG00673.hp1 HG02129.hp2 NA18942.hp1 others(9): Show |
intron_variant | MODIFIER | c.72+961G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101465816 | ||||||
| chr2:101465818
|
C | T | 2 | a0002c0002t0001g0195a0002c0002t0001g0196 | 2 | NA19080.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.72+959G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101465818 | ||||||
| chr2:101465938
|
G | A | 1 | a0001c0001t0002g0041 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.72+839C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101465938 | ||||||
| chr2:101466029
|
G | C | 1 | a0007c0010t0001g0260 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.72+748C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101466029 | ||||||
| chr2:101466130
|
T | C | 1 | a0001c0001t0001g0313 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.72+647A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101466130 | ||||||
| chr2:101466168
|
C | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0122a0001c0001t0001g0190others(133): Show | 149 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.72+609G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101466168 | ||||||
| chr2:101466246
|
T | C | 1 | a0002c0002t0005g0022 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.72+531A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101466246 | ||||||
| chr2:101466276
|
T | C | 300 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(297): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.72+501A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101466276 | ||||||
| chr2:101466309
|
G | GA | 97 | a0001c0001t0001g0193a0001c0001t0001g0197a0001c0001t0001g0200others(94): Show | 103 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.72+467dupT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101466309 | ||||||
| chr2:101466309
|
GA | G | 61 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0109others(58): Show | 64 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.72+467delT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101466309 | ||||||
| chr2:101466309
|
GAA | G | 41 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(38): Show | 53 | HG00639.hp2 HG00735.hp2 HG01099.hp1 others(50): Show |
intron_variant | MODIFIER | c.72+466_72+467delTT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101466309 | ||||||
| chr2:101466423
|
T | C | 120 | a0001c0001t0001g0002a0001c0001t0001g0193a0001c0001t0001g0197others(117): Show | 130 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.72+354A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101466423 | ||||||
| chr2:101466471
|
C | A | 1 | a0001c0001t0001g0120 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.72+306G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101466471 | ||||||
| chr2:101466498
|
C | T | 1 | a0008c0009t0002g0032 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.72+279G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101466498 | ||||||
| chr2:101466719
|
A | C | 1 | a0001c0001t0001g0237 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.72+58T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101466719 | ||||||
| chr2:101466721
|
T | C | 142 | a0001c0001t0001g0002a0001c0001t0001g0190a0001c0001t0001g0193others(139): Show | 154 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.72+56A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101466721 | ||||||
| chr2:101466739
|
CT | C | 3 | a0003c0003t0001g0189a0011c0014t0001g0188a0021c0018t0001g0187 | 3 | HG02451.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.72+37delA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101466739 | ||||||
| chr2:101466924
|
G | A | 1 | a0010c0007t0003g0097 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-52-24C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101466924 | ||||||
| chr2:101466931
|
T | C | 75 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0009others(72): Show | 86 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.-52-31A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101466931 | ||||||
| chr2:101467146
|
T | C | 1 | a0002c0002t0001g0294 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-52-246A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101467146 | ||||||
| chr2:101467154
|
T | C | 1 | a0021c0018t0001g0187 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-52-254A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101467154 | ||||||
| chr2:101467205
|
C | T | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-52-305G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101467205 | ||||||
| chr2:101467405
|
A | T | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-52-505T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101467405 | ||||||
| chr2:101467449
|
G | C | 1 | a0002c0002t0005g0022 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-52-549C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101467449 | ||||||
| chr2:101467458
|
G | A | 1 | a0002c0002t0001g0295 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-52-558C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101467458 | ||||||
| chr2:101467578
|
C | T | 1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-52-678G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101467578 | ||||||
| chr2:101467721
|
G | C | 205 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(202): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.-52-821C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101467721 | ||||||
| chr2:101467854
|
C | T | 304 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(301): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.-52-954G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101467854 | ||||||
| chr2:101467869
|
T | TA | 14 | a0001c0001t0003g0094a0001c0001t0003g0096a0001c0001t0003g0098others(11): Show | 14 | HG01167.hp2 HG01891.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-52-970dupT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101467869 | ||||||
