Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9295 |
| ensemblid | ENSG00000116754.14 |
| hgncid | 10782 |
| symbol | SRSF11 |
| name | serine and arginine rich splicing factor 11 |
| refseq_nuc | NM_001350605.2 |
| refseq_prot | NP_001337534.1 |
| ensembl_nuc | ENST00000370949.2 |
| ensembl_prot | ENSP00000359987.2 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 70221380 |
| end | 70253052 |
| strand | + |
| ver | v1.2 |
| region | chr1:70221380-70253052 |
| region5000 | chr1:70216380-70258052 |
| regionname0 | SRSF11_chr1_70221380_70253052 |
| regionname5000 | SRSF11_chr1_70216380_70258052 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1452 | 334 | 62 | 63 | 153 | 12 | 42 | SRSF11_chr1_70216380_70258052 | SRSF11 | ATGAG others(1447): Show |
chr1 | 70216380 | 70258052 | ||
| a0001c0002 | 0/0 | 1452 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | ATGAG others(1447): Show |
chr1 | 70216380 | 70258052 | ||
| a0001c0003 | 0/0 | 1452 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | ATGAG others(1447): Show |
chr1 | 70216380 | 70258052 | ||
| a0001c0004 | 0/0 | 1452 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | ATGAG others(1447): Show |
chr1 | 70216380 | 70258052 | ||
| a0001c0005 | 0/0 | 1452 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | ATGAG others(1447): Show |
chr1 | 70216380 | 70258052 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3959 | 305 | 46 | 60 | 147 | 12 | 39 | SRSF11_chr1_70216380_70258052 | SRSF11 | AGTGT others(3954): Show |
chr1 | 70216380 | 70258052 |
| a0001c0001t0002 | 0/0 | 3959 | 11 | 9 | 2 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | AGTGT others(3954): Show |
chr1 | 70216380 | 70258052 |
| a0001c0001t0003 | 0/0 | 3958 | 4 | 4 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | AGTGT others(3953): Show |
chr1 | 70216380 | 70258052 |
| a0001c0001t0004 | 0/0 | 3959 | 3 | 0 | 0 | 0 | 0 | 3 | SRSF11_chr1_70216380_70258052 | SRSF11 | AGTGT others(3954): Show |
chr1 | 70216380 | 70258052 |
| a0001c0001t0005 | 0/0 | 3959 | 3 | 0 | 0 | 3 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | AGTGT others(3954): Show |
chr1 | 70216380 | 70258052 |
| a0001c0001t0006 | 0/0 | 3959 | 2 | 2 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | AGTGT others(3954): Show |
chr1 | 70216380 | 70258052 |
| a0001c0001t0007 | 0/0 | 3959 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | AGTGT others(3954): Show |
chr1 | 70216380 | 70258052 |
| a0001c0001t0008 | 0/0 | 3959 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | AGTGT others(3954): Show |
chr1 | 70216380 | 70258052 |
| a0001c0001t0009 | 0/1 | 3961 | 1 | 0 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | AGTGT others(3956): Show |
chr1 | 70216380 | 70258052 |
| a0001c0001t0011 | 0/0 | 3959 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | AGTGT others(3954): Show |
chr1 | 70216380 | 70258052 |
| a0001c0001t0012 | 0/0 | 3959 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | AGTGT others(3954): Show |
chr1 | 70216380 | 70258052 |
| a0001c0001t0013 | 0/0 | 3959 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | AGTGT others(3954): Show |
chr1 | 70216380 | 70258052 |
| a0001c0002t0001 | 0/0 | 3959 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | AGTGT others(3954): Show |
chr1 | 70216380 | 70258052 |
| a0001c0003t0010 | 0/0 | 3959 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | AGTGT others(3954): Show |
chr1 | 70216380 | 70258052 |
| a0001c0004t0001 | 0/0 | 3959 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | AGTGT others(3954): Show |
chr1 | 70216380 | 70258052 |
| a0001c0005t0001 | 0/0 | 3959 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | AGTGT others(3954): Show |
chr1 | 70216380 | 70258052 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0002 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0004 | 0/0 | 7 | 0 | 5 | 0 | 1 | 1 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0005 | 0/0 | 6 | 1 | 1 | 4 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0006 | 0/0 | 6 | 1 | 0 | 5 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0007 | 0/0 | 6 | 1 | 2 | 0 | 0 | 3 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0010 | 0/0 | 5 | 1 | 2 | 2 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0092 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0002g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0003g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0005g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0005g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0006g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0006g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0007g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0008g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0009g0105 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0011g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0012g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0001t0013g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0003t0010g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0004t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| a0001c0005t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0155 | EUR | GBR | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | GBR | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0174 | EUR | GBR | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0119 | EUR | FIN | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | FIN | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01106 | hp1 | a0001 | c0004 | t0001 | g0029 | AMR | PUR | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01346 | hp2 | a0001 | c0001 | t0008 | g0089 | AMR | CLM | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | IBS | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | PEL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02080 | hp2 | a0001 | c0001 | t0012 | g0001 | EAS | KHV | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CDX | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CDX | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CDX | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02165 | hp2 | a0001 | c0001 | t0007 | g0075 | EAS | CDX | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02622 | hp2 | a0001 | c0003 | t0010 | g0044 | AFR | GWD | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | GWD | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02647 | hp2 | a0001 | c0001 | t0011 | g0140 | AFR | GWD | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0096 | SAS | PJL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | GWD | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0234 | AFR | ESN | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02976 | hp1 | a0001 | c0005 | t0001 | g0062 | AFR | ESN | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | ESN | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | GWD | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | ESN | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | MSL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0239 | AFR | MSL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | GWD | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | STU | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | STU | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0097 | SAS | PJL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | BEB | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | BEB | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0098 | SAS | BEB | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | BEB | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | STU | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | STU | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | BEB | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | STU | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | STU | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | YRI | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHB | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHB | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHB | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | YRI | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18972 | hp1 | a0001 | c0001 | t0005 | g0047 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19000 | hp2 | a0001 | c0001 | t0005 | g0045 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19063 | hp1 | a0001 | c0001 | t0013 | g0224 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19075 | hp2 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19086 | hp1 | a0001 | c0001 | t0005 | g0046 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | YRI | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | YRI | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0124 | AFR | ASW | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ASW | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0147 | EUR | TSI | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0112 | EUR | TSI | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | TSI | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | TSI | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | GIH | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | GIH | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0235 | AFR | ACB | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | USA | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | USA | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | USA | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | USA | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0009 | g0105 | REF | REF | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0092 | REF | REF | SRSF11_chr1_70216380_70258052 | SRSF11 | chr1 | 70216380 | 70258052 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:70221651 | C | A | 1 | a0001c0002 | 1 | NA19075.hp2 | synonymous_variant | LOW | c.15C>A | p.Thr5Thr | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/12 | 272/3959 | 15/1455 | 5/484 | chr1 | 70221651 | |||
| chr1:70232365 | C | T | 1 | a0001c0005 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.435C>T | p.Asn145Asn | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 3/12 | 692/3959 | 435/1455 | 145/484 | chr1 | 70232365 | |||
| chr1:70246860 | A | C | 1 | a0001c0004 | 1 | HG01106.hp1 | synonymous_variant | LOW | c.975A>C | p.Thr325Thr | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 9/12 | 1232/3959 | 975/1455 | 325/484 | chr1 | 70246860 | |||
| chr1:70250407 | T | C | 1 | a0001c0003 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.1161T>C | p.Ser387Ser | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 11/12 | 1418/3959 | 1161/1455 | 387/484 | chr1 | 70250407 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:70251306 | T | C | 1 | a0001c0001t0006 | 2 | HG02486.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*501T>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 12/12 | 501 | chr1 | 70251306 | ||||||
| chr1:70251543 | G | C | 1 | a0001c0001t0007 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*738G>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 12/12 | 738 | chr1 | 70251543 | ||||||
| chr1:70251617 | A | G | 1 | a0001c0001t0013 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*812A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 12/12 | 812 | chr1 | 70251617 | ||||||
| chr1:70251618 | G | A | 1 | a0001c0001t0013 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*813G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 12/12 | 813 | chr1 | 70251618 | ||||||
| chr1:70251908 | A | G | 1 | a0001c0001t0012 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1103A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 12/12 | 1103 | chr1 | 70251908 | ||||||
| chr1:70252320 | C | G | 1 | a0001c0001t0011 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1515C>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 12/12 | 1515 | chr1 | 70252320 | ||||||
| chr1:70252415 | G | A | 1 | a0001c0001t0002 | 11 | HG00738.hp2 HG01884.hp2 HG01934.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1610G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 12/12 | 1610 | chr1 | 70252415 | ||||||
| chr1:70252503 | A | G | 2 | a0001c0001t0005 a0001c0003t0010 |
4 | HG02622.hp2 NA18972.hp1 NA19000.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1698A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 12/12 | 1698 | chr1 | 70252503 | ||||||
| chr1:70252539 | T | C | 1 | a0001c0003t0010 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1734T>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 12/12 | 1734 | chr1 | 70252539 | ||||||
| chr1:70252712 | C | T | 1 | a0001c0001t0008 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1907C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 12/12 | 1907 | chr1 | 70252712 | ||||||
| chr1:70252724 | TG | T | 1 | a0001c0001t0003 | 4 | HG02976.hp2 HG03041.hp1 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1920delG | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 12/12 | 1920 | chr1 | 70252724 | ||||||
| chr1:70252769 | A | T | 1 | a0001c0001t0004 | 3 | HG02683.hp2 HG03710.hp1 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1964A>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 12/12 | 1964 | chr1 | 70252769 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:70221867 | T | C | 1 | a0001c0001t0001g0043 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.203+28T>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70221867 | |||||||
| chr1:70221962 | G | A | 4 | a0001c0001t0005g0045 a0001c0001t0005g0046 a0001c0001t0005g0047 others(1): Show |
4 | HG02622.hp2 NA18972.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.203+123G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70221962 | |||||||
| chr1:70222059 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.203+220C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70222059 | |||||||
| chr1:70222095 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.203+256A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70222095 | |||||||
| chr1:70222185 | G | C | 1 | a0001c0001t0001g0048 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.203+346G>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70222185 | |||||||
| chr1:70222204 | T | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(52): Show |
87 | HG00597.hp2 HG00621.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.203+365T>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70222204 | |||||||
| chr1:70222543 | T | C | 1 | a0001c0001t0001g0025 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.203+704T>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70222543 | |||||||
| chr1:70222684 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.203+845G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70222684 | |||||||
| chr1:70222778 | C | G | 2 | a0001c0001t0001g0236 a0001c0001t0001g0237 |
2 | NA18953.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.203+939C>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70222778 | |||||||
| chr1:70222869 | A | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(52): Show |
87 | HG00597.hp2 HG00621.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.203+1030A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70222869 | |||||||
| chr1:70222878 | C | G | 2 | a0001c0001t0006g0234 a0001c0001t0006g0235 |
2 | HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.203+1039C>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70222878 | |||||||
| chr1:70222973 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.203+1134G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70222973 | |||||||
| chr1:70223259 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.203+1420T>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70223259 | |||||||
| chr1:70223263 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.203+1424A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70223263 | |||||||
| chr1:70223281 | T | G | 4 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0090 others(1): Show |
5 | HG01346.hp2 HG03490.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.203+1442T>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70223281 | |||||||
| chr1:70223294 | C | T | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | NA18960.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.203+1455C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70223294 | |||||||
