Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2130 |
| ensemblid | ENSG00000182944.18 |
| hgncid | 3508 |
| symbol | EWSR1 |
| name | EWS RNA binding protein 1 |
| refseq_nuc | NM_005243.4 |
| refseq_prot | NP_005234.1 |
| ensembl_nuc | ENST00000397938.7 |
| ensembl_prot | ENSP00000381031.2 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 29268268 |
| end | 29300521 |
| strand | + |
| ver | v1.2 |
| region | chr22:29268268-29300521 |
| region5000 | chr22:29263268-29305521 |
| regionname0 | EWSR1_chr22_29268268_29300521 |
| regionname5000 | EWSR1_chr22_29263268_29305521 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 656 | 388 | 95 | 61 | 176 | 12 | 42 | 134 | EWSR1_chr22_29263268_29305521 | EWSR1 | MASTD others(651): Show |
chr22 | 29263268 | 29305521 |
| a0002 | 0/0 | 656 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | MASTD others(651): Show |
chr22 | 29263268 | 29305521 |
| a0003 | 0/0 | 656 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | MASTD others(651): Show |
chr22 | 29263268 | 29305521 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1968 | 386 | 95 | 61 | 175 | 12 | 42 | EWSR1_chr22_29263268_29305521 | EWSR1 | ATGGC others(1963): Show |
chr22 | 29263268 | 29305521 | ||
| a0001c0002 | 0/1 | 1968 | 1 | 0 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | ATGGC others(1963): Show |
chr22 | 29263268 | 29305521 | ||
| a0001c0005 | 0/0 | 1968 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | ATGGC others(1963): Show |
chr22 | 29263268 | 29305521 | ||
| a0002c0003 | 0/0 | 1968 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | ATGGC others(1963): Show |
chr22 | 29263268 | 29305521 | ||
| a0003c0004 | 0/0 | 1968 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | ATGGC others(1963): Show |
chr22 | 29263268 | 29305521 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2400 | 378 | 92 | 59 | 174 | 12 | 40 | EWSR1_chr22_29263268_29305521 | EWSR1 | GCAGT others(2395): Show |
chr22 | 29263268 | 29305521 |
| a0001c0001t0002 | 0/0 | 2400 | 3 | 2 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | GCAGT others(2395): Show |
chr22 | 29263268 | 29305521 |
| a0001c0001t0003 | 0/0 | 2400 | 2 | 0 | 0 | 0 | 0 | 2 | EWSR1_chr22_29263268_29305521 | EWSR1 | GCAGT others(2395): Show |
chr22 | 29263268 | 29305521 |
| a0001c0001t0004 | 0/0 | 2400 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | GCAGT others(2395): Show |
chr22 | 29263268 | 29305521 |
| a0001c0001t0005 | 0/0 | 2400 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | GCAGT others(2395): Show |
chr22 | 29263268 | 29305521 |
| a0001c0001t0006 | 0/0 | 2400 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | GCAGT others(2395): Show |
chr22 | 29263268 | 29305521 |
| a0001c0002t0001 | 0/1 | 2400 | 1 | 0 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | GCAGT others(2395): Show |
chr22 | 29263268 | 29305521 |
| a0001c0005t0001 | 0/0 | 2400 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | GCAGT others(2395): Show |
chr22 | 29263268 | 29305521 |
| a0002c0003t0001 | 0/0 | 2400 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | GCAGT others(2395): Show |
chr22 | 29263268 | 29305521 |
| a0003c0004t0001 | 0/0 | 2400 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | GCAGT others(2395): Show |
chr22 | 29263268 | 29305521 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 26 | 2 | 3 | 18 | 2 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0002 | 0/0 | 14 | 0 | 0 | 13 | 0 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0003 | 0/0 | 10 | 0 | 0 | 8 | 0 | 2 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0010 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0054 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0163 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0001t0006g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0002t0001g0205 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0001c0005t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0002c0003t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| a0003c0004t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | GBR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | GBR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0043 | EUR | FIN | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | FIN | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0047 | EUR | FIN | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | FIN | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01255 | hp2 | a0002 | c0003 | t0001 | g0021 | AMR | CLM | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0244 | EUR | IBS | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0085 | EUR | IBS | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0094 | AMR | PEL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CDX | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CDX | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CDX | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02451 | hp1 | a0003 | c0004 | t0001 | g0232 | AFR | ACB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0239 | AFR | ACB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | MSL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | MSL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ESN | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | STU | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | STU | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | BEB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | BEB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | STU | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | STU | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | STU | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | STU | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | STU | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | YRI | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | YRI | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | YRI | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | YRI | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18980 | hp2 | a0001 | c0005 | t0001 | g0143 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19001 | hp1 | a0001 | c0001 | t0006 | g0090 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | LWK | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | LWK | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0172 | AFR | LWK | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | LWK | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | YRI | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | YRI | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | GIH | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | GIH | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | USA | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | USA | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | USA | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | LWK | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0205 | REF | REF | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0163 | REF | REF | EWSR1_chr22_29263268_29305521 | EWSR1 | chr22 | 29263268 | 29305521 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:29297925 | G | A | 1 | a0002 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.1393G>A | p.Gly465Ser | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 13/17 | 1462/2400 | 1393/1971 | 465/656 | chr22 | 29297925 | |||
| chr22:29300123 | G | A | 1 | a0003 | 1 | HG02451.hp1 | missense_variant&splice_region_variant | MODERATE | c.1933G>A | p.Gly645Ser | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 17/17 | 2002/2400 | 1933/1971 | 645/656 | chr22 | 29300123 | |||
| chr22:29300520 | G | C | 1 | a0001 | 1 | NA19043.hp1 | splice_region_variant | LOW | c.*359G>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 17/17 | chr22 | 29300520 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:29287109 | A | G | 1 | a0001c0005 | 1 | NA18980.hp2 | synonymous_variant | LOW | c.768A>G | p.Gln256Gln | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 7/17 | 837/2400 | 768/1971 | 256/656 | chr22 | 29287109 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:29268292 | C | A | 1 | a0001c0001t0003 | 2 | HG03239.hp1 HG04204.hp1 |
5_prime_UTR_variant | MODIFIER | c.-45C>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/17 | 45 | chr22 | 29268292 | ||||||
| chr22:29300282 | G | A | 1 | a0001c0001t0004 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*121G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 17/17 | 121 | chr22 | 29300282 | ||||||
| chr22:29300356 | C | T | 1 | a0001c0001t0006 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*195C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 17/17 | 195 | chr22 | 29300356 | ||||||
| chr22:29300357 | T | C | 1 | a0001c0001t0006 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*196T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 17/17 | 196 | chr22 | 29300357 | ||||||
| chr22:29300359 | C | T | 1 | a0001c0001t0006 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*198C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 17/17 | 198 | chr22 | 29300359 | ||||||
| chr22:29300494 | T | A | 1 | a0001c0001t0002 | 3 | HG01243.hp1 HG02451.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*333T>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 17/17 | 333 | chr22 | 29300494 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:29268419 | G | A | 4 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(1): Show |
4 | HG02109.hp2 HG02886.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.13+70G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29268419 | |||||||
| chr22:29268434 | G | A | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(115): Show |
179 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.13+85G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29268434 | |||||||
| chr22:29268459 | G | A | 4 | a0001c0001t0001g0038 a0001c0001t0001g0150 a0001c0001t0001g0151 others(1): Show |
5 | NA18947.hp1 NA18952.hp2 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.13+110G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29268459 | |||||||
| chr22:29268602 | G | T | 1 | a0001c0001t0001g0260 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.13+253G>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29268602 | |||||||
| chr22:29268636 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | NA18981.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.13+287C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29268636 | |||||||
| chr22:29268787 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.13+438G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29268787 | |||||||
