Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 27248 |
| ensemblid | ENSG00000068912.15 |
| hgncid | 25222 |
| symbol | ERLEC1 |
| name | endoplasmic reticulum lectin 1 |
| refseq_nuc | NM_015701.5 |
| refseq_prot | NP_056516.2 |
| ensembl_nuc | ENST00000185150.9 |
| ensembl_prot | ENSP00000185150.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 53787044 |
| end | 53818796 |
| strand | + |
| ver | v1.2 |
| region | chr2:53787044-53818796 |
| region5000 | chr2:53782044-53823796 |
| regionname0 | ERLEC1_chr2_53787044_53818796 |
| regionname5000 | ERLEC1_chr2_53782044_53823796 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 483 | 316 | 83 | 51 | 133 | 12 | 35 | 103 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | MEEGG others(478): Show |
chr2 | 53782044 | 53823796 |
| a0002 | 0/0 | 483 | 53 | 7 | 10 | 31 | 2 | 3 | 23 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | MEEGG others(478): Show |
chr2 | 53782044 | 53823796 |
| a0003 | 0/0 | 483 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | MEEGG others(478): Show |
chr2 | 53782044 | 53823796 |
| a0004 | 0/0 | 483 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | MEEGG others(478): Show |
chr2 | 53782044 | 53823796 |
| a0005 | 0/0 | 483 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | MEEGG others(478): Show |
chr2 | 53782044 | 53823796 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1449 | 256 | 74 | 33 | 110 | 12 | 26 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | ATGGA others(1444): Show |
chr2 | 53782044 | 53823796 | ||
| a0001c0002 | 0/1 | 1449 | 57 | 6 | 18 | 23 | 0 | 9 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | ATGGA others(1444): Show |
chr2 | 53782044 | 53823796 | ||
| a0001c0004 | 0/0 | 1449 | 3 | 3 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | ATGGA others(1444): Show |
chr2 | 53782044 | 53823796 | ||
| a0002c0003 | 0/0 | 1449 | 53 | 7 | 10 | 31 | 2 | 3 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | ATGGA others(1444): Show |
chr2 | 53782044 | 53823796 | ||
| a0003c0005 | 0/0 | 1449 | 3 | 0 | 0 | 3 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | ATGGA others(1444): Show |
chr2 | 53782044 | 53823796 | ||
| a0004c0006 | 0/0 | 1449 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | ATGGA others(1444): Show |
chr2 | 53782044 | 53823796 | ||
| a0005c0007 | 0/0 | 1449 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | ATGGA others(1444): Show |
chr2 | 53782044 | 53823796 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2446 | 213 | 51 | 28 | 98 | 10 | 25 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | GGAGG others(2441): Show |
chr2 | 53782044 | 53823796 |
| a0001c0001t0002 | 0/0 | 2446 | 33 | 21 | 5 | 4 | 2 | 1 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | GGAGG others(2441): Show |
chr2 | 53782044 | 53823796 |
| a0001c0001t0003 | 0/0 | 2446 | 7 | 0 | 0 | 7 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | GGAGG others(2441): Show |
chr2 | 53782044 | 53823796 |
| a0001c0001t0004 | 0/0 | 2446 | 2 | 2 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | GGAGG others(2441): Show |
chr2 | 53782044 | 53823796 |
| a0001c0001t0005 | 0/0 | 2446 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | GGAGG others(2441): Show |
chr2 | 53782044 | 53823796 |
| a0001c0002t0001 | 0/1 | 2446 | 57 | 6 | 18 | 23 | 0 | 9 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | GGAGG others(2441): Show |
chr2 | 53782044 | 53823796 |
| a0001c0004t0002 | 0/0 | 2446 | 3 | 3 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | GGAGG others(2441): Show |
chr2 | 53782044 | 53823796 |
| a0002c0003t0001 | 0/0 | 2446 | 6 | 6 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | GGAGG others(2441): Show |
chr2 | 53782044 | 53823796 |
| a0002c0003t0002 | 0/0 | 2446 | 45 | 1 | 9 | 30 | 2 | 3 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | GGAGG others(2441): Show |
chr2 | 53782044 | 53823796 |
| a0002c0003t0006 | 0/0 | 2446 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | GGAGG others(2441): Show |
chr2 | 53782044 | 53823796 |
| a0002c0003t0007 | 0/0 | 2446 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | GGAGG others(2441): Show |
chr2 | 53782044 | 53823796 |
| a0003c0005t0001 | 0/0 | 2446 | 3 | 0 | 0 | 3 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | GGAGG others(2441): Show |
chr2 | 53782044 | 53823796 |
| a0004c0006t0002 | 0/0 | 2446 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | GGAGG others(2441): Show |
chr2 | 53782044 | 53823796 |
| a0005c0007t0001 | 0/0 | 2446 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | GGAGG others(2441): Show |
