Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1996 |
| ensemblid | ENSG00000162374.18 |
| hgncid | 3315 |
| symbol | ELAVL4 |
| name | ELAV like RNA binding protein 4 |
| refseq_nuc | NM_001144774.3 |
| refseq_prot | NP_001138246.1 |
| ensembl_nuc | ENST00000371824.7 |
| ensembl_prot | ENSP00000360889.2 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 50108920 |
| end | 50203772 |
| strand | + |
| ver | v1.2 |
| region | chr1:50108920-50203772 |
| region5000 | chr1:50103920-50208772 |
| regionname0 | ELAVL4_chr1_50108920_50203772 |
| regionname5000 | ELAVL4_chr1_50103920_50208772 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1098 | 215 | 37 | 39 | 102 | 12 | 24 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | ATGGT others(1093): Show |
chr1 | 50103920 | 50208772 | ||
| a0001c0002 | 1/0 | 1098 | 61 | 53 | 7 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | ATGGT others(1093): Show |
chr1 | 50103920 | 50208772 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3965 | 159 | 33 | 34 | 63 | 10 | 18 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | GAGCC others(3960): Show |
chr1 | 50103920 | 50208772 |
| a0001c0001t0002 | 0/0 | 3965 | 48 | 2 | 1 | 38 | 2 | 5 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | GAGCC others(3960): Show |
chr1 | 50103920 | 50208772 |
| a0001c0001t0006 | 0/0 | 3965 | 3 | 0 | 3 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | GAGCC others(3960): Show |
chr1 | 50103920 | 50208772 |
| a0001c0001t0009 | 0/0 | 3965 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | GAGCC others(3960): Show |
chr1 | 50103920 | 50208772 |
| a0001c0001t0010 | 0/0 | 3965 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | GAGCC others(3960): Show |
chr1 | 50103920 | 50208772 |
| a0001c0001t0011 | 0/0 | 3965 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | GAGCC others(3960): Show |
chr1 | 50103920 | 50208772 |
| a0001c0001t0012 | 0/0 | 3965 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | GAGCC others(3960): Show |
chr1 | 50103920 | 50208772 |
| a0001c0001t0014 | 0/0 | 3965 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | GAGCC others(3960): Show |
chr1 | 50103920 | 50208772 |
| a0001c0002t0001 | 1/0 | 3965 | 28 | 24 | 3 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | GAGCC others(3960): Show |
chr1 | 50103920 | 50208772 |
| a0001c0002t0003 | 0/0 | 3964 | 16 | 13 | 3 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | GAGCC others(3959): Show |
chr1 | 50103920 | 50208772 |
| a0001c0002t0004 | 0/0 | 3965 | 8 | 7 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | GAGCC others(3960): Show |
chr1 | 50103920 | 50208772 |
| a0001c0002t0005 | 0/0 | 3965 | 4 | 4 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | GAGCC others(3960): Show |
chr1 | 50103920 | 50208772 |
| a0001c0002t0007 | 0/0 | 3965 | 3 | 3 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | GAGCC others(3960): Show |
chr1 | 50103920 | 50208772 |
| a0001c0002t0008 | 0/0 | 3965 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | GAGCC others(3960): Show |
chr1 | 50103920 | 50208772 |
| a0001c0002t0013 | 0/0 | 3964 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | GAGCC others(3959): Show |
chr1 | 50103920 | 50208772 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0219 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0006g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0006g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0009g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0010g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0011g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0012g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0001t0014g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0001g0068 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0003g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0005g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0005g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0007g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0007g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0007g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0008g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| a0001c0002t0013g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | GBR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0139 | EUR | GBR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0221 | EUR | GBR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | GBR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0143 | EUR | FIN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | FIN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0019 | EUR | FIN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0187 | EUR | FIN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | CHS | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0246 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | CHS | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0056 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01168 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01169 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0107 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01243 | hp2 | a0001 | c0002 | t0004 | g0059 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01346 | hp2 | a0001 | c0002 | t0003 | g0031 | AMR | CLM | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0032 | EUR | IBS | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0222 | EUR | IBS | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01891 | hp1 | a0001 | c0002 | t0004 | g0089 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | KHV | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02055 | hp2 | a0001 | c0001 | t0010 | g0108 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | KHV | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | KHV | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02135 | hp2 | a0001 | c0001 | t0012 | g0137 | EAS | KHV | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02145 | hp2 | a0001 | c0002 | t0004 | g0265 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0261 | AMR | PEL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CDX | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CDX | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02257 | hp1 | a0001 | c0002 | t0003 | g0263 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0177 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02258 | hp1 | a0001 | c0002 | t0004 | g0009 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02273 | hp2 | a0001 | c0001 | t0006 | g0003 | AMR | PEL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02293 | hp2 | a0001 | c0001 | t0006 | g0003 | AMR | PEL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0229 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02572 | hp2 | a0001 | c0002 | t0003 | g0008 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02622 | hp1 | a0001 | c0002 | t0003 | g0172 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02630 | hp1 | a0001 | c0002 | t0003 | g0170 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0268 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0098 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02723 | hp1 | a0001 | c0002 | t0004 | g0239 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0240 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0191 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0199 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0067 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02895 | hp2 | a0001 | c0002 | t0004 | g0102 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0105 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02922 | hp1 | a0001 | c0002 | t0005 | g0232 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02922 | hp2 | a0001 | c0002 | t0004 | g0072 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02965 | hp2 | a0001 | c0002 | t0003 | g0244 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0106 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02970 | hp2 | a0001 | c0002 | t0005 | g0236 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0211 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0167 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0186 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03098 | hp1 | a0001 | c0002 | t0007 | g0237 | AFR | MSL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03098 | hp2 | a0001 | c0002 | t0003 | g0010 | AFR | MSL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03130 | hp1 | a0001 | c0002 | t0004 | g0231 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0126 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0060 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03139 | hp2 | a0001 | c0002 | t0003 | g0192 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03195 | hp1 | a0001 | c0002 | t0003 | g0247 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03195 | hp2 | a0001 | c0002 | t0008 | g0115 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0096 | AFR | MSL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0093 | AFR | MSL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0208 | SAS | PJL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0228 | AFR | MSL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | MSL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0114 | AFR | MSL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0159 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03540 | hp1 | a0001 | c0002 | t0007 | g0234 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03579 | hp1 | a0001 | c0002 | t0003 | g0163 | AFR | MSL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03669 | hp1 | a0001 | c0001 | t0011 | g0212 | SAS | PJL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0145 | SAS | BEB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0037 | SAS | BEB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0209 | SAS | STU | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | STU | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | STU | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | STU | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | STU | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | STU | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18522 | hp1 | a0001 | c0002 | t0003 | g0008 | AFR | YRI | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18522 | hp2 | a0001 | c0002 | t0005 | g0235 | AFR | YRI | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | YRI | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19030 | hp1 | a0001 | c0002 | t0013 | g0095 | AFR | LWK | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | LWK | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19043 | hp1 | a0001 | c0002 | t0007 | g0233 | AFR | LWK | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | LWK | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0075 | AFR | YRI | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | YRI | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0092 | AFR | ASW | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ASW | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0166 | EUR | TSI | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0248 | EUR | TSI | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | GIH | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | GIH | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01123 | hp1 | a0001 | c0001 | t0014 | g0028 | AMR | CLM | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG01123 | hp2 | a0001 | c0001 | t0006 | g0118 | AMR | CLM | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0091 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02486 | hp1 | a0001 | c0002 | t0003 | g0220 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02486 | hp2 | a0001 | c0002 | t0005 | g0238 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02559 | hp1 | a0001 | c0001 | t0009 | g0116 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG06807 | hp1 | a0001 | c0002 | t0003 | g0243 | AFR | USA | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | USA | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0110 | AFR | USA | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0162 | AFR | USA | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | LWK | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0219 | REF | REF | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0068 | REF | REF | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:50195739 | C | T | 1 | a0001c0001 | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
synonymous_variant | LOW | c.687C>T | p.Pro229Pro | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/7 | 957/3965 | 687/1101 | 229/366 | chr1 | 50195739 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:50108973 | G | A | 3 | a0001c0001t0009 a0001c0001t0010 a0001c0002t0008 |
3 | HG02055.hp2 HG02559.hp1 HG03195.hp2 |
5_prime_UTR_variant | MODIFIER | c.-217G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/7 | 217 | chr1 | 50108973 | ||||||
| chr1:50201234 | C | T | 1 | a0001c0002t0003 | 16 | HG01168.hp1 HG01169.hp1 HG01346.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*56C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 7/7 | 56 | chr1 | 50201234 | ||||||
| chr1:50201290 | A | T | 1 | a0001c0001t0014 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*112A>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 7/7 | 112 | chr1 | 50201290 | ||||||
| chr1:50201390 | GA | G | 2 | a0001c0002t0003 a0001c0002t0013 |
17 | HG01168.hp1 HG01169.hp1 HG01346.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*224delA | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 7/7 | 224 | INFO_REALIGN_3_PRIME | chr1 | 50201390 | |||||
| chr1:50202183 | C | T | 1 | a0001c0001t0012 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1005C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 7/7 | 1005 | chr1 | 50202183 | ||||||
| chr1:50202874 | G | A | 1 | a0001c0002t0005 | 4 | HG02486.hp2 HG02922.hp1 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1696G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 7/7 | 1696 | chr1 | 50202874 | ||||||
| chr1:50202958 | G | A | 1 | a0001c0001t0006 | 3 | HG01123.hp2 HG02273.hp2 HG02293.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1780G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 7/7 | 1780 | chr1 | 50202958 | ||||||
| chr1:50202973 | C | T | 2 | a0001c0001t0010 a0001c0002t0004 |
9 | HG01243.hp2 HG01891.hp1 HG02055.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1795C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 7/7 | 1795 | chr1 | 50202973 | ||||||
| chr1:50203286 | T | C | 2 | a0001c0001t0002 a0001c0001t0011 |
49 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*2108T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 7/7 | 2108 | chr1 | 50203286 | ||||||
| chr1:50203481 | T | C | 1 | a0001c0002t0008 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2303T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 7/7 | 2303 | chr1 | 50203481 | ||||||
| chr1:50203698 | T | C | 2 | a0001c0001t0002 a0001c0001t0011 |
49 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*2520T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 7/7 | 2520 | chr1 | 50203698 | ||||||
| chr1:50203707 | T | A | 1 | a0001c0002t0007 | 3 | HG03098.hp1 HG03540.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2529T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 7/7 | 2529 | chr1 | 50203707 | ||||||
| chr1:50203741 | T | C | 1 | a0001c0001t0011 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2563T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 7/7 | 2563 | chr1 | 50203741 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:50109452 | G | T | 1 | a0001c0002t0001g0268 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.9+254G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50109452 | |||||||
| chr1:50109540 | G | A | 1 | a0001c0002t0004g0009 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.9+342G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50109540 | |||||||
| chr1:50109604 | C | G | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG00609.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.9+406C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50109604 | |||||||
| chr1:50109736 | A | T | 1 | a0001c0002t0004g0265 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.9+538A>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50109736 | |||||||
| chr1:50110003 | C | CTG | 33 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0245 others(30): Show |
34 | HG00642.hp1 HG02083.hp1 HG02148.hp2 others(31): Show |
intron_variant | MODIFIER | c.9+828_9+829dupTG | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50110003 | ||||||
| chr1:50110003 | C | CTGTG | 3 | a0001c0001t0002g0264 a0001c0002t0003g0263 a0001c0002t0004g0265 |
3 | HG02145.hp2 HG02257.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.9+826_9+829dupTGTG | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50110003 | ||||||
| chr1:50110459 | G | A | 1 | a0001c0002t0003g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.9+1261G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50110459 | |||||||
| chr1:50110461 | A | G | 1 | a0001c0002t0004g0231 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.9+1263A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50110461 | |||||||
| chr1:50110710 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.9+1512C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50110710 | |||||||
| chr1:50110843 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.9+1645G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50110843 | |||||||
| chr1:50111038 | T | A | 41 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(38): Show |
42 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.9+1840T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50111038 | |||||||
| chr1:50111362 | A | G | 4 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0002t0001g0228 others(1): Show |
4 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+2164A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50111362 | |||||||
| chr1:50111663 | C | G | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | NA18959.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.9+2465C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50111663 | |||||||
| chr1:50111845 | T | G | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.9+2647T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50111845 | |||||||
| chr1:50111886 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.9+2688C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50111886 | |||||||
| chr1:50111982 | G | T | 62 | a0001c0001t0001g0176 a0001c0001t0001g0178 a0001c0001t0001g0179 others(59): Show |
63 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.9+2784G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50111982 | |||||||
| chr1:50112004 | C | T | 31 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0168 others(28): Show |
32 | HG00642.hp1 HG01891.hp2 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.9+2806C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50112004 | |||||||
| chr1:50112401 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.9+3203A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50112401 | |||||||
| chr1:50112665 | A | T | 1 | a0001c0001t0001g0165 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.9+3467A>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50112665 | |||||||
| chr1:50112784 | T | A | 1 | a0001c0002t0004g0239 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.9+3586T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50112784 | |||||||
| chr1:50112796 | G | A | 4 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0002t0001g0228 others(1): Show |
4 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+3598G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50112796 | |||||||
| chr1:50112905 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.9+3707G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50112905 | |||||||
| chr1:50113116 | G | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.9+3918G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50113116 | |||||||
| chr1:50113220 | C | CT | 8 | a0001c0001t0001g0164 a0001c0002t0005g0232 a0001c0002t0005g0235 others(5): Show |
8 | HG02486.hp2 HG02922.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.9+4033dupT | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50113220 | ||||||