| chr1:70223532 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(52): Show |
87 | HG00597.hp2 HG00621.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.203+1693T>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70223532 | |||||||
| chr1:70223538 | A | C | 1 | a0001c0001t0001g0230 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.203+1699A>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70223538 | |||||||
| chr1:70223602 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.203+1763C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70223602 | |||||||
| chr1:70223994 | A | G | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(234): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.203+2155A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70223994 | |||||||
| chr1:70224077 | A | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(46): Show |
81 | HG00597.hp2 HG00621.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.203+2238A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70224077 | |||||||
| chr1:70224177 | G | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(52): Show |
87 | HG00597.hp2 HG00621.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.203+2338G>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70224177 | |||||||
| chr1:70224210 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.203+2371G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70224210 | |||||||
| chr1:70224339 | A | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(52): Show |
87 | HG00597.hp2 HG00621.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.203+2500A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70224339 | |||||||
| chr1:70224782 | G | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(58): Show |
94 | HG00597.hp2 HG00621.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.203+2943G>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70224782 | |||||||
| chr1:70224857 | C | T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(94): Show |
141 | HG00597.hp2 HG00621.hp1 HG00639.hp2 others(138): Show |
intron_variant | MODIFIER | c.203+3018C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70224857 | |||||||
| chr1:70224886 | T | C | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.203+3047T>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70224886 | |||||||
| chr1:70225215 | C | T | 5 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0004g0096 others(2): Show |
5 | HG02683.hp2 HG03225.hp2 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.204-3207C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70225215 | |||||||
| chr1:70225396 | A | G | 28 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(25): Show |
28 | HG00621.hp2 HG02738.hp1 HG03654.hp2 others(25): Show |
intron_variant | MODIFIER | c.204-3026A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70225396 | |||||||
| chr1:70225437 | T | G | 1 | a0001c0001t0001g0101 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.204-2985T>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70225437 | |||||||
| chr1:70225486 | G | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0102 a0001c0001t0001g0103 others(1): Show |
5 | HG02280.hp2 HG02486.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.204-2936G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70225486 | |||||||
| chr1:70225496 | A | T | 1 | a0001c0001t0001g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.204-2926A>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70225496 | |||||||
| chr1:70225564 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.204-2858G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70225564 | |||||||
| chr1:70225910 | CTT | C | 4 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(1): Show |
4 | HG02683.hp1 HG03017.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.204-2511_204-2510d others(4): Show |
SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70225910 | |||||||
| chr1:70226131 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0087 |
3 | HG02622.hp1 HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.204-2291C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70226131 | |||||||
| chr1:70226204 | A | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(52): Show |
87 | HG00597.hp2 HG00621.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.204-2218A>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70226204 | |||||||
| chr1:70226216 | A | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(52): Show |
87 | HG00597.hp2 HG00621.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.204-2206A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70226216 | |||||||
| chr1:70226309 | A | G | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.204-2113A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70226309 | |||||||
| chr1:70226874 | T | G | 3 | a0001c0001t0004g0096 a0001c0001t0004g0097 a0001c0001t0004g0098 |
3 | HG02683.hp2 HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.204-1548T>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70226874 | |||||||
| chr1:70226993 | A | C | 1 | a0001c0001t0001g0085 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.204-1429A>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70226993 | |||||||
| chr1:70227004 | A | G | 4 | a0001c0001t0005g0045 a0001c0001t0005g0046 a0001c0001t0005g0047 others(1): Show |
4 | HG02622.hp2 NA18972.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.204-1418A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70227004 | |||||||
| chr1:70227133 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.204-1289G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70227133 | |||||||
| chr1:70227404 | G | C | 1 | a0001c0001t0001g0026 | 2 | HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.204-1018G>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70227404 | |||||||
| chr1:70227479 | C | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.204-943C>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70227479 | |||||||
| chr1:70227502 | T | G | 1 | a0001c0001t0001g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.204-920T>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70227502 | |||||||
| chr1:70227903 | T | C | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.204-519T>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70227903 | |||||||
| chr1:70228048 | A | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(46): Show |
81 | HG00597.hp2 HG00621.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.204-374A>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70228048 | |||||||
| chr1:70228209 | G | C | 1 | a0001c0001t0001g0179 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.204-213G>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 1/11 | chr1 | 70228209 | |||||||
| chr1:70228876 | G | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0058 others(1): Show |
6 | HG00597.hp2 HG02129.hp2 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.337+321G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 2/11 | chr1 | 70228876 | |||||||
| chr1:70228998 | GA | G | 57 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(54): Show |
90 | HG00597.hp2 HG00621.hp1 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.337+455delA | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 70228998 | ||||||
| chr1:70229550 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.337+995C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 2/11 | chr1 | 70229550 | |||||||
| chr1:70229613 | A | T | 1 | a0001c0001t0002g0176 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.337+1058A>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 2/11 | chr1 | 70229613 | |||||||
| chr1:70229796 | A | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.337+1241A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 2/11 | chr1 | 70229796 | |||||||
| chr1:70229801 | T | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG01433.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.337+1246T>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 2/11 | chr1 | 70229801 | |||||||