| chr2:101467980
|
A | T | 2 | a0001c0001t0001g0312a0003c0003t0001g0235 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-52-1080T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101467980 | ||||||
| chr2:101468006
|
T | C | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-52-1106A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468006 | ||||||
| chr2:101468278
|
G | A | 1 | a0001c0001t0001g0313 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-52-1378C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468278 | ||||||
| chr2:101468354
|
GGTGTTCC others(3): Show |
G | 1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-52-1464_-52-1455d others(12): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468354 | ||||||
| chr2:101468364
|
A | G | 64 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0109others(61): Show | 68 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.-52-1464T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468364 | ||||||
| chr2:101468580
|
G | A | 2 | a0003c0003t0001g0317a0003c0003t0001g0318 | 2 | HG02622.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-52-1680C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468580 | ||||||
| chr2:101468671
|
T | C | 14 | a0001c0001t0003g0094a0001c0001t0003g0096a0001c0001t0003g0098others(11): Show | 14 | HG01167.hp2 HG01891.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-52-1771A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468671 | ||||||
| chr2:101468745
|
G | A | 1 | a0014c0017t0001g0186 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-52-1845C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468745 | ||||||
| chr2:101468785
|
A | G | 1 | a0007c0010t0001g0234 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-52-1885T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468785 | ||||||
| chr2:101468794
|
T | A | 1 | a0001c0001t0002g0086 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-52-1894A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468794 | ||||||
| chr2:101468961
|
C | CAT | 3 | a0001c0001t0001g0016a0001c0001t0001g0151a0014c0017t0001g0186 | 4 | HG02717.hp2 HG02886.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52-2063_-52-2062d others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468961 | ||||||
| chr2:101468980
|
A | G | 3 | a0006c0011t0001g0018a0006c0011t0001g0183a0017c0024t0001g0184 | 4 | HG01884.hp1 HG02109.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52-2080T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468980 | ||||||
| chr2:101468980
|
ATATATAT others(123): Show |
A | 1 | a0001c0001t0001g0141 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-52-2210_-52-2081d others(2): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468980 | ||||||
| chr2:101468990
|
A | G | 1 | a0001c0001t0003g0103 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-52-2090T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468990 | ||||||
| chr2:101468991
|
A | C | 1 | a0014c0017t0001g0186 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-52-2091T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468991 | ||||||
| chr2:101468991
|
A | T | 2 | a0001c0001t0003g0103a0001c0015t0001g0185 | 2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-52-2091T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468991 | ||||||
| chr2:101468991
|
AGTATATA others(19): Show |
A | 5 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0312others(2): Show | 5 | HG01069.hp2 HG02965.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52-2117_-52-2092d others(28): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468991 | ||||||
| chr2:101468991
|
AGTATATA others(43): Show |
A | 125 | a0001c0001t0001g0002a0001c0001t0001g0193a0001c0001t0001g0197others(122): Show | 135 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.-52-2141_-52-2092d others(52): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468991 | ||||||
| chr2:101468992
|
G | A | 1 | a0001c0001t0003g0103 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-52-2092C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468992 | ||||||
| chr2:101468996
|
ATATATAC others(1): Show |
A | 5 | a0001c0001t0001g0190a0001c0001t0001g0210a0002c0002t0001g0006others(2): Show | 7 | HG02056.hp2 NA18612.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.-52-2104_-52-2097d others(10): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468996 | ||||||
| chr2:101469003
|
C | G | 1 | a0001c0001t0003g0103 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-52-2103G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469003 | ||||||
| chr2:101469003
|
C | T | 58 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0109others(55): Show | 61 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.-52-2103G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469003 | ||||||
| chr2:101469006
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0003g0103 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-52-2107_-52-2106i others(14): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469006 | ||||||
| chr2:101469007
|
T | C | 2 | a0001c0001t0001g0298a0004c0004t0001g0206 | 2 | HG00558.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-52-2107A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469007 | ||||||
| chr2:101469008
|
A | G | 2 | a0001c0001t0001g0298a0004c0004t0001g0206 | 2 | HG00558.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-52-2108T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469008 | ||||||
| chr2:101469014
|
A | G | 6 | a0001c0001t0001g0190a0001c0001t0001g0210a0002c0002t0001g0006others(3): Show | 8 | HG02056.hp2 HG02523.hp1 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.-52-2114T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469014 | ||||||
| chr2:101469017
|
G | A | 5 | a0001c0001t0001g0190a0001c0001t0001g0210a0002c0002t0001g0006others(2): Show | 7 | HG02056.hp2 NA18612.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.-52-2117C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469017 | ||||||
