Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6429 |
| ensemblid | ENSG00000116350.18 |
| hgncid | 10786 |
| symbol | SRSF4 |
| name | serine and arginine rich splicing factor 4 |
| refseq_nuc | NM_005626.5 |
| refseq_prot | NP_005617.2 |
| ensembl_nuc | ENST00000373795.7 |
| ensembl_prot | ENSP00000362900.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 29147743 |
| end | 29181900 |
| strand | - |
| ver | v1.2 |
| region | chr1:29147743-29181900 |
| region5000 | chr1:29142743-29186900 |
| regionname0 | SRSF4_chr1_29147743_29181900 |
| regionname5000 | SRSF4_chr1_29142743_29186900 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 494 | 140 | 47 | 45 | 23 | 6 | 19 | 18 | SRSF4_chr1_29142743_29186900 | SRSF4 | MPRVY others(489): Show |
chr1 | 29142743 | 29186900 |
| a0002 | 1/1 | 494 | 125 | 24 | 21 | 71 | 0 | 7 | 53 | SRSF4_chr1_29142743_29186900 | SRSF4 | MPRVY others(489): Show |
chr1 | 29142743 | 29186900 |
| a0003 | 0/0 | 494 | 95 | 12 | 8 | 63 | 2 | 10 | 46 | SRSF4_chr1_29142743_29186900 | SRSF4 | MPRVY others(489): Show |
chr1 | 29142743 | 29186900 |
| a0004 | 0/0 | 494 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | MPRVY others(489): Show |
chr1 | 29142743 | 29186900 |
| a0005 | 0/0 | 494 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | MPRVY others(489): Show |
chr1 | 29142743 | 29186900 |
| a0006 | 0/0 | 494 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | MPRVY others(489): Show |
chr1 | 29142743 | 29186900 |
| a0007 | 0/0 | 494 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | MPRVY others(489): Show |
chr1 | 29142743 | 29186900 |
| a0008 | 0/0 | 494 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | MPRVY others(489): Show |
chr1 | 29142743 | 29186900 |
| a0009 | 0/0 | 494 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | MPRVY others(489): Show |
chr1 | 29142743 | 29186900 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1482 | 140 | 47 | 45 | 23 | 6 | 19 | SRSF4_chr1_29142743_29186900 | SRSF4 | ATGCC others(1477): Show |
chr1 | 29142743 | 29186900 | ||
| a0002c0002 | 1/1 | 1482 | 125 | 24 | 21 | 71 | 0 | 7 | SRSF4_chr1_29142743_29186900 | SRSF4 | ATGCC others(1477): Show |
chr1 | 29142743 | 29186900 | ||
| a0003c0003 | 0/0 | 1482 | 87 | 12 | 8 | 55 | 2 | 10 | SRSF4_chr1_29142743_29186900 | SRSF4 | ATGCC others(1477): Show |
chr1 | 29142743 | 29186900 | ||
| a0003c0004 | 0/0 | 1482 | 8 | 0 | 0 | 8 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | ATGCC others(1477): Show |
chr1 | 29142743 | 29186900 | ||
| a0004c0006 | 0/0 | 1482 | 2 | 0 | 2 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | ATGCC others(1477): Show |
chr1 | 29142743 | 29186900 | ||
| a0005c0005 | 0/0 | 1482 | 2 | 1 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | ATGCC others(1477): Show |
chr1 | 29142743 | 29186900 | ||
| a0006c0009 | 0/0 | 1482 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | ATGCC others(1477): Show |
chr1 | 29142743 | 29186900 | ||
| a0007c0008 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | ATGCC others(1477): Show |
chr1 | 29142743 | 29186900 | ||
| a0008c0010 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | ATGCC others(1477): Show |
chr1 | 29142743 | 29186900 | ||
| a0009c0007 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | ATGCC others(1477): Show |
chr1 | 29142743 | 29186900 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2300 | 68 | 18 | 22 | 15 | 3 | 10 | SRSF4_chr1_29142743_29186900 | SRSF4 | GCGTG others(2295): Show |
chr1 | 29142743 | 29186900 |
| a0001c0001t0002 | 0/0 | 2300 | 42 | 8 | 16 | 8 | 1 | 9 | SRSF4_chr1_29142743_29186900 | SRSF4 | GCGTG others(2295): Show |
chr1 | 29142743 | 29186900 |
| a0001c0001t0003 | 0/0 | 2300 | 30 | 21 | 7 | 0 | 2 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | GCGTG others(2295): Show |
chr1 | 29142743 | 29186900 |
| a0002c0002t0001 | 1/1 | 2300 | 118 | 24 | 21 | 64 | 0 | 7 | SRSF4_chr1_29142743_29186900 | SRSF4 | GCGTG others(2295): Show |
chr1 | 29142743 | 29186900 |
| a0002c0002t0004 | 0/0 | 2300 | 2 | 0 | 0 | 2 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | GCGTG others(2295): Show |
chr1 | 29142743 | 29186900 |
| a0002c0002t0005 | 0/0 | 2300 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | CCGTG others(2295): Show |
chr1 | 29142743 | 29186900 |
| a0002c0002t0006 | 0/0 | 2300 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | GCGTG others(2295): Show |
chr1 | 29142743 | 29186900 |
| a0002c0002t0007 | 0/0 | 2300 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | GCGTG others(2295): Show |
chr1 | 29142743 | 29186900 |
| a0002c0002t0008 | 0/0 | 2300 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | GCGTG others(2295): Show |
chr1 | 29142743 | 29186900 |
| a0002c0002t0009 | 0/0 | 2325 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | GCGTG others(2320): Show |
chr1 | 29142743 | 29186900 |
| a0003c0003t0001 | 0/0 | 2300 | 87 | 12 | 8 | 55 | 2 | 10 | SRSF4_chr1_29142743_29186900 | SRSF4 | GCGTG others(2295): Show |
chr1 | 29142743 | 29186900 |
| a0003c0004t0001 | 0/0 | 2300 | 8 | 0 | 0 | 8 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | GCGTG others(2295): Show |
chr1 | 29142743 | 29186900 |
| a0004c0006t0001 | 0/0 | 2300 | 2 | 0 | 2 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | GCGTG others(2295): Show |
chr1 | 29142743 | 29186900 |
| a0005c0005t0001 | 0/0 | 2300 | 2 | 1 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | GCGTG others(2295): Show |
chr1 | 29142743 | 29186900 |
| a0006c0009t0001 | 0/0 | 2300 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | GCGTG others(2295): Show |
chr1 | 29142743 | 29186900 |
| a0007c0008t0001 | 0/0 | 2300 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | GCGTG others(2295): Show |
chr1 | 29142743 | 29186900 |
| a0008c0010t0001 | 0/0 | 2300 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | GCGTG others(2295): Show |
chr1 | 29142743 | 29186900 |
| a0009c0007t0002 | 0/0 | 2300 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | GCGTG others(2295): Show |
chr1 | 29142743 | 29186900 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0003g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0001 | 0/0 | 8 | 1 | 2 | 5 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0003 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0215 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0001g0321 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0005g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0006g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0007g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0008g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0002c0002t0009g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0003t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0004t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0004t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0004t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0004t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0004t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0003c0004t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0004c0006t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0004c0006t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0005c0005t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0005c0005t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0006c0009t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0007c0008t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0008c0010t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| a0009c0007t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0082 | EUR | FIN | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | FIN | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG00408 | hp1 | a0003 | c0003 | t0001 | g0315 | EAS | CHS | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG00423 | hp1 | a0003 | c0003 | t0001 | g0025 | EAS | CHS | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG00423 | hp2 | a0003 | c0004 | t0001 | g0249 | EAS | CHS | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG00544 | hp2 | a0003 | c0003 | t0001 | g0281 | EAS | CHS | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | CHS | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG00558 | hp2 | a0003 | c0003 | t0001 | g0297 | EAS | CHS | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG00597 | hp2 | a0003 | c0003 | t0001 | g0027 | EAS | CHS | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0239 | EAS | CHS | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | CHS | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG00621 | hp1 | a0003 | c0003 | t0001 | g0282 | EAS | CHS | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0227 | EAS | CHS | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG00639 | hp1 | a0003 | c0003 | t0001 | g0254 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG00639 | hp2 | a0003 | c0003 | t0001 | g0309 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0222 | EAS | CHS | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG00673 | hp2 | a0003 | c0003 | t0001 | g0026 | EAS | CHS | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0020 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG00733 | hp2 | a0003 | c0003 | t0001 | g0100 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0193 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0076 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0158 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0020 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0208 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01106 | hp1 | a0006 | c0009 | t0001 | g0177 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0087 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01168 | hp1 | a0003 | c0003 | t0001 | g0294 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0093 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0091 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01175 | hp1 | a0003 | c0003 | t0001 | g0256 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0075 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | CLM | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01256 | hp1 | a0004 | c0006 | t0001 | g0311 | AMR | CLM | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0188 | AMR | CLM | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01258 | hp2 | a0004 | c0006 | t0001 | g0291 | AMR | CLM | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0217 | AMR | CLM | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0169 | AMR | CLM | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | CLM | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0234 | AMR | CLM | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0085 | AMR | CLM | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0172 | AMR | CLM | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01433 | hp1 | a0003 | c0003 | t0001 | g0028 | AMR | CLM | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0204 | AMR | CLM | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01515 | hp1 | a0003 | c0003 | t0001 | g0287 | EUR | IBS | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0121 | EUR | IBS | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0211 | AFR | ACB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0089 | AFR | ACB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01891 | hp2 | a0003 | c0003 | t0001 | g0265 | AFR | ACB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0238 | AMR | PEL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01934 | hp2 | a0005 | c0005 | t0001 | g0314 | AMR | PEL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0185 | AMR | PEL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01952 | hp1 | a0003 | c0003 | t0001 | g0316 | AMR | PEL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0218 | AMR | PEL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01975 | hp1 | a0003 | c0003 | t0001 | g0305 | AMR | PEL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0191 | AMR | PEL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PEL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0205 | AMR | PEL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0018 | AMR | PEL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02015 | hp2 | a0003 | c0004 | t0001 | g0247 | EAS | KHV | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0243 | EAS | KHV | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | KHV | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02055 | hp1 | a0003 | c0003 | t0001 | g0099 | AFR | ACB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0086 | AFR | ACB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02056 | hp1 | a0003 | c0003 | t0001 | g0260 | EAS | KHV | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | KHV | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02071 | hp1 | a0003 | c0003 | t0001 | g0262 | EAS | KHV | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0220 | EAS | KHV | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | KHV | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02074 | hp2 | a0003 | c0003 | t0001 | g0027 | EAS | KHV | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0225 | EAS | KHV | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02080 | hp2 | a0003 | c0003 | t0001 | g0253 | EAS | KHV | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0233 | EAS | KHV | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02132 | hp2 | a0003 | c0003 | t0001 | g0251 | EAS | KHV | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | ACB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0235 | AFR | ACB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CDX | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0203 | EAS | CDX | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02165 | hp1 | a0002 | c0002 | t0004 | g0214 | EAS | CDX | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02165 | hp2 | a0003 | c0003 | t0001 | g0252 | EAS | CDX | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | ACB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0178 | AFR | ACB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | ACB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0221 | AFR | ACB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | ACB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0189 | AFR | ACB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0224 | AMR | PEL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02451 | hp1 | a0003 | c0003 | t0001 | g0098 | AFR | ACB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0090 | AFR | ACB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | PJL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02622 | hp1 | a0003 | c0003 | t0001 | g0029 | AFR | GWD | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | GWD | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | GWD | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0229 | AFR | GWD | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0023 | SAS | PJL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02698 | hp1 | a0003 | c0003 | t0001 | g0267 | SAS | PJL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0210 | SAS | PJL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0182 | AFR | GWD | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0080 | AFR | GWD | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0237 | SAS | PJL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02809 | hp1 | a0003 | c0003 | t0001 | g0307 | AFR | GWD | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0081 | AFR | GWD | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02886 | hp2 | a0003 | c0003 | t0001 | g0029 | AFR | GWD | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0024 | AFR | GWD | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0094 | AFR | GWD | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0184 | AFR | GWD | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0092 | AFR | GWD | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0183 | AFR | ESN | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0088 | AFR | ESN | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0163 | AFR | ESN | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02970 | hp2 | a0003 | c0003 | t0001 | g0101 | AFR | ESN | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | ESN | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0084 | AFR | ESN | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03017 | hp1 | a0003 | c0003 | t0001 | g0313 | SAS | PJL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03041 | hp1 | a0003 | c0003 | t0001 | g0263 | AFR | GWD | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0070 | AFR | MSL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0179 | AFR | MSL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03130 | hp1 | a0003 | c0003 | t0001 | g0319 | AFR | ESN | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | ESN | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0186 | AFR | ESN | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0180 | AFR | ESN | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0078 | AFR | MSL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0095 | AFR | MSL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0162 | AFR | MSL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0071 | AFR | MSL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0181 | AFR | MSL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0063 | SAS | PJL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0023 | SAS | PJL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0241 | SAS | PJL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0199 | SAS | PJL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | ESN | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0077 | AFR | GWD | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | MSL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03669 | hp1 | a0003 | c0003 | t0001 | g0301 | SAS | PJL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | PJL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03704 | hp1 | a0003 | c0003 | t0001 | g0299 | SAS | PJL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03710 | hp1 | a0003 | c0003 | t0001 | g0300 | SAS | PJL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03834 | hp2 | a0003 | c0003 | t0001 | g0276 | SAS | BEB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0174 | SAS | BEB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03927 | hp2 | a0003 | c0003 | t0001 | g0266 | SAS | BEB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG04115 | hp1 | a0003 | c0003 | t0001 | g0303 | SAS | STU | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | STU | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG04184 | hp1 | a0003 | c0003 | t0001 | g0258 | SAS | BEB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | BEB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0055 | SAS | STU | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | STU | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0212 | AFR | YRI | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18522 | hp2 | a0003 | c0003 | t0001 | g0308 | AFR | YRI | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18747 | hp1 | a0003 | c0003 | t0001 | g0280 | EAS | CHB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18747 | hp2 | a0003 | c0003 | t0001 | g0277 | EAS | CHB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0176 | AFR | YRI | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18940 | hp1 | a0003 | c0004 | t0001 | g0245 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0226 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18942 | hp1 | a0003 | c0003 | t0001 | g0259 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18943 | hp1 | a0003 | c0003 | t0001 | g0255 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18948 | hp2 | a0003 | c0003 | t0001 | g0310 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18949 | hp1 | a0003 | c0003 | t0001 | g0279 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18950 | hp1 | a0003 | c0004 | t0001 | g0007 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18953 | hp1 | a0007 | c0008 | t0001 | g0206 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18953 | hp2 | a0003 | c0003 | t0001 | g0295 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18954 | hp2 | a0003 | c0003 | t0001 | g0268 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18956 | hp1 | a0003 | c0003 | t0001 | g0304 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18961 | hp2 | a0003 | c0003 | t0001 | g0288 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18962 | hp2 | a0003 | c0003 | t0001 | g0200 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18964 | hp1 | a0003 | c0003 | t0001 | g0278 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18969 | hp2 | a0003 | c0003 | t0001 | g0284 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18973 | hp1 | a0002 | c0002 | t0005 | g0219 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18973 | hp2 | a0003 | c0003 | t0001 | g0290 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18977 | hp2 | a0003 | c0003 | t0001 | g0261 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18979 | hp1 | a0003 | c0003 | t0001 | g0270 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18980 | hp1 | a0003 | c0003 | t0001 | g0275 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18981 | hp2 | a0003 | c0003 | t0001 | g0025 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18984 | hp2 | a0003 | c0003 | t0001 | g0008 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18986 | hp1 | a0003 | c0003 | t0001 | g0271 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18986 | hp2 | a0002 | c0002 | t0004 | g0213 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18988 | hp1 | a0003 | c0003 | t0001 | g0293 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18989 | hp1 | a0003 | c0003 | t0001 | g0286 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18993 | hp1 | a0003 | c0003 | t0001 | g0272 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18995 | hp1 | a0003 | c0003 | t0001 | g0283 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19001 | hp2 | a0003 | c0003 | t0001 | g0250 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19004 | hp2 | a0003 | c0003 | t0001 | g0257 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19005 | hp1 | a0002 | c0002 | t0008 | g0322 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19005 | hp2 | a0003 | c0004 | t0001 | g0007 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19010 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19011 | hp1 | a0003 | c0003 | t0001 | g0008 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19012 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19012 | hp2 | a0003 | c0004 | t0001 | g0246 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0024 | AFR | LWK | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | LWK | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19056 | hp2 | a0003 | c0003 | t0001 | g0292 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19057 | hp1 | a0002 | c0002 | t0006 | g0244 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19057 | hp2 | a0003 | c0004 | t0001 | g0248 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19060 | hp1 | a0002 | c0002 | t0009 | g0323 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19063 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19063 | hp2 | a0002 | c0002 | t0007 | g0240 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19065 | hp1 | a0003 | c0003 | t0001 | g0008 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19067 | hp2 | a0003 | c0003 | t0001 | g0264 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19072 | hp1 | a0003 | c0003 | t0001 | g0273 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19074 | hp1 | a0003 | c0004 | t0001 | g0007 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19079 | hp2 | a0008 | c0010 | t0001 | g0289 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19080 | hp2 | a0003 | c0003 | t0001 | g0274 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19081 | hp2 | a0003 | c0003 | t0001 | g0298 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19084 | hp1 | a0003 | c0003 | t0001 | g0306 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19085 | hp1 | a0003 | c0003 | t0001 | g0028 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19085 | hp2 | a0009 | c0007 | t0002 | g0060 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19087 | hp1 | a0003 | c0003 | t0001 | g0296 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0242 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19089 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19090 | hp2 | a0003 | c0003 | t0001 | g0026 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19240 | hp1 | a0003 | c0003 | t0001 | g0102 | AFR | YRI | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0072 | AFR | YRI | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ASW | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | ASW | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | TSI | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0079 | EUR | TSI | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA20805 | hp1 | a0003 | c0003 | t0001 | g0312 | EUR | TSI | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0052 | EUR | TSI | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0050 | SAS | GIH | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA20905 | hp2 | a0003 | c0003 | t0001 | g0302 | SAS | GIH | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | ACB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0198 | AFR | ACB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02486 | hp1 | a0003 | c0003 | t0001 | g0285 | AFR | ACB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02486 | hp2 | a0005 | c0005 | t0001 | g0320 | AFR | ACB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | ACB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0073 | AFR | ACB | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0083 | AFR | MSL | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | USA | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | USA | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA18955 | hp2 | a0003 | c0003 | t0001 | g0269 | EAS | JPT | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | USA | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0016 | AFR | USA | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | LWK | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0321 | REF | REF | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0215 | REF | REF | SRSF4_chr1_29142743_29186900 | SRSF4 | chr1 | 29142743 | 29186900 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:29148447 | G | C | 1 | a0006 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.1448C>G | p.Pro483Arg | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 6/6 | 1596/2300 | 1448/1485 | 483/494 | chr1 | 29148447 | |||
| chr1:29148664 | C | T | 1 | a0005 | 2 | HG01934.hp2 HG02486.hp2 |
missense_variant | MODERATE | c.1231G>A | p.Val411Met | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 6/6 | 1379/2300 | 1231/1485 | 411/494 | chr1 | 29148664 | |||
| chr1:29148709 | T | C | 1 | a0008 | 1 | NA19079.hp2 | missense_variant | MODERATE | c.1186A>G | p.Lys396Glu | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 6/6 | 1334/2300 | 1186/1485 | 396/494 | chr1 | 29148709 | |||
| chr1:29148762 | C | T | 1 | a0007 | 1 | NA18953.hp1 | missense_variant | MODERATE | c.1133G>A | p.Arg378Lys | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 6/6 | 1281/2300 | 1133/1485 | 378/494 | chr1 | 29148762 | |||
| chr1:29148829 | C | T | 2 | a0001 a0009 |
141 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(138): Show |
missense_variant | MODERATE | c.1066G>A | p.Gly356Ser | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 6/6 | 1214/2300 | 1066/1485 | 356/494 | chr1 | 29148829 | |||
| chr1:29148882 | C | G | 2 | a0001 a0009 |
141 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(138): Show |
missense_variant | MODERATE | c.1013G>C | p.Gly338Ala | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 6/6 | 1161/2300 | 1013/1485 | 338/494 | chr1 | 29148882 | |||
| chr1:29149030 | G | A | 1 | a0004 | 2 | HG01256.hp1 HG01258.hp2 |
missense_variant | MODERATE | c.865C>T | p.Arg289Trp | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 6/6 | 1013/2300 | 865/1485 | 289/494 | chr1 | 29149030 | |||
| chr1:29149136 | T | G | 6 | a0001 a0003 a0004 others(3): Show |
241 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(238): Show |
missense_variant | MODERATE | c.759A>C | p.Glu253Asp | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 6/6 | 907/2300 | 759/1485 | 253/494 | chr1 | 29149136 | |||
| chr1:29150181 | C | T | 1 | a0009 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.590G>A | p.Arg197Gln | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 5/6 | 738/2300 | 590/1485 | 197/494 | chr1 | 29150181 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:29148874 | T | G | 1 | a0003c0004 | 8 | HG00423.hp2 HG02015.hp2 NA18940.hp1 others(5): Show |