chr2 | 53782044 | 53823796 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 15 | 3 | 3 | 6 | 0 | 3 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0003 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 0 | 2 | 3 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0012 | 1/0 | 3 | 0 | 0 | 0 | 0 | 2 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0022 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0002g0010 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0002g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0001t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0005 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0008 | 0/1 | 5 | 0 | 3 | 0 | 0 | 1 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0040 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0004t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0004t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0001c0004t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0002g0002 | 0/0 | 12 | 0 | 1 | 10 | 0 | 1 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0002g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0006g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0002c0003t0007g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0003c0005t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0003c0005t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0003c0005t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0004c0006t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| a0005c0007t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | GBR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0069 | EUR | GBR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | FIN | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | FIN | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | FIN | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | FIN | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG00408 | hp2 | a0002 | c0003 | t0002 | g0002 | EAS | CHS | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | CHS | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | CHS | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | CHS | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG00621 | hp1 | a0003 | c0005 | t0001 | g0191 | EAS | CHS | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG00621 | hp2 | a0002 | c0003 | t0002 | g0125 | EAS | CHS | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0210 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0204 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01070 | hp2 | a0002 | c0003 | t0002 | g0131 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0203 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01074 | hp2 | a0002 | c0003 | t0007 | g0170 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01109 | hp1 | a0002 | c0003 | t0002 | g0119 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0208 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0211 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0207 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0221 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01175 | hp2 | a0002 | c0003 | t0002 | g0120 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0213 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01243 | hp1 | a0004 | c0006 | t0002 | g0148 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01256 | hp1 | a0002 | c0003 | t0002 | g0138 | AMR | CLM | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0212 | AMR | CLM | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0209 | AMR | CLM | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01257 | hp2 | a0002 | c0003 | t0002 | g0002 | AMR | CLM | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | CLM | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01358 | hp2 | a0002 | c0003 | t0002 | g0135 | AMR | CLM | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0196 | EUR | IBS | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01515 | hp2 | a0002 | c0003 | t0002 | g0019 | EUR | IBS | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0034 | EUR | IBS | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01517 | hp1 | a0002 | c0003 | t0002 | g0019 | EUR | IBS | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | ACB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | ACB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0039 | AMR | PEL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01928 | hp2 | a0002 | c0003 | t0002 | g0141 | AMR | PEL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0040 | AMR | PEL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0220 | AMR | PEL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0039 | AMR | PEL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0174 | AMR | PEL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02004 | hp2 | a0002 | c0003 | t0002 | g0117 | AMR | PEL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02040 | hp2 | a0002 | c0003 | t0002 | g0002 | EAS | KHV | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0240 | EAS | KHV | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02056 | hp2 | a0002 | c0003 | t0002 | g0134 | EAS | KHV | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | KHV | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02080 | hp1 | a0002 | c0003 | t0002 | g0035 | EAS | KHV | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02080 | hp2 | a0002 | c0003 | t0002 | g0041 | EAS | KHV | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | KHV | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02132 | hp2 | a0002 | c0003 | t0002 | g0124 | EAS | KHV | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0227 | AFR | ACB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | PEL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | CDX | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CDX | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | CDX | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | CDX | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02293 | hp1 | a0002 | c0003 | t0002 | g0132 | AMR | PEL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02523 | hp2 | a0003 | c0005 | t0001 | g0189 | EAS | KHV | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02572 | hp2 | a0001 | c0004 | t0002 | g0156 | AFR | GWD | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0178 | SAS | PJL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02683 | hp1 | a0002 | c0003 | t0002 | g0222 | SAS | PJL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02717 | hp1 | a0002 | c0003 | t0001 | g0016 | AFR | GWD | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | GWD | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0008 | SAS | PJL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02735 | hp2 | a0002 | c0003 | t0002 | g0002 | SAS | PJL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0179 | AFR | GWD | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0186 | AFR | GWD | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02818 | hp1 | a0002 | c0003 | t0001 | g0167 | AFR | GWD | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02886 | hp1 | a0002 | c0003 | t0002 | g0137 | AFR | GWD | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02922 | hp2 | a0001 | c0004 | t0002 | g0158 | AFR | ESN | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | ESN | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | ESN | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0047 | AFR | GWD | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03139 | hp1 | a0002 | c0003 | t0001 | g0016 | AFR | ESN | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0142 | AFR | ESN | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0143 | AFR | MSL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03453 | hp1 | a0002 | c0003 | t0001 | g0016 | AFR | MSL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03516 | hp2 | a0002 | c0003 | t0001 | g0168 | AFR | ESN | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03540 | hp2 | a0002 | c0003 | t0001 | g0169 | AFR | GWD | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | MSL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0040 | SAS | STU | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0214 | SAS | STU | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0147 | SAS | PJL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03831 | hp2 | a0002 | c0003 | t0002 | g0118 | SAS | BEB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0188 | SAS | BEB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | BEB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | BEB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | BEB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0201 | SAS | BEB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | STU | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0206 | SAS | STU | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0175 | SAS | STU | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | STU | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | STU | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | YRI | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18747 | hp1 | a0002 | c0003 | t0002 | g0140 | EAS | CHB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18941 | hp1 | a0002 | c0003 | t0006 | g0136 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18944 | hp1 | a0002 | c0003 | t0002 | g0015 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18950 | hp1 | a0002 | c0003 | t0002 | g0154 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18954 | hp1 | a0002 | c0003 | t0002 | g0002 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18963 | hp2 | a0002 | c0003 | t0002 | g0015 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18964 | hp1 | a0002 | c0003 | t0002 | g0002 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18971 | hp2 | a0002 | c0003 | t0002 | g0041 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18986 | hp2 | a0002 | c0003 | t0002 | g0150 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18987 | hp1 | a0002 | c0003 | t0002 | g0223 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18990 | hp2 | a0005 | c0007 | t0001 | g0244 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18993 | hp2 | a0002 | c0003 | t0002 | g0133 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19000 | hp2 | a0002 | c0003 | t0002 | g0111 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19002 | hp2 | a0002 | c0003 | t0002 | g0130 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19004 | hp1 | a0002 | c0003 | t0002 | g0015 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19009 | hp1 | a0002 | c0003 | t0002 | g0035 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | LWK | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | LWK | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | LWK | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | LWK | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19055 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19057 | hp2 | a0002 | c0003 | t0002 | g0002 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19063 | hp2 | a0003 | c0005 | t0001 | g0190 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19065 | hp1 | a0002 | c0003 | t0002 | g0002 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19066 | hp2 | a0002 | c0003 | t0002 | g0002 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19076 | hp1 | a0001 | c0001 | t0005 | g0090 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19078 | hp2 | a0002 | c0003 | t0002 | g0224 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19079 | hp1 | a0002 | c0003 | t0002 | g0129 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19080 | hp1 | a0002 | c0003 | t0002 | g0002 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19082 | hp1 | a0002 | c0003 | t0002 | g0002 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19086 | hp2 | a0002 | c0003 | t0002 | g0126 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | ASW | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0226 | AFR | ASW | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | TSI | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0010 | EUR | TSI | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | CLM | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | ACB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | ACB | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03471 | hp1 | a0001 | c0004 | t0002 | g0157 | AFR | MSL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | MSL | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | USA | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0200 | AFR | USA | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA18955 | hp2 | a0002 | c0003 | t0002 | g0002 | EAS | JPT | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | USA | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | USA | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | LWK | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | LWK | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0008 | REF | REF | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0012 | REF | REF | ERLEC1_chr2_53782044_53823796 | ERLEC1 | chr2 | 53782044 | 53823796 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:53795996 | A | G | 1 | a0003 | 3 | HG00621.hp1 HG02523.hp2 NA19063.hp2 |
missense_variant | MODERATE | c.331A>G | p.Ser111Gly | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 3/14 | 498/2446 | 331/1452 | 111/483 | chr2 | 53795996 | |||
| chr2:53808371 | G | C | 1 | a0002 | 53 | HG00408.hp2 HG00621.hp2 HG01070.hp2 others(50): Show |
missense_variant | MODERATE | c.952G>C | p.Val318Leu | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 9/14 | 1119/2446 | 952/1452 | 318/483 | chr2 | 53808371 | |||
| chr2:53808401 | A | C | 1 | a0005 | 1 | NA18990.hp2 | missense_variant | MODERATE | c.982A>C | p.Lys328Gln | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 9/14 | 1149/2446 | 982/1452 | 328/483 | chr2 | 53808401 | |||
| chr2:53814879 | C | T | 1 | a0004 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.1324C>T | p.Pro442Ser | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/14 | 1491/2446 | 1324/1452 | 442/483 | chr2 | 53814879 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:53808310 | A | G | 2 | a0001c0002 a0003c0005 |
59 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(56): Show |
synonymous_variant | LOW | c.891A>G | p.Gln297Gln | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 9/14 | 1058/2446 | 891/1452 | 297/483 | chr2 | 53808310 | |||
| chr2:53809234 | T | C | 1 | a0001c0004 | 3 | HG02572.hp2 HG02922.hp2 HG03471.hp1 |
synonymous_variant | LOW | c.1062T>C | p.Tyr354Tyr | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/14 | 1229/2446 | 1062/1452 | 354/483 | chr2 | 53809234 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:53787114 | A | G | 1 | a0001c0001t0004 | 2 | HG02145.hp2 NA20129.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-97A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/14 | chr2 | 53787114 | |||||||
| chr2:53787135 | C | T | 1 | a0002c0003t0007 | 1 | HG01074.hp2 | 5_prime_UTR_variant | MODIFIER | c.-76C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/14 | 76 | chr2 | 53787135 | ||||||
| chr2:53787166 | A | G | 6 | a0001c0001t0002 a0001c0001t0004 a0001c0004t0002 others(3): Show |
85 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(82): Show |
5_prime_UTR_variant | MODIFIER | c.-45A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/14 | 45 | chr2 | 53787166 | ||||||
| chr2:53818298 | A | G | 1 | a0001c0001t0003 | 7 | HG02056.hp1 NA18971.hp1 NA18978.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*329A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 14/14 | 329 | chr2 | 53818298 | ||||||
| chr2:53818499 | T | A | 1 | a0001c0001t0005 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*530T>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 14/14 | 530 | chr2 | 53818499 | ||||||
| chr2:53818510 | A | G | 1 | a0002c0003t0006 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*541A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 14/14 | 541 | chr2 | 53818510 | ||||||
| chr2:53818595 | T | A | 1 | a0001c0001t0005 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*626T>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 14/14 | 626 | chr2 | 53818595 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:53787396 | A | C | 3 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 |
