Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1994 |
| ensemblid | ENSG00000066044.15 |
| hgncid | 3312 |
| symbol | ELAVL1 |
| name | ELAV like RNA binding protein 1 |
| refseq_nuc | NM_001419.3 |
| refseq_prot | NP_001410.2 |
| ensembl_nuc | ENST00000407627.7 |
| ensembl_prot | ENSP00000385269.1 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 7958573 |
| end | 8005641 |
| strand | - |
| ver | v1.2 |
| region | chr19:7958573-8005641 |
| region5000 | chr19:7953573-8010641 |
| regionname0 | ELAVL1_chr19_7958573_8005641 |
| regionname5000 | ELAVL1_chr19_7953573_8010641 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 978 | 223 | 66 | 43 | 75 | 10 | 27 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | ATGTC others(973): Show |
chr19 | 7953573 | 8010641 | ||
| a0001c0002 | 0/0 | 978 | 49 | 14 | 15 | 11 | 6 | 3 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | ATGTC others(973): Show |
chr19 | 7953573 | 8010641 | ||
| a0001c0003 | 0/0 | 978 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | ATGTC others(973): Show |
chr19 | 7953573 | 8010641 | ||
| a0001c0004 | 0/0 | 978 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | ATGTC others(973): Show |
chr19 | 7953573 | 8010641 | ||
| a0001c0005 | 0/0 | 978 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | ATGTC others(973): Show |
chr19 | 7953573 | 8010641 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 6054 | 104 | 37 | 18 | 23 | 7 | 18 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6049): Show |
chr19 | 7953573 | 8010641 |
| a0001c0001t0002 | 0/1 | 6053 | 32 | 2 | 6 | 14 | 2 | 7 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6048): Show |
chr19 | 7953573 | 8010641 |
| a0001c0001t0003 | 0/0 | 6026 | 21 | 1 | 11 | 8 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6021): Show |
chr19 | 7953573 | 8010641 |
| a0001c0001t0006 | 0/0 | 6054 | 11 | 10 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6049): Show |
chr19 | 7953573 | 8010641 |
| a0001c0001t0007 | 0/0 | 6053 | 8 | 0 | 2 | 6 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6048): Show |
chr19 | 7953573 | 8010641 |
| a0001c0001t0008 | 0/0 | 6054 | 7 | 0 | 0 | 7 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6049): Show |
chr19 | 7953573 | 8010641 |
| a0001c0001t0010 | 0/0 | 6053 | 5 | 0 | 0 | 5 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6048): Show |
chr19 | 7953573 | 8010641 |
| a0001c0001t0012 | 0/0 | 6053 | 3 | 1 | 0 | 2 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6048): Show |
chr19 | 7953573 | 8010641 |
| a0001c0001t0013 | 0/0 | 6054 | 3 | 3 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6049): Show |
chr19 | 7953573 | 8010641 |
| a0001c0001t0014 | 0/0 | 6054 | 3 | 3 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6049): Show |
chr19 | 7953573 | 8010641 |
| a0001c0001t0015 | 0/0 | 6138 | 3 | 3 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6133): Show |
chr19 | 7953573 | 8010641 |
| a0001c0001t0017 | 0/0 | 6054 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6049): Show |
chr19 | 7953573 | 8010641 |
| a0001c0001t0018 | 0/0 | 6082 | 2 | 1 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6077): Show |
chr19 | 7953573 | 8010641 |
| a0001c0001t0019 | 0/0 | 6054 | 2 | 0 | 0 | 2 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6049): Show |
chr19 | 7953573 | 8010641 |
| a0001c0001t0020 | 0/0 | 6053 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6048): Show |
chr19 | 7953573 | 8010641 |
| a0001c0001t0021 | 0/0 | 6053 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6048): Show |
chr19 | 7953573 | 8010641 |
| a0001c0001t0022 | 0/0 | 6054 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6049): Show |
chr19 | 7953573 | 8010641 |
| a0001c0001t0023 | 0/0 | 6054 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6049): Show |
chr19 | 7953573 | 8010641 |
| a0001c0001t0024 | 0/0 | 6054 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6049): Show |
chr19 | 7953573 | 8010641 |
| a0001c0001t0025 | 0/0 | 6053 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6048): Show |
chr19 | 7953573 | 8010641 |
| a0001c0001t0030 | 0/0 | 6054 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6049): Show |
chr19 | 7953573 | 8010641 |
| a0001c0001t0031 | 0/0 | 6026 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6021): Show |
chr19 | 7953573 | 8010641 |
| a0001c0001t0032 | 0/0 | 6054 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6049): Show |
chr19 | 7953573 | 8010641 |
| a0001c0001t0033 | 0/0 | 6054 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6049): Show |
chr19 | 7953573 | 8010641 |
| a0001c0001t0034 | 0/0 | 6053 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6048): Show |
chr19 | 7953573 | 8010641 |
| a0001c0001t0035 | 0/0 | 6054 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6049): Show |
chr19 | 7953573 | 8010641 |
| a0001c0001t0036 | 0/0 | 6082 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6077): Show |
chr19 | 7953573 | 8010641 |
| a0001c0001t0037 | 0/0 | 6110 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6105): Show |
chr19 | 7953573 | 8010641 |
| a0001c0001t0038 | 0/0 | 6054 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6049): Show |
chr19 | 7953573 | 8010641 |
| a0001c0001t0039 | 0/0 | 6077 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6072): Show |
chr19 | 7953573 | 8010641 |
| a0001c0001t0040 | 0/0 | 6053 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6048): Show |
chr19 | 7953573 | 8010641 |
| a0001c0002t0004 | 0/0 | 6054 | 19 | 2 | 10 | 0 | 4 | 3 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6049): Show |
chr19 | 7953573 | 8010641 |
| a0001c0002t0005 | 0/0 | 6026 | 15 | 0 | 3 | 10 | 2 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6021): Show |
chr19 | 7953573 | 8010641 |
| a0001c0002t0009 | 0/0 | 6054 | 5 | 5 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6049): Show |
chr19 | 7953573 | 8010641 |
| a0001c0002t0011 | 0/0 | 6026 | 4 | 4 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6021): Show |
chr19 | 7953573 | 8010641 |
| a0001c0002t0016 | 0/0 | 6054 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6049): Show |
chr19 | 7953573 | 8010641 |
| a0001c0002t0026 | 0/0 | 6026 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6021): Show |
chr19 | 7953573 | 8010641 |
| a0001c0002t0027 | 0/0 | 6026 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6021): Show |
chr19 | 7953573 | 8010641 |
| a0001c0002t0028 | 0/0 | 6026 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6021): Show |
chr19 | 7953573 | 8010641 |
| a0001c0002t0029 | 0/0 | 6026 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6021): Show |
chr19 | 7953573 | 8010641 |
| a0001c0003t0001 | 0/0 | 6054 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6049): Show |
chr19 | 7953573 | 8010641 |
| a0001c0004t0001 | 0/0 | 6054 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6049): Show |
chr19 | 7953573 | 8010641 |
| a0001c0005t0001 | 0/0 | 6054 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | GTGCG others(6049): Show |
chr19 | 7953573 | 8010641 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 1 | 0 | 4 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0008 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0061 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0002g0003 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0002g0006 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0002g0166 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0003g0001 | 0/0 | 8 | 0 | 6 | 2 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0006g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0006g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0006g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0006g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0006g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0006g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0007g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0007g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0007g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0007g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0007g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0007g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0007g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0007g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0008g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0008g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0008g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0008g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0008g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0008g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0008g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0010g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0010g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0010g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0010g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0010g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0012g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0012g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0012g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0013g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0013g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0013g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0014g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0014g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0015g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0015g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0015g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0017g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0018g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0018g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0019g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0019g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0020g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0021g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0022g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0023g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0024g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0025g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0030g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0031g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0032g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0033g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0034g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0035g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0036g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0037g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0038g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0039g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0001t0040g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0004g0004 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0004g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0004g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0004g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0004g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0004g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0004g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0004g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0004g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0004g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0004g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0005g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0005g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0005g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0005g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0005g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0005g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0005g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0005g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0005g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0005g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0009g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0009g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0009g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0009g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0011g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0011g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0011g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0011g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0016g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0016g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0026g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0027g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0028g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0002t0029g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0003t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0004t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| a0001c0005t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0006 | EUR | GBR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | GBR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG00140 | hp1 | a0001 | c0002 | t0004 | g0020 | EUR | GBR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | GBR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG00280 | hp1 | a0001 | c0002 | t0005 | g0017 | EUR | FIN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG00280 | hp2 | a0001 | c0002 | t0004 | g0238 | EUR | FIN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | FIN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | FIN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG00408 | hp1 | a0001 | c0001 | t0021 | g0151 | EAS | CHS | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | CHS | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG00544 | hp2 | a0001 | c0001 | t0010 | g0193 | EAS | CHS | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG00609 | hp1 | a0001 | c0001 | t0007 | g0170 | EAS | CHS | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | CHS | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG00621 | hp2 | a0001 | c0001 | t0010 | g0154 | EAS | CHS | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG00642 | hp1 | a0001 | c0002 | t0026 | g0209 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0105 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG00733 | hp1 | a0001 | c0002 | t0004 | g0225 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG00733 | hp2 | a0001 | c0002 | t0005 | g0016 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG00738 | hp2 | a0001 | c0002 | t0004 | g0019 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01070 | hp1 | a0001 | c0002 | t0004 | g0004 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01071 | hp2 | a0001 | c0002 | t0004 | g0004 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0077 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01106 | hp1 | a0001 | c0001 | t0035 | g0059 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01109 | hp1 | a0001 | c0002 | t0004 | g0004 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01109 | hp2 | a0001 | c0002 | t0005 | g0017 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01168 | hp1 | a0001 | c0001 | t0033 | g0121 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01243 | hp1 | a0001 | c0002 | t0004 | g0223 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01256 | hp2 | a0001 | c0002 | t0004 | g0221 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01257 | hp1 | a0001 | c0002 | t0004 | g0222 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01261 | hp1 | a0001 | c0001 | t0007 | g0108 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01261 | hp2 | a0001 | c0001 | t0006 | g0199 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01346 | hp1 | a0001 | c0002 | t0028 | g0205 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0087 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01433 | hp1 | a0001 | c0001 | t0023 | g0177 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01433 | hp2 | a0001 | c0002 | t0004 | g0224 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | IBS | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | IBS | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01517 | hp2 | a0001 | c0002 | t0004 | g0020 | EUR | IBS | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01891 | hp1 | a0001 | c0002 | t0009 | g0232 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01928 | hp1 | a0001 | c0001 | t0007 | g0156 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01934 | hp1 | a0001 | c0001 | t0038 | g0084 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0181 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01981 | hp2 | a0001 | c0001 | t0020 | g0169 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02004 | hp1 | a0001 | c0002 | t0005 | g0207 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0101 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02027 | hp1 | a0001 | c0001 | t0010 | g0194 | EAS | KHV | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02055 | hp2 | a0001 | c0001 | t0015 | g0041 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | KHV | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02135 | hp1 | a0001 | c0001 | t0031 | g0073 | EAS | KHV | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02135 | hp2 | a0001 | c0001 | t0007 | g0195 | EAS | KHV | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02145 | hp1 | a0001 | c0001 | t0015 | g0198 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0159 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0201 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02257 | hp2 | a0001 | c0002 | t0009 | g0231 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02280 | hp1 | a0001 | c0001 | t0013 | g0043 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0161 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0082 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02300 | hp2 | a0001 | c0002 | t0004 | g0019 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0145 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02523 | hp2 | a0001 | c0002 | t0005 | g0206 | EAS | KHV | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0203 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02602 | hp1 | a0001 | c0002 | t0004 | g0237 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0160 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02622 | hp1 | a0001 | c0002 | t0011 | g0024 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0200 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02647 | hp1 | a0001 | c0001 | t0013 | g0037 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02698 | hp1 | a0001 | c0002 | t0004 | g0228 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02717 | hp2 | a0001 | c0002 | t0011 | g0027 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0202 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02723 | hp2 | a0001 | c0001 | t0014 | g0014 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02809 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02922 | hp1 | a0001 | c0002 | t0027 | g0204 | AFR | ESN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0162 | AFR | ESN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02976 | hp1 | a0001 | c0001 | t0017 | g0009 | AFR | ESN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03041 | hp1 | a0001 | c0002 | t0009 | g0230 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03041 | hp2 | a0001 | c0001 | t0012 | g0236 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03098 | hp1 | a0001 | c0001 | t0025 | g0038 | AFR | MSL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03130 | hp2 | a0001 | c0002 | t0011 | g0026 | AFR | ESN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03139 | hp1 | a0001 | c0002 | t0009 | g0021 | AFR | ESN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03139 | hp2 | a0001 | c0001 | t0015 | g0044 | AFR | ESN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03195 | hp2 | a0001 | c0001 | t0014 | g0014 | AFR | ESN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03209 | hp1 | a0001 | c0002 | t0016 | g0233 | AFR | MSL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0136 | AFR | MSL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03486 | hp1 | a0001 | c0001 | t0017 | g0009 | AFR | MSL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03516 | hp2 | a0001 | c0002 | t0011 | g0025 | AFR | ESN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03579 | hp1 | a0001 | c0001 | t0036 | g0040 | AFR | MSL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03579 | hp2 | a0001 | c0002 | t0016 | g0220 | AFR | MSL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0192 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | STU | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0153 | SAS | STU | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0186 | SAS | BEB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03927 | hp1 | a0001 | c0002 | t0004 | g0004 | SAS | BEB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | BEB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0171 | SAS | STU | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | YRI | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18522 | hp2 | a0001 | c0001 | t0034 | g0143 | AFR | YRI | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18612 | hp1 | a0001 | c0001 | t0010 | g0168 | EAS | CHB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | CHB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | YRI | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | YRI | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18941 | hp2 | a0001 | c0001 | t0008 | g0100 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18946 | hp1 | a0001 | c0001 | t0024 | g0176 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18946 | hp2 | a0001 | c0004 | t0001 | g0107 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18952 | hp1 | a0001 | c0002 | t0005 | g0216 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18952 | hp2 | a0001 | c0001 | t0008 | g0080 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18953 | hp1 | a0001 | c0001 | t0007 | g0197 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18953 | hp2 | a0001 | c0001 | t0008 | g0079 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18959 | hp1 | a0001 | c0002 | t0005 | g0218 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18960 | hp1 | a0001 | c0002 | t0005 | g0217 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18961 | hp2 | a0001 | c0001 | t0012 | g0235 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18962 | hp2 | a0001 | c0002 | t0005 | g0215 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18964 | hp1 | a0001 | c0001 | t0032 | g0058 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18964 | hp2 | a0001 | c0002 | t0005 | g0018 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18966 | hp1 | a0001 | c0001 | t0037 | g0051 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18966 | hp2 | a0001 | c0001 | t0007 | g0174 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18968 | hp1 | a0001 | c0001 | t0039 | g0066 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18968 | hp2 | a0001 | c0001 | t0012 | g0234 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18969 | hp2 | a0001 | c0002 | t0005 | g0214 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18970 | hp2 | a0001 | c0001 | t0008 | g0023 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18971 | hp1 | a0001 | c0001 | t0007 | g0028 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18971 | hp2 | a0001 | c0001 | t0008 | g0022 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18973 | hp1 | a0001 | c0001 | t0040 | g0179 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18980 | hp2 | a0001 | c0002 | t0029 | g0213 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18982 | hp1 | a0001 | c0001 | t0008 | g0106 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA19007 | hp1 | a0001 | c0001 | t0008 | g0137 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA19009 | hp1 | a0001 | c0002 | t0005 | g0208 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA19012 | hp1 | a0001 | c0001 | t0007 | g0155 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA19012 | hp2 | a0001 | c0005 | t0001 | g0114 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA19030 | hp1 | a0001 | c0001 | t0013 | g0045 | AFR | LWK | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | LWK | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | LWK | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA19043 | hp2 | a0001 | c0002 | t0009 | g0021 | AFR | LWK | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA19065 | hp2 | a0001 | c0002 | t0005 | g0018 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA19077 | hp1 | a0001 | c0001 | t0022 | g0165 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA19079 | hp2 | a0001 | c0001 | t0010 | g0149 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA19082 | hp2 | a0001 | c0001 | t0019 | g0240 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA19090 | hp1 | a0001 | c0002 | t0005 | g0212 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA19090 | hp2 | a0001 | c0001 | t0019 | g0239 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA20129 | hp1 | a0001 | c0002 | t0004 | g0229 | AFR | ASW | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA20129 | hp2 | a0001 | c0001 | t0014 | g0124 | AFR | ASW | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA20752 | hp1 | a0001 | c0001 | t0018 | g0119 | EUR | TSI | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA20752 | hp2 | a0001 | c0002 | t0005 | g0016 | EUR | TSI | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | TSI | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA20805 | hp2 | a0001 | c0002 | t0004 | g0227 | EUR | TSI | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA20905 | hp2 | a0001 | c0001 | t0030 | g0099 | SAS | GIH | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02486 | hp1 | a0001 | c0002 | t0004 | g0226 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0139 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03471 | hp1 | a0001 | c0001 | t0018 | g0039 | AFR | MSL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | USA | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | USA | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0166 | REF | REF | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0061 | REF | REF | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:7963660 | A | G | 1 | a0001c0002 | 49 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(46): Show |
synonymous_variant | LOW | c.804T>C | p.Gly268Gly | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 967/6054 | 804/981 | 268/326 | chr19 | 7963660 | |||
| chr19:7963696 | G | A | 1 | a0001c0004 | 1 | NA18946.hp2 | synonymous_variant | LOW | c.768C>T | p.Asp256Asp | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 931/6054 | 768/981 | 256/326 | chr19 | 7963696 | |||
| chr19:7963765 | G | A | 1 | a0001c0005 | 1 | NA19012.hp2 | synonymous_variant | LOW | c.699C>T | p.Gly233Gly | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 862/6054 | 699/981 | 233/326 | chr19 | 7963765 | |||
| chr19:7991657 | C | G | 1 | a0001c0003 | 2 | HG02622.hp2 HG02809.hp2 |
synonymous_variant | LOW | c.159G>C | p.Arg53Arg | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/6 | 322/6054 | 159/981 | 53/326 | chr19 | 7991657 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:7958588 | T | A | 1 | a0001c0001t0024 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4895A>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 4895 | chr19 | 7958588 | ||||||
| chr19:7959057 | TA | T | 10 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(7): Show |
53 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*4425delT | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 4425 | chr19 | 7959057 | ||||||
| chr19:7959064 | A | T | 2 | a0001c0001t0017 a0001c0001t0031 |
3 | HG02135.hp1 HG02976.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4419T>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 4419 | chr19 | 7959064 | ||||||
| chr19:7959071 | A | T | 1 | a0001c0001t0022 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4412T>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 4412 | chr19 | 7959071 | ||||||
| chr19:7959101 | A | C | 1 | a0001c0001t0022 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4382T>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 4382 | chr19 | 7959101 | ||||||
