Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 54845 |
|---|---|
| ensemblid | ENSG00000104413.18 |
| hgncid | 25966 |
| symbol | ESRP1 |
| name | epithelial splicing regulatory protein 1 |
| refseq_nuc | NM_017697.4 |
| refseq_prot | NP_060167.2 |
| ensembl_nuc | ENST00000433389.8 |
| ensembl_prot | ENSP00000405738.2 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 94641174 |
| end | 94707466 |
| strand | + |
| ver | v1.2 |
| region | chr8:94641174-94707466 |
| region5000 | chr8:94636174-94712466 |
| regionname0 | ESRP1_chr8_94641174_94707466 |
| regionname5000 | ESRP1_chr8_94636174_94712466 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 681 | 371 | 95 | 68 | 156 | 9 | 41 | 116 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0002 | 0/0 | 681 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0003 | 0/0 | 681 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0004 | 0/0 | 681 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 2046 | 217 | 74 | 34 | 90 | 5 | 13 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| c0002 | 0/0 | 2046 | 88 | 2 | 8 | 65 | 0 | 13 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| c0003 | 0/1 | 2046 | 39 | 8 | 19 | 0 | 2 | 9 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| c0004 | 0/0 | 2046 | 16 | 1 | 7 | 0 | 2 | 6 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| c0005 | 0/0 | 2046 | 4 | 4 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| c0006 | 0/0 | 2046 | 2 | 2 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| c0007 | 0/0 | 2046 | 2 | 2 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| c0008 | 0/0 | 2046 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| c0009 | 0/0 | 2046 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| c0010 | 0/0 | 2046 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| c0011 | 0/0 | 2046 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| c0012 | 0/0 | 2046 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| c0013 | 0/0 | 2046 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 1723 | 251 | 78 | 55 | 87 | 8 | 22 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| t0002 | 1/0 | 1723 | 97 | 1 | 13 | 61 | 2 | 19 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| t0003 | 0/0 | 1723 | 6 | 6 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| t0004 | 0/0 | 1723 | 5 | 5 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| t0005 | 0/0 | 1723 | 4 | 0 | 0 | 4 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| t0006 | 0/0 | 1723 | 3 | 3 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| t0007 | 0/0 | 1723 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| t0008 | 0/0 | 1723 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| t0009 | 0/0 | 1723 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| t0010 | 0/0 | 1723 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| t0011 | 0/0 | 1723 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| t0012 | 0/0 | 1723 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| t0013 | 0/0 | 1723 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| t0014 | 0/0 | 1723 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0135 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0319 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2046 | 217 | 74 | 34 | 90 | 5 | 13 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0002 | 0/0 | 2046 | 88 | 2 | 8 | 65 | 0 | 13 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0003 | 0/1 | 2046 | 39 | 8 | 19 | 0 | 2 | 9 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0004 | 0/0 | 2046 | 16 | 1 | 7 | 0 | 2 | 6 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0005 | 0/0 | 2046 | 4 | 4 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0006 | 0/0 | 2046 | 2 | 2 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0007 | 0/0 | 2046 | 2 | 2 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0008 | 0/0 | 2046 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0009 | 0/0 | 2046 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0011 | 0/0 | 2046 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0002c0012 | 0/0 | 2046 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0003c0010 | 0/0 | 2046 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0004c0013 | 0/0 | 2046 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3768 | 195 | 58 | 34 | 85 | 5 | 13 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0001t0002 | 1/0 | 3768 | 1 | 0 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0001t0003 | 0/0 | 3768 | 6 | 6 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0001t0004 | 0/0 | 3768 | 5 | 5 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0001t0005 | 0/0 | 3768 | 4 | 0 | 0 | 4 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0001t0006 | 0/0 | 3768 | 3 | 3 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0001t0009 | 0/0 | 3768 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0001t0010 | 0/0 | 3768 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0001t0011 | 0/0 | 3768 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0002t0001 | 0/0 | 3768 | 4 | 1 | 2 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0002t0002 | 0/0 | 3768 | 80 | 0 | 6 | 61 | 0 | 13 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0002t0008 | 0/0 | 3768 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0002t0012 | 0/0 | 3768 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0002t0013 | 0/0 | 3768 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0002t0014 | 0/0 | 3768 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0003t0001 | 0/1 | 3768 | 39 | 8 | 19 | 0 | 2 | 9 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0004t0002 | 0/0 | 3768 | 15 | 1 | 7 | 0 | 2 | 5 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0004t0007 | 0/0 | 3768 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0005t0001 | 0/0 | 3768 | 4 | 4 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0006t0001 | 0/0 | 3768 | 2 | 2 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0007t0001 | 0/0 | 3768 | 2 | 2 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0008t0001 | 0/0 | 3768 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0009t0001 | 0/0 | 3768 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0001c0011t0001 | 0/0 | 3768 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0002c0012t0002 | 0/0 | 3768 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0003c0010t0001 | 0/0 | 3768 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| a0004c0013t0001 | 0/0 | 3768 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | copy fasta | chr8 | 94636174 | 94712466 |
| 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 | 2 | 0 | 2 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0002g0319 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0005g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0005g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0005g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0006g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0006g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0009g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0010g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0011g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0008g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0012g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0013g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0014g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0135 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0007g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0005t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0005t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0005t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0005t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0006t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0006t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0007t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0007t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0008t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0009t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0011t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0002c0012t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0003c0010t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0004c0013t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | GBR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00140 | hp2 | a0004 | c0013 | t0001 | g0145 | EUR | GBR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00323 | hp1 | a0001 | c0004 | t0002 | g0090 | EUR | FIN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0342 | EUR | FIN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | CHS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0055 | EAS | CHS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00423 | hp1 | a0001 | c0001 | t0005 | g0298 | EAS | CHS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | CHS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0061 | EAS | CHS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0098 | EAS | CHS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0053 | EAS | CHS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0332 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00642 | hp2 | a0001 | c0003 | t0001 | g0334 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0082 | EAS | CHS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | CHS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0019 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0037 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00735 | hp2 | a0001 | c0003 | t0001 | g0339 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0051 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00741 | hp2 | a0001 | c0003 | t0001 | g0241 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01069 | hp2 | a0001 | c0003 | t0001 | g0330 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01070 | hp1 | a0001 | c0004 | t0002 | g0093 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01070 | hp2 | a0001 | c0003 | t0001 | g0351 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01071 | hp1 | a0001 | c0003 | t0001 | g0328 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01071 | hp2 | a0001 | c0004 | t0002 | g0096 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01074 | hp1 | a0001 | c0004 | t0002 | g0095 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01074 | hp2 | a0001 | c0003 | t0001 | g0325 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01081 | hp1 | a0001 | c0003 | t0001 | g0348 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0120 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01099 | hp2 | a0001 | c0003 | t0001 | g0324 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01167 | hp2 | a0001 | c0003 | t0001 | g0369 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01168 | hp2 | a0001 | c0004 | t0002 | g0094 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01175 | hp2 | a0001 | c0003 | t0001 | g0337 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01243 | hp2 | a0001 | c0004 | t0002 | g0099 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0343 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01256 | hp2 | a0001 | c0004 | t0002 | g0091 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01257 | hp2 | a0001 | c0003 | t0001 | g0001 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01258 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0240 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01346 | hp1 | a0001 | c0003 | t0001 | g0134 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01433 | hp1 | a0001 | c0003 | t0001 | g0151 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0078 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01516 | hp1 | a0001 | c0004 | t0002 | g0101 | EUR | IBS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0154 | EUR | IBS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01517 | hp1 | a0001 | c0003 | t0001 | g0088 | EUR | IBS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | IBS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PEL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0085 | AMR | PEL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0097 | AMR | PEL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01978 | hp2 | a0001 | c0003 | t0001 | g0341 | AMR | PEL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0071 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02015 | hp2 | a0001 | c0001 | t0005 | g0302 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0031 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02040 | hp1 | a0001 | c0001 | t0005 | g0274 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0028 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02056 | hp1 | a0001 | c0001 | t0005 | g0306 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0075 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0077 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02080 | hp1 | a0001 | c0002 | t0014 | g0042 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0059 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0027 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0121 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02145 | hp1 | a0001 | c0009 | t0001 | g0150 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0029 | EAS | CDX | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CDX | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0217 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0364 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0214 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02451 | hp1 | a0001 | c0004 | t0002 | g0007 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0350 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0064 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0167 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02572 | hp2 | a0001 | c0005 | t0001 | g0183 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0009 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0360 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0366 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0323 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02683 | hp1 | a0001 | c0003 | t0001 | g0335 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0050 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0030 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0358 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0322 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02723 | hp2 | a0001 | c0001 | t0011 | g0136 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02735 | hp1 | a0001 | c0004 | t0002 | g0036 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02738 | hp1 | a0001 | c0003 | t0001 | g0333 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02809 | hp1 | a0001 | c0005 | t0001 | g0181 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0362 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02818 | hp1 | a0001 | c0006 | t0001 | g0352 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0368 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0365 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02965 | hp1 | a0001 | c0006 | t0001 | g0345 | AFR | ESN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02970 | hp2 | a0001 | c0003 | t0001 | g0318 | AFR | ESN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ESN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0349 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0196 | AFR | MSL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03130 | hp1 | a0001 | c0002 | t0012 | g0141 | AFR | ESN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03130 | hp2 | a0001 | c0005 | t0001 | g0182 | AFR | ESN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0194 | AFR | ESN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0347 | AFR | ESN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03209 | hp1 | a0001 | c0007 | t0001 | g0346 | AFR | MSL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0363 | AFR | MSL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | MSL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03239 | hp1 | a0001 | c0003 | t0001 | g0329 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0062 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0353 | AFR | MSL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | MSL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0124 | AFR | MSL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0049 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03491 | hp2 | a0001 | c0004 | t0002 | g0035 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03492 | hp1 | a0001 | c0004 | t0002 | g0034 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0047 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0359 | AFR | ESN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0254 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0367 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | MSL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | MSL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03654 | hp1 | a0001 | c0003 | t0001 | g0340 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0022 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03688 | hp1 | a0001 | c0003 | t0001 | g0331 | SAS | STU | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0044 | SAS | STU | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03710 | hp1 | a0001 | c0003 | t0001 | g0336 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03710 | hp2 | a0001 | c0004 | t0002 | g0033 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03831 | hp1 | a0001 | c0004 | t0007 | g0032 | SAS | BEB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03831 | hp2 | a0001 | c0003 | t0001 | g0371 | SAS | BEB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03927 | hp1 | a0001 | c0004 | t0002 | g0086 | SAS | BEB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0089 | SAS | BEB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0020 | SAS | STU | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG04115 | hp2 | a0001 | c0003 | t0001 | g0326 | SAS | STU | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0074 | SAS | STU | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | STU | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0021 | SAS | STU | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG04204 | hp2 | a0001 | c0003 | t0001 | g0327 | SAS | STU | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG04228 | hp1 | a0002 | c0012 | t0002 | g0122 | SAS | STU | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0284 | SAS | STU | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | YRI | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18522 | hp2 | a0001 | c0007 | t0001 | g0344 | AFR | YRI | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0057 | EAS | CHB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0060 | EAS | CHB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0361 | AFR | YRI | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | YRI | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18939 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18943 | hp2 | a0001 | c0002 | t0002 | g0372 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0081 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0357 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0272 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18965 | hp2 | a0001 | c0008 | t0001 | g0276 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18968 | hp1 | a0001 | c0002 | t0008 | g0012 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0056 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0281 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18972 | hp2 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18974 | hp2 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18982 | hp1 | a0001 | c0001 | t0009 | g0356 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18985 | hp2 | a0001 | c0002 | t0002 | g0102 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18988 | hp2 | a0001 | c0002 | t0002 | g0084 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18992 | hp1 | a0001 | c0002 | t0013 | g0018 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0080 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0280 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0370 | AFR | LWK | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0354 | AFR | LWK | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19043 | hp1 | a0001 | c0001 | t0010 | g0005 | AFR | LWK | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | LWK | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19054 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0313 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0079 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19065 | hp2 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19078 | hp1 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0282 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19090 | hp2 | a0001 | c0002 | t0002 | g0100 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19240 | hp1 | a0003 | c0010 | t0001 | g0321 | AFR | YRI | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | YRI | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ASW | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA20129 | hp2 | a0001 | c0005 | t0001 | g0184 | AFR | ASW | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA20752 | hp1 | a0001 | c0003 | t0001 | g0338 | EUR | TSI | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | TSI | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0023 | SAS | GIH | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01123 | hp1 | a0001 | c0004 | t0002 | g0092 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01123 | hp2 | a0001 | c0003 | t0001 | g0239 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0195 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0166 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0355 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0271 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0215 | AFR | MSL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | USA | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | USA | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | USA | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | USA | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | LWK | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA21309 | hp2 | a0001 | c0011 | t0001 | g0251 | AFR | LWK | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0135 | REF | REF | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0319 | REF | REF | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:94643357
|
C | G | 1 | a0004 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.316C>G | p.Leu106Val | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/16 | 461/3768 | 316/2046 | 106/681 | chr8 | 94643357 | ||
| chr8:94646267
|
G | A | 1 | a0003 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.475G>A | p.Ala159Thr | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/16 | 620/3768 | 475/2046 | 159/681 | chr8 | 94646267 | ||
| chr8:94646273
|
A | G | 1 | a0002 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.481A>G | p.Met161Val | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/16 | 626/3768 | 481/2046 | 161/681 | chr8 | 94646273 | ||
| chr8:94667958
|
A | G | 1 | a0002 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.941A>G | p.Asn314Ser | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/16 | 1086/3768 | 941/2046 | 314/681 | chr8 | 94667958 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:94642060
|
G | A | 1 | a0001c0008 | 1 | NA18965.hp2 | synonymous_variant | LOW | c.237G>A | p.Ser79Ser | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/16 | 382/3768 | 237/2046 | 79/681 | chr8 | 94642060 | ||
| chr8:94643344
|
G | A | 1 | a0001c0009 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.303G>A | p.Gly101Gly | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/16 | 448/3768 | 303/2046 | 101/681 | chr8 | 94643344 | ||
| chr8:94643368
|
T | C | 1 | a0001c0004 | 16 | HG00323.hp1 HG01070.hp1 HG01071.hp2 others(13): Show |
synonymous_variant | LOW | c.327T>C | p.Asp109Asp | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/16 | 472/3768 | 327/2046 | 109/681 | chr8 | 94643368 | ||
| chr8:94646179
|
A | G | 3 | a0001c0005a0001c0006a0001c0007 | 8 | HG02572.hp2 HG02809.hp1 HG02818.hp1 others(5): Show |
synonymous_variant | LOW | c.387A>G | p.Leu129Leu | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/16 | 532/3768 | 387/2046 | 129/681 | chr8 | 94646179 | ||
| chr8:94668001
|
C | T | 3 | a0001c0002a0001c0004a0002c0012 | 105 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(102): Show |
synonymous_variant | LOW | c.984C>T | p.Val328Val | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/16 | 1129/3768 | 984/2046 | 328/681 | chr8 | 94668001 | ||
| chr8:94668229
|
C | T | 2 | a0001c0007a0001c0011 | 3 | HG03209.hp1 NA18522.hp2 NA21309.hp2 |
synonymous_variant | LOW | c.1212C>T | p.Ser404Ser | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/16 | 1357/3768 | 1212/2046 | 404/681 | chr8 | 94668229 | ||
| chr8:94678351
|
T | C | 5 | a0001c0002a0001c0003a0001c0004others(2): Show | 146 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(143): Show |
synonymous_variant | LOW | c.1800T>C | p.Asn600Asn | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/16 | 1945/3768 | 1800/2046 | 600/681 | chr8 | 94678351 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:94641201
|
G | C | 1 | a0001c0004t0007 | 1 | HG03831.hp1 | 5_prime_UTR_variant | MODIFIER | c.-118G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 1/16 | 118 | chr8 | 94641201 | |||||
| chr8:94641290
|
C | T | 1 | a0001c0002t0014 | 1 | HG02080.hp1 | 5_prime_UTR_variant | MODIFIER | c.-29C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 1/16 | 29 | chr8 | 94641290 | |||||
| chr8:94705982
|
A | T | 1 | a0001c0001t0006 | 3 | HG02109.hp2 HG02572.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*93A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 9056 | chr8 | 94705982 | |||||
| chr8:94706009
|
G | C | 1 | a0001c0002t0008 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*120G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 9083 | chr8 | 94706009 | |||||
| chr8:94706086
|
T | C | 19 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(16): Show | 273 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(270): Show |
3_prime_UTR_variant | MODIFIER | c.*197T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 9160 | chr8 | 94706086 | |||||
| chr8:94706220
|
T | C | 18 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(15): Show | 272 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*331T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 9294 | chr8 | 94706220 | |||||
| chr8:94706227
|
T | G | 1 | a0001c0001t0009 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*338T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 9301 | chr8 | 94706227 | |||||
| chr8:94706305
|
T | C | 18 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(15): Show | 272 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*416T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 9379 | chr8 | 94706305 | |||||
| chr8:94706306
|
G | A | 1 | a0001c0001t0010 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*417G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 9380 | chr8 | 94706306 | |||||
| chr8:94706308
|
A | G | 1 | a0001c0002t0013 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*419A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 9382 | chr8 | 94706308 | |||||
| chr8:94706401
|
T | C | 1 | a0001c0001t0006 | 3 | HG02109.hp2 HG02572.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*512T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 9475 | chr8 | 94706401 | |||||
| chr8:94706453
|
T | C | 1 | a0001c0001t0011 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*564T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 9527 | chr8 | 94706453 | |||||
| chr8:94706505
|
A | T | 18 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(15): Show | 272 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*616A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 9579 | chr8 | 94706505 | |||||
| chr8:94706670
|
A | G | 1 | a0001c0001t0003 | 6 | HG02257.hp1 HG02280.hp1 HG02647.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*781A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 9744 | chr8 | 94706670 | |||||
| chr8:94706869
|
A | G | 1 | a0001c0001t0005 | 4 | HG00423.hp1 HG02015.hp2 HG02040.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*980A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 9943 | chr8 | 94706869 | |||||
| chr8:94707065
|
G | A | 1 | a0001c0001t0006 | 3 | HG02109.hp2 HG02572.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1176G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 10139 | chr8 | 94707065 | |||||
| chr8:94707099
|
A | C | 18 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(15): Show | 272 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*1210A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 10173 | chr8 | 94707099 | |||||
| chr8:94707110
|
A | T | 1 | a0001c0001t0004 | 5 | HG02109.hp1 HG02486.hp2 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1221A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 10184 | chr8 | 94707110 | |||||
| chr8:94707159
|
A | T | 18 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(15): Show | 272 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*1270A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 10233 | chr8 | 94707159 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:94641516
|
C | T | 1 | a0001c0002t0002g0372 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.132+66C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 1/15 | chr8 | 94641516 | ||||||
| chr8:94641633
|
C | T | 1 | a0001c0003t0001g0371 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.132+183C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 1/15 | chr8 | 94641633 | ||||||
| chr8:94641716
|
C | G | 1 | a0001c0001t0001g0370 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.133-240C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 1/15 | chr8 | 94641716 | ||||||
| chr8:94641717
|
G | A | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(132): Show | 135 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.133-239G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 1/15 | chr8 | 94641717 | ||||||
| chr8:94641804
|
C | T | 12 | a0001c0001t0001g0358a0001c0001t0001g0359a0001c0001t0001g0360others(9): Show | 12 | HG01167.hp2 HG02257.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.133-152C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 1/15 | chr8 | 94641804 | ||||||
| chr8:94641815
|
C | T | 137 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(134): Show | 137 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.133-141C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 1/15 | chr8 | 94641815 | ||||||
| chr8:94641847
|
C | T | 3 | a0001c0003t0001g0353a0001c0003t0001g0354a0001c0003t0001g0355 | 3 | HG02486.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.133-109C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 1/15 | chr8 | 94641847 | ||||||
| chr8:94641861
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.133-95G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 1/15 | chr8 | 94641861 | ||||||
| chr8:94641935
|
C | G | 1 | a0001c0001t0011g0136 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.133-21C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 1/15 | chr8 | 94641935 | ||||||
| chr8:94642119
|
T | A | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG02258.hp2 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.261+35T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94642119 | ||||||
| chr8:94642206
|
G | T | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.261+122G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94642206 | ||||||
| chr8:94642304
|
A | G | 23 | a0001c0001t0001g0358a0001c0001t0001g0359a0001c0001t0001g0360others(20): Show | 23 | HG01070.hp2 HG01081.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.261+220A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94642304 | ||||||
| chr8:94642347
|
A | C | 185 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(182): Show | 187 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.261+263A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94642347 | ||||||
| chr8:94642400
|
C | T | 34 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(31): Show | 36 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.261+316C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94642400 | ||||||
| chr8:94642495
|
T | C | 317 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(314): Show | 319 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(316): Show |
intron_variant | MODIFIER | c.261+411T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94642495 | ||||||
| chr8:94642575
|
C | T | 20 | a0001c0001t0001g0358a0001c0001t0001g0359a0001c0001t0001g0360others(17): Show | 20 | HG01070.hp2 HG01081.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.261+491C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94642575 | ||||||
| chr8:94642658
|
G | A | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.261+574G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94642658 | ||||||
| chr8:94642669
|
T | G | 371 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(368): Show | 373 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(370): Show |
intron_variant | MODIFIER | c.261+585T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94642669 | ||||||
| chr8:94642670
|
G | T | 5 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(2): Show | 5 | HG00438.hp1 HG00609.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.261+586G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94642670 | ||||||
| chr8:94642724
|
GGCT | G | 16 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(13): Show | 16 | HG01891.hp1 HG02559.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.262-577_262-575del others(3): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr8 | 94642724 | |||||
| chr8:94642802
|
G | T | 7 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(4): Show | 7 | HG02559.hp2 HG02818.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.262-501G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94642802 | ||||||
| chr8:94642822
|
A | G | 278 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(275): Show | 280 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.262-481A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94642822 | ||||||
| chr8:94642978
|
G | A | 8 | a0001c0003t0001g0347a0001c0003t0001g0348a0001c0003t0001g0349others(5): Show | 8 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.262-325G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94642978 | ||||||
| chr8:94643056
|
A | G | 3 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246 | 3 | HG01361.hp1 HG01433.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.262-247A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94643056 | ||||||
| chr8:94643109
|