synonymous_variant | LOW | c.1021A>C | p.Arg341Arg | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 6/6 | 1169/2300 | 1021/1485 | 341/494 | chr1 | 29148874 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:29147903 | T | C | 1 | a0002c0002t0007 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*507A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 6/6 | 507 | chr1 | 29147903 | ||||||
| chr1:29148032 | G | A | 1 | a0002c0002t0004 | 2 | HG02165.hp1 NA18986.hp2 |
3_prime_UTR_variant | MODIFIER | c.*378C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 6/6 | 378 | chr1 | 29148032 | ||||||
| chr1:29148381 | C | T | 1 | a0002c0002t0006 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*29G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 6/6 | 29 | chr1 | 29148381 | ||||||
| chr1:29181815 | C | G | 1 | a0001c0001t0003 | 30 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(27): Show |
5_prime_UTR_variant | MODIFIER | c.-63G>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/6 | 63 | chr1 | 29181815 | ||||||
| chr1:29181838 | C | T | 2 | a0001c0001t0002 a0009c0007t0002 |
43 | HG00609.hp2 HG00642.hp1 HG00735.hp1 others(40): Show |
5_prime_UTR_variant | MODIFIER | c.-86G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/6 | 86 | chr1 | 29181838 | ||||||
| chr1:29181839 | G | A | 1 | a0002c0002t0008 | 1 | NA19005.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-87C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/6 | chr1 | 29181839 | |||||||
| chr1:29181861 | G | GACGGACG others(18): Show |
1 | a0002c0002t0009 | 1 | NA19060.hp1 | 5_prime_UTR_variant | MODIFIER | c.-134_-110dupGTCGCC others(19): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/6 | 110 | chr1 | 29181861 | ||||||
| chr1:29181900 | C | G | 1 | a0002c0002t0005 | 1 | NA18973.hp1 | 5_prime_UTR_variant | MODIFIER | c.-148G>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/6 | 148 | chr1 | 29181900 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:29149247 | G | A | 1 | a0003c0003t0001g0254 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.669-21C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 5/5 | chr1 | 29149247 | |||||||
| chr1:29149279 | G | A | 1 | a0003c0004t0001g0246 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.669-53C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 5/5 | chr1 | 29149279 | |||||||
| chr1:29149404 | G | C | 1 | a0003c0003t0001g0319 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.669-178C>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 5/5 | chr1 | 29149404 | |||||||
| chr1:29149463 | G | A | 61 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(58): Show |
66 | HG00280.hp2 HG00438.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.669-237C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 5/5 | chr1 | 29149463 | |||||||
| chr1:29149509 | G | A | 1 | a0005c0005t0001g0320 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.669-283C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 5/5 | chr1 | 29149509 | |||||||
| chr1:29149642 | C | T | 3 | a0003c0003t0001g0287 a0004c0006t0001g0291 a0004c0006t0001g0311 |
3 | HG01256.hp1 HG01258.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.669-416G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 5/5 | chr1 | 29149642 | |||||||
| chr1:29149668 | G | A | 69 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0030 others(66): Show |
73 | HG00280.hp1 HG00609.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.668+435C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 5/5 | chr1 | 29149668 | |||||||
| chr1:29149682 | AG | A | 18 | a0001c0001t0002g0035 a0001c0001t0002g0044 a0001c0001t0003g0071 others(15): Show |
18 | HG00280.hp1 HG01074.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.668+420delC | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 5/5 | chr1 | 29149682 | |||||||
| chr1:29149687 | G | GA | 20 | a0001c0001t0002g0033 a0001c0001t0002g0036 a0001c0001t0002g0037 others(17): Show |
20 | HG00642.hp1 HG00735.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.668+415_668+416ins others(1): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 5/5 | chr1 | 29149687 | |||||||
| chr1:29149688 | G | A | 152 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0030 others(149): Show |
179 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(176): Show |
intron_variant | MODIFIER | c.668+415C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 5/5 | chr1 | 29149688 | |||||||
| chr1:29149688 | GA | G | 80 | a0003c0003t0001g0004 a0003c0003t0001g0008 a0003c0003t0001g0025 others(77): Show |
92 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.668+414delT | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 5/5 | chr1 | 29149688 | |||||||
| chr1:29149704 | AAG | A | 32 | a0001c0001t0001g0013 a0001c0001t0001g0097 a0001c0001t0001g0103 others(29): Show |
33 | HG00438.hp1 HG00642.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.668+397_668+398del others(2): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 5/5 | chr1 | 29149704 | |||||||
| chr1:29149705 | AG | A | 19 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0104 others(16): Show |
21 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.668+397delC | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 5/5 | chr1 | 29149705 | |||||||
| chr1:29149706 | G | A | 80 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0105 others(77): Show |
86 | HG00280.hp1 HG00609.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.668+397C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 5/5 | chr1 | 29149706 | |||||||
| chr1:29149716 | C | T | 82 | a0003c0003t0001g0004 a0003c0003t0001g0008 a0003c0003t0001g0025 others(79): Show |
94 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.668+387G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 5/5 | chr1 | 29149716 | |||||||
| chr1:29149804 | G | T | 82 | a0003c0003t0001g0004 a0003c0003t0001g0008 a0003c0003t0001g0025 others(79): Show |
94 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.668+299C>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 5/5 | chr1 | 29149804 | |||||||
| chr1:29149884 | C | G | 1 | a0005c0005t0001g0320 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.668+219G>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 5/5 | chr1 | 29149884 | |||||||
| chr1:29149977 | A | T | 1 | a0002c0002t0001g0017 | 2 | NA19056.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.668+126T>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 5/5 | chr1 | 29149977 | |||||||
| chr1:29150009 | C | T | 1 | a0003c0003t0001g0250 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.668+94G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 5/5 | chr1 | 29150009 | |||||||
| chr1:29150200 | G | T | 1 | a0003c0003t0001g0275 | 1 | NA18980.hp1 | splice_region_variant&intron_variant | LOW | c.579-8C>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29150200 | |||||||
| chr1:29150434 | T | C | 1 | a0002c0002t0001g0201 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.579-242A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29150434 | |||||||
| chr1:29150594 | G | A | 1 | a0002c0002t0001g0205 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.579-402C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29150594 | |||||||
| chr1:29150596 | C | T | 1 | a0003c0003t0001g0293 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.579-404G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29150596 | |||||||
| chr1:29150673 | G | A | 1 | a0001c0001t0003g0068 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.579-481C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29150673 | |||||||
| chr1:29150715 | C | T | 14 | a0001c0001t0003g0070 a0001c0001t0003g0071 a0001c0001t0003g0072 others(11): Show |
14 | HG00280.hp1 HG01168.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.579-523G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29150715 | |||||||
| chr1:29150953 | C | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0106 others(1): Show |
6 | HG01243.hp2 HG01891.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.579-761G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29150953 | |||||||
| chr1:29150960 | T | C | 2 | a0001c0001t0001g0109 a0001c0001t0001g0156 |
2 | HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.579-768A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29150960 | |||||||
| chr1:29151107 | G | A | 2 | a0001c0001t0001g0109 a0001c0001t0001g0156 |
2 | HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.579-915C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29151107 | |||||||
| chr1:29151238 | C | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0147 |
2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.579-1046G>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29151238 | |||||||
| chr1:29151257 | T | C | 1 | a0001c0001t0003g0080 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.579-1065A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29151257 | |||||||
| chr1:29151292 | G | A | 2 | a0001c0001t0001g0109 a0001c0001t0001g0156 |
2 | HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.579-1100C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29151292 | |||||||
| chr1:29151372 | C | T | 5 | a0003c0003t0001g0098 a0003c0003t0001g0099 a0003c0003t0001g0100 others(2): Show |
5 | HG00733.hp2 HG02055.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.579-1180G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29151372 | |||||||
| chr1:29151528 | A | C | 1 | a0001c0001t0001g0127 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.579-1336T>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29151528 | |||||||
| chr1:29151542 | G | A | 1 | a0001c0001t0002g0061 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.579-1350C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29151542 | |||||||
| chr1:29151802 | T | C | 28 | a0001c0001t0003g0010 a0001c0001t0003g0068 a0001c0001t0003g0070 others(25): Show |
29 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.579-1610A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29151802 | |||||||
| chr1:29151872 | A | G | 1 | a0001c0001t0001g0103 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.579-1680T>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29151872 | |||||||
| chr1:29151907 | C | T | 132 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(129): Show |
141 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.579-1715G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29151907 | |||||||
| chr1:29151966 | A | G | 17 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0096 others(14): Show |
22 | HG00408.hp2 HG00558.hp1 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.579-1774T>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29151966 | |||||||
| chr1:29152124 | A | C | 2 | a0001c0001t0003g0080 a0001c0001t0003g0090 |
2 | HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.579-1932T>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29152124 | |||||||
| chr1:29152137 | T | C | 1 | a0002c0002t0009g0323 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.579-1945A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29152137 | |||||||
| chr1:29152296 | G | A | 1 | a0005c0005t0001g0320 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.579-2104C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29152296 | |||||||
| chr1:29152492 | T | G | 9 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(6): Show |
12 | HG01243.hp2 HG01255.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.578+2204A>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29152492 | |||||||
| chr1:29152621 | T | C | 1 | a0003c0003t0001g0101 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.578+2075A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29152621 | |||||||
| chr1:29152635 | C | A | 1 | a0002c0002t0001g0017 | 2 | NA19056.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.578+2061G>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29152635 | |||||||
| chr1:29152643 | G | A | 1 | a0002c0002t0001g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.578+2053C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29152643 | |||||||
| chr1:29152647 | G | A | 1 | a0002c0002t0001g0158 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.578+2049C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29152647 | |||||||
| chr1:29152684 | C | G | 1 | a0001c0001t0001g0114 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.578+2012G>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29152684 | |||||||
| chr1:29152706 | G | A | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(3): Show |
9 | HG01243.hp2 HG01255.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.578+1990C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29152706 | |||||||
| chr1:29152918 | G | T | 2 | a0002c0002t0001g0229 a0006c0009t0001g0177 |
2 | HG01106.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.578+1778C>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29152918 | |||||||
| chr1:29152922 | C | CA | 122 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0097 others(119): Show |
128 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.578+1773dupT | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29152922 | |||||||
| chr1:29153530 | T | C | 5 | a0003c0003t0001g0098 a0003c0003t0001g0099 a0003c0003t0001g0100 others(2): Show |
5 | HG00733.hp2 HG02055.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.578+1166A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29153530 | |||||||
| chr1:29153542 | C | A | 1 | a0002c0002t0001g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.578+1154G>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29153542 | |||||||
| chr1:29153600 | A | AT | 11 | a0001c0001t0001g0110 a0001c0001t0001g0128 a0001c0001t0001g0150 others(8): Show |
11 | HG00558.hp2 HG00642.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.578+1095dupA | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29153600 | |||||||
| chr1:29153685 | G | A | 2 | a0001c0001t0003g0087 a0001c0001t0003g0088 |
2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.578+1011C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29153685 | |||||||
| chr1:29153792 | C | T | 4 | a0001c0001t0003g0082 a0001c0001t0003g0085 a0001c0001t0003g0091 others(1): Show |
4 | HG00280.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.578+904G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29153792 | |||||||
| chr1:29153830 | A | G | 40 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0030 others(37): Show |
43 | HG00609.hp2 HG00642.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.578+866T>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29153830 | |||||||