| chr19:7959383 | C | T | 1 | a0001c0001t0040 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4100G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 4100 | chr19 | 7959383 | ||||||
| chr19:7959384 | T | C | 1 | a0001c0001t0040 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4099A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 4099 | chr19 | 7959384 | ||||||
| chr19:7959387 | C | T | 1 | a0001c0001t0036 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4096G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 4096 | chr19 | 7959387 | ||||||
| chr19:7959403 | G | A | 1 | a0001c0002t0026 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4080C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 4080 | chr19 | 7959403 | ||||||
| chr19:7959453 | G | T | 1 | a0001c0001t0033 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4030C>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 4030 | chr19 | 7959453 | ||||||
| chr19:7959554 | A | T | 1 | a0001c0001t0014 | 3 | HG02723.hp2 HG03195.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3929T>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 3929 | chr19 | 7959554 | ||||||
| chr19:7959605 | G | A | 1 | a0001c0002t0011 | 4 | HG02622.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3878C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 3878 | chr19 | 7959605 | ||||||
| chr19:7959715 | G | A | 5 | a0001c0002t0005 a0001c0002t0026 a0001c0002t0027 others(2): Show |
19 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3768C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 3768 | chr19 | 7959715 | ||||||
| chr19:7959800 | A | C | 2 | a0001c0002t0004 a0001c0002t0009 |
24 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*3683T>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 3683 | chr19 | 7959800 | ||||||
| chr19:7959998 | G | T | 1 | a0001c0001t0032 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3485C>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 3485 | chr19 | 7959998 | ||||||
| chr19:7960127 | G | A | 1 | a0001c0001t0012 | 3 | HG03041.hp2 NA18961.hp2 NA18968.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3356C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 3356 | chr19 | 7960127 | ||||||
| chr19:7960607 | T | C | 9 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(6): Show |
60 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*2876A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 2876 | chr19 | 7960607 | ||||||
| chr19:7961047 | C | T | 1 | a0001c0002t0004 | 19 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2436G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 2436 | chr19 | 7961047 | ||||||
| chr19:7961051 | G | A | 1 | a0001c0001t0035 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2432C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 2432 | chr19 | 7961051 | ||||||
| chr19:7961182 | G | A | 1 | a0001c0002t0011 | 4 | HG02622.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2301C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 2301 | chr19 | 7961182 | ||||||
| chr19:7961286 | T | C | 2 | a0001c0001t0012 a0001c0001t0025 |
4 | HG03041.hp2 HG03098.hp1 NA18961.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2197A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 2197 | chr19 | 7961286 | ||||||
| chr19:7961303 | G | GCCTTCCA others(21): Show |
2 | a0001c0001t0018 a0001c0001t0036 |
3 | HG03471.hp1 HG03579.hp1 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2152_*2179dupTGGG others(24): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 2179 | chr19 | 7961303 | ||||||
| chr19:7961303 | G | GCCTTCCA others(49): Show |
1 | a0001c0001t0037 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2124_*2179dupTGGG others(52): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 2179 | chr19 | 7961303 | ||||||
| chr19:7961303 | G | GCCTTCCA others(77): Show |
1 | a0001c0001t0015 | 3 | HG02055.hp2 HG02145.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2096_*2179dupTGGG others(80): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 2179 | chr19 | 7961303 | ||||||
| chr19:7961303 | GCCTTCCA others(21): Show |
G | 8 | a0001c0001t0003 a0001c0001t0031 a0001c0002t0005 others(5): Show |
45 | HG00280.hp1 HG00408.hp2 HG00642.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2152_*2179delTGGG others(24): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 2152 | chr19 | 7961303 | ||||||
| chr19:7961341 | A | G | 4 | a0001c0002t0005 a0001c0002t0026 a0001c0002t0028 others(1): Show |
18 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2142T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 2142 | chr19 | 7961341 | ||||||
| chr19:7961534 | G | A | 5 | a0001c0002t0005 a0001c0002t0026 a0001c0002t0027 others(2): Show |
19 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1949C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 1949 | chr19 | 7961534 | ||||||
| chr19:7961562 | C | T | 1 | a0001c0001t0013 | 3 | HG02280.hp1 HG02647.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1921G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 1921 | chr19 | 7961562 | ||||||
| chr19:7961665 | A | G | 9 | a0001c0002t0004 a0001c0002t0005 a0001c0002t0009 others(6): Show |
49 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1818T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 1818 | chr19 | 7961665 | ||||||
| chr19:7961668 | C | T | 1 | a0001c0001t0030 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1815G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 1815 | chr19 | 7961668 | ||||||
| chr19:7961797 | T | C | 1 | a0001c0001t0039 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1686A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 1686 | chr19 | 7961797 | ||||||
| chr19:7961798 | G | T | 1 | a0001c0001t0039 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1685C>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 1685 | chr19 | 7961798 | ||||||
| chr19:7962056 | C | A | 1 | a0001c0002t0028 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1427G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 1427 | chr19 | 7962056 | ||||||
| chr19:7962171 | G | T | 9 | a0001c0002t0004 a0001c0002t0005 a0001c0002t0009 others(6): Show |
49 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1312C>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 1312 | chr19 | 7962171 | ||||||
| chr19:7962181 | T | C | 1 | a0001c0001t0038 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1302A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 1302 | chr19 | 7962181 | ||||||
| chr19:7962295 | T | TTAATGGT others(17): Show |
1 | a0001c0001t0039 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1164_*1187dupTTAC others(20): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 1187 | chr19 | 7962295 | ||||||
| chr19:7962648 | G | A | 1 | a0001c0002t0029 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*835C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 835 | chr19 | 7962648 | ||||||
| chr19:7962719 | G | T | 3 | a0001c0001t0010 a0001c0001t0020 a0001c0001t0040 |
7 | HG00544.hp2 HG00621.hp2 HG01981.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*764C>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 764 | chr19 | 7962719 | ||||||
| chr19:7962870 | C | A | 5 | a0001c0002t0005 a0001c0002t0026 a0001c0002t0027 others(2): Show |
19 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*613G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 613 | chr19 | 7962870 | ||||||
| chr19:7962878 | A | G | 20 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(17): Show |
103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*605T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 605 | chr19 | 7962878 | ||||||
| chr19:7962900 | T | G | 4 | a0001c0001t0007 a0001c0001t0010 a0001c0001t0020 others(1): Show |
15 | HG00544.hp2 HG00609.hp1 HG00621.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*583A>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 583 | chr19 | 7962900 | ||||||
| chr19:7962923 | C | T | 1 | a0001c0001t0020 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*560G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 560 | chr19 | 7962923 | ||||||
| chr19:7963058 | G | A | 1 | a0001c0001t0008 | 7 | NA18941.hp2 NA18952.hp2 NA18953.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*425C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 425 | chr19 | 7963058 | ||||||
| chr19:8005534 | G | A | 1 | a0001c0001t0019 | 2 | NA19082.hp2 NA19090.hp2 |
5_prime_UTR_variant | MODIFIER | c.-56C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/6 | 13719 | chr19 | 8005534 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:7963827 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.657-20G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7963827 | |||||||
| chr19:7963897 | T | C | 2 | a0001c0001t0018g0039 a0001c0001t0036g0040 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.657-90A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7963897 | |||||||
| chr19:7964004 | G | C | 4 | a0001c0002t0009g0021 a0001c0002t0009g0230 a0001c0002t0009g0231 others(1): Show |
5 | HG01891.hp1 HG02257.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.657-197C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7964004 | |||||||
| chr19:7964040 | G | C | 3 | a0001c0002t0009g0021 a0001c0002t0009g0230 a0001c0002t0009g0232 |
4 | HG01891.hp1 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.657-233C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7964040 | |||||||
| chr19:7964043 | C | T | 3 | a0001c0002t0009g0021 a0001c0002t0009g0230 a0001c0002t0009g0232 |
4 | HG01891.hp1 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.657-236G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7964043 | |||||||
| chr19:7964047 | AC | A | 4 | a0001c0002t0009g0021 a0001c0002t0009g0230 a0001c0002t0009g0231 others(1): Show |
5 | HG01891.hp1 HG02257.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.657-241delG | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7964047 | |||||||
| chr19:7964103 | A | G | 4 | a0001c0002t0011g0024 a0001c0002t0011g0025 a0001c0002t0011g0026 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-296T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7964103 | |||||||
| chr19:7964435 | T | C | 2 | a0001c0002t0016g0220 a0001c0002t0016g0233 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.657-628A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7964435 | |||||||
| chr19:7964504 | G | A | 8 | a0001c0001t0007g0028 a0001c0001t0007g0108 a0001c0001t0007g0155 others(5): Show |
8 | HG00609.hp1 HG01261.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.657-697C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7964504 | |||||||
| chr19:7965352 | A | G | 4 | a0001c0002t0011g0024 a0001c0002t0011g0025 a0001c0002t0011g0026 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-1545T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7965352 | |||||||
| chr19:7965638 | G | A | 7 | a0001c0001t0010g0149 a0001c0001t0010g0154 a0001c0001t0010g0168 others(4): Show |
7 | HG00544.hp2 HG00621.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.657-1831C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7965638 | |||||||
| chr19:7965758 | C | T | 4 | a0001c0001t0012g0234 a0001c0001t0012g0235 a0001c0001t0012g0236 others(1): Show |
4 | HG03041.hp2 HG03098.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.656+1807G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7965758 | |||||||
| chr19:7966013 | G | A | 10 | a0001c0001t0003g0001 a0001c0001t0003g0015 a0001c0001t0003g0076 others(7): Show |
18 | HG00408.hp2 HG01069.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.656+1552C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7966013 | |||||||
| chr19:7966086 | C | T | 3 | a0001c0001t0001g0131 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG02647.hp2 HG02886.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.656+1479G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7966086 | |||||||
| chr19:7966708 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.656+857G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7966708 | |||||||
| chr19:7966827 | C | T | 1 | a0001c0001t0003g0153 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.656+738G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7966827 | |||||||
| chr19:7966883 | G | C | 7 | a0001c0001t0010g0149 a0001c0001t0010g0154 a0001c0001t0010g0168 others(4): Show |
7 | HG00544.hp2 HG00621.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.656+682C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7966883 | |||||||
| chr19:7967025 | CT | C | 5 | a0001c0001t0001g0031 a0001c0001t0001g0110 a0001c0001t0001g0122 others(2): Show |
5 | HG00099.hp2 HG01069.hp2 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.656+539delA | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7967025 | |||||||
| chr19:7967049 | A | G | 1 | a0001c0005t0001g0114 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.656+516T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7967049 | |||||||
| chr19:7967228 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.656+337A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7967228 | |||||||
| chr19:7967373 | A | C | 201 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(198): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.656+192T>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7967373 | |||||||
| chr19:7967548 | G | A | 44 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0069 others(41): Show |
49 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.656+17C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7967548 | |||||||
| chr19:7967796 | C | T | 56 | a0001c0001t0001g0042 a0001c0001t0001g0046 a0001c0001t0001g0047 others(53): Show |
65 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(62): Show |
splice_region_variant&intron_variant | LOW | c.431-6G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7967796 | |||||||
| chr19:7968088 | G | A | 18 | a0001c0002t0004g0004 a0001c0002t0004g0019 a0001c0002t0004g0020 others(15): Show |
24 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.431-298C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7968088 | |||||||
| chr19:7968233 | A | C | 1 | a0001c0002t0005g0016 | 2 | HG00733.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.431-443T>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7968233 | |||||||