| chr1:50113220 | CT | C | 32 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0168 others(29): Show |
33 | HG00642.hp1 HG01167.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.9+4033delT | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50113220 | ||||||
| chr1:50113375 | A | T | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.9+4177A>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50113375 | |||||||
| chr1:50113542 | A | G | 2 | a0001c0002t0001g0162 a0001c0002t0003g0163 |
2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.9+4344A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50113542 | |||||||
| chr1:50113565 | A | C | 119 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
124 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.9+4367A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50113565 | |||||||
| chr1:50113653 | G | A | 1 | a0001c0002t0013g0095 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.9+4455G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50113653 | |||||||
| chr1:50113748 | A | G | 1 | a0001c0001t0001g0094 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.9+4550A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50113748 | |||||||
| chr1:50114070 | C | A | 11 | a0001c0001t0002g0097 a0001c0002t0001g0096 a0001c0002t0001g0268 others(8): Show |
11 | HG02055.hp1 HG02486.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.9+4872C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50114070 | |||||||
| chr1:50114125 | T | C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | NA18948.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.9+4927T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50114125 | |||||||
| chr1:50114247 | G | A | 4 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0002t0001g0228 others(1): Show |
4 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+5049G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50114247 | |||||||
| chr1:50114394 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.9+5196A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50114394 | |||||||
| chr1:50114429 | G | A | 1 | a0001c0002t0001g0162 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.9+5231G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50114429 | |||||||
| chr1:50114602 | C | T | 2 | a0001c0001t0001g0262 a0001c0002t0003g0220 |
2 | HG02486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.9+5404C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50114602 | |||||||
| chr1:50114603 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.9+5405G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50114603 | |||||||
| chr1:50115056 | G | C | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.9+5858G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50115056 | |||||||
| chr1:50115060 | C | G | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.9+5862C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50115060 | |||||||
| chr1:50115074 | G | C | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.9+5876G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50115074 | |||||||
| chr1:50115120 | T | C | 11 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0168 others(8): Show |
11 | HG02145.hp1 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.9+5922T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50115120 | |||||||
| chr1:50115151 | C | T | 88 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
92 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.9+5953C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50115151 | |||||||
| chr1:50115155 | C | A | 1 | a0001c0002t0001g0268 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.9+5957C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50115155 | |||||||
| chr1:50115406 | G | A | 27 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0168 others(24): Show |
28 | HG00642.hp1 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.9+6208G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50115406 | |||||||
| chr1:50115446 | A | G | 1 | a0001c0001t0002g0097 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.9+6248A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50115446 | |||||||
| chr1:50115637 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.9+6439G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50115637 | |||||||
| chr1:50115787 | G | T | 88 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
92 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.9+6589G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50115787 | |||||||
| chr1:50115962 | A | G | 3 | a0001c0002t0001g0091 a0001c0002t0001g0092 a0001c0002t0001g0093 |
3 | HG02109.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.9+6764A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50115962 | |||||||
| chr1:50115971 | G | T | 1 | a0001c0001t0001g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.9+6773G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50115971 | |||||||
| chr1:50116395 | GGT | G | 10 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0002t0003g0008 others(7): Show |
11 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.9+7213_9+7214delTG | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50116395 | ||||||
| chr1:50116397 | T | G | 1 | a0001c0001t0001g0149 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.9+7199T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50116397 | |||||||
| chr1:50116409 | TGTGC | T | 86 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(83): Show |
90 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.9+7215_9+7218delCG others(2): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50116409 | ||||||
| chr1:50116411 | T | C | 5 | a0001c0001t0001g0245 a0001c0001t0001g0248 a0001c0001t0001g0249 others(2): Show |
5 | HG00642.hp1 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+7213T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50116411 | |||||||
| chr1:50116411 | TGC | T | 62 | a0001c0001t0001g0176 a0001c0001t0001g0178 a0001c0001t0001g0179 others(59): Show |
63 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.9+7215_9+7216delCG | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50116411 | ||||||
| chr1:50116413 | C | CGTGT | 4 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0002t0001g0228 others(1): Show |
4 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+7238_9+7241dupGT others(2): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50116413 | ||||||
| chr1:50116413 | C | T | 6 | a0001c0001t0001g0245 a0001c0001t0001g0248 a0001c0001t0001g0249 others(3): Show |
6 | HG00642.hp1 HG02818.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.9+7215C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50116413 | |||||||
| chr1:50116413 | CGT | C | 11 | a0001c0001t0001g0015 a0001c0001t0001g0164 a0001c0001t0001g0168 others(8): Show |
11 | HG01891.hp1 HG01993.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.9+7240_9+7241delGT | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50116413 | ||||||
| chr1:50116415 | T | C | 1 | a0001c0002t0001g0096 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.9+7217T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50116415 | |||||||
| chr1:50116417 | T | C | 62 | a0001c0001t0001g0176 a0001c0001t0001g0178 a0001c0001t0001g0179 others(59): Show |
63 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.9+7219T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50116417 | |||||||
| chr1:50116419 | T | C | 86 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(83): Show |
90 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.9+7221T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50116419 | |||||||
| chr1:50116500 | A | C | 149 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(146): Show |
154 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.9+7302A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50116500 | |||||||
| chr1:50117066 | G | A | 1 | a0001c0002t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.9+7868G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50117066 | |||||||
| chr1:50117407 | C | T | 31 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0168 others(28): Show |
32 | HG00642.hp1 HG01891.hp2 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.9+8209C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50117407 | |||||||
| chr1:50117469 | G | A | 1 | a0001c0002t0004g0231 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.9+8271G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50117469 | |||||||
| chr1:50117518 | C | T | 31 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0168 others(28): Show |
32 | HG00642.hp1 HG01891.hp2 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.9+8320C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50117518 | |||||||
| chr1:50117565 | C | T | 5 | a0001c0001t0001g0245 a0001c0001t0001g0248 a0001c0001t0001g0249 others(2): Show |
5 | HG00642.hp1 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+8367C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50117565 | |||||||
| chr1:50117753 | G | A | 1 | a0001c0002t0003g0240 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.9+8555G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50117753 | |||||||
| chr1:50117813 | C | A | 4 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0002t0001g0228 others(1): Show |
4 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+8615C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50117813 | |||||||
| chr1:50117946 | A | G | 4 | a0001c0001t0001g0006 a0001c0001t0001g0160 a0001c0001t0001g0161 others(1): Show |
5 | HG01069.hp1 HG01109.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.9+8748A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50117946 | |||||||
| chr1:50117950 | G | T | 1 | a0001c0001t0002g0261 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.9+8752G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50117950 | |||||||
| chr1:50118140 | T | G | 1 | a0001c0002t0001g0098 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.9+8942T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50118140 | |||||||
| chr1:50118204 | T | A | 1 | a0001c0001t0001g0099 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.9+9006T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50118204 | |||||||
| chr1:50118207 | A | AT | 10 | a0001c0001t0002g0097 a0001c0002t0001g0096 a0001c0002t0005g0232 others(7): Show |
10 | HG02055.hp1 HG02486.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.9+9017dupT | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50118207 | ||||||
| chr1:50118263 | A | G | 1 | a0001c0002t0013g0095 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.9+9065A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50118263 | |||||||
| chr1:50118494 | GA | G | 13 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0158 others(10): Show |
13 | HG02145.hp1 HG02615.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.9+9305delA | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50118494 | ||||||
| chr1:50118503 | AG | A | 163 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(160): Show |
169 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.9+9306delG | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50118503 | |||||||
| chr1:50118516 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.9+9318A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50118516 | |||||||
| chr1:50118723 | C | T | 3 | a0001c0001t0001g0157 a0001c0002t0001g0098 a0001c0002t0004g0231 |
3 | HG02717.hp2 HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.9+9525C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50118723 | |||||||
| chr1:50118944 | A | AAG | 78 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(75): Show |
82 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.9+9765_9+9766dupAG | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50118944 | ||||||
| chr1:50118961 | A | AGAGAGG | 10 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0168 others(7): Show |
10 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.9+9766_9+9767insAG others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50118961 | ||||||
| chr1:50118961 | A | AGAGAGGG others(3): Show |
1 | a0001c0001t0001g0173 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.9+9766_9+9767insAG others(8): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50118961 | ||||||
| chr1:50118981 | G | GGA | 4 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0002t0001g0228 others(1): Show |
4 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+9798_9+9799dupGA | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50118981 | ||||||
| chr1:50119010 | A | G | 61 | a0001c0001t0001g0176 a0001c0001t0001g0178 a0001c0001t0001g0179 others(58): Show |
62 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.9+9812A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50119010 | |||||||
| chr1:50119034 | G | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.9+9836G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50119034 | |||||||
| chr1:50119036 | A | AAAAG | 27 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(24): Show |
27 | HG00140.hp2 HG00609.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.9+9894_9+9897dupGA others(2): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119036 | ||||||
| chr1:50119036 | A | AAAAGAAA others(1): Show |
27 | a0001c0001t0001g0001 a0001c0001t0001g0042 a0001c0001t0001g0043 others(24): Show |
29 | HG00099.hp1 HG00438.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.9+9890_9+9897dupGA others(6): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119036 | ||||||
| chr1:50119036 | A | AAAAGAAA others(5): Show |
12 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0173 others(9): Show |
12 | HG02615.hp1 HG02965.hp2 HG03098.hp2 others(9): Show |
intron_variant | MODIFIER | c.9+9886_9+9897dupGA others(10): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119036 | ||||||
| chr1:50119036 | A | AAAAGAAA others(9): Show |
1 | a0001c0001t0002g0259 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.9+9882_9+9897dupGA others(14): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119036 | ||||||
| chr1:50119036 | A | AAAAGAAA others(13): Show |
2 | a0001c0001t0002g0050 a0001c0002t0003g0172 |
2 | HG02622.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.9+9878_9+9897dupGA others(18): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119036 | ||||||
| chr1:50119036 | A | AAAGAAAG others(8): Show |
1 | a0001c0001t0001g0090 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.9+9840_9+9841insGA others(13): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119036 | ||||||
| chr1:50119036 | A | AAGAAAGA others(3): Show |
1 | a0001c0001t0002g0260 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.9+9839_9+9840insGA others(8): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119036 | ||||||
| chr1:50119036 | A | G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.9+9838A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50119036 | |||||||
| chr1:50119036 | AAAAG | A | 17 | a0001c0001t0001g0016 a0001c0001t0001g0064 a0001c0001t0001g0065 others(14): Show |
17 | HG00140.hp1 HG02717.hp1 HG02723.hp1 others(14): Show |
intron_variant | MODIFIER | c.9+9894_9+9897delGA others(2): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119036 | ||||||
| chr1:50119036 | AAAAGAAA others(1): Show |
A | 26 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(23): Show |
27 | HG01167.hp2 HG01169.hp2 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.9+9890_9+9897delGA others(6): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119036 | ||||||
| chr1:50119036 | AAAAGAAA others(5): Show |
A | 18 | a0001c0001t0001g0011 a0001c0001t0001g0190 a0001c0001t0001g0193 others(15): Show |
18 | HG01243.hp2 HG01361.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.9+9886_9+9897delGA others(10): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119036 | ||||||
| chr1:50119036 | AAAAGAAA others(9): Show |
A | 7 | a0001c0001t0001g0182 a0001c0001t0001g0184 a0001c0001t0001g0185 others(4): Show |
7 | HG00323.hp2 HG01255.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.9+9882_9+9897delGA others(14): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119036 | ||||||
| chr1:50119036 | AAAAGAAA others(13): Show |
A | 5 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0181 others(2): Show |
5 | HG00438.hp1 HG00673.hp1 HG00673.hp2 others(2): Show |
intron_variant | MODIFIER | c.9+9878_9+9897delGA others(18): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119036 | ||||||
| chr1:50119036 | AAAAGAAA others(17): Show |
A | 1 | a0001c0002t0001g0177 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.9+9874_9+9897delGA others(22): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119036 | ||||||
| chr1:50119036 | AAAAGAAA others(25): Show |
A | 1 | a0001c0001t0001g0176 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.9+9866_9+9897delGA others(30): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119036 | ||||||
| chr1:50119072 | GAAAGAAA others(15): Show |
G | 3 | a0001c0001t0001g0103 a0001c0001t0001g0189 a0001c0002t0004g0102 |
3 | HG02895.hp2 NA19043.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.9+9882_9+9903delGA others(20): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119072 | ||||||
| chr1:50119076 | GAAAGAAA others(11): Show |
G | 1 | a0001c0001t0001g0149 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.9+9886_9+9903delGA others(16): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119076 | ||||||
| chr1:50119080 | GAAAGAAA others(7): Show |
G | 2 | a0001c0001t0002g0113 a0001c0001t0006g0003 |
2 | HG02273.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.9+9890_9+9903delGA others(12): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119080 | ||||||
| chr1:50119084 | GAAAGAAA others(3): Show |
G | 5 | a0001c0001t0001g0111 a0001c0001t0001g0132 a0001c0001t0001g0136 others(2): Show |
5 | HG02896.hp1 HG03579.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+9894_9+9903delGA others(8): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119084 | ||||||
| chr1:50119088 | GAAAGAA | G | 13 | a0001c0001t0001g0005 a0001c0001t0001g0094 a0001c0001t0001g0104 others(10): Show |
13 | HG00280.hp1 HG00642.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.9+9902_9+9907delAA others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119088 | ||||||
| chr1:50119092 | GAA | G | 17 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0109 others(14): Show |
17 | HG00099.hp2 HG00609.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.9+9898_9+9899delAA | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119092 | ||||||
| chr1:50119094 | A | AAG | 26 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0099 others(23): Show |
26 | HG00423.hp2 HG01069.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.9+9897_9+9898insGA | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119094 | ||||||
| chr1:50119094 | A | AAGAAAG | 11 | a0001c0001t0001g0006 a0001c0001t0001g0130 a0001c0001t0001g0138 others(8): Show |
12 | HG00741.hp2 HG01243.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.9+9897_9+9898insGA others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119094 | ||||||
| chr1:50119094 | A | AAGAAAGA others(3): Show |
5 | a0001c0001t0001g0004 a0001c0001t0001g0146 a0001c0001t0001g0153 others(2): Show |
5 | HG01261.hp2 HG02647.hp1 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.9+9897_9+9898insGA others(8): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119094 | ||||||
| chr1:50119095 | A | AGAAAGAA others(6): Show |
1 | a0001c0001t0001g0217 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.9+9897_9+9898insGA others(11): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50119095 | |||||||
| chr1:50119343 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.9+10145T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50119343 | |||||||
| chr1:50119566 | G | C | 1 | a0001c0001t0001g0017 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.9+10368G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50119566 | |||||||
| chr1:50119611 | A | C | 79 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(76): Show |
83 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.9+10413A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50119611 | |||||||
| chr1:50120046 | T | C | 17 | a0001c0001t0001g0109 a0001c0001t0001g0111 a0001c0001t0001g0112 others(14): Show |
17 | HG01167.hp1 HG01243.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.9+10848T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50120046 | |||||||