| chr1:29153892 | T | C | 5 | a0003c0003t0001g0098 a0003c0003t0001g0099 a0003c0003t0001g0100 others(2): Show |
5 | HG00733.hp2 HG02055.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.578+804A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29153892 | |||||||
| chr1:29154099 | G | A | 1 | a0003c0003t0001g0281 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.578+597C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29154099 | |||||||
| chr1:29154315 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.578+381G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29154315 | |||||||
| chr1:29154376 | T | C | 1 | a0003c0003t0001g0252 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.578+320A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29154376 | |||||||
| chr1:29154474 | C | T | 2 | a0001c0001t0001g0109 a0001c0001t0001g0156 |
2 | HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.578+222G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 4/5 | chr1 | 29154474 | |||||||
| chr1:29155104 | A | G | 3 | a0001c0001t0002g0038 a0001c0001t0002g0047 a0001c0001t0002g0057 |
3 | HG01109.hp2 HG02280.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.364-194T>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29155104 | |||||||
| chr1:29155191 | C | T | 1 | a0001c0001t0003g0090 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.364-281G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29155191 | |||||||
| chr1:29155202 | G | A | 1 | a0001c0001t0003g0069 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.364-292C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29155202 | |||||||
| chr1:29155299 | A | C | 1 | a0005c0005t0001g0320 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.364-389T>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29155299 | |||||||
| chr1:29155309 | G | A | 1 | a0003c0003t0001g0263 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.364-399C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29155309 | |||||||
| chr1:29155377 | G | T | 5 | a0003c0003t0001g0098 a0003c0003t0001g0099 a0003c0003t0001g0100 others(2): Show |
5 | HG00733.hp2 HG02055.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.364-467C>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29155377 | |||||||
| chr1:29155379 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.364-469G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29155379 | |||||||
| chr1:29155594 | G | A | 1 | a0003c0003t0001g0299 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.364-684C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29155594 | |||||||
| chr1:29155677 | G | C | 1 | a0001c0001t0002g0067 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.364-767C>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29155677 | |||||||
| chr1:29156019 | C | A | 1 | a0001c0001t0002g0052 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.364-1109G>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29156019 | |||||||
| chr1:29156217 | G | T | 3 | a0003c0003t0001g0251 a0003c0003t0001g0252 a0003c0003t0001g0253 |
3 | HG02080.hp2 HG02132.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.364-1307C>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29156217 | |||||||
| chr1:29156218 | G | T | 3 | a0003c0003t0001g0251 a0003c0003t0001g0252 a0003c0003t0001g0253 |
3 | HG02080.hp2 HG02132.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.364-1308C>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29156218 | |||||||
| chr1:29156353 | C | CA | 79 | a0001c0001t0001g0155 a0001c0001t0002g0030 a0002c0002t0001g0169 others(76): Show |
90 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.364-1444dupT | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29156353 | |||||||
| chr1:29156353 | C | CAA | 139 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(136): Show |
149 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.364-1445_364-1444d others(4): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29156353 | |||||||
| chr1:29156369 | T | A | 8 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(5): Show |
11 | HG01243.hp2 HG01255.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.364-1459A>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29156369 | |||||||
| chr1:29156474 | A | G | 1 | a0003c0003t0001g0100 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.364-1564T>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29156474 | |||||||
| chr1:29156749 | A | ACAC | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0106 others(1): Show |
6 | HG01243.hp2 HG01891.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.364-1842_364-1840d others(5): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29156749 | |||||||
| chr1:29156855 | G | C | 1 | a0003c0003t0001g0295 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.364-1945C>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29156855 | |||||||
| chr1:29156903 | A | G | 1 | a0002c0002t0001g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.364-1993T>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29156903 | |||||||
| chr1:29157318 | C | T | 1 | a0003c0003t0001g0258 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.363+2056G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29157318 | |||||||
| chr1:29157389 | C | T | 3 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0139 |
3 | HG02027.hp2 NA18983.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.363+1985G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29157389 | |||||||
| chr1:29157674 | A | G | 1 | a0003c0003t0001g0277 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.363+1700T>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29157674 | |||||||
| chr1:29157683 | G | A | 1 | a0003c0003t0001g0287 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.363+1691C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29157683 | |||||||
| chr1:29157856 | T | C | 1 | a0002c0002t0009g0323 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.363+1518A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29157856 | |||||||
| chr1:29157891 | C | T | 2 | a0002c0002t0001g0021 a0002c0002t0001g0223 |
3 | HG02040.hp1 NA18943.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.363+1483G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29157891 | |||||||
| chr1:29157907 | C | A | 5 | a0003c0003t0001g0098 a0003c0003t0001g0099 a0003c0003t0001g0100 others(2): Show |
5 | HG00733.hp2 HG02055.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+1467G>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29157907 | |||||||
| chr1:29157927 | T | G | 1 | a0001c0001t0001g0127 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.363+1447A>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29157927 | |||||||
| chr1:29157932 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0149 |
3 | HG01255.hp1 HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.363+1442C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29157932 | |||||||
| chr1:29158054 | C | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0149 |
3 | HG01255.hp1 HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.363+1320G>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29158054 | |||||||
| chr1:29158106 | T | A | 1 | a0001c0001t0001g0104 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.363+1268A>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29158106 | |||||||
| chr1:29158168 | C | CA | 9 | a0001c0001t0002g0061 a0002c0002t0001g0163 a0002c0002t0001g0168 others(6): Show |
9 | HG02970.hp1 NA18955.hp2 NA18978.hp1 others(6): Show |
intron_variant | MODIFIER | c.363+1205dupT | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29158168 | |||||||
| chr1:29158200 | G | C | 2 | a0001c0001t0002g0058 a0009c0007t0002g0060 |
2 | NA19010.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.363+1174C>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29158200 | |||||||
| chr1:29158433 | C | CT | 63 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(60): Show |
68 | HG00280.hp2 HG00438.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.363+940dupA | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29158433 | |||||||
| chr1:29158434 | T | C | 1 | a0001c0001t0003g0078 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.363+940A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29158434 | |||||||
| chr1:29158795 | G | A | 82 | a0003c0003t0001g0004 a0003c0003t0001g0008 a0003c0003t0001g0025 others(79): Show |
94 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.363+579C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29158795 | |||||||
| chr1:29158809 | G | A | 2 | a0002c0002t0001g0022 a0002c0002t0001g0175 |
3 | NA18983.hp2 NA18990.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.363+565C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29158809 | |||||||
| chr1:29158963 | C | T | 53 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0097 others(50): Show |
55 | HG00280.hp2 HG00438.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.363+411G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29158963 | |||||||
| chr1:29158964 | G | A | 2 | a0001c0001t0001g0109 a0001c0001t0001g0156 |
2 | HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.363+410C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29158964 | |||||||
| chr1:29158975 | C | T | 5 | a0003c0003t0001g0098 a0003c0003t0001g0099 a0003c0003t0001g0100 others(2): Show |
5 | HG00733.hp2 HG02055.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+399G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29158975 | |||||||
| chr1:29159031 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0149 a0003c0003t0001g0287 |
4 | HG01255.hp1 HG01515.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+343C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29159031 | |||||||
| chr1:29159092 | C | T | 1 | a0005c0005t0001g0320 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.363+282G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29159092 | |||||||
| chr1:29159108 | A | ACAAAC | 169 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(166): Show |
186 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.363+261_363+265dup others(5): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29159108 | |||||||
| chr1:29159108 | A | ACAAACCA others(3): Show |
10 | a0001c0001t0001g0107 a0001c0001t0001g0121 a0001c0001t0001g0123 others(7): Show |
11 | HG00280.hp2 HG01433.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.363+256_363+265dup others(10): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29159108 | |||||||
| chr1:29159108 | A | ACAAACCA others(8): Show |
1 | a0005c0005t0001g0320 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.363+251_363+265dup others(15): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29159108 | |||||||
| chr1:29159108 | A | C | 1 | a0003c0004t0001g0247 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.363+266T>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29159108 | |||||||
| chr1:29159108 | ACAAAC | A | 6 | a0001c0001t0002g0046 a0001c0001t0002g0048 a0001c0001t0003g0068 others(3): Show |
6 | HG02109.hp1 HG02622.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.363+261_363+265del others(5): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29159108 | |||||||
| chr1:29159108 | ACAAACCA others(3): Show |
A | 2 | a0002c0002t0001g0159 a0002c0002t0001g0221 |
2 | HG02258.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.363+256_363+265del others(10): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29159108 | |||||||
| chr1:29159108 | ACAAACCA others(8): Show |
A | 7 | a0001c0001t0003g0087 a0001c0001t0003g0088 a0003c0003t0001g0098 others(4): Show |
7 | HG00733.hp2 HG01109.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.363+251_363+265del others(15): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29159108 | |||||||
| chr1:29159108 | ACAAACCA others(13): Show |
A | 1 | a0003c0003t0001g0283 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.363+246_363+265del others(20): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29159108 | |||||||
| chr1:29159122 | A | T | 1 | a0002c0002t0001g0210 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.363+252T>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29159122 | |||||||
| chr1:29159270 | A | C | 2 | a0001c0001t0001g0131 a0001c0001t0001g0157 |
2 | HG00642.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.363+104T>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 3/5 | chr1 | 29159270 | |||||||
| chr1:29159511 | A | G | 1 | a0002c0002t0001g0234 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.251-25T>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 2/5 | chr1 | 29159511 | |||||||
| chr1:29159560 | C | G | 1 | a0001c0001t0003g0095 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.251-74G>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 2/5 | chr1 | 29159560 | |||||||
| chr1:29159599 | C | T | 1 | a0001c0001t0002g0038 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.251-113G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 2/5 | chr1 | 29159599 | |||||||
| chr1:29159616 | C | T | 5 | a0001c0001t0002g0036 a0001c0001t0002g0040 a0001c0001t0002g0054 others(2): Show |
5 | HG00735.hp1 HG00741.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.251-130G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 2/5 | chr1 | 29159616 | |||||||
| chr1:29159800 | G | A | 1 | a0002c0002t0001g0191 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.251-314C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 2/5 | chr1 | 29159800 | |||||||
| chr1:29159841 | G | GA | 317 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(314): Show |
362 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(359): Show |
intron_variant | MODIFIER | c.251-356dupT | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 2/5 | chr1 | 29159841 | |||||||
| chr1:29159941 | G | A | 1 | a0003c0003t0001g0276 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.250+434C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 2/5 | chr1 | 29159941 | |||||||
| chr1:29160673 | G | A | 1 | a0001c0001t0003g0069 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.108-156C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29160673 | |||||||
| chr1:29160685 | C | T | 1 | a0005c0005t0001g0314 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.108-168G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29160685 | |||||||
| chr1:29160719 | T | C | 1 | a0003c0003t0001g0299 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.108-202A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29160719 | |||||||