| chr19:7968349 | G | C | 1 | a0001c0001t0001g0158 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.431-559C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7968349 | |||||||
| chr19:7968464 | A | G | 40 | a0001c0002t0004g0004 a0001c0002t0004g0019 a0001c0002t0004g0020 others(37): Show |
49 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.431-674T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7968464 | |||||||
| chr19:7968541 | G | A | 2 | a0001c0002t0005g0212 a0001c0002t0029g0213 |
2 | NA18980.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.431-751C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7968541 | |||||||
| chr19:7968616 | C | A | 1 | a0001c0001t0006g0202 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.431-826G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7968616 | |||||||
| chr19:7968647 | C | T | 15 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(12): Show |
18 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.431-857G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7968647 | |||||||
| chr19:7968658 | A | C | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 |
3 | HG01891.hp2 HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.431-868T>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7968658 | |||||||
| chr19:7968674 | A | G | 3 | a0001c0002t0004g0019 a0001c0002t0004g0226 a0001c0002t0004g0227 |
4 | HG00738.hp2 HG02300.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.431-884T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7968674 | |||||||
| chr19:7968690 | A | C | 232 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(229): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.431-900T>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7968690 | |||||||
| chr19:7968805 | G | A | 7 | a0001c0001t0001g0042 a0001c0001t0001g0046 a0001c0001t0001g0047 others(4): Show |
7 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.431-1015C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7968805 | |||||||
| chr19:7968849 | C | T | 2 | a0001c0001t0015g0041 a0001c0001t0015g0044 |
2 | HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.431-1059G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7968849 | |||||||
| chr19:7969012 | A | G | 40 | a0001c0002t0004g0004 a0001c0002t0004g0019 a0001c0002t0004g0020 others(37): Show |
49 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.431-1222T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7969012 | |||||||
| chr19:7969171 | A | G | 4 | a0001c0002t0011g0024 a0001c0002t0011g0025 a0001c0002t0011g0026 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-1381T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7969171 | |||||||
| chr19:7969623 | C | T | 1 | a0001c0001t0001g0031 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.431-1833G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7969623 | |||||||
| chr19:7969680 | G | A | 1 | a0001c0001t0023g0177 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.431-1890C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7969680 | |||||||
| chr19:7969686 | C | T | 4 | a0001c0001t0012g0234 a0001c0001t0012g0235 a0001c0001t0012g0236 others(1): Show |
4 | HG03041.hp2 HG03098.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-1896G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7969686 | |||||||
| chr19:7969745 | G | A | 1 | a0001c0002t0027g0204 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.431-1955C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7969745 | |||||||
| chr19:7969980 | A | G | 49 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0069 others(46): Show |
54 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.431-2190T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7969980 | |||||||
| chr19:7969984 | T | C | 1 | a0001c0001t0001g0130 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.431-2194A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7969984 | |||||||
| chr19:7970012 | G | A | 1 | a0001c0001t0003g0076 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.431-2222C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7970012 | |||||||
| chr19:7970225 | G | A | 1 | a0001c0001t0003g0076 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.431-2435C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7970225 | |||||||
| chr19:7970258 | C | T | 1 | a0001c0001t0015g0198 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.431-2468G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7970258 | |||||||
| chr19:7970397 | C | T | 1 | a0001c0001t0015g0198 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.431-2607G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7970397 | |||||||
| chr19:7970527 | C | T | 16 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(13): Show |
19 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.431-2737G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7970527 | |||||||
| chr19:7970614 | C | T | 1 | a0001c0001t0038g0084 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.431-2824G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7970614 | |||||||
| chr19:7970664 | G | C | 1 | a0001c0001t0001g0141 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.431-2874C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7970664 | |||||||
| chr19:7970738 | T | TA | 5 | a0001c0002t0004g0238 a0001c0002t0009g0021 a0001c0002t0009g0230 others(2): Show |
6 | HG00280.hp2 HG01891.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-2949dupT | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7970738 | |||||||
| chr19:7970820 | C | T | 4 | a0001c0002t0011g0024 a0001c0002t0011g0025 a0001c0002t0011g0026 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+2905G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7970820 | |||||||
| chr19:7970911 | A | G | 1 | a0001c0001t0001g0029 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.430+2814T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7970911 | |||||||
| chr19:7970957 | T | C | 1 | a0001c0001t0030g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.430+2768A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7970957 | |||||||
| chr19:7971162 | T | A | 1 | a0001c0001t0014g0124 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.430+2563A>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7971162 | |||||||
| chr19:7971227 | T | G | 1 | a0001c0001t0006g0161 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.430+2498A>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7971227 | |||||||
| chr19:7971697 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.430+2028G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7971697 | |||||||
| chr19:7971903 | C | T | 16 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(13): Show |
19 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.430+1822G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7971903 | |||||||
| chr19:7971904 | A | G | 16 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(13): Show |
19 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.430+1821T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7971904 | |||||||
| chr19:7972125 | C | T | 16 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(13): Show |
19 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.430+1600G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972125 | |||||||
| chr19:7972156 | T | C | 158 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(155): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.430+1569A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972156 | |||||||
| chr19:7972160 | T | C | 1 | a0001c0001t0001g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.430+1565A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972160 | |||||||
| chr19:7972352 | C | T | 4 | a0001c0001t0012g0234 a0001c0001t0012g0235 a0001c0001t0012g0236 others(1): Show |
4 | HG03041.hp2 HG03098.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+1373G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972352 | |||||||
| chr19:7972617 | CTTTTT | C | 11 | a0001c0001t0001g0042 a0001c0001t0001g0046 a0001c0001t0001g0047 others(8): Show |
11 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.430+1103_430+1107d others(7): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972617 | |||||||
| chr19:7972633 | CT | C | 41 | a0001c0001t0003g0077 a0001c0002t0004g0004 a0001c0002t0004g0019 others(38): Show |
50 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.430+1091delA | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972633 | |||||||
| chr19:7972689 | C | T | 15 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(12): Show |
18 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.430+1036G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972689 | |||||||
| chr19:7972696 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.430+1029C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972696 | |||||||
| chr19:7972708 | C | G | 1 | a0001c0001t0001g0031 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.430+1017G>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972708 | |||||||
| chr19:7972800 | C | CT | 72 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(69): Show |
89 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.430+924dupA | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972800 | |||||||
| chr19:7972800 | C | CTT | 47 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0074 others(44): Show |
53 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.430+923_430+924dup others(2): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972800 | |||||||
| chr19:7972800 | C | CTTT | 18 | a0001c0001t0001g0089 a0001c0001t0001g0144 a0001c0001t0002g0150 others(15): Show |
18 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.430+922_430+924dup others(3): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972800 | |||||||
| chr19:7972800 | C | T | 1 | a0001c0002t0004g0225 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.430+925G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972800 | |||||||
| chr19:7972800 | CTT | C | 23 | a0001c0001t0001g0057 a0001c0001t0001g0062 a0001c0001t0001g0063 others(20): Show |
27 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.430+923_430+924del others(2): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972800 | |||||||
| chr19:7972800 | CTTT | C | 23 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0050 others(20): Show |
24 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.430+922_430+924del others(3): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972800 | |||||||
| chr19:7972800 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0012g0234 a0001c0001t0025g0038 |
2 | HG03098.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.430+915_430+924del others(10): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972800 | |||||||
| chr19:7972800 | CTTTTTTT others(4): Show |
C | 7 | a0001c0001t0007g0108 a0001c0001t0007g0155 a0001c0001t0007g0156 others(4): Show |
7 | HG00609.hp1 HG01261.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+914_430+924del others(11): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972800 | |||||||
| chr19:7972898 | G | A | 1 | a0001c0002t0005g0214 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.430+827C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972898 | |||||||
| chr19:7972915 | C | G | 3 | a0001c0002t0004g0223 a0001c0002t0004g0224 a0001c0002t0004g0225 |
3 | HG00733.hp1 HG01243.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.430+810G>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972915 | |||||||
| chr19:7972916 | G | A | 1 | a0001c0002t0009g0021 | 2 | HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+809C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972916 | |||||||
| chr19:7973025 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.430+700G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7973025 | |||||||
| chr19:7973212 | G | A | 1 | a0001c0002t0004g0004 | 4 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+513C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7973212 | |||||||
| chr19:7973229 | C | CT | 6 | a0001c0001t0001g0097 a0001c0001t0001g0112 a0001c0001t0012g0234 others(3): Show |
6 | HG02055.hp2 HG02572.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.430+495dupA | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7973229 | |||||||
| chr19:7973229 | CTT | C | 12 | a0001c0002t0004g0004 a0001c0002t0004g0019 a0001c0002t0004g0020 others(9): Show |
17 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.430+494_430+495del others(2): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7973229 | |||||||
| chr19:7973510 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.430+215C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7973510 | |||||||
| chr19:7973930 | T | C | 1 | a0001c0001t0015g0198 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.277-52A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7973930 | |||||||
| chr19:7974206 | G | A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0138 |
2 | HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.277-328C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7974206 | |||||||
| chr19:7974207 | G | A | 16 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(13): Show |
19 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.277-329C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7974207 | |||||||
| chr19:7974211 | C | A | 4 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0187 others(1): Show |
4 | HG00639.hp1 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.277-333G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7974211 | |||||||
| chr19:7974212 | AG | A | 20 | a0001c0002t0004g0004 a0001c0002t0004g0019 a0001c0002t0004g0020 others(17): Show |
26 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.277-335delC | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7974212 | |||||||
| chr19:7974283 | G | A | 18 | a0001c0002t0004g0004 a0001c0002t0004g0019 a0001c0002t0004g0020 others(15): Show |
24 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.277-405C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7974283 | |||||||
| chr19:7974800 | G | A | 4 | a0001c0002t0011g0024 a0001c0002t0011g0025 a0001c0002t0011g0026 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.277-922C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7974800 | |||||||