| chr1:70229802 | A | G | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | NA19067.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.337+1247A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 2/11 | chr1 | 70229802 | |||||||
| chr1:70230130 | G | T | 1 | a0001c0001t0001g0175 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.337+1575G>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 2/11 | chr1 | 70230130 | |||||||
| chr1:70230270 | A | G | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | HG00140.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.337+1715A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 2/11 | chr1 | 70230270 | |||||||
| chr1:70230288 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.337+1733T>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 2/11 | chr1 | 70230288 | |||||||
| chr1:70230433 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.338-1835C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 2/11 | chr1 | 70230433 | |||||||
| chr1:70230849 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.338-1419A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 2/11 | chr1 | 70230849 | |||||||
| chr1:70231439 | CAGAT | C | 3 | a0001c0001t0004g0096 a0001c0001t0004g0097 a0001c0001t0004g0098 |
3 | HG02683.hp2 HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.338-827_338-824del others(4): Show |
SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 70231439 | ||||||
| chr1:70231694 | G | A | 1 | a0001c0003t0010g0044 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.338-574G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 2/11 | chr1 | 70231694 | |||||||
| chr1:70232636 | C | T | 3 | a0001c0001t0004g0096 a0001c0001t0004g0097 a0001c0001t0004g0098 |
3 | HG02683.hp2 HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.447+259C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 3/11 | chr1 | 70232636 | |||||||
| chr1:70232868 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.447+491T>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 3/11 | chr1 | 70232868 | |||||||
| chr1:70232943 | T | C | 1 | a0001c0001t0001g0110 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.447+566T>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 3/11 | chr1 | 70232943 | |||||||
| chr1:70233143 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.447+766C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 3/11 | chr1 | 70233143 | |||||||
| chr1:70233193 | A | C | 1 | a0001c0001t0001g0041 | 2 | HG02129.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.447+816A>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 3/11 | chr1 | 70233193 | |||||||
| chr1:70233215 | G | GT | 9 | a0001c0001t0001g0083 a0001c0001t0001g0171 a0001c0001t0001g0172 others(6): Show |
9 | HG01109.hp2 NA18941.hp1 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.447+847dupT | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 70233215 | ||||||
| chr1:70233298 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.447+921G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 3/11 | chr1 | 70233298 | |||||||
| chr1:70233373 | C | A | 1 | a0001c0001t0001g0111 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.447+996C>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 3/11 | chr1 | 70233373 | |||||||
| chr1:70233432 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0063 |
2 | HG01167.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.447+1055G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 3/11 | chr1 | 70233432 | |||||||
| chr1:70233509 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.447+1132G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 3/11 | chr1 | 70233509 | |||||||
| chr1:70233551 | A | G | 3 | a0001c0001t0004g0096 a0001c0001t0004g0097 a0001c0001t0004g0098 |
3 | HG02683.hp2 HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.448-1145A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 3/11 | chr1 | 70233551 | |||||||
| chr1:70233593 | A | G | 2 | a0001c0001t0004g0097 a0001c0001t0004g0098 |
2 | HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.448-1103A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 3/11 | chr1 | 70233593 | |||||||
| chr1:70233606 | A | C | 3 | a0001c0001t0004g0096 a0001c0001t0004g0097 a0001c0001t0004g0098 |
3 | HG02683.hp2 HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.448-1090A>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 3/11 | chr1 | 70233606 | |||||||
| chr1:70233664 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.448-1032A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 3/11 | chr1 | 70233664 | |||||||
| chr1:70233666 | A | G | 9 | a0001c0001t0001g0037 a0001c0001t0001g0167 a0001c0001t0001g0168 others(6): Show |
10 | HG00558.hp2 HG00609.hp2 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.448-1030A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 3/11 | chr1 | 70233666 | |||||||
| chr1:70233808 | A | C | 1 | a0001c0001t0001g0198 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.448-888A>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 3/11 | chr1 | 70233808 | |||||||
| chr1:70233880 | A | G | 2 | a0001c0001t0006g0234 a0001c0001t0006g0235 |
2 | HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.448-816A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 3/11 | chr1 | 70233880 | |||||||
| chr1:70233900 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.448-796A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 3/11 | chr1 | 70233900 | |||||||
| chr1:70234481 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.448-215T>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 3/11 | chr1 | 70234481 | |||||||
| chr1:70234508 | C | T | 4 | a0001c0001t0001g0207 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG02559.hp1 HG02630.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.448-188C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 3/11 | chr1 | 70234508 | |||||||
| chr1:70234808 | A | G | 3 | a0001c0001t0004g0096 a0001c0001t0004g0097 a0001c0001t0004g0098 |
3 | HG02683.hp2 HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.540+20A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 4/11 | chr1 | 70234808 | |||||||
| chr1:70234935 | C | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0165 |
3 | HG02896.hp2 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.540+147C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 4/11 | chr1 | 70234935 | |||||||
| chr1:70235000 | A | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(52): Show |
87 | HG00597.hp2 HG00621.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.540+212A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 4/11 | chr1 | 70235000 | |||||||
| chr1:70235019 | A | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(52): Show |
87 | HG00597.hp2 HG00621.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.540+231A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 4/11 | chr1 | 70235019 | |||||||
| chr1:70235257 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.541-244A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 4/11 | chr1 | 70235257 | |||||||
| chr1:70235319 | TTTTTG | T | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0163 others(1): Show |
4 | HG01884.hp1 HG02055.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.541-162_541-158del others(5): Show |
SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 70235319 | ||||||
| chr1:70235576 | T | G | 1 | a0001c0001t0006g0234 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.590+26T>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 5/11 | chr1 | 70235576 | |||||||
| chr1:70235668 | A | G | 1 | a0001c0001t0013g0224 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.590+118A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 5/11 | chr1 | 70235668 | |||||||
| chr1:70235687 | CAAG | C | 4 | a0001c0001t0005g0045 a0001c0001t0005g0046 a0001c0001t0005g0047 others(1): Show |
4 | HG02622.hp2 NA18972.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.590+138_590+140del others(3): Show |
SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 5/11 | chr1 | 70235687 | |||||||
| chr1:70235898 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.590+348G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 5/11 | chr1 | 70235898 | |||||||