| chr2:101469017
|
G | C | 1 | a0001c0001t0003g0103 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-52-2117C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469017 | ||||||
| chr2:101469017
|
G | T | 2 | a0001c0001t0001g0298a0004c0004t0001g0206 | 2 | HG00558.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-52-2117C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469017 | ||||||
| chr2:101469018
|
G | GTA | 5 | a0006c0011t0001g0018a0006c0011t0001g0183a0009c0006t0001g0164others(2): Show | 6 | HG01884.hp1 HG02109.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-52-2120_-52-2119d others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469018 | ||||||
| chr2:101469020
|
A | ATATATAT others(15): Show |
3 | a0002c0002t0001g0112a0003c0003t0001g0113a0003c0003t0001g0114 | 3 | NA18944.hp2 NA18971.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-52-2121_-52-2120i others(24): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469020 | ||||||
| chr2:101469022
|
ATATATAT others(3): Show |
A | 5 | a0001c0001t0001g0190a0001c0001t0001g0210a0002c0002t0001g0006others(2): Show | 7 | HG02056.hp2 NA18612.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.-52-2132_-52-2123d others(12): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469022 | ||||||
| chr2:101469029
|
TAC | T | 42 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0109others(39): Show | 45 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.-52-2131_-52-2130d others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469029 | ||||||
| chr2:101469031
|
C | A | 5 | a0001c0001t0001g0298a0002c0002t0001g0301a0003c0003t0002g0030others(2): Show | 5 | HG00558.hp1 HG02523.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52-2131G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469031 | ||||||
| chr2:101469041
|
T | A | 5 | a0001c0001t0001g0190a0001c0001t0001g0210a0002c0002t0001g0006others(2): Show | 7 | HG02056.hp2 NA18612.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.-52-2141A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469041 | ||||||
| chr2:101469041
|
T | TAC | 14 | a0001c0001t0003g0094a0001c0001t0003g0096a0001c0001t0003g0098others(11): Show | 14 | HG01167.hp2 HG01891.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-52-2142_-52-2141i others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469041 | ||||||
| chr2:101469041
|
T | TACGTATA others(9): Show |
2 | a0003c0003t0002g0030a0014c0017t0002g0031 | 2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-52-2142_-52-2141i others(18): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469041 | ||||||
| chr2:101469041
|
T | TATACGTA others(33): Show |
1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-52-2142_-52-2141i others(42): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469041 | ||||||
| chr2:101469042
|
G | A | 42 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0109others(39): Show | 45 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.-52-2142C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469042 | ||||||
| chr2:101469043
|
T | G | 42 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0109others(39): Show | 45 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.-52-2143A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469043 | ||||||
| chr2:101469044
|
A | G | 42 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0109others(39): Show | 45 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.-52-2144T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469044 | ||||||
| chr2:101469044
|
ATATATAT others(59): Show |
A | 1 | a0004c0004t0001g0206 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-52-2210_-52-2145d others(68): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469044 | ||||||
| chr2:101469049
|
T | G | 1 | a0001c0001t0002g0027 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-52-2149A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469049 | ||||||
| chr2:101469055
|
C | A | 6 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0312others(3): Show | 6 | HG01069.hp2 HG01884.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-52-2155G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469055 | ||||||
| chr2:101469055
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-52-2155G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469055 | ||||||
| chr2:101469056
|
G | T | 12 | a0001c0001t0001g0226a0001c0001t0001g0231a0002c0002t0001g0207others(9): Show | 12 | HG00558.hp2 HG01361.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.-52-2156C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469056 | ||||||
| chr2:101469056
|
GTA | G | 4 | a0001c0001t0001g0151a0002c0002t0005g0022a0002c0008t0004g0008others(1): Show | 5 | HG02630.hp1 HG02630.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-52-2158_-52-2157d others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469056 | ||||||
| chr2:101469063
|
T | A | 2 | a0001c0001t0001g0298a0002c0002t0001g0301 | 2 | HG02523.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-52-2163A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469063 | ||||||
| chr2:101469063
|
TATGTATA others(23): Show |
T | 10 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(7): Show | 14 | HG01257.hp1 HG01258.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.-52-2193_-52-2164d others(32): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469063 | ||||||
| chr2:101469064
|
A | G | 2 | a0001c0001t0001g0298a0002c0002t0001g0301 | 2 | HG02523.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-52-2164T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469064 | ||||||
| chr2:101469065
|
T | C | 1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-52-2165A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469065 | ||||||
| chr2:101469065
|
TGTATATA others(21): Show |
T | 12 | a0001c0001t0001g0107a0001c0001t0001g0181a0001c0001t0002g0033others(9): Show | 12 | HG01175.hp1 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-52-2193_-52-2166d others(30): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469065 | ||||||