| chr1:50120060 | A | AAT | 124 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0094 others(121): Show |
128 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.9+10880_9+10881dup others(2): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50120060 | ||||||
| chr1:50120060 | A | AATAT | 6 | a0001c0001t0001g0006 a0001c0001t0001g0103 a0001c0001t0001g0155 others(3): Show |
7 | HG02280.hp1 HG02723.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.9+10878_9+10881dup others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50120060 | ||||||
| chr1:50120078 | T | C | 2 | a0001c0001t0001g0061 a0001c0001t0001g0074 |
2 | NA18975.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.9+10880T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50120078 | |||||||
| chr1:50120402 | G | A | 4 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0002t0001g0228 others(1): Show |
4 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+11204G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50120402 | |||||||
| chr1:50120852 | G | C | 2 | a0001c0001t0001g0182 a0001c0001t0002g0183 |
2 | NA19060.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.9+11654G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50120852 | |||||||
| chr1:50120956 | G | A | 1 | a0001c0002t0003g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.9+11758G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50120956 | |||||||
| chr1:50121611 | G | C | 5 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0002g0117 others(2): Show |
6 | HG01123.hp2 HG01358.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.9+12413G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50121611 | |||||||
| chr1:50121622 | G | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(38): Show |
42 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.9+12424G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50121622 | |||||||
| chr1:50121853 | C | T | 79 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(76): Show |
83 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.9+12655C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50121853 | |||||||
| chr1:50121907 | C | T | 1 | a0001c0002t0001g0268 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.9+12709C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50121907 | |||||||
| chr1:50122013 | C | T | 7 | a0001c0002t0005g0232 a0001c0002t0005g0235 a0001c0002t0005g0236 others(4): Show |
7 | HG02486.hp2 HG02922.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.9+12815C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50122013 | |||||||
| chr1:50122114 | A | G | 2 | a0001c0002t0001g0162 a0001c0002t0003g0163 |
2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.9+12916A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50122114 | |||||||
| chr1:50122117 | G | T | 1 | a0001c0001t0001g0181 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.9+12919G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50122117 | |||||||
| chr1:50122210 | C | T | 79 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(76): Show |
83 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.9+13012C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50122210 | |||||||
| chr1:50122217 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.9+13019T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50122217 | |||||||
| chr1:50122421 | A | G | 61 | a0001c0001t0001g0176 a0001c0001t0001g0178 a0001c0001t0001g0179 others(58): Show |
62 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.9+13223A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50122421 | |||||||
| chr1:50122754 | G | C | 1 | a0001c0002t0001g0096 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.9+13556G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50122754 | |||||||
| chr1:50122913 | A | G | 3 | a0001c0001t0001g0182 a0001c0001t0001g0223 a0001c0001t0002g0183 |
3 | HG01361.hp1 NA19060.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.9+13715A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50122913 | |||||||
| chr1:50122971 | T | C | 1 | a0001c0002t0001g0096 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.9+13773T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50122971 | |||||||
| chr1:50122993 | C | T | 183 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(180): Show |
189 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.9+13795C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50122993 | |||||||
| chr1:50123053 | C | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0018 |
3 | HG00280.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.9+13855C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50123053 | |||||||
| chr1:50123171 | G | T | 102 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0168 others(99): Show |
104 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.9+13973G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50123171 | |||||||
| chr1:50123173 | G | A | 4 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0002t0001g0228 others(1): Show |
4 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+13975G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50123173 | |||||||
| chr1:50123354 | A | G | 15 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0245 others(12): Show |
16 | HG00642.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.9+14156A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50123354 | |||||||
| chr1:50123485 | T | TA | 79 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(76): Show |
83 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.9+14292dupA | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50123485 | ||||||
| chr1:50123766 | T | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.9+14568T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50123766 | |||||||
| chr1:50124034 | G | A | 1 | a0001c0001t0002g0259 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.9+14836G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50124034 | |||||||
| chr1:50124070 | C | G | 48 | a0001c0001t0001g0176 a0001c0001t0001g0178 a0001c0001t0001g0179 others(45): Show |
49 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.9+14872C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50124070 | |||||||
| chr1:50124119 | C | T | 1 | a0001c0002t0001g0096 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.9+14921C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50124119 | |||||||
| chr1:50124126 | G | A | 79 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(76): Show |
83 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.9+14928G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50124126 | |||||||
| chr1:50124802 | C | T | 1 | a0001c0002t0001g0268 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.9+15604C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50124802 | |||||||
| chr1:50124848 | G | A | 79 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(76): Show |
83 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.9+15650G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50124848 | |||||||
| chr1:50124934 | A | G | 1 | a0001c0001t0001g0154 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.9+15736A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50124934 | |||||||
| chr1:50124966 | G | A | 78 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(75): Show |
82 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.9+15768G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50124966 | |||||||
| chr1:50124977 | G | A | 1 | a0001c0002t0001g0177 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.9+15779G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50124977 | |||||||
| chr1:50125049 | T | C | 1 | a0001c0002t0001g0105 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.9+15851T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50125049 | |||||||
| chr1:50125060 | G | A | 78 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(75): Show |
82 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.9+15862G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50125060 | |||||||
| chr1:50125130 | C | G | 1 | a0001c0001t0001g0262 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.9+15932C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50125130 | |||||||
| chr1:50125733 | G | T | 102 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0168 others(99): Show |
104 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.9+16535G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50125733 | |||||||
| chr1:50125893 | G | A | 59 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(56): Show |
63 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.9+16695G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50125893 | |||||||
| chr1:50126032 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.9+16834C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50126032 | |||||||
| chr1:50126033 | C | G | 79 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(76): Show |
83 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.9+16835C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50126033 | |||||||
| chr1:50126071 | C | T | 102 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0168 others(99): Show |
104 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.9+16873C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50126071 | |||||||
| chr1:50126179 | G | A | 74 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0094 others(71): Show |
77 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.9+16981G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50126179 | |||||||
| chr1:50126419 | G | A | 102 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0168 others(99): Show |
104 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.9+17221G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50126419 | |||||||
| chr1:50126568 | A | C | 1 | a0001c0002t0003g0220 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.9+17370A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50126568 | |||||||
| chr1:50126776 | C | T | 264 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(261): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.9+17578C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50126776 | |||||||
| chr1:50126929 | G | C | 142 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(139): Show |
147 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.9+17731G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50126929 | |||||||
| chr1:50126998 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.9+17800G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50126998 | |||||||
| chr1:50127334 | C | A | 10 | a0001c0001t0001g0112 a0001c0001t0001g0174 a0001c0002t0001g0056 others(7): Show |
10 | HG01167.hp1 HG01243.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.10-17623C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50127334 | |||||||
| chr1:50127460 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.10-17497G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50127460 | |||||||
| chr1:50127469 | T | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0151 a0001c0001t0001g0153 others(1): Show |
5 | NA18954.hp1 NA18977.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.10-17488T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50127469 | |||||||
| chr1:50127569 | C | T | 21 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0073 others(18): Show |
23 | HG00642.hp1 HG00741.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.10-17388C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50127569 | |||||||
| chr1:50127725 | T | C | 2 | a0001c0002t0001g0096 a0001c0002t0001g0268 |
2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.10-17232T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50127725 | |||||||
| chr1:50127857 | A | G | 1 | a0001c0001t0009g0116 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.10-17100A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50127857 | |||||||
| chr1:50127939 | C | T | 12 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0073 others(9): Show |
13 | HG00642.hp1 HG00741.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.10-17018C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50127939 | |||||||
| chr1:50127949 | G | A | 1 | a0001c0001t0001g0267 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.10-17008G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50127949 | |||||||
| chr1:50127988 | G | T | 1 | a0001c0002t0003g0220 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.10-16969G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50127988 | |||||||
| chr1:50127994 | ATTGGCT | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0156 |
2 | HG02129.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.10-16941_10-16936d others(8): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50127994 | ||||||
| chr1:50128137 | C | T | 1 | a0001c0002t0008g0115 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.10-16820C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50128137 | |||||||
| chr1:50128166 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.10-16791G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50128166 | |||||||
| chr1:50128520 | G | A | 1 | a0001c0002t0001g0096 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.10-16437G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50128520 | |||||||
| chr1:50128755 | G | A | 1 | a0001c0002t0001g0162 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.10-16202G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50128755 | |||||||
| chr1:50128764 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.10-16193T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50128764 | |||||||
| chr1:50128810 | T | C | 7 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(4): Show |
7 | HG00673.hp1 HG01109.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.10-16147T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50128810 | |||||||
| chr1:50128810 | T | G | 3 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0002t0001g0228 |
3 | HG01891.hp2 HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.10-16147T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50128810 | |||||||
| chr1:50128913 | A | C | 10 | a0001c0001t0001g0006 a0001c0001t0001g0101 a0001c0001t0001g0111 others(7): Show |
11 | HG01069.hp1 HG01109.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.10-16044A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50128913 | |||||||
| chr1:50128925 | C | G | 2 | a0001c0002t0001g0096 a0001c0002t0001g0268 |
2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.10-16032C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50128925 | |||||||
| chr1:50129274 | G | A | 100 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0017 others(97): Show |
105 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.10-15683G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50129274 | |||||||
| chr1:50129514 | T | C | 2 | a0001c0001t0001g0174 a0001c0002t0001g0167 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.10-15443T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50129514 | |||||||
| chr1:50129867 | T | C | 2 | a0001c0001t0001g0109 a0001c0002t0013g0095 |
2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.10-15090T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50129867 | |||||||
| chr1:50130006 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.10-14951T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50130006 | |||||||
| chr1:50130063 | C | T | 1 | a0001c0002t0004g0059 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.10-14894C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50130063 | |||||||
| chr1:50130115 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.10-14842A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50130115 | |||||||
| chr1:50130311 | G | A | 150 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(147): Show |
157 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.10-14646G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50130311 | |||||||
| chr1:50130324 | G | A | 152 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
159 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.10-14633G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50130324 | |||||||
| chr1:50130725 | A | G | 2 | a0001c0002t0001g0096 a0001c0002t0001g0268 |
2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.10-14232A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50130725 | |||||||
| chr1:50130785 | A | G | 152 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
159 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.10-14172A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50130785 | |||||||
| chr1:50131015 | T | C | 49 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0142 others(46): Show |
51 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.10-13942T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50131015 | |||||||
| chr1:50131172 | C | A | 50 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0142 others(47): Show |
52 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.10-13785C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50131172 | |||||||
| chr1:50131330 | A | G | 2 | a0001c0001t0001g0109 a0001c0002t0013g0095 |
2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.10-13627A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50131330 | |||||||
| chr1:50131408 | T | C | 2 | a0001c0001t0001g0188 a0001c0001t0001g0207 |
2 | HG01255.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.10-13549T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50131408 | |||||||
| chr1:50131781 | T | C | 1 | a0001c0001t0002g0125 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.10-13176T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50131781 | |||||||
| chr1:50131886 | TA | T | 30 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0035 others(27): Show |
32 | HG00642.hp1 HG00741.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.10-13055delA | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50131886 | ||||||
| chr1:50131946 | A | G | 1 | a0001c0002t0004g0059 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.10-13011A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50131946 | |||||||
| chr1:50132063 | A | G | 6 | a0001c0001t0001g0053 a0001c0001t0001g0241 a0001c0002t0004g0009 others(3): Show |
6 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.10-12894A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50132063 | |||||||
| chr1:50132082 | A | T | 1 | a0001c0001t0002g0180 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.10-12875A>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50132082 | |||||||
| chr1:50132696 | C | T | 100 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0017 others(97): Show |
105 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.10-12261C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50132696 | |||||||
| chr1:50133078 | G | T | 49 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0142 others(46): Show |
51 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.10-11879G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50133078 | |||||||
| chr1:50133215 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.10-11742T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50133215 | |||||||
| chr1:50133598 | G | GA | 3 | a0001c0001t0001g0242 a0001c0002t0003g0172 a0001c0002t0003g0263 |
3 | HG02257.hp1 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.10-11355dupA | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133598 | ||||||
| chr1:50133599 | A | AAAAAG | 3 | a0001c0002t0003g0243 a0001c0002t0003g0244 a0001c0002t0004g0072 |
3 | HG02922.hp2 HG02965.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.10-11355_10-11354i others(7): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133599 | ||||||
| chr1:50133599 | A | AAAAAGAA others(6): Show |
1 | a0001c0002t0003g0240 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.10-11355_10-11354i others(15): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133599 | ||||||
| chr1:50133599 | A | AAAAG | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0018 others(40): Show |
45 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.10-11308_10-11305d others(6): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133599 | ||||||
| chr1:50133599 | A | AAAAGAAA others(1): Show |
56 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(53): Show |