| chr19:7974812 | C | T | 2 | a0001c0002t0016g0220 a0001c0002t0016g0233 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.277-934G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7974812 | |||||||
| chr19:7974813 | G | A | 2 | a0001c0001t0002g0180 a0001c0001t0002g0190 |
2 | NA18970.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.277-935C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7974813 | |||||||
| chr19:7974842 | C | T | 4 | a0001c0001t0001g0042 a0001c0001t0013g0037 a0001c0001t0013g0043 others(1): Show |
4 | HG02280.hp1 HG02486.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.277-964G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7974842 | |||||||
| chr19:7974843 | G | A | 2 | a0001c0002t0016g0220 a0001c0002t0016g0233 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.277-965C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7974843 | |||||||
| chr19:7975038 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.277-1160C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7975038 | |||||||
| chr19:7975199 | C | A | 1 | a0001c0001t0008g0137 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.277-1321G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7975199 | |||||||
| chr19:7975213 | G | A | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 |
3 | HG02886.hp2 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.277-1335C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7975213 | |||||||
| chr19:7975222 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.277-1344G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7975222 | |||||||
| chr19:7975399 | C | G | 1 | a0001c0001t0012g0236 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.277-1521G>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7975399 | |||||||
| chr19:7975529 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.277-1651C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7975529 | |||||||
| chr19:7975615 | T | C | 3 | a0001c0001t0001g0117 a0001c0001t0001g0120 a0001c0001t0001g0122 |
3 | HG00099.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.277-1737A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7975615 | |||||||
| chr19:7976051 | T | C | 104 | a0001c0001t0001g0042 a0001c0001t0001g0046 a0001c0001t0001g0047 others(101): Show |
118 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.277-2173A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7976051 | |||||||
| chr19:7976294 | C | T | 1 | a0001c0002t0005g0207 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.277-2416G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7976294 | |||||||
| chr19:7976334 | G | A | 2 | a0001c0002t0016g0220 a0001c0002t0016g0233 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.277-2456C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7976334 | |||||||
| chr19:7976489 | T | G | 43 | a0001c0001t0001g0141 a0001c0001t0001g0210 a0001c0001t0001g0211 others(40): Show |
52 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.277-2611A>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7976489 | |||||||
| chr19:7976499 | G | A | 17 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(14): Show |
20 | HG00544.hp1 HG00558.hp1 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.277-2621C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7976499 | |||||||
| chr19:7976511 | C | T | 2 | a0001c0002t0016g0220 a0001c0002t0016g0233 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.277-2633G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7976511 | |||||||
| chr19:7976517 | G | A | 1 | a0001c0002t0009g0231 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.277-2639C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7976517 | |||||||
| chr19:7976534 | G | C | 158 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(155): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.277-2656C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7976534 | |||||||
| chr19:7976637 | T | C | 4 | a0001c0002t0011g0024 a0001c0002t0011g0025 a0001c0002t0011g0026 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.277-2759A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7976637 | |||||||
| chr19:7976650 | T | G | 7 | a0001c0001t0001g0042 a0001c0001t0001g0046 a0001c0001t0001g0047 others(4): Show |
7 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.277-2772A>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7976650 | |||||||
| chr19:7976816 | G | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0030 a0001c0001t0001g0035 others(3): Show |
7 | HG00544.hp1 HG00558.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.277-2938C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7976816 | |||||||
| chr19:7976840 | A | AT | 25 | a0001c0001t0001g0094 a0001c0001t0001g0141 a0001c0001t0001g0210 others(22): Show |
29 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.277-2963dupA | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7976840 | |||||||
| chr19:7976840 | AT | A | 8 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0064 others(5): Show |
8 | HG01168.hp2 HG01257.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.277-2963delA | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7976840 | |||||||
| chr19:7976860 | GT | G | 14 | a0001c0001t0001g0005 a0001c0001t0001g0070 a0001c0001t0001g0071 others(11): Show |
16 | HG01884.hp1 HG02559.hp2 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.277-2983delA | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7976860 | |||||||
| chr19:7977064 | C | T | 4 | a0001c0002t0011g0024 a0001c0002t0011g0025 a0001c0002t0011g0026 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.277-3186G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7977064 | |||||||
| chr19:7977093 | G | A | 11 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0081 others(8): Show |
13 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.277-3215C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7977093 | |||||||
| chr19:7977139 | C | T | 1 | a0001c0002t0028g0205 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.277-3261G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7977139 | |||||||
| chr19:7977156 | G | A | 1 | a0001c0001t0001g0031 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.277-3278C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7977156 | |||||||
| chr19:7977527 | CAG | C | 11 | a0001c0001t0006g0139 a0001c0001t0006g0145 a0001c0001t0006g0159 others(8): Show |
11 | HG01261.hp2 HG02145.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.276+3554_276+3555d others(4): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7977527 | |||||||
| chr19:7977547 | A | G | 101 | a0001c0001t0001g0042 a0001c0001t0001g0046 a0001c0001t0001g0047 others(98): Show |
115 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.276+3536T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7977547 | |||||||
| chr19:7977563 | T | G | 1 | a0001c0001t0001g0118 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.276+3520A>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7977563 | |||||||
| chr19:7977886 | G | T | 20 | a0001c0002t0004g0004 a0001c0002t0004g0019 a0001c0002t0004g0020 others(17): Show |
26 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.276+3197C>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7977886 | |||||||
| chr19:7978029 | C | A | 1 | a0001c0001t0017g0009 | 2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.276+3054G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7978029 | |||||||
| chr19:7978103 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.276+2980G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7978103 | |||||||
| chr19:7978154 | C | T | 1 | a0001c0001t0002g0185 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.276+2929G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7978154 | |||||||
| chr19:7978161 | C | T | 21 | a0001c0001t0025g0038 a0001c0002t0005g0016 a0001c0002t0005g0017 others(18): Show |
24 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.276+2922G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7978161 | |||||||
| chr19:7978238 | T | C | 1 | a0001c0001t0002g0183 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.276+2845A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7978238 | |||||||
| chr19:7978293 | A | G | 5 | a0001c0001t0025g0038 a0001c0002t0011g0024 a0001c0002t0011g0025 others(2): Show |
5 | HG02622.hp1 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.276+2790T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7978293 | |||||||
| chr19:7978341 | G | A | 1 | a0001c0001t0040g0179 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.276+2742C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7978341 | |||||||
| chr19:7978355 | G | A | 1 | a0001c0001t0018g0119 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.276+2728C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7978355 | |||||||
| chr19:7978357 | G | A | 16 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(13): Show |
19 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.276+2726C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7978357 | |||||||
| chr19:7978672 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.276+2411T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7978672 | |||||||
| chr19:7978693 | G | C | 25 | a0001c0001t0025g0038 a0001c0002t0004g0004 a0001c0002t0004g0019 others(22): Show |
31 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.276+2390C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7978693 | |||||||
| chr19:7978721 | A | G | 2 | a0001c0001t0002g0163 a0001c0001t0002g0175 |
2 | NA18944.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.276+2362T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7978721 | |||||||
| chr19:7978852 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.276+2231A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7978852 | |||||||
| chr19:7978909 | T | G | 1 | a0001c0002t0005g0216 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.276+2174A>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7978909 | |||||||
| chr19:7979092 | C | A | 4 | a0001c0002t0009g0021 a0001c0002t0009g0230 a0001c0002t0009g0231 others(1): Show |
5 | HG01891.hp1 HG02257.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.276+1991G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7979092 | |||||||
| chr19:7979241 | G | A | 1 | a0001c0001t0003g0087 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.276+1842C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7979241 | |||||||
| chr19:7979264 | G | A | 1 | a0001c0001t0019g0239 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.276+1819C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7979264 | |||||||
| chr19:7979339 | G | A | 2 | a0001c0002t0005g0206 a0001c0002t0028g0205 |
2 | HG01346.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.276+1744C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7979339 | |||||||
| chr19:7979555 | G | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0070 a0001c0001t0001g0071 others(4): Show |
9 | HG01884.hp1 HG02559.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.276+1528C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7979555 | |||||||
| chr19:7979616 | G | C | 7 | a0001c0001t0001g0042 a0001c0001t0001g0046 a0001c0001t0001g0047 others(4): Show |
7 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.276+1467C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7979616 | |||||||
| chr19:7979627 | C | T | 2 | a0001c0002t0016g0220 a0001c0002t0016g0233 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.276+1456G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7979627 | |||||||
| chr19:7979673 | C | T | 14 | a0001c0002t0004g0004 a0001c0002t0004g0019 a0001c0002t0004g0020 others(11): Show |
19 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.276+1410G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7979673 | |||||||
| chr19:7979726 | C | T | 18 | a0001c0002t0004g0004 a0001c0002t0004g0019 a0001c0002t0004g0020 others(15): Show |
24 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.276+1357G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7979726 | |||||||
| chr19:7979831 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.276+1252A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7979831 | |||||||
| chr19:7979855 | G | C | 1 | a0001c0001t0013g0045 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.276+1228C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7979855 | |||||||
| chr19:7979923 | A | G | 1 | a0001c0001t0001g0033 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.276+1160T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7979923 | |||||||
| chr19:7980071 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.276+1012A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7980071 | |||||||
| chr19:7980163 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.276+920G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7980163 | |||||||
| chr19:7980269 | G | A | 16 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(13): Show |
19 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.276+814C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7980269 | |||||||
| chr19:7980397 | C | T | 1 | a0001c0002t0016g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.276+686G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7980397 | |||||||
| chr19:7980508 | C | T | 1 | a0001c0001t0031g0073 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.276+575G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7980508 | |||||||
| chr19:7980524 | ACTATGGC others(1): Show |
A | 3 | a0001c0001t0012g0234 a0001c0001t0012g0235 a0001c0001t0012g0236 |
3 | HG03041.hp2 NA18961.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.276+551_276+558del others(8): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7980524 | |||||||
| chr19:7980653 | G | C | 1 | a0001c0001t0001g0065 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.276+430C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7980653 | |||||||
| chr19:7980665 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.276+418C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7980665 | |||||||
| chr19:7980978 | G | A | 17 | a0001c0002t0004g0004 a0001c0002t0004g0019 a0001c0002t0004g0020 others(14): Show |