| chr1:29161392 | TA | T | 132 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(129): Show |
141 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.108-876delT | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29161392 | |||||||
| chr1:29161398 | C | G | 1 | a0005c0005t0001g0320 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.108-881G>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29161398 | |||||||
| chr1:29161535 | G | A | 82 | a0003c0003t0001g0004 a0003c0003t0001g0008 a0003c0003t0001g0025 others(79): Show |
94 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.108-1018C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29161535 | |||||||
| chr1:29161691 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.108-1174A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29161691 | |||||||
| chr1:29161691 | T | G | 1 | a0001c0001t0003g0090 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.108-1174A>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29161691 | |||||||
| chr1:29161778 | T | C | 40 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0030 others(37): Show |
43 | HG00609.hp2 HG00642.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.108-1261A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29161778 | |||||||
| chr1:29161783 | G | C | 2 | a0003c0003t0001g0098 a0003c0003t0001g0099 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.108-1266C>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29161783 | |||||||
| chr1:29161785 | G | C | 1 | a0002c0002t0001g0158 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.108-1268C>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29161785 | |||||||
| chr1:29161956 | T | G | 1 | a0003c0003t0001g0280 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.108-1439A>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29161956 | |||||||
| chr1:29162087 | T | A | 1 | a0001c0001t0002g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.108-1570A>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29162087 | |||||||
| chr1:29162138 | G | C | 1 | a0003c0004t0001g0246 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.108-1621C>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29162138 | |||||||
| chr1:29162516 | A | G | 4 | a0003c0003t0001g0025 a0003c0003t0001g0270 a0003c0003t0001g0277 others(1): Show |
5 | HG00423.hp1 HG00544.hp2 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.108-1999T>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29162516 | |||||||
| chr1:29162602 | C | A | 2 | a0001c0001t0001g0109 a0001c0001t0001g0156 |
2 | HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.108-2085G>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29162602 | |||||||
| chr1:29162697 | G | A | 3 | a0001c0001t0002g0038 a0001c0001t0002g0047 a0001c0001t0002g0057 |
3 | HG01109.hp2 HG02280.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.108-2180C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29162697 | |||||||
| chr1:29162988 | A | C | 4 | a0002c0002t0001g0187 a0002c0002t0001g0203 a0002c0002t0001g0222 others(1): Show |
4 | HG00673.hp1 HG02155.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.108-2471T>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29162988 | |||||||
| chr1:29163179 | C | T | 3 | a0002c0002t0001g0020 a0002c0002t0001g0169 a0002c0002t0001g0172 |
4 | HG00733.hp1 HG01074.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.108-2662G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29163179 | |||||||
| chr1:29163505 | G | C | 82 | a0003c0003t0001g0004 a0003c0003t0001g0008 a0003c0003t0001g0025 others(79): Show |
94 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.108-2988C>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29163505 | |||||||
| chr1:29163531 | C | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0317 |
2 | HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.108-3014G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29163531 | |||||||
| chr1:29163627 | G | A | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.108-3110C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29163627 | |||||||
| chr1:29163865 | T | C | 1 | a0003c0003t0001g0102 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.108-3348A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29163865 | |||||||
| chr1:29163891 | A | G | 5 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0048 others(2): Show |
5 | HG02109.hp1 HG02258.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.108-3374T>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29163891 | |||||||
| chr1:29163972 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.108-3455G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29163972 | |||||||
| chr1:29163977 | A | C | 1 | a0001c0001t0002g0067 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.108-3460T>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29163977 | |||||||
| chr1:29164186 | T | C | 1 | a0005c0005t0001g0320 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.108-3669A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29164186 | |||||||
| chr1:29164220 | A | G | 1 | a0003c0003t0001g0287 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.108-3703T>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29164220 | |||||||
| chr1:29164428 | T | C | 1 | a0002c0002t0001g0174 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.108-3911A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29164428 | |||||||
| chr1:29164576 | C | T | 69 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0030 others(66): Show |
73 | HG00280.hp1 HG00609.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.108-4059G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29164576 | |||||||
| chr1:29164640 | T | C | 2 | a0003c0003t0001g0098 a0003c0003t0001g0099 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.108-4123A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29164640 | |||||||
| chr1:29164689 | G | A | 7 | a0002c0002t0001g0168 a0002c0002t0001g0171 a0002c0002t0001g0192 others(4): Show |
7 | NA18960.hp1 NA18978.hp1 NA18993.hp2 others(4): Show |
intron_variant | MODIFIER | c.108-4172C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29164689 | |||||||
| chr1:29164757 | G | A | 1 | a0002c0002t0001g0174 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.108-4240C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29164757 | |||||||
| chr1:29164758 | CG | C | 82 | a0003c0003t0001g0004 a0003c0003t0001g0008 a0003c0003t0001g0025 others(79): Show |
94 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.108-4242delC | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29164758 | |||||||
| chr1:29164880 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.108-4363A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29164880 | |||||||
| chr1:29164983 | T | G | 4 | a0002c0002t0001g0167 a0002c0002t0001g0197 a0002c0002t0001g0209 others(1): Show |
4 | NA18945.hp2 NA18984.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-4466A>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29164983 | |||||||
| chr1:29165040 | C | CA | 12 | a0001c0001t0003g0069 a0001c0001t0003g0070 a0001c0001t0003g0071 others(9): Show |
12 | HG02145.hp1 HG02886.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.108-4524dupT | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29165040 | |||||||
| chr1:29165154 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.108-4637C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29165154 | |||||||
| chr1:29165194 | C | T | 1 | a0002c0002t0001g0234 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.108-4677G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29165194 | |||||||
| chr1:29165452 | T | G | 1 | a0001c0001t0001g0145 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.108-4935A>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29165452 | |||||||
| chr1:29165713 | T | C | 219 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(216): Show |
240 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.108-5196A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29165713 | |||||||
| chr1:29165716 | C | A | 1 | a0001c0001t0002g0050 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.108-5199G>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29165716 | |||||||
| chr1:29165731 | A | G | 2 | a0003c0003t0001g0100 a0003c0003t0001g0102 |
2 | HG00733.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.108-5214T>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29165731 | |||||||
| chr1:29166227 | C | T | 1 | a0005c0005t0001g0320 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.108-5710G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29166227 | |||||||
| chr1:29166340 | T | G | 8 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(5): Show |
11 | HG01243.hp2 HG01255.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.108-5823A>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29166340 | |||||||
| chr1:29166559 | C | T | 1 | a0001c0001t0002g0061 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.108-6042G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29166559 | |||||||
| chr1:29166650 | G | A | 1 | a0003c0003t0001g0271 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.108-6133C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29166650 | |||||||
| chr1:29167058 | T | C | 3 | a0002c0002t0001g0023 a0002c0002t0001g0199 a0002c0002t0001g0210 |
4 | HG02683.hp2 HG02698.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-6541A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29167058 | |||||||
| chr1:29167071 | A | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(3): Show |
9 | HG01243.hp2 HG01255.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.108-6554T>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29167071 | |||||||
| chr1:29167354 | T | C | 55 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0097 others(52): Show |
57 | HG00280.hp2 HG00438.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.108-6837A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29167354 | |||||||
| chr1:29167390 | T | TTTTG | 8 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(5): Show |
11 | HG01243.hp2 HG01255.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.108-6874_108-6873i others(6): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29167390 | |||||||
| chr1:29167507 | C | T | 40 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0030 others(37): Show |
43 | HG00609.hp2 HG00642.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.108-6990G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29167507 | |||||||
| chr1:29167625 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.108-7108A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29167625 | |||||||
| chr1:29167995 | C | T | 82 | a0003c0003t0001g0004 a0003c0003t0001g0008 a0003c0003t0001g0025 others(79): Show |
94 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.108-7478G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29167995 | |||||||
| chr1:29168012 | C | CT | 54 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0097 others(51): Show |
56 | HG00438.hp1 HG00642.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.108-7496dupA | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29168012 | |||||||
| chr1:29168012 | C | CTTT | 15 | a0003c0003t0001g0029 a0003c0003t0001g0102 a0003c0003t0001g0254 others(12): Show |
16 | HG00639.hp1 HG00639.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.108-7498_108-7496d others(5): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29168012 | |||||||
| chr1:29168029 | T | A | 14 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(11): Show |
17 | HG01243.hp2 HG01255.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.108-7512A>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29168029 | |||||||
| chr1:29168029 | T | TA | 65 | a0001c0001t0001g0105 a0001c0001t0001g0110 a0001c0001t0001g0124 others(62): Show |
69 | HG00280.hp1 HG00609.hp2 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.108-7513dupT | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29168029 | |||||||
| chr1:29168029 | T | TTA | 8 | a0001c0001t0002g0036 a0001c0001t0002g0040 a0001c0001t0002g0054 others(5): Show |
8 | HG00735.hp1 HG00741.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.108-7513_108-7512i others(4): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29168029 | |||||||
| chr1:29168029 | T | TTTA | 58 | a0003c0003t0001g0004 a0003c0003t0001g0008 a0003c0003t0001g0025 others(55): Show |
69 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.108-7513_108-7512i others(5): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29168029 | |||||||
| chr1:29168030 | A | T | 4 | a0001c0001t0001g0111 a0001c0001t0001g0126 a0002c0002t0001g0237 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-7513T>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29168030 | |||||||
| chr1:29168047 | G | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0106 others(1): Show |
6 | HG01243.hp2 HG01891.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.108-7530C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29168047 | |||||||
| chr1:29168068 | C | T | 1 | a0003c0003t0001g0274 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.108-7551G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29168068 | |||||||
| chr1:29168073 | C | T | 1 | a0003c0003t0001g0286 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.108-7556G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29168073 | |||||||
| chr1:29168191 | A | AT | 68 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0103 others(65): Show |
71 | HG00280.hp2 HG00438.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.108-7675dupA | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29168191 | |||||||
| chr1:29168191 | ATT | A | 80 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(77): Show |
87 | HG00280.hp1 HG00609.hp2 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.108-7676_108-7675d others(4): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29168191 | |||||||
| chr1:29168222 | G | A | 1 | a0005c0005t0001g0320 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.108-7705C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29168222 | |||||||
| chr1:29168399 | T | C | 1 | a0001c0001t0002g0065 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.108-7882A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29168399 | |||||||
| chr1:29168492 | A | C | 1 | a0002c0002t0001g0096 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108-7975T>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29168492 | |||||||