G | A | 1 | a0001c0001t0010g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.262-194G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94643109 | ||||||
| chr8:94643175
|
C | T | 5 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(2): Show | 5 | HG02559.hp1 HG02647.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.262-128C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94643175 | ||||||
| chr8:94643187
|
T | A | 122 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0087others(119): Show | 122 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.262-116T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94643187 | ||||||
| chr8:94643525
|
T | C | 1 | a0001c0001t0001g0190 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.375+109T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94643525 | ||||||
| chr8:94643727
|
C | T | 8 | a0001c0005t0001g0181a0001c0005t0001g0182a0001c0005t0001g0183others(5): Show | 8 | HG02572.hp2 HG02809.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.375+311C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94643727 | ||||||
| chr8:94643751
|
A | ACT | 354 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(351): Show | 356 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(353): Show |
intron_variant | MODIFIER | c.375+336_375+337dup others(2): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr8 | 94643751 | |||||
| chr8:94644045
|
G | A | 48 | a0001c0001t0001g0003a0001c0001t0001g0137a0001c0001t0001g0273others(45): Show | 48 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.375+629G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94644045 | ||||||
| chr8:94644110
|
A | T | 1 | a0001c0003t0001g0318 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.375+694A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94644110 | ||||||
| chr8:94644471
|
T | C | 365 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(362): Show | 367 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(364): Show |
intron_variant | MODIFIER | c.375+1055T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94644471 | ||||||
| chr8:94644482
|
C | T | 1 | a0001c0001t0001g0343 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.375+1066C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94644482 | ||||||
| chr8:94644555
|
C | A | 2 | a0001c0003t0001g0368a0001c0003t0001g0369 | 2 | HG01167.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.375+1139C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94644555 | ||||||
| chr8:94644575
|
T | C | 120 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0087others(117): Show | 120 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.375+1159T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94644575 | ||||||
| chr8:94644659
|
C | T | 2 | a0001c0003t0001g0368a0001c0003t0001g0369 | 2 | HG01167.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.375+1243C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94644659 | ||||||
| chr8:94644702
|
A | G | 1 | a0001c0001t0001g0242 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.375+1286A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94644702 | ||||||
| chr8:94644793
|
G | A | 1 | a0001c0003t0001g0318 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.376-1375G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94644793 | ||||||
| chr8:94644934
|
C | CAGAGCAT others(37377): Show |
1 | a0001c0005t0001g0181 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.376-1233_376-1232i others(37386): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr8 | 94644934 | |||||
| chr8:94644934
|
CAA | C | 7 | a0001c0005t0001g0182a0001c0005t0001g0183a0001c0005t0001g0184others(4): Show | 7 | HG02572.hp2 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.376-1232_376-1231d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr8 | 94644934 | |||||
| chr8:94644936
|
A | C | 1 | a0001c0005t0001g0181 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.376-1232A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94644936 | ||||||
| chr8:94644953
|
G | A | 8 | a0001c0003t0001g0347a0001c0003t0001g0348a0001c0003t0001g0349others(5): Show | 8 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.376-1215G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94644953 | ||||||
| chr8:94645008
|
A | C | 10 | a0001c0001t0001g0358a0001c0001t0001g0359a0001c0001t0001g0360others(7): Show | 10 | HG02257.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.376-1160A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94645008 | ||||||
| chr8:94645427
|
G | GA | 8 | a0001c0001t0001g0180a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | HG02145.hp2 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.376-730dupA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr8 | 94645427 | |||||
| chr8:94645427
|
GA | G | 216 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(213): Show | 218 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.376-730delA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr8 | 94645427 | |||||
| chr8:94645443
|
G | A | 371 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(368): Show | 373 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(370): Show |
intron_variant | MODIFIER | c.376-725G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94645443 | ||||||
| chr8:94645686
|
AC | A | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(206): Show | 211 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.376-481delC | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94645686 | ||||||
| chr8:94645728
|
A | G | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(206): Show | 211 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.376-440A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94645728 | ||||||
| chr8:94645737
|
G | A | 1 | a0003c0010t0001g0321 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.376-431G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94645737 | ||||||
| chr8:94645744
|
C | A | 1 | a0001c0003t0001g0318 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.376-424C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94645744 | ||||||
| chr8:94645811
|
A | G | 4 | a0001c0005t0001g0181a0001c0005t0001g0182a0001c0005t0001g0183others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.376-357A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94645811 | ||||||
| chr8:94645831
|
G | T | 1 | a0001c0001t0001g0003 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.376-337G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94645831 | ||||||
| chr8:94645986
|
A | C | 8 | a0001c0005t0001g0181a0001c0005t0001g0182a0001c0005t0001g0183others(5): Show | 8 | HG02572.hp2 HG02809.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.376-182A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94645986 | ||||||
| chr8:94645997
|
G | T | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(206): Show | 211 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.376-171G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94645997 | ||||||
| chr8:94646042
|
T | C | 218 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(215): Show | 220 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.376-126T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94646042 | ||||||
| chr8:94646059
|
A | AT | 218 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(215): Show | 220 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.376-104dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr8 | 94646059 | |||||
| chr8:94646068
|
T | C | 8 | a0001c0005t0001g0181a0001c0005t0001g0182a0001c0005t0001g0183others(5): Show | 8 | HG02572.hp2 HG02809.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.376-100T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94646068 | ||||||
| chr8:94646298
|
T | C | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(207): Show | 212 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.490+16T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94646298 | ||||||
| chr8:94646334
|
A | AAAAT | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(207): Show | 212 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.490+52_490+53insAA others(2): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94646334 | ||||||
| chr8:94646477
|
G | A | 1 | a0001c0001t0010g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.490+195G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94646477 | ||||||
| chr8:94646480
|
C | T | 324 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(321): Show | 326 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.490+198C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94646480 | ||||||
| chr8:94646515
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.490+233C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94646515 | ||||||
| chr8:94646573
|
A | G | 5 | a0001c0001t0001g0180a0001c0001t0001g0267a0001c0001t0001g0268others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.490+291A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94646573 | ||||||
| chr8:94646597
|
A | G | 157 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0043others(154): Show | 159 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.490+315A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94646597 | ||||||
| chr8:94646688
|
C | T | 1 | a0002c0012t0002g0122 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.490+406C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94646688 | ||||||
| chr8:94646709
|
T | C | 1 | a0004c0013t0001g0145 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.490+427T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94646709 | ||||||
| chr8:94646716
|
G | A | 1 | a0001c0002t0002g0006 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.490+434G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94646716 | ||||||
| chr8:94646724
|
C | A | 9 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(6): Show | 9 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.490+442C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94646724 | ||||||
| chr8:94646731
|
T | C | 7 | a0001c0001t0001g0247a0001c0001t0001g0256a0001c0001t0001g0257others(4): Show | 7 | HG02559.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.490+449T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94646731 | ||||||
| chr8:94646897
|
A | G | 1 | a0001c0001t0001g0317 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.490+615A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94646897 | ||||||
| chr8:94647037
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.490+755A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94647037 | ||||||
| chr8:94647123
|
G | C | 106 | a0001c0001t0001g0004a0001c0001t0001g0129a0001c0001t0001g0130others(103): Show | 106 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.490+841G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94647123 | ||||||
| chr8:94647138
|
T | G | 1 | a0001c0001t0001g0248 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.490+856T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94647138 | ||||||
| chr8:94647161
|
T | C | 10 | a0001c0001t0001g0358a0001c0001t0001g0359a0001c0001t0001g0360others(7): Show | 10 | HG02257.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.490+879T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94647161 | ||||||
| chr8:94647201
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.490+919G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94647201 | ||||||
| chr8:94647213
|
C | G | 49 | a0001c0001t0001g0003a0001c0001t0001g0137a0001c0001t0001g0193others(46): Show | 49 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.490+931C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94647213 | ||||||
| chr8:94647307
|
C | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.490+1025C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94647307 | ||||||
| chr8:94647408
|
C | G | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(207): Show | 212 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.490+1126C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94647408 | ||||||
| chr8:94647414
|
A | G | 157 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0043others(154): Show | 159 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.490+1132A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94647414 | ||||||
| chr8:94647456
|
T | C | 4 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(1): Show | 4 | HG02280.hp2 HG02622.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.490+1174T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94647456 | ||||||
| chr8:94647621
|
A | C | 324 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(321): Show | 326 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.490+1339A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94647621 | ||||||
| chr8:94647672
|
G | A | 1 | a0001c0004t0002g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.490+1390G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94647672 | ||||||
| chr8:94647790
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.490+1508T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94647790 | ||||||
| chr8:94647860
|
G | T | 1 | a0001c0002t0002g0121 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.490+1578G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94647860 | ||||||
| chr8:94648174
|
T | C | 268 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(265): Show | 270 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.490+1892T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94648174 | ||||||
| chr8:94648301
|
G | A | 1 | a0001c0001t0001g0198 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.490+2019G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94648301 | ||||||
| chr8:94648543
|
C | T | 2 | a0001c0001t0001g0315a0001c0001t0001g0316 | 2 | HG00738.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.490+2261C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94648543 | ||||||
| chr8:94648544
|
C | T | 264 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(261): Show | 266 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.490+2262C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94648544 | ||||||
| chr8:94648574
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.490+2292G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94648574 | ||||||
| chr8:94648584
|
A | C | 9 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(6): Show | 9 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.490+2302A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94648584 | ||||||
| chr8:94648590
|
C | T | 1 | a0001c0001t0004g0271 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.490+2308C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94648590 | ||||||
| chr8:94648611
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.490+2329G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94648611 | ||||||
| chr8:94648737
|
C | T | 6 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(3): Show | 6 | HG00423.hp2 NA18944.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.490+2455C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94648737 | ||||||
| chr8:94648780
|
C | T | 1 | a0001c0001t0001g0238 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.490+2498C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94648780 | ||||||
| chr8:94648835
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0171 | 2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.490+2553A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94648835 | ||||||
| chr8:94648850
|
G | A | 1 | a0001c0002t0002g0008 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.490+2568G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94648850 | ||||||
| chr8:94648924
|
C | T | 348 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(345): Show | 350 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(347): Show |
intron_variant | MODIFIER | c.490+2642C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94648924 | ||||||
| chr8:94648963
|
G | A | 1 | a0001c0002t0002g0009 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.490+2681G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94648963 | ||||||
| chr8:94648984
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.490+2702G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94648984 | ||||||
| chr8:94649047
|
C | G | 1 | a0001c0002t0002g0120 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.490+2765C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94649047 | ||||||
| chr8:94649050
|
G | A | 19 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(16): Show | 19 | HG01257.hp1 HG02004.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.490+2768G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94649050 | ||||||
| chr8:94649091
|
C | G | 1 | a0001c0001t0001g0170 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.490+2809C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94649091 | ||||||
| chr8:94649232
|
G | A | 140 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0043others(137): Show | 142 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.490+2950G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94649232 | ||||||
| chr8:94649274
|
T | C | 3 | a0001c0003t0001g0318a0001c0003t0001g0368a0001c0003t0001g0369 | 3 | HG01167.hp2 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.490+2992T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94649274 | ||||||
| chr8:94649285
|
C | G | 3 | a0001c0006t0001g0345a0001c0007t0001g0344a0001c0007t0001g0346 | 3 | HG02965.hp1 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.490+3003C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94649285 | ||||||
| chr8:94649349
|
C | T | 1 | a0001c0001t0001g0190 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.490+3067C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94649349 | ||||||
| chr8:94649356
|
T | G | 1 | a0001c0001t0001g0273 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.490+3074T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94649356 | ||||||
| chr8:94649440
|
T | TCTC | 268 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(265): Show | 270 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.490+3160_490+3161i others(5): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94649440 | |||||
| chr8:94649489
|
C | T | 268 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(265): Show | 270 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.490+3207C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94649489 | ||||||
| chr8:94649544
|
C | G | 141 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0043others(138): Show | 143 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.490+3262C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94649544 | ||||||
| chr8:94649598
|
C | T | 57 | a0001c0001t0001g0003a0001c0001t0001g0137a0001c0001t0001g0212others(54): Show | 57 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.490+3316C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94649598 | ||||||
| chr8:94649613
|
A | T | 1 | a0001c0001t0001g0138 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.490+3331A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94649613 | ||||||
| chr8:94649659
|
C | T | 1 | a0001c0001t0001g0255 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.490+3377C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94649659 | ||||||
| chr8:94649762
|
C | A | 267 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(264): Show | 269 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.490+3480C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94649762 | ||||||
| chr8:94649809
|
G | A | 15 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(12): Show | 15 | HG01891.hp1 HG02559.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.490+3527G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94649809 | ||||||
| chr8:94649992
|
CCTCTTCC others(14): Show |
C | 1 | a0001c0001t0001g0358 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.490+3712_490+3732d others(23): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94649992 | |||||
| chr8:94650051
|
G | C | 371 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(368): Show | 373 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(370): Show |
intron_variant | MODIFIER | c.490+3769G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94650051 | ||||||
| chr8:94650111
|
A | T | 287 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(284): Show | 288 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.490+3829A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94650111 | ||||||
| chr8:94650164
|
T | C | 106 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0087others(103): Show | 106 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.490+3882T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94650164 | ||||||
| chr8:94650167
|
A | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.490+3885A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94650167 | ||||||
| chr8:94650259
|
TTTTG | T | 93 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0104others(90): Show | 94 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.490+3981_490+3984d others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94650259 | |||||
| chr8:94650263
|
G | GT | 144 | a0001c0001t0001g0043a0001c0001t0001g0087a0001c0001t0001g0123others(141): Show | 145 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.490+3990dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94650263 | |||||
| chr8:94650263
|
GT | G | 50 | a0001c0001t0001g0003a0001c0001t0001g0137a0001c0001t0001g0193others(47): Show | 50 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.490+3990delT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94650263 | |||||
| chr8:94650352
|
C | T | 25 | a0001c0003t0001g0001a0001c0003t0001g0134a0001c0003t0001g0135others(22): Show | 26 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.490+4070C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94650352 | ||||||
| chr8:94650408
|
G | C | 281 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(278): Show | 283 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.490+4126G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94650408 | ||||||
| chr8:94650488
|
T | C | 1 | a0001c0002t0002g0011 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.490+4206T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94650488 | ||||||
| chr8:94650558
|
TGGTTTGT others(12): Show |
T | 8 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220others(5): Show | 8 | HG00438.hp2 NA18747.hp2 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.490+4291_490+4309d others(21): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94650558 | |||||
| chr8:94650616
|
T | C | 298 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(295): Show | 300 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(297): Show |
intron_variant | MODIFIER | c.490+4334T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94650616 | ||||||
| chr8:94650678
|
C | T | 11 | a0001c0003t0001g0318a0001c0003t0001g0347a0001c0003t0001g0348others(8): Show | 11 | HG01070.hp2 HG01081.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.490+4396C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94650678 | ||||||
| chr8:94650721
|
A | AT | 88 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0104others(85): Show | 89 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.490+4448dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94650721 | |||||
| chr8:94650736
|
G | A | 3 | a0001c0006t0001g0345a0001c0007t0001g0344a0001c0007t0001g0346 | 3 | HG02965.hp1 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.490+4454G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94650736 | ||||||
| chr8:94650770
|
G | T | 1 | a0001c0001t0001g0314 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.490+4488G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94650770 | ||||||
| chr8:94650802
|
T | TC | 76 | a0001c0001t0001g0003a0001c0001t0001g0137a0001c0001t0001g0193others(73): Show | 77 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.490+4522dupC | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94650802 | |||||
| chr8:94650843
|
C | G | 1 | a0001c0005t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.490+4561C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94650843 | ||||||
| chr8:94650951
|
C | T | 10 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(7): Show | 10 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.490+4669C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94650951 | ||||||
| chr8:94651058
|
T | G | 1 | a0001c0001t0001g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.490+4776T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94651058 | ||||||
| chr8:94651143
|
A | G | 26 | a0001c0003t0001g0001a0001c0003t0001g0134a0001c0003t0001g0135others(23): Show | 27 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.490+4861A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94651143 | ||||||
| chr8:94651143
|
A | T | 107 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0087others(104): Show | 107 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.490+4861A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94651143 | ||||||
| chr8:94651239
|
C | CT | 96 | a0001c0001t0001g0004a0001c0001t0001g0116a0001c0001t0001g0117others(93): Show | 96 | HG00140.hp2 HG00423.hp2 HG00735.hp2 others(93): Show |
intron_variant | MODIFIER | c.490+4979dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94651239 | |||||
| chr8:94651239
|
CT | C | 110 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0087others(107): Show | 110 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.490+4979delT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94651239 | |||||
| chr8:94651271
|
C | T | 10 | a0001c0001t0001g0358a0001c0001t0001g0359a0001c0001t0001g0360others(7): Show | 10 | HG02257.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.490+4989C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94651271 | ||||||
| chr8:94651305
|
G | A | 3 | a0001c0006t0001g0345a0001c0007t0001g0344a0001c0007t0001g0346 | 3 | HG02965.hp1 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.490+5023G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94651305 | ||||||
| chr8:94651378
|
C | T | 26 | a0001c0003t0001g0001a0001c0003t0001g0088a0001c0003t0001g0134others(23): Show | 27 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.490+5096C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94651378 | ||||||
| chr8:94651397
|
T | C | 1 | a0001c0008t0001g0276 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.490+5115T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94651397 | ||||||
| chr8:94651441
|
A | G | 1 | a0001c0003t0001g0318 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.490+5159A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94651441 | ||||||
| chr8:94651531
|
T | C | 1 | a0001c0001t0001g0359 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.490+5249T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94651531 | ||||||
| chr8:94651594
|
T | C | 91 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0104others(88): Show | 92 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.490+5312T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94651594 | ||||||
| chr8:94651607
|
G | C | 27 | a0001c0003t0001g0001a0001c0003t0001g0088a0001c0003t0001g0134others(24): Show | 28 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.490+5325G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94651607 | ||||||
| chr8:94651616
|
A | AT | 92 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0104others(89): Show | 93 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.490+5343dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94651616 | |||||
| chr8:94651806
|
T | A | 282 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(279): Show | 283 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.490+5524T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94651806 | ||||||
| chr8:94651922
|
G | A | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.490+5640G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94651922 | ||||||
| chr8:94651987
|
C | CT | 61 | a0001c0001t0001g0003a0001c0001t0001g0137a0001c0001t0001g0159others(58): Show | 61 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.490+5728dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94651987 | |||||
| chr8:94651987
|
C | CTT | 134 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0146others(131): Show | 134 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.490+5727_490+5728d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94651987 | |||||
| chr8:94651987
|
C | CTTT | 87 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0104others(84): Show | 88 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.490+5726_490+5728d others(5): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94651987 | |||||
| chr8:94651987
|
C | CTTTT | 17 | a0001c0001t0001g0087a0001c0001t0001g0115a0001c0001t0001g0118others(14): Show | 17 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(14): Show |
intron_variant | MODIFIER | c.490+5725_490+5728d others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94651987 | |||||
| chr8:94652010
|
T | TTTTTTGA | 9 | a0001c0001t0001g0247a0001c0001t0001g0252a0001c0001t0001g0253others(6): Show | 9 | HG02559.hp2 HG02630.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.490+5728_490+5729i others(9): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94652010 | ||||||
| chr8:94652172
|
G | C | 13 | a0001c0001t0001g0247a0001c0001t0001g0249a0001c0001t0001g0250others(10): Show | 13 | HG02559.hp2 HG02630.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.490+5890G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94652172 | ||||||
| chr8:94652239
|
C | A | 1 | a0001c0001t0001g0211 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.490+5957C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94652239 | ||||||
| chr8:94652275
|
A | G | 1 | a0001c0002t0001g0085 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.490+5993A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94652275 | ||||||
| chr8:94652290
|
C | A | 13 | a0001c0001t0001g0247a0001c0001t0001g0249a0001c0001t0001g0250others(10): Show | 13 | HG02559.hp2 HG02630.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.490+6008C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94652290 | ||||||
| chr8:94652324
|
G | A | 1 | a0001c0002t0001g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.490+6042G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94652324 | ||||||
| chr8:94652441
|
G | T | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.490+6159G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94652441 | ||||||
| chr8:94652459
|
T | C | 2 | a0001c0003t0001g0368a0001c0003t0001g0369 | 2 | HG01167.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.490+6177T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94652459 | ||||||
| chr8:94652479
|
G | GT | 92 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0104others(89): Show | 93 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.490+6208dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94652479 | |||||
| chr8:94652479
|
G | GTT | 6 | a0001c0001t0001g0169a0001c0001t0001g0185a0001c0001t0001g0186others(3): Show | 6 | HG02559.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.490+6207_490+6208d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94652479 | |||||
| chr8:94652574
|
A | T | 65 | a0001c0001t0001g0003a0001c0001t0001g0137a0001c0001t0001g0193others(62): Show | 65 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.490+6292A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94652574 | ||||||
| chr8:94652601
|
C | A | 13 | a0001c0001t0001g0247a0001c0001t0001g0249a0001c0001t0001g0250others(10): Show | 13 | HG02559.hp2 HG02630.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.490+6319C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94652601 | ||||||
| chr8:94652630
|
T | C | 282 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(279): Show | 283 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.490+6348T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94652630 | ||||||
| chr8:94652681
|
C | A | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.490+6399C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94652681 | ||||||
| chr8:94652737
|
C | A | 13 | a0001c0001t0001g0247a0001c0001t0001g0249a0001c0001t0001g0250others(10): Show | 13 | HG02559.hp2 HG02630.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.490+6455C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94652737 | ||||||
| chr8:94652910
|
T | C | 1 | a0001c0001t0003g0142 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.490+6628T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94652910 | ||||||
| chr8:94653009
|
G | A | 8 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220others(5): Show | 8 | HG00438.hp2 NA18747.hp2 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.490+6727G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94653009 | ||||||
| chr8:94653064
|
T | C | 1 | a0001c0002t0002g0013 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.490+6782T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94653064 | ||||||
| chr8:94653142
|
G | GA | 295 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(292): Show | 296 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(293): Show |
intron_variant | MODIFIER | c.490+6869dupA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94653142 | |||||
| chr8:94653198
|
T | C | 1 | a0001c0001t0004g0194 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.490+6916T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94653198 | ||||||
| chr8:94653215
|
TG | T | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.490+6939delG | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94653215 | |||||
| chr8:94653246
|
A | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0103others(97): Show | 101 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.490+6964A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94653246 | ||||||
| chr8:94653545
|
T | G | 13 | a0001c0001t0001g0247a0001c0001t0001g0249a0001c0001t0001g0250others(10): Show | 13 | HG02559.hp2 HG02630.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.490+7263T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94653545 | ||||||
| chr8:94653802
|
G | GAT | 106 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0087others(103): Show | 106 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.490+7534_490+7535d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94653802 | |||||
| chr8:94654140
|
G | A | 4 | a0001c0005t0001g0181a0001c0005t0001g0182a0001c0005t0001g0183others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.490+7858G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94654140 | ||||||
| chr8:94654164
|
C | CA | 290 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(287): Show | 291 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(288): Show |
intron_variant | MODIFIER | c.490+7886dupA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94654164 | |||||
| chr8:94654176
|
G | A | 6 | a0001c0003t0001g0001a0001c0003t0001g0134a0001c0003t0001g0324others(3): Show | 7 | HG00642.hp1 HG01074.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.490+7894G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94654176 | ||||||
| chr8:94654189
|