| chr22:29268888 | A | C | 2 | a0001c0001t0001g0017 a0001c0001t0001g0147 |
4 | HG00099.hp2 HG00642.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.13+539A>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29268888 | |||||||
| chr22:29268917 | C | T | 30 | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0038 others(27): Show |
39 | HG00544.hp1 HG00642.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.13+568C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29268917 | |||||||
| chr22:29269253 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.13+904C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29269253 | |||||||
| chr22:29269281 | G | T | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.13+932G>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29269281 | |||||||
| chr22:29269296 | A | G | 1 | a0001c0001t0002g0239 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.13+947A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29269296 | |||||||
| chr22:29269533 | C | T | 1 | a0001c0001t0001g0238 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.13+1184C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29269533 | |||||||
| chr22:29269541 | A | T | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG02056.hp1 HG02071.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.13+1192A>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29269541 | |||||||
| chr22:29269685 | GGGATACC others(7): Show |
G | 8 | a0001c0001t0001g0021 a0001c0001t0001g0052 a0001c0001t0001g0154 others(5): Show |
10 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.13+1352_13+1365del others(14): Show |
EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr22 | 29269685 | ||||||
| chr22:29269777 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.13+1428G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29269777 | |||||||
| chr22:29269893 | C | A | 1 | a0001c0001t0001g0061 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.13+1544C>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29269893 | |||||||
| chr22:29269915 | T | C | 3 | a0001c0001t0001g0008 a0001c0001t0001g0156 a0001c0001t0001g0157 |
6 | HG01243.hp2 HG02055.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.13+1566T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29269915 | |||||||
| chr22:29269949 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.13+1600C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29269949 | |||||||
| chr22:29269960 | C | G | 5 | a0001c0001t0001g0051 a0001c0001t0001g0234 a0001c0001t0001g0235 others(2): Show |
6 | HG02572.hp2 HG02622.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.13+1611C>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29269960 | |||||||
| chr22:29269979 | G | T | 1 | a0001c0001t0001g0059 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.13+1630G>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29269979 | |||||||
| chr22:29270021 | T | C | 2 | a0001c0001t0001g0053 a0001c0001t0001g0246 |
3 | HG01891.hp2 HG02647.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.13+1672T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29270021 | |||||||
| chr22:29270129 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.13+1780T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29270129 | |||||||
| chr22:29270185 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0023 |
7 | HG00673.hp2 NA18941.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.13+1836G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29270185 | |||||||
| chr22:29270216 | A | G | 1 | a0001c0001t0001g0233 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.13+1867A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29270216 | |||||||
| chr22:29270231 | G | T | 1 | a0001c0005t0001g0143 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.13+1882G>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29270231 | |||||||
| chr22:29270270 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.13+1921A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29270270 | |||||||
| chr22:29270461 | C | G | 1 | a0003c0004t0001g0232 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.14-1755C>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29270461 | |||||||
| chr22:29270653 | T | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.14-1563T>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29270653 | |||||||
| chr22:29270806 | TCTGCATT others(26): Show |
T | 1 | a0001c0001t0001g0231 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.14-1407_14-1375del others(33): Show |
EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr22 | 29270806 | ||||||
| chr22:29270905 | A | T | 1 | a0001c0001t0001g0051 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.14-1311A>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29270905 | |||||||
| chr22:29271020 | G | C | 6 | a0001c0001t0001g0051 a0001c0001t0001g0160 a0001c0001t0001g0234 others(3): Show |
7 | HG02080.hp2 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.14-1196G>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29271020 | |||||||
| chr22:29271104 | A | T | 1 | a0001c0001t0001g0142 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.14-1112A>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29271104 | |||||||
| chr22:29271327 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.14-889A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29271327 | |||||||
| chr22:29271504 | A | G | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG01891.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.14-712A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29271504 | |||||||
| chr22:29271665 | G | C | 1 | a0001c0001t0001g0063 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.14-551G>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29271665 | |||||||
| chr22:29272015 | C | T | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.14-201C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29272015 | |||||||
| chr22:29272210 | C | T | 12 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0135 others(9): Show |
14 | HG01884.hp1 HG02723.hp2 HG02809.hp2 others(11): Show |
splice_region_variant&intron_variant | LOW | c.14-6C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 1/16 | chr22 | 29272210 | |||||||
| chr22:29272274 | G | A | 1 | a0001c0001t0001g0052 | 2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.50+22G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 2/16 | chr22 | 29272274 | |||||||
| chr22:29272577 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.102+146G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 3/16 | chr22 | 29272577 | |||||||
| chr22:29272721 | T | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0067 |
4 | HG02257.hp1 HG02572.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+290T>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 3/16 | chr22 | 29272721 | |||||||
| chr22:29272759 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.102+328A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 3/16 | chr22 | 29272759 | |||||||
| chr22:29272799 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.102+368T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 3/16 | chr22 | 29272799 | |||||||
| chr22:29272833 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.102+402C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 3/16 | chr22 | 29272833 | |||||||
| chr22:29273050 | A | G | 1 | a0001c0001t0001g0035 | 2 | NA18961.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.102+619A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 3/16 | chr22 | 29273050 | |||||||
| chr22:29273220 | T | C | 1 | a0001c0001t0002g0164 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.103-521T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 3/16 | chr22 | 29273220 | |||||||
| chr22:29273228 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.103-513G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 3/16 | chr22 | 29273228 | |||||||
| chr22:29273466 | CT | C | 5 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(2): Show |
5 | HG02109.hp1 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.103-267delT | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr22 | 29273466 | ||||||
| chr22:29273488 | A | C | 1 | a0001c0001t0001g0226 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.103-253A>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 3/16 | chr22 | 29273488 | |||||||
| chr22:29273525 | T | C | 1 | a0001c0001t0002g0164 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.103-216T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 3/16 | chr22 | 29273525 | |||||||
| chr22:29273653 | G | T | 1 | a0001c0001t0001g0132 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.103-88G>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 3/16 | chr22 | 29273653 | |||||||
| chr22:29273659 | G | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(62): Show |
109 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.103-82G>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 3/16 | chr22 | 29273659 | |||||||
| chr22:29273704 | T | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(71): Show |
123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.103-37T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 3/16 | chr22 | 29273704 | |||||||
| chr22:29273723 | C | G | 1 | a0001c0001t0001g0016 | 3 | HG00639.hp1 HG01099.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.103-18C>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 3/16 | chr22 | 29273723 | |||||||
| chr22:29273896 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.226+32G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29273896 | |||||||
| chr22:29273991 | A | T | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | HG01081.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.226+127A>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29273991 | |||||||
| chr22:29274028 | T | C | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | NA19060.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.226+164T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29274028 | |||||||
| chr22:29274047 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.226+183A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29274047 | |||||||
| chr22:29274478 | G | GT | 5 | a0001c0001t0001g0021 a0001c0001t0001g0052 a0001c0001t0001g0244 others(2): Show |
7 | HG01255.hp2 HG01257.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.226+621dupT | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr22 | 29274478 | ||||||