3 | HG00597.hp1 NA18939.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.162+24A>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53787396 | |||||||
| chr2:53787421 | G | T | 45 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0042 others(42): Show |
59 | HG00280.hp2 HG00323.hp2 HG01255.hp2 others(56): Show |
intron_variant | MODIFIER | c.162+49G>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53787421 | |||||||
| chr2:53787443 | T | C | 1 | a0002c0003t0002g0019 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.162+71T>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53787443 | |||||||
| chr2:53787533 | G | T | 2 | a0001c0001t0004g0226 a0001c0001t0004g0227 |
2 | HG02145.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.162+161G>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53787533 | |||||||
| chr2:53787797 | C | T | 1 | a0001c0001t0002g0225 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.162+425C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53787797 | |||||||
| chr2:53787863 | A | G | 3 | a0002c0003t0002g0041 a0002c0003t0002g0223 a0002c0003t0002g0224 |
4 | HG02080.hp2 NA18971.hp2 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+491A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53787863 | |||||||
| chr2:53788039 | G | A | 2 | a0001c0002t0001g0020 a0001c0002t0001g0047 |
3 | HG03041.hp1 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.162+667G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53788039 | |||||||
| chr2:53788075 | C | T | 1 | a0002c0003t0002g0222 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.162+703C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53788075 | |||||||
| chr2:53788266 | C | T | 181 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(178): Show |
236 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.162+894C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53788266 | |||||||
| chr2:53788391 | T | G | 62 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0034 others(59): Show |
85 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.162+1019T>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53788391 | |||||||
| chr2:53788725 | G | A | 2 | a0001c0001t0004g0226 a0001c0001t0004g0227 |
2 | HG02145.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.162+1353G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53788725 | |||||||
| chr2:53788804 | A | G | 3 | a0001c0004t0002g0156 a0001c0004t0002g0157 a0001c0004t0002g0158 |
3 | HG02572.hp2 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.162+1432A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53788804 | |||||||
| chr2:53788839 | A | C | 176 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(173): Show |
230 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.162+1467A>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53788839 | |||||||
| chr2:53788840 | C | T | 176 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(173): Show |
230 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.162+1468C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53788840 | |||||||
| chr2:53788870 | A | G | 1 | a0001c0001t0002g0155 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.162+1498A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53788870 | |||||||
| chr2:53788911 | T | A | 1 | a0001c0001t0001g0228 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.162+1539T>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53788911 | |||||||
| chr2:53788990 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.162+1618G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53788990 | |||||||
| chr2:53788991 | C | T | 1 | a0002c0003t0002g0154 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.162+1619C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53788991 | |||||||
| chr2:53789077 | C | A | 5 | a0002c0003t0001g0016 a0002c0003t0001g0167 a0002c0003t0001g0168 others(2): Show |
7 | HG01074.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.162+1705C>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53789077 | |||||||
| chr2:53789205 | C | A | 1 | a0001c0001t0001g0099 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.162+1833C>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53789205 | |||||||
| chr2:53789319 | G | A | 3 | a0002c0003t0002g0002 a0002c0003t0002g0130 a0002c0003t0002g0150 |
4 | NA18955.hp2 NA18986.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+1947G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53789319 | |||||||
| chr2:53789393 | C | CA | 18 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(15): Show |
21 | HG00423.hp1 HG01243.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.162+2044dupA | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 53789393 | ||||||
| chr2:53789393 | CA | C | 94 | a0001c0001t0001g0038 a0001c0001t0001g0104 a0001c0001t0001g0105 others(91): Show |
123 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.162+2044delA | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 53789393 | ||||||
| chr2:53789393 | CAA | C | 6 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0001c0001t0002g0153 others(3): Show |
6 | HG00738.hp1 HG01884.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+2043_162+2044d others(4): Show |
ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 53789393 | ||||||