G | A | 1 | a0001c0001t0003g0142 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.490+7907G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94654189 | ||||||
| chr8:94654259
|
G | A | 1 | a0001c0001t0001g0360 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.490+7977G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94654259 | ||||||
| chr8:94654275
|
A | G | 277 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(274): Show | 278 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(275): Show |
intron_variant | MODIFIER | c.490+7993A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94654275 | ||||||
| chr8:94654393
|
G | A | 277 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(274): Show | 278 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(275): Show |
intron_variant | MODIFIER | c.491-7879G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94654393 | ||||||
| chr8:94654406
|
C | T | 294 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(291): Show | 295 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.491-7866C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94654406 | ||||||
| chr8:94654450
|
CTT | C | 86 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0104others(83): Show | 87 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.491-7818_491-7817d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94654450 | |||||
| chr8:94654494
|
C | T | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.491-7778C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94654494 | ||||||
| chr8:94654495
|
C | T | 13 | a0001c0001t0001g0247a0001c0001t0001g0249a0001c0001t0001g0250others(10): Show | 13 | HG02559.hp2 HG02630.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.491-7777C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94654495 | ||||||
| chr8:94654676
|
C | T | 1 | a0001c0002t0001g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.491-7596C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94654676 | ||||||
| chr8:94654852
|
G | A | 4 | a0001c0005t0001g0181a0001c0005t0001g0182a0001c0005t0001g0183others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.491-7420G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94654852 | ||||||
| chr8:94654919
|
C | CA | 36 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(33): Show | 37 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.491-7340dupA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94654919 | |||||
| chr8:94655044
|
CTG | C | 7 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0002g0015others(4): Show | 7 | HG01943.hp2 HG01978.hp1 NA18984.hp2 others(4): Show |
intron_variant | MODIFIER | c.491-7225_491-7224d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94655044 | |||||
| chr8:94655060
|
G | GTT | 9 | a0001c0001t0001g0275a0001c0001t0001g0279a0001c0001t0001g0303others(6): Show | 9 | HG00738.hp2 HG01099.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.491-7207_491-7206d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94655060 | |||||
| chr8:94655060
|
G | GTTTT | 8 | a0001c0001t0004g0254a0001c0002t0002g0070a0001c0002t0002g0071others(5): Show | 8 | HG02015.hp1 HG03540.hp1 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.491-7209_491-7206d others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94655060 | |||||
| chr8:94655060
|
G | GTTTTT | 89 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0104others(86): Show | 90 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.491-7210_491-7206d others(7): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94655060 | |||||
| chr8:94655060
|
G | GTTTTTT | 9 | a0001c0001t0001g0119a0001c0001t0001g0189a0001c0001t0001g0193others(6): Show | 9 | HG00597.hp2 HG02055.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.491-7211_491-7206d others(8): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94655060 | |||||
| chr8:94655063
|
T | TTG | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG02258.hp2 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.491-7208_491-7207i others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94655063 | |||||
| chr8:94655065
|
T | G | 33 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(30): Show | 34 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.491-7207T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655065 | ||||||
| chr8:94655065
|
T | TGTGTG | 3 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 3 | HG02886.hp1 HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.491-7207_491-7206i others(7): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655065 | ||||||
| chr8:94655065
|
T | TTGTG | 7 | a0001c0002t0002g0019a0001c0002t0002g0020a0001c0002t0002g0021others(4): Show | 7 | HG00733.hp1 HG03654.hp2 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.491-7187_491-7184d others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94655065 | |||||
| chr8:94655065
|
T | TTTGTG | 4 | a0001c0001t0001g0149a0001c0001t0011g0136a0001c0002t0002g0025others(1): Show | 4 | HG01109.hp1 HG02145.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.491-7206_491-7205i others(7): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94655065 | |||||
| chr8:94655065
|
T | TTTTG | 87 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0087others(84): Show | 87 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.491-7206_491-7205i others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94655065 | |||||
| chr8:94655067
|
G | T | 171 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0103others(168): Show | 172 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.491-7205G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655067 | ||||||
| chr8:94655069
|
G | T | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0103others(138): Show | 142 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.491-7203G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655069 | ||||||
| chr8:94655071
|
G | T | 7 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0203others(4): Show | 7 | HG02004.hp1 NA18949.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.491-7201G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655071 | ||||||
| chr8:94655087
|
G | T | 13 | a0001c0001t0001g0247a0001c0001t0001g0249a0001c0001t0001g0250others(10): Show | 13 | HG02559.hp2 HG02630.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.491-7185G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655087 | ||||||
| chr8:94655106
|
A | T | 4 | a0001c0002t0002g0021a0001c0002t0002g0022a0001c0002t0002g0023others(1): Show | 4 | HG03654.hp2 HG04204.hp1 NA20905.hp1 others(1): Show |
intron_variant | MODIFIER | c.491-7166A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655106 | ||||||
| chr8:94655120
|
C | T | 2 | a0001c0001t0001g0360a0001c0001t0001g0367 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.491-7152C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655120 | ||||||
| chr8:94655352
|
G | A | 62 | a0001c0001t0001g0003a0001c0001t0001g0137a0001c0001t0001g0212others(59): Show | 62 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.491-6920G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655352 | ||||||
| chr8:94655388
|
C | CT | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0103others(163): Show | 167 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.491-6870dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94655388 | |||||
| chr8:94655444
|
A | G | 3 | a0001c0006t0001g0345a0001c0007t0001g0344a0001c0007t0001g0346 | 3 | HG02965.hp1 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.491-6828A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655444 | ||||||
| chr8:94655466
|
G | A | 62 | a0001c0001t0001g0003a0001c0001t0001g0137a0001c0001t0001g0212others(59): Show | 62 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.491-6806G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655466 | ||||||
| chr8:94655603
|
G | T | 99 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0104others(96): Show | 100 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.491-6669G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655603 | ||||||
| chr8:94655711
|
T | C | 12 | a0001c0001t0001g0256a0001c0001t0006g0166a0001c0001t0006g0167others(9): Show | 12 | HG01070.hp2 HG01081.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.491-6561T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655711 | ||||||
| chr8:94655727
|
CA | C | 4 | a0001c0005t0001g0181a0001c0005t0001g0182a0001c0005t0001g0183others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.491-6539delA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94655727 | |||||
| chr8:94655814
|
C | T | 1 | a0001c0005t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.491-6458C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655814 | ||||||
| chr8:94655815
|
C | T | 27 | a0001c0003t0001g0001a0001c0003t0001g0088a0001c0003t0001g0134others(24): Show | 28 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.491-6457C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655815 | ||||||
| chr8:94655889
|
G | A | 1 | a0001c0002t0002g0024 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.491-6383G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655889 | ||||||
| chr8:94655996
|
T | G | 1 | a0001c0002t0012g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.491-6276T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655996 | ||||||
| chr8:94656003
|
C | T | 59 | a0001c0001t0001g0003a0001c0001t0001g0137a0001c0001t0001g0212others(56): Show | 59 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.491-6269C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94656003 | ||||||
| chr8:94656087
|
G | T | 44 | a0001c0001t0001g0003a0001c0001t0001g0137a0001c0001t0001g0212others(41): Show | 44 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.491-6185G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94656087 | ||||||
| chr8:94656138
|
C | G | 1 | a0001c0002t0012g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.491-6134C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94656138 | ||||||
| chr8:94656145
|
G | A | 2 | a0001c0002t0002g0026a0001c0002t0002g0027 | 2 | HG02083.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.491-6127G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94656145 | ||||||
| chr8:94656207
|
C | CA | 74 | a0001c0001t0001g0118a0001c0001t0001g0137a0001c0001t0001g0138others(71): Show | 74 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.491-6043dupA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94656207 | |||||
| chr8:94656207
|
C | CAA | 15 | a0001c0001t0001g0247a0001c0001t0001g0249a0001c0001t0001g0250others(12): Show | 15 | HG02559.hp2 HG02630.hp2 HG02896.hp1 others(12): Show |
intron_variant | MODIFIER | c.491-6044_491-6043d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94656207 | |||||
| chr8:94656207
|
CA | C | 29 | a0001c0001t0001g0245a0001c0002t0001g0085a0001c0002t0002g0009others(26): Show | 30 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.491-6043delA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94656207 | |||||
| chr8:94656229
|
A | T | 31 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0231others(28): Show | 32 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.491-6043A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94656229 | ||||||
| chr8:94656230
|
T | A | 5 | a0001c0001t0001g0180a0001c0001t0001g0342a0001c0001t0001g0343others(2): Show | 5 | HG00323.hp1 HG00323.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.491-6042T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94656230 | ||||||
| chr8:94656241
|
C | T | 1 | a0001c0001t0003g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.491-6031C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94656241 | ||||||
| chr8:94656311
|
C | T | 6 | a0001c0003t0001g0368a0001c0003t0001g0369a0001c0006t0001g0345others(3): Show | 6 | HG01167.hp2 HG02818.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.491-5961C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94656311 | ||||||
| chr8:94656364
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.491-5908G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94656364 | ||||||
| chr8:94656410
|
CG | C | 17 | a0001c0003t0001g0088a0001c0003t0001g0135a0001c0003t0001g0151others(14): Show | 17 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.491-5857delG | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94656410 | |||||
| chr8:94656440
|
C | T | 10 | a0001c0001t0001g0358a0001c0001t0001g0359a0001c0001t0001g0360others(7): Show | 10 | HG02257.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.491-5832C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94656440 | ||||||
| chr8:94656511
|
A | G | 2 | a0001c0001t0001g0238a0001c0003t0001g0340 | 2 | HG03654.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.491-5761A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94656511 | ||||||
| chr8:94656529
|
T | C | 103 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0104others(100): Show | 104 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.491-5743T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94656529 | ||||||
| chr8:94656657
|
G | A | 1 | a0001c0003t0001g0318 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.491-5615G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94656657 | ||||||
| chr8:94657034
|
A | G | 27 | a0001c0003t0001g0001a0001c0003t0001g0088a0001c0003t0001g0134others(24): Show | 28 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.491-5238A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94657034 | ||||||
| chr8:94657292
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.491-4980G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94657292 | ||||||
| chr8:94657311
|
T | G | 1 | a0001c0003t0001g0318 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.491-4961T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94657311 | ||||||
| chr8:94657414
|
C | T | 1 | a0001c0002t0002g0069 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.491-4858C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94657414 | ||||||
| chr8:94657472
|
C | CGT | 35 | a0001c0001t0001g0004a0001c0001t0001g0130a0001c0001t0001g0149others(32): Show | 35 | HG00140.hp2 HG00423.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.491-4769_491-4768d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94657472 | |||||
| chr8:94657472
|
C | CGTGT | 73 | a0001c0001t0001g0123a0001c0001t0001g0129a0001c0001t0001g0131others(70): Show | 74 | HG00408.hp1 HG00642.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.491-4771_491-4768d others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94657472 | |||||
| chr8:94657472
|
C | CGTGTGT | 126 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0087others(123): Show | 127 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.491-4773_491-4768d others(8): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94657472 | |||||
| chr8:94657472
|
C | CGTGTGTG others(1): Show |
29 | a0001c0001t0001g0114a0001c0001t0001g0118a0001c0001t0001g0228others(26): Show | 29 | HG00597.hp2 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.491-4775_491-4768d others(10): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94657472 | |||||
| chr8:94657472
|
C | CGTGTGTG others(3): Show |
18 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0128others(15): Show | 18 | HG01070.hp2 HG01167.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.491-4777_491-4768d others(12): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94657472 | |||||
| chr8:94657472
|
C | CGTGTGTG others(5): Show |
4 | a0001c0001t0001g0250a0001c0001t0001g0253a0001c0001t0003g0216others(1): Show | 4 | HG02630.hp2 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.491-4779_491-4768d others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94657472 | |||||
| chr8:94657472
|
C | CGTGTGTG others(7): Show |
2 | a0001c0001t0001g0010a0001c0001t0001g0190 | 2 | NA18946.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.491-4781_491-4768d others(16): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94657472 | |||||
| chr8:94657472
|
C | T | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.491-4800C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94657472 | ||||||
| chr8:94657472
|
CGT | C | 6 | a0001c0001t0001g0137a0001c0001t0001g0180a0001c0001t0001g0267others(3): Show | 6 | HG00140.hp1 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.491-4769_491-4768d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94657472 | |||||
| chr8:94657472
|
CGTGT | C | 40 | a0001c0001t0001g0003a0001c0001t0001g0212a0001c0001t0001g0273others(37): Show | 40 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.491-4771_491-4768d others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94657472 | |||||
| chr8:94657472
|
CGTGTGT | C | 3 | a0001c0001t0001g0284a0001c0001t0001g0305a0001c0008t0001g0276 | 3 | HG02738.hp2 HG04228.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.491-4773_491-4768d others(8): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94657472 | |||||
| chr8:94657472
|
CGTGTGTG others(7): Show |
C | 1 | a0001c0001t0001g0277 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.491-4781_491-4768d others(16): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94657472 | |||||
| chr8:94657522
|
A | C | 1 | a0001c0004t0002g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.491-4750A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94657522 | ||||||
| chr8:94657545
|
A | T | 1 | a0001c0001t0001g0359 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.491-4727A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94657545 | ||||||
| chr8:94657586
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.491-4686C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94657586 | ||||||
| chr8:94657729
|
C | A | 1 | a0001c0001t0001g0370 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.491-4543C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94657729 | ||||||
| chr8:94657930
|
C | A | 298 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(295): Show | 299 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(296): Show |
intron_variant | MODIFIER | c.491-4342C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94657930 | ||||||
| chr8:94657954
|
G | A | 2 | a0001c0007t0001g0344a0001c0007t0001g0346 | 2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.491-4318G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94657954 | ||||||
| chr8:94658015
|
G | A | 4 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(1): Show | 4 | HG01891.hp2 HG02723.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.491-4257G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94658015 | ||||||
| chr8:94658057
|
G | A | 3 | a0001c0003t0001g0368a0001c0003t0001g0369a0001c0006t0001g0345 | 3 | HG01167.hp2 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.491-4215G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94658057 | ||||||
| chr8:94658073
|
G | A | 45 | a0001c0001t0001g0003a0001c0001t0001g0137a0001c0001t0001g0212others(42): Show | 45 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.491-4199G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94658073 | ||||||
| chr8:94658091
|
T | C | 1 | a0001c0008t0001g0276 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.491-4181T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94658091 | ||||||
| chr8:94658174
|
A | G | 4 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(1): Show | 4 | HG01891.hp2 HG02723.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.491-4098A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94658174 | ||||||
| chr8:94658176
|
GTGCTGGG others(18): Show |
G | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.491-4095_491-4071d others(27): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94658176 | ||||||
| chr8:94658275
|
G | A | 1 | a0001c0002t0002g0037 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.491-3997G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94658275 | ||||||
| chr8:94658452
|
A | G | 3 | a0001c0001t0001g0159a0001c0001t0001g0163a0001c0001t0001g0165 | 3 | HG01261.hp2 HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.491-3820A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94658452 | ||||||
| chr8:94658483
|
C | T | 27 | a0001c0003t0001g0001a0001c0003t0001g0088a0001c0003t0001g0134others(24): Show | 28 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.491-3789C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94658483 | ||||||
| chr8:94658516
|
T | C | 5 | a0001c0001t0001g0256a0001c0001t0006g0166a0001c0001t0006g0167others(2): Show | 5 | HG02109.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.491-3756T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94658516 | ||||||
| chr8:94658681
|
A | G | 1 | a0001c0002t0002g0061 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.491-3591A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94658681 | ||||||
| chr8:94658691
|
T | C | 46 | a0001c0001t0001g0003a0001c0001t0001g0137a0001c0001t0001g0193others(43): Show | 46 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.491-3581T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94658691 | ||||||
| chr8:94658889
|
A | C | 298 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(295): Show | 299 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(296): Show |
intron_variant | MODIFIER | c.491-3383A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94658889 | ||||||
| chr8:94658959
|
T | C | 1 | a0001c0002t0002g0121 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.491-3313T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94658959 | ||||||
| chr8:94659002
|
G | T | 1 | a0001c0001t0001g0148 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.491-3270G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94659002 | ||||||
| chr8:94659109
|
G | A | 2 | a0001c0007t0001g0344a0001c0007t0001g0346 | 2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.491-3163G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94659109 | ||||||
| chr8:94659170
|
C | T | 1 | a0001c0001t0010g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.491-3102C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94659170 | ||||||
| chr8:94659190
|
T | G | 1 | a0001c0003t0001g0347 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.491-3082T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94659190 | ||||||
| chr8:94659195
|
T | TA | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.491-3068dupA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94659195 | |||||
| chr8:94659325
|
G | A | 5 | a0001c0001t0001g0228a0001c0001t0001g0231a0001c0001t0001g0233others(2): Show | 5 | HG00597.hp2 NA18612.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.491-2947G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94659325 | ||||||
| chr8:94659342
|
C | T | 1 | a0001c0001t0001g0317 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.491-2930C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94659342 | ||||||
| chr8:94659428
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.491-2844C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94659428 | ||||||
| chr8:94659429
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.491-2843G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94659429 | ||||||
| chr8:94659577
|
A | T | 1 | a0001c0001t0001g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.491-2695A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94659577 | ||||||
| chr8:94659614
|
G | A | 2 | a0001c0003t0001g0368a0001c0003t0001g0369 | 2 | HG01167.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.491-2658G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94659614 | ||||||
| chr8:94659805
|
T | C | 328 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(325): Show | 330 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(327): Show |
intron_variant | MODIFIER | c.491-2467T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94659805 | ||||||
| chr8:94659805
|
T | G | 4 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(1): Show | 4 | NA18943.hp1 NA18957.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.491-2467T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94659805 | ||||||
| chr8:94660269
|
T | C | 13 | a0001c0001t0001g0256a0001c0001t0006g0166a0001c0001t0006g0167others(10): Show | 13 | HG01070.hp2 HG01081.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.491-2003T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94660269 | ||||||
| chr8:94660325
|
G | A | 1 | a0001c0002t0002g0022 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.491-1947G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94660325 | ||||||
| chr8:94660461
|
G | A | 1 | a0001c0001t0001g0362 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.491-1811G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94660461 | ||||||
| chr8:94660678
|
T | C | 371 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(368): Show | 373 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(370): Show |
intron_variant | MODIFIER | c.491-1594T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94660678 | ||||||
| chr8:94660709
|
C | CA | 11 | a0001c0001t0001g0154a0001c0001t0001g0165a0001c0001t0001g0174others(8): Show | 11 | HG00423.hp2 HG01123.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.491-1529dupA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660709 | |||||
| chr8:94660709
|
C | CAA | 9 | a0001c0001t0001g0163a0001c0001t0001g0172a0001c0001t0001g0173others(6): Show | 9 | HG01261.hp2 HG02486.hp1 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.491-1530_491-1529d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660709 | |||||
| chr8:94660709
|
C | CAAA | 6 | a0001c0001t0001g0178a0001c0003t0001g0339a0001c0003t0001g0348others(3): Show | 6 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.491-1531_491-1529d others(5): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660709 | |||||
| chr8:94660709
|
CA | C | 16 | a0001c0001t0001g0004a0001c0001t0001g0138a0001c0001t0001g0155others(13): Show | 16 | HG00140.hp2 HG01069.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.491-1529delA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660709 | |||||
| chr8:94660709
|
CAA | C | 8 | a0001c0001t0001g0127a0001c0001t0001g0139a0001c0001t0006g0166others(5): Show | 8 | HG01069.hp2 HG01071.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.491-1530_491-1529d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660709 | |||||
| chr8:94660709
|
CAAA | C | 13 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0128others(10): Show | 13 | HG01891.hp2 HG02257.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.491-1531_491-1529d others(5): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660709 | |||||
| chr8:94660709
|
CAAAA | C | 32 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0114others(29): Show | 32 | HG00438.hp1 HG00438.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.491-1532_491-1529d others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660709 | |||||
| chr8:94660709
|
CAAAAA | C | 73 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(70): Show | 73 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.491-1533_491-1529d others(7): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660709 | |||||
| chr8:94660709
|
CAAAAAA | C | 17 | a0001c0001t0001g0002a0001c0001t0001g0242a0001c0001t0001g0247others(14): Show | 18 | HG00323.hp2 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.491-1534_491-1529d others(8): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660709 | |||||
| chr8:94660709
|
CAAAAAAA | C | 43 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0248others(40): Show | 43 | HG00733.hp1 HG01109.hp2 HG01123.hp1 others(40): Show |
intron_variant | MODIFIER | c.491-1535_491-1529d others(9): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660709 | |||||
| chr8:94660709
|
CAAAAAAA others(1): Show |
C | 78 | a0001c0001t0001g0087a0001c0001t0001g0212a0001c0001t0001g0257others(75): Show | 78 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.491-1536_491-1529d others(10): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660709 | |||||
| chr8:94660709
|
CAAAAAAA others(2): Show |
C | 41 | a0001c0001t0001g0003a0001c0001t0001g0137a0001c0001t0001g0273others(38): Show | 41 | HG00140.hp1 HG00423.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.491-1537_491-1529d others(11): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660709 | |||||
| chr8:94660709
|
CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0001g0277a0001c0001t0001g0300a0001c0001t0001g0301 | 3 | HG00558.hp1 HG01928.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.491-1538_491-1529d others(12): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660709 | |||||
| chr8:94660709
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.491-1540_491-1529d others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660709 | |||||
| chr8:94660740
|
A | C | 1 | a0001c0001t0001g0270 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.491-1532A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94660740 | ||||||
| chr8:94660744
|
C | A | 1 | a0001c0001t0001g0270 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.491-1528C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94660744 | ||||||
| chr8:94660745
|
C | A | 3 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269 | 3 | HG02280.hp2 HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.491-1527C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94660745 | ||||||
| chr8:94660746
|
A | AAAC | 3 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269 | 3 | HG02280.hp2 HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.491-1524_491-1523i others(5): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660746 | |||||
| chr8:94660746
|
AAAACAAA others(1): Show |
A | 108 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0087others(105): Show | 108 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.491-1514_491-1507d others(10): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660746 | |||||
| chr8:94660805
|
C | T | 1 | a0001c0002t0002g0067 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.491-1467C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94660805 | ||||||
| chr8:94660836
|
G | A | 4 | a0001c0005t0001g0181a0001c0005t0001g0182a0001c0005t0001g0183others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.491-1436G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94660836 | ||||||
| chr8:94661032
|
C | T | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.491-1240C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94661032 | ||||||
| chr8:94661446
|
A | C | 347 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(344): Show | 349 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(346): Show |
intron_variant | MODIFIER | c.491-826A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94661446 | ||||||
| chr8:94661498
|
G | A | 1 | a0001c0001t0011g0136 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.491-774G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94661498 | ||||||
| chr8:94661528
|
A | G | 1 | a0001c0003t0001g0135 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.491-744A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94661528 | ||||||
| chr8:94661651
|
A | G | 5 | a0001c0002t0002g0046a0001c0002t0002g0077a0001c0002t0002g0272others(2): Show | 5 | HG02074.hp2 NA18943.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.491-621A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94661651 | ||||||
| chr8:94661657
|
A | C | 13 | a0001c0001t0001g0256a0001c0001t0006g0166a0001c0001t0006g0167others(10): Show | 13 | HG01070.hp2 HG01081.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.491-615A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94661657 | ||||||
| chr8:94661717
|
A | G | 108 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0087others(105): Show | 108 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.491-555A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94661717 | ||||||
| chr8:94661897
|
A | C | 1 | a0001c0001t0001g0320 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.491-375A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94661897 | ||||||
| chr8:94662025
|
C | T | 2 | a0001c0002t0002g0020a0001c0002t0002g0030 | 2 | HG02698.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.491-247C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94662025 | ||||||
| chr8:94662204
|
G | C | 107 | a0001c0001t0001g0043a0001c0001t0001g0087a0001c0002t0001g0014others(104): Show | 107 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.491-68G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94662204 | ||||||
| chr8:94662380
|
G | T | 4 | a0001c0003t0001g0368a0001c0003t0001g0369a0001c0006t0001g0345others(1): Show | 4 | HG01167.hp2 HG02818.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.589+10G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 5/15 | chr8 | 94662380 | ||||||
| chr8:94662382
|
T | G | 6 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(3): Show | 6 | HG00741.hp1 HG02523.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.589+12T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 5/15 | chr8 | 94662382 | ||||||
| chr8:94662595
|
G | GT | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(244): Show | 248 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.644+52dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr8 | 94662595 | |||||
| chr8:94662702
|
G | C | 253 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0043others(250): Show | 255 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.644+147G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94662702 | ||||||
| chr8:94662733
|
G | A | 4 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(1): Show | 4 | HG01891.hp2 HG02723.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.644+178G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94662733 | ||||||
| chr8:94663017
|
T | C | 4 | a0001c0003t0001g0368a0001c0003t0001g0369a0001c0006t0001g0345others(1): Show | 4 | HG01167.hp2 HG02818.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.644+462T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94663017 | ||||||
| chr8:94663058
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.644+503A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94663058 | ||||||
| chr8:94663127
|
G | T | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.644+572G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94663127 | ||||||
| chr8:94663144
|
G | A | 172 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0087others(169): Show | 172 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.644+589G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94663144 | ||||||
| chr8:94663241
|
C | CATTT | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.644+703_644+706dup others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr8 | 94663241 | |||||
| chr8:94663302
|
G | A | 1 | a0001c0001t0010g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.644+747G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94663302 | ||||||
| chr8:94663338
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.644+783C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94663338 | ||||||
| chr8:94663460
|
G | C | 2 | a0001c0007t0001g0344a0001c0007t0001g0346 | 2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.644+905G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94663460 | ||||||
| chr8:94663723
|
G | T | 17 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(14): Show | 17 | HG01361.hp2 HG01928.hp2 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.645-974G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94663723 | ||||||