| chr22:29274653 | A | G | 5 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
5 | NA18944.hp1 NA18974.hp1 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.226+789A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29274653 | |||||||
| chr22:29274734 | TA | T | 12 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0125 others(9): Show |
13 | HG01099.hp1 HG01109.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.226+871delA | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29274734 | |||||||
| chr22:29274925 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.226+1061A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29274925 | |||||||
| chr22:29274950 | T | C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(65): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.226+1086T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29274950 | |||||||
| chr22:29275034 | A | G | 5 | a0001c0001t0001g0048 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
6 | HG02145.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.226+1170A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29275034 | |||||||
| chr22:29275046 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.226+1182T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29275046 | |||||||
| chr22:29275047 | T | G | 5 | a0001c0001t0001g0048 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
6 | HG02145.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.226+1183T>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29275047 | |||||||
| chr22:29275226 | C | G | 2 | a0001c0001t0001g0037 a0001c0001t0001g0139 |
3 | HG03139.hp2 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.226+1362C>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29275226 | |||||||
| chr22:29275251 | A | G | 5 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(2): Show |
5 | HG02647.hp1 HG02717.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.226+1387A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29275251 | |||||||
| chr22:29275390 | C | G | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.226+1526C>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29275390 | |||||||
| chr22:29275483 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.226+1619T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29275483 | |||||||
| chr22:29275593 | A | G | 1 | a0001c0001t0001g0199 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.226+1729A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29275593 | |||||||
| chr22:29275621 | C | T | 6 | a0001c0001t0001g0051 a0001c0001t0001g0160 a0001c0001t0001g0234 others(3): Show |
7 | HG02080.hp2 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.226+1757C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29275621 | |||||||
| chr22:29275914 | CTTT | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0052 a0001c0001t0001g0244 others(2): Show |
7 | HG01255.hp2 HG01257.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.226+2052_226+2054d others(5): Show |
EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr22 | 29275914 | ||||||
| chr22:29275926 | T | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0147 |
4 | HG00099.hp2 HG00642.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.226+2062T>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29275926 | |||||||
| chr22:29275935 | G | GT | 90 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(87): Show |
142 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.226+2081dupT | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr22 | 29275935 | ||||||
| chr22:29275935 | G | GTT | 7 | a0001c0001t0001g0046 a0001c0001t0001g0051 a0001c0001t0001g0160 others(4): Show |
9 | HG02080.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.226+2080_226+2081d others(4): Show |
EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr22 | 29275935 | ||||||
| chr22:29275935 | G | T | 1 | a0001c0001t0001g0123 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.226+2071G>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29275935 | |||||||
| chr22:29275936 | T | G | 1 | a0001c0001t0001g0231 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.226+2072T>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29275936 | |||||||
| chr22:29276128 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.227-1902T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29276128 | |||||||
| chr22:29276304 | A | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0119 others(1): Show |
8 | HG00140.hp2 HG01074.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.227-1726A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29276304 | |||||||
| chr22:29276412 | CTG | C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0154 a0001c0001t0001g0155 |
5 | HG00639.hp1 HG01099.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.227-1614_227-1613d others(4): Show |
EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr22 | 29276412 | ||||||
| chr22:29276451 | A | G | 2 | a0001c0001t0001g0197 a0001c0001t0001g0198 |
2 | NA18972.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.227-1579A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29276451 | |||||||
| chr22:29276454 | G | C | 1 | a0001c0001t0001g0168 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.227-1576G>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29276454 | |||||||
| chr22:29276805 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.227-1225C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29276805 | |||||||
| chr22:29276841 | G | A | 1 | a0001c0001t0001g0039 | 2 | HG00741.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.227-1189G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29276841 | |||||||
| chr22:29276991 | GGTT | G | 39 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(36): Show |
65 | HG00280.hp2 HG00558.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.227-1036_227-1034d others(5): Show |
EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr22 | 29276991 | ||||||
| chr22:29277094 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.227-936C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29277094 | |||||||
| chr22:29277317 | T | A | 1 | a0001c0001t0001g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.227-713T>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29277317 | |||||||
| chr22:29277371 | A | C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0115 |
3 | HG02886.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.227-659A>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29277371 | |||||||
| chr22:29277492 | C | G | 1 | a0001c0001t0001g0231 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.227-538C>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29277492 | |||||||
| chr22:29277593 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.227-437A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29277593 | |||||||
| chr22:29277880 | T | C | 5 | a0001c0001t0001g0048 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
6 | HG02145.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.227-150T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29277880 | |||||||
| chr22:29277895 | C | T | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.227-135C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29277895 | |||||||
| chr22:29277932 | T | C | 6 | a0001c0001t0001g0024 a0001c0001t0001g0064 a0001c0001t0001g0144 others(3): Show |
7 | HG00323.hp2 HG02056.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.227-98T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29277932 | |||||||
| chr22:29277952 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.227-78A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 4/16 | chr22 | 29277952 | |||||||
| chr22:29278517 | G | A | 1 | a0001c0001t0001g0036 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.413+301G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29278517 | |||||||
| chr22:29278533 | C | CA | 10 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0116 others(7): Show |
10 | HG00741.hp2 HG01109.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.413+322dupA | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr22 | 29278533 | ||||||
| chr22:29278545 | G | C | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.413+329G>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29278545 | |||||||
| chr22:29278546 | G | C | 1 | a0001c0001t0001g0114 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.413+330G>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29278546 | |||||||
| chr22:29278604 | C | T | 1 | a0001c0001t0001g0055 | 2 | NA18747.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.413+388C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29278604 | |||||||
| chr22:29278642 | G | C | 1 | a0001c0001t0001g0170 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.413+426G>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29278642 | |||||||
| chr22:29278656 | C | G | 1 | a0001c0001t0001g0058 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.413+440C>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29278656 | |||||||
| chr22:29278777 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.413+561A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29278777 | |||||||
| chr22:29278818 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.413+602C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29278818 | |||||||
| chr22:29278824 | C | CA | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(120): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.413+621dupA | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr22 | 29278824 | ||||||
| chr22:29278997 | A | C | 1 | a0001c0001t0001g0204 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.413+781A>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29278997 | |||||||
| chr22:29279024 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.413+808C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29279024 | |||||||
| chr22:29279086 | G | A | 11 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0125 others(8): Show |
12 | HG01109.hp2 HG01243.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.413+870G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29279086 | |||||||
| chr22:29279108 | A | G | 5 | a0001c0001t0001g0008 a0001c0001t0001g0156 a0001c0001t0001g0157 others(2): Show |
8 | HG01243.hp2 HG02055.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.413+892A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29279108 | |||||||
| chr22:29279132 | A | AGT | 3 | a0001c0001t0001g0085 a0001c0001t0001g0227 a0001c0001t0001g0228 |
3 | HG01515.hp2 HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.413+931_413+932dup others(2): Show |
EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr22 | 29279132 | ||||||
| chr22:29279219 | T | C | 1 | a0001c0001t0001g0051 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.413+1003T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29279219 | |||||||
| chr22:29279412 | A | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(55): Show |
105 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.413+1196A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29279412 | |||||||
| chr22:29279419 | A | T | 1 | a0001c0001t0001g0231 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.413+1203A>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29279419 | |||||||
| chr22:29279434 | A | T | 5 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(2): Show |
5 | HG02647.hp1 HG02717.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+1218A>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29279434 | |||||||
| chr22:29279470 | C | G | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.413+1254C>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29279470 | |||||||
| chr22:29279477 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.413+1261A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29279477 | |||||||
| chr22:29279559 | C | T | 1 | a0001c0001t0001g0012 | 3 | HG02257.hp1 HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.413+1343C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29279559 | |||||||
| chr22:29279699 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.413+1483C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29279699 | |||||||
| chr22:29279866 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.413+1650C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29279866 | |||||||
| chr22:29279926 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.413+1710A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29279926 | |||||||
| chr22:29279947 | T | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(52): Show |
101 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.413+1731T>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29279947 | |||||||
| chr22:29280138 | A | G | 5 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(2): Show |
8 | HG00280.hp1 HG01123.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.413+1922A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29280138 | |||||||
| chr22:29280302 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.413+2086A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29280302 | |||||||
| chr22:29280357 | C | T | 1 | a0001c0001t0001g0036 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.414-2033C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29280357 | |||||||
| chr22:29280363 | C | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0210 |
5 | HG02630.hp1 HG02896.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.414-2027C>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29280363 | |||||||
| chr22:29280410 | C | G | 5 | a0001c0001t0001g0048 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
6 | HG02145.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.414-1980C>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29280410 | |||||||
| chr22:29280505 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.414-1885C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29280505 | |||||||
| chr22:29280647 | T | A | 1 | a0001c0001t0001g0246 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.414-1743T>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29280647 | |||||||
| chr22:29280674 | G | GT | 7 | a0001c0001t0001g0068 a0001c0001t0001g0083 a0001c0001t0001g0112 others(4): Show |
7 | HG00597.hp2 HG02015.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.414-1700dupT | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr22 | 29280674 | ||||||
| chr22:29280706 | T | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(55): Show |
105 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.414-1684T>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29280706 | |||||||
| chr22:29280759 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.414-1631C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29280759 | |||||||
| chr22:29280765 | C | T | 1 | a0001c0001t0001g0046 | 2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.414-1625C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29280765 | |||||||
| chr22:29280822 | C | T | 7 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0208 others(4): Show |
7 | HG01884.hp1 HG01884.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.414-1568C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29280822 | |||||||
| chr22:29280843 | T | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0154 a0001c0001t0001g0155 |
5 | HG00639.hp1 HG01099.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.414-1547T>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29280843 | |||||||
| chr22:29280843 | T | TTGTG | 2 | a0001c0001t0001g0028 a0001c0001t0001g0065 |
3 | NA18960.hp2 NA18984.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.414-1533_414-1530d others(6): Show |
EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr22 | 29280843 | ||||||
| chr22:29280860 | T | G | 1 | a0001c0001t0001g0083 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.414-1530T>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29280860 | |||||||
| chr22:29280862 | G | GT | 10 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0018 others(7): Show |
11 | HG00323.hp1 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.414-1491dupT | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr22 | 29280862 | ||||||
| chr22:29280862 | G | T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG01891.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.414-1528G>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29280862 | |||||||
| chr22:29280862 | GT | G | 20 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(17): Show |
23 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(20): Show |
intron_variant | MODIFIER | c.414-1491delT | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr22 | 29280862 | ||||||
| chr22:29280862 | GTT | G | 16 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0041 others(13): Show |
20 | HG00544.hp2 HG01123.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.414-1492_414-1491d others(4): Show |
EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr22 | 29280862 | ||||||
| chr22:29280862 | GTTT | G | 13 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0040 others(10): Show |
16 | HG00741.hp1 HG01496.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.414-1493_414-1491d others(5): Show |
EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr22 | 29280862 | ||||||
| chr22:29280862 | GTTTT | G | 23 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(20): Show |
30 | HG00423.hp2 HG00558.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.414-1494_414-1491d others(6): Show |
EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr22 | 29280862 | ||||||
| chr22:29280862 | GTTTTT | G | 25 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(22): Show |
34 | HG00673.hp1 HG01109.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.414-1495_414-1491d others(7): Show |
EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr22 | 29280862 | ||||||
| chr22:29280862 | GTTTTTT | G | 36 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0035 others(33): Show |
39 | HG00741.hp2 HG01099.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.414-1496_414-1491d others(8): Show |
EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr22 | 29280862 | ||||||
| chr22:29280862 | GTTTTTTT | G | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(98): Show |
161 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.414-1497_414-1491d others(9): Show |
EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr22 | 29280862 | ||||||
| chr22:29280862 | GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0001g0171 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.414-1501_414-1491d others(13): Show |
EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr22 | 29280862 | ||||||
| chr22:29280862 | GTTTTTTT others(9): Show |
G | 1 | a0001c0001t0001g0001 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.414-1506_414-1491d others(18): Show |
EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr22 | 29280862 | ||||||
| chr22:29280862 | GTTTTTTT others(10): Show |
G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0070 |
2 | HG02004.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.414-1507_414-1491d others(19): Show |
EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr22 | 29280862 | ||||||
| chr22:29280862 | GTTTTTTT others(11): Show |
G | 6 | a0001c0001t0001g0033 a0001c0001t0001g0085 a0001c0001t0001g0109 others(3): Show |
7 | HG01261.hp1 HG01515.hp2 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.414-1508_414-1491d others(20): Show |
EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr22 | 29280862 | ||||||
| chr22:29280864 | T | G | 1 | a0001c0001t0001g0069 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.414-1526T>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29280864 | |||||||
| chr22:29280866 | T | G | 1 | a0001c0001t0001g0069 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.414-1524T>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29280866 | |||||||
| chr22:29280869 | T | G | 1 | a0001c0001t0001g0069 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.414-1521T>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29280869 | |||||||
| chr22:29280873 | T | G | 2 | a0001c0001t0001g0040 a0001c0001t0001g0168 |
3 | HG01496.hp2 HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.414-1517T>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29280873 | |||||||
| chr22:29280876 | T | G | 2 | a0001c0001t0001g0040 a0001c0001t0001g0168 |
3 | HG01496.hp2 HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.414-1514T>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29280876 | |||||||
| chr22:29280877 | T | G | 8 | a0001c0001t0001g0046 a0001c0001t0001g0051 a0001c0001t0001g0056 others(5): Show |
10 | HG02109.hp1 HG02486.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.414-1513T>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29280877 | |||||||
| chr22:29280878 | T | G | 20 | a0001c0001t0001g0009 a0001c0001t0001g0057 a0001c0001t0001g0058 others(17): Show |
23 | HG01109.hp2 HG01243.hp2 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.414-1512T>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29280878 | |||||||