| chr2:101469066
|
G | A | 6 | a0001c0001t0001g0298a0001c0001t0003g0103a0002c0002t0001g0112others(3): Show | 6 | HG02523.hp1 HG03516.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.-52-2166C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469066 | ||||||
| chr2:101469066
|
G | GTA | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0002c0002t0001g0297 | 3 | HG01069.hp2 HG04115.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-52-2168_-52-2167d others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469066 | ||||||
| chr2:101469066
|
GTATATAT others(23): Show |
G | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-52-2196_-52-2167d others(32): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469066 | ||||||
| chr2:101469067
|
T | C | 1 | a0001c0001t0003g0103 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-52-2167A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469067 | ||||||
| chr2:101469068
|
A | ATATATAC others(3): Show |
1 | a0011c0014t0003g0093 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-52-2169_-52-2168i others(12): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469068 | ||||||
| chr2:101469068
|
A | ATATATAT others(3): Show |
12 | a0001c0001t0003g0094a0001c0001t0003g0096a0001c0001t0003g0098others(9): Show | 12 | HG01167.hp2 HG01891.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-52-2169_-52-2168i others(12): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469068 | ||||||
| chr2:101469068
|
A | G | 4 | a0001c0001t0003g0103a0002c0002t0001g0112a0003c0003t0001g0113others(1): Show | 4 | HG03516.hp1 NA18944.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52-2168T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469068 | ||||||
| chr2:101469077
|
TAAGTGTA others(9): Show |
T | 3 | a0006c0011t0001g0018a0006c0011t0001g0183a0017c0024t0001g0184 | 4 | HG01884.hp1 HG02109.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52-2193_-52-2178d others(18): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469077 | ||||||
| chr2:101469078
|
A | G | 1 | a0001c0001t0002g0036 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-52-2178T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469078 | ||||||
| chr2:101469078
|
AAG | A | 41 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0109others(38): Show | 44 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.-52-2180_-52-2179d others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469078 | ||||||
| chr2:101469079
|
A | C | 25 | a0001c0001t0001g0115a0001c0001t0002g0037a0001c0001t0003g0094others(22): Show | 26 | HG01167.hp2 HG01891.hp1 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.-52-2179T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469079 | ||||||
| chr2:101469079
|
A | T | 3 | a0001c0001t0001g0312a0001c0001t0002g0036a0003c0003t0001g0296 | 3 | HG01255.hp1 HG02965.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-52-2179T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469079 | ||||||
| chr2:101469080
|
G | A | 2 | a0001c0001t0001g0312a0003c0003t0001g0296 | 2 | HG02965.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-52-2180C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469080 | ||||||
| chr2:101469080
|
G | GTA | 5 | a0001c0001t0001g0151a0001c0001t0001g0224a0001c0001t0001g0225others(2): Show | 5 | HG01069.hp2 HG02572.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52-2181_-52-2180i others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469080 | ||||||
| chr2:101469080
|
GTGTA | G | 3 | a0003c0003t0002g0030a0014c0017t0001g0186a0014c0017t0002g0031 | 3 | HG02965.hp2 HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-52-2184_-52-2181d others(6): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469080 | ||||||
| chr2:101469081
|
T | A | 2 | a0001c0001t0001g0312a0003c0003t0001g0296 | 2 | HG02965.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-52-2181A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469081 | ||||||
| chr2:101469081
|
T | C | 41 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0109others(38): Show | 44 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.-52-2181A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469081 | ||||||
| chr2:101469081
|
T | TATATATA others(39): Show |
1 | a0016c0025t0001g0159 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-52-2182_-52-2181i others(48): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469081 | ||||||
| chr2:101469082
|
G | A | 146 | a0001c0001t0001g0002a0001c0001t0001g0115a0001c0001t0001g0151others(143): Show | 159 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.-52-2182C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469082 | ||||||
| chr2:101469082
|
G | GTA | 67 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0009others(64): Show | 78 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.-52-2184_-52-2183d others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469082 | ||||||
| chr2:101469082
|
G | GTATATAT others(23): Show |
1 | a0015c0012t0001g0177 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-52-2212_-52-2183d others(32): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469082 | ||||||
| chr2:101469088
|
A | ATATG | 3 | a0002c0002t0001g0112a0003c0003t0001g0113a0003c0003t0001g0114 | 3 | NA18944.hp2 NA18971.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-52-2189_-52-2188i others(6): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469088 | ||||||
| chr2:101469090
|
A | G | 131 | a0001c0001t0001g0002a0001c0001t0001g0190a0001c0001t0001g0193others(128): Show | 143 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.-52-2190T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469090 | ||||||
| chr2:101469092
|
A | G | 2 | a0001c0001t0001g0312a0003c0003t0001g0296 | 2 | HG02965.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-52-2192T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469092 | ||||||
| chr2:101469092
|