| chr8:94663854
|
T | C | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.645-843T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94663854 | ||||||
| chr8:94663992
|
A | C | 8 | a0001c0003t0001g0347a0001c0003t0001g0348a0001c0003t0001g0349others(5): Show | 8 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.645-705A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94663992 | ||||||
| chr8:94664120
|
C | CT | 37 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(34): Show | 37 | HG01070.hp2 HG01109.hp1 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.645-556dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr8 | 94664120 | |||||
| chr8:94664120
|
C | CTT | 8 | a0001c0001t0001g0169a0001c0001t0001g0256a0001c0001t0001g0266others(5): Show | 8 | HG00609.hp1 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.645-557_645-556dup others(2): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr8 | 94664120 | |||||
| chr8:94664120
|
CT | C | 105 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0155others(102): Show | 105 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.645-556delT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr8 | 94664120 | |||||
| chr8:94664120
|
CTT | C | 8 | a0001c0002t0002g0031a0001c0002t0002g0071a0001c0002t0002g0078others(5): Show | 8 | HG01167.hp2 HG01496.hp1 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.645-557_645-556del others(2): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr8 | 94664120 | |||||
| chr8:94664141
|
T | TTTTTG | 25 | a0001c0003t0001g0001a0001c0003t0001g0088a0001c0003t0001g0134others(22): Show | 26 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.645-556_645-555ins others(5): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94664141 | ||||||
| chr8:94664150
|
G | C | 5 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(2): Show | 5 | HG02559.hp1 HG02647.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.645-547G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94664150 | ||||||
| chr8:94664188
|
A | G | 27 | a0001c0003t0001g0001a0001c0003t0001g0088a0001c0003t0001g0134others(24): Show | 28 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.645-509A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94664188 | ||||||
| chr8:94664342
|
G | C | 1 | a0001c0011t0001g0251 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645-355G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94664342 | ||||||
| chr8:94664428
|
T | A | 1 | a0001c0001t0010g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.645-269T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94664428 | ||||||
| chr8:94664442
|
T | C | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0213 | 3 | HG02615.hp1 HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.645-255T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94664442 | ||||||
| chr8:94664557
|
G | A | 27 | a0001c0003t0001g0001a0001c0003t0001g0088a0001c0003t0001g0134others(24): Show | 28 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.645-140G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94664557 | ||||||
| chr8:94664633
|
G | A | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.645-64G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94664633 | ||||||
| chr8:94664666
|
C | G | 27 | a0001c0003t0001g0001a0001c0003t0001g0088a0001c0003t0001g0134others(24): Show | 28 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.645-31C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94664666 | ||||||
| chr8:94664904
|
T | C | 254 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0043others(251): Show | 256 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.756-23T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 7/15 | chr8 | 94664904 | ||||||
| chr8:94665352
|
G | A | 1 | a0001c0006t0001g0345 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.931+156G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94665352 | ||||||
| chr8:94665547
|
G | A | 10 | a0001c0001t0001g0358a0001c0001t0001g0359a0001c0001t0001g0360others(7): Show | 10 | HG02257.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.931+351G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94665547 | ||||||
| chr8:94665556
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.931+360A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94665556 | ||||||
| chr8:94665566
|
G | A | 1 | a0001c0011t0001g0251 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.931+370G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94665566 | ||||||
| chr8:94665570
|
C | T | 215 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0043others(212): Show | 216 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.931+374C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94665570 | ||||||
| chr8:94665615
|
C | T | 3 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196 | 3 | HG02109.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.931+419C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94665615 | ||||||
| chr8:94665641
|
G | A | 4 | a0001c0005t0001g0181a0001c0005t0001g0182a0001c0005t0001g0183others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.931+445G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94665641 | ||||||
| chr8:94665790
|
G | A | 14 | a0001c0001t0001g0169a0001c0001t0001g0247a0001c0001t0001g0249others(11): Show | 14 | HG02559.hp2 HG02622.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.931+594G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94665790 | ||||||
| chr8:94665812
|
A | AT | 4 | a0001c0005t0001g0181a0001c0005t0001g0182a0001c0005t0001g0183others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.931+616_931+617ins others(1): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94665812 | ||||||
| chr8:94665813
|
A | T | 4 | a0001c0005t0001g0181a0001c0005t0001g0182a0001c0005t0001g0183others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.931+617A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94665813 | ||||||
| chr8:94665814
|
A | C | 4 | a0001c0005t0001g0181a0001c0005t0001g0182a0001c0005t0001g0183others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.931+618A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94665814 | ||||||
| chr8:94665853
|
C | A | 1 | a0001c0002t0001g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.931+657C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94665853 | ||||||
| chr8:94666084
|
T | C | 250 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0043others(247): Show | 252 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.931+888T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94666084 | ||||||
| chr8:94666250
|
A | G | 1 | a0001c0001t0001g0310 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.931+1054A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94666250 | ||||||
| chr8:94666348
|
G | A | 14 | a0001c0001t0001g0169a0001c0001t0001g0247a0001c0001t0001g0249others(11): Show | 14 | HG02559.hp2 HG02622.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.931+1152G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94666348 | ||||||
| chr8:94666389
|
A | G | 2 | a0001c0001t0011g0136a0001c0009t0001g0150 | 2 | HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.931+1193A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94666389 | ||||||
| chr8:94666568
|
A | G | 1 | a0001c0002t0002g0121 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.931+1372A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94666568 | ||||||
| chr8:94666676
|
G | T | 1 | a0001c0001t0001g0304 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.932-1273G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94666676 | ||||||
| chr8:94666774
|
A | C | 1 | a0001c0001t0001g0235 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.932-1175A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94666774 | ||||||
| chr8:94666786
|
GGTTGCT | G | 27 | a0001c0003t0001g0001a0001c0003t0001g0088a0001c0003t0001g0134others(24): Show | 28 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.932-1160_932-1155d others(8): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94666786 | |||||
| chr8:94666950
|
G | C | 332 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(329): Show | 334 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(331): Show |
intron_variant | MODIFIER | c.932-999G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94666950 | ||||||
| chr8:94667040
|
T | G | 6 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(3): Show | 6 | HG00741.hp1 HG02523.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.932-909T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94667040 | ||||||
| chr8:94667043
|
T | C | 35 | a0001c0003t0001g0001a0001c0003t0001g0088a0001c0003t0001g0134others(32): Show | 36 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.932-906T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94667043 | ||||||
| chr8:94667052
|
A | G | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.932-897A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94667052 | ||||||
| chr8:94667068
|
G | GGGGGGTG others(13): Show |
4 | a0001c0003t0001g0368a0001c0003t0001g0369a0001c0006t0001g0345others(1): Show | 4 | HG01167.hp2 HG02818.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.932-880_932-879ins others(20): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | |||||
| chr8:94667068
|
G | GGGGGGTG others(17): Show |
1 | a0001c0003t0001g0354 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.932-880_932-879ins others(24): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | |||||
| chr8:94667068
|
G | GGGGTGTG others(7): Show |
11 | a0001c0003t0001g0001a0001c0003t0001g0134a0001c0003t0001g0135others(8): Show | 12 | HG00642.hp2 HG01257.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.932-880_932-879ins others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | |||||
| chr8:94667068
|
G | GGGGTGTG others(9): Show |
6 | a0001c0003t0001g0088a0001c0003t0001g0151a0001c0003t0001g0239others(3): Show | 6 | HG00741.hp2 HG01123.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.932-880_932-879ins others(16): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | |||||
| chr8:94667068
|
G | GGGGTGTG others(11): Show |
1 | a0001c0003t0001g0338 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.932-880_932-879ins others(18): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | |||||
| chr8:94667068
|
G | GGGGTGTG others(13): Show |
1 | a0001c0003t0001g0355 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.932-880_932-879ins others(20): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | |||||
| chr8:94667068
|
G | GGGGTGTG others(17): Show |
3 | a0001c0003t0001g0349a0001c0003t0001g0350a0001c0003t0001g0351 | 3 | HG01070.hp2 HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.932-880_932-879ins others(24): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | |||||
| chr8:94667068
|
G | GGGGTGTG others(19): Show |
1 | a0001c0003t0001g0353 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.932-880_932-879ins others(26): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | |||||
| chr8:94667068
|
G | GGGGTGTG others(25): Show |
2 | a0001c0003t0001g0347a0001c0003t0001g0348 | 2 | HG01081.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.932-880_932-879ins others(32): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | |||||
| chr8:94667068
|
G | GGT | 5 | a0001c0001t0001g0173a0001c0001t0001g0175a0001c0001t0004g0194others(2): Show | 5 | HG02109.hp1 HG03098.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-856_932-855dup others(2): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | |||||
| chr8:94667068
|
G | GGTGT | 98 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0043others(95): Show | 99 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.932-858_932-855dup others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | |||||
| chr8:94667068
|
G | GGTGTGT | 91 | a0001c0001t0001g0105a0001c0001t0001g0235a0001c0001t0001g0246others(88): Show | 91 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.932-860_932-855dup others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | |||||
| chr8:94667068
|
G | GGTGTGTG others(1): Show |
20 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(17): Show | 20 | HG00597.hp1 HG00733.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.932-862_932-855dup others(8): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | |||||
| chr8:94667068
|
G | GGTGTGTG others(3): Show |
13 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0252others(10): Show | 13 | HG00735.hp2 HG02074.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.932-864_932-855dup others(10): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | |||||
| chr8:94667068
|
G | GGTGTGTG others(5): Show |
1 | a0001c0002t0002g0074 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.932-866_932-855dup others(12): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | |||||
| chr8:94667068
|
G | GGTGTGTG others(7): Show |
46 | a0001c0001t0001g0003a0001c0001t0001g0137a0001c0001t0001g0267others(43): Show | 46 | HG00140.hp1 HG00558.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.932-868_932-855dup others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | |||||
| chr8:94667068
|
G | GGTGTGTG others(9): Show |
10 | a0001c0001t0001g0212a0001c0001t0001g0297a0001c0001t0001g0299others(7): Show | 10 | HG00423.hp1 HG00738.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.932-870_932-855dup others(16): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | |||||
| chr8:94667068
|
G | GGTGTGTG others(11): Show |
13 | a0001c0001t0001g0138a0001c0001t0001g0169a0001c0001t0001g0180others(10): Show | 13 | HG02109.hp2 HG02145.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.932-872_932-855dup others(18): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | |||||
| chr8:94667068
|
G | GGTGTGTG others(13): Show |
13 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0143others(10): Show | 13 | HG02615.hp1 HG02615.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.932-874_932-855dup others(20): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | |||||
| chr8:94667068
|
G | GGTGTGTG others(15): Show |
3 | a0001c0001t0001g0358a0001c0001t0001g0359a0001c0001t0001g0364 | 3 | HG02257.hp2 HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.932-876_932-855dup others(22): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | |||||
| chr8:94667068
|
G | GGTGTGTG others(17): Show |
3 | a0001c0001t0001g0363a0001c0007t0001g0344a0001c0007t0001g0346 | 3 | HG03209.hp1 HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.932-878_932-855dup others(24): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | |||||
| chr8:94667068
|
G | GTGTGTGT others(16): Show |
1 | a0001c0001t0001g0362 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.932-881_932-880ins others(23): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94667068 | ||||||
| chr8:94667098
|
C | T | 2 | a0001c0001t0001g0262a0001c0001t0001g0263 | 2 | HG00438.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.932-851C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94667098 | ||||||
| chr8:94667147
|
G | A | 3 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 3 | HG02886.hp1 HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.932-802G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94667147 | ||||||
| chr8:94667173
|
G | A | 216 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0043others(213): Show | 217 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.932-776G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94667173 | ||||||
| chr8:94667217
|
C | CA | 21 | a0001c0001t0001g0358a0001c0001t0001g0359a0001c0001t0001g0360others(18): Show | 21 | HG00323.hp1 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.932-722dupA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667217 | |||||
| chr8:94667217
|
CA | C | 110 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0043others(107): Show | 111 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.932-722delA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667217 | |||||
| chr8:94667251
|
C | T | 42 | a0001c0002t0002g0008a0001c0002t0002g0011a0001c0002t0002g0013others(39): Show | 42 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.932-698C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94667251 | ||||||
| chr8:94667393
|
T | C | 1 | a0001c0003t0001g0318 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.932-556T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94667393 | ||||||
| chr8:94667435
|
T | TA | 142 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0043others(139): Show | 144 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.932-502dupA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667435 | |||||
| chr8:94667435
|
T | TAA | 108 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(105): Show | 108 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.932-503_932-502dup others(2): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667435 | |||||
| chr8:94667704
|
C | A | 54 | a0001c0001t0001g0002a0001c0001t0001g0087a0001c0001t0001g0103others(51): Show | 55 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.932-245C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94667704 | ||||||
| chr8:94667771
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.932-178A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94667771 | ||||||
| chr8:94667772
|
G | A | 1 | a0001c0001t0001g0370 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.932-177G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94667772 | ||||||
| chr8:94667845
|
C | T | 1 | a0001c0011t0001g0251 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.932-104C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94667845 | ||||||
| chr8:94667890
|
C | T | 4 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(1): Show | 4 | HG01891.hp2 HG02723.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.932-59C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94667890 | ||||||
| chr8:94668431
|
A | G | 9 | a0001c0001t0001g0256a0001c0001t0006g0166a0001c0001t0006g0167others(6): Show | 9 | HG01167.hp2 HG02109.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1233+181A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668431 | ||||||
| chr8:94668445
|
G | A | 105 | a0001c0002t0001g0014a0001c0002t0001g0085a0001c0002t0001g0097others(102): Show | 105 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.1233+195G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668445 | ||||||
| chr8:94668528
|
A | G | 1 | a0001c0003t0001g0318 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1233+278A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668528 | ||||||
| chr8:94668601
|
T | A | 5 | a0001c0001t0001g0256a0001c0001t0006g0166a0001c0001t0006g0167others(2): Show | 5 | HG02109.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1233+351T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668601 | ||||||
| chr8:94668632
|
A | T | 4 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(1): Show | 4 | HG02280.hp2 HG02622.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1233+382A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668632 | ||||||
| chr8:94668655
|
T | A | 2 | a0001c0002t0002g0013a0001c0002t0002g0067 | 2 | NA18965.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1233+405T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668655 | ||||||
| chr8:94668707
|
G | A | 1 | a0001c0001t0001g0307 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1233+457G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668707 | ||||||
| chr8:94668788
|
C | CGTGTGTG others(1): Show |
23 | a0001c0003t0001g0001a0001c0003t0001g0088a0001c0003t0001g0134others(20): Show | 24 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.1233+538_1233+539i others(10): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668788 | ||||||
| chr8:94668788
|
C | CGTGTGTG others(3): Show |
1 | a0001c0003t0001g0151 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1233+538_1233+539i others(12): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668788 | ||||||
| chr8:94668788
|
C | CGTGTGTG others(7): Show |
3 | a0001c0003t0001g0239a0001c0003t0001g0240a0001c0003t0001g0241 | 3 | HG00741.hp2 HG01123.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1233+538_1233+539i others(16): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668788 | ||||||
| chr8:94668788
|
C | CGTGTGTG others(31): Show |
1 | a0001c0001t0001g0197 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1233+538_1233+539i others(40): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668788 | ||||||
| chr8:94668789
|
A | ATGTG | 8 | a0001c0003t0001g0347a0001c0003t0001g0348a0001c0003t0001g0349others(5): Show | 8 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1233+555_1233+558d others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94668789 | |||||
| chr8:94668789
|
A | ATGTGTGT others(7): Show |
1 | a0001c0002t0002g0062 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1233+545_1233+558d others(16): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94668789 | |||||
| chr8:94668789
|
A | ATGTGTGT others(9): Show |
88 | a0001c0002t0001g0014a0001c0002t0002g0006a0001c0002t0002g0008others(85): Show | 88 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1233+543_1233+558d others(18): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94668789 | |||||
| chr8:94668789
|
A | ATGTGTGT others(11): Show |
11 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(8): Show | 11 | HG00733.hp1 HG01943.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.1233+541_1233+558d others(20): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94668789 | |||||
| chr8:94668789
|
A | ATGTGTGT others(13): Show |
4 | a0001c0002t0002g0040a0001c0002t0002g0079a0001c0002t0013g0018others(1): Show | 4 | HG01243.hp2 NA18941.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.1233+558_1233+559i others(22): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94668789 | |||||
| chr8:94668789
|
A | ATGTGTGT others(19): Show |
4 | a0001c0001t0001g0114a0001c0001t0001g0230a0001c0001t0004g0254others(1): Show | 4 | HG03130.hp1 HG03540.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1233+558_1233+559i others(28): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94668789 | |||||
| chr8:94668789
|
A | ATGTGTGT others(21): Show |
2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1233+558_1233+559i others(30): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94668789 | |||||
| chr8:94668789
|
A | ATGTGTGT others(23): Show |
13 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(10): Show | 13 | HG00741.hp1 HG02145.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1233+558_1233+559i others(32): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94668789 | |||||
| chr8:94668789
|
A | ATGTGTGT others(25): Show |
7 | a0001c0001t0001g0087a0001c0001t0001g0123a0001c0001t0001g0185others(4): Show | 7 | HG01243.hp1 HG02109.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1233+558_1233+559i others(34): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94668789 | |||||
| chr8:94668789
|
A | ATGTGTGT others(27): Show |
27 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(24): Show | 27 | HG00438.hp2 HG00609.hp1 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.1233+558_1233+559i others(36): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94668789 | |||||
| chr8:94668789
|
A | ATGTGTGT others(29): Show |
21 | a0001c0001t0001g0002a0001c0001t0001g0110a0001c0001t0001g0116others(18): Show | 22 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.1233+558_1233+559i others(38): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94668789 | |||||
| chr8:94668789
|
A | ATGTGTGT others(31): Show |
18 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(15): Show | 18 | HG01175.hp1 HG01256.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1233+558_1233+559i others(40): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94668789 | |||||
| chr8:94668789
|
A | ATGTGTGT others(33): Show |
4 | a0001c0001t0001g0106a0001c0001t0001g0152a0001c0001t0001g0204others(1): Show | 4 | HG03942.hp1 HG06807.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1233+558_1233+559i others(42): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94668789 | |||||
| chr8:94668789
|
A | ATGTGTGT others(35): Show |
8 | a0001c0001t0001g0043a0001c0001t0001g0117a0001c0001t0001g0190others(5): Show | 8 | HG01891.hp1 HG02004.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.1233+558_1233+559i others(44): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94668789 | |||||
| chr8:94668789
|
A | ATGTGTGT others(37): Show |
2 | a0001c0001t0001g0010a0001c0001t0001g0201 | 2 | NA18974.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1233+558_1233+559i others(46): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94668789 | |||||
| chr8:94668789
|
A | G | 28 | a0001c0001t0001g0197a0001c0003t0001g0001a0001c0003t0001g0088others(25): Show | 29 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.1233+539A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668789 | ||||||
| chr8:94668808
|
T | TGTGTGTG others(28): Show |
2 | a0001c0001t0001g0228a0001c0001t0001g0246 | 2 | HG01934.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1233+558_1233+559i others(37): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668808 | ||||||
| chr8:94668808
|
T | TGTGTGTG others(30): Show |
3 | a0001c0001t0001g0234a0001c0001t0001g0245a0001c0001t0001g0343 | 3 | HG01255.hp2 HG01433.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1233+558_1233+559i others(39): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668808 | ||||||
| chr8:94668928
|
C | T | 8 | a0001c0003t0001g0347a0001c0003t0001g0348a0001c0003t0001g0349others(5): Show | 8 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1233+678C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668928 | ||||||
| chr8:94668950
|
A | G | 4 | a0001c0005t0001g0181a0001c0005t0001g0182a0001c0005t0001g0183others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1233+700A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668950 | ||||||
| chr8:94668978
|
A | G | 1 | a0001c0001t0010g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1233+728A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668978 | ||||||
| chr8:94669196
|
G | A | 238 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0043others(235): Show | 240 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1233+946G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94669196 | ||||||
| chr8:94669565
|
C | G | 1 | a0001c0002t0002g0023 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1233+1315C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94669565 | ||||||
| chr8:94669587
|
C | T | 45 | a0001c0001t0001g0003a0001c0001t0001g0137a0001c0001t0001g0212others(42): Show | 45 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1233+1337C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94669587 | ||||||
| chr8:94669712
|
A | G | 246 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0043others(243): Show | 248 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.1233+1462A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94669712 | ||||||
| chr8:94669725
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1233+1475G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94669725 | ||||||
| chr8:94669874
|
C | CA | 24 | a0001c0001t0001g0043a0001c0001t0001g0118a0001c0001t0001g0119others(21): Show | 24 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.1234-1557dupA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94669874 | |||||
| chr8:94669874
|
C | CAA | 8 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0143others(5): Show | 8 | HG02109.hp2 HG02258.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1234-1558_1234-155 others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94669874 | |||||
| chr8:94669874
|
CA | C | 47 | a0001c0001t0001g0114a0001c0001t0001g0123a0001c0001t0001g0146others(44): Show | 48 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.1234-1557delA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94669874 | |||||
| chr8:94669874
|
CAAAAAAA others(1): Show |
C | 8 | a0001c0003t0001g0347a0001c0003t0001g0348a0001c0003t0001g0349others(5): Show | 8 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1234-1564_1234-155 others(12): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94669874 | |||||
| chr8:94670065
|
G | A | 4 | a0001c0005t0001g0181a0001c0005t0001g0182a0001c0005t0001g0183others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1234-1388G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94670065 | ||||||
| chr8:94670068
|
G | A | 238 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0043others(235): Show | 240 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1234-1385G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94670068 | ||||||
| chr8:94670354
|
A | T | 1 | a0001c0003t0001g0318 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1234-1099A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94670354 | ||||||
| chr8:94670526
|
G | C | 100 | a0001c0002t0001g0014a0001c0002t0001g0085a0001c0002t0001g0097others(97): Show | 100 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1234-927G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94670526 | ||||||
| chr8:94670548
|
A | G | 1 | a0001c0001t0001g0295 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1234-905A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94670548 | ||||||
| chr8:94670684
|
A | G | 1 | a0001c0009t0001g0150 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1234-769A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94670684 | ||||||
| chr8:94671040
|
T | C | 1 | a0001c0002t0002g0074 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1234-413T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94671040 | ||||||
| chr8:94671041
|
A | C | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1234-412A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94671041 | ||||||
| chr8:94671211
|
C | T | 5 | a0001c0001t0001g0256a0001c0001t0006g0166a0001c0001t0006g0167others(2): Show | 5 | HG02109.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1234-242C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94671211 | ||||||
| chr8:94671296
|
C | T | 110 | a0001c0002t0001g0014a0001c0002t0001g0085a0001c0002t0001g0097others(107): Show | 110 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.1234-157C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94671296 | ||||||
| chr8:94671333
|
A | C | 10 | a0001c0003t0001g0001a0001c0003t0001g0134a0001c0003t0001g0324others(7): Show | 11 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1234-120A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94671333 | ||||||
| chr8:94671366
|
C | T | 8 | a0001c0001t0001g0256a0001c0001t0006g0166a0001c0001t0006g0167others(5): Show | 8 | HG02109.hp2 HG02572.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1234-87C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94671366 | ||||||
| chr8:94671700
|
T | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0277a0001c0001t0001g0297others(3): Show | 6 | HG00733.hp2 HG00738.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.1452+29T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94671700 | ||||||
| chr8:94671740
|
G | GATATTAG others(21): Show |
2 | a0001c0001t0001g0297a0001c0001t0001g0299 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1452+80_1452+107du others(29): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr8 | 94671740 | |||||
| chr8:94671953
|
T | C | 95 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0043others(92): Show | 96 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1452+282T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94671953 | ||||||
| chr8:94671975
|
C | T | 4 | a0001c0005t0001g0181a0001c0005t0001g0182a0001c0005t0001g0183others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1452+304C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94671975 | ||||||
| chr8:94672046
|
T | C | 1 | a0001c0009t0001g0150 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1452+375T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94672046 | ||||||
| chr8:94672143
|
A | G | 45 | a0001c0001t0001g0003a0001c0001t0001g0137a0001c0001t0001g0212others(42): Show | 45 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1452+472A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94672143 | ||||||
| chr8:94672220
|
T | A | 4 | a0001c0005t0001g0181a0001c0005t0001g0182a0001c0005t0001g0183others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1452+549T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94672220 | ||||||
| chr8:94672249
|
A | T | 10 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(7): Show | 10 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1452+578A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94672249 | ||||||
| chr8:94672350
|
C | A | 4 | a0001c0005t0001g0181a0001c0005t0001g0182a0001c0005t0001g0183others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1452+679C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94672350 | ||||||
| chr8:94672381
|
A | G | 10 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(7): Show | 10 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1452+710A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94672381 | ||||||
| chr8:94672520
|
A | G | 244 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0043others(241): Show | 246 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.1452+849A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94672520 | ||||||
| chr8:94672536
|
C | CT | 12 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0149others(9): Show | 12 | HG01109.hp1 HG02040.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1452+879dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr8 | 94672536 | |||||
| chr8:94672536
|
CT | C | 9 | a0001c0003t0001g0318a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1452+879delT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr8 | 94672536 | |||||
| chr8:94672551
|
G | C | 35 | a0001c0003t0001g0001a0001c0003t0001g0088a0001c0003t0001g0134others(32): Show | 36 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.1452+880G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94672551 | ||||||
| chr8:94672693
|
C | T | 2 | a0001c0005t0001g0182a0001c0005t0001g0183 | 2 | HG02572.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1452+1022C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94672693 | ||||||
| chr8:94672820
|
G | T | 105 | a0001c0002t0001g0014a0001c0002t0001g0085a0001c0002t0001g0097others(102): Show | 105 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.1452+1149G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94672820 | ||||||
| chr8:94672871
|
G | A | 1 | a0001c0002t0002g0008 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1452+1200G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94672871 | ||||||
| chr8:94672914
|
T | A | 4 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(1): Show | 4 | HG02280.hp2 HG02622.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1452+1243T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94672914 | ||||||
| chr8:94672919
|
A | C | 141 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0043others(138): Show | 143 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.1452+1248A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94672919 | ||||||