| chr1:70236249 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0087 |
3 | HG02622.hp1 HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.590+699T>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 5/11 | chr1 | 70236249 | |||||||
| chr1:70236332 | C | CT | 8 | a0001c0001t0001g0016 a0001c0001t0001g0083 a0001c0001t0001g0159 others(5): Show |
10 | HG02486.hp1 HG02895.hp1 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.590+799dupT | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 70236332 | ||||||
| chr1:70236332 | CT | C | 8 | a0001c0001t0001g0012 a0001c0001t0001g0065 a0001c0001t0001g0066 others(5): Show |
11 | HG02572.hp1 HG02735.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.590+799delT | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 70236332 | ||||||
| chr1:70236391 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.590+841C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 5/11 | chr1 | 70236391 | |||||||
| chr1:70236414 | T | A | 1 | a0001c0001t0002g0113 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.590+864T>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 5/11 | chr1 | 70236414 | |||||||
| chr1:70236438 | C | A | 1 | a0001c0001t0001g0115 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.590+888C>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 5/11 | chr1 | 70236438 | |||||||
| chr1:70236453 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.590+903C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 5/11 | chr1 | 70236453 | |||||||
| chr1:70236517 | A | C | 1 | a0001c0001t0001g0064 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.591-908A>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 5/11 | chr1 | 70236517 | |||||||
| chr1:70236531 | C | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.591-894C>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 5/11 | chr1 | 70236531 | |||||||
| chr1:70236625 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.591-800C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 5/11 | chr1 | 70236625 | |||||||
| chr1:70236746 | C | T | 1 | a0001c0005t0001g0062 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.591-679C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 5/11 | chr1 | 70236746 | |||||||
| chr1:70236752 | A | G | 1 | a0001c0001t0001g0204 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.591-673A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 5/11 | chr1 | 70236752 | |||||||
| chr1:70236792 | A | AT | 72 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(69): Show |
104 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.591-604dupT | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 70236792 | ||||||
| chr1:70236792 | A | ATT | 15 | a0001c0001t0001g0018 a0001c0001t0001g0036 a0001c0001t0001g0153 others(12): Show |
18 | HG00099.hp1 HG02015.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.591-605_591-604dup others(2): Show |
SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 70236792 | ||||||
| chr1:70236792 | AT | A | 12 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0067 others(9): Show |
12 | HG00323.hp2 HG00735.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.591-604delT | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 70236792 | ||||||
| chr1:70236834 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.591-591C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 5/11 | chr1 | 70236834 | |||||||
| chr1:70236952 | T | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.591-473T>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 5/11 | chr1 | 70236952 | |||||||
| chr1:70236954 | G | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.591-471G>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 5/11 | chr1 | 70236954 | |||||||
| chr1:70237082 | G | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.591-343G>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 5/11 | chr1 | 70237082 | |||||||
| chr1:70237104 | A | G | 3 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 |
3 | HG00558.hp1 NA18747.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.591-321A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 5/11 | chr1 | 70237104 | |||||||
| chr1:70237176 | G | T | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | NA18960.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.591-249G>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 5/11 | chr1 | 70237176 | |||||||
| chr1:70237196 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.591-229A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 5/11 | chr1 | 70237196 | |||||||
| chr1:70237315 | T | G | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.591-110T>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 5/11 | chr1 | 70237315 | |||||||
| chr1:70237677 | A | G | 1 | a0001c0001t0001g0135 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.718+125A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 6/11 | chr1 | 70237677 | |||||||
| chr1:70237755 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0119 |
3 | HG00099.hp2 HG00323.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.718+203G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 6/11 | chr1 | 70237755 | |||||||
| chr1:70238039 | C | T | 29 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0035 others(26): Show |
43 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.718+487C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 6/11 | chr1 | 70238039 | |||||||
| chr1:70238302 | G | A | 4 | a0001c0001t0005g0045 a0001c0001t0005g0046 a0001c0001t0005g0047 others(1): Show |
4 | HG02622.hp2 NA18972.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.718+750G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 6/11 | chr1 | 70238302 | |||||||
| chr1:70238327 | A | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.718+775A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 6/11 | chr1 | 70238327 | |||||||
| chr1:70238381 | C | G | 1 | a0001c0005t0001g0062 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.718+829C>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 6/11 | chr1 | 70238381 | |||||||
| chr1:70238502 | A | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0087 |
3 | HG02622.hp1 HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.719-937A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 6/11 | chr1 | 70238502 | |||||||
| chr1:70238622 | A | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.719-817A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 6/11 | chr1 | 70238622 | |||||||
| chr1:70238692 | A | C | 1 | a0001c0001t0001g0238 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.719-747A>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 6/11 | chr1 | 70238692 | |||||||
| chr1:70238721 | G | C | 1 | a0001c0001t0001g0048 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.719-718G>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 6/11 | chr1 | 70238721 | |||||||
| chr1:70238754 | C | A | 4 | a0001c0001t0001g0207 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG02559.hp1 HG02630.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.719-685C>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 6/11 | chr1 | 70238754 | |||||||
| chr1:70239123 | A | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0119 |
3 | HG00099.hp2 HG00323.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.719-316A>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 6/11 | chr1 | 70239123 | |||||||
| chr1:70239243 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.719-196C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 6/11 | chr1 | 70239243 | |||||||
| chr1:70239318 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.719-121C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 6/11 | chr1 | 70239318 | |||||||
| chr1:70239327 | A | G | 1 | a0001c0001t0001g0033 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.719-112A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 6/11 | chr1 | 70239327 | |||||||
| chr1:70239632 | C | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(46): Show |
81 | HG00597.hp2 HG00621.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.800+112C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70239632 | |||||||