| chr22:29280879 | T | G | 38 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0029 others(35): Show |
44 | HG00741.hp2 HG01099.hp1 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.414-1511T>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29280879 | |||||||
| chr22:29280880 | T | G | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(98): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.414-1510T>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29280880 | |||||||
| chr22:29280881 | T | G | 2 | a0001c0001t0001g0067 a0001c0001t0001g0155 |
2 | HG01167.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.414-1509T>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29280881 | |||||||
| chr22:29280886 | T | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0049 |
4 | HG02257.hp2 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.414-1504T>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29280886 | |||||||
| chr22:29280887 | T | G | 1 | a0001c0001t0001g0212 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.414-1503T>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29280887 | |||||||
| chr22:29280888 | T | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0119 others(1): Show |
8 | HG00140.hp2 HG01074.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.414-1502T>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29280888 | |||||||
| chr22:29280946 | C | T | 2 | a0001c0001t0001g0248 a0001c0001t0001g0260 |
2 | HG00642.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.414-1444C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29280946 | |||||||
| chr22:29280969 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.414-1421T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29280969 | |||||||
| chr22:29280998 | G | A | 1 | a0001c0001t0001g0022 | 2 | NA18941.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.414-1392G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29280998 | |||||||
| chr22:29281126 | G | T | 1 | a0001c0001t0001g0052 | 2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.414-1264G>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29281126 | |||||||
| chr22:29281175 | A | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.414-1215A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29281175 | |||||||
| chr22:29281203 | C | T | 1 | a0001c0001t0001g0036 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.414-1187C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29281203 | |||||||
| chr22:29281237 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.414-1153A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29281237 | |||||||
| chr22:29281305 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.414-1085G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29281305 | |||||||
| chr22:29281319 | G | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0039 |
5 | HG00741.hp1 HG02004.hp1 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-1071G>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29281319 | |||||||
| chr22:29281321 | T | C | 8 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0064 others(5): Show |
10 | HG02056.hp1 HG02071.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.414-1069T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29281321 | |||||||
| chr22:29281380 | T | G | 1 | a0001c0001t0001g0109 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.414-1010T>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29281380 | |||||||
| chr22:29281562 | C | T | 5 | a0001c0001t0001g0048 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
6 | HG02145.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.414-828C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29281562 | |||||||
| chr22:29281573 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0156 a0001c0001t0001g0157 |
6 | HG01243.hp2 HG02055.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-817G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29281573 | |||||||
| chr22:29281581 | T | G | 1 | a0001c0001t0001g0067 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.414-809T>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29281581 | |||||||
| chr22:29281639 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.414-751G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29281639 | |||||||
| chr22:29281657 | T | G | 1 | a0001c0001t0001g0147 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.414-733T>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29281657 | |||||||
| chr22:29281757 | T | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(63): Show |
114 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.414-633T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29281757 | |||||||
| chr22:29281836 | C | T | 5 | a0001c0001t0001g0048 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
6 | HG02145.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.414-554C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29281836 | |||||||
| chr22:29281978 | C | A | 43 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(40): Show |
72 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.414-412C>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29281978 | |||||||
| chr22:29282288 | T | C | 7 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0208 others(4): Show |
7 | HG01884.hp1 HG01884.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.414-102T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29282288 | |||||||
| chr22:29282330 | G | A | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | HG02698.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.414-60G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 5/16 | chr22 | 29282330 | |||||||
| chr22:29282572 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.581+15T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29282572 | |||||||
| chr22:29282669 | GTGATAAG others(5): Show |
G | 7 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0208 others(4): Show |
7 | HG01884.hp1 HG01884.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.581+116_581+127del others(12): Show |
EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr22 | 29282669 | ||||||
| chr22:29282760 | C | CT | 10 | a0001c0001t0001g0072 a0001c0001t0001g0075 a0001c0001t0001g0080 others(7): Show |
10 | HG01981.hp1 HG02129.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.581+218dupT | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr22 | 29282760 | ||||||
| chr22:29282775 | T | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0052 a0001c0001t0001g0176 others(3): Show |
8 | HG01255.hp2 HG01257.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.581+218T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29282775 | |||||||
| chr22:29282835 | T | C | 2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.581+278T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29282835 | |||||||
| chr22:29282875 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0156 a0001c0001t0001g0157 others(1): Show |
7 | HG01243.hp2 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.581+318G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29282875 | |||||||
| chr22:29282948 | G | A | 11 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0125 others(8): Show |
12 | HG01109.hp2 HG01243.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.581+391G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29282948 | |||||||
| chr22:29283233 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0079 |
2 | NA19070.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.581+676C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29283233 | |||||||
| chr22:29283419 | GATCTCCG others(2475): Show |
G | 7 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0208 others(4): Show |
7 | HG01884.hp1 HG01884.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.581+868_582-1017de others(1): Show |
EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr22 | 29283419 | ||||||
| chr22:29283467 | G | C | 1 | a0001c0005t0001g0143 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.581+910G>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29283467 | |||||||
| chr22:29283532 | A | G | 1 | a0001c0001t0001g0117 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.581+975A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29283532 | |||||||
| chr22:29283577 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0220 |
2 | NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.581+1020G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29283577 | |||||||
| chr22:29283661 | G | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0100 |
4 | HG02683.hp2 HG03710.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.581+1104G>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29283661 | |||||||
| chr22:29283694 | AT | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(86): Show |
141 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.581+1148delT | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr22 | 29283694 | ||||||
| chr22:29283724 | G | A | 40 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0014 others(37): Show |
61 | HG00140.hp2 HG00423.hp1 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.581+1167G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29283724 | |||||||
| chr22:29284148 | T | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0210 |
5 | HG02630.hp1 HG02896.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.581+1591T>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29284148 | |||||||
| chr22:29284353 | A | G | 1 | a0001c0001t0003g0004 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.581+1796A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29284353 | |||||||
| chr22:29284354 | G | T | 1 | a0001c0001t0001g0103 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.581+1797G>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29284354 | |||||||
| chr22:29284450 | C | G | 5 | a0001c0001t0001g0008 a0001c0001t0001g0156 a0001c0001t0001g0157 others(2): Show |
8 | HG01243.hp2 HG02055.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.581+1893C>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29284450 | |||||||
| chr22:29284624 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.581+2067T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29284624 | |||||||
| chr22:29284842 | G | A | 1 | a0001c0001t0001g0002 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.582-2081G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29284842 | |||||||
| chr22:29284876 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.582-2047A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29284876 | |||||||