56 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.10-11312_10-11305d others(10): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133599 | ||||||
| chr1:50133599 | A | AAAAGAAA others(5): Show |
27 | a0001c0001t0001g0038 a0001c0001t0001g0053 a0001c0001t0001g0085 others(24): Show |
27 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.10-11316_10-11305d others(14): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133599 | ||||||
| chr1:50133599 | A | AAAAGAAA others(9): Show |
9 | a0001c0001t0001g0057 a0001c0001t0001g0064 a0001c0001t0001g0196 others(6): Show |
9 | HG02056.hp1 HG02109.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.10-11320_10-11305d others(18): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133599 | ||||||
| chr1:50133599 | A | AAAGAAAG others(8): Show |
1 | a0001c0002t0003g0010 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.10-11356_10-11355i others(17): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133599 | ||||||
| chr1:50133599 | A | AAAGAAAG others(12): Show |
1 | a0001c0001t0001g0179 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.10-11356_10-11355i others(21): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133599 | ||||||
| chr1:50133599 | AAAAG | A | 25 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0022 others(22): Show |
26 | HG00735.hp1 HG01069.hp2 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.10-11308_10-11305d others(6): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133599 | ||||||
| chr1:50133599 | AAAAGAAA others(1): Show |
A | 22 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0030 others(19): Show |
22 | HG00609.hp2 HG01167.hp1 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.10-11312_10-11305d others(10): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133599 | ||||||
| chr1:50133599 | AAAAGAAA others(5): Show |
A | 13 | a0001c0001t0001g0066 a0001c0001t0001g0080 a0001c0001t0001g0082 others(10): Show |
13 | HG00642.hp1 HG02132.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.10-11316_10-11305d others(14): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133599 | ||||||
| chr1:50133599 | AAAAGAAA others(9): Show |
A | 1 | a0001c0002t0013g0095 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.10-11320_10-11305d others(18): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133599 | ||||||
| chr1:50133599 | AAAAGAAA others(13): Show |
A | 2 | a0001c0001t0001g0069 a0001c0002t0001g0107 |
2 | HG01243.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.10-11324_10-11305d others(22): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133599 | ||||||
| chr1:50133635 | GAAAGAAA others(3): Show |
G | 3 | a0001c0001t0001g0184 a0001c0001t0001g0189 a0001c0001t0001g0190 |
3 | HG02280.hp2 NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.10-11320_10-11311d others(12): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133635 | ||||||
| chr1:50133649 | AAG | A | 4 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0189 others(1): Show |
4 | HG02280.hp2 HG03540.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-11304_10-11303d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133649 | ||||||
| chr1:50133651 | G | GAA | 3 | a0001c0001t0002g0041 a0001c0001t0002g0183 a0001c0002t0001g0268 |
3 | HG00438.hp2 HG02647.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.10-11305_10-11304i others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133651 | ||||||
| chr1:50133651 | G | GAAAGAAA others(3): Show |
1 | a0001c0001t0001g0182 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.10-11305_10-11304i others(12): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133651 | ||||||
| chr1:50133651 | G | GAAAGAAG others(3): Show |
1 | a0001c0001t0002g0076 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.10-11305_10-11304i others(12): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133651 | ||||||
| chr1:50133652 | A | G | 1 | a0001c0001t0002g0050 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.10-11305A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50133652 | |||||||
| chr1:50133653 | G | A | 2 | a0001c0001t0002g0215 a0001c0002t0001g0096 |
2 | HG03209.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.10-11304G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50133653 | |||||||
| chr1:50133655 | A | AAG | 4 | a0001c0001t0001g0182 a0001c0001t0002g0041 a0001c0001t0002g0183 others(1): Show |
4 | HG00438.hp2 HG02647.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-11300_10-11299d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133655 | ||||||
| chr1:50133655 | A | G | 2 | a0001c0001t0002g0215 a0001c0002t0001g0096 |
2 | HG03209.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.10-11302A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50133655 | |||||||
| chr1:50133746 | A | G | 1 | a0001c0002t0001g0107 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.10-11211A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50133746 | |||||||
| chr1:50133872 | T | G | 1 | a0001c0001t0001g0196 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.10-11085T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50133872 | |||||||
| chr1:50133905 | A | G | 1 | a0001c0001t0009g0116 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.10-11052A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50133905 | |||||||
| chr1:50134320 | G | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0101 a0001c0001t0001g0111 others(6): Show |
10 | HG01069.hp1 HG01109.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.10-10637G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50134320 | |||||||
| chr1:50134663 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.10-10294G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50134663 | |||||||
| chr1:50134911 | G | T | 1 | a0001c0002t0005g0238 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.10-10046G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50134911 | |||||||
| chr1:50134967 | T | G | 1 | a0001c0001t0001g0020 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.10-9990T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50134967 | |||||||
| chr1:50134972 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.10-9985A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50134972 | |||||||
| chr1:50135209 | C | T | 10 | a0001c0001t0001g0112 a0001c0002t0001g0056 a0001c0002t0001g0105 others(7): Show |
10 | HG01167.hp1 HG01243.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.10-9748C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50135209 | |||||||
| chr1:50135595 | T | G | 4 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0189 others(1): Show |
4 | HG02280.hp2 HG03540.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-9362T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50135595 | |||||||
| chr1:50136064 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.10-8893G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50136064 | |||||||
| chr1:50136074 | G | A | 1 | a0001c0002t0013g0095 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.10-8883G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50136074 | |||||||
| chr1:50136452 | T | C | 1 | a0001c0001t0002g0258 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.10-8505T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50136452 | |||||||
| chr1:50136748 | A | G | 2 | a0001c0002t0001g0096 a0001c0002t0001g0268 |
2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.10-8209A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50136748 | |||||||
| chr1:50136749 | T | C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0221 a0001c0001t0001g0223 |
3 | HG00140.hp1 HG01361.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.10-8208T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50136749 | |||||||
| chr1:50136823 | G | A | 79 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0023 others(76): Show |
82 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.10-8134G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50136823 | |||||||
| chr1:50137006 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.10-7951T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50137006 | |||||||
| chr1:50137078 | A | G | 1 | a0001c0001t0011g0212 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.10-7879A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50137078 | |||||||
| chr1:50137112 | G | C | 1 | a0001c0001t0001g0062 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.10-7845G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50137112 | |||||||
| chr1:50137172 | T | G | 1 | a0001c0002t0004g0059 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.10-7785T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50137172 | |||||||
| chr1:50137390 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.10-7567T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50137390 | |||||||
| chr1:50137955 | A | T | 1 | a0001c0001t0001g0141 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.10-7002A>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50137955 | |||||||
| chr1:50138072 | G | A | 1 | a0001c0001t0009g0116 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.10-6885G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50138072 | |||||||
| chr1:50138214 | A | G | 1 | a0001c0002t0003g0163 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.10-6743A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50138214 | |||||||
| chr1:50138323 | A | C | 76 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0023 others(73): Show |
79 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.10-6634A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50138323 | |||||||
| chr1:50138465 | CT | C | 99 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0017 others(96): Show |
104 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.10-6480delT | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50138465 | ||||||
| chr1:50138546 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.10-6411G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50138546 | |||||||
| chr1:50139565 | C | G | 1 | a0001c0001t0001g0001 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.10-5392C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50139565 | |||||||
| chr1:50139665 | T | C | 152 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
159 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.10-5292T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50139665 | |||||||
| chr1:50139689 | G | A | 2 | a0001c0002t0001g0096 a0001c0002t0001g0268 |
2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.10-5268G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50139689 | |||||||
| chr1:50139805 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.10-5152G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50139805 | |||||||
| chr1:50139976 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.10-4981T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50139976 | |||||||
| chr1:50140072 | C | T | 2 | a0001c0002t0001g0096 a0001c0002t0001g0268 |
2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.10-4885C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50140072 | |||||||
| chr1:50140245 | G | C | 2 | a0001c0002t0001g0098 a0001c0002t0001g0114 |
2 | HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.10-4712G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50140245 | |||||||
| chr1:50140255 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.10-4702T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50140255 | |||||||
| chr1:50140801 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.10-4156T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50140801 | |||||||
| chr1:50141204 | A | G | 177 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(174): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.10-3753A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50141204 | |||||||
| chr1:50141357 | T | G | 10 | a0001c0001t0001g0112 a0001c0002t0001g0056 a0001c0002t0001g0105 others(7): Show |
10 | HG01167.hp1 HG01243.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.10-3600T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50141357 | |||||||
| chr1:50141688 | G | T | 1 | a0001c0002t0001g0107 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.10-3269G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50141688 | |||||||
| chr1:50141958 | C | T | 1 | a0001c0002t0003g0220 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.10-2999C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50141958 | |||||||
| chr1:50141998 | T | G | 2 | a0001c0002t0001g0060 a0001c0002t0001g0211 |
2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.10-2959T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50141998 | |||||||
| chr1:50142194 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.10-2763A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50142194 | |||||||
| chr1:50142454 | C | T | 2 | a0001c0001t0001g0109 a0001c0002t0013g0095 |
2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.10-2503C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50142454 | |||||||
| chr1:50142493 | G | A | 1 | a0001c0001t0002g0117 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.10-2464G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50142493 | |||||||
| chr1:50142665 | G | T | 1 | a0001c0001t0001g0017 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.10-2292G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50142665 | |||||||
| chr1:50143492 | T | A | 1 | a0001c0002t0013g0095 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.10-1465T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50143492 | |||||||
| chr1:50143527 | C | T | 1 | a0001c0001t0002g0257 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.10-1430C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50143527 | |||||||
| chr1:50143537 | C | T | 1 | a0001c0002t0001g0246 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.10-1420C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50143537 | |||||||
| chr1:50143592 | C | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0222 |
3 | HG01167.hp2 HG01169.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.10-1365C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50143592 | |||||||
| chr1:50143779 | G | T | 2 | a0001c0002t0001g0186 a0001c0002t0001g0199 |
2 | HG02818.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.10-1178G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50143779 | |||||||
| chr1:50143811 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.10-1146T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50143811 | |||||||
| chr1:50143834 | A | G | 1 | a0001c0002t0007g0237 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.10-1123A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50143834 | |||||||
| chr1:50144437 | G | A | 1 | a0001c0002t0001g0162 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.10-520G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50144437 | |||||||
| chr1:50145326 | T | G | 1 | a0001c0002t0001g0229 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.250+129T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50145326 | |||||||
| chr1:50145366 | T | C | 1 | a0001c0001t0001g0248 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.250+169T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50145366 | |||||||
| chr1:50145619 | C | G | 1 | a0001c0002t0007g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.250+422C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50145619 | |||||||
| chr1:50145866 | T | A | 1 | a0001c0001t0002g0145 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.250+669T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50145866 | |||||||
| chr1:50146028 | G | T | 1 | a0001c0001t0001g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.250+831G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50146028 | |||||||
| chr1:50146154 | GT | G | 148 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(145): Show |
155 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.250+970delT | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50146154 | ||||||
| chr1:50146154 | GTT | G | 5 | a0001c0001t0001g0128 a0001c0001t0001g0147 a0001c0002t0001g0096 others(2): Show |
5 | HG01070.hp2 HG01168.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.250+969_250+970del others(2): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50146154 | ||||||
| chr1:50146238 | A | ATG | 3 | a0001c0001t0001g0071 a0001c0001t0001g0213 a0001c0001t0001g0214 |
3 | NA18959.hp1 NA18985.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.250+1051_250+1052d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50146238 | ||||||
| chr1:50146248 | G | A | 1 | a0001c0002t0004g0231 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.250+1051G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50146248 | |||||||
| chr1:50146506 | A | G | 4 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0006g0003 others(1): Show |
5 | HG01123.hp2 HG01358.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.250+1309A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50146506 | |||||||
| chr1:50146578 | A | G | 57 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0024 others(54): Show |
59 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.250+1381A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50146578 | |||||||
| chr1:50147042 | C | T | 2 | a0001c0001t0002g0041 a0001c0001t0002g0215 |
2 | HG00438.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.250+1845C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50147042 | |||||||
| chr1:50147203 | A | C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0245 |
2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.250+2006A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50147203 | |||||||
| chr1:50147232 | G | T | 1 | a0001c0002t0003g0163 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.250+2035G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50147232 | |||||||
| chr1:50147359 | C | A | 1 | a0001c0002t0001g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.250+2162C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50147359 | |||||||
| chr1:50147508 | A | C | 1 | a0001c0001t0001g0187 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.250+2311A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50147508 | |||||||
| chr1:50147587 | G | A | 2 | a0001c0002t0001g0096 a0001c0002t0001g0268 |
2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.250+2390G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50147587 | |||||||
| chr1:50147728 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.250+2531A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50147728 | |||||||
| chr1:50148004 | T | G | 99 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0017 others(96): Show |
104 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.250+2807T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50148004 | |||||||
| chr1:50148017 | G | A | 2 | a0001c0001t0001g0188 a0001c0001t0001g0207 |
2 | HG01255.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.250+2820G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50148017 | |||||||
| chr1:50148100 | G | A | 50 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0142 others(47): Show |
52 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.250+2903G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50148100 | |||||||
| chr1:50148429 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.250+3232A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50148429 | |||||||
| chr1:50148873 | T | G | 3 | a0001c0001t0001g0080 a0001c0001t0001g0083 a0001c0001t0001g0195 |
3 | HG02132.hp1 NA18965.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.250+3676T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50148873 | |||||||
| chr1:50149062 | G | A | 1 | a0001c0002t0001g0162 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.250+3865G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50149062 | |||||||
| chr1:50149136 | G | A | 6 | a0001c0001t0001g0053 a0001c0001t0001g0241 a0001c0002t0004g0009 others(3): Show |
6 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.250+3939G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50149136 | |||||||
| chr1:50149303 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.250+4106C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50149303 | |||||||
| chr1:50149499 | G | A | 15 | a0001c0001t0001g0081 a0001c0001t0001g0112 a0001c0002t0001g0056 others(12): Show |