22 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.276+105C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7980978 | |||||||
| chr19:7981060 | C | T | 3 | a0001c0001t0007g0028 a0001c0001t0007g0174 a0001c0001t0007g0197 |
3 | NA18953.hp1 NA18966.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.276+23G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7981060 | |||||||
| chr19:7981314 | C | A | 1 | a0001c0001t0001g0095 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.173-128G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7981314 | |||||||
| chr19:7981355 | C | CT | 5 | a0001c0001t0002g0167 a0001c0001t0002g0180 a0001c0001t0010g0154 others(2): Show |
5 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(2): Show |
intron_variant | MODIFIER | c.173-170dupA | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7981355 | |||||||
| chr19:7981355 | CT | C | 27 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0001t0001g0110 others(24): Show |
32 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.173-170delA | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7981355 | |||||||
| chr19:7981355 | CTT | C | 18 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0002t0005g0016 others(15): Show |
21 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.173-171_173-170del others(2): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7981355 | |||||||
| chr19:7981410 | T | C | 2 | a0001c0001t0001g0115 a0001c0001t0033g0121 |
2 | HG01168.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.173-224A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7981410 | |||||||
| chr19:7981415 | C | A | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.173-229G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7981415 | |||||||
| chr19:7981622 | C | T | 1 | a0001c0002t0005g0207 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.173-436G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7981622 | |||||||
| chr19:7981673 | G | A | 1 | a0001c0001t0002g0173 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.173-487C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7981673 | |||||||
| chr19:7981731 | T | A | 214 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(211): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.173-545A>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7981731 | |||||||
| chr19:7981795 | G | C | 1 | a0001c0001t0001g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.173-609C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7981795 | |||||||
| chr19:7981835 | GGACA | G | 11 | a0001c0001t0001g0210 a0001c0002t0005g0016 a0001c0002t0005g0017 others(8): Show |
13 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.173-653_173-650del others(4): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7981835 | |||||||
| chr19:7982364 | C | T | 20 | a0001c0001t0001g0096 a0001c0001t0001g0138 a0001c0001t0001g0210 others(17): Show |
23 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.173-1178G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7982364 | |||||||
| chr19:7982465 | G | A | 2 | a0001c0001t0002g0180 a0001c0001t0002g0190 |
2 | NA18970.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.173-1279C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7982465 | |||||||
| chr19:7982787 | C | T | 18 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0002t0005g0016 others(15): Show |
21 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.173-1601G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7982787 | |||||||
| chr19:7982812 | G | A | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0002t0009g0231 |
3 | HG02257.hp2 HG02897.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.173-1626C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7982812 | |||||||
| chr19:7982836 | G | A | 1 | a0001c0001t0002g0192 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.173-1650C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7982836 | |||||||
| chr19:7982848 | C | T | 1 | a0001c0001t0002g0069 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.173-1662G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7982848 | |||||||
| chr19:7982892 | C | T | 2 | a0001c0001t0015g0041 a0001c0001t0015g0044 |
2 | HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.173-1706G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7982892 | |||||||
| chr19:7982902 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.173-1716C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7982902 | |||||||
| chr19:7983040 | G | A | 48 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0069 others(45): Show |
53 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.173-1854C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7983040 | |||||||
| chr19:7983155 | C | T | 1 | a0001c0001t0034g0143 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.173-1969G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7983155 | |||||||
| chr19:7983197 | T | G | 2 | a0001c0001t0002g0181 a0001c0001t0002g0191 |
2 | HG01975.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.173-2011A>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7983197 | |||||||
| chr19:7983258 | C | T | 1 | a0001c0001t0006g0199 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.173-2072G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7983258 | |||||||
| chr19:7983478 | C | A | 2 | a0001c0001t0015g0041 a0001c0001t0015g0044 |
2 | HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.173-2292G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7983478 | |||||||
| chr19:7983489 | G | C | 18 | a0001c0001t0001g0141 a0001c0001t0001g0210 a0001c0001t0001g0211 others(15): Show |
21 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.173-2303C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7983489 | |||||||
| chr19:7983995 | C | T | 5 | a0001c0001t0025g0038 a0001c0002t0011g0024 a0001c0002t0011g0025 others(2): Show |
5 | HG02622.hp1 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.173-2809G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7983995 | |||||||
| chr19:7984013 | T | C | 5 | a0001c0001t0025g0038 a0001c0002t0011g0024 a0001c0002t0011g0025 others(2): Show |
5 | HG02622.hp1 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.173-2827A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7984013 | |||||||
| chr19:7984196 | C | T | 1 | a0001c0002t0011g0024 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.173-3010G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7984196 | |||||||
| chr19:7984254 | C | T | 1 | a0001c0002t0027g0204 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.173-3068G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7984254 | |||||||
| chr19:7984268 | A | G | 18 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0002t0005g0016 others(15): Show |
21 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.173-3082T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7984268 | |||||||
| chr19:7984277 | A | G | 91 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0002g0003 others(88): Show |
105 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.173-3091T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7984277 | |||||||
| chr19:7984480 | G | A | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.173-3294C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7984480 | |||||||
| chr19:7984558 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.173-3372C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7984558 | |||||||
| chr19:7984699 | C | T | 27 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0032 others(24): Show |
34 | HG00099.hp2 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.173-3513G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7984699 | |||||||
| chr19:7984968 | C | G | 11 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0081 others(8): Show |
13 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.173-3782G>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7984968 | |||||||
| chr19:7985208 | C | T | 18 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0002t0005g0016 others(15): Show |
21 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.173-4022G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7985208 | |||||||
| chr19:7985210 | G | A | 1 | a0001c0001t0001g0010 | 2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.173-4024C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7985210 | |||||||
| chr19:7985212 | G | A | 3 | a0001c0001t0012g0234 a0001c0001t0012g0235 a0001c0001t0012g0236 |
3 | HG03041.hp2 NA18961.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.173-4026C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7985212 | |||||||
| chr19:7985324 | C | T | 7 | a0001c0001t0008g0022 a0001c0001t0008g0023 a0001c0001t0008g0079 others(4): Show |
7 | NA18941.hp2 NA18952.hp2 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.173-4138G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7985324 | |||||||
| chr19:7985427 | C | A | 1 | a0001c0001t0015g0198 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.173-4241G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7985427 | |||||||
| chr19:7985597 | G | C | 1 | a0001c0001t0013g0045 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.173-4411C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7985597 | |||||||
| chr19:7985635 | G | A | 2 | a0001c0001t0008g0079 a0001c0001t0008g0106 |
2 | NA18953.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.173-4449C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7985635 | |||||||
| chr19:7985814 | C | T | 1 | a0001c0001t0007g0028 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.173-4628G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7985814 | |||||||
| chr19:7985838 | G | A | 1 | a0001c0001t0014g0014 | 2 | HG02723.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.173-4652C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7985838 | |||||||
| chr19:7985935 | T | C | 1 | a0001c0001t0002g0182 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.173-4749A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7985935 | |||||||
| chr19:7986203 | G | A | 2 | a0001c0002t0016g0220 a0001c0002t0016g0233 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.173-5017C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7986203 | |||||||
| chr19:7986370 | G | C | 1 | a0001c0001t0006g0201 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.173-5184C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7986370 | |||||||
| chr19:7986417 | T | G | 15 | a0001c0001t0001g0005 a0001c0001t0001g0070 a0001c0001t0001g0071 others(12): Show |
17 | HG01884.hp1 HG02559.hp2 HG02647.hp2 others(14): Show |
intron_variant | MODIFIER | c.172+5227A>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7986417 | |||||||
| chr19:7986477 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.172+5167C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7986477 | |||||||
| chr19:7986525 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.172+5119A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7986525 | |||||||
| chr19:7986559 | C | T | 1 | a0001c0002t0027g0204 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.172+5085G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7986559 | |||||||
| chr19:7986570 | G | C | 16 | a0001c0001t0001g0005 a0001c0001t0001g0070 a0001c0001t0001g0071 others(13): Show |
18 | HG01884.hp1 HG02559.hp2 HG02647.hp2 others(15): Show |
intron_variant | MODIFIER | c.172+5074C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7986570 | |||||||
| chr19:7986574 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.172+5070C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7986574 | |||||||
| chr19:7986582 | G | A | 2 | a0001c0002t0016g0220 a0001c0002t0016g0233 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.172+5062C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7986582 | |||||||
| chr19:7986590 | C | T | 3 | a0001c0001t0012g0234 a0001c0001t0012g0235 a0001c0001t0012g0236 |
3 | HG03041.hp2 NA18961.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.172+5054G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7986590 | |||||||
| chr19:7986762 | G | A | 18 | a0001c0002t0004g0004 a0001c0002t0004g0019 a0001c0002t0004g0020 others(15): Show |
24 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.172+4882C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7986762 | |||||||
| chr19:7986983 | C | A | 1 | a0001c0002t0004g0227 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.172+4661G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7986983 | |||||||
| chr19:7987035 | A | G | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.172+4609T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7987035 | |||||||
| chr19:7987116 | C | CG | 72 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0054 others(69): Show |
75 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.172+4527dupC | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7987116 | |||||||
| chr19:7987116 | C | CGG | 36 | a0001c0001t0001g0005 a0001c0001t0001g0042 a0001c0001t0001g0046 others(33): Show |
41 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.172+4526_172+4527d others(4): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7987116 | |||||||
| chr19:7987116 | CG | C | 41 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0002t0004g0004 others(38): Show |
50 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.172+4527delC | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7987116 | |||||||
| chr19:7987120 | G | T | 3 | a0001c0001t0001g0057 a0001c0001t0001g0146 a0001c0001t0037g0051 |
3 | NA18966.hp1 NA18977.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.172+4524C>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7987120 | |||||||
| chr19:7987137 | C | T | 1 | a0001c0001t0003g0072 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.172+4507G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7987137 | |||||||
| chr19:7987171 | C | T | 1 | a0001c0002t0027g0204 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.172+4473G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7987171 | |||||||
| chr19:7987283 | T | A | 1 | a0001c0001t0003g0153 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.172+4361A>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7987283 | |||||||