AAG | A | 131 | a0001c0001t0001g0002a0001c0001t0001g0190a0001c0001t0001g0193others(128): Show | 143 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.-52-2194_-52-2193d others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469092 | ||||||
| chr2:101469093
|
A | C | 14 | a0001c0001t0003g0094a0001c0001t0003g0096a0001c0001t0003g0098others(11): Show | 14 | HG01167.hp2 HG01891.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-52-2193T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469093 | ||||||
| chr2:101469093
|
A | T | 51 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0109others(48): Show | 54 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.-52-2193T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469093 | ||||||
| chr2:101469094
|
G | A | 6 | a0001c0001t0001g0312a0002c0002t0001g0112a0002c0002t0001g0297others(3): Show | 6 | HG02965.hp1 NA18944.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.-52-2194C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469094 | ||||||
| chr2:101469096
|
A | ATATATAT others(51): Show |
2 | a0001c0001t0003g0096a0002c0002t0003g0095 | 2 | HG02257.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-52-2197_-52-2196i others(60): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469096 | ||||||
| chr2:101469096
|
A | ATATATAT others(51): Show |
2 | a0001c0001t0003g0094a0001c0001t0008g0320 | 2 | HG01167.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.-52-2197_-52-2196i others(60): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469096 | ||||||
| chr2:101469096
|
A | ATATATAT others(51): Show |
6 | a0001c0001t0003g0103a0005c0005t0003g0099a0005c0005t0003g0100others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-52-2197_-52-2196i others(60): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469096 | ||||||
| chr2:101469096
|
A | ATATATAT others(51): Show |
2 | a0001c0001t0003g0098a0001c0001t0003g0105 | 2 | HG02735.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-52-2197_-52-2196i others(60): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469096 | ||||||
| chr2:101469096
|
A | ATATATAT others(53): Show |
1 | a0010c0007t0003g0097 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-52-2197_-52-2196i others(62): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469096 | ||||||
| chr2:101469096
|
A | ATATATAT others(27): Show |
1 | a0011c0014t0003g0093 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-52-2197_-52-2196i others(36): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469096 | ||||||
| chr2:101469096
|
A | G | 2 | a0001c0001t0001g0115a0016c0025t0001g0159 | 2 | HG03471.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.-52-2196T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469096 | ||||||
| chr2:101469098
|
ATATATAT others(5): Show |
A | 1 | a0001c0001t0001g0298 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-52-2210_-52-2199d others(14): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469098 | ||||||
| chr2:101469104
|
A | ACG | 34 | a0001c0001t0001g0015a0001c0001t0001g0121a0001c0001t0001g0122others(31): Show | 36 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.-52-2205_-52-2204i others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469104 | ||||||
| chr2:101469105
|
T | C | 7 | a0001c0001t0001g0013a0001c0001t0001g0109a0001c0001t0001g0116others(4): Show | 8 | NA18942.hp1 NA18945.hp1 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.-52-2205A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469105 | ||||||
| chr2:101469106
|
A | G | 7 | a0001c0001t0001g0013a0001c0001t0001g0109a0001c0001t0001g0116others(4): Show | 8 | NA18942.hp1 NA18945.hp1 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.-52-2206T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469106 | ||||||
| chr2:101469107
|
A | C | 22 | a0001c0001t0001g0115a0001c0001t0003g0094a0001c0001t0003g0096others(19): Show | 23 | HG01167.hp2 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.-52-2207T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469107 | ||||||
| chr2:101469107
|
A | T | 41 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0109others(38): Show | 44 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.-52-2207T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469107 | ||||||
| chr2:101469107
|
AGT | A | 3 | a0002c0002t0001g0301a0014c0017t0001g0186a0021c0018t0001g0187 | 3 | HG02523.hp1 HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-52-2209_-52-2208d others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469107 | ||||||
| chr2:101469108
|
G | A | 41 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0109others(38): Show | 44 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.-52-2208C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469108 | ||||||
| chr2:101469110
|
G | A | 219 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(216): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.-52-2210C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469110 | ||||||
| chr2:101469116
|
A | ATATG | 3 | a0002c0002t0001g0112a0003c0003t0001g0113a0003c0003t0001g0114 | 3 | NA18944.hp2 NA18971.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-52-2217_-52-2216i others(6): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469116 | ||||||
| chr2:101469116
|
A | G | 34 | a0001c0001t0001g0015a0001c0001t0001g0121a0001c0001t0001g0122others(31): Show | 36 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.-52-2216T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469116 | ||||||
| chr2:101469118
|
A | G | 7 | a0001c0001t0001g0013a0001c0001t0001g0109a0001c0001t0001g0116others(4): Show | 8 | NA18942.hp1 NA18945.hp1 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.-52-2218T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469118 | ||||||
| chr2:101469120
|
A | G | 1 | a0001c0001t0001g0115 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-52-2220T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469120 | ||||||
| chr2:101469123
|