15 | HG01167.hp1 HG01243.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.250+4302G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50149499 | |||||||
| chr1:50149542 | C | CT | 63 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0035 others(60): Show |
65 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.250+4364dupT | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50149542 | ||||||
| chr1:50149543 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.250+4346T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50149543 | |||||||
| chr1:50149694 | CCACCACG others(3): Show |
C | 1 | a0001c0002t0008g0115 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.250+4498_250+4507d others(12): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50149694 | |||||||
| chr1:50149705 | G | C | 1 | a0001c0001t0001g0128 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.250+4508G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50149705 | |||||||
| chr1:50149955 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.250+4758T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50149955 | |||||||
| chr1:50150042 | A | AAAAGC | 8 | a0001c0001t0001g0004 a0001c0001t0001g0130 a0001c0001t0001g0131 others(5): Show |
9 | HG00735.hp1 HG00741.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.250+4850_250+4854d others(7): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50150042 | ||||||
| chr1:50150055 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.250+4858T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50150055 | |||||||
| chr1:50150189 | C | G | 1 | a0001c0001t0001g0175 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.250+4992C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50150189 | |||||||
| chr1:50150266 | G | A | 2 | a0001c0002t0001g0096 a0001c0002t0001g0268 |
2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.250+5069G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50150266 | |||||||
| chr1:50150293 | G | A | 16 | a0001c0001t0001g0081 a0001c0001t0001g0090 a0001c0001t0001g0112 others(13): Show |
16 | HG01167.hp1 HG01243.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.250+5096G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50150293 | |||||||
| chr1:50150703 | G | T | 2 | a0001c0002t0003g0002 a0001c0002t0003g0031 |
3 | HG01168.hp1 HG01169.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.250+5506G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50150703 | |||||||
| chr1:50151115 | C | T | 1 | a0001c0002t0001g0268 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.250+5918C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50151115 | |||||||
| chr1:50151303 | G | A | 1 | a0001c0001t0001g0267 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.250+6106G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50151303 | |||||||
| chr1:50151618 | G | C | 169 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(166): Show |
176 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.250+6421G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50151618 | |||||||
| chr1:50151824 | G | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0043 |
2 | HG00140.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.250+6627G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50151824 | |||||||
| chr1:50151878 | G | A | 12 | a0001c0001t0002g0251 a0001c0001t0002g0252 a0001c0001t0002g0253 others(9): Show |
12 | HG02148.hp2 NA18948.hp1 NA18950.hp1 others(9): Show |
intron_variant | MODIFIER | c.250+6681G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50151878 | |||||||
| chr1:50152021 | CAG | C | 16 | a0001c0001t0001g0081 a0001c0001t0001g0109 a0001c0001t0001g0112 others(13): Show |
16 | HG01167.hp1 HG01243.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.250+6828_250+6829d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50152021 | ||||||
| chr1:50152102 | A | C | 2 | a0001c0002t0001g0096 a0001c0002t0001g0268 |
2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.250+6905A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50152102 | |||||||
| chr1:50152182 | G | T | 1 | a0001c0002t0004g0231 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.250+6985G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50152182 | |||||||
| chr1:50152191 | C | G | 4 | a0001c0001t0001g0081 a0001c0002t0001g0091 a0001c0002t0001g0092 others(1): Show |
4 | HG02109.hp1 HG02622.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.250+6994C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50152191 | |||||||
| chr1:50152202 | A | C | 1 | a0001c0002t0001g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.250+7005A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50152202 | |||||||
| chr1:50152411 | A | AAC | 5 | a0001c0001t0001g0100 a0001c0001t0001g0149 a0001c0001t0002g0117 others(2): Show |
5 | HG01256.hp1 HG02559.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.250+7233_250+7234d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50152411 | ||||||
| chr1:50152430 | A | C | 1 | a0001c0001t0001g0173 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.250+7233A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50152430 | |||||||
| chr1:50152556 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.250+7359C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50152556 | |||||||
| chr1:50152689 | C | A | 2 | a0001c0001t0001g0188 a0001c0001t0001g0207 |
2 | HG01255.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.250+7492C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50152689 | |||||||
| chr1:50152766 | G | A | 3 | a0001c0001t0002g0145 a0001c0002t0001g0060 a0001c0002t0001g0211 |
3 | HG02976.hp1 HG03139.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.250+7569G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50152766 | |||||||
| chr1:50152829 | A | G | 6 | a0001c0001t0001g0053 a0001c0001t0001g0241 a0001c0002t0004g0009 others(3): Show |
6 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.250+7632A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50152829 | |||||||
| chr1:50153095 | C | T | 7 | a0001c0001t0001g0157 a0001c0001t0001g0248 a0001c0001t0001g0249 others(4): Show |
7 | HG00642.hp1 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.250+7898C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50153095 | |||||||
| chr1:50153096 | G | A | 53 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0142 others(50): Show |
55 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.250+7899G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50153096 | |||||||
| chr1:50153248 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0002g0143 |
2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.250+8051G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50153248 | |||||||
| chr1:50153336 | T | A | 1 | a0001c0001t0002g0210 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.250+8139T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50153336 | |||||||
| chr1:50153368 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.250+8171G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50153368 | |||||||
| chr1:50153403 | A | T | 1 | a0001c0001t0002g0210 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.250+8206A>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50153403 | |||||||
| chr1:50153453 | G | A | 1 | a0001c0001t0006g0118 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.250+8256G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50153453 | |||||||
| chr1:50153677 | T | C | 51 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0142 others(48): Show |
53 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.250+8480T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50153677 | |||||||
| chr1:50153918 | A | G | 11 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(8): Show |
11 | HG00140.hp1 HG00280.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.250+8721A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50153918 | |||||||
| chr1:50154020 | T | A | 1 | a0001c0001t0001g0016 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.250+8823T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50154020 | |||||||
| chr1:50154044 | C | T | 1 | a0001c0002t0004g0231 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.250+8847C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50154044 | |||||||
| chr1:50154056 | A | C | 1 | a0001c0002t0004g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.250+8859A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50154056 | |||||||
| chr1:50154125 | C | T | 1 | a0001c0002t0004g0059 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.250+8928C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50154125 | |||||||
| chr1:50154312 | G | A | 1 | a0001c0002t0004g0059 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.250+9115G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50154312 | |||||||
| chr1:50154358 | C | A | 1 | a0001c0001t0001g0196 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.250+9161C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50154358 | |||||||
| chr1:50154389 | T | TAA | 152 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
159 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.250+9193_250+9194i others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50154389 | ||||||
| chr1:50154493 | G | T | 1 | a0001c0002t0001g0162 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.250+9296G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50154493 | |||||||
| chr1:50154522 | C | T | 1 | a0001c0002t0001g0056 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.250+9325C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50154522 | |||||||
| chr1:50154523 | G | A | 2 | a0001c0002t0001g0096 a0001c0002t0001g0268 |
2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.250+9326G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50154523 | |||||||
| chr1:50154752 | T | TTG | 28 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(25): Show |
28 | HG00140.hp1 HG00280.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.250+9587_250+9588d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50154752 | ||||||
| chr1:50154752 | T | TTGTG | 3 | a0001c0001t0001g0063 a0001c0001t0001g0187 a0001c0002t0004g0265 |
3 | HG00323.hp2 HG02145.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.250+9585_250+9588d others(6): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50154752 | ||||||
| chr1:50154752 | TTG | T | 119 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
124 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.250+9587_250+9588d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50154752 | ||||||
| chr1:50154861 | T | C | 1 | a0001c0001t0002g0259 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.250+9664T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50154861 | |||||||
| chr1:50154908 | T | A | 6 | a0001c0001t0001g0053 a0001c0001t0001g0241 a0001c0002t0004g0009 others(3): Show |
6 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.250+9711T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50154908 | |||||||
| chr1:50155005 | C | G | 1 | a0001c0001t0001g0161 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.250+9808C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50155005 | |||||||
| chr1:50155034 | T | C | 1 | a0001c0002t0001g0162 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.250+9837T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50155034 | |||||||
| chr1:50155058 | A | C | 1 | a0001c0002t0004g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.250+9861A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50155058 | |||||||
| chr1:50155070 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.250+9873T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50155070 | |||||||
| chr1:50155172 | C | T | 2 | a0001c0002t0001g0096 a0001c0002t0001g0268 |
2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.250+9975C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50155172 | |||||||
| chr1:50155273 | A | G | 22 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0073 others(19): Show |
24 | HG00642.hp1 HG00741.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.250+10076A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50155273 | |||||||
| chr1:50155440 | ACATGGAA others(11): Show |
A | 1 | a0001c0001t0002g0259 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.250+10244_250+1026 others(22): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50155440 | |||||||
| chr1:50155621 | G | A | 51 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0142 others(48): Show |
53 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.250+10424G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50155621 | |||||||
| chr1:50155636 | G | T | 1 | a0001c0001t0002g0210 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.250+10439G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50155636 | |||||||
| chr1:50155666 | T | C | 1 | a0001c0001t0009g0116 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.250+10469T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50155666 | |||||||
| chr1:50155785 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.250+10588C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50155785 | |||||||
| chr1:50155964 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.250+10767C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50155964 | |||||||
| chr1:50156019 | G | A | 2 | a0001c0001t0001g0109 a0001c0001t0001g0168 |
2 | HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.250+10822G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50156019 | |||||||
| chr1:50156027 | G | A | 2 | a0001c0001t0001g0119 a0001c0001t0002g0210 |
2 | HG01358.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.250+10830G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50156027 | |||||||
| chr1:50156031 | G | A | 50 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0142 others(47): Show |
52 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.250+10834G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50156031 | |||||||
| chr1:50156031 | G | GCA | 82 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0023 others(79): Show |
85 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.250+10853_250+1085 others(6): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50156031 | ||||||
| chr1:50156302 | A | C | 1 | a0001c0001t0002g0259 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.250+11105A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50156302 | |||||||
| chr1:50156303 | C | A | 1 | a0001c0001t0002g0259 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.250+11106C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50156303 | |||||||
| chr1:50156614 | G | A | 1 | a0001c0002t0013g0095 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.250+11417G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50156614 | |||||||
| chr1:50156754 | C | G | 1 | a0001c0001t0002g0210 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.250+11557C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50156754 | |||||||
| chr1:50156756 | G | C | 1 | a0001c0001t0002g0210 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.250+11559G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50156756 | |||||||
| chr1:50156898 | A | T | 1 | a0001c0001t0002g0259 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.250+11701A>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50156898 | |||||||
| chr1:50157295 | C | T | 1 | a0001c0002t0003g0163 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.250+12098C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50157295 | |||||||
| chr1:50157652 | A | G | 3 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0002t0001g0246 |
3 | HG00642.hp1 HG02818.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.250+12455A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50157652 | |||||||
| chr1:50157838 | C | G | 1 | a0001c0001t0002g0259 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.250+12641C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50157838 | |||||||
| chr1:50157839 | A | C | 1 | a0001c0001t0002g0259 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.250+12642A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50157839 | |||||||
| chr1:50157840 | C | A | 1 | a0001c0001t0002g0259 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.250+12643C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50157840 | |||||||
| chr1:50158042 | T | G | 1 | a0001c0001t0002g0210 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.250+12845T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50158042 | |||||||
| chr1:50158068 | T | C | 152 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
159 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.250+12871T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50158068 | |||||||
| chr1:50158191 | A | G | 1 | a0001c0001t0002g0210 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.250+12994A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50158191 | |||||||
| chr1:50158464 | T | A | 1 | a0001c0002t0001g0177 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.250+13267T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50158464 | |||||||
| chr1:50158594 | C | T | 20 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0073 others(17): Show |
22 | HG00642.hp1 HG00741.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.250+13397C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50158594 | |||||||
| chr1:50158711 | A | G | 1 | a0001c0001t0001g0241 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.250+13514A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50158711 | |||||||
| chr1:50158776 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.250+13579C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50158776 | |||||||
| chr1:50158823 | G | A | 1 | a0001c0001t0012g0137 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.250+13626G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50158823 | |||||||
| chr1:50158916 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.250+13719T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50158916 | |||||||
| chr1:50159039 | C | CA | 34 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0073 others(31): Show |
36 | HG00642.hp1 HG00741.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.250+13860dupA | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50159039 | ||||||
| chr1:50159054 | A | AG | 73 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0023 others(70): Show |
76 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.250+13857_250+1385 others(5): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50159054 | |||||||
| chr1:50159054 | A | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0082 a0001c0001t0001g0158 |
3 | HG02698.hp1 NA18962.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.250+13857A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50159054 | |||||||
| chr1:50159092 | A | T | 1 | a0001c0002t0005g0236 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.250+13895A>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50159092 | |||||||
| chr1:50159116 | A | T | 2 | a0001c0001t0001g0100 a0001c0002t0001g0126 |
2 | HG02559.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.250+13919A>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50159116 | |||||||
| chr1:50159242 | T | A | 1 | a0001c0001t0002g0259 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.250+14045T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50159242 | |||||||
| chr1:50159371 | A | G | 169 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(166): Show |
176 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.250+14174A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50159371 | |||||||
| chr1:50159437 | A | C | 2 | a0001c0001t0001g0198 a0001c0001t0002g0152 |
2 | NA19010.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.250+14240A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50159437 | |||||||
| chr1:50159482 | G | C | 2 | a0001c0002t0001g0096 a0001c0002t0001g0268 |
2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.250+14285G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50159482 | |||||||
| chr1:50159508 | C | G | 20 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0073 others(17): Show |
22 | HG00642.hp1 HG00741.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.250+14311C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50159508 | |||||||