| chr8:94672926
|
A | AT | 370 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(367): Show | 372 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(369): Show |
intron_variant | MODIFIER | c.1452+1262dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr8 | 94672926 | |||||
| chr8:94673113
|
T | C | 2 | a0001c0001t0001g0206a0001c0001t0001g0209 | 2 | NA18971.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1453-1195T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94673113 | ||||||
| chr8:94673172
|
A | C | 230 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0043others(227): Show | 231 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.1453-1136A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94673172 | ||||||
| chr8:94673172
|
A | T | 6 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(3): Show | 6 | HG01175.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1453-1136A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94673172 | ||||||
| chr8:94673306
|
T | G | 1 | a0001c0001t0001g0230 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1453-1002T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94673306 | ||||||
| chr8:94673312
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1453-996C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94673312 | ||||||
| chr8:94673359
|
C | T | 113 | a0001c0002t0001g0014a0001c0002t0001g0085a0001c0002t0001g0097others(110): Show | 113 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.1453-949C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94673359 | ||||||
| chr8:94673490
|
A | G | 1 | a0001c0001t0004g0271 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1453-818A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94673490 | ||||||
| chr8:94673494
|
A | T | 10 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(7): Show | 10 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1453-814A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94673494 | ||||||
| chr8:94673546
|
A | T | 1 | a0001c0003t0001g0135 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1453-762A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94673546 | ||||||
| chr8:94673722
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1453-586A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94673722 | ||||||
| chr8:94673832
|
T | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0043others(108): Show | 112 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1453-476T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94673832 | ||||||
| chr8:94673959
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1453-349C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94673959 | ||||||
| chr8:94673986
|
G | T | 54 | a0001c0001t0001g0002a0001c0001t0001g0087a0001c0001t0001g0103others(51): Show | 55 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1453-322G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94673986 | ||||||
| chr8:94674027
|
C | A | 1 | a0001c0001t0001g0289 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1453-281C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94674027 | ||||||
| chr8:94674030
|
T | C | 3 | a0001c0003t0001g0368a0001c0003t0001g0369a0001c0006t0001g0345 | 3 | HG01167.hp2 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1453-278T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94674030 | ||||||
| chr8:94674051
|
T | C | 132 | a0001c0002t0001g0014a0001c0002t0001g0085a0001c0002t0001g0097others(129): Show | 133 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1453-257T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94674051 | ||||||
| chr8:94674058
|
T | G | 10 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(7): Show | 10 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1453-250T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94674058 | ||||||
| chr8:94674081
|
T | C | 1 | a0001c0003t0001g0088 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1453-227T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94674081 | ||||||
| chr8:94674094
|
C | A | 8 | a0001c0003t0001g0347a0001c0003t0001g0348a0001c0003t0001g0349others(5): Show | 8 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1453-214C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94674094 | ||||||
| chr8:94674167
|
G | A | 2 | a0001c0001t0001g0247a0001c0001t0001g0259 | 2 | HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1453-141G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94674167 | ||||||
| chr8:94674572
|
G | A | 3 | a0001c0001t0001g0287a0001c0001t0001g0290a0001c0001t0001g0312 | 3 | HG01934.hp2 HG01943.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1651+66G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94674572 | ||||||
| chr8:94674622
|
A | G | 28 | a0001c0003t0001g0001a0001c0003t0001g0088a0001c0003t0001g0134others(25): Show | 29 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.1651+116A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94674622 | ||||||
| chr8:94674739
|
G | A | 13 | a0001c0003t0001g0318a0001c0003t0001g0347a0001c0003t0001g0348others(10): Show | 13 | HG01070.hp2 HG01081.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.1651+233G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94674739 | ||||||
| chr8:94674948
|
A | AT | 13 | a0001c0003t0001g0318a0001c0003t0001g0347a0001c0003t0001g0348others(10): Show | 13 | HG01070.hp2 HG01081.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.1651+449dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr8 | 94674948 | |||||
| chr8:94675037
|
A | C | 2 | a0001c0001t0001g0249a0001c0001t0001g0252 | 2 | HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1651+531A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94675037 | ||||||
| chr8:94675107
|
C | T | 191 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(188): Show | 192 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.1651+601C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94675107 | ||||||
| chr8:94675177
|
GT | G | 132 | a0001c0002t0001g0014a0001c0002t0001g0085a0001c0002t0001g0097others(129): Show | 133 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1651+673delT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr8 | 94675177 | |||||
| chr8:94675232
|
T | C | 8 | a0001c0003t0001g0347a0001c0003t0001g0348a0001c0003t0001g0349others(5): Show | 8 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1651+726T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94675232 | ||||||
| chr8:94675252
|
A | C | 132 | a0001c0002t0001g0014a0001c0002t0001g0085a0001c0002t0001g0097others(129): Show | 133 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1651+746A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94675252 | ||||||
| chr8:94675364
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1651+858G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94675364 | ||||||
| chr8:94675506
|
T | C | 3 | a0001c0007t0001g0344a0001c0007t0001g0346a0001c0011t0001g0251 | 3 | HG03209.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1651+1000T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94675506 | ||||||
| chr8:94675776
|
T | C | 28 | a0001c0001t0011g0136a0001c0003t0001g0001a0001c0003t0001g0088others(25): Show | 29 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.1651+1270T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94675776 | ||||||
| chr8:94675798
|
C | T | 27 | a0001c0003t0001g0001a0001c0003t0001g0088a0001c0003t0001g0134others(24): Show | 28 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1651+1292C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94675798 | ||||||
| chr8:94675848
|
A | G | 2 | a0001c0007t0001g0344a0001c0007t0001g0346 | 2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1651+1342A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94675848 | ||||||
| chr8:94675898
|
G | A | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1651+1392G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94675898 | ||||||
| chr8:94675953
|
G | A | 6 | a0001c0001t0001g0168a0001c0001t0001g0185a0001c0001t0001g0186others(3): Show | 6 | HG02559.hp1 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1651+1447G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94675953 | ||||||
| chr8:94676059
|
C | T | 13 | a0001c0003t0001g0318a0001c0003t0001g0347a0001c0003t0001g0348others(10): Show | 13 | HG01070.hp2 HG01081.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.1651+1553C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676059 | ||||||
| chr8:94676086
|
A | T | 4 | a0001c0005t0001g0181a0001c0005t0001g0182a0001c0005t0001g0183others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1651+1580A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676086 | ||||||
| chr8:94676132
|
A | T | 1 | a0001c0001t0001g0191 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1651+1626A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676132 | ||||||
| chr8:94676171
|
G | A | 1 | a0001c0001t0001g0304 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1651+1665G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676171 | ||||||
| chr8:94676230
|
G | A | 3 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196 | 3 | HG02109.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1651+1724G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676230 | ||||||
| chr8:94676252
|
T | A | 105 | a0001c0002t0001g0014a0001c0002t0001g0085a0001c0002t0001g0097others(102): Show | 105 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.1651+1746T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676252 | ||||||
| chr8:94676266
|
T | C | 13 | a0001c0003t0001g0318a0001c0003t0001g0347a0001c0003t0001g0348others(10): Show | 13 | HG01070.hp2 HG01081.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.1651+1760T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676266 | ||||||
| chr8:94676330
|
C | G | 132 | a0001c0002t0001g0014a0001c0002t0001g0085a0001c0002t0001g0097others(129): Show | 133 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1651+1824C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676330 | ||||||
| chr8:94676333
|
C | T | 1 | a0001c0002t0014g0042 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1651+1827C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676333 | ||||||
| chr8:94676343
|
C | A | 7 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(4): Show | 7 | HG01109.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1651+1837C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676343 | ||||||
| chr8:94676349
|
C | CA | 167 | a0001c0001t0001g0169a0001c0001t0001g0171a0001c0001t0001g0207others(164): Show | 168 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.1652-1838dupA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr8 | 94676349 | |||||
| chr8:94676349
|
C | CAA | 11 | a0001c0001t0001g0146a0001c0001t0001g0359a0001c0001t0004g0194others(8): Show | 11 | HG02109.hp1 HG03098.hp2 HG03139.hp1 others(8): Show |
intron_variant | MODIFIER | c.1652-1839_1652-183 others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr8 | 94676349 | |||||
| chr8:94676349
|
C | CAAA | 11 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149others(8): Show | 11 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1652-1840_1652-183 others(7): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr8 | 94676349 | |||||
| chr8:94676422
|
C | T | 3 | a0001c0007t0001g0344a0001c0007t0001g0346a0001c0011t0001g0251 | 3 | HG03209.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1652-1781C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676422 | ||||||
| chr8:94676499
|
T | G | 1 | a0001c0001t0004g0271 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1652-1704T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676499 | ||||||
| chr8:94676574
|
G | A | 27 | a0001c0003t0001g0001a0001c0003t0001g0088a0001c0003t0001g0134others(24): Show | 28 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1652-1629G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676574 | ||||||
| chr8:94676749
|
C | T | 12 | a0001c0003t0001g0318a0001c0003t0001g0347a0001c0003t0001g0348others(9): Show | 12 | HG01070.hp2 HG01081.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.1652-1454C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676749 | ||||||
| chr8:94676777
|
C | T | 132 | a0001c0002t0001g0014a0001c0002t0001g0085a0001c0002t0001g0097others(129): Show | 133 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1652-1426C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676777 | ||||||
| chr8:94676778
|
G | A | 1 | a0001c0004t0002g0086 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1652-1425G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676778 | ||||||
| chr8:94676928
|
A | G | 145 | a0001c0002t0001g0014a0001c0002t0001g0085a0001c0002t0001g0097others(142): Show | 146 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.1652-1275A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676928 | ||||||
| chr8:94676929
|
G | T | 1 | a0001c0003t0001g0001 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1652-1274G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676929 | ||||||
| chr8:94676939
|
A | C | 9 | a0001c0001t0001g0256a0001c0001t0006g0166a0001c0001t0006g0167others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1652-1264A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676939 | ||||||
| chr8:94676999
|
A | T | 132 | a0001c0002t0001g0014a0001c0002t0001g0085a0001c0002t0001g0097others(129): Show | 133 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1652-1204A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676999 | ||||||
| chr8:94677084
|
A | G | 132 | a0001c0002t0001g0014a0001c0002t0001g0085a0001c0002t0001g0097others(129): Show | 133 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1652-1119A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94677084 | ||||||
| chr8:94677108
|
C | G | 12 | a0001c0003t0001g0318a0001c0003t0001g0347a0001c0003t0001g0348others(9): Show | 12 | HG01070.hp2 HG01081.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.1652-1095C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94677108 | ||||||
| chr8:94677172
|
G | A | 145 | a0001c0002t0001g0014a0001c0002t0001g0085a0001c0002t0001g0097others(142): Show | 146 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.1652-1031G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94677172 | ||||||
| chr8:94677198
|
G | A | 2 | a0001c0001t0001g0360a0001c0001t0001g0367 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1652-1005G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94677198 | ||||||
| chr8:94677453
|
T | G | 145 | a0001c0002t0001g0014a0001c0002t0001g0085a0001c0002t0001g0097others(142): Show | 146 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.1652-750T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94677453 | ||||||
| chr8:94677529
|
G | A | 1 | a0001c0002t0002g0019 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1652-674G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94677529 | ||||||
| chr8:94677594
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1652-609C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94677594 | ||||||
| chr8:94677796
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1652-407G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94677796 | ||||||
| chr8:94677918
|
A | G | 1 | a0001c0002t0012g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1652-285A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94677918 | ||||||
| chr8:94677960
|
T | C | 3 | a0001c0003t0001g0368a0001c0003t0001g0369a0001c0006t0001g0345 | 3 | HG01167.hp2 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1652-243T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94677960 | ||||||
| chr8:94677999
|
C | A | 11 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(8): Show | 11 | HG01361.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.1652-204C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94677999 | ||||||
| chr8:94678033
|
C | T | 12 | a0001c0003t0001g0318a0001c0003t0001g0347a0001c0003t0001g0348others(9): Show | 12 | HG01070.hp2 HG01081.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.1652-170C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94678033 | ||||||
| chr8:94678100
|
T | A | 10 | a0001c0001t0001g0358a0001c0001t0001g0359a0001c0001t0001g0360others(7): Show | 10 | HG02257.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1652-103T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94678100 | ||||||
| chr8:94678488
|
A | G | 1 | a0001c0001t0001g0231 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1820+117A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94678488 | ||||||
| chr8:94678601
|
C | G | 1 | a0001c0001t0001g0278 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1820+230C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94678601 | ||||||
| chr8:94678768
|
A | C | 8 | a0001c0003t0001g0347a0001c0003t0001g0348a0001c0003t0001g0349others(5): Show | 8 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1820+397A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94678768 | ||||||
| chr8:94678838
|
T | C | 132 | a0001c0002t0001g0014a0001c0002t0001g0085a0001c0002t0001g0097others(129): Show | 133 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1820+467T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94678838 | ||||||
| chr8:94678973
|
T | A | 8 | a0001c0003t0001g0347a0001c0003t0001g0348a0001c0003t0001g0349others(5): Show | 8 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1820+602T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94678973 | ||||||
| chr8:94679188
|
A | T | 6 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(3): Show | 6 | HG01109.hp1 HG02145.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1820+817A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94679188 | ||||||
| chr8:94679497
|
G | A | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1820+1126G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94679497 | ||||||
| chr8:94679514
|
A | T | 7 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(4): Show | 7 | HG01109.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1820+1143A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94679514 | ||||||
| chr8:94679571
|
T | C | 2 | a0001c0002t0001g0085a0001c0002t0001g0097 | 2 | HG01943.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1820+1200T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94679571 | ||||||
| chr8:94679596
|
A | G | 132 | a0001c0002t0001g0014a0001c0002t0001g0085a0001c0002t0001g0097others(129): Show | 133 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1820+1225A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94679596 | ||||||
| chr8:94679598
|
G | T | 6 | a0001c0001t0001g0168a0001c0001t0001g0185a0001c0001t0001g0186others(3): Show | 6 | HG02559.hp1 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1820+1227G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94679598 | ||||||
| chr8:94679783
|
C | T | 145 | a0001c0002t0001g0014a0001c0002t0001g0085a0001c0002t0001g0097others(142): Show | 146 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.1820+1412C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94679783 | ||||||
| chr8:94679862
|
T | C | 4 | a0001c0005t0001g0181a0001c0005t0001g0182a0001c0005t0001g0183others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1820+1491T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94679862 | ||||||
| chr8:94679911
|
T | C | 132 | a0001c0002t0001g0014a0001c0002t0001g0085a0001c0002t0001g0097others(129): Show | 133 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1820+1540T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94679911 | ||||||
| chr8:94679919
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1820+1548G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94679919 | ||||||
| chr8:94679988
|
A | T | 46 | a0001c0001t0001g0003a0001c0001t0001g0137a0001c0001t0001g0198others(43): Show | 46 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.1820+1617A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94679988 | ||||||
| chr8:94680162
|
A | G | 282 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0125others(279): Show | 283 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.1820+1791A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94680162 | ||||||
| chr8:94680166
|
T | C | 1 | a0001c0002t0002g0313 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1820+1795T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94680166 | ||||||
| chr8:94680568
|
C | T | 3 | a0001c0003t0001g0368a0001c0003t0001g0369a0001c0006t0001g0345 | 3 | HG01167.hp2 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1820+2197C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94680568 | ||||||
| chr8:94680635
|
G | A | 4 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(1): Show | 4 | HG02109.hp1 HG03098.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1820+2264G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94680635 | ||||||
| chr8:94680774
|
A | G | 1 | a0001c0002t0012g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1820+2403A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94680774 | ||||||
| chr8:94680847
|
G | C | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1820+2476G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94680847 | ||||||
| chr8:94680926
|
T | C | 123 | a0001c0001t0001g0256a0001c0001t0006g0166a0001c0001t0006g0167others(120): Show | 123 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1820+2555T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94680926 | ||||||
| chr8:94680956
|
G | A | 123 | a0001c0001t0001g0256a0001c0001t0006g0166a0001c0001t0006g0167others(120): Show | 123 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1820+2585G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94680956 | ||||||
| chr8:94680999
|
T | C | 123 | a0001c0001t0001g0256a0001c0001t0006g0166a0001c0001t0006g0167others(120): Show | 123 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1820+2628T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94680999 | ||||||
| chr8:94681063
|
C | T | 6 | a0001c0001t0001g0242a0001c0001t0003g0214a0001c0001t0003g0216others(3): Show | 6 | HG02257.hp1 HG02280.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1820+2692C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681063 | ||||||
| chr8:94681064
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | NA19084.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1820+2693G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681064 | ||||||
| chr8:94681099
|
A | G | 1 | a0001c0011t0001g0251 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1820+2728A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681099 | ||||||
| chr8:94681107
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1820+2736C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681107 | ||||||
| chr8:94681110
|
G | T | 1 | a0001c0001t0001g0172 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1820+2739G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681110 | ||||||
| chr8:94681126
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1820+2755C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681126 | ||||||
| chr8:94681140
|
A | G | 5 | a0001c0005t0001g0181a0001c0005t0001g0182a0001c0005t0001g0183others(2): Show | 5 | HG02572.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1820+2769A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681140 | ||||||
| chr8:94681141
|
T | C | 2 | a0001c0002t0002g0072a0001c0002t0002g0084 | 2 | NA18988.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1820+2770T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681141 | ||||||
| chr8:94681152
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1820+2781C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681152 | ||||||
| chr8:94681154
|
T | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0043others(86): Show | 90 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1820+2783T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681154 | ||||||
| chr8:94681161
|
TA | T | 29 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0152others(26): Show | 29 | HG01070.hp2 HG01081.hp1 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.1820+2796delA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94681161 | |||||
| chr8:94681198
|
T | C | 3 | a0001c0001t0001g0159a0001c0001t0001g0163a0001c0001t0001g0165 | 3 | HG01261.hp2 HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1820+2827T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681198 | ||||||
| chr8:94681208
|
C | A | 4 | a0001c0003t0001g0318a0001c0003t0001g0368a0001c0003t0001g0369others(1): Show | 4 | HG01167.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1820+2837C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681208 | ||||||
| chr8:94681225
|
C | G | 1 | a0001c0005t0001g0181 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1820+2854C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681225 | ||||||
| chr8:94681251
|
G | A | 117 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(114): Show | 117 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.1820+2880G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681251 | ||||||
| chr8:94681283
|
G | A | 1 | a0001c0003t0001g0318 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1820+2912G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681283 | ||||||
| chr8:94681304
|
T | C | 117 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(114): Show | 117 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.1820+2933T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681304 | ||||||
| chr8:94681325
|
C | CA | 42 | a0001c0001t0001g0043a0001c0001t0001g0123a0001c0001t0001g0129others(39): Show | 42 | HG00423.hp2 HG00642.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.1820+2982dupA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94681325 | |||||
| chr8:94681325
|
C | CAA | 19 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(16): Show | 19 | HG00741.hp1 HG01346.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.1820+2981_1820+298 others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94681325 | |||||
| chr8:94681325
|
C | CAAAAAA | 19 | a0001c0001t0001g0137a0001c0001t0001g0140a0001c0001t0001g0169others(16): Show | 19 | HG00140.hp1 HG00738.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.1820+2977_1820+298 others(10): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94681325 | |||||
| chr8:94681325
|
C | CAAAAAAA | 28 | a0001c0001t0001g0003a0001c0001t0001g0139a0001c0001t0001g0144others(25): Show | 28 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.1820+2976_1820+298 others(11): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94681325 | |||||
| chr8:94681325
|
C | CAAAAAAA others(1): Show |
8 | a0001c0001t0001g0143a0001c0001t0001g0159a0001c0001t0001g0165others(5): Show | 8 | HG02004.hp1 HG02055.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1820+2975_1820+298 others(12): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94681325 | |||||
| chr8:94681325
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0163a0001c0001t0001g0308 | 2 | HG01261.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.1820+2973_1820+298 others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94681325 | |||||
| chr8:94681325
|
CA | C | 114 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0104others(111): Show | 115 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.1820+2982delA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94681325 | |||||
| chr8:94681325
|
CAAAAAAA others(7): Show |
C | 3 | a0001c0001t0001g0234a0001c0001t0001g0287a0001c0001t0001g0312 | 3 | HG01934.hp2 HG02300.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1820+2969_1820+298 others(18): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94681325 | |||||
| chr8:94681325
|
CAAAAAAA others(9): Show |
C | 4 | a0001c0005t0001g0181a0001c0005t0001g0182a0001c0005t0001g0183others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1820+2967_1820+298 others(20): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94681325 | |||||
| chr8:94681435
|
T | C | 117 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(114): Show | 117 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.1820+3064T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681435 | ||||||
| chr8:94681704
|
C | T | 104 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(101): Show | 104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1820+3333C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681704 | ||||||
| chr8:94681721
|
G | A | 9 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(6): Show | 9 | HG00597.hp2 HG01256.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1820+3350G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681721 | ||||||
| chr8:94681742
|
G | A | 102 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0002g0006others(99): Show | 102 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.1820+3371G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681742 | ||||||
| chr8:94681827
|
C | T | 1 | a0001c0003t0001g0334 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1820+3456C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681827 | ||||||
| chr8:94681910
|
G | T | 116 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(113): Show | 116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1820+3539G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681910 | ||||||
| chr8:94681953
|
T | C | 116 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(113): Show | 116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1820+3582T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681953 | ||||||
| chr8:94681981
|
G | A | 2 | a0001c0002t0002g0041a0001c0002t0002g0100 | 2 | NA19054.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1820+3610G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681981 | ||||||
| chr8:94681997
|
G | A | 116 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(113): Show | 116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1820+3626G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681997 | ||||||
| chr8:94682041
|
C | T | 104 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(101): Show | 104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1820+3670C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682041 | ||||||
| chr8:94682068
|
A | G | 4 | a0001c0003t0001g0318a0001c0003t0001g0368a0001c0003t0001g0369others(1): Show | 4 | HG01167.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1820+3697A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682068 | ||||||
| chr8:94682072
|
T | A | 156 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0159others(153): Show | 156 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.1820+3701T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682072 | ||||||
| chr8:94682096
|
G | C | 2 | a0001c0001t0001g0163a0001c0001t0001g0165 | 2 | HG01261.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1820+3725G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682096 | ||||||
| chr8:94682316
|
A | C | 1 | a0001c0002t0002g0051 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1820+3945A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682316 | ||||||
| chr8:94682364
|
A | T | 116 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(113): Show | 116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1820+3993A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682364 | ||||||
| chr8:94682403
|
A | G | 103 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(100): Show | 103 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1820+4032A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682403 | ||||||
| chr8:94682639
|
T | G | 104 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(101): Show | 104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1820+4268T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682639 | ||||||
| chr8:94682641
|
A | AATCCTCC | 104 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(101): Show | 104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1820+4270_1820+427 others(11): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682641 | ||||||
| chr8:94682643
|
A | AATGT | 104 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(101): Show | 104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1820+4272_1820+427 others(8): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682643 | ||||||
| chr8:94682645
|
G | C | 104 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(101): Show | 104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1820+4274G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682645 | ||||||
| chr8:94682648
|
T | G | 104 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(101): Show | 104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1820+4277T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682648 | ||||||
| chr8:94682651
|
GCCA | G | 104 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(101): Show | 104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1820+4284_1820+428 others(7): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682651 | |||||
| chr8:94682655
|
C | T | 104 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(101): Show | 104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1820+4284C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682655 | ||||||
| chr8:94682656
|
C | A | 104 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(101): Show | 104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1820+4285C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682656 | ||||||
| chr8:94682683
|
C | T | 1 | a0001c0001t0010g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1820+4312C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682683 | ||||||
| chr8:94682748
|
C | T | 7 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(4): Show | 7 | HG01109.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1820+4377C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682748 | ||||||
| chr8:94682869
|
C | CAT | 4 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(1): Show | 4 | HG01891.hp2 HG02723.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1820+4507_1820+450 others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682869 | |||||
| chr8:94682888
|
C | T | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1820+4517C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682888 | ||||||
| chr8:94682889
|
A | T | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1820+4518A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682889 | ||||||
| chr8:94682896
|
T | A | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1820+4525T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682896 | ||||||
| chr8:94682897
|
C | T | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1820+4526C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682897 | ||||||
| chr8:94682900
|
T | A | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1820+4529T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682900 | ||||||
| chr8:94682901
|
A | T | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1820+4530A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682901 | ||||||
| chr8:94682902
|
T | A | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1820+4531T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682902 | ||||||
| chr8:94682904
|
T | A | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1820+4533T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682904 | ||||||