| chr1:29168680 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.108-8163G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29168680 | |||||||
| chr1:29168776 | T | C | 1 | a0003c0003t0001g0267 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.108-8259A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29168776 | |||||||
| chr1:29169035 | A | G | 1 | a0005c0005t0001g0320 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.108-8518T>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29169035 | |||||||
| chr1:29169132 | C | A | 1 | a0002c0002t0001g0222 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.108-8615G>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29169132 | |||||||
| chr1:29169832 | A | G | 1 | a0002c0002t0001g0187 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.108-9315T>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29169832 | |||||||
| chr1:29169995 | T | C | 1 | a0002c0002t0001g0238 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.108-9478A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29169995 | |||||||
| chr1:29170260 | CGA | C | 8 | a0001c0001t0003g0010 a0001c0001t0003g0068 a0001c0001t0003g0073 others(5): Show |
9 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.108-9745_108-9744d others(4): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29170260 | |||||||
| chr1:29170321 | C | T | 1 | a0002c0002t0001g0165 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.108-9804G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29170321 | |||||||
| chr1:29170544 | T | G | 2 | a0003c0003t0001g0100 a0003c0003t0001g0102 |
2 | HG00733.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.108-10027A>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29170544 | |||||||
| chr1:29170666 | A | C | 4 | a0001c0001t0001g0128 a0001c0001t0001g0131 a0001c0001t0001g0135 others(1): Show |
4 | HG00642.hp2 HG00738.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.108-10149T>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29170666 | |||||||
| chr1:29170703 | A | AAGTCCAT others(8): Show |
1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.108-10201_108-1018 others(19): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29170703 | |||||||
| chr1:29170738 | T | C | 69 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0030 others(66): Show |
73 | HG00280.hp1 HG00609.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.108-10221A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29170738 | |||||||
| chr1:29171076 | G | A | 1 | a0002c0002t0001g0211 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.108-10559C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29171076 | |||||||
| chr1:29171115 | T | C | 1 | a0003c0003t0001g0290 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.107+10531A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29171115 | |||||||
| chr1:29171193 | T | C | 2 | a0002c0002t0001g0023 a0002c0002t0001g0199 |
3 | HG02683.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.107+10453A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29171193 | |||||||
| chr1:29171308 | C | T | 132 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(129): Show |
141 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.107+10338G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29171308 | |||||||
| chr1:29171374 | A | G | 1 | a0003c0003t0001g0100 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.107+10272T>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29171374 | |||||||
| chr1:29171469 | C | T | 6 | a0001c0001t0001g0125 a0001c0001t0001g0130 a0001c0001t0001g0137 others(3): Show |
6 | HG01123.hp2 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.107+10177G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29171469 | |||||||
| chr1:29171725 | G | A | 1 | a0002c0002t0001g0188 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.107+9921C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29171725 | |||||||
| chr1:29171878 | T | G | 1 | a0001c0001t0002g0052 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.107+9768A>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29171878 | |||||||
| chr1:29172059 | CAGAAAAA others(22): Show |
C | 1 | a0001c0001t0001g0146 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.107+9558_107+9586d others(31): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29172059 | |||||||
| chr1:29172061 | G | GA | 69 | a0002c0002t0001g0159 a0003c0003t0001g0004 a0003c0003t0001g0008 others(66): Show |
80 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.107+9584dupT | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29172061 | |||||||
| chr1:29172085 | T | C | 1 | a0002c0002t0001g0016 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.107+9561A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29172085 | |||||||
| chr1:29172394 | C | T | 2 | a0003c0003t0001g0100 a0003c0003t0001g0102 |
2 | HG00733.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.107+9252G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29172394 | |||||||
| chr1:29172395 | G | A | 1 | a0002c0002t0001g0212 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.107+9251C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29172395 | |||||||
| chr1:29172497 | G | C | 1 | a0003c0003t0001g0303 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.107+9149C>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29172497 | |||||||
| chr1:29172641 | G | A | 3 | a0001c0001t0002g0038 a0001c0001t0002g0047 a0001c0001t0002g0057 |
3 | HG01109.hp2 HG02280.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.107+9005C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29172641 | |||||||
| chr1:29172871 | A | G | 1 | a0002c0002t0001g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.107+8775T>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29172871 | |||||||
| chr1:29172891 | A | G | 2 | a0002c0002t0001g0226 a0003c0003t0001g0200 |
2 | NA18940.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.107+8755T>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29172891 | |||||||
| chr1:29172913 | T | G | 220 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(217): Show |
241 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.107+8733A>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29172913 | |||||||
| chr1:29173015 | C | T | 28 | a0001c0001t0003g0010 a0001c0001t0003g0068 a0001c0001t0003g0070 others(25): Show |
29 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.107+8631G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173015 | |||||||
| chr1:29173130 | C | CT | 30 | a0001c0001t0001g0112 a0001c0001t0003g0071 a0001c0001t0003g0081 others(27): Show |
31 | HG00621.hp2 HG00673.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.107+8515dupA | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173130 | |||||||
| chr1:29173130 | C | CTT | 6 | a0001c0001t0001g0156 a0001c0001t0003g0010 a0001c0001t0003g0069 others(3): Show |
7 | HG01071.hp1 HG02080.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.107+8514_107+8515d others(4): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173130 | |||||||
| chr1:29173130 | C | T | 1 | a0003c0003t0001g0101 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.107+8516G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173130 | |||||||
| chr1:29173130 | CT | C | 82 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(79): Show |
89 | HG00280.hp2 HG00609.hp2 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.107+8515delA | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173130 | |||||||
| chr1:29173130 | CTTTTT | C | 9 | a0003c0003t0001g0269 a0003c0003t0001g0273 a0003c0003t0001g0297 others(6): Show |
9 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.107+8511_107+8515d others(7): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173130 | |||||||
| chr1:29173130 | CTTTTTT | C | 69 | a0002c0002t0001g0159 a0003c0003t0001g0004 a0003c0003t0001g0008 others(66): Show |
81 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.107+8510_107+8515d others(8): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173130 | |||||||
| chr1:29173346 | A | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0126 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.107+8300T>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173346 | |||||||
| chr1:29173378 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.107+8268A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173378 | |||||||
| chr1:29173462 | T | C | 1 | a0001c0001t0003g0069 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.107+8184A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173462 | |||||||
| chr1:29173465 | TC | T | 78 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(75): Show |
90 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.107+8180delG | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173465 | |||||||
| chr1:29173466 | C | T | 4 | a0003c0003t0001g0281 a0003c0003t0001g0288 a0003c0003t0001g0303 others(1): Show |
4 | HG00544.hp2 HG04115.hp1 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+8180G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173466 | |||||||
| chr1:29173466 | CT | C | 6 | a0001c0001t0001g0105 a0001c0001t0001g0146 a0001c0001t0001g0151 others(3): Show |
6 | HG00438.hp1 HG02280.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.107+8179delA | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173466 | |||||||
| chr1:29173466 | CTT | C | 101 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(98): Show |
109 | HG00280.hp2 HG00609.hp2 HG00642.hp1 others(106): Show |
intron_variant | MODIFIER | c.107+8178_107+8179d others(4): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173466 | |||||||
| chr1:29173466 | CTTT | C | 27 | a0001c0001t0003g0010 a0001c0001t0003g0068 a0001c0001t0003g0070 others(24): Show |
28 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.107+8177_107+8179d others(5): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173466 | |||||||
| chr1:29173467 | T | C | 1 | a0003c0004t0001g0245 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.107+8179A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173467 | |||||||
| chr1:29173468 | T | C | 82 | a0001c0001t0001g0108 a0001c0001t0001g0134 a0001c0001t0001g0135 others(79): Show |
94 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.107+8178A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173468 | |||||||
| chr1:29173469 | T | C | 3 | a0001c0001t0003g0094 a0003c0003t0001g0252 a0003c0003t0001g0306 |
3 | HG02165.hp2 HG02895.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.107+8177A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173469 | |||||||
| chr1:29173494 | T | C | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.107+8152A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173494 | |||||||
| chr1:29173817 | T | G | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7829A>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173817 | |||||||
| chr1:29173818 | T | A | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7828A>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173818 | |||||||
| chr1:29173819 | C | A | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7827G>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173819 | |||||||
| chr1:29173820 | C | A | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7826G>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173820 | |||||||
| chr1:29173833 | C | G | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7813G>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173833 | |||||||
| chr1:29173834 | T | G | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7812A>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173834 | |||||||
| chr1:29173835 | A | C | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7811T>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173835 | |||||||
| chr1:29173837 | A | G | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7809T>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173837 | |||||||
| chr1:29173839 | A | C | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7807T>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173839 | |||||||
| chr1:29173843 | T | A | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7803A>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173843 | |||||||
| chr1:29173845 | A | G | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7801T>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173845 | |||||||
| chr1:29173846 | T | G | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7800A>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173846 | |||||||
| chr1:29173847 | T | C | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7799A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173847 | |||||||
| chr1:29173848 | A | T | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7798T>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173848 | |||||||
| chr1:29173849 | G | T | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7797C>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173849 | |||||||
| chr1:29173850 | A | G | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7796T>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173850 | |||||||
| chr1:29173851 | A | T | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7795T>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173851 | |||||||
| chr1:29173852 | A | C | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7794T>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173852 | |||||||
| chr1:29173853 | A | T | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7793T>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173853 | |||||||
| chr1:29173855 | A | T | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7791T>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173855 | |||||||
| chr1:29173860 | T | C | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7786A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173860 | |||||||
| chr1:29173861 | T | A | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7785A>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173861 | |||||||
| chr1:29173864 | A | T | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7782T>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173864 | |||||||
| chr1:29173865 | A | C | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7781T>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173865 | |||||||
| chr1:29173869 | T | G | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7777A>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173869 | |||||||