| chr22:29284928 | T | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0156 a0001c0001t0001g0157 others(2): Show |
8 | HG01243.hp2 HG02055.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.582-1995T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29284928 | |||||||
| chr22:29284992 | T | C | 1 | a0001c0001t0001g0039 | 2 | HG00741.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.582-1931T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29284992 | |||||||
| chr22:29285040 | A | G | 1 | a0001c0001t0001g0002 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.582-1883A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29285040 | |||||||
| chr22:29285087 | G | T | 1 | a0001c0001t0001g0231 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.582-1836G>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29285087 | |||||||
| chr22:29285119 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.582-1804C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29285119 | |||||||
| chr22:29285122 | G | GT | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(108): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.582-1782dupT | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr22 | 29285122 | ||||||
| chr22:29285122 | G | GTT | 33 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(30): Show |
48 | HG00597.hp2 HG00609.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.582-1783_582-1782d others(4): Show |
EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr22 | 29285122 | ||||||
| chr22:29285122 | G | GTTT | 7 | a0001c0001t0001g0016 a0001c0001t0001g0048 a0001c0001t0001g0156 others(4): Show |
8 | HG01175.hp1 HG02055.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.582-1784_582-1782d others(5): Show |
EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr22 | 29285122 | ||||||
| chr22:29285185 | G | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.582-1738G>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29285185 | |||||||
| chr22:29285195 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.582-1728C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29285195 | |||||||
| chr22:29285227 | A | G | 26 | a0001c0001t0001g0010 a0001c0001t0001g0038 a0001c0001t0001g0053 others(23): Show |
33 | HG00544.hp1 HG00642.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.582-1696A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29285227 | |||||||
| chr22:29285239 | G | T | 1 | a0001c0001t0001g0153 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.582-1684G>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29285239 | |||||||
| chr22:29285714 | T | A | 1 | a0001c0001t0001g0054 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.582-1209T>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29285714 | |||||||
| chr22:29285732 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.582-1191G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29285732 | |||||||
| chr22:29285770 | T | C | 1 | a0001c0001t0001g0006 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.582-1153T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29285770 | |||||||
| chr22:29285868 | C | G | 1 | a0001c0001t0001g0201 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.582-1055C>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29285868 | |||||||
| chr22:29285919 | G | T | 1 | a0001c0001t0001g0257 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.582-1004G>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29285919 | |||||||
| chr22:29286048 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.582-875C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29286048 | |||||||
| chr22:29286143 | T | C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0095 a0001c0001t0001g0114 |
4 | HG02698.hp2 NA18612.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.582-780T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29286143 | |||||||
| chr22:29286150 | G | GT | 69 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(66): Show |
99 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.582-764dupT | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr22 | 29286150 | ||||||
| chr22:29286191 | G | A | 2 | a0001c0001t0001g0252 a0001c0001t0001g0259 |
2 | HG01070.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.582-732G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29286191 | |||||||
| chr22:29286420 | G | C | 5 | a0001c0001t0001g0024 a0001c0001t0001g0144 a0001c0001t0001g0145 others(2): Show |
6 | HG00323.hp2 HG02056.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.582-503G>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29286420 | |||||||
| chr22:29286670 | G | C | 9 | a0001c0001t0001g0008 a0001c0001t0001g0156 a0001c0001t0001g0157 others(6): Show |
12 | HG01243.hp2 HG02055.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.582-253G>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29286670 | |||||||
| chr22:29286686 | CA | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(69): Show |
119 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.582-211delA | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr22 | 29286686 | ||||||
| chr22:29286686 | CAA | C | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(130): Show |
198 | HG00099.hp2 HG00140.hp2 HG00558.hp2 others(195): Show |
intron_variant | MODIFIER | c.582-212_582-211del others(2): Show |
EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr22 | 29286686 | ||||||
| chr22:29286686 | CAAA | C | 27 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(24): Show |
36 | HG00408.hp2 HG00597.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.582-213_582-211del others(3): Show |
EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr22 | 29286686 | ||||||
| chr22:29286686 | CAAAAAAA others(2): Show |
C | 7 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0208 others(4): Show |
7 | HG01884.hp1 HG01884.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.582-219_582-211del others(9): Show |
EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr22 | 29286686 | ||||||
| chr22:29286711 | A | T | 5 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(2): Show |
5 | HG00741.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.582-212A>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29286711 | |||||||
| chr22:29286712 | A | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(79): Show |
113 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.582-211A>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 6/16 | chr22 | 29286712 | |||||||
| chr22:29287218 | T | C | 1 | a0001c0001t0001g0238 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.793+84T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 7/16 | chr22 | 29287218 | |||||||
| chr22:29287295 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.793+161G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 7/16 | chr22 | 29287295 | |||||||
| chr22:29287345 | T | A | 1 | a0001c0001t0001g0231 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.793+211T>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 7/16 | chr22 | 29287345 | |||||||
| chr22:29287427 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.793+293C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 7/16 | chr22 | 29287427 | |||||||
| chr22:29287455 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.793+321G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 7/16 | chr22 | 29287455 | |||||||
| chr22:29287569 | A | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0052 a0001c0001t0001g0244 others(2): Show |
7 | HG01255.hp2 HG01257.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.793+435A>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 7/16 | chr22 | 29287569 | |||||||
| chr22:29288171 | A | G | 4 | a0001c0001t0001g0048 a0001c0001t0001g0218 a0001c0001t0001g0219 others(1): Show |
5 | HG02145.hp1 HG02965.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-435A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 7/16 | chr22 | 29288171 | |||||||
| chr22:29288388 | T | A | 1 | a0001c0001t0001g0026 | 2 | HG02165.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.794-218T>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 7/16 | chr22 | 29288388 | |||||||
| chr22:29288842 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.974+56A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 8/16 | chr22 | 29288842 | |||||||
| chr22:29288940 | T | C | 1 | a0001c0001t0001g0177 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.974+154T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 8/16 | chr22 | 29288940 | |||||||
| chr22:29289086 | G | C | 2 | a0001c0001t0001g0235 a0001c0001t0001g0237 |
2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.974+300G>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 8/16 | chr22 | 29289086 | |||||||
| chr22:29289174 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.974+388A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 8/16 | chr22 | 29289174 | |||||||
| chr22:29289309 | A | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0112 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.974+523A>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 8/16 | chr22 | 29289309 | |||||||
| chr22:29289310 | T | C | 5 | a0001c0001t0001g0029 a0001c0001t0001g0066 a0001c0001t0001g0086 others(2): Show |
6 | HG02027.hp2 HG02083.hp1 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.974+524T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 8/16 | chr22 | 29289310 | |||||||
| chr22:29289420 | T | C | 5 | a0001c0001t0001g0048 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
6 | HG02145.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.974+634T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 8/16 | chr22 | 29289420 | |||||||
| chr22:29289438 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.974+652T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 8/16 | chr22 | 29289438 | |||||||
| chr22:29289619 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.974+833T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 8/16 | chr22 | 29289619 | |||||||
| chr22:29289662 | T | A | 1 | a0001c0001t0001g0052 | 2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.974+876T>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 8/16 | chr22 | 29289662 | |||||||
| chr22:29289663 | T | A | 1 | a0001c0001t0001g0052 | 2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.974+877T>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 8/16 | chr22 | 29289663 | |||||||
| chr22:29289664 | T | A | 1 | a0001c0001t0001g0052 | 2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.974+878T>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 8/16 | chr22 | 29289664 | |||||||