| chr1:50159683 | A | C | 1 | a0001c0002t0001g0060 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.250+14486A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50159683 | |||||||
| chr1:50160021 | T | C | 1 | a0001c0002t0001g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.250+14824T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50160021 | |||||||
| chr1:50160034 | C | A | 1 | a0001c0002t0004g0231 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.250+14837C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50160034 | |||||||
| chr1:50160307 | C | T | 79 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0023 others(76): Show |
82 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.250+15110C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50160307 | |||||||
| chr1:50160317 | A | G | 1 | a0001c0001t0002g0206 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.250+15120A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50160317 | |||||||
| chr1:50160352 | T | G | 1 | a0001c0001t0002g0259 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.250+15155T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50160352 | |||||||
| chr1:50160582 | C | CAGATATT others(23): Show |
1 | a0001c0001t0002g0259 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.250+15386_250+1541 others(34): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50160582 | ||||||
| chr1:50160720 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.250+15523A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50160720 | |||||||
| chr1:50160777 | A | T | 1 | a0001c0002t0001g0186 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.250+15580A>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50160777 | |||||||
| chr1:50160793 | T | G | 1 | a0001c0001t0001g0185 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.250+15596T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50160793 | |||||||
| chr1:50161122 | C | A | 2 | a0001c0001t0002g0048 a0001c0001t0002g0050 |
2 | NA18977.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.250+15925C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50161122 | |||||||
| chr1:50161563 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.251-15526A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50161563 | |||||||
| chr1:50161749 | A | G | 1 | a0001c0002t0001g0093 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.251-15340A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50161749 | |||||||
| chr1:50161843 | G | C | 5 | a0001c0001t0001g0006 a0001c0001t0001g0101 a0001c0001t0001g0111 others(2): Show |
6 | HG01069.hp1 HG01109.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.251-15246G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50161843 | |||||||
| chr1:50161952 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.251-15137G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50161952 | |||||||
| chr1:50162430 | G | A | 1 | a0001c0002t0013g0095 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.251-14659G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50162430 | |||||||
| chr1:50162554 | T | G | 9 | a0001c0001t0001g0006 a0001c0001t0001g0101 a0001c0001t0001g0111 others(6): Show |
10 | HG01069.hp1 HG01109.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.251-14535T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50162554 | |||||||
| chr1:50162587 | C | T | 1 | a0001c0002t0005g0238 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.251-14502C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50162587 | |||||||
| chr1:50162829 | C | G | 3 | a0001c0002t0001g0067 a0001c0002t0001g0075 a0001c0002t0001g0229 |
3 | HG02572.hp1 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.251-14260C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50162829 | |||||||
| chr1:50162852 | AG | A | 8 | a0001c0001t0001g0053 a0001c0001t0001g0241 a0001c0002t0003g0220 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.251-14235delG | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50162852 | ||||||
| chr1:50163098 | C | G | 1 | a0001c0001t0001g0016 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.251-13991C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50163098 | |||||||
| chr1:50163113 | C | T | 1 | a0001c0002t0001g0056 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.251-13976C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50163113 | |||||||
| chr1:50163179 | G | A | 79 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0023 others(76): Show |
82 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.251-13910G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50163179 | |||||||
| chr1:50163451 | G | A | 1 | a0001c0002t0003g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.251-13638G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50163451 | |||||||
| chr1:50163550 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.251-13539G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50163550 | |||||||
| chr1:50163565 | G | A | 1 | a0001c0002t0003g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.251-13524G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50163565 | |||||||
| chr1:50163608 | T | C | 1 | a0001c0002t0004g0231 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.251-13481T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50163608 | |||||||
| chr1:50163719 | G | A | 2 | a0001c0002t0001g0096 a0001c0002t0001g0268 |
2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.251-13370G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50163719 | |||||||
| chr1:50163877 | T | C | 1 | a0001c0002t0004g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.251-13212T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50163877 | |||||||
| chr1:50163929 | C | T | 1 | a0001c0002t0003g0220 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.251-13160C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50163929 | |||||||
| chr1:50164172 | G | C | 2 | a0001c0002t0001g0096 a0001c0002t0001g0268 |
2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.251-12917G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50164172 | |||||||
| chr1:50164207 | G | C | 1 | a0001c0001t0001g0132 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.251-12882G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50164207 | |||||||
| chr1:50164354 | C | G | 2 | a0001c0002t0001g0096 a0001c0002t0001g0268 |
2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.251-12735C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50164354 | |||||||
| chr1:50164732 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.251-12357C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50164732 | |||||||
| chr1:50165108 | G | A | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG00609.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.251-11981G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50165108 | |||||||
| chr1:50165359 | T | G | 1 | a0001c0001t0001g0140 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.251-11730T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50165359 | |||||||
| chr1:50165377 | T | C | 2 | a0001c0001t0002g0252 a0001c0001t0002g0257 |
2 | NA18948.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.251-11712T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50165377 | |||||||
| chr1:50165427 | G | GAT | 57 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0036 others(54): Show |
59 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.251-11648_251-1164 others(6): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50165427 | ||||||
| chr1:50165437 | T | G | 6 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0171 others(3): Show |
6 | HG02145.hp1 HG02647.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.251-11652T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50165437 | |||||||
| chr1:50165437 | TATATAG | T | 8 | a0001c0001t0001g0053 a0001c0001t0001g0241 a0001c0002t0003g0220 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.251-11636_251-1163 others(10): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50165437 | ||||||
| chr1:50165439 | T | G | 1 | a0001c0002t0001g0096 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.251-11650T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50165439 | |||||||
| chr1:50165457 | T | TAC | 4 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0189 others(1): Show |
4 | HG02280.hp2 HG03540.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.251-11617_251-1161 others(6): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50165457 | ||||||
| chr1:50165521 | G | A | 100 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0017 others(97): Show |
105 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.251-11568G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50165521 | |||||||
| chr1:50165529 | A | T | 1 | a0001c0002t0013g0095 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.251-11560A>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50165529 | |||||||
| chr1:50165752 | A | G | 49 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0142 others(46): Show |
51 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.251-11337A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50165752 | |||||||
| chr1:50165762 | G | GTGTGTAT others(3): Show |
247 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(244): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.251-11318_251-1131 others(14): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50165762 | ||||||
| chr1:50165762 | G | GTGTGTAT others(73): Show |
2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.251-11318_251-1131 others(84): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50165762 | ||||||
| chr1:50165772 | G | A | 1 | a0001c0002t0001g0162 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.251-11317G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50165772 | |||||||
| chr1:50165822 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.251-11267A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50165822 | |||||||
| chr1:50166303 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.251-10786A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50166303 | |||||||
| chr1:50166760 | C | T | 3 | a0001c0002t0001g0191 a0001c0002t0003g0192 a0001c0002t0003g0247 |
3 | HG02809.hp2 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.251-10329C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50166760 | |||||||
| chr1:50166930 | A | G | 1 | a0001c0001t0001g0020 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.251-10159A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50166930 | |||||||
| chr1:50166998 | A | T | 1 | a0001c0002t0013g0095 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.251-10091A>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50166998 | |||||||
| chr1:50167023 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.251-10066T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50167023 | |||||||
| chr1:50167406 | G | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.251-9683G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50167406 | |||||||
| chr1:50167704 | G | T | 51 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0142 others(48): Show |
53 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.251-9385G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50167704 | |||||||
| chr1:50168682 | G | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.251-8407G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50168682 | |||||||
| chr1:50168724 | C | T | 15 | a0001c0001t0001g0242 a0001c0002t0003g0008 a0001c0002t0003g0163 others(12): Show |
16 | HG02257.hp1 HG02486.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.251-8365C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50168724 | |||||||
| chr1:50168946 | G | GTA | 9 | a0001c0001t0001g0021 a0001c0001t0001g0066 a0001c0001t0001g0120 others(6): Show |
9 | HG01167.hp1 HG02148.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.251-8126_251-8125d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50168946 | ||||||
| chr1:50168946 | G | GTATA | 40 | a0001c0001t0001g0038 a0001c0001t0001g0142 a0001c0001t0001g0196 others(37): Show |
41 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.251-8128_251-8125d others(6): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50168946 | ||||||
| chr1:50168946 | G | GTATATA | 10 | a0001c0001t0001g0005 a0001c0001t0001g0151 a0001c0001t0001g0153 others(7): Show |
11 | HG00609.hp1 HG02135.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.251-8130_251-8125d others(8): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50168946 | ||||||
| chr1:50168963 | T | C | 1 | a0001c0001t0001g0193 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.251-8126T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50168963 | |||||||
| chr1:50168963 | TAC | T | 3 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0002t0001g0228 |
3 | HG01891.hp2 HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.251-8116_251-8115d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50168963 | ||||||
| chr1:50168984 | G | GTA | 13 | a0001c0001t0001g0053 a0001c0001t0001g0063 a0001c0001t0001g0084 others(10): Show |
13 | HG01891.hp1 HG02145.hp2 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.251-8090_251-8089d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50168984 | ||||||
| chr1:50169029 | A | G | 1 | a0001c0001t0002g0205 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.251-8060A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50169029 | |||||||
| chr1:50169101 | G | A | 1 | a0001c0002t0008g0115 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.251-7988G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50169101 | |||||||
| chr1:50169371 | C | T | 1 | a0001c0001t0002g0087 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.251-7718C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50169371 | |||||||
| chr1:50169849 | A | G | 2 | a0001c0001t0001g0074 a0001c0001t0001g0079 |
2 | HG02040.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.251-7240A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50169849 | |||||||
| chr1:50169859 | T | C | 4 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0189 others(1): Show |
4 | HG02280.hp2 HG03540.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.251-7230T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50169859 | |||||||
| chr1:50170109 | G | A | 1 | a0001c0002t0001g0162 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.251-6980G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50170109 | |||||||
| chr1:50170161 | G | A | 1 | a0001c0002t0004g0059 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.251-6928G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50170161 | |||||||
| chr1:50170520 | C | G | 1 | a0001c0001t0001g0175 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.251-6569C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50170520 | |||||||
| chr1:50170838 | G | A | 50 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0142 others(47): Show |
52 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.251-6251G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50170838 | |||||||
| chr1:50170999 | C | G | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.251-6090C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50170999 | |||||||
| chr1:50171010 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.251-6079G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50171010 | |||||||
| chr1:50171039 | A | G | 7 | a0001c0001t0001g0053 a0001c0001t0001g0241 a0001c0002t0003g0220 others(4): Show |
7 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.251-6050A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50171039 | |||||||
| chr1:50171418 | T | G | 1 | a0001c0001t0001g0112 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.251-5671T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50171418 | |||||||
| chr1:50171532 | A | G | 91 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0017 others(88): Show |
95 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.251-5557A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50171532 | |||||||
| chr1:50171652 | A | G | 1 | a0001c0001t0002g0145 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.251-5437A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50171652 | |||||||
| chr1:50171670 | A | G | 1 | a0001c0002t0004g0059 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.251-5419A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50171670 | |||||||
| chr1:50171843 | G | T | 1 | a0001c0001t0001g0026 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.251-5246G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50171843 | |||||||
| chr1:50171882 | C | T | 152 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
159 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.251-5207C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50171882 | |||||||
| chr1:50172013 | A | G | 2 | a0001c0002t0001g0096 a0001c0002t0001g0268 |
2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.251-5076A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50172013 | |||||||
| chr1:50172079 | GAT | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0025 others(8): Show |
12 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.251-5009_251-5008d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50172079 | |||||||
| chr1:50172179 | AG | A | 4 | a0001c0001t0001g0242 a0001c0002t0003g0172 a0001c0002t0003g0244 others(1): Show |
4 | HG02257.hp1 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.251-4908delG | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50172179 | ||||||
| chr1:50172350 | C | T | 49 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0142 others(46): Show |
51 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.251-4739C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50172350 | |||||||
| chr1:50172362 | A | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(96): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.251-4727A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50172362 | |||||||
| chr1:50172965 | T | C | 1 | a0001c0002t0003g0192 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.251-4124T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50172965 | |||||||
| chr1:50173303 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.251-3786G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50173303 | |||||||
| chr1:50173405 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.251-3684C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50173405 | |||||||
| chr1:50173668 | T | C | 249 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(246): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.251-3421T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50173668 | |||||||
| chr1:50173792 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.251-3297C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50173792 | |||||||
| chr1:50173877 | G | T | 1 | a0001c0001t0001g0104 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.251-3212G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50173877 | |||||||
| chr1:50173990 | C | T | 1 | a0001c0002t0003g0031 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.251-3099C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50173990 | |||||||
| chr1:50173991 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.251-3098G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50173991 | |||||||
| chr1:50174085 | T | C | 7 | a0001c0002t0005g0232 a0001c0002t0005g0235 a0001c0002t0005g0236 others(4): Show |
7 | HG02486.hp2 HG02922.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.251-3004T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50174085 | |||||||
| chr1:50174449 | C | A | 1 | a0001c0001t0001g0040 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.251-2640C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50174449 | |||||||
| chr1:50174488 | G | GT | 86 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0023 others(83): Show |
90 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.251-2588dupT | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50174488 | ||||||
| chr1:50174488 | GT | G | 6 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0218 others(3): Show |
6 | HG01074.hp1 HG01123.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.251-2588delT | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50174488 | ||||||
| chr1:50174990 | C | T | 49 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0142 others(46): Show |
51 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.251-2099C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50174990 | |||||||