A | T | 45 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0109others(42): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.-52-2223T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469123 | ||||||
| chr2:101469124
|
G | A | 45 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0109others(42): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.-52-2224C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469124 | ||||||
| chr2:101469126
|
ATATATAT others(5): Show |
A | 1 | a0002c0002t0001g0301 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-52-2238_-52-2227d others(14): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469126 | ||||||
| chr2:101469134
|
A | G | 1 | a0001c0001t0001g0141 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-52-2234T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469134 | ||||||
| chr2:101469135
|
T | C | 45 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0109others(42): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.-52-2235A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469135 | ||||||
| chr2:101469137
|
A | C | 45 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0109others(42): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.-52-2237T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469137 | ||||||
| chr2:101469137
|
A | T | 1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-52-2237T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469137 | ||||||
| chr2:101469138
|
G | A | 1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-52-2238C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469138 | ||||||
| chr2:101469153
|
T | C | 16 | a0001c0001t0003g0094a0001c0001t0003g0096a0001c0001t0003g0098others(13): Show | 16 | HG01167.hp2 HG01891.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-52-2253A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469153 | ||||||
| chr2:101469214
|
G | A | 1 | a0002c0002t0001g0299 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-52-2314C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469214 | ||||||
| chr2:101469236
|
C | G | 1 | a0002c0002t0001g0223 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-52-2336G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469236 | ||||||
| chr2:101469321
|
TA | T | 138 | a0001c0001t0001g0002a0001c0001t0001g0190a0001c0001t0001g0193others(135): Show | 150 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.-52-2422delT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469321 | ||||||
| chr2:101469401
|
C | G | 1 | a0014c0017t0001g0186 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-52-2501G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469401 | ||||||
| chr2:101469538
|
G | A | 8 | a0001c0001t0001g0107a0001c0001t0001g0181a0003c0003t0001g0180others(5): Show | 8 | HG01175.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-52-2638C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469538 | ||||||
| chr2:101469685
|
T | C | 1 | a0020c0023t0001g0142 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-52-2785A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469685 | ||||||
| chr2:101469735
|
A | G | 4 | a0006c0011t0001g0018a0006c0011t0001g0183a0016c0025t0001g0159others(1): Show | 5 | HG01884.hp1 HG02109.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-52-2835T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469735 | ||||||
| chr2:101469908
|
T | C | 1 | a0003c0003t0001g0300 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-52-3008A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469908 | ||||||
| chr2:101469915
|
G | A | 1 | a0002c0002t0001g0301 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-52-3015C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469915 | ||||||
| chr2:101470068
|
TTGTCACC others(22): Show |
T | 1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-52-3197_-52-3169d others(31): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470068 | ||||||
| chr2:101470137
|
CAT | C | 14 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(11): Show | 19 | HG01257.hp1 HG01258.hp2 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.-52-3239_-52-3238d others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470137 | ||||||
| chr2:101470303
|
G | T | 64 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0109others(61): Show | 68 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.-52-3403C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470303 | ||||||
| chr2:101470320
|
T | C | 6 | a0001c0001t0001g0145a0001c0001t0001g0149a0002c0002t0001g0108others(3): Show | 6 | HG00140.hp2 HG00323.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.-52-3420A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470320 | ||||||
| chr2:101470420
|
T | C | 1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-52-3520A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470420 | ||||||
| chr2:101470493
|
A | G | 14 | a0001c0001t0003g0094a0001c0001t0003g0096a0001c0001t0003g0098others(11): Show | 14 | HG01167.hp2 HG01891.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-52-3593T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470493 | ||||||
| chr2:101470581
|
C | A | 1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-52-3681G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470581 | ||||||
| chr2:101470587
|
G | A | 3 | a0001c0001t0001g0303a0002c0002t0001g0302a0012c0013t0001g0319 | 3 | HG00738.hp1 HG02300.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-52-3687C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470587 | ||||||
| chr2:101470659
|
A | G | 3 | a0001c0001t0001g0201a0001c0001t0001g0222a0002c0002t0001g0221 | 3 | HG02040.hp2 HG02083.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.-52-3759T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470659 | ||||||
| chr2:101470709
|
C | CT | 31 | a0001c0001t0001g0109a0001c0001t0001g0210a0001c0001t0001g0214others(28): Show | 32 | HG00408.hp1 HG00558.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.-52-3810dupA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470709 | ||||||