| chr22:29289722 | C | T | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
264 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.974+936C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 8/16 | chr22 | 29289722 | |||||||
| chr22:29289763 | A | G | 54 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(51): Show |
87 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.974+977A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 8/16 | chr22 | 29289763 | |||||||
| chr22:29289765 | T | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0156 a0001c0001t0001g0157 others(1): Show |
7 | HG01243.hp2 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.974+979T>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 8/16 | chr22 | 29289765 | |||||||
| chr22:29289857 | A | C | 1 | a0001c0001t0001g0187 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.974+1071A>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 8/16 | chr22 | 29289857 | |||||||
| chr22:29289908 | A | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | NA19060.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.974+1122A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 8/16 | chr22 | 29289908 | |||||||
| chr22:29289925 | ATACTC | A | 11 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0125 others(8): Show |
12 | HG01109.hp2 HG01243.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.974+1142_974+1146d others(7): Show |
EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr22 | 29289925 | ||||||
| chr22:29290358 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.975-1204T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 8/16 | chr22 | 29290358 | |||||||
| chr22:29290503 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.975-1059G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 8/16 | chr22 | 29290503 | |||||||
| chr22:29290899 | A | G | 1 | a0001c0001t0001g0023 | 2 | HG00673.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.975-663A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 8/16 | chr22 | 29290899 | |||||||
| chr22:29290929 | T | C | 1 | a0001c0001t0001g0255 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.975-633T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 8/16 | chr22 | 29290929 | |||||||
| chr22:29290955 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.975-607G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 8/16 | chr22 | 29290955 | |||||||
| chr22:29291293 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.975-269G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 8/16 | chr22 | 29291293 | |||||||
| chr22:29292230 | A | C | 1 | a0001c0001t0001g0230 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1045+61A>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 10/16 | chr22 | 29292230 | |||||||
| chr22:29292363 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1046-125C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 10/16 | chr22 | 29292363 | |||||||
| chr22:29292471 | CTTG | C | 5 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(2): Show |
5 | HG02647.hp1 HG02717.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1046-12_1046-10del others(3): Show |
EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr22 | 29292471 | ||||||
| chr22:29292643 | T | G | 40 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0014 others(37): Show |
61 | HG00140.hp2 HG00423.hp1 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.1164+37T>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29292643 | |||||||
| chr22:29292762 | C | CT | 5 | a0001c0001t0001g0054 a0001c0001t0001g0227 a0001c0001t0001g0228 others(2): Show |
6 | HG00735.hp1 HG01081.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.1164+175dupT | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr22 | 29292762 | ||||||
| chr22:29292762 | CT | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(171): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1164+175delT | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr22 | 29292762 | ||||||
| chr22:29292762 | CTT | C | 37 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0014 others(34): Show |
57 | HG00423.hp1 HG01074.hp2 HG01261.hp1 others(54): Show |
intron_variant | MODIFIER | c.1164+174_1164+175d others(4): Show |
EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr22 | 29292762 | ||||||
| chr22:29292883 | A | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0210 |
5 | HG02630.hp1 HG02896.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1164+277A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29292883 | |||||||
| chr22:29292952 | G | T | 5 | a0001c0001t0001g0024 a0001c0001t0001g0064 a0001c0001t0001g0144 others(2): Show |
6 | HG02056.hp1 HG02071.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.1164+346G>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29292952 | |||||||
| chr22:29293044 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1164+438G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29293044 | |||||||
| chr22:29293069 | A | C | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1164+463A>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29293069 | |||||||
| chr22:29293216 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1164+610C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29293216 | |||||||
| chr22:29293520 | CT | C | 16 | a0001c0001t0001g0008 a0001c0001t0001g0049 a0001c0001t0001g0050 others(13): Show |
20 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.1164+921delT | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr22 | 29293520 | ||||||
| chr22:29293549 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0210 |
5 | HG02630.hp1 HG02896.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1164+943C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29293549 | |||||||
| chr22:29293627 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1164+1021C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29293627 | |||||||
| chr22:29293725 | C | T | 1 | a0003c0004t0001g0232 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1164+1119C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29293725 | |||||||
| chr22:29293754 | G | A | 1 | a0001c0001t0001g0046 | 2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1164+1148G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29293754 | |||||||
| chr22:29293848 | A | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(227): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1164+1242A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29293848 | |||||||
| chr22:29293903 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1164+1297G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29293903 | |||||||
| chr22:29293938 | C | T | 1 | a0001c0001t0001g0042 | 2 | NA18944.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.1164+1332C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29293938 | |||||||
| chr22:29293983 | C | G | 1 | a0001c0001t0001g0036 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1164+1377C>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29293983 | |||||||
| chr22:29294190 | G | A | 7 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0208 others(4): Show |
7 | HG01884.hp1 HG01884.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1164+1584G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29294190 | |||||||
| chr22:29294198 | TA | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0115 |
3 | HG02886.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1164+1595delA | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr22 | 29294198 | ||||||
| chr22:29294201 | A | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0115 |
3 | HG02886.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1164+1595A>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29294201 | |||||||
| chr22:29294202 | G | C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0115 |
3 | HG02886.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1164+1596G>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29294202 | |||||||
| chr22:29294257 | G | A | 39 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(36): Show |
66 | HG00280.hp2 HG00558.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.1164+1651G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29294257 | |||||||
| chr22:29294356 | T | C | 208 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(205): Show |
289 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.1164+1750T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29294356 | |||||||
| chr22:29294498 | C | G | 1 | a0001c0001t0005g0172 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1165-1741C>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29294498 | |||||||
| chr22:29294604 | C | CA | 9 | a0001c0001t0001g0061 a0001c0001t0001g0084 a0001c0001t0001g0100 others(6): Show |
9 | HG01109.hp1 HG01175.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.1165-1619dupA | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr22 | 29294604 | ||||||
| chr22:29294604 | CA | C | 16 | a0001c0001t0001g0040 a0001c0001t0001g0048 a0001c0001t0001g0064 others(13): Show |
18 | HG01167.hp1 HG01496.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1165-1619delA | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr22 | 29294604 | ||||||
| chr22:29294637 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1165-1602C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29294637 | |||||||
| chr22:29294802 | A | C | 4 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(1): Show |
4 | HG02109.hp2 HG02886.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1165-1437A>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29294802 | |||||||
| chr22:29294849 | G | T | 1 | a0001c0001t0001g0192 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1165-1390G>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29294849 | |||||||
| chr22:29294859 | G | C | 1 | a0001c0001t0001g0105 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1165-1380G>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29294859 | |||||||
| chr22:29294911 | C | CA | 9 | a0001c0001t0001g0051 a0001c0001t0001g0103 a0001c0001t0001g0112 others(6): Show |
10 | HG02080.hp2 HG02258.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1165-1317dupA | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr22 | 29294911 | ||||||
| chr22:29294998 | T | C | 11 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0125 others(8): Show |
12 | HG01109.hp2 HG01243.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.1165-1241T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29294998 | |||||||