| chr8:94682904
|
T | TTA | 18 | a0001c0001t0001g0115a0001c0001t0001g0148a0001c0001t0001g0225others(15): Show | 19 | HG00323.hp2 HG00609.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.1820+4561_1820+456 others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682904 | |||||
| chr8:94682904
|
T | TTATA | 22 | a0001c0001t0001g0002a0001c0001t0001g0087a0001c0001t0001g0103others(19): Show | 23 | HG00741.hp2 HG01168.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.1820+4559_1820+456 others(8): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682904 | |||||
| chr8:94682904
|
T | TTATATA | 8 | a0001c0001t0001g0123a0001c0001t0001g0127a0001c0001t0001g0199others(5): Show | 8 | HG00438.hp1 HG01243.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.1820+4557_1820+456 others(10): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682904 | |||||
| chr8:94682904
|
T | TTATATAT others(1): Show |
7 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0206others(4): Show | 7 | HG01256.hp1 HG01258.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1820+4555_1820+456 others(12): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682904 | |||||
| chr8:94682904
|
T | TTATATAT others(3): Show |
1 | a0001c0001t0001g0218 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1820+4553_1820+456 others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682904 | |||||
| chr8:94682904
|
T | TTATATAT others(5): Show |
3 | a0001c0001t0001g0197a0001c0001t0001g0309a0001c0006t0001g0345 | 3 | HG02965.hp1 HG03195.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1820+4551_1820+456 others(16): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682904 | |||||
| chr8:94682904
|
T | TTATATAT others(7): Show |
1 | a0001c0003t0001g0368 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1820+4549_1820+456 others(18): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682904 | |||||
| chr8:94682904
|
T | TTATATAT others(11): Show |
2 | a0001c0001t0001g0168a0001c0001t0001g0186 | 2 | HG02965.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1820+4545_1820+456 others(22): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682904 | |||||
| chr8:94682904
|
T | TTATATAT others(13): Show |
1 | a0001c0001t0001g0187 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1820+4543_1820+456 others(24): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682904 | |||||
| chr8:94682904
|
T | TTATATAT others(23): Show |
1 | a0001c0001t0001g0189 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1820+4562_1820+456 others(34): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682904 | |||||
| chr8:94682904
|
TTA | T | 7 | a0001c0001t0001g0291a0001c0004t0002g0086a0001c0004t0002g0091others(4): Show | 7 | HG01071.hp2 HG01074.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.1820+4561_1820+456 others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682904 | |||||
| chr8:94682904
|
TTATATAT others(5): Show |
T | 1 | a0001c0003t0001g0350 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1820+4551_1820+456 others(16): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682904 | |||||
| chr8:94682906
|
A | T | 7 | a0001c0001t0001g0138a0001c0001t0001g0144a0001c0002t0002g0026others(4): Show | 7 | HG02083.hp2 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1820+4535A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682906 | ||||||
| chr8:94682908
|
A | T | 2 | a0001c0001t0001g0360a0001c0001t0001g0367 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1820+4537A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682908 | ||||||
| chr8:94682921
|
TATATATA others(4): Show |
T | 6 | a0001c0003t0001g0347a0001c0003t0001g0348a0001c0003t0001g0349others(3): Show | 6 | HG01070.hp2 HG01081.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1820+4551_1820+456 others(15): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682921 | ||||||
| chr8:94682922
|
ATATATAT others(4): Show |
A | 1 | a0001c0003t0001g0354 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1820+4553_1820+456 others(15): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682922 | |||||
| chr8:94682922
|
ATATATAT others(5): Show |
A | 1 | a0001c0003t0001g0151 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1820+4553_1820+456 others(16): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682922 | |||||
| chr8:94682924
|
ATATATAT others(3): Show |
A | 4 | a0001c0005t0001g0181a0001c0005t0001g0182a0001c0005t0001g0183others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1820+4555_1820+456 others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682924 | |||||
| chr8:94682928
|
A | T | 3 | a0001c0001t0001g0154a0001c0001t0001g0161a0003c0010t0001g0321 | 3 | HG01516.hp2 HG01517.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1820+4557A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682928 | ||||||
| chr8:94682930
|
A | AT | 8 | a0001c0002t0002g0006a0001c0002t0002g0015a0001c0002t0002g0016others(5): Show | 8 | HG01109.hp2 HG02040.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.1820+4560dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682930 | |||||
| chr8:94682930
|
A | ATT | 5 | a0001c0002t0002g0013a0001c0002t0002g0041a0001c0002t0002g0282others(2): Show | 5 | HG02451.hp1 HG03710.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.1820+4560_1820+456 others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682930 | |||||
| chr8:94682930
|
A | ATTTTTT | 4 | a0001c0001t0001g0153a0001c0001t0001g0160a0001c0001t0001g0171others(1): Show | 4 | HG01255.hp1 HG01346.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1820+4560_1820+456 others(10): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682930 | |||||
| chr8:94682930
|
A | T | 7 | a0001c0001t0001g0154a0001c0001t0001g0161a0001c0001t0001g0256others(4): Show | 7 | HG01516.hp2 HG01517.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1820+4559A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682930 | ||||||
| chr8:94682931
|
TA | T | 4 | a0001c0001t0001g0165a0001c0001t0001g0320a0001c0002t0002g0065others(1): Show | 4 | HG00741.hp1 HG02055.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.1820+4561delA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682931 | ||||||
| chr8:94682932
|
A | AT | 23 | a0001c0001t0001g0147a0001c0001t0001g0180a0001c0002t0001g0097others(20): Show | 23 | HG00673.hp1 HG00733.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.1820+4590dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | |||||
| chr8:94682932
|
A | ATAT | 10 | a0001c0001t0001g0146a0001c0001t0001g0226a0001c0002t0002g0037others(7): Show | 10 | HG00735.hp1 HG02015.hp1 HG03710.hp2 others(7): Show |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(7): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | |||||
| chr8:94682932
|
A | ATATAT | 11 | a0001c0001t0001g0169a0001c0001t0001g0204a0001c0001t0001g0227others(8): Show | 11 | HG01175.hp1 HG01433.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(9): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | |||||
| chr8:94682932
|
A | ATATATAT others(4): Show |
3 | a0001c0001t0001g0210a0001c0001t0001g0268a0001c0001t0001g0360 | 3 | HG02615.hp2 HG03579.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(15): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | |||||
| chr8:94682932
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0202 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1820+4562_1820+456 others(17): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | |||||
| chr8:94682932
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0247 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1820+4562_1820+456 others(21): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | |||||
| chr8:94682932
|
A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0358 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1820+4562_1820+456 others(31): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | |||||
| chr8:94682932
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0365 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1820+4562_1820+456 others(27): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | |||||
| chr8:94682932
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0363 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1820+4562_1820+456 others(30): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | |||||
| chr8:94682932
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0366 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1820+4562_1820+456 others(23): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | |||||
| chr8:94682932
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0004g0271 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1820+4562_1820+456 others(24): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | |||||
| chr8:94682932
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0362 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1820+4562_1820+456 others(23): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | |||||
| chr8:94682932
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0367 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1820+4562_1820+456 others(19): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | |||||
| chr8:94682932
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0359 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1820+4562_1820+456 others(23): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | |||||
| chr8:94682932
|
A | ATATATAT others(13): Show |
1 | a0001c0002t0012g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1820+4562_1820+456 others(24): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | |||||
| chr8:94682932
|
A | ATATATAT others(3): Show |
2 | a0001c0001t0001g0043a0001c0001t0001g0162 | 2 | HG01069.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | |||||
| chr8:94682932
|
A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(15): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | |||||
| chr8:94682932
|
A | ATATATAT others(3): Show |
3 | a0001c0001t0001g0164a0001c0001t0001g0205a0001c0001t0001g0229 | 3 | HG02004.hp2 HG02300.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | |||||
| chr8:94682932
|
A | ATATATTT others(3): Show |
2 | a0001c0001t0001g0174a0001c0001t0001g0207 | 2 | NA18949.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | |||||
| chr8:94682932
|
A | ATATTTT | 6 | a0001c0001t0001g0173a0001c0001t0001g0175a0001c0001t0001g0177others(3): Show | 6 | HG02647.hp2 HG02717.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(10): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | |||||
| chr8:94682932
|
A | T | 38 | a0001c0001t0001g0143a0001c0001t0001g0153a0001c0001t0001g0154others(35): Show | 38 | HG01109.hp2 HG01255.hp1 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.1820+4561A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682932 | ||||||
| chr8:94682932
|
AT | A | 11 | a0001c0001t0001g0163a0001c0001t0001g0212a0001c0001t0001g0283others(8): Show | 11 | HG00423.hp1 HG00558.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.1820+4590delT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | |||||
| chr8:94682932
|
ATT | A | 13 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0137others(10): Show | 13 | HG00140.hp1 HG01934.hp2 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.1820+4589_1820+459 others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | |||||
| chr8:94682932
|
ATTT | A | 13 | a0001c0001t0001g0129a0001c0001t0001g0132a0001c0001t0001g0133others(10): Show | 13 | HG00673.hp2 HG00738.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.1820+4588_1820+459 others(7): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | |||||
| chr8:94682932
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0243 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1820+4581_1820+459 others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | |||||
| chr8:94682933
|
T | TA | 11 | a0001c0001t0001g0198a0001c0001t0001g0220a0001c0001t0001g0223others(8): Show | 11 | HG00558.hp2 HG00609.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(5): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682933 | ||||||
| chr8:94682933
|
T | TATA | 17 | a0001c0001t0001g0105a0001c0001t0001g0116a0001c0001t0001g0270others(14): Show | 17 | HG00642.hp1 HG00735.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(7): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682933 | ||||||
| chr8:94682933
|
T | TATATA | 10 | a0001c0001t0001g0125a0001c0001t0001g0128a0001c0001t0001g0221others(7): Show | 10 | HG00408.hp1 HG01891.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(9): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682933 | ||||||
| chr8:94682933
|
T | TATATATA | 7 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(4): Show | 7 | HG01167.hp2 NA18944.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(11): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682933 | ||||||
| chr8:94682933
|
T | TATATATA others(2): Show |
3 | a0001c0001t0001g0193a0001c0001t0001g0364a0001c0003t0001g0338 | 3 | HG02257.hp2 NA20300.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(13): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682933 | ||||||
| chr8:94682933
|
T | TATATATA others(4): Show |
3 | a0001c0001t0001g0179a0001c0001t0001g0209a0001c0001t0001g0259 | 3 | HG02165.hp2 HG02976.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(15): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682933 | ||||||
| chr8:94682933
|
T | TATATATA others(6): Show |
2 | a0001c0001t0001g0269a0001c0003t0001g0334 | 2 | HG00642.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(17): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682933 | ||||||
| chr8:94682933
|
T | TATATATA others(10): Show |
1 | a0001c0001t0001g0149 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1820+4562_1820+456 others(21): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682933 | ||||||
| chr8:94682933
|
T | TATATATA others(12): Show |
2 | a0001c0001t0001g0010a0001c0001t0001g0361 | 2 | NA18906.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(23): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682933 | ||||||
| chr8:94682933
|
T | TATATATA others(14): Show |
1 | a0001c0001t0001g0284 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1820+4562_1820+456 others(25): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682933 | ||||||
| chr8:94682934
|
T | A | 38 | a0001c0001t0001g0002a0001c0001t0001g0103a0001c0001t0001g0126others(35): Show | 40 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.1820+4563T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682934 | ||||||
| chr8:94682935
|
T | A | 28 | a0001c0001t0001g0107a0001c0001t0001g0128a0001c0001t0001g0149others(25): Show | 28 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.1820+4564T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682935 | ||||||
| chr8:94682936
|
T | A | 28 | a0001c0001t0001g0137a0001c0001t0001g0168a0001c0001t0001g0186others(25): Show | 29 | HG00140.hp1 HG00323.hp2 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.1820+4565T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682936 | ||||||
| chr8:94682937
|
T | A | 22 | a0001c0001t0001g0149a0001c0001t0001g0185a0001c0001t0001g0198others(19): Show | 22 | HG00673.hp2 HG00735.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1820+4566T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682937 | ||||||
| chr8:94682938
|
T | A | 8 | a0001c0001t0001g0137a0001c0001t0001g0186a0001c0001t0001g0188others(5): Show | 8 | HG00140.hp1 HG01928.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.1820+4567T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682938 | ||||||
| chr8:94682939
|
T | A | 4 | a0001c0001t0001g0149a0001c0001t0001g0275a0001c0001t0001g0283others(1): Show | 4 | HG01109.hp1 HG02257.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.1820+4568T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682939 | ||||||
| chr8:94682940
|
T | A | 4 | a0001c0001t0001g0186a0001c0001t0001g0295a0001c0003t0001g0368others(1): Show | 4 | HG02818.hp2 HG02965.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1820+4569T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682940 | ||||||
| chr8:94682941
|
T | A | 1 | a0001c0001t0001g0364 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1820+4570T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682941 | ||||||
| chr8:94682942
|
T | A | 1 | a0001c0001t0001g0295 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1820+4571T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682942 | ||||||
| chr8:94682943
|
T | A | 1 | a0001c0001t0001g0364 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1820+4572T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682943 | ||||||
| chr8:94682944
|
T | A | 1 | a0001c0001t0001g0243 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1820+4573T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682944 | ||||||
| chr8:94682946
|
T | A | 1 | a0001c0001t0001g0243 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1820+4575T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682946 | ||||||
| chr8:94682961
|
T | G | 1 | a0001c0001t0001g0204 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1820+4590T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682961 | ||||||
| chr8:94682967
|
G | A | 4 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(1): Show | 4 | HG02280.hp2 HG02622.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1820+4596G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682967 | ||||||
| chr8:94683133
|
G | A | 154 | a0001c0001t0001g0159a0001c0001t0001g0163a0001c0001t0001g0165others(151): Show | 154 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.1820+4762G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683133 | ||||||
| chr8:94683186
|
C | T | 1 | a0001c0001t0001g0365 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1820+4815C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683186 | ||||||
| chr8:94683187
|
G | T | 1 | a0001c0001t0001g0224 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1820+4816G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683187 | ||||||
| chr8:94683232
|
C | T | 5 | a0001c0001t0001g0256a0001c0001t0006g0166a0001c0001t0006g0167others(2): Show | 5 | HG02109.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1820+4861C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683232 | ||||||
| chr8:94683235
|
C | T | 4 | a0001c0003t0001g0318a0001c0003t0001g0368a0001c0003t0001g0369others(1): Show | 4 | HG01167.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1820+4864C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683235 | ||||||
| chr8:94683252
|
T | A | 4 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(1): Show | 4 | HG01891.hp2 HG02723.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1820+4881T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683252 | ||||||
| chr8:94683289
|
T | C | 116 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(113): Show | 116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1820+4918T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683289 | ||||||
| chr8:94683320
|
A | G | 1 | a0001c0002t0002g0078 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1820+4949A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683320 | ||||||
| chr8:94683371
|
G | T | 115 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(112): Show | 115 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.1820+5000G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683371 | ||||||
| chr8:94683372
|
G | A | 3 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196 | 3 | HG02109.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1820+5001G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683372 | ||||||
| chr8:94683385
|
A | G | 103 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(100): Show | 103 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1820+5014A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683385 | ||||||
| chr8:94683424
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1820+5053C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683424 | ||||||
| chr8:94683434
|
G | T | 116 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(113): Show | 116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1820+5063G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683434 | ||||||
| chr8:94683448
|
A | G | 116 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(113): Show | 116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1820+5077A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683448 | ||||||
| chr8:94683494
|
C | T | 10 | a0001c0001t0001g0159a0001c0001t0001g0163a0001c0001t0001g0165others(7): Show | 10 | HG01261.hp2 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1820+5123C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683494 | ||||||
| chr8:94683515
|
A | G | 8 | a0001c0003t0001g0347a0001c0003t0001g0348a0001c0003t0001g0349others(5): Show | 8 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1820+5144A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683515 | ||||||
| chr8:94683607
|
A | G | 1 | a0001c0003t0001g0354 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1820+5236A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683607 | ||||||
| chr8:94683654
|
C | G | 1 | a0001c0001t0001g0159 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1820+5283C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683654 | ||||||
| chr8:94683725
|
T | C | 116 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(113): Show | 116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1820+5354T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683725 | ||||||
| chr8:94683760
|
A | G | 1 | a0001c0001t0001g0314 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1820+5389A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683760 | ||||||
| chr8:94683846
|
T | C | 116 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(113): Show | 116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1820+5475T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683846 | ||||||
| chr8:94683902
|
C | T | 201 | a0001c0001t0001g0003a0001c0001t0001g0137a0001c0001t0001g0159others(198): Show | 201 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.1820+5531C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683902 | ||||||
| chr8:94684033
|
G | A | 28 | a0001c0001t0001g0159a0001c0001t0001g0163a0001c0001t0001g0165others(25): Show | 28 | HG01261.hp2 HG02055.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1820+5662G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94684033 | ||||||
| chr8:94684126
|
T | C | 116 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(113): Show | 116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1820+5755T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94684126 | ||||||
| chr8:94684141
|
A | C | 154 | a0001c0001t0001g0159a0001c0001t0001g0163a0001c0001t0001g0165others(151): Show | 154 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.1820+5770A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94684141 | ||||||
| chr8:94684142
|
C | CG | 153 | a0001c0001t0001g0159a0001c0001t0001g0163a0001c0001t0001g0165others(150): Show | 153 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.1820+5772dupG | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94684142 | |||||
| chr8:94684469
|
C | T | 116 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(113): Show | 116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1820+6098C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94684469 | ||||||
| chr8:94684533
|
C | T | 1 | a0001c0011t0001g0251 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1820+6162C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94684533 | ||||||
| chr8:94684623
|
T | C | 104 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(101): Show | 104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1820+6252T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94684623 | ||||||
| chr8:94684643
|
A | G | 4 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(1): Show | 4 | HG02280.hp2 HG02622.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1820+6272A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94684643 | ||||||
| chr8:94684713
|
A | G | 4 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(1): Show | 4 | HG02280.hp2 HG02622.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1820+6342A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94684713 | ||||||
| chr8:94684863
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1820+6492C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94684863 | ||||||
| chr8:94684965
|
C | T | 6 | a0001c0003t0001g0001a0001c0003t0001g0134a0001c0003t0001g0324others(3): Show | 7 | HG00642.hp1 HG01074.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.1820+6594C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94684965 | ||||||
| chr8:94685022
|
TA | T | 149 | a0001c0001t0001g0159a0001c0001t0001g0163a0001c0001t0001g0165others(146): Show | 149 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.1820+6664delA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94685022 | |||||
| chr8:94685051
|
A | G | 104 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(101): Show | 104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1820+6680A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94685051 | ||||||
| chr8:94685130
|
A | G | 1 | a0001c0001t0003g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1820+6759A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94685130 | ||||||
| chr8:94685205
|
A | G | 5 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0252others(2): Show | 5 | HG02630.hp2 HG03041.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1820+6834A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94685205 | ||||||
| chr8:94685236
|
G | T | 4 | a0001c0005t0001g0181a0001c0005t0001g0182a0001c0005t0001g0183others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1820+6865G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94685236 | ||||||
| chr8:94685482
|
T | A | 4 | a0001c0003t0001g0318a0001c0003t0001g0368a0001c0003t0001g0369others(1): Show | 4 | HG01167.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1820+7111T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94685482 | ||||||
| chr8:94685570
|
G | A | 116 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(113): Show | 116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-7107G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94685570 | ||||||
| chr8:94685662
|
T | C | 4 | a0001c0003t0001g0324a0001c0003t0001g0325a0001c0003t0001g0332others(1): Show | 4 | HG00642.hp1 HG01074.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.1821-7015T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94685662 | ||||||
| chr8:94685687
|
C | G | 2 | a0001c0001t0001g0163a0001c0001t0001g0165 | 2 | HG01261.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1821-6990C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94685687 | ||||||
| chr8:94685786
|
CA | C | 108 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(105): Show | 108 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.1821-6880delA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94685786 | |||||
| chr8:94685797
|
A | G | 116 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(113): Show | 116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-6880A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94685797 | ||||||
| chr8:94686001
|
G | T | 103 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(100): Show | 103 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1821-6676G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94686001 | ||||||
| chr8:94686209
|
A | G | 1 | a0001c0002t0012g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1821-6468A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94686209 | ||||||
| chr8:94686244
|
T | G | 3 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196 | 3 | HG02109.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1821-6433T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94686244 | ||||||
| chr8:94686254
|
A | G | 4 | a0001c0005t0001g0181a0001c0005t0001g0182a0001c0005t0001g0183others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1821-6423A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94686254 | ||||||
| chr8:94686386
|
C | T | 120 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(117): Show | 120 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.1821-6291C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94686386 | ||||||
| chr8:94686542
|
C | T | 4 | a0001c0003t0001g0327a0001c0003t0001g0328a0001c0003t0001g0329others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.1821-6135C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94686542 | ||||||
| chr8:94686647
|
A | G | 116 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(113): Show | 116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-6030A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94686647 | ||||||
| chr8:94686724
|
T | A | 1 | a0001c0002t0002g0041 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1821-5953T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94686724 | ||||||
| chr8:94686991
|
G | A | 103 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(100): Show | 103 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1821-5686G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94686991 | ||||||
| chr8:94687093
|
T | C | 27 | a0001c0003t0001g0001a0001c0003t0001g0088a0001c0003t0001g0134others(24): Show | 28 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1821-5584T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94687093 | ||||||
| chr8:94687114
|
C | G | 5 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0252others(2): Show | 5 | HG02630.hp2 HG03041.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1821-5563C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94687114 | ||||||
| chr8:94687169
|
C | A | 6 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0252others(3): Show | 6 | HG02630.hp2 HG03041.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1821-5508C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94687169 | ||||||
| chr8:94687261
|
A | T | 1 | a0001c0001t0001g0246 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1821-5416A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94687261 | ||||||
| chr8:94687340
|
G | A | 116 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(113): Show | 116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-5337G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94687340 | ||||||
| chr8:94687350
|
G | A | 1 | a0001c0002t0002g0009 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1821-5327G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94687350 | ||||||
| chr8:94687400
|
T | C | 28 | a0001c0001t0001g0159a0001c0001t0001g0163a0001c0001t0001g0165others(25): Show | 28 | HG01261.hp2 HG02055.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1821-5277T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94687400 | ||||||
| chr8:94687447
|
T | C | 116 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(113): Show | 116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-5230T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94687447 | ||||||
| chr8:94687530
|
A | G | 103 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(100): Show | 103 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1821-5147A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94687530 | ||||||
| chr8:94688114
|
G | A | 27 | a0001c0003t0001g0001a0001c0003t0001g0088a0001c0003t0001g0134others(24): Show | 28 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1821-4563G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94688114 | ||||||
| chr8:94688142
|
C | T | 116 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(113): Show | 116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-4535C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94688142 | ||||||
| chr8:94688175
|
A | G | 116 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(113): Show | 116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-4502A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94688175 | ||||||
| chr8:94688237
|
AT | A | 154 | a0001c0001t0001g0159a0001c0001t0001g0163a0001c0001t0001g0165others(151): Show | 154 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.1821-4438delT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94688237 | |||||
| chr8:94688410
|
T | C | 1 | a0001c0011t0001g0251 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1821-4267T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94688410 | ||||||
| chr8:94688460
|
C | T | 277 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0125others(274): Show | 278 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.1821-4217C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94688460 | ||||||
| chr8:94688524
|
A | T | 13 | a0001c0001t0001g0159a0001c0001t0001g0163a0001c0001t0001g0165others(10): Show | 13 | HG01261.hp2 HG02055.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1821-4153A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94688524 | ||||||
| chr8:94688675
|
G | C | 1 | a0001c0001t0001g0212 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1821-4002G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94688675 | ||||||
| chr8:94688726
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1821-3951C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94688726 | ||||||
| chr8:94688918
|
G | A | 116 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(113): Show | 116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-3759G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94688918 | ||||||
| chr8:94688989
|
G | A | 1 | a0001c0002t0002g0024 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1821-3688G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94688989 | ||||||
| chr8:94689042
|
G | A | 4 | a0001c0005t0001g0181a0001c0005t0001g0182a0001c0005t0001g0183others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1821-3635G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689042 | ||||||
| chr8:94689173
|
T | C | 116 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(113): Show | 116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-3504T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689173 | ||||||
| chr8:94689236
|
G | A | 163 | a0001c0001t0001g0003a0001c0001t0001g0137a0001c0001t0001g0198others(160): Show | 163 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.1821-3441G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689236 | ||||||
| chr8:94689249
|
C | CA | 81 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0087others(78): Show | 81 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1821-3403dupA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689249 | |||||
| chr8:94689249
|
C | CAA | 34 | a0001c0001t0001g0131a0001c0001t0001g0148a0001c0001t0001g0149others(31): Show | 34 | HG00423.hp1 HG01109.hp1 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.1821-3404_1821-340 others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689249 | |||||
| chr8:94689249
|
C | CAAA | 12 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0159others(9): Show | 12 | HG00673.hp2 HG02055.hp1 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1821-3405_1821-340 others(7): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689249 | |||||
| chr8:94689249
|