| chr1:50175066 | A | G | 2 | a0001c0001t0001g0066 a0001c0001t0001g0245 |
2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.251-2023A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50175066 | |||||||
| chr1:50175160 | A | G | 2 | a0001c0001t0001g0197 a0001c0001t0002g0194 |
2 | HG02056.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.251-1929A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50175160 | |||||||
| chr1:50175284 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.251-1805A>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50175284 | |||||||
| chr1:50175311 | T | C | 1 | a0001c0001t0001g0090 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.251-1778T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50175311 | |||||||
| chr1:50175387 | T | TAC | 17 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0073 others(14): Show |
18 | HG00323.hp2 HG00642.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.251-1667_251-1666d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50175387 | ||||||
| chr1:50175387 | T | TACAC | 5 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0009g0116 others(2): Show |
5 | HG02559.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.251-1669_251-1666d others(6): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50175387 | ||||||
| chr1:50175387 | TAC | T | 31 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(28): Show |
32 | HG00280.hp2 HG01074.hp1 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.251-1667_251-1666d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50175387 | ||||||
| chr1:50175387 | TACAC | T | 91 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(88): Show |
94 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.251-1669_251-1666d others(6): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50175387 | ||||||
| chr1:50175387 | TACACAC | T | 25 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0025 others(22): Show |
26 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(23): Show |
intron_variant | MODIFIER | c.251-1671_251-1666d others(8): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50175387 | ||||||
| chr1:50175387 | TACACACA others(7): Show |
T | 1 | a0001c0001t0001g0063 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.251-1679_251-1666d others(16): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50175387 | ||||||
| chr1:50175946 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.251-1143G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50175946 | |||||||
| chr1:50175984 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0130 |
3 | HG00741.hp2 HG01261.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.251-1105G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50175984 | |||||||
| chr1:50176160 | C | T | 1 | a0001c0002t0001g0229 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.251-929C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50176160 | |||||||
| chr1:50176272 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(82): Show |
86 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.251-817C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50176272 | |||||||
| chr1:50176295 | C | T | 1 | a0001c0001t0010g0108 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.251-794C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50176295 | |||||||
| chr1:50176430 | C | G | 1 | a0001c0001t0002g0041 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.251-659C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50176430 | |||||||
| chr1:50176450 | G | T | 1 | a0001c0001t0001g0038 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.251-639G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50176450 | |||||||
| chr1:50176547 | G | A | 1 | a0001c0002t0001g0067 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.251-542G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50176547 | |||||||
| chr1:50176557 | C | T | 1 | a0001c0001t0002g0264 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.251-532C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50176557 | |||||||
| chr1:50176916 | T | G | 1 | a0001c0001t0002g0077 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.251-173T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50176916 | |||||||
| chr1:50177000 | A | G | 1 | a0001c0001t0002g0204 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.251-89A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50177000 | |||||||
| chr1:50177829 | A | G | 1 | a0001c0001t0002g0019 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.354+637A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50177829 | |||||||
| chr1:50177994 | A | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(247): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.354+802A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50177994 | |||||||
| chr1:50178019 | G | A | 1 | a0001c0002t0004g0059 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.354+827G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50178019 | |||||||
| chr1:50178062 | T | G | 1 | a0001c0001t0001g0120 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.354+870T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50178062 | |||||||
| chr1:50178378 | G | A | 1 | a0001c0002t0013g0095 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.354+1186G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50178378 | |||||||
| chr1:50178841 | G | A | 1 | a0001c0001t0001g0267 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.354+1649G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50178841 | |||||||
| chr1:50178962 | T | G | 1 | a0001c0001t0001g0138 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.354+1770T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50178962 | |||||||
| chr1:50178963 | G | C | 1 | a0001c0001t0001g0138 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.354+1771G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50178963 | |||||||
| chr1:50178964 | C | CT | 142 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(139): Show |
147 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.354+1784dupT | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50178964 | ||||||
| chr1:50178964 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.354+1772C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50178964 | |||||||
| chr1:50179148 | G | A | 45 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0027 others(42): Show |
46 | HG00423.hp2 HG00438.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.354+1956G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50179148 | |||||||
| chr1:50179219 | C | T | 19 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0016 others(16): Show |
19 | HG00609.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.354+2027C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50179219 | |||||||
| chr1:50179506 | A | T | 11 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0029 others(8): Show |
11 | HG00280.hp2 HG00323.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.354+2314A>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50179506 | |||||||
| chr1:50179594 | A | C | 1 | a0001c0001t0010g0108 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.354+2402A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50179594 | |||||||
| chr1:50179789 | T | A | 1 | a0001c0002t0007g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.354+2597T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50179789 | |||||||
| chr1:50179925 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.354+2733T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50179925 | |||||||
| chr1:50180219 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.354+3027A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50180219 | |||||||
| chr1:50180403 | A | G | 7 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0161 others(4): Show |
7 | HG01069.hp1 HG02145.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.354+3211A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50180403 | |||||||
| chr1:50180463 | C | A | 15 | a0001c0002t0001g0191 a0001c0002t0003g0002 a0001c0002t0003g0008 others(12): Show |
17 | HG01168.hp1 HG01169.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.354+3271C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50180463 | |||||||
| chr1:50180817 | G | A | 1 | a0001c0002t0001g0096 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.354+3625G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50180817 | |||||||
| chr1:50180941 | A | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(224): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.354+3749A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50180941 | |||||||
| chr1:50181354 | T | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(238): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.354+4162T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50181354 | |||||||
| chr1:50181568 | G | T | 1 | a0001c0001t0001g0221 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.354+4376G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50181568 | |||||||
| chr1:50181675 | G | GTTTGT | 226 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(223): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.354+4502_354+4506d others(7): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50181675 | ||||||
| chr1:50181803 | C | A | 15 | a0001c0002t0001g0191 a0001c0002t0003g0002 a0001c0002t0003g0008 others(12): Show |
17 | HG01168.hp1 HG01169.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.354+4611C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50181803 | |||||||
| chr1:50181841 | G | A | 1 | a0001c0002t0001g0107 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.354+4649G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50181841 | |||||||
| chr1:50181875 | G | T | 7 | a0001c0002t0004g0009 a0001c0002t0004g0059 a0001c0002t0004g0072 others(4): Show |
7 | HG01243.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.354+4683G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50181875 | |||||||
| chr1:50181972 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0079 |
2 | HG02040.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.354+4780C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50181972 | |||||||
| chr1:50182117 | C | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0130 |
3 | HG00741.hp2 HG01261.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.354+4925C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50182117 | |||||||
| chr1:50182309 | G | A | 1 | a0001c0002t0001g0228 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.354+5117G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50182309 | |||||||
| chr1:50182360 | A | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(240): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.354+5168A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50182360 | |||||||
| chr1:50182802 | G | A | 226 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(223): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.354+5610G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50182802 | |||||||
| chr1:50182870 | CT | C | 18 | a0001c0001t0002g0202 a0001c0001t0009g0116 a0001c0002t0001g0191 others(15): Show |
20 | HG01168.hp1 HG01169.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.354+5690delT | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50182870 | ||||||
| chr1:50182875 | T | C | 1 | a0001c0001t0001g0011 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.354+5683T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50182875 | |||||||
| chr1:50182982 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.354+5790C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50182982 | |||||||
| chr1:50183085 | T | G | 11 | a0001c0002t0001g0092 a0001c0002t0001g0096 a0001c0002t0001g0229 others(8): Show |
11 | HG01243.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.354+5893T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50183085 | |||||||
| chr1:50183123 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.354+5931G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50183123 | |||||||
| chr1:50183465 | G | A | 11 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0025 others(8): Show |
12 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.354+6273G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50183465 | |||||||
| chr1:50183794 | T | C | 1 | a0001c0001t0001g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.354+6602T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50183794 | |||||||
| chr1:50183938 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.354+6746G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50183938 | |||||||
| chr1:50184027 | C | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0014 others(56): Show |
61 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.354+6835C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50184027 | |||||||
| chr1:50184142 | G | A | 1 | a0001c0002t0001g0162 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.354+6950G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50184142 | |||||||
| chr1:50184144 | G | C | 1 | a0001c0002t0013g0095 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.354+6952G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50184144 | |||||||
| chr1:50184197 | C | A | 1 | a0001c0001t0001g0081 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.354+7005C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50184197 | |||||||
| chr1:50184226 | C | T | 12 | a0001c0002t0001g0067 a0001c0002t0001g0075 a0001c0002t0001g0093 others(9): Show |
12 | HG02486.hp2 HG02895.hp1 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.354+7034C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50184226 | |||||||
| chr1:50184257 | G | A | 4 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0218 others(1): Show |
4 | HG01074.hp1 HG01123.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.354+7065G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50184257 | |||||||
| chr1:50184398 | C | CA | 220 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(217): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.354+7222dupA | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50184398 | ||||||
| chr1:50184398 | C | CAA | 13 | a0001c0001t0001g0080 a0001c0001t0001g0083 a0001c0001t0001g0100 others(10): Show |
13 | HG00642.hp1 HG01243.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.354+7221_354+7222d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50184398 | ||||||
| chr1:50184527 | G | A | 41 | a0001c0001t0001g0038 a0001c0001t0001g0200 a0001c0001t0002g0007 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.354+7335G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50184527 | |||||||
| chr1:50185284 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.354+8092C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50185284 | |||||||
| chr1:50185522 | T | A | 4 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0188 others(1): Show |
4 | HG01255.hp1 HG01261.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.355-8243T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50185522 | |||||||
| chr1:50185616 | A | G | 5 | a0001c0001t0001g0064 a0001c0001t0001g0176 a0001c0001t0001g0178 others(2): Show |
5 | HG00423.hp1 HG00438.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.355-8149A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50185616 | |||||||
| chr1:50185731 | G | A | 1 | a0001c0002t0001g0228 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.355-8034G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50185731 | |||||||
| chr1:50185958 | C | T | 1 | a0001c0002t0005g0235 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.355-7807C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50185958 | |||||||
| chr1:50186107 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.355-7658A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50186107 | |||||||
| chr1:50186440 | G | A | 6 | a0001c0002t0003g0008 a0001c0002t0003g0010 a0001c0002t0003g0163 others(3): Show |
7 | HG02572.hp2 HG02630.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.355-7325G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50186440 | |||||||
| chr1:50186565 | G | C | 1 | a0001c0001t0001g0156 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.355-7200G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50186565 | |||||||
| chr1:50186627 | CATAGAA | C | 15 | a0001c0002t0001g0191 a0001c0002t0003g0002 a0001c0002t0003g0008 others(12): Show |
17 | HG01168.hp1 HG01169.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.355-7129_355-7124d others(8): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50186627 | ||||||
| chr1:50186646 | T | G | 221 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(218): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.355-7119T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50186646 | |||||||
| chr1:50186671 | T | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.355-7094T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50186671 | |||||||
| chr1:50186697 | G | A | 1 | a0001c0001t0002g0077 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.355-7068G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50186697 | |||||||
| chr1:50186800 | G | A | 1 | a0001c0001t0002g0117 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.355-6965G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50186800 | |||||||
| chr1:50186842 | A | AAAG | 226 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(223): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.355-6921_355-6920i others(5): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50186842 | ||||||
| chr1:50186895 | A | G | 1 | a0001c0001t0009g0116 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.355-6870A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50186895 | |||||||
| chr1:50186919 | A | G | 4 | a0001c0001t0001g0065 a0001c0001t0001g0124 a0001c0001t0001g0150 others(1): Show |
4 | HG02056.hp2 HG02135.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.355-6846A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50186919 | |||||||
| chr1:50186973 | C | T | 6 | a0001c0002t0001g0060 a0001c0002t0001g0091 a0001c0002t0001g0186 others(3): Show |
6 | HG00642.hp1 HG02109.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.355-6792C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50186973 | |||||||
| chr1:50187160 | G | T | 1 | a0001c0001t0002g0215 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.355-6605G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50187160 | |||||||
| chr1:50187260 | A | G | 1 | a0001c0002t0004g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.355-6505A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50187260 | |||||||
| chr1:50187371 | T | C | 3 | a0001c0001t0001g0149 a0001c0001t0001g0221 a0001c0001t0001g0223 |
3 | HG00140.hp1 HG01256.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.355-6394T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50187371 | |||||||
| chr1:50187460 | A | G | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG02647.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.355-6305A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50187460 | |||||||
| chr1:50188159 | T | A | 1 | a0001c0002t0004g0239 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.355-5606T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50188159 | |||||||
| chr1:50188460 | G | A | 1 | a0001c0002t0001g0107 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.355-5305G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50188460 | |||||||
| chr1:50188487 | T | C | 4 | a0001c0002t0003g0172 a0001c0002t0003g0220 a0001c0002t0003g0244 others(1): Show |
4 | HG02257.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.355-5278T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50188487 | |||||||
| chr1:50189167 | G | A | 15 | a0001c0002t0001g0191 a0001c0002t0003g0002 a0001c0002t0003g0008 others(12): Show |
17 | HG01168.hp1 HG01169.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.355-4598G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50189167 | |||||||
| chr1:50189249 | C | T | 1 | a0001c0002t0004g0239 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.355-4516C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50189249 | |||||||
| chr1:50189305 | C | G | 6 | a0001c0002t0001g0060 a0001c0002t0001g0091 a0001c0002t0001g0186 others(3): Show |