| chr2:53789417 | T | A | 1 | a0001c0001t0001g0230 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.162+2045T>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53789417 | |||||||
| chr2:53789419 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.162+2047C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53789419 | |||||||
| chr2:53789420 | T | C | 1 | a0001c0001t0001g0230 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.162+2048T>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53789420 | |||||||
| chr2:53789625 | C | G | 1 | a0001c0001t0002g0149 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.162+2253C>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53789625 | |||||||
| chr2:53789632 | C | T | 2 | a0001c0002t0001g0220 a0001c0002t0001g0221 |
2 | HG01175.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.162+2260C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53789632 | |||||||
| chr2:53789697 | A | G | 7 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0100 others(4): Show |
9 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.162+2325A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53789697 | |||||||
| chr2:53789880 | A | G | 51 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0042 others(48): Show |
65 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.162+2508A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53789880 | |||||||
| chr2:53789967 | C | T | 1 | a0001c0001t0002g0147 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.162+2595C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53789967 | |||||||
| chr2:53790015 | C | CA | 59 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0024 others(56): Show |
76 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.162+2659dupA | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 53790015 | ||||||
| chr2:53790225 | C | G | 48 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0042 others(45): Show |
62 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.162+2853C>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53790225 | |||||||
| chr2:53790260 | AT | A | 175 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(172): Show |
229 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.162+2897delT | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 53790260 | ||||||
| chr2:53790400 | G | A | 2 | a0001c0001t0002g0115 a0001c0001t0002g0116 |
2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.162+3028G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53790400 | |||||||
| chr2:53790776 | A | C | 1 | a0001c0002t0001g0188 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.162+3404A>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53790776 | |||||||
| chr2:53790948 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.163-3397A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53790948 | |||||||
| chr2:53790999 | A | G | 2 | a0001c0001t0001g0057 a0001c0001t0001g0097 |
2 | NA18981.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.163-3346A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53790999 | |||||||
| chr2:53791164 | G | A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.163-3181G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53791164 | |||||||
| chr2:53791206 | G | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0187 |
4 | HG02818.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-3139G>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53791206 | |||||||
| chr2:53791523 | T | G | 10 | a0001c0001t0001g0038 a0001c0001t0001g0110 a0001c0001t0001g0171 others(7): Show |
11 | HG00408.hp1 HG01069.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.163-2822T>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53791523 | |||||||
| chr2:53791695 | C | G | 60 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0034 others(57): Show |
83 | HG00408.hp2 HG00621.hp2 HG00738.hp1 others(80): Show |
intron_variant | MODIFIER | c.163-2650C>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53791695 | |||||||
| chr2:53791777 | T | C | 3 | a0001c0004t0002g0156 a0001c0004t0002g0157 a0001c0004t0002g0158 |
3 | HG02572.hp2 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.163-2568T>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53791777 | |||||||
| chr2:53791778 | G | A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0187 others(1): Show |
7 | HG02258.hp2 HG02818.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-2567G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53791778 | |||||||
| chr2:53791787 | C | T | 170 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(167): Show |
222 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.163-2558C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53791787 | |||||||
| chr2:53791789 | T | C | 1 | a0002c0003t0002g0117 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.163-2556T>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53791789 | |||||||
| chr2:53791906 | T | A | 1 | a0001c0001t0001g0017 | 3 | HG02818.hp2 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.163-2439T>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53791906 | |||||||
| chr2:53791906 | T | TA | 16 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0027 others(13): Show |