CA | C | 6 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0143others(3): Show | 6 | HG01261.hp1 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1821-3403delA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689249 | |||||
| chr8:94689249
|
CAAAAAAA others(1): Show |
C | 8 | a0001c0003t0001g0347a0001c0003t0001g0348a0001c0003t0001g0349others(5): Show | 8 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1821-3410_1821-340 others(12): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689249 | |||||
| chr8:94689249
|
CAAAAAAA others(2): Show |
C | 14 | a0001c0001t0001g0358a0001c0001t0001g0359a0001c0001t0001g0360others(11): Show | 14 | HG02257.hp2 HG02451.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1821-3411_1821-340 others(13): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689249 | |||||
| chr8:94689249
|
CAAAAAAA others(3): Show |
C | 100 | a0001c0001t0001g0365a0001c0002t0001g0085a0001c0002t0001g0097others(97): Show | 100 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1821-3412_1821-340 others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689249 | |||||
| chr8:94689319
|
CTT | C | 116 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(113): Show | 116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-3353_1821-335 others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689319 | |||||
| chr8:94689321
|
TTTTTC | T | 3 | a0001c0001t0001g0155a0001c0001t0001g0162a0001c0001t0001g0164 | 3 | HG01069.hp1 HG02300.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1821-3351_1821-334 others(9): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689321 | |||||
| chr8:94689407
|
T | C | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0213 | 3 | HG02615.hp1 HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1821-3270T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689407 | ||||||
| chr8:94689599
|
A | G | 4 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(1): Show | 4 | HG02109.hp1 HG03098.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1821-3078A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689599 | ||||||
| chr8:94689657
|
A | G | 244 | a0001c0001t0001g0003a0001c0001t0001g0125a0001c0001t0001g0126others(241): Show | 245 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.1821-3020A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689657 | ||||||
| chr8:94689657
|
A | T | 1 | a0001c0002t0002g0067 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1821-3020A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689657 | ||||||
| chr8:94689673
|
A | G | 2 | a0001c0001t0001g0154a0001c0001t0001g0161 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1821-3004A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689673 | ||||||
| chr8:94689715
|
T | G | 116 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(113): Show | 116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-2962T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689715 | ||||||
| chr8:94689788
|
C | G | 104 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(101): Show | 104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1821-2889C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689788 | ||||||
| chr8:94689806
|
C | T | 3 | a0001c0003t0001g0368a0001c0003t0001g0369a0001c0006t0001g0345 | 3 | HG01167.hp2 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1821-2871C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689806 | ||||||
| chr8:94689811
|
C | CT | 25 | a0001c0001t0001g0107a0001c0001t0001g0112a0001c0001t0001g0113others(22): Show | 25 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.1821-2841dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | |||||
| chr8:94689811
|
C | CTTTTTTT others(3): Show |
4 | a0001c0001t0001g0169a0001c0001t0001g0258a0001c0001t0001g0259others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1821-2850_1821-284 others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | |||||
| chr8:94689811
|
C | CTTTTTTT others(4): Show |
5 | a0001c0001t0001g0159a0001c0001t0001g0163a0001c0001t0001g0165others(2): Show | 5 | HG01261.hp2 HG02055.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1821-2851_1821-284 others(15): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | |||||
| chr8:94689811
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0186 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1821-2852_1821-284 others(16): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | |||||
| chr8:94689811
|
C | CTTTTTTT others(6): Show |
5 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0003t0001g0333others(2): Show | 5 | HG02647.hp1 HG02738.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1821-2853_1821-284 others(17): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | |||||
| chr8:94689811
|
C | CTTTTTTT others(7): Show |
8 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0270others(5): Show | 8 | HG01069.hp2 HG01099.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1821-2854_1821-284 others(18): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | |||||
| chr8:94689811
|
C | CTTTTTTT others(8): Show |
27 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(24): Show | 27 | HG00140.hp1 HG00642.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.1821-2855_1821-284 others(19): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | |||||
| chr8:94689811
|
C | CTTTTTTT others(9): Show |
17 | a0001c0001t0001g0128a0001c0001t0001g0143a0001c0001t0001g0144others(14): Show | 17 | HG00423.hp1 HG01346.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1821-2856_1821-284 others(20): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | |||||
| chr8:94689811
|
C | CTTTTTTT others(10): Show |
9 | a0001c0001t0001g0278a0001c0001t0001g0284a0001c0001t0001g0307others(6): Show | 9 | HG02004.hp1 HG02015.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.1821-2857_1821-284 others(21): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | |||||
| chr8:94689811
|
C | CTTTTTTT others(11): Show |
9 | a0001c0001t0001g0139a0001c0001t0001g0292a0001c0001t0001g0297others(6): Show | 9 | HG00738.hp2 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1821-2858_1821-284 others(22): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | |||||
| chr8:94689811
|
C | CTTTTTTT others(12): Show |
4 | a0001c0001t0001g0140a0001c0001t0001g0180a0001c0001t0001g0256others(1): Show | 4 | HG01099.hp1 HG02145.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1821-2859_1821-284 others(23): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | |||||
| chr8:94689811
|
C | CTTTTTTT others(13): Show |
2 | a0001c0001t0001g0003a0001c0003t0001g0340 | 2 | HG00733.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1821-2860_1821-284 others(24): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | |||||
| chr8:94689811
|
C | CTTTTTTT others(14): Show |
1 | a0001c0003t0001g0338 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1821-2861_1821-284 others(25): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | |||||
| chr8:94689811
|
C | CTTTTTTT others(15): Show |
3 | a0001c0001t0001g0277a0001c0001t0001g0295a0001c0001t0001g0301 | 3 | HG00558.hp1 HG03017.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1821-2862_1821-284 others(26): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | |||||
| chr8:94689811
|
C | CTTTTTTT others(16): Show |
2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | NA18957.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1821-2863_1821-284 others(27): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | |||||
| chr8:94689811
|
C | CTTTTTTT others(19): Show |
1 | a0001c0003t0001g0135 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1821-2841_1821-284 others(30): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | |||||
| chr8:94689811
|
C | CTTTTTTT others(20): Show |
1 | a0001c0003t0001g0339 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1821-2841_1821-284 others(31): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | |||||
| chr8:94689811
|
C | CTTTTTTT others(24): Show |
1 | a0001c0001t0001g0138 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1821-2841_1821-284 others(35): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | |||||
| chr8:94689811
|
CT | C | 24 | a0001c0001t0001g0004a0001c0001t0001g0153a0001c0001t0001g0154others(21): Show | 25 | HG00140.hp2 HG00423.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.1821-2841delT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | |||||
| chr8:94689811
|
CTTTT | C | 7 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(4): Show | 7 | HG01109.hp1 HG02486.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1821-2844_1821-284 others(8): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | |||||
| chr8:94689811
|
CTTTTT | C | 7 | a0001c0001t0001g0275a0001c0001t0001g0279a0001c0001t0001g0286others(4): Show | 7 | HG00673.hp2 HG02602.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.1821-2845_1821-284 others(9): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | |||||
| chr8:94689811
|
CTTTTTTT others(3): Show |
C | 116 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(113): Show | 116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-2850_1821-284 others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | |||||
| chr8:94689851
|
C | G | 116 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(113): Show | 116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-2826C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689851 | ||||||
| chr8:94689877
|
C | T | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1821-2800C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689877 | ||||||
| chr8:94689878
|
G | A | 98 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0043others(95): Show | 99 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1821-2799G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689878 | ||||||
| chr8:94689892
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1821-2785C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689892 | ||||||
| chr8:94689912
|
G | A | 116 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(113): Show | 116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-2765G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689912 | ||||||
| chr8:94690020
|
G | A | 5 | a0001c0001t0001g0180a0001c0001t0001g0267a0001c0001t0001g0268others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1821-2657G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94690020 | ||||||
| chr8:94690107
|
C | T | 3 | a0001c0001t0001g0159a0001c0001t0001g0163a0001c0001t0001g0165 | 3 | HG01261.hp2 HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1821-2570C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94690107 | ||||||
| chr8:94690120
|
A | AT | 115 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(112): Show | 115 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.1821-2549dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94690120 | |||||
| chr8:94690152
|
GTTTTTTA | G | 21 | a0001c0001t0001g0004a0001c0001t0001g0153a0001c0001t0001g0154others(18): Show | 21 | HG00140.hp2 HG00423.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.1821-2524_1821-251 others(11): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94690152 | ||||||
| chr8:94690267
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0171 | 2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1821-2410G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94690267 | ||||||
| chr8:94690276
|
A | AT | 63 | a0001c0001t0001g0115a0001c0001t0001g0148a0001c0001t0001g0149others(60): Show | 63 | HG00423.hp1 HG00558.hp1 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.1821-2373dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94690276 | |||||
| chr8:94690276
|
A | ATT | 49 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0123others(46): Show | 50 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.1821-2374_1821-237 others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94690276 | |||||
| chr8:94690276
|
A | ATTT | 26 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0143others(23): Show | 26 | HG00642.hp1 HG00735.hp2 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.1821-2375_1821-237 others(7): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94690276 | |||||
| chr8:94690276
|
A | ATTTT | 9 | a0001c0001t0001g0258a0001c0001t0001g0360a0001c0003t0001g0151others(6): Show | 9 | HG00642.hp2 HG00741.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1821-2376_1821-237 others(8): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94690276 | |||||
| chr8:94690276
|
A | ATTTTT | 11 | a0001c0001t0001g0159a0001c0001t0001g0163a0001c0001t0001g0169others(8): Show | 11 | HG01261.hp2 HG01517.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1821-2377_1821-237 others(9): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94690276 | |||||
| chr8:94690276
|
AT | A | 12 | a0001c0001t0001g0002a0001c0001t0001g0106a0001c0001t0001g0190others(9): Show | 13 | HG01168.hp1 HG01169.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.1821-2373delT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94690276 | |||||
| chr8:94690294
|
TTTTTTTT others(4): Show |
T | 1 | a0001c0003t0001g0348 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1821-2382_1821-237 others(15): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94690294 | ||||||
| chr8:94690295
|
TTTTTTTT others(3): Show |
T | 8 | a0001c0003t0001g0318a0001c0003t0001g0347a0001c0003t0001g0349others(5): Show | 8 | HG01070.hp2 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1821-2381_1821-237 others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94690295 | ||||||
| chr8:94690298
|
TTTTTTTG | T | 9 | a0001c0002t0002g0030a0001c0002t0002g0038a0001c0002t0002g0066others(6): Show | 9 | HG01070.hp1 HG01256.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.1821-2378_1821-237 others(11): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94690298 | ||||||
| chr8:94690299
|
TTTTTTG | T | 92 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0002g0006others(89): Show | 92 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1821-2377_1821-237 others(10): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94690299 | ||||||
| chr8:94690623
|
G | A | 8 | a0001c0003t0001g0347a0001c0003t0001g0348a0001c0003t0001g0349others(5): Show | 8 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1821-2054G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94690623 | ||||||
| chr8:94690707
|
C | T | 4 | a0001c0004t0002g0090a0001c0004t0002g0091a0001c0004t0002g0099others(1): Show | 4 | HG00323.hp1 HG01243.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.1821-1970C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94690707 | ||||||
| chr8:94690741
|
T | C | 283 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0125others(280): Show | 284 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.1821-1936T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94690741 | ||||||
| chr8:94690895
|
T | C | 116 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(113): Show | 116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-1782T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94690895 | ||||||
| chr8:94690920
|
A | G | 104 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(101): Show | 104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1821-1757A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94690920 | ||||||
| chr8:94690932
|
T | C | 116 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(113): Show | 116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-1745T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94690932 | ||||||
| chr8:94691034
|
C | T | 4 | a0001c0005t0001g0181a0001c0005t0001g0182a0001c0005t0001g0183others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1821-1643C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94691034 | ||||||
| chr8:94691096
|
T | G | 1 | a0001c0001t0004g0254 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1821-1581T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94691096 | ||||||
| chr8:94691129
|
C | G | 1 | a0001c0004t0002g0092 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1821-1548C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94691129 | ||||||
| chr8:94691170
|
G | A | 1 | a0001c0002t0002g0008 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1821-1507G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94691170 | ||||||
| chr8:94691360
|
G | A | 150 | a0001c0001t0001g0159a0001c0001t0001g0163a0001c0001t0001g0165others(147): Show | 150 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.1821-1317G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94691360 | ||||||
| chr8:94691369
|
T | A | 4 | a0001c0005t0001g0181a0001c0005t0001g0182a0001c0005t0001g0183others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1821-1308T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94691369 | ||||||
| chr8:94691390
|
G | A | 5 | a0001c0001t0001g0256a0001c0001t0006g0166a0001c0001t0006g0167others(2): Show | 5 | HG02109.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1821-1287G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94691390 | ||||||
| chr8:94691395
|
C | T | 1 | a0001c0002t0002g0023 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1821-1282C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94691395 | ||||||
| chr8:94691517
|
T | C | 3 | a0001c0003t0001g0368a0001c0003t0001g0369a0001c0006t0001g0345 | 3 | HG01167.hp2 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1821-1160T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94691517 | ||||||
| chr8:94691582
|
G | T | 103 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(100): Show | 103 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1821-1095G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94691582 | ||||||
| chr8:94691692
|
G | A | 1 | a0001c0002t0001g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1821-985G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94691692 | ||||||
| chr8:94691833
|
C | T | 4 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0206others(1): Show | 4 | NA18971.hp1 NA19062.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.1821-844C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94691833 | ||||||
| chr8:94691869
|
T | G | 4 | a0001c0001t0001g0212a0001c0001t0001g0275a0001c0001t0001g0279others(1): Show | 4 | NA18962.hp1 NA18972.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1821-808T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94691869 | ||||||
| chr8:94691975
|
C | G | 3 | a0001c0001t0006g0166a0001c0001t0006g0167a0001c0001t0006g0215 | 3 | HG02109.hp2 HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1821-702C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94691975 | ||||||
| chr8:94692054
|
C | G | 1 | a0001c0001t0001g0138 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1821-623C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94692054 | ||||||
| chr8:94692126
|
C | T | 4 | a0001c0003t0001g0318a0001c0003t0001g0368a0001c0003t0001g0369others(1): Show | 4 | HG01167.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1821-551C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94692126 | ||||||
| chr8:94692187
|
G | A | 103 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(100): Show | 103 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1821-490G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94692187 | ||||||
| chr8:94692390
|
G | A | 2 | a0001c0001t0001g0158a0001c0001t0001g0170 | 2 | NA18947.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1821-287G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94692390 | ||||||
| chr8:94692478
|
T | G | 2 | a0001c0001t0001g0154a0001c0001t0001g0161 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1821-199T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94692478 | ||||||
| chr8:94692496
|
T | G | 1 | a0001c0001t0001g0211 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1821-181T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94692496 | ||||||
| chr8:94693007
|
C | T | 3 | a0001c0001t0006g0166a0001c0001t0006g0167a0001c0001t0006g0215 | 3 | HG02109.hp2 HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1971+180C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94693007 | ||||||
| chr8:94693008
|
C | T | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1971+181C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94693008 | ||||||
| chr8:94693026
|
CT | C | 150 | a0001c0001t0001g0159a0001c0001t0001g0163a0001c0001t0001g0165others(147): Show | 150 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.1971+204delT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr8 | 94693026 | |||||
| chr8:94693100
|
G | A | 4 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(1): Show | 4 | HG02109.hp1 HG03098.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1971+273G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94693100 | ||||||
| chr8:94693182
|
A | G | 104 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0001g0124others(101): Show | 104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1971+355A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94693182 | ||||||
| chr8:94693313
|
G | GT | 4 | a0001c0003t0001g0318a0001c0003t0001g0368a0001c0003t0001g0369others(1): Show | 4 | HG01167.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1971+487dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr8 | 94693313 | |||||
| chr8:94693545
|
A | G | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1971+718A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94693545 | ||||||
| chr8:94693681
|
A | G | 1 | a0001c0002t0002g0075 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1971+854A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94693681 | ||||||
| chr8:94693904
|
A | G | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1971+1077A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94693904 | ||||||
| chr8:94694027
|
C | A | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1971+1200C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94694027 | ||||||
| chr8:94694042
|
A | G | 1 | a0001c0011t0001g0251 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1971+1215A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94694042 | ||||||
| chr8:94694106
|
T | C | 10 | a0001c0001t0001g0256a0001c0002t0012g0141a0001c0003t0001g0347others(7): Show | 10 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1971+1279T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94694106 | ||||||
| chr8:94694132
|
T | C | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1971+1305T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94694132 | ||||||
| chr8:94694182
|
G | T | 4 | a0001c0003t0001g0318a0001c0003t0001g0368a0001c0003t0001g0369others(1): Show | 4 | HG01167.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1971+1355G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94694182 | ||||||
| chr8:94694344
|
C | A | 1 | a0001c0003t0001g0353 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1971+1517C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94694344 | ||||||
| chr8:94694349
|
G | C | 2 | a0001c0002t0002g0066a0001c0002t0002g0076 | 2 | NA18994.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1971+1522G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94694349 | ||||||
| chr8:94694433
|
G | A | 1 | a0001c0002t0012g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1971+1606G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94694433 | ||||||
| chr8:94694561
|
T | G | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1971+1734T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94694561 | ||||||
| chr8:94694598
|
T | C | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1971+1771T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94694598 | ||||||
| chr8:94694651
|
A | G | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1971+1824A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94694651 | ||||||
| chr8:94694662
|
G | A | 1 | a0001c0007t0001g0346 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1971+1835G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94694662 | ||||||
| chr8:94695005
|
T | C | 10 | a0001c0001t0001g0358a0001c0001t0001g0359a0001c0001t0001g0360others(7): Show | 10 | HG02257.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1972-1847T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695005 | ||||||
| chr8:94695039
|
A | T | 1 | a0001c0001t0001g0204 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1972-1813A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695039 | ||||||
| chr8:94695055
|
G | A | 103 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0002g0006others(100): Show | 103 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1972-1797G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695055 | ||||||
| chr8:94695106
|
T | C | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-1746T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695106 | ||||||
| chr8:94695128
|
T | A | 3 | a0001c0001t0001g0307a0001c0001t0001g0309a0001c0001t0001g0311 | 3 | NA18994.hp1 NA19002.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1972-1724T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695128 | ||||||
| chr8:94695240
|
G | A | 47 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0043others(44): Show | 47 | HG00140.hp2 HG00423.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.1972-1612G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695240 | ||||||
| chr8:94695348
|
C | CT | 92 | a0001c0002t0001g0085a0001c0002t0001g0097a0001c0002t0002g0006others(89): Show | 92 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1972-1480dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr8 | 94695348 | |||||
| chr8:94695348
|
C | CTT | 8 | a0001c0001t0010g0005a0001c0002t0002g0013a0001c0002t0002g0047others(5): Show | 8 | HG00597.hp1 HG02080.hp1 HG03490.hp2 others(5): Show |
intron_variant | MODIFIER | c.1972-1481_1972-148 others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr8 | 94695348 | |||||
| chr8:94695348
|
CT | C | 14 | a0001c0001t0001g0159a0001c0001t0001g0163a0001c0001t0001g0165others(11): Show | 14 | HG01167.hp2 HG01261.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1972-1480delT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr8 | 94695348 | |||||
| chr8:94695348
|
CTT | C | 8 | a0001c0001t0001g0169a0001c0001t0001g0247a0001c0001t0001g0257others(5): Show | 8 | HG02559.hp2 HG02622.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1972-1481_1972-148 others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr8 | 94695348 | |||||
| chr8:94695348
|
CTTTTTTT others(1): Show |
C | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-1487_1972-148 others(12): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr8 | 94695348 | |||||
| chr8:94695371
|
T | C | 4 | a0001c0001t0006g0166a0001c0001t0006g0167a0001c0001t0006g0215others(1): Show | 4 | HG02109.hp2 HG02572.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1972-1481T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695371 | ||||||
| chr8:94695371
|
T | TTC | 9 | a0001c0001t0001g0125a0001c0001t0001g0127a0001c0001t0001g0128others(6): Show | 9 | HG00558.hp1 HG01891.hp2 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-1480_1972-147 others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr8 | 94695371 | |||||
| chr8:94695371
|
T | TTTC | 91 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0043others(88): Show | 91 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.1972-1480_1972-147 others(7): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr8 | 94695371 | |||||
| chr8:94695371
|
T | TTTTC | 102 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0087others(99): Show | 104 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.1972-1480_1972-147 others(8): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr8 | 94695371 | |||||
| chr8:94695371
|
T | TTTTTC | 15 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0118others(12): Show | 15 | HG00438.hp2 HG01175.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.1972-1480_1972-147 others(9): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr8 | 94695371 | |||||
| chr8:94695395
|
C | T | 222 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(219): Show | 224 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.1972-1457C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695395 | ||||||
| chr8:94695416
|
G | A | 1 | a0001c0011t0001g0251 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1972-1436G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695416 | ||||||
| chr8:94695424
|
G | A | 4 | a0001c0003t0001g0318a0001c0003t0001g0368a0001c0003t0001g0369others(1): Show | 4 | HG01167.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1972-1428G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695424 | ||||||
| chr8:94695497
|
C | T | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-1355C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695497 | ||||||
| chr8:94695499
|
T | C | 268 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(265): Show | 270 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.1972-1353T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695499 | ||||||
| chr8:94695520
|
T | C | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-1332T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695520 | ||||||
| chr8:94695599
|
G | A | 1 | a0001c0003t0001g0334 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1972-1253G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695599 | ||||||
| chr8:94695606
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1972-1246G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695606 | ||||||
| chr8:94695612
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1972-1240G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695612 | ||||||
| chr8:94695633
|
G | A | 1 | a0001c0003t0001g0318 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1972-1219G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695633 | ||||||
| chr8:94695642
|
C | A | 1 | a0001c0003t0001g0326 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1972-1210C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695642 | ||||||
| chr8:94695713
|
A | ATTCTGTC others(56): Show |
9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-1138_1972-113 others(67): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr8 | 94695713 | |||||
| chr8:94695715
|
C | T | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-1137C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695715 | ||||||
| chr8:94695776
|
C | T | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-1076C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695776 | ||||||
| chr8:94695783
|
C | T | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-1069C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695783 | ||||||
| chr8:94695789
|
A | G | 13 | a0001c0001t0001g0256a0001c0003t0001g0318a0001c0003t0001g0347others(10): Show | 13 | HG01070.hp2 HG01081.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.1972-1063A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695789 | ||||||
| chr8:94695796
|
T | C | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-1056T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695796 | ||||||
| chr8:94695882
|
G | T | 7 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(4): Show | 7 | HG01109.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1972-970G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695882 | ||||||
| chr8:94695905
|
A | C | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-947A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695905 | ||||||
| chr8:94695921
|
C | T | 1 | a0001c0004t0002g0091 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1972-931C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695921 | ||||||
| chr8:94695928
|
T | C | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-924T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695928 | ||||||
| chr8:94695961
|
G | A | 4 | a0001c0003t0001g0318a0001c0003t0001g0368a0001c0003t0001g0369others(1): Show | 4 | HG01167.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1972-891G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695961 | ||||||
| chr8:94696063
|
AAAAC | A | 30 | a0001c0001t0001g0137a0001c0001t0001g0198a0001c0001t0001g0212others(27): Show | 30 | HG00140.hp1 HG00558.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.1972-777_1972-774d others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr8 | 94696063 | |||||
| chr8:94696087
|
C | G | 10 | a0001c0001t0001g0358a0001c0001t0001g0359a0001c0001t0001g0360others(7): Show | 10 | HG02257.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1972-765C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94696087 | ||||||
| chr8:94696092
|
T | C | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-760T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94696092 | ||||||
| chr8:94696269
|
A | G | 1 | a0001c0001t0003g0323 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1972-583A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94696269 | ||||||
| chr8:94696330
|
C | G | 13 | a0001c0001t0001g0159a0001c0001t0001g0163a0001c0001t0001g0165others(10): Show | 13 | HG01261.hp2 HG02055.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1972-522C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94696330 | ||||||
| chr8:94696423
|
T | C | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | NA19064.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1972-429T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94696423 | ||||||
| chr8:94696495
|
T | C | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-357T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94696495 | ||||||
| chr8:94696496
|
G | A | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-356G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94696496 | ||||||
| chr8:94696532
|
A | G | 3 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196 | 3 | HG02109.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1972-320A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94696532 | ||||||
| chr8:94696704
|
A | T | 1 | a0001c0001t0001g0148 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1972-148A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94696704 | ||||||
| chr8:94696708
|
G | A | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-144G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94696708 | ||||||
| chr8:94696774
|
G | C | 1 | a0001c0001t0001g0173 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1972-78G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94696774 | ||||||
| chr8:94696977
|
G | A | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+16G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94696977 | ||||||
| chr8:94697079
|
C | A | 2 | a0001c0001t0003g0214a0001c0001t0003g0217 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.*35+118C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94697079 | ||||||
| chr8:94697189
|
C | T | 5 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(2): Show | 5 | HG02559.hp1 HG02647.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.*35+228C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94697189 | ||||||
| chr8:94697219
|
C | T | 1 | a0001c0001t0003g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.*35+258C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94697219 | ||||||
| chr8:94697272
|
A | G | 3 | a0001c0001t0001g0159a0001c0001t0001g0163a0001c0001t0001g0165 | 3 | HG01261.hp2 HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.*35+311A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94697272 | ||||||