| chr2:101470709
|
CT | C | 17 | a0001c0001t0001g0107a0001c0001t0001g0148a0001c0001t0001g0149others(14): Show | 17 | HG00140.hp2 HG01175.hp1 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.-52-3810delA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470709 | ||||||
| chr2:101470709
|
CTTTTTTT | C | 5 | a0001c0001t0001g0313a0001c0015t0001g0185a0002c0002t0005g0022others(2): Show | 6 | HG01884.hp2 HG02630.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-52-3816_-52-3810d others(9): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470709 | ||||||
| chr2:101470709
|
CTTTTTTT others(1): Show |
C | 9 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(6): Show | 13 | HG01257.hp1 HG01258.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.-52-3817_-52-3810d others(10): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470709 | ||||||
| chr2:101470709
|
CTTTTTTT others(6): Show |
C | 75 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0009others(72): Show | 86 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.-52-3822_-52-3810d others(15): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470709 | ||||||
| chr2:101470782
|
C | T | 3 | a0001c0001t0001g0107a0001c0001t0001g0181a0003c0003t0001g0180 | 3 | HG01175.hp1 HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-53+3854G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470782 | ||||||
| chr2:101470788
|
C | T | 18 | a0001c0001t0003g0094a0001c0001t0003g0096a0001c0001t0003g0098others(15): Show | 19 | HG01167.hp2 HG01884.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.-53+3848G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470788 | ||||||
| chr2:101470789
|
G | C | 1 | a0011c0014t0001g0188 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-53+3847C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470789 | ||||||
| chr2:101470833
|
C | T | 4 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026others(1): Show | 4 | HG02074.hp2 HG02523.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53+3803G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470833 | ||||||
| chr2:101470864
|
C | T | 4 | a0003c0003t0001g0202a0003c0003t0001g0203a0003c0003t0001g0204others(1): Show | 4 | HG02896.hp2 HG03041.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-53+3772G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470864 | ||||||
| chr2:101470928
|
C | G | 1 | a0014c0017t0001g0186 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-53+3708G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470928 | ||||||
| chr2:101470931
|
G | A | 5 | a0001c0001t0001g0314a0002c0002t0001g0316a0003c0003t0001g0315others(2): Show | 5 | HG02145.hp1 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-53+3705C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470931 | ||||||
| chr2:101470938
|
C | A | 3 | a0001c0001t0002g0012a0001c0001t0002g0087a0002c0002t0002g0088 | 4 | HG00544.hp1 HG02155.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53+3698G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470938 | ||||||
| chr2:101471008
|
C | T | 45 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0109others(42): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.-53+3628G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101471008 | ||||||
| chr2:101471062
|
G | C | 1 | a0001c0001t0002g0089 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-53+3574C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101471062 | ||||||
| chr2:101471071
|
T | C | 3 | a0002c0002t0005g0022a0002c0008t0004g0008a0002c0008t0004g0021 | 4 | HG02630.hp1 HG02630.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53+3565A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101471071 | ||||||
| chr2:101471129
|
T | C | 1 | a0014c0017t0001g0186 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-53+3507A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101471129 | ||||||
| chr2:101471132
|
A | G | 1 | a0008c0009t0001g0182 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-53+3504T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101471132 | ||||||
| chr2:101471303
|
C | T | 14 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(11): Show | 19 | HG01257.hp1 HG01258.hp2 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.-53+3333G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101471303 | ||||||
| chr2:101471307
|
C | A | 1 | a0001c0001t0002g0090 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-53+3329G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101471307 | ||||||
| chr2:101471682
|
T | A | 3 | a0006c0011t0001g0018a0006c0011t0001g0183a0017c0024t0001g0184 | 4 | HG01884.hp1 HG02109.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53+2954A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101471682 | ||||||
| chr2:101471882
|
G | T | 11 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(8): Show | 15 | HG01257.hp1 HG01258.hp2 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.-53+2754C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101471882 | ||||||
| chr2:101471908
|
G | A | 226 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(223): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.-53+2728C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101471908 | ||||||
| chr2:101472068
|
G | A | 1 | a0001c0001t0003g0105 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-53+2568C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101472068 | ||||||
| chr2:101472100
|
G | T | 4 | a0001c0001t0003g0094a0001c0001t0003g0096a0001c0001t0008g0320others(1): Show | 4 | HG01167.hp2 HG01891.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-53+2536C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101472100 | ||||||
| chr2:101472210
|
T | C | 301 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(298): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.-53+2426A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101472210 | ||||||
| chr2:101472250
|