| chr19:7987425 | A | G | 42 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0002t0004g0004 others(39): Show |
51 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.172+4219T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7987425 | |||||||
| chr19:7987762 | C | T | 51 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(48): Show |
60 | HG00099.hp2 HG01069.hp2 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.172+3882G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7987762 | |||||||
| chr19:7987868 | C | T | 2 | a0001c0002t0004g0221 a0001c0002t0004g0222 |
2 | HG01256.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.172+3776G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7987868 | |||||||
| chr19:7987890 | A | G | 4 | a0001c0002t0011g0024 a0001c0002t0011g0025 a0001c0002t0011g0026 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.172+3754T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7987890 | |||||||
| chr19:7987977 | C | T | 3 | a0001c0001t0012g0234 a0001c0001t0012g0235 a0001c0001t0012g0236 |
3 | HG03041.hp2 NA18961.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.172+3667G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7987977 | |||||||
| chr19:7988299 | C | G | 1 | a0001c0002t0016g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.172+3345G>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7988299 | |||||||
| chr19:7988431 | A | T | 2 | a0001c0002t0005g0206 a0001c0002t0028g0205 |
2 | HG01346.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.172+3213T>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7988431 | |||||||
| chr19:7988479 | A | G | 18 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0002t0005g0016 others(15): Show |
21 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.172+3165T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7988479 | |||||||
| chr19:7988537 | AGAGGATG others(10): Show |
A | 8 | a0001c0002t0005g0018 a0001c0002t0005g0212 a0001c0002t0005g0214 others(5): Show |
9 | NA18952.hp1 NA18959.hp1 NA18960.hp1 others(6): Show |
intron_variant | MODIFIER | c.172+3090_172+3106d others(19): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7988537 | |||||||
| chr19:7988645 | G | T | 2 | a0001c0001t0001g0089 a0001c0004t0001g0107 |
2 | HG00558.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.172+2999C>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7988645 | |||||||
| chr19:7988877 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.172+2767C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7988877 | |||||||
| chr19:7988897 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.172+2747G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7988897 | |||||||
| chr19:7988963 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.172+2681G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7988963 | |||||||
| chr19:7989056 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.172+2588G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7989056 | |||||||
| chr19:7989226 | G | A | 1 | a0001c0001t0015g0198 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.172+2418C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7989226 | |||||||
| chr19:7989234 | G | A | 3 | a0001c0002t0009g0021 a0001c0002t0009g0230 a0001c0002t0009g0232 |
4 | HG01891.hp1 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.172+2410C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7989234 | |||||||
| chr19:7989463 | C | A | 1 | a0001c0002t0027g0204 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.172+2181G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7989463 | |||||||
| chr19:7989551 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.172+2093T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7989551 | |||||||
| chr19:7989956 | G | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0032 others(22): Show |
31 | HG00099.hp2 HG01069.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.172+1688C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7989956 | |||||||
| chr19:7990098 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.172+1546A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7990098 | |||||||
| chr19:7990338 | G | GTT | 18 | a0001c0002t0004g0004 a0001c0002t0004g0019 a0001c0002t0004g0020 others(15): Show |
24 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.172+1304_172+1305d others(4): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7990338 | |||||||
| chr19:7990404 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.172+1240A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7990404 | |||||||
| chr19:7990967 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.172+677C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7990967 | |||||||
| chr19:7991174 | G | A | 1 | a0001c0002t0005g0215 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.172+470C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7991174 | |||||||
| chr19:7991225 | G | A | 2 | a0001c0001t0002g0184 a0001c0001t0002g0185 |
2 | HG01074.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.172+419C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7991225 | |||||||
| chr19:7991264 | C | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.172+380G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7991264 | |||||||
| chr19:7991873 | T | C | 3 | a0001c0002t0005g0214 a0001c0002t0005g0215 a0001c0002t0005g0216 |
3 | NA18952.hp1 NA18962.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.-16-42A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7991873 | |||||||
| chr19:7991898 | T | G | 4 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
4 | HG01884.hp1 HG02559.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16-67A>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7991898 | |||||||
| chr19:7991932 | C | CT | 99 | a0001c0001t0001g0042 a0001c0001t0001g0046 a0001c0001t0001g0047 others(96): Show |
114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.-16-102dupA | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7991932 | |||||||
| chr19:7992183 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-16-352G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7992183 | |||||||
| chr19:7992221 | A | G | 42 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0002t0004g0004 others(39): Show |
51 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-16-390T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7992221 | |||||||
| chr19:7992589 | G | C | 1 | a0001c0001t0001g0090 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-16-758C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7992589 | |||||||
| chr19:7992740 | G | A | 4 | a0001c0001t0006g0159 a0001c0001t0006g0160 a0001c0001t0006g0161 others(1): Show |
4 | HG02145.hp2 HG02280.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16-909C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7992740 | |||||||
| chr19:7992829 | C | T | 42 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0002t0004g0004 others(39): Show |
51 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-16-998G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7992829 | |||||||
| chr19:7992889 | C | G | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-16-1058G>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7992889 | |||||||
| chr19:7992915 | G | A | 1 | a0001c0001t0003g0091 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-16-1084C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7992915 | |||||||
| chr19:7992936 | C | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
3 | HG03239.hp1 HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-16-1105G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7992936 | |||||||
| chr19:7992937 | G | A | 24 | a0001c0002t0004g0004 a0001c0002t0004g0019 a0001c0002t0004g0020 others(21): Show |
30 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.-16-1106C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7992937 | |||||||
| chr19:7993636 | A | T | 1 | a0001c0001t0015g0041 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-16-1805T>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7993636 | |||||||
| chr19:7993794 | G | A | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-16-1963C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7993794 | |||||||
| chr19:7993801 | C | T | 2 | a0001c0002t0016g0220 a0001c0002t0016g0233 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-16-1970G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7993801 | |||||||
| chr19:7993855 | C | T | 1 | a0001c0001t0014g0124 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-16-2024G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7993855 | |||||||
| chr19:7993997 | C | A | 1 | a0001c0001t0001g0054 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-16-2166G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7993997 | |||||||
| chr19:7994237 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-16-2406C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7994237 | |||||||
| chr19:7994544 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-16-2713C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7994544 | |||||||
| chr19:7994771 | G | A | 1 | a0001c0001t0008g0137 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-16-2940C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7994771 | |||||||
| chr19:7994907 | T | G | 4 | a0001c0002t0011g0024 a0001c0002t0011g0025 a0001c0002t0011g0026 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16-3076A>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7994907 | |||||||
| chr19:7994987 | AC | A | 12 | a0001c0001t0001g0042 a0001c0001t0001g0046 a0001c0001t0001g0047 others(9): Show |
12 | HG01891.hp2 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-16-3157delG | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7994987 | |||||||
| chr19:7995012 | A | T | 1 | a0001c0002t0027g0204 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-16-3181T>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7995012 | |||||||
| chr19:7995462 | C | T | 42 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0002t0004g0004 others(39): Show |
51 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-16-3631G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7995462 | |||||||
| chr19:7995536 | T | C | 214 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(211): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.-16-3705A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7995536 | |||||||
| chr19:7995562 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-16-3731A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7995562 | |||||||
| chr19:7995662 | C | A | 1 | a0001c0001t0001g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-16-3831G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7995662 | |||||||
| chr19:7995690 | A | C | 2 | a0001c0002t0016g0220 a0001c0002t0016g0233 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-16-3859T>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7995690 | |||||||
| chr19:7995783 | T | TA | 11 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0094 others(8): Show |
13 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-16-3953dupT | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7995783 | |||||||
| chr19:7995783 | TA | T | 43 | a0001c0001t0001g0030 a0001c0001t0001g0053 a0001c0001t0001g0054 others(40): Show |
52 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.-16-3953delT | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7995783 | |||||||
| chr19:7995818 | C | T | 18 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0002t0005g0016 others(15): Show |
21 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.-16-3987G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7995818 | |||||||
| chr19:7995916 | C | CT | 16 | a0001c0001t0001g0030 a0001c0001t0010g0154 a0001c0002t0004g0004 others(13): Show |
21 | HG00140.hp1 HG00280.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.-16-4086dupA | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7995916 | |||||||
| chr19:7996003 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-16-4172G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7996003 | |||||||
| chr19:7996126 | T | C | 1 | a0001c0001t0015g0198 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-16-4295A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7996126 | |||||||
| chr19:7996156 | G | A | 1 | a0001c0001t0030g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-16-4325C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7996156 | |||||||
| chr19:7996183 | CT | C | 21 | a0001c0001t0001g0048 a0001c0001t0001g0210 a0001c0001t0001g0211 others(18): Show |
25 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.-16-4353delA | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7996183 | |||||||
| chr19:7996250 | C | T | 3 | a0001c0001t0012g0234 a0001c0001t0012g0235 a0001c0001t0012g0236 |
3 | HG03041.hp2 NA18961.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.-16-4419G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7996250 | |||||||
| chr19:7996374 | G | C | 1 | a0001c0001t0001g0157 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-16-4543C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7996374 | |||||||
| chr19:7996468 | C | T | 2 | a0001c0001t0018g0039 a0001c0001t0036g0040 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-16-4637G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7996468 | |||||||
| chr19:7996469 | G | A | 24 | a0001c0002t0004g0004 a0001c0002t0004g0019 a0001c0002t0004g0020 others(21): Show |
30 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.-16-4638C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7996469 | |||||||
| chr19:7996485 | G | A | 1 | a0001c0002t0004g0238 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-16-4654C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7996485 | |||||||
| chr19:7996671 | G | A | 1 | a0001c0001t0008g0100 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-16-4840C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7996671 | |||||||
| chr19:7996694 | T | C | 1 | a0001c0001t0014g0124 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-16-4863A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7996694 | |||||||
| chr19:7996785 | A | C | 42 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0002t0004g0004 others(39): Show |