| chr1:70239770 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.800+250T>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70239770 | |||||||
| chr1:70239839 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.800+319A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70239839 | |||||||
| chr1:70239905 | T | G | 1 | a0001c0001t0001g0048 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.800+385T>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70239905 | |||||||
| chr1:70239908 | T | C | 1 | a0001c0001t0011g0140 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.800+388T>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70239908 | |||||||
| chr1:70239973 | A | C | 4 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0058 others(1): Show |
6 | HG00597.hp2 HG02129.hp2 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.800+453A>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70239973 | |||||||
| chr1:70240135 | T | C | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.800+615T>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70240135 | |||||||
| chr1:70240487 | C | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(57): Show |
93 | HG00597.hp2 HG00621.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.800+967C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70240487 | |||||||
| chr1:70240592 | TATTTC | T | 29 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0025 others(26): Show |
39 | HG01168.hp2 HG01192.hp1 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.800+1074_800+1078d others(7): Show |
SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 70240592 | ||||||
| chr1:70240750 | C | A | 1 | a0001c0001t0001g0053 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.800+1230C>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70240750 | |||||||
| chr1:70240770 | C | CT | 21 | a0001c0001t0001g0032 a0001c0001t0001g0043 a0001c0001t0001g0050 others(18): Show |
22 | HG00597.hp1 HG01192.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.800+1272dupT | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 70240770 | ||||||
| chr1:70240770 | C | CTT | 9 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0189 others(6): Show |
9 | HG02622.hp2 NA18952.hp2 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.800+1271_800+1272d others(4): Show |
SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 70240770 | ||||||
| chr1:70240770 | CT | C | 57 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(54): Show |
90 | HG00597.hp2 HG00621.hp1 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.800+1272delT | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 70240770 | ||||||
| chr1:70240831 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.800+1311A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70240831 | |||||||
| chr1:70240834 | G | C | 2 | a0001c0001t0001g0061 a0001c0005t0001g0062 |
2 | HG02895.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.800+1314G>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70240834 | |||||||
| chr1:70240862 | G | A | 15 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0039 others(12): Show |
23 | HG01168.hp2 HG01192.hp1 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.800+1342G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70240862 | |||||||
| chr1:70241261 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.800+1741C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70241261 | |||||||
| chr1:70241356 | C | CA | 2 | a0001c0001t0001g0038 a0001c0001t0001g0165 |
3 | HG02896.hp2 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.800+1837dupA | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 70241356 | ||||||
| chr1:70241404 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.800+1884G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70241404 | |||||||
| chr1:70241503 | C | T | 1 | a0001c0001t0002g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.800+1983C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70241503 | |||||||
| chr1:70241578 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.800+2058G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70241578 | |||||||
| chr1:70241598 | C | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.800+2078C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70241598 | |||||||
| chr1:70241627 | G | A | 1 | a0001c0001t0001g0026 | 2 | HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.800+2107G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70241627 | |||||||
| chr1:70241774 | T | C | 3 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0001g0171 |
3 | HG00735.hp1 HG01109.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.800+2254T>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70241774 | |||||||
| chr1:70242099 | G | A | 2 | a0001c0001t0001g0123 a0001c0001t0001g0144 |
2 | NA18992.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.800+2579G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70242099 | |||||||
| chr1:70242165 | T | TA | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(85): Show |
130 | HG00597.hp2 HG00621.hp1 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.801-2503dupA | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 70242165 | ||||||
| chr1:70242226 | T | G | 2 | a0001c0001t0001g0032 a0001c0001t0001g0109 |
3 | HG01192.hp2 HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.801-2458T>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70242226 | |||||||
| chr1:70242353 | C | T | 4 | a0001c0001t0005g0045 a0001c0001t0005g0046 a0001c0001t0005g0047 others(1): Show |
4 | HG02622.hp2 NA18972.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.801-2331C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70242353 | |||||||
| chr1:70242392 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.801-2292C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70242392 | |||||||
| chr1:70242472 | C | CTTTTTTT others(5): Show |
5 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0051 others(2): Show |
6 | HG00639.hp2 HG01256.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.801-2202_801-2201i others(14): Show |
SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 70242472 | ||||||
| chr1:70242472 | C | CTTTTTTT others(6): Show |
66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(63): Show |
108 | HG00597.hp2 HG00621.hp1 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.801-2202_801-2201i others(15): Show |
SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 70242472 | ||||||
| chr1:70242472 | C | CTTTTTTT others(7): Show |
13 | a0001c0001t0001g0048 a0001c0001t0001g0066 a0001c0001t0001g0073 others(10): Show |
13 | HG01978.hp2 HG02145.hp1 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.801-2202_801-2201i others(16): Show |
SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 70242472 | ||||||
| chr1:70242472 | C | CTTTTTTT others(8): Show |
5 | a0001c0001t0004g0096 a0001c0001t0004g0098 a0001c0001t0005g0045 others(2): Show |
5 | HG02622.hp2 HG02683.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.801-2202_801-2201i others(17): Show |
SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 70242472 | ||||||
| chr1:70242689 | A | G | 2 | a0001c0001t0004g0097 a0001c0001t0004g0098 |
2 | HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.801-1995A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70242689 | |||||||
| chr1:70242739 | T | G | 2 | a0001c0001t0006g0234 a0001c0001t0006g0235 |
2 | HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.801-1945T>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70242739 | |||||||
| chr1:70242848 | T | C | 6 | a0001c0001t0001g0022 a0001c0001t0001g0072 a0001c0001t0001g0076 others(3): Show |
7 | HG01943.hp2 HG01975.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.801-1836T>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70242848 | |||||||
| chr1:70242856 | AGGCAGTG others(8): Show |
A | 1 | a0001c0001t0003g0124 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.801-1826_801-1812d others(17): Show |
SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 70242856 | ||||||