| chr8:94697337
|
C | T | 2 | a0001c0001t0001g0225a0001c0001t0001g0227 | 2 | HG01175.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.*35+376C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94697337 | ||||||
| chr8:94697607
|
T | G | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+646T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94697607 | ||||||
| chr8:94697746
|
G | A | 1 | a0001c0003t0001g0318 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*35+785G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94697746 | ||||||
| chr8:94697860
|
C | A | 6 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(3): Show | 6 | HG00741.hp1 HG02523.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.*35+899C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94697860 | ||||||
| chr8:94697941
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.*35+980T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94697941 | ||||||
| chr8:94698120
|
A | G | 1 | a0003c0010t0001g0321 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.*35+1159A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94698120 | ||||||
| chr8:94698181
|
G | A | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+1220G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94698181 | ||||||
| chr8:94698348
|
T | G | 1 | a0001c0001t0001g0284 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.*35+1387T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94698348 | ||||||
| chr8:94698390
|
TTA | T | 3 | a0001c0001t0006g0166a0001c0001t0006g0167a0001c0001t0006g0215 | 3 | HG02109.hp2 HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.*35+1431_*35+1432d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94698390 | |||||
| chr8:94698398
|
T | A | 26 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(23): Show | 26 | HG00438.hp2 HG01361.hp2 HG01928.hp2 others(23): Show |
intron_variant | MODIFIER | c.*35+1437T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94698398 | ||||||
| chr8:94698463
|
G | A | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+1502G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94698463 | ||||||
| chr8:94698505
|
C | T | 1 | a0001c0001t0001g0231 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.*35+1544C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94698505 | ||||||
| chr8:94698664
|
A | G | 1 | a0001c0002t0002g0357 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.*35+1703A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94698664 | ||||||
| chr8:94698819
|
T | G | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*35+1858T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94698819 | ||||||
| chr8:94698871
|
A | T | 3 | a0001c0003t0001g0368a0001c0003t0001g0369a0001c0006t0001g0345 | 3 | HG01167.hp2 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.*35+1910A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94698871 | ||||||
| chr8:94699002
|
A | C | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*35+2041A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699002 | ||||||
| chr8:94699003
|
C | A | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*35+2042C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699003 | ||||||
| chr8:94699004
|
A | T | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*35+2043A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699004 | ||||||
| chr8:94699054
|
A | G | 1 | a0001c0002t0002g0100 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.*35+2093A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699054 | ||||||
| chr8:94699190
|
C | T | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+2229C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699190 | ||||||
| chr8:94699240
|
G | C | 222 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(219): Show | 224 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.*35+2279G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699240 | ||||||
| chr8:94699287
|
T | G | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+2326T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699287 | ||||||
| chr8:94699304
|
T | C | 3 | a0001c0003t0001g0368a0001c0003t0001g0369a0001c0006t0001g0345 | 3 | HG01167.hp2 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.*35+2343T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699304 | ||||||
| chr8:94699415
|
C | T | 5 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(2): Show | 5 | HG02258.hp2 HG02615.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.*35+2454C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699415 | ||||||
| chr8:94699478
|
C | A | 5 | a0001c0001t0001g0180a0001c0001t0001g0267a0001c0001t0001g0268others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.*35+2517C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699478 | ||||||
| chr8:94699479
|
GA | G | 10 | a0001c0001t0001g0179a0001c0001t0001g0256a0001c0003t0001g0347others(7): Show | 10 | HG01070.hp2 HG01081.hp1 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.*35+2526delA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94699479 | |||||
| chr8:94699487
|
A | G | 2 | a0001c0001t0001g0203a0001c0001t0001g0207 | 2 | NA18949.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.*35+2526A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699487 | ||||||
| chr8:94699524
|
C | T | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+2563C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699524 | ||||||
| chr8:94699613
|
C | T | 75 | a0001c0001t0001g0002a0001c0001t0001g0087a0001c0001t0001g0103others(72): Show | 76 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.*35+2652C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699613 | ||||||
| chr8:94699658
|
A | G | 1 | a0003c0010t0001g0321 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.*35+2697A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699658 | ||||||
| chr8:94699755
|
A | T | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+2794A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699755 | ||||||
| chr8:94699907
|
A | AT | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+2953dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94699907 | |||||
| chr8:94699908
|
T | TA | 261 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(258): Show | 263 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.*35+2947_*35+2948i others(3): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699908 | ||||||
| chr8:94699918
|
G | C | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*35+2957G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699918 | ||||||
| chr8:94700005
|
A | T | 1 | a0001c0001t0003g0142 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*35+3044A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700005 | ||||||
| chr8:94700006
|
C | T | 4 | a0001c0003t0001g0327a0001c0003t0001g0328a0001c0003t0001g0329others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.*35+3045C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700006 | ||||||
| chr8:94700020
|
A | G | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+3059A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700020 | ||||||
| chr8:94700024
|
G | A | 11 | a0001c0001t0001g0159a0001c0001t0001g0163a0001c0001t0001g0165others(8): Show | 11 | HG01261.hp2 HG02055.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.*35+3063G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700024 | ||||||
| chr8:94700033
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.*35+3072G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700033 | ||||||
| chr8:94700166
|
A | T | 1 | a0001c0001t0005g0298 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.*35+3205A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700166 | ||||||
| chr8:94700208
|
T | C | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+3247T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700208 | ||||||
| chr8:94700219
|
G | A | 1 | a0001c0001t0003g0142 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*35+3258G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700219 | ||||||
| chr8:94700301
|
C | T | 1 | a0001c0001t0001g0314 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.*35+3340C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700301 | ||||||
| chr8:94700436
|
G | A | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+3475G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700436 | ||||||
| chr8:94700522
|
T | C | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+3561T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700522 | ||||||
| chr8:94700741
|
A | T | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*35+3780A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700741 | ||||||
| chr8:94700757
|
G | A | 1 | a0001c0003t0001g0334 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.*35+3796G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700757 | ||||||
| chr8:94700796
|
G | A | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+3835G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700796 | ||||||
| chr8:94700810
|
C | T | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+3849C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700810 | ||||||
| chr8:94700853
|
C | T | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+3892C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700853 | ||||||
| chr8:94700856
|
A | G | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+3895A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700856 | ||||||
| chr8:94700920
|
C | T | 3 | a0001c0001t0001g0172a0001c0001t0001g0174a0001c0001t0001g0177 | 3 | NA18961.hp2 NA19083.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.*35+3959C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700920 | ||||||
| chr8:94700923
|
C | T | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(64): Show | 67 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.*35+3962C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700923 | ||||||
| chr8:94700924
|
G | A | 1 | a0001c0002t0002g0058 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.*35+3963G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700924 | ||||||
| chr8:94700937
|
ATGTGTGT others(11): Show |
A | 1 | a0001c0002t0002g0044 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.*35+3992_*35+4009d others(20): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94700937 | |||||
| chr8:94700937
|
ATGTGTGT others(25): Show |
A | 8 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220others(5): Show | 8 | HG00438.hp2 NA18747.hp2 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.*35+3992_*35+4023d others(34): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94700937 | |||||
| chr8:94700951
|
GTA | G | 3 | a0001c0001t0001g0149a0001c0001t0001g0257a0001c0001t0001g0258 | 3 | HG01109.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.*35+3992_*35+3993d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94700951 | |||||
| chr8:94700953
|
A | ATG | 9 | a0001c0002t0002g0015a0001c0002t0002g0016a0001c0002t0002g0017others(6): Show | 9 | HG00642.hp2 HG02015.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.*35+4022_*35+4023d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94700953 | |||||
| chr8:94700953
|
A | G | 16 | a0001c0001t0001g0179a0001c0001t0001g0256a0001c0003t0001g0318others(13): Show | 16 | HG01070.hp2 HG01081.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.*35+3992A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700953 | ||||||
| chr8:94700953
|
ATG | A | 91 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(88): Show | 91 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.*35+4022_*35+4023d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94700953 | |||||
| chr8:94700953
|
ATGTG | A | 62 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(59): Show | 62 | HG00140.hp1 HG00558.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.*35+4020_*35+4023d others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94700953 | |||||
| chr8:94700953
|
ATGTGTG | A | 41 | a0001c0001t0001g0002a0001c0001t0001g0087a0001c0001t0001g0103others(38): Show | 42 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.*35+4018_*35+4023d others(8): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94700953 | |||||
| chr8:94700953
|
ATGTGTGT others(1): Show |
A | 19 | a0001c0001t0001g0168a0001c0001t0001g0185a0001c0001t0001g0186others(16): Show | 19 | HG01175.hp1 HG01361.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.*35+4016_*35+4023d others(10): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94700953 | |||||
| chr8:94700953
|
ATGTGTGT others(5): Show |
A | 1 | a0001c0004t0002g0086 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.*35+4012_*35+4023d others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94700953 | |||||
| chr8:94700957
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.*35+3996G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700957 | ||||||
| chr8:94700959
|
G | GTGTGTGT others(3): Show |
9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+4007_*35+4008i others(12): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94700959 | |||||
| chr8:94700962
|
T | A | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*35+4001T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700962 | ||||||
| chr8:94700963
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*35+4002G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700963 | ||||||
| chr8:94700969
|
G | A | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+4008G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700969 | ||||||
| chr8:94700979
|
G | A | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+4018G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700979 | ||||||
| chr8:94700995
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.*35+4034G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700995 | ||||||
| chr8:94701089
|
G | A | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+4128G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701089 | ||||||
| chr8:94701274
|
C | CA | 20 | a0001c0001t0001g0208a0001c0001t0001g0256a0001c0001t0001g0303others(17): Show | 20 | HG01070.hp2 HG01081.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.*35+4328dupA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94701274 | |||||
| chr8:94701289
|
AG | A | 21 | a0001c0001t0001g0159a0001c0001t0001g0163a0001c0001t0001g0165others(18): Show | 21 | HG01261.hp2 HG02055.hp1 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.*35+4329delG | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701289 | ||||||
| chr8:94701290
|
G | A | 250 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(247): Show | 252 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.*35+4329G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701290 | ||||||
| chr8:94701301
|
T | A | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+4340T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701301 | ||||||
| chr8:94701315
|
G | A | 30 | a0001c0001t0001g0137a0001c0001t0001g0198a0001c0001t0001g0212others(27): Show | 30 | HG00140.hp1 HG00558.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.*35+4354G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701315 | ||||||
| chr8:94701319
|
A | G | 3 | a0001c0001t0006g0166a0001c0001t0006g0167a0001c0001t0006g0215 | 3 | HG02109.hp2 HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.*35+4358A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701319 | ||||||
| chr8:94701420
|
C | T | 3 | a0001c0001t0006g0166a0001c0001t0006g0167a0001c0001t0006g0215 | 3 | HG02109.hp2 HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.*35+4459C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701420 | ||||||
| chr8:94701421
|
G | A | 9 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(6): Show | 9 | HG02258.hp2 HG02615.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+4460G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701421 | ||||||
| chr8:94701509
|
G | A | 6 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(3): Show | 6 | HG01175.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.*36-4416G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701509 | ||||||
| chr8:94701511
|
G | T | 2 | a0001c0002t0002g0040a0001c0002t0002g0079 | 2 | NA18941.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.*36-4414G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701511 | ||||||
| chr8:94701532
|
G | T | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*36-4393G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701532 | ||||||
| chr8:94701689
|
C | G | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*36-4236C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701689 | ||||||
| chr8:94701690
|
T | C | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*36-4235T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701690 | ||||||
| chr8:94701735
|
G | T | 1 | a0001c0001t0001g0283 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.*36-4190G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701735 | ||||||
| chr8:94701869
|
G | T | 4 | a0001c0005t0001g0181a0001c0005t0001g0182a0001c0005t0001g0183others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.*36-4056G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701869 | ||||||
| chr8:94701886
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.*36-4039C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701886 | ||||||
| chr8:94701989
|
G | A | 6 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(3): Show | 6 | HG01175.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.*36-3936G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701989 | ||||||
| chr8:94702018
|
C | T | 2 | a0001c0002t0002g0072a0001c0002t0002g0084 | 2 | NA18988.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.*36-3907C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94702018 | ||||||
| chr8:94702048
|
A | G | 221 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(218): Show | 223 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.*36-3877A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94702048 | ||||||
| chr8:94702160
|
G | GT | 9 | a0001c0001t0001g0179a0001c0001t0001g0267a0001c0001t0001g0268others(6): Show | 9 | HG02165.hp2 HG02280.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.*36-3758dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94702160 | |||||
| chr8:94702226
|
C | T | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*36-3699C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94702226 | ||||||
| chr8:94702416
|
G | C | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*36-3509G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94702416 | ||||||
| chr8:94702417
|
T | G | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*36-3508T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94702417 | ||||||
| chr8:94702418
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*36-3507C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94702418 | ||||||
| chr8:94702441
|
A | C | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*36-3484A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94702441 | ||||||
| chr8:94702448
|
A | T | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*36-3477A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94702448 | ||||||
| chr8:94702590
|
G | A | 4 | a0001c0003t0001g0318a0001c0003t0001g0368a0001c0003t0001g0369others(1): Show | 4 | HG01167.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.*36-3335G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94702590 | ||||||
| chr8:94702770
|
G | C | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*36-3155G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94702770 | ||||||
| chr8:94702771
|
C | G | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*36-3154C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94702771 | ||||||
| chr8:94702955
|
T | C | 3 | a0001c0001t0006g0166a0001c0001t0006g0167a0001c0001t0006g0215 | 3 | HG02109.hp2 HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.*36-2970T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94702955 | ||||||
| chr8:94703105
|
A | AT | 5 | a0001c0001t0001g0180a0001c0001t0001g0267a0001c0001t0001g0268others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.*36-2818dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94703105 | |||||
| chr8:94703108
|
G | GT | 32 | a0001c0001t0001g0159a0001c0001t0001g0163a0001c0001t0001g0165others(29): Show | 32 | HG01070.hp2 HG01081.hp1 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.*36-2801dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94703108 | |||||
| chr8:94703108
|
G | GTT | 38 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0001g0198others(35): Show | 38 | HG00140.hp1 HG00558.hp1 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.*36-2802_*36-2801d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94703108 | |||||
| chr8:94703108
|
G | GTTT | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(160): Show | 165 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.*36-2803_*36-2801d others(5): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94703108 | |||||
| chr8:94703108
|
G | GTTTT | 12 | a0001c0001t0001g0010a0001c0001t0001g0105a0001c0001t0001g0119others(9): Show | 12 | HG01261.hp1 HG01934.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.*36-2804_*36-2801d others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94703108 | |||||
| chr8:94703108
|
G | T | 7 | a0001c0001t0001g0168a0001c0001t0001g0180a0001c0001t0001g0267others(4): Show | 7 | HG02145.hp2 HG02280.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.*36-2817G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94703108 | ||||||
| chr8:94703153
|
T | TTTG | 17 | a0001c0001t0001g0159a0001c0001t0001g0163a0001c0001t0001g0165others(14): Show | 17 | HG01261.hp2 HG02055.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.*36-2753_*36-2751d others(5): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94703153 | |||||
| chr8:94703153
|
TTTG | T | 9 | a0001c0001t0001g0256a0001c0003t0001g0347a0001c0003t0001g0348others(6): Show | 9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*36-2753_*36-2751d others(5): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94703153 | |||||
| chr8:94703279
|
C | T | 30 | a0001c0001t0001g0137a0001c0001t0001g0198a0001c0001t0001g0212others(27): Show | 30 | HG00140.hp1 HG00558.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.*36-2646C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94703279 | ||||||
| chr8:94703335
|
G | C | 1 | a0002c0012t0002g0122 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.*36-2590G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94703335 | ||||||
| chr8:94703441
|
C | A | 1 | a0001c0002t0002g0120 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.*36-2484C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94703441 | ||||||
| chr8:94703574
|
A | G | 1 | a0001c0002t0012g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.*36-2351A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94703574 | ||||||
| chr8:94703599
|
A | C | 1 | a0001c0001t0001g0242 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.*36-2326A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94703599 | ||||||
| chr8:94703757
|
G | A | 1 | a0001c0001t0001g0293 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.*36-2168G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94703757 | ||||||
| chr8:94703824
|
T | C | 266 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(263): Show | 268 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.*36-2101T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94703824 | ||||||
| chr8:94703894
|
T | A | 222 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(219): Show | 224 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.*36-2031T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94703894 | ||||||
| chr8:94703907
|
A | G | 1 | a0001c0001t0001g0311 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.*36-2018A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94703907 | ||||||
| chr8:94703937
|
G | C | 270 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(267): Show | 272 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(269): Show |
intron_variant | MODIFIER | c.*36-1988G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94703937 | ||||||
| chr8:94704001
|
T | C | 1 | a0001c0001t0001g0361 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.*36-1924T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94704001 | ||||||
| chr8:94704040
|
C | T | 1 | a0001c0004t0002g0086 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.*36-1885C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94704040 | ||||||
| chr8:94704064
|
A | G | 270 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(267): Show | 272 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(269): Show |
intron_variant | MODIFIER | c.*36-1861A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94704064 | ||||||
| chr8:94704175
|
C | CTT | 15 | a0001c0001t0001g0003a0001c0001t0001g0109a0001c0001t0001g0153others(12): Show | 15 | HG00733.hp2 HG00738.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.*36-1735_*36-1734d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94704175 | |||||
| chr8:94704175
|
C | CTTT | 187 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(184): Show | 189 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.*36-1736_*36-1734d others(5): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94704175 | |||||
| chr8:94704175
|
C | CTTTT | 56 | a0001c0001t0001g0087a0001c0001t0001g0108a0001c0001t0001g0119others(53): Show | 56 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.*36-1737_*36-1734d others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94704175 | |||||
| chr8:94704263
|
T | C | 270 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(267): Show | 272 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(269): Show |
intron_variant | MODIFIER | c.*36-1662T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94704263 | ||||||
| chr8:94704359
|
C | T | 1 | a0001c0002t0002g0019 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.*36-1566C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94704359 | ||||||
| chr8:94704481
|
G | T | 75 | a0001c0001t0001g0002a0001c0001t0001g0087a0001c0001t0001g0103others(72): Show | 76 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.*36-1444G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94704481 | ||||||
| chr8:94704504
|
T | C | 270 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(267): Show | 272 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(269): Show |
intron_variant | MODIFIER | c.*36-1421T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94704504 | ||||||
| chr8:94704542
|
T | C | 270 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(267): Show | 272 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(269): Show |
intron_variant | MODIFIER | c.*36-1383T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94704542 | ||||||
| chr8:94704551
|
G | T | 1 | a0001c0001t0001g0210 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.*36-1374G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94704551 | ||||||
| chr8:94704766
|
G | GA | 29 | a0001c0002t0002g0009a0001c0002t0002g0011a0001c0002t0002g0020others(26): Show | 29 | HG00597.hp1 HG00673.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.*36-1132dupA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94704766 | |||||
| chr8:94704766
|
G | GAAA | 11 | a0001c0004t0002g0007a0001c0004t0002g0033a0001c0004t0002g0035others(8): Show | 11 | HG00323.hp1 HG01070.hp1 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.*36-1134_*36-1132d others(5): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94704766 | |||||
| chr8:94704766
|
GAAAAAAA | G | 40 | a0001c0001t0001g0110a0001c0001t0001g0118a0001c0001t0001g0119others(37): Show | 40 | HG00741.hp2 HG01069.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.*36-1138_*36-1132d others(9): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94704766 | |||||
| chr8:94704766
|
GAAAAAAA others(1): Show |
G | 192 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(189): Show | 194 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.*36-1139_*36-1132d others(10): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94704766 | |||||
| chr8:94704766
|
GAAAAAAA others(2): Show |
G | 35 | a0001c0001t0001g0139a0001c0001t0001g0149a0001c0001t0001g0159others(32): Show | 35 | HG01109.hp1 HG01167.hp1 HG01261.hp2 others(32): Show |
intron_variant | MODIFIER | c.*36-1140_*36-1132d others(11): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94704766 | |||||
| chr8:94704773
|
A | G | 2 | a0001c0003t0001g0333a0001c0003t0001g0371 | 2 | HG02738.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.*36-1152A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94704773 | ||||||
| chr8:94704774
|
A | G | 6 | a0001c0003t0001g0135a0001c0003t0001g0241a0001c0003t0001g0326others(3): Show | 6 | HG00741.hp2 HG01175.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.*36-1151A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94704774 | ||||||
| chr8:94704775
|
A | G | 19 | a0001c0003t0001g0001a0001c0003t0001g0088a0001c0003t0001g0134others(16): Show | 20 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.*36-1150A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94704775 | ||||||
| chr8:94704937
|
A | G | 270 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(267): Show | 272 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(269): Show |
intron_variant | MODIFIER | c.*36-988A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94704937 | ||||||
| chr8:94705022
|
G | T | 1 | a0001c0001t0001g0129 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.*36-903G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94705022 | ||||||
| chr8:94705117
|
A | G | 31 | a0001c0001t0001g0149a0001c0001t0001g0159a0001c0001t0001g0163others(28): Show | 31 | HG01109.hp1 HG01261.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.*36-808A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94705117 | ||||||
| chr8:94705156
|
C | CT | 50 | a0001c0001t0006g0166a0001c0001t0006g0215a0001c0002t0002g0006others(47): Show | 50 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.*36-740dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94705156 | |||||
| chr8:94705156
|
C | CTT | 13 | a0001c0001t0001g0358a0001c0001t0001g0360a0001c0001t0001g0361others(10): Show | 13 | HG00323.hp1 HG00735.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.*36-741_*36-740dup others(2): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94705156 | |||||
| chr8:94705156
|
C | CTTT | 7 | a0001c0001t0001g0359a0001c0001t0001g0362a0001c0001t0001g0363others(4): Show | 7 | HG02257.hp2 HG02809.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.*36-742_*36-740dup others(3): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94705156 | |||||
| chr8:94705156
|
CTT | C | 6 | a0001c0001t0001g0159a0001c0001t0001g0165a0001c0001t0001g0247others(3): Show | 6 | HG01167.hp2 HG02055.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.*36-741_*36-740del others(2): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94705156 | |||||
| chr8:94705156
|
CTTT | C | 12 | a0001c0001t0001g0163a0001c0001t0001g0169a0001c0001t0001g0257others(9): Show | 12 | HG01261.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.*36-742_*36-740del others(3): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94705156 | |||||
| chr8:94705156
|
CTTTTTTT others(3): Show |
C | 27 | a0001c0001t0001g0002a0001c0001t0001g0131a0001c0001t0001g0137others(24): Show | 28 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.*36-749_*36-740del others(10): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94705156 | |||||
| chr8:94705156
|
CTTTTTTT others(4): Show |
C | 190 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(187): Show | 191 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.*36-750_*36-740del others(11): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94705156 | |||||
| chr8:94705156
|
CTTTTTTT others(5): Show |
C | 4 | a0001c0001t0001g0155a0001c0001t0001g0162a0001c0001t0001g0301others(1): Show | 4 | HG00558.hp1 HG01069.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.*36-751_*36-740del others(12): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94705156 | |||||
| chr8:94705245
|
G | A | 1 | a0001c0011t0001g0251 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*36-680G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94705245 | ||||||
| chr8:94705473
|
T | A | 1 | a0001c0001t0001g0129 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.*36-452T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94705473 | ||||||
| chr8:94705633
|
A | G | 269 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(266): Show | 271 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.*36-292A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94705633 | ||||||
| chr8:94705633
|
A | T | 1 | a0001c0001t0001g0261 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.*36-292A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94705633 | ||||||
| chr8:94705637
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.*36-288G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94705637 | ||||||
| chr8:94705654
|
A | T | 1 | a0001c0001t0001g0129 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.*36-271A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94705654 | ||||||
| chr8:94705677
|
G | A | 7 | a0001c0002t0002g0011a0001c0002t0002g0025a0001c0002t0002g0054others(4): Show | 7 | HG00408.hp2 HG00558.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.*36-248G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94705677 | ||||||
| chr8:94705680
|
T | C | 28 | a0001c0002t0002g0074a0001c0003t0001g0001a0001c0003t0001g0088others(25): Show | 29 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.*36-245T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94705680 | ||||||
| chr8:94705902
|
A | G | 2 | a0001c0007t0001g0344a0001c0007t0001g0346 | 2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.*36-23A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94705902 | ||||||
| chr8:94705903
|
C | CT | 6 | a0001c0002t0002g0040a0001c0002t0002g0058a0001c0002t0002g0079others(3): Show | 6 | HG02451.hp1 HG03942.hp2 NA18941.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.*36-4dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94705903 | |||||
| chr8:94705903
|
CTT | C | 22 | a0001c0001t0001g0148a0001c0001t0001g0157a0001c0001t0001g0256others(19): Show | 22 | HG01070.hp2 HG01081.hp1 HG01993.hp2 others(19): Show |
splice_region_variant&intron_variant | LOW | c.*36-5_*36-4delTT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94705903 | |||||
| chr8:94705903
|
CTTT | C | 187 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(184): Show | 188 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(185): Show |
splice_region_variant&intron_variant | LOW | c.*36-6_*36-4delTTT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94705903 | |||||
| chr8:94705903
|
CTTTT | C | 61 | a0001c0001t0001g0137a0001c0001t0001g0198a0001c0001t0001g0212others(58): Show | 62 | HG00140.hp1 HG00558.hp1 HG00642.hp1 others(59): Show |
splice_region_variant&intron_variant | LOW | c.*36-7_*36-4delTTTT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94705903 |