6 | HG00642.hp1 HG02109.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.355-4460C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50189305 | |||||||
| chr1:50189329 | G | A | 6 | a0001c0001t0001g0242 a0001c0001t0001g0262 a0001c0002t0001g0092 others(3): Show |
6 | HG02572.hp1 HG02647.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.355-4436G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50189329 | |||||||
| chr1:50189535 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.355-4230G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50189535 | |||||||
| chr1:50189629 | T | G | 1 | a0001c0002t0001g0246 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.355-4136T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50189629 | |||||||
| chr1:50189666 | G | C | 1 | a0001c0001t0001g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.355-4099G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50189666 | |||||||
| chr1:50189992 | G | T | 1 | a0001c0001t0010g0108 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.355-3773G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50189992 | |||||||
| chr1:50190034 | G | C | 1 | a0001c0002t0004g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.355-3731G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50190034 | |||||||
| chr1:50190204 | G | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0079 |
2 | HG02040.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.355-3561G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50190204 | |||||||
| chr1:50190319 | CTTTCAGC others(14): Show |
C | 1 | a0001c0001t0001g0185 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.355-3445_355-3425d others(23): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50190319 | |||||||
| chr1:50190401 | G | A | 228 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(225): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.355-3364G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50190401 | |||||||
| chr1:50190469 | C | T | 8 | a0001c0002t0001g0060 a0001c0002t0001g0091 a0001c0002t0001g0162 others(5): Show |
8 | HG00642.hp1 HG02109.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.355-3296C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50190469 | |||||||
| chr1:50190574 | T | C | 1 | a0001c0001t0001g0142 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.355-3191T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50190574 | |||||||
| chr1:50190761 | C | T | 5 | a0001c0002t0004g0009 a0001c0002t0004g0089 a0001c0002t0004g0231 others(2): Show |
5 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.355-3004C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50190761 | |||||||
| chr1:50190787 | A | G | 59 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0014 others(56): Show |
61 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.355-2978A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50190787 | |||||||
| chr1:50190921 | T | A | 14 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0010 others(11): Show |
16 | HG01168.hp1 HG01169.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.355-2844T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50190921 | |||||||
| chr1:50190992 | T | G | 1 | a0001c0001t0001g0061 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.355-2773T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50190992 | |||||||
| chr1:50191044 | C | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0101 a0001c0001t0001g0111 others(3): Show |
7 | HG01069.hp1 HG01109.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.355-2721C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50191044 | |||||||
| chr1:50191249 | A | G | 5 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0171 others(2): Show |
5 | HG02145.hp1 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.355-2516A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50191249 | |||||||
| chr1:50191649 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.355-2116A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50191649 | |||||||
| chr1:50191656 | A | G | 1 | a0001c0002t0001g0228 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.355-2109A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50191656 | |||||||
| chr1:50191748 | G | A | 1 | a0001c0002t0003g0192 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.355-2017G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50191748 | |||||||
| chr1:50191753 | G | A | 223 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(220): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.355-2012G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50191753 | |||||||
| chr1:50191754 | G | C | 5 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0171 others(2): Show |
5 | HG02145.hp1 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.355-2011G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50191754 | |||||||
| chr1:50191794 | G | A | 1 | a0001c0002t0003g0243 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.355-1971G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50191794 | |||||||
| chr1:50191855 | C | T | 14 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0010 others(11): Show |
16 | HG01168.hp1 HG01169.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.355-1910C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50191855 | |||||||
| chr1:50192178 | C | T | 4 | a0001c0002t0001g0092 a0001c0002t0001g0096 a0001c0002t0001g0229 others(1): Show |
4 | HG02572.hp1 HG02647.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.355-1587C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50192178 | |||||||
| chr1:50192245 | G | A | 1 | a0001c0001t0001g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.355-1520G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50192245 | |||||||
| chr1:50192398 | C | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(4): Show |
7 | HG00280.hp2 HG00741.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.355-1367C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50192398 | |||||||
| chr1:50192519 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.355-1246G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50192519 | |||||||
| chr1:50192519 | G | GCA | 36 | a0001c0001t0001g0023 a0001c0001t0001g0055 a0001c0001t0001g0061 others(33): Show |
37 | HG00438.hp1 HG00642.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.355-1202_355-1201d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50192519 | ||||||
| chr1:50192519 | G | GCACA | 46 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(43): Show |
47 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.355-1204_355-1201d others(6): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50192519 | ||||||
| chr1:50192519 | G | GCACACA | 37 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(34): Show |
40 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.355-1206_355-1201d others(8): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50192519 | ||||||
| chr1:50192519 | G | GCACACAC others(1): Show |
24 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(21): Show |
24 | HG00609.hp1 HG00609.hp2 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.355-1208_355-1201d others(10): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50192519 | ||||||
| chr1:50192519 | G | GCACACAC others(3): Show |
9 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0124 others(6): Show |
9 | HG01071.hp2 HG02056.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.355-1210_355-1201d others(12): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50192519 | ||||||
| chr1:50192519 | G | GCACACAC others(5): Show |
3 | a0001c0001t0001g0069 a0001c0001t0001g0129 a0001c0001t0001g0157 |
3 | HG01346.hp1 HG01361.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.355-1212_355-1201d others(14): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50192519 | ||||||
| chr1:50192519 | G | GCACGCAC others(3): Show |
1 | a0001c0001t0001g0151 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.355-1243_355-1242i others(12): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50192519 | ||||||
| chr1:50192519 | GCA | G | 15 | a0001c0001t0001g0090 a0001c0001t0002g0047 a0001c0001t0002g0050 others(12): Show |
15 | HG00280.hp1 HG00673.hp2 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.355-1202_355-1201d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50192519 | ||||||
| chr1:50192519 | GCACA | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0025 others(50): Show |
55 | HG00099.hp1 HG00438.hp2 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.355-1204_355-1201d others(6): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50192519 | ||||||
| chr1:50192519 | GCACACA | G | 6 | a0001c0001t0002g0019 a0001c0002t0001g0075 a0001c0002t0001g0092 others(3): Show |
6 | HG00323.hp1 HG01243.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.355-1206_355-1201d others(8): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50192519 | ||||||
| chr1:50192519 | GCACACAC others(1): Show |
G | 4 | a0001c0001t0001g0038 a0001c0001t0002g0183 a0001c0001t0002g0258 others(1): Show |
4 | HG02922.hp2 NA18962.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.355-1208_355-1201d others(10): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50192519 | ||||||
| chr1:50192519 | GCACACAC others(7): Show |
G | 1 | a0001c0002t0001g0107 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.355-1214_355-1201d others(16): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50192519 | ||||||
| chr1:50192519 | GCACACAC others(9): Show |
G | 1 | a0001c0001t0010g0108 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.355-1216_355-1201d others(18): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50192519 | ||||||
| chr1:50192519 | GCACACAC others(17): Show |
G | 1 | a0001c0001t0002g0076 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.355-1224_355-1201d others(26): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50192519 | ||||||
| chr1:50192523 | A | G | 2 | a0001c0002t0003g0002 a0001c0002t0013g0095 |
3 | HG01168.hp1 HG01169.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.355-1242A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50192523 | |||||||
| chr1:50192801 | T | C | 1 | a0001c0001t0001g0248 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.355-964T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50192801 | |||||||
| chr1:50192922 | A | G | 5 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0171 others(2): Show |
5 | HG02145.hp1 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.355-843A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50192922 | |||||||
| chr1:50193114 | C | T | 1 | a0001c0001t0002g0113 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.355-651C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50193114 | |||||||
| chr1:50193366 | G | GT | 230 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(227): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.355-385dupT | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50193366 | ||||||
| chr1:50193406 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.355-359G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50193406 | |||||||
| chr1:50193407 | T | C | 2 | a0001c0001t0001g0040 a0001c0001t0001g0043 |
2 | HG00140.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.355-358T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50193407 | |||||||
| chr1:50193442 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.355-323G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50193442 | |||||||
| chr1:50193744 | G | A | 1 | a0001c0002t0001g0107 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.355-21G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50193744 | |||||||
| chr1:50194256 | A | G | 5 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0053 others(2): Show |
5 | HG01074.hp1 HG01123.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.508+338A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 4/6 | chr1 | 50194256 | |||||||
| chr1:50194469 | T | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.508+551T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 4/6 | chr1 | 50194469 | |||||||
| chr1:50194960 | G | T | 1 | a0001c0001t0001g0081 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.509-601G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 4/6 | chr1 | 50194960 | |||||||
| chr1:50194974 | A | G | 7 | a0001c0002t0005g0232 a0001c0002t0005g0235 a0001c0002t0005g0236 others(4): Show |
7 | HG02486.hp2 HG02922.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.509-587A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 4/6 | chr1 | 50194974 | |||||||
| chr1:50195071 | TGTTA | T | 223 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(220): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.509-489_509-486del others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 4/6 | chr1 | 50195071 | |||||||
| chr1:50195309 | A | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(240): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.509-252A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 4/6 | chr1 | 50195309 | |||||||
| chr1:50195352 | G | C | 14 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0010 others(11): Show |
16 | HG01168.hp1 HG01169.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.509-209G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 4/6 | chr1 | 50195352 | |||||||
| chr1:50195466 | C | T | 14 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0010 others(11): Show |
16 | HG01168.hp1 HG01169.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.509-95C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 4/6 | chr1 | 50195466 | |||||||
| chr1:50195857 | T | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0039 a0001c0001t0002g0045 |
3 | NA18973.hp1 NA19057.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.734+71T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50195857 | |||||||
| chr1:50195911 | C | T | 7 | a0001c0002t0001g0060 a0001c0002t0001g0091 a0001c0002t0001g0186 others(4): Show |
7 | HG00642.hp1 HG02109.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.734+125C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50195911 | |||||||
| chr1:50196016 | T | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(220): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.734+230T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50196016 | |||||||
| chr1:50196067 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.734+281C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50196067 | |||||||
| chr1:50196085 | A | G | 1 | a0001c0001t0002g0202 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.734+299A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50196085 | |||||||
| chr1:50196168 | G | A | 4 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0218 others(1): Show |
4 | HG01074.hp1 HG01123.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.734+382G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50196168 | |||||||
| chr1:50196769 | C | A | 1 | a0001c0001t0002g0041 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.735-660C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50196769 | |||||||
| chr1:50196976 | T | C | 5 | a0001c0002t0001g0092 a0001c0002t0001g0096 a0001c0002t0001g0107 others(2): Show |
5 | HG01243.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-453T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50196976 | |||||||
| chr1:50197164 | A | AAT | 6 | a0001c0002t0001g0092 a0001c0002t0001g0096 a0001c0002t0001g0107 others(3): Show |
6 | HG01243.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.735-265_735-264ins others(2): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50197164 | |||||||
| chr1:50197167 | T | TATTAA | 6 | a0001c0002t0001g0092 a0001c0002t0001g0096 a0001c0002t0001g0107 others(3): Show |
6 | HG01243.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.735-262_735-261ins others(5): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50197167 | |||||||
| chr1:50197168 | G | T | 6 | a0001c0002t0001g0092 a0001c0002t0001g0096 a0001c0002t0001g0107 others(3): Show |
6 | HG01243.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.735-261G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50197168 | |||||||
| chr1:50197169 | G | T | 6 | a0001c0002t0001g0092 a0001c0002t0001g0096 a0001c0002t0001g0107 others(3): Show |
6 | HG01243.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.735-260G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50197169 | |||||||
| chr1:50197170 | G | C | 6 | a0001c0002t0001g0092 a0001c0002t0001g0096 a0001c0002t0001g0107 others(3): Show |
6 | HG01243.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.735-259G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50197170 | |||||||
| chr1:50197171 | G | A | 6 | a0001c0002t0001g0092 a0001c0002t0001g0096 a0001c0002t0001g0107 others(3): Show |
6 | HG01243.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.735-258G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50197171 | |||||||
| chr1:50197226 | T | C | 1 | a0001c0002t0003g0240 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.735-203T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50197226 | |||||||
| chr1:50197283 | G | A | 1 | a0001c0002t0004g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.735-146G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50197283 | |||||||
| chr1:50197861 | T | C | 1 | a0001c0001t0002g0097 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.773+394T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 6/6 | chr1 | 50197861 | |||||||
| chr1:50198179 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.773+712G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 6/6 | chr1 | 50198179 | |||||||
| chr1:50198193 | C | T | 1 | a0001c0002t0003g0163 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.773+726C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 6/6 | chr1 | 50198193 | |||||||
| chr1:50198435 | C | T | 263 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(260): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.773+968C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 6/6 | chr1 | 50198435 | |||||||
| chr1:50198939 | T | C | 6 | a0001c0002t0001g0092 a0001c0002t0001g0096 a0001c0002t0001g0107 others(3): Show |
6 | HG01243.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.773+1472T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 6/6 | chr1 | 50198939 | |||||||
| chr1:50199507 | A | G | 1 | a0001c0001t0001g0057 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.774-1344A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 6/6 | chr1 | 50199507 | |||||||
| chr1:50199633 | G | A | 14 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0010 others(11): Show |
16 | HG01168.hp1 HG01169.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.774-1218G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 6/6 | chr1 | 50199633 | |||||||
| chr1:50199734 | G | GA | 14 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0010 others(11): Show |
16 | HG01168.hp1 HG01169.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.774-1108dupA | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 50199734 | ||||||
| chr1:50200242 | C | T | 14 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0010 others(11): Show |
16 | HG01168.hp1 HG01169.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.774-609C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 6/6 | chr1 | 50200242 | |||||||
| chr1:50200401 | A | G | 1 | a0001c0002t0001g0228 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.774-450A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 6/6 | chr1 | 50200401 | |||||||
| chr1:50200495 | A | C | 1 | a0001c0001t0001g0085 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.774-356A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 6/6 | chr1 | 50200495 | |||||||
| chr1:50200517 | G | A | 15 | a0001c0001t0001g0154 a0001c0002t0003g0002 a0001c0002t0003g0008 others(12): Show |
17 | HG01168.hp1 HG01169.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.774-334G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 6/6 | chr1 | 50200517 | |||||||
| chr1:50200548 | A | G | 1 | a0001c0001t0002g0215 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.774-303A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 6/6 | chr1 | 50200548 | |||||||
| chr1:50200843 | C | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
splice_region_variant&intron_variant | LOW | c.774-8C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 6/6 | chr1 | 50200843 |