| chr1:70242873 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.801-1811C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70242873 | |||||||
| chr1:70243336 | C | CA | 7 | a0001c0001t0001g0035 a0001c0001t0001g0120 a0001c0001t0001g0133 others(4): Show |
8 | HG01361.hp1 HG01433.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.801-1311dupA | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 70243336 | ||||||
| chr1:70243336 | CA | C | 33 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0029 others(30): Show |
43 | HG00323.hp1 HG00558.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.801-1311delA | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 70243336 | ||||||
| chr1:70243336 | CAA | C | 45 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(42): Show |
65 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.801-1312_801-1311d others(4): Show |
SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 70243336 | ||||||
| chr1:70243336 | CAAA | C | 46 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0018 others(43): Show |
59 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.801-1313_801-1311d others(5): Show |
SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 70243336 | ||||||
| chr1:70243336 | CAAAA | C | 21 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(18): Show |
39 | HG00597.hp2 HG00741.hp2 HG01123.hp2 others(36): Show |
intron_variant | MODIFIER | c.801-1314_801-1311d others(6): Show |
SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 70243336 | ||||||
| chr1:70243336 | CAAAAA | C | 19 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0032 others(16): Show |
28 | HG00621.hp1 HG00639.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.801-1315_801-1311d others(7): Show |
SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 70243336 | ||||||
| chr1:70243336 | CAAAAAA | C | 22 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0014 others(19): Show |
40 | HG01943.hp2 HG01975.hp2 HG02015.hp1 others(37): Show |
intron_variant | MODIFIER | c.801-1316_801-1311d others(8): Show |
SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 70243336 | ||||||
| chr1:70243336 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.801-1320_801-1311d others(12): Show |
SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 70243336 | ||||||
| chr1:70243336 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0158 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.801-1322_801-1311d others(14): Show |
SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 70243336 | ||||||
| chr1:70243336 | CAAAAAAA others(9): Show |
C | 4 | a0001c0001t0001g0129 a0001c0001t0001g0226 a0001c0001t0005g0047 others(1): Show |
4 | HG01081.hp1 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.801-1326_801-1311d others(18): Show |
SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 70243336 | ||||||
| chr1:70243336 | CAAAAAAA others(10): Show |
C | 8 | a0001c0001t0001g0042 a0001c0001t0001g0061 a0001c0001t0001g0087 others(5): Show |
9 | HG02622.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.801-1327_801-1311d others(19): Show |
SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 70243336 | ||||||
| chr1:70243336 | CAAAAAAA others(11): Show |
C | 10 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0130 others(7): Show |
15 | HG01123.hp1 HG01261.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.801-1328_801-1311d others(20): Show |
SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 70243336 | ||||||
| chr1:70243336 | CAAAAAAA others(14): Show |
C | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.801-1331_801-1311d others(23): Show |
SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 70243336 | ||||||
| chr1:70243336 | CAAAAAAA others(15): Show |
C | 1 | a0001c0001t0001g0031 | 2 | HG01167.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.801-1332_801-1311d others(24): Show |
SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 70243336 | ||||||
| chr1:70243359 | A | C | 1 | a0001c0001t0001g0230 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.801-1325A>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70243359 | |||||||
| chr1:70243385 | G | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(58): Show |
94 | HG00597.hp2 HG00621.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.801-1299G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70243385 | |||||||
| chr1:70243686 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.801-998G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70243686 | |||||||
| chr1:70243816 | A | C | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.801-868A>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70243816 | |||||||
| chr1:70244036 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.801-648T>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70244036 | |||||||
| chr1:70244068 | A | G | 4 | a0001c0001t0005g0045 a0001c0001t0005g0046 a0001c0001t0005g0047 others(1): Show |
4 | HG02622.hp2 NA18972.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.801-616A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70244068 | |||||||
| chr1:70244076 | G | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(58): Show |
94 | HG00597.hp2 HG00621.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.801-608G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70244076 | |||||||
| chr1:70244111 | G | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0087 |
3 | HG02622.hp1 HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.801-573G>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70244111 | |||||||
| chr1:70244129 | A | T | 4 | a0001c0001t0005g0045 a0001c0001t0005g0046 a0001c0001t0005g0047 others(1): Show |
4 | HG02622.hp2 NA18972.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.801-555A>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70244129 | |||||||
| chr1:70244141 | G | T | 1 | a0001c0001t0001g0082 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.801-543G>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | chr1 | 70244141 | |||||||
| chr1:70244495 | AAAGGTAT others(11): Show |
A | 3 | a0001c0001t0004g0096 a0001c0001t0004g0097 a0001c0001t0004g0098 |
3 | HG02683.hp2 HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.801-183_801-166del others(18): Show |
SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 70244495 | ||||||
| chr1:70244890 | G | T | 46 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(43): Show |
78 | HG00597.hp2 HG00621.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.932+75G>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 8/11 | chr1 | 70244890 | |||||||
| chr1:70245016 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0074 |
4 | NA18965.hp2 NA18974.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.932+201G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 8/11 | chr1 | 70245016 | |||||||
| chr1:70245126 | C | G | 1 | a0001c0001t0001g0147 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.932+311C>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 8/11 | chr1 | 70245126 | |||||||
| chr1:70245135 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.932+320C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 8/11 | chr1 | 70245135 | |||||||
| chr1:70245136 | G | A | 3 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 |
3 | HG00558.hp1 NA18747.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.932+321G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 8/11 | chr1 | 70245136 | |||||||
| chr1:70245160 | T | TATAAATT others(26): Show |
2 | a0001c0001t0001g0127 a0001c0001t0001g0185 |
2 | NA18949.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.932+346_932+347ins others(33): Show |
SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 70245160 | ||||||
| chr1:70245162 | G | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0185 |
2 | NA18949.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.932+347G>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 8/11 | chr1 | 70245162 | |||||||
| chr1:70245170 | C | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0185 |
2 | NA18949.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.932+355C>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 8/11 | chr1 | 70245170 | |||||||