51 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-16-4954T>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7996785 | |||||||
| chr19:7996792 | G | A | 3 | a0001c0001t0010g0154 a0001c0001t0010g0193 a0001c0001t0010g0194 |
3 | HG00544.hp2 HG00621.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.-16-4961C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7996792 | |||||||
| chr19:7996854 | A | C | 1 | a0001c0002t0027g0204 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-16-5023T>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7996854 | |||||||
| chr19:7996969 | G | A | 20 | a0001c0002t0004g0004 a0001c0002t0004g0019 a0001c0002t0004g0020 others(17): Show |
26 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.-16-5138C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7996969 | |||||||
| chr19:7997031 | C | G | 1 | a0001c0002t0009g0230 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-16-5200G>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7997031 | |||||||
| chr19:7997050 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-16-5219C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7997050 | |||||||
| chr19:7997120 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-16-5289G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7997120 | |||||||
| chr19:7997457 | G | A | 1 | a0001c0001t0003g0101 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-16-5626C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7997457 | |||||||
| chr19:7997468 | C | T | 1 | a0001c0001t0037g0051 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-16-5637G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7997468 | |||||||
| chr19:7997672 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-16-5841C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7997672 | |||||||
| chr19:7997725 | A | G | 1 | a0001c0001t0025g0038 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-16-5894T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7997725 | |||||||
| chr19:7997881 | G | A | 1 | a0001c0002t0016g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-16-6050C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7997881 | |||||||
| chr19:7998177 | A | G | 1 | a0001c0001t0001g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-16-6346T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7998177 | |||||||
| chr19:7998264 | A | C | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG01884.hp1 HG02559.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-16-6433T>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7998264 | |||||||
| chr19:7998305 | G | A | 7 | a0001c0001t0006g0139 a0001c0001t0006g0145 a0001c0001t0006g0159 others(4): Show |
7 | HG01261.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-16-6474C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7998305 | |||||||
| chr19:7998308 | G | C | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG01884.hp1 HG02559.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-16-6477C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7998308 | |||||||
| chr19:7998355 | A | C | 42 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0002t0004g0004 others(39): Show |
51 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-16-6524T>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7998355 | |||||||
| chr19:7998391 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-16-6560G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7998391 | |||||||
| chr19:7998413 | G | A | 1 | a0001c0001t0002g0192 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-16-6582C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7998413 | |||||||
| chr19:7998733 | TTGGCCTC others(37): Show |
T | 1 | a0001c0002t0016g0220 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-17+6718_-17+6761d others(46): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7998733 | |||||||
| chr19:7998796 | C | T | 42 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0002t0004g0004 others(39): Show |
51 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-17+6699G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7998796 | |||||||
| chr19:7998966 | A | G | 1 | a0001c0001t0022g0165 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-17+6529T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7998966 | |||||||
| chr19:7999099 | G | A | 1 | a0001c0001t0034g0143 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-17+6396C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7999099 | |||||||
| chr19:7999190 | T | C | 1 | a0001c0001t0002g0192 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-17+6305A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7999190 | |||||||
| chr19:7999386 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-17+6109T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7999386 | |||||||
| chr19:7999494 | G | C | 2 | a0001c0001t0010g0193 a0001c0001t0010g0194 |
2 | HG00544.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.-17+6001C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7999494 | |||||||
| chr19:7999740 | G | A | 19 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0007g0195 others(16): Show |
22 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.-17+5755C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7999740 | |||||||
| chr19:7999978 | C | T | 27 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0032 others(24): Show |
34 | HG00099.hp2 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-17+5517G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7999978 | |||||||
| chr19:8000054 | A | G | 42 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0002t0004g0004 others(39): Show |
51 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-17+5441T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8000054 | |||||||
| chr19:8000106 | G | A | 18 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0002t0005g0016 others(15): Show |
21 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.-17+5389C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8000106 | |||||||
| chr19:8000301 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-17+5194A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8000301 | |||||||
| chr19:8000310 | T | A | 3 | a0001c0002t0004g0228 a0001c0002t0004g0229 a0001c0002t0004g0237 |
3 | HG02602.hp1 HG02698.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-17+5185A>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8000310 | |||||||
| chr19:8000345 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-17+5150C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8000345 | |||||||
| chr19:8000860 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-17+4635C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8000860 | |||||||
| chr19:8001063 | C | T | 6 | a0001c0001t0006g0145 a0001c0001t0006g0159 a0001c0001t0006g0160 others(3): Show |
6 | HG01261.hp2 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17+4432G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8001063 | |||||||
| chr19:8001113 | G | T | 1 | a0001c0001t0001g0158 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-17+4382C>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8001113 | |||||||
| chr19:8001633 | A | C | 20 | a0001c0002t0004g0004 a0001c0002t0004g0019 a0001c0002t0004g0020 others(17): Show |
26 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.-17+3862T>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8001633 | |||||||
| chr19:8001634 | A | AT | 17 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0002t0005g0016 others(14): Show |
20 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-17+3860dupA | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8001634 | |||||||
| chr19:8001634 | A | T | 2 | a0001c0001t0001g0033 a0001c0001t0002g0164 |
2 | HG03491.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.-17+3861T>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8001634 | |||||||
| chr19:8001634 | AT | A | 5 | a0001c0001t0001g0104 a0001c0001t0001g0144 a0001c0001t0003g0105 others(2): Show |
5 | HG00642.hp2 NA18942.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17+3860delA | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8001634 | |||||||
| chr19:8001648 | T | A | 2 | a0001c0001t0002g0196 a0001c0001t0007g0197 |
2 | HG00639.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.-17+3847A>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8001648 | |||||||
| chr19:8001648 | T | TA | 48 | a0001c0001t0001g0152 a0001c0001t0001g0188 a0001c0001t0002g0003 others(45): Show |
54 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.-17+3846dupT | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8001648 | |||||||
| chr19:8001760 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-17+3735G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8001760 | |||||||
| chr19:8001791 | G | C | 1 | a0001c0001t0012g0236 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-17+3704C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8001791 | |||||||
| chr19:8002066 | C | G | 3 | a0001c0001t0007g0108 a0001c0001t0007g0155 a0001c0001t0007g0156 |
3 | HG01261.hp1 HG01928.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-17+3429G>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8002066 | |||||||
| chr19:8002241 | C | T | 13 | a0001c0001t0001g0042 a0001c0001t0001g0046 a0001c0001t0001g0047 others(10): Show |
13 | HG01891.hp2 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-17+3254G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8002241 | |||||||
| chr19:8003027 | C | T | 1 | a0001c0001t0013g0037 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-17+2468G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8003027 | |||||||
| chr19:8003113 | C | T | 4 | a0001c0002t0011g0024 a0001c0002t0011g0025 a0001c0002t0011g0026 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17+2382G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8003113 | |||||||
| chr19:8003355 | C | CA | 96 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(93): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.-17+2139dupT | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8003355 | |||||||
| chr19:8003355 | CA | C | 28 | a0001c0001t0001g0029 a0001c0001t0001g0033 a0001c0001t0001g0034 others(25): Show |
34 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.-17+2139delT | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8003355 | |||||||
| chr19:8003355 | CAA | C | 21 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0002t0004g0221 others(18): Show |
24 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.-17+2138_-17+2139d others(4): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8003355 | |||||||
| chr19:8003371 | A | G | 4 | a0001c0002t0009g0021 a0001c0002t0009g0230 a0001c0002t0009g0231 others(1): Show |
5 | HG01891.hp1 HG02257.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17+2124T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8003371 | |||||||
| chr19:8003381 | GA | G | 19 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(16): Show |
24 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.-17+2113delT | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8003381 | |||||||
| chr19:8003381 | GAA | G | 16 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0002t0005g0016 others(13): Show |
19 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.-17+2112_-17+2113d others(4): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8003381 | |||||||
| chr19:8003691 | C | CA | 63 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0152 others(60): Show |
69 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.-17+1803dupT | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8003691 | |||||||
| chr19:8003691 | C | CAA | 7 | a0001c0001t0006g0199 a0001c0001t0006g0200 a0001c0001t0006g0201 others(4): Show |
7 | HG01261.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17+1802_-17+1803d others(4): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8003691 | |||||||
| chr19:8003819 | G | A | 42 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0002t0004g0004 others(39): Show |
51 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-17+1676C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8003819 | |||||||
| chr19:8004062 | G | T | 18 | a0001c0002t0004g0004 a0001c0002t0004g0019 a0001c0002t0004g0020 others(15): Show |
24 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.-17+1433C>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8004062 | |||||||
| chr19:8004066 | C | T | 18 | a0001c0002t0004g0004 a0001c0002t0004g0019 a0001c0002t0004g0020 others(15): Show |
24 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.-17+1429G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8004066 | |||||||
| chr19:8004435 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-17+1060C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8004435 | |||||||
| chr19:8004485 | T | C | 3 | a0001c0001t0012g0234 a0001c0001t0012g0235 a0001c0001t0012g0236 |
3 | HG03041.hp2 NA18961.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.-17+1010A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8004485 | |||||||
| chr19:8004565 | C | A | 1 | a0001c0002t0004g0237 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-17+930G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8004565 | |||||||
| chr19:8004643 | G | T | 1 | a0001c0001t0007g0028 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-17+852C>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8004643 | |||||||
| chr19:8004806 | C | T | 5 | a0001c0002t0011g0024 a0001c0002t0011g0025 a0001c0002t0011g0026 others(2): Show |
5 | HG02622.hp1 HG02717.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17+689G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8004806 | |||||||
| chr19:8004807 | C | T | 2 | a0001c0001t0008g0022 a0001c0001t0008g0023 |
2 | NA18970.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.-17+688G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8004807 | |||||||
| chr19:8005265 | C | A | 1 | a0001c0002t0004g0238 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-17+230G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8005265 | |||||||
| chr19:8005285 | G | A | 23 | a0001c0001t0012g0234 a0001c0001t0012g0235 a0001c0001t0012g0236 others(20): Show |
29 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.-17+210C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8005285 |