19 | HG00423.hp1 HG00597.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.163-2414dupA | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 53791906 | ||||||
| chr2:53791906 | TA | T | 83 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0042 others(80): Show |
117 | HG00408.hp2 HG00423.hp2 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.163-2414delA | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 53791906 | ||||||
| chr2:53791906 | TAA | T | 28 | a0001c0001t0001g0037 a0001c0001t0001g0045 a0001c0001t0001g0046 others(25): Show |
35 | HG00280.hp2 HG00323.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.163-2415_163-2414d others(4): Show |
ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 53791906 | ||||||
| chr2:53791906 | TAAA | T | 38 | a0001c0001t0001g0194 a0001c0001t0001g0230 a0001c0002t0001g0005 others(35): Show |
48 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.163-2416_163-2414d others(5): Show |
ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 53791906 | ||||||
| chr2:53791906 | TAAAAAAA | T | 9 | a0001c0001t0001g0038 a0001c0001t0001g0171 a0001c0001t0001g0192 others(6): Show |
10 | HG01081.hp1 HG01515.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.163-2420_163-2414d others(9): Show |
ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 53791906 | ||||||
| chr2:53791907 | A | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0050 a0001c0001t0001g0057 others(2): Show |
6 | NA18959.hp1 NA18978.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-2438A>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53791907 | |||||||
| chr2:53791908 | A | T | 1 | a0001c0001t0001g0096 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.163-2437A>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53791908 | |||||||
| chr2:53791983 | C | G | 41 | a0001c0001t0002g0010 a0001c0001t0002g0034 a0001c0001t0002g0112 others(38): Show |
61 | HG00408.hp2 HG00621.hp2 HG01070.hp2 others(58): Show |
intron_variant | MODIFIER | c.163-2362C>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53791983 | |||||||
| chr2:53791993 | G | T | 5 | a0001c0001t0001g0036 a0001c0001t0001g0159 a0001c0001t0001g0164 others(2): Show |
6 | HG01255.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-2352G>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53791993 | |||||||
| chr2:53792035 | C | T | 1 | a0002c0003t0007g0170 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.163-2310C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53792035 | |||||||
| chr2:53792050 | T | G | 4 | a0001c0001t0001g0032 a0001c0001t0001g0100 a0001c0001t0001g0101 others(1): Show |
5 | HG01109.hp2 HG01884.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.163-2295T>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53792050 | |||||||
| chr2:53792090 | A | C | 1 | a0001c0002t0001g0217 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.163-2255A>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53792090 | |||||||
| chr2:53792154 | T | A | 2 | a0002c0003t0002g0124 a0002c0003t0002g0125 |
2 | HG00621.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.163-2191T>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53792154 | |||||||
| chr2:53792165 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.163-2180T>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53792165 | |||||||
| chr2:53792193 | C | T | 5 | a0002c0003t0001g0016 a0002c0003t0001g0167 a0002c0003t0001g0168 others(2): Show |
7 | HG01074.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-2152C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53792193 | |||||||
| chr2:53792216 | CT | C | 59 | a0001c0001t0001g0050 a0001c0001t0001g0104 a0001c0001t0001g0234 others(56): Show |
81 | HG00408.hp2 HG00438.hp1 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.163-2112delT | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 53792216 | ||||||
| chr2:53792520 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.163-1825T>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53792520 | |||||||
| chr2:53792637 | G | GT | 4 | a0001c0001t0001g0037 a0001c0001t0001g0199 a0001c0001t0001g0218 others(1): Show |
5 | HG02258.hp2 HG02970.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-1700dupT | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 53792637 | ||||||
| chr2:53792850 | C | T | 42 | a0001c0001t0002g0010 a0001c0001t0002g0034 a0001c0001t0002g0112 others(39): Show |
62 | HG00408.hp2 HG00621.hp2 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.163-1495C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53792850 | |||||||
| chr2:53793005 | C | CA | 64 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0070 others(61): Show |
77 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.163-1325dupA | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 53793005 | ||||||
| chr2:53793114 | C | T | 1 | a0002c0003t0002g0140 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.163-1231C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53793114 | |||||||
| chr2:53793449 | T | G | 1 | a0001c0001t0001g0241 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.163-896T>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53793449 | |||||||
| chr2:53793604 | CT | C | 47 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0042 others(44): Show |