| chr1:29173870 | T | C | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7776A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173870 | |||||||
| chr1:29173875 | T | C | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7771A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173875 | |||||||
| chr1:29173891 | G | A | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7755C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173891 | |||||||
| chr1:29173892 | A | G | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7754T>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173892 | |||||||
| chr1:29173896 | G | T | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7750C>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173896 | |||||||
| chr1:29173909 | G | C | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7737C>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173909 | |||||||
| chr1:29173910 | T | A | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7736A>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173910 | |||||||
| chr1:29173910 | T | C | 232 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(229): Show |
254 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.107+7736A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173910 | |||||||
| chr1:29173913 | G | T | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+7733C>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173913 | |||||||
| chr1:29173926 | C | T | 1 | a0003c0003t0001g0315 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.107+7720G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173926 | |||||||
| chr1:29173927 | G | A | 1 | a0003c0003t0001g0261 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.107+7719C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173927 | |||||||
| chr1:29173937 | C | T | 132 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(129): Show |
141 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.107+7709G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173937 | |||||||
| chr1:29173958 | G | A | 1 | a0002c0002t0001g0234 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.107+7688C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29173958 | |||||||
| chr1:29174043 | G | C | 3 | a0003c0003t0001g0251 a0003c0003t0001g0252 a0003c0003t0001g0253 |
3 | HG02080.hp2 HG02132.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.107+7603C>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29174043 | |||||||
| chr1:29174193 | C | CA | 15 | a0001c0001t0003g0070 a0001c0001t0003g0071 a0001c0001t0003g0072 others(12): Show |
15 | HG00280.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.107+7452dupT | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29174193 | |||||||
| chr1:29174212 | GA | G | 318 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(315): Show |
362 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(359): Show |
intron_variant | MODIFIER | c.107+7433delT | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29174212 | |||||||
| chr1:29174270 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.107+7376G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29174270 | |||||||
| chr1:29174303 | T | C | 220 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(217): Show |
241 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.107+7343A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29174303 | |||||||
| chr1:29174483 | T | C | 132 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(129): Show |
141 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.107+7163A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29174483 | |||||||
| chr1:29174503 | G | A | 3 | a0003c0003t0001g0098 a0003c0003t0001g0099 a0003c0003t0001g0101 |
3 | HG02055.hp1 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.107+7143C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29174503 | |||||||
| chr1:29174617 | G | GA | 19 | a0003c0003t0001g0026 a0003c0003t0001g0027 a0003c0003t0001g0260 others(16): Show |
23 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.107+7028dupT | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29174617 | |||||||
| chr1:29174655 | AGAGACTG others(10): Show |
A | 1 | a0001c0001t0001g0118 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.107+6974_107+6990d others(19): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29174655 | |||||||
| chr1:29174675 | G | GT | 117 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0106 others(114): Show |
128 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.107+6970dupA | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29174675 | |||||||
| chr1:29174675 | G | GTT | 30 | a0001c0001t0001g0111 a0002c0002t0001g0159 a0002c0002t0001g0191 others(27): Show |
34 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.107+6969_107+6970d others(4): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29174675 | |||||||
| chr1:29174681 | T | G | 2 | a0001c0001t0001g0109 a0001c0001t0001g0156 |
2 | HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.107+6965A>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29174681 | |||||||
| chr1:29174736 | C | T | 82 | a0002c0002t0001g0159 a0003c0003t0001g0004 a0003c0003t0001g0008 others(79): Show |
94 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.107+6910G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29174736 | |||||||
| chr1:29174854 | A | G | 1 | a0002c0002t0001g0190 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.107+6792T>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29174854 | |||||||
| chr1:29174971 | C | T | 1 | a0002c0002t0001g0189 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.107+6675G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29174971 | |||||||
| chr1:29174987 | T | TA | 82 | a0001c0001t0001g0137 a0002c0002t0001g0159 a0003c0003t0001g0004 others(79): Show |
94 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.107+6658dupT | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29174987 | |||||||
| chr1:29174987 | TA | T | 17 | a0001c0001t0001g0150 a0001c0001t0002g0009 a0001c0001t0002g0030 others(14): Show |
18 | HG00735.hp2 HG01074.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.107+6658delT | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29174987 | |||||||
| chr1:29174997 | A | G | 1 | a0001c0001t0003g0070 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.107+6649T>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29174997 | |||||||
| chr1:29175004 | AAAG | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(2): Show |
8 | HG01255.hp1 HG01891.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.107+6639_107+6641d others(5): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29175004 | |||||||
| chr1:29175005 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.107+6641T>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29175005 | |||||||
| chr1:29175007 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.107+6639C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29175007 | |||||||
| chr1:29175327 | C | T | 1 | a0002c0002t0001g0017 | 2 | NA19056.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.107+6319G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29175327 | |||||||
| chr1:29175418 | G | A | 1 | a0002c0002t0001g0158 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.107+6228C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29175418 | |||||||
| chr1:29175422 | G | A | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(3): Show |
9 | HG01243.hp2 HG01255.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.107+6224C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29175422 | |||||||
| chr1:29175431 | C | T | 1 | a0005c0005t0001g0320 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.107+6215G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29175431 | |||||||
| chr1:29175492 | G | A | 1 | a0001c0001t0003g0079 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.107+6154C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29175492 | |||||||
| chr1:29175522 | C | G | 1 | a0001c0001t0001g0139 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.107+6124G>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29175522 | |||||||
| chr1:29175525 | C | A | 1 | a0002c0002t0001g0236 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.107+6121G>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29175525 | |||||||
| chr1:29175558 | G | T | 1 | a0003c0003t0001g0254 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.107+6088C>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29175558 | |||||||
| chr1:29175617 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0138 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.107+6029G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29175617 | |||||||
| chr1:29175629 | A | G | 5 | a0003c0003t0001g0098 a0003c0003t0001g0099 a0003c0003t0001g0100 others(2): Show |
5 | HG00733.hp2 HG02055.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.107+6017T>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29175629 | |||||||
| chr1:29175694 | C | CA | 55 | a0001c0001t0001g0011 a0001c0001t0001g0106 a0001c0001t0001g0149 others(52): Show |
62 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.107+5951dupT | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29175694 | |||||||
| chr1:29175694 | C | CAA | 43 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(40): Show |
46 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.107+5950_107+5951d others(4): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29175694 | |||||||
| chr1:29175694 | C | CAAA | 33 | a0001c0001t0001g0013 a0001c0001t0001g0104 a0001c0001t0001g0109 others(30): Show |
34 | HG00609.hp1 HG00733.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.107+5949_107+5951d others(5): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29175694 | |||||||
| chr1:29175694 | C | CAAAA | 19 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(16): Show |
19 | HG00438.hp1 HG00642.hp1 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.107+5948_107+5951d others(6): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29175694 | |||||||
| chr1:29175694 | C | CAAAAA | 11 | a0001c0001t0002g0009 a0001c0001t0002g0032 a0001c0001t0002g0033 others(8): Show |
12 | HG00609.hp2 HG01074.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.107+5947_107+5951d others(7): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29175694 | |||||||
| chr1:29175694 | C | CAAAAAA | 5 | a0001c0001t0001g0117 a0001c0001t0002g0005 a0001c0001t0002g0061 others(2): Show |
7 | HG02074.hp1 HG03490.hp1 NA18978.hp2 others(4): Show |
intron_variant | MODIFIER | c.107+5946_107+5951d others(8): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29175694 | |||||||
| chr1:29175694 | C | CAAAAAAA others(1): Show |
15 | a0003c0003t0001g0028 a0003c0003t0001g0263 a0003c0003t0001g0264 others(12): Show |
16 | HG00408.hp1 HG01433.hp1 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.107+5944_107+5951d others(10): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29175694 | |||||||
| chr1:29175694 | C | CAAAAAAA others(2): Show |
12 | a0003c0003t0001g0029 a0003c0003t0001g0255 a0003c0003t0001g0265 others(9): Show |
13 | HG00639.hp2 HG01168.hp1 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.107+5943_107+5951d others(11): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29175694 | |||||||
| chr1:29175694 | C | CAAAAAAA others(3): Show |
11 | a0003c0003t0001g0256 a0003c0003t0001g0257 a0003c0003t0001g0266 others(8): Show |
11 | HG00558.hp2 HG01175.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.107+5942_107+5951d others(12): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29175694 | |||||||
| chr1:29175694 | C | CAAAAAAA others(4): Show |
2 | a0003c0003t0001g0301 a0003c0003t0001g0302 |
2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.107+5941_107+5951d others(13): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29175694 | |||||||
| chr1:29175694 | C | CAAAAAAA others(5): Show |
1 | a0003c0003t0001g0303 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.107+5940_107+5951d others(14): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29175694 | |||||||
| chr1:29175694 | CAAA | C | 9 | a0003c0003t0001g0027 a0003c0003t0001g0253 a0003c0003t0001g0261 others(6): Show |
10 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(7): Show |
intron_variant | MODIFIER | c.107+5949_107+5951d others(5): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29175694 | |||||||
| chr1:29175694 | CAAAA | C | 27 | a0002c0002t0001g0159 a0003c0003t0001g0004 a0003c0003t0001g0008 others(24): Show |
36 | HG00423.hp1 HG00673.hp2 HG02015.hp2 others(33): Show |
intron_variant | MODIFIER | c.107+5948_107+5951d others(6): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29175694 | |||||||
| chr1:29175694 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0002g0045 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.107+5942_107+5951d others(12): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29175694 | |||||||
| chr1:29175711 | A | AAG | 7 | a0001c0001t0001g0110 a0001c0001t0001g0119 a0001c0001t0001g0121 others(4): Show |
7 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.107+5934_107+5935i others(4): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29175711 | |||||||
| chr1:29175722 | A | C | 1 | a0003c0004t0001g0246 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.107+5924T>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29175722 | |||||||
| chr1:29175724 | T | A | 1 | a0001c0001t0002g0040 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.107+5922A>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29175724 | |||||||
| chr1:29176016 | G | C | 1 | a0002c0002t0001g0182 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.107+5630C>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29176016 | |||||||
| chr1:29176056 | T | A | 1 | a0001c0001t0003g0086 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.107+5590A>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29176056 | |||||||
| chr1:29176060 | G | T | 11 | a0001c0001t0002g0009 a0001c0001t0002g0030 a0001c0001t0002g0031 others(8): Show |
12 | HG00735.hp2 HG01074.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.107+5586C>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29176060 | |||||||
| chr1:29176079 | T | C | 1 | a0003c0003t0001g0304 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.107+5567A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29176079 | |||||||
| chr1:29176111 | G | C | 1 | a0003c0003t0001g0100 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.107+5535C>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29176111 | |||||||