| chr22:29295156 | C | G | 1 | a0001c0001t0001g0111 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1165-1083C>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29295156 | |||||||
| chr22:29295171 | C | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0156 a0001c0001t0001g0157 others(2): Show |
8 | HG01243.hp2 HG02055.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1165-1068C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29295171 | |||||||
| chr22:29295246 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1165-993A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29295246 | |||||||
| chr22:29295246 | A | T | 1 | a0001c0001t0001g0012 | 3 | HG02257.hp1 HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1165-993A>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29295246 | |||||||
| chr22:29295280 | A | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0210 |
5 | HG02630.hp1 HG02896.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1165-959A>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29295280 | |||||||
| chr22:29295358 | T | C | 5 | a0001c0001t0001g0048 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
6 | HG02145.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1165-881T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29295358 | |||||||
| chr22:29295393 | A | T | 169 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(166): Show |
242 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1165-846A>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29295393 | |||||||
| chr22:29295408 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1165-831G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29295408 | |||||||
| chr22:29295488 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1165-751C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29295488 | |||||||
| chr22:29295705 | ATACAAGG others(7): Show |
A | 7 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0135 others(4): Show |
9 | HG02723.hp2 HG02895.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1165-532_1165-519d others(16): Show |
EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr22 | 29295705 | ||||||
| chr22:29295930 | G | A | 6 | a0001c0001t0001g0033 a0001c0001t0001g0070 a0001c0001t0001g0085 others(3): Show |
7 | HG01261.hp1 HG01515.hp2 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.1165-309G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29295930 | |||||||
| chr22:29296045 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1165-194T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29296045 | |||||||
| chr22:29296062 | A | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
4 | NA18944.hp2 NA18977.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.1165-177A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29296062 | |||||||
| chr22:29296119 | G | C | 2 | a0001c0001t0001g0040 a0001c0001t0001g0168 |
3 | HG01496.hp2 HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1165-120G>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29296119 | |||||||
| chr22:29296122 | G | A | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1165-117G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 11/16 | chr22 | 29296122 | |||||||
| chr22:29296498 | G | T | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1294+130G>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 12/16 | chr22 | 29296498 | |||||||
| chr22:29296507 | G | T | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(231): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.1294+139G>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 12/16 | chr22 | 29296507 | |||||||
| chr22:29296728 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1294+360A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 12/16 | chr22 | 29296728 | |||||||
| chr22:29296798 | T | C | 6 | a0001c0001t0001g0031 a0001c0001t0001g0082 a0001c0001t0001g0091 others(3): Show |
7 | NA18957.hp2 NA18965.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.1294+430T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 12/16 | chr22 | 29296798 | |||||||
| chr22:29297272 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1295-555A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 12/16 | chr22 | 29297272 | |||||||
| chr22:29297275 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1295-552C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 12/16 | chr22 | 29297275 | |||||||
| chr22:29297541 | A | G | 1 | a0001c0001t0001g0210 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1295-286A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 12/16 | chr22 | 29297541 | |||||||
| chr22:29297650 | G | A | 50 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(47): Show |
81 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.1295-177G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 12/16 | chr22 | 29297650 | |||||||
| chr22:29297786 | G | A | 1 | a0001c0001t0001g0024 | 2 | NA18981.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1295-41G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 12/16 | chr22 | 29297786 | |||||||
| chr22:29298000 | A | G | 60 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(57): Show |
88 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.1417+51A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 13/16 | chr22 | 29298000 | |||||||
| chr22:29298256 | A | T | 1 | a0003c0004t0001g0232 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1417+307A>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 13/16 | chr22 | 29298256 | |||||||
| chr22:29298322 | G | A | 184 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(181): Show |
261 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.1417+373G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 13/16 | chr22 | 29298322 | |||||||
| chr22:29298332 | T | C | 2 | a0001c0001t0001g0223 a0001c0001t0001g0242 |
2 | HG01109.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1417+383T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 13/16 | chr22 | 29298332 | |||||||
| chr22:29298418 | A | T | 1 | a0001c0001t0001g0026 | 2 | HG02165.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1418-315A>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 13/16 | chr22 | 29298418 | |||||||
| chr22:29298431 | G | C | 1 | a0001c0001t0001g0111 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1418-302G>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 13/16 | chr22 | 29298431 | |||||||
| chr22:29298493 | T | C | 189 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(186): Show |
266 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.1418-240T>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 13/16 | chr22 | 29298493 | |||||||
| chr22:29298507 | C | CA | 90 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(87): Show |
123 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.1418-208dupA | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr22 | 29298507 | ||||||
| chr22:29298509 | A | C | 1 | a0001c0001t0001g0115 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1418-224A>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 13/16 | chr22 | 29298509 | |||||||
| chr22:29298510 | A | C | 1 | a0001c0001t0001g0034 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1418-223A>C | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 13/16 | chr22 | 29298510 | |||||||
| chr22:29298526 | T | A | 1 | a0001c0001t0001g0238 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1418-207T>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 13/16 | chr22 | 29298526 | |||||||
| chr22:29298562 | C | T | 3 | a0001c0001t0001g0037 a0001c0001t0001g0135 a0001c0001t0001g0139 |
4 | HG02895.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1418-171C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 13/16 | chr22 | 29298562 | |||||||
| chr22:29298698 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1418-35A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 13/16 | chr22 | 29298698 | |||||||
| chr22:29298902 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG01070.hp2 | splice_region_variant&intron_variant | LOW | c.1580+7A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 14/16 | chr22 | 29298902 | |||||||
| chr22:29298927 | A | G | 4 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(1): Show |
4 | HG02723.hp2 HG02895.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1580+32A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 14/16 | chr22 | 29298927 | |||||||
| chr22:29299202 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1581-32G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 14/16 | chr22 | 29299202 | |||||||
| chr22:29299431 | C | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0156 a0001c0001t0001g0157 others(2): Show |
8 | HG01243.hp2 HG02055.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1678+100C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 15/16 | chr22 | 29299431 | |||||||
| chr22:29299495 | G | A | 1 | a0003c0004t0001g0232 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1679-104G>A | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 15/16 | chr22 | 29299495 | |||||||
| chr22:29299881 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1931+30C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 16/16 | chr22 | 29299881 | |||||||
| chr22:29299939 | T | G | 26 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0047 others(23): Show |
35 | HG00323.hp1 HG00544.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.1931+88T>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 16/16 | chr22 | 29299939 | |||||||
| chr22:29299954 | A | G | 1 | a0001c0001t0001g0044 | 2 | HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1931+103A>G | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 16/16 | chr22 | 29299954 | |||||||
| chr22:29299960 | G | GTTGGGAG others(63): Show |
4 | a0001c0001t0001g0185 a0001c0001t0001g0227 a0001c0001t0001g0228 others(1): Show |
4 | HG01884.hp1 HG02809.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1932-91_1932-22dup others(70): Show |
EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr22 | 29299960 | ||||||
| chr22:29299960 | GTTGGGAG others(63): Show |
G | 187 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
268 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.1932-91_1932-22del others(70): Show |
EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr22 | 29299960 | ||||||
| chr22:29300079 | C | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0139 |
3 | HG03139.hp2 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1932-43C>T | EWSR1 | ENSG00000182944.18 | transcript | ENST00000397938.7 | protein_coding | 16/16 | chr22 | 29300079 |