C | T | 3 | a0001c0001t0001g0107a0001c0001t0001g0181a0003c0003t0001g0180 | 3 | HG01175.hp1 HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-53+2386G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101472250 | ||||||
| chr2:101472302
|
A | G | 1 | a0014c0017t0001g0186 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-53+2334T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101472302 | ||||||
| chr2:101472384
|
G | C | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-53+2252C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101472384 | ||||||
| chr2:101472420
|
T | C | 1 | a0002c0002t0001g0179 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-53+2216A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101472420 | ||||||
| chr2:101472464
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-53+2172T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101472464 | ||||||
| chr2:101472501
|
C | T | 1 | a0002c0002t0005g0022 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-53+2135G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101472501 | ||||||
| chr2:101472518
|
GAGTGGCC others(3): Show |
G | 138 | a0001c0001t0001g0002a0001c0001t0001g0190a0001c0001t0001g0193others(135): Show | 150 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.-53+2108_-53+2117d others(12): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101472518 | ||||||
| chr2:101472559
|
G | A | 225 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(222): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.-53+2077C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101472559 | ||||||
| chr2:101472691
|
A | G | 1 | a0014c0017t0001g0186 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-53+1945T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101472691 | ||||||
| chr2:101472775
|
T | A | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-53+1861A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101472775 | ||||||
| chr2:101473185
|
G | T | 3 | a0006c0011t0001g0018a0006c0011t0001g0183a0017c0024t0001g0184 | 4 | HG01884.hp1 HG02109.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53+1451C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101473185 | ||||||
| chr2:101473276
|
C | T | 138 | a0001c0001t0001g0002a0001c0001t0001g0190a0001c0001t0001g0193others(135): Show | 150 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.-53+1360G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101473276 | ||||||
| chr2:101473355
|
C | T | 3 | a0001c0001t0001g0200a0002c0002t0001g0198a0002c0002t0001g0199 | 3 | HG01070.hp1 HG01071.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-53+1281G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101473355 | ||||||
| chr2:101473416
|
C | T | 217 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(214): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.-53+1220G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101473416 | ||||||
| chr2:101473482
|
G | A | 1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-53+1154C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101473482 | ||||||
| chr2:101473504
|
C | T | 1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-53+1132G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101473504 | ||||||
| chr2:101473593
|
C | G | 14 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(11): Show | 19 | HG01257.hp1 HG01258.hp2 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.-53+1043G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101473593 | ||||||
| chr2:101473995
|
G | A | 1 | a0012c0013t0001g0319 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-53+641C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101473995 | ||||||
| chr2:101474112
|
G | A | 3 | a0006c0011t0001g0018a0006c0011t0001g0183a0017c0024t0001g0184 | 4 | HG01884.hp1 HG02109.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53+524C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101474112 | ||||||
| chr2:101474157
|
G | A | 1 | a0002c0002t0005g0022 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-53+479C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101474157 | ||||||
| chr2:101474221
|
G | T | 4 | a0001c0001t0001g0197a0002c0002t0001g0195a0002c0002t0001g0196others(1): Show | 4 | HG02683.hp2 HG03017.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53+415C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101474221 | ||||||
| chr2:101474296
|
G | A | 1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-53+340C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101474296 | ||||||
| chr2:101474308
|
G | A | 1 | a0014c0017t0001g0186 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-53+328C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101474308 | ||||||
| chr2:101474393
|
C | CG | 7 | a0001c0001t0001g0190a0001c0001t0001g0193a0002c0002t0001g0108others(4): Show | 7 | HG01261.hp1 HG02056.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.-53+242dupC | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101474393 | ||||||
| chr2:101474473
|
G | C | 3 | a0003c0003t0001g0189a0011c0014t0001g0188a0021c0018t0001g0187 | 3 | HG02451.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-53+163C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101474473 | ||||||
| chr2:101474523
|
C | G | 45 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0109others(42): Show | 48 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.-53+113G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101474523 | ||||||
| chr2:101474524
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-53+112G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101474524 | ||||||
| chr2:101474547
|
C | G | 1 | a0002c0002t0002g0023 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-53+89G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101474547 | ||||||
| chr2:101474613
|
G | A | 137 | a0001c0001t0001g0002a0001c0001t0001g0190a0001c0001t0001g0193others(134): Show | 149 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.-53+23C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101474613 |