| chr1:29176184 | G | A | 2 | a0001c0001t0003g0087 a0001c0001t0003g0088 |
2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.107+5462C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29176184 | |||||||
| chr1:29176229 | G | C | 1 | a0003c0003t0001g0305 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.107+5417C>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29176229 | |||||||
| chr1:29176341 | T | C | 1 | a0002c0002t0001g0183 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.107+5305A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29176341 | |||||||
| chr1:29176486 | CT | C | 3 | a0001c0001t0001g0109 a0001c0001t0001g0156 a0001c0001t0003g0090 |
3 | HG02451.hp2 HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.107+5159delA | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29176486 | |||||||
| chr1:29176489 | TA | T | 98 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(95): Show |
106 | HG00280.hp1 HG00408.hp1 HG00609.hp2 others(103): Show |
intron_variant | MODIFIER | c.107+5156delT | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29176489 | |||||||
| chr1:29176490 | A | T | 1 | a0003c0003t0001g0099 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.107+5156T>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29176490 | |||||||
| chr1:29176545 | A | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(3): Show |
9 | HG01243.hp2 HG01255.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.107+5101T>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29176545 | |||||||
| chr1:29176702 | G | A | 40 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0030 others(37): Show |
43 | HG00609.hp2 HG00642.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.107+4944C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29176702 | |||||||
| chr1:29176801 | A | G | 1 | a0005c0005t0001g0320 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.107+4845T>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29176801 | |||||||
| chr1:29177007 | G | GT | 49 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0097 others(46): Show |
51 | HG00280.hp2 HG00438.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.107+4638dupA | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29177007 | |||||||
| chr1:29177164 | C | G | 5 | a0003c0003t0001g0098 a0003c0003t0001g0099 a0003c0003t0001g0100 others(2): Show |
5 | HG00733.hp2 HG02055.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.107+4482G>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29177164 | |||||||
| chr1:29177182 | CCA | C | 10 | a0002c0002t0001g0016 a0002c0002t0001g0162 a0002c0002t0001g0163 others(7): Show |
11 | HG02257.hp2 HG02717.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.107+4462_107+4463d others(4): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29177182 | |||||||
| chr1:29177189 | G | C | 1 | a0003c0003t0001g0102 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.107+4457C>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29177189 | |||||||
| chr1:29177237 | T | C | 1 | a0005c0005t0001g0320 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.107+4409A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29177237 | |||||||
| chr1:29177245 | G | A | 82 | a0002c0002t0001g0159 a0003c0003t0001g0004 a0003c0003t0001g0008 others(79): Show |
94 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.107+4401C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29177245 | |||||||
| chr1:29177283 | G | GT | 51 | a0001c0001t0001g0110 a0001c0001t0001g0118 a0001c0001t0002g0005 others(48): Show |
54 | HG00609.hp2 HG00642.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.107+4362dupA | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29177283 | |||||||
| chr1:29177283 | G | GTT | 29 | a0001c0001t0003g0010 a0001c0001t0003g0068 a0001c0001t0003g0069 others(26): Show |
30 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.107+4361_107+4362d others(4): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29177283 | |||||||
| chr1:29177814 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.107+3832A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29177814 | |||||||
| chr1:29177893 | A | AT | 86 | a0001c0001t0001g0013 a0001c0001t0001g0110 a0001c0001t0001g0111 others(83): Show |
91 | HG00280.hp1 HG00735.hp2 HG01069.hp1 others(88): Show |
intron_variant | MODIFIER | c.107+3752dupA | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29177893 | |||||||
| chr1:29177893 | A | ATT | 22 | a0001c0001t0001g0109 a0001c0001t0002g0030 a0001c0001t0002g0031 others(19): Show |
22 | HG00609.hp2 HG00642.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.107+3751_107+3752d others(4): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29177893 | |||||||
| chr1:29177893 | A | ATTTT | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0105 others(3): Show |
8 | HG01243.hp2 HG01891.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.107+3749_107+3752d others(6): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29177893 | |||||||
| chr1:29177893 | AT | A | 10 | a0001c0001t0001g0097 a0001c0001t0001g0150 a0001c0001t0001g0153 others(7): Show |
10 | HG01934.hp2 HG01981.hp2 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.107+3752delA | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29177893 | |||||||
| chr1:29177893 | ATT | A | 8 | a0002c0002t0001g0158 a0003c0003t0001g0099 a0003c0003t0001g0100 others(5): Show |
8 | HG00639.hp2 HG00733.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.107+3751_107+3752d others(4): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29177893 | |||||||
| chr1:29178001 | G | C | 2 | a0002c0002t0001g0243 a0002c0002t0006g0244 |
2 | HG02027.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.107+3645C>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29178001 | |||||||
| chr1:29178244 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.107+3402G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29178244 | |||||||
| chr1:29178353 | C | CTTCTCTT others(5): Show |
1 | a0001c0001t0003g0068 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.107+3292_107+3293i others(14): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29178353 | |||||||
| chr1:29178353 | C | CTTCTTTT others(4): Show |
105 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(102): Show |
113 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.107+3292_107+3293i others(13): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29178353 | |||||||
| chr1:29178353 | C | CTTCTTTT others(5): Show |
26 | a0001c0001t0001g0151 a0001c0001t0003g0010 a0001c0001t0003g0070 others(23): Show |
27 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.107+3292_107+3293i others(14): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29178353 | |||||||
| chr1:29178353 | C | CTTCTTTT others(8): Show |
5 | a0003c0003t0001g0310 a0003c0003t0001g0312 a0003c0003t0001g0313 others(2): Show |
5 | HG01256.hp1 HG01934.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.107+3292_107+3293i others(17): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29178353 | |||||||
| chr1:29178353 | C | CTTCTTTT others(9): Show |
68 | a0003c0003t0001g0004 a0003c0003t0001g0008 a0003c0003t0001g0025 others(65): Show |
80 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.107+3292_107+3293i others(18): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29178353 | |||||||
| chr1:29178353 | C | CTTCTTTT others(10): Show |
9 | a0002c0002t0001g0159 a0003c0003t0001g0250 a0003c0003t0001g0251 others(6): Show |
9 | HG00639.hp1 HG01175.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.107+3292_107+3293i others(19): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29178353 | |||||||
| chr1:29178353 | C | CTTCTTTT others(13): Show |
1 | a0005c0005t0001g0320 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.107+3292_107+3293i others(22): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29178353 | |||||||
| chr1:29178353 | C | CTTTTTTT others(6): Show |
5 | a0003c0003t0001g0098 a0003c0003t0001g0099 a0003c0003t0001g0100 others(2): Show |
5 | HG00733.hp2 HG02055.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.107+3292_107+3293i others(15): Show |
SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29178353 | |||||||
| chr1:29178406 | C | T | 2 | a0003c0003t0001g0098 a0003c0003t0001g0099 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.107+3240G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29178406 | |||||||
| chr1:29178518 | T | A | 1 | a0001c0001t0001g0151 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.107+3128A>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29178518 | |||||||
| chr1:29178558 | A | G | 219 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(216): Show |
240 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.107+3088T>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29178558 | |||||||
| chr1:29178617 | A | G | 1 | a0005c0005t0001g0320 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.107+3029T>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29178617 | |||||||
| chr1:29178639 | C | T | 6 | a0003c0004t0001g0007 a0003c0004t0001g0245 a0003c0004t0001g0246 others(3): Show |
8 | HG00423.hp2 HG02015.hp2 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.107+3007G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29178639 | |||||||
| chr1:29178749 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.107+2897G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29178749 | |||||||
| chr1:29178919 | G | T | 1 | a0001c0001t0001g0104 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.107+2727C>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29178919 | |||||||
| chr1:29178925 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.107+2721A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29178925 | |||||||
| chr1:29179101 | A | G | 29 | a0001c0001t0003g0010 a0001c0001t0003g0068 a0001c0001t0003g0069 others(26): Show |
30 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.107+2545T>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29179101 | |||||||
| chr1:29179164 | G | A | 1 | a0003c0003t0001g0315 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.107+2482C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29179164 | |||||||
| chr1:29179190 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.107+2456G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29179190 | |||||||
| chr1:29179450 | C | G | 5 | a0003c0003t0001g0098 a0003c0003t0001g0099 a0003c0003t0001g0100 others(2): Show |
5 | HG00733.hp2 HG02055.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.107+2196G>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29179450 | |||||||
| chr1:29179907 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.107+1739A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29179907 | |||||||
| chr1:29180047 | G | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.107+1599C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29180047 | |||||||
| chr1:29180091 | A | G | 1 | a0002c0002t0001g0158 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.107+1555T>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29180091 | |||||||
| chr1:29180497 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.107+1149A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29180497 | |||||||
| chr1:29180555 | T | C | 1 | a0003c0003t0001g0316 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.107+1091A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29180555 | |||||||
| chr1:29180562 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.107+1084C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29180562 | |||||||
| chr1:29180588 | A | C | 190 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(187): Show |
210 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.107+1058T>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29180588 | |||||||
| chr1:29180588 | A | T | 29 | a0001c0001t0003g0010 a0001c0001t0003g0068 a0001c0001t0003g0069 others(26): Show |
30 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.107+1058T>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29180588 | |||||||
| chr1:29180595 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.107+1051G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29180595 | |||||||
| chr1:29180604 | G | A | 81 | a0003c0003t0001g0004 a0003c0003t0001g0008 a0003c0003t0001g0025 others(78): Show |
93 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.107+1042C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29180604 | |||||||
| chr1:29180803 | T | C | 1 | a0001c0001t0001g0317 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.107+843A>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29180803 | |||||||
| chr1:29180806 | C | G | 1 | a0002c0002t0001g0096 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.107+840G>C | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29180806 | |||||||
| chr1:29180820 | G | C | 2 | a0003c0003t0001g0029 a0003c0003t0001g0319 |
3 | HG02622.hp1 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.107+826C>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29180820 | |||||||
| chr1:29180941 | C | T | 1 | a0001c0001t0003g0069 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.107+705G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29180941 | |||||||
| chr1:29181059 | G | C | 3 | a0001c0001t0001g0318 a0003c0003t0001g0029 a0003c0003t0001g0319 |
4 | HG02622.hp1 HG02886.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+587C>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29181059 | |||||||
| chr1:29181124 | C | A | 1 | a0001c0001t0003g0095 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.107+522G>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29181124 | |||||||
| chr1:29181135 | G | C | 69 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0030 others(66): Show |
73 | HG00280.hp1 HG00609.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.107+511C>G | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29181135 | |||||||
| chr1:29181183 | G | A | 1 | a0005c0005t0001g0320 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.107+463C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29181183 | |||||||
| chr1:29181472 | G | A | 1 | a0001c0001t0002g0067 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.107+174C>T | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29181472 | |||||||
| chr1:29181485 | C | T | 1 | a0001c0001t0003g0068 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.107+161G>A | SRSF4 | ENSG00000116350.18 | transcript | ENST00000373795.7 | protein_coding | 1/5 | chr1 | 29181485 |