| chr1:70245266 | T | C | 1 | a0001c0001t0001g0172 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.932+451T>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 8/11 | chr1 | 70245266 | |||||||
| chr1:70245363 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.932+548C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 8/11 | chr1 | 70245363 | |||||||
| chr1:70245469 | G | C | 1 | a0001c0001t0001g0229 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.932+654G>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 8/11 | chr1 | 70245469 | |||||||
| chr1:70245553 | A | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(94): Show |
141 | HG00597.hp2 HG00621.hp1 HG00639.hp2 others(138): Show |
intron_variant | MODIFIER | c.932+738A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 8/11 | chr1 | 70245553 | |||||||
| chr1:70245615 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.932+800G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 8/11 | chr1 | 70245615 | |||||||
| chr1:70245740 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.932+925G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 8/11 | chr1 | 70245740 | |||||||
| chr1:70245962 | G | A | 2 | a0001c0001t0001g0167 a0001c0001t0001g0178 |
2 | NA18943.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.933-856G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 8/11 | chr1 | 70245962 | |||||||
| chr1:70246175 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.933-643G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 8/11 | chr1 | 70246175 | |||||||
| chr1:70246262 | T | TA | 45 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(42): Show |
77 | HG00597.hp2 HG00621.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.933-544dupA | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 70246262 | ||||||
| chr1:70246693 | T | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.933-125T>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 8/11 | chr1 | 70246693 | |||||||
| chr1:70247037 | GTTAT | G | 4 | a0001c0001t0005g0045 a0001c0001t0005g0046 a0001c0001t0005g0047 others(1): Show |
4 | HG02622.hp2 NA18972.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.1022+134_1022+137d others(6): Show |
SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 70247037 | ||||||
| chr1:70247069 | A | C | 3 | a0001c0001t0005g0045 a0001c0001t0005g0046 a0001c0001t0005g0047 |
3 | NA18972.hp1 NA19000.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1022+162A>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 9/11 | chr1 | 70247069 | |||||||
| chr1:70247228 | A | C | 2 | a0001c0001t0002g0126 a0001c0001t0002g0146 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1022+321A>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 9/11 | chr1 | 70247228 | |||||||
| chr1:70247428 | A | G | 1 | a0001c0001t0001g0038 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1022+521A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 9/11 | chr1 | 70247428 | |||||||
| chr1:70247503 | A | G | 2 | a0001c0001t0006g0234 a0001c0001t0006g0235 |
2 | HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1022+596A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 9/11 | chr1 | 70247503 | |||||||
| chr1:70247702 | G | A | 6 | a0001c0001t0002g0030 a0001c0001t0002g0034 a0001c0001t0002g0113 others(3): Show |
8 | HG00738.hp2 HG01884.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1022+795G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 9/11 | chr1 | 70247702 | |||||||
| chr1:70247884 | A | G | 2 | a0001c0001t0003g0017 a0001c0001t0003g0124 |
4 | HG02976.hp2 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1022+977A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 9/11 | chr1 | 70247884 | |||||||
| chr1:70248208 | T | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(46): Show |
81 | HG00597.hp2 HG00621.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.1022+1301T>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 9/11 | chr1 | 70248208 | |||||||
| chr1:70248330 | A | G | 28 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0025 others(25): Show |
38 | HG01168.hp2 HG01192.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.1022+1423A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 9/11 | chr1 | 70248330 | |||||||
| chr1:70248368 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1022+1461A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 9/11 | chr1 | 70248368 | |||||||
| chr1:70248532 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(52): Show |
87 | HG00597.hp2 HG00621.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.1023-1420T>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 9/11 | chr1 | 70248532 | |||||||
| chr1:70248647 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1023-1305C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 9/11 | chr1 | 70248647 | |||||||
| chr1:70248934 | T | C | 2 | a0001c0001t0001g0186 a0001c0002t0001g0183 |
2 | NA18951.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.1023-1018T>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 9/11 | chr1 | 70248934 | |||||||
| chr1:70248939 | A | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0119 |
3 | HG00099.hp2 HG00323.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.1023-1013A>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 9/11 | chr1 | 70248939 | |||||||
| chr1:70248959 | CACAGAGG others(17): Show |
C | 1 | a0001c0001t0001g0156 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1023-991_1023-968d others(26): Show |
SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 70248959 | ||||||
| chr1:70248959 | CACAGAGG others(18): Show |
C | 2 | a0001c0001t0001g0151 a0001c0001t0001g0157 |
2 | NA19003.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1023-991_1023-967d others(27): Show |
SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 70248959 | ||||||
| chr1:70248967 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1023-985G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 9/11 | chr1 | 70248967 | |||||||
| chr1:70248984 | A | T | 1 | a0001c0001t0001g0156 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1023-968A>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 9/11 | chr1 | 70248984 | |||||||
| chr1:70248985 | A | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0157 |
2 | NA19003.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1023-967A>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 9/11 | chr1 | 70248985 | |||||||
| chr1:70248987 | G | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0157 |
2 | NA19003.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1023-965G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 9/11 | chr1 | 70248987 | |||||||
| chr1:70248988 | C | T | 3 | a0001c0001t0001g0151 a0001c0001t0001g0156 a0001c0001t0001g0157 |
3 | NA19003.hp1 NA19066.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1023-964C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 9/11 | chr1 | 70248988 | |||||||
| chr1:70249410 | G | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(58): Show |
94 | HG00597.hp2 HG00621.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.1023-542G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 9/11 | chr1 | 70249410 | |||||||
| chr1:70249484 | A | G | 6 | a0001c0001t0001g0042 a0001c0001t0001g0087 a0001c0001t0001g0207 others(3): Show |
7 | HG02559.hp1 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1023-468A>G | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 9/11 | chr1 | 70249484 | |||||||
| chr1:70249582 | G | A | 1 | a0001c0001t0003g0017 | 3 | HG02976.hp2 HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1023-370G>A | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 9/11 | chr1 | 70249582 | |||||||
| chr1:70249855 | T | C | 1 | a0001c0001t0002g0113 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1023-97T>C | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 9/11 | chr1 | 70249855 | |||||||
| chr1:70250201 | C | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(58): Show |
94 | HG00597.hp2 HG00621.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.1118+154C>T | SRSF11 | ENSG00000116754.14 | transcript | ENST00000370949.2 | protein_coding | 10/11 | chr1 | 70250201 |