61 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.163-734delT | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 53793604 | ||||||
| chr2:53793952 | G | A | 1 | a0001c0001t0002g0127 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.163-393G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53793952 | |||||||
| chr2:53793956 | G | A | 5 | a0001c0001t0002g0010 a0001c0001t0002g0034 a0001c0001t0002g0147 others(2): Show |
9 | HG01099.hp1 HG01106.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.163-389G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53793956 | |||||||
| chr2:53793994 | A | G | 1 | a0001c0001t0001g0257 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.163-351A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53793994 | |||||||
| chr2:53794088 | C | G | 61 | a0001c0001t0001g0038 a0001c0001t0001g0110 a0001c0001t0001g0171 others(58): Show |
73 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.163-257C>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53794088 | |||||||
| chr2:53794324 | T | TAC | 4 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0187 others(1): Show |
7 | HG02258.hp2 HG02818.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-21_163-20insAC | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 1/13 | chr2 | 53794324 | |||||||
| chr2:53794542 | G | C | 2 | a0002c0003t0002g0019 a0002c0003t0002g0118 |
3 | HG01515.hp2 HG01517.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.267+93G>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 2/13 | chr2 | 53794542 | |||||||
| chr2:53794694 | C | T | 3 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0230 |
5 | HG00280.hp2 HG00323.hp2 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.267+245C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 2/13 | chr2 | 53794694 | |||||||
| chr2:53794732 | G | A | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.267+283G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 2/13 | chr2 | 53794732 | |||||||
| chr2:53794777 | C | T | 1 | a0001c0002t0001g0175 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.267+328C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 2/13 | chr2 | 53794777 | |||||||
| chr2:53794802 | A | C | 5 | a0002c0003t0001g0016 a0002c0003t0001g0167 a0002c0003t0001g0168 others(2): Show |
7 | HG01074.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.267+353A>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 2/13 | chr2 | 53794802 | |||||||
| chr2:53794945 | G | A | 1 | a0004c0006t0002g0148 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.267+496G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 2/13 | chr2 | 53794945 | |||||||
| chr2:53795033 | TA | T | 179 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0017 others(176): Show |
235 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.267+586delA | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 53795033 | ||||||
| chr2:53795110 | C | T | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.267+661C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 2/13 | chr2 | 53795110 | |||||||
| chr2:53795131 | C | G | 60 | a0001c0001t0001g0038 a0001c0001t0001g0171 a0001c0001t0001g0192 others(57): Show |
72 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.267+682C>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 2/13 | chr2 | 53795131 | |||||||
| chr2:53795239 | G | A | 42 | a0001c0001t0002g0010 a0001c0001t0002g0034 a0001c0001t0002g0112 others(39): Show |
62 | HG00408.hp2 HG00621.hp2 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.268-694G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 2/13 | chr2 | 53795239 | |||||||
| chr2:53795375 | A | G | 1 | a0001c0001t0002g0149 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.268-558A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 2/13 | chr2 | 53795375 | |||||||
| chr2:53795445 | G | GAC | 2 | a0001c0001t0001g0037 a0001c0001t0001g0199 |
3 | HG02258.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.268-475_268-474dup others(2): Show |
ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 53795445 | ||||||
| chr2:53795460 | G | A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0187 others(1): Show |
7 | HG02258.hp2 HG02818.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.268-473G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 2/13 | chr2 | 53795460 | |||||||
| chr2:53795494 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.268-439A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 2/13 | chr2 | 53795494 | |||||||
| chr2:53795509 | G | T | 1 | a0001c0001t0001g0092 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.268-424G>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 2/13 | chr2 | 53795509 | |||||||
| chr2:53795561 | T | A | 2 | a0001c0001t0002g0128 a0004c0006t0002g0148 |
2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.268-372T>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 2/13 | chr2 | 53795561 | |||||||
| chr2:53795695 | T | A | 58 | a0001c0001t0001g0038 a0001c0001t0001g0110 a0001c0001t0001g0171 others(55): Show |
70 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.268-238T>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 2/13 | chr2 | 53795695 | |||||||
| chr2:53795832 | T | G | 1 | a0001c0001t0001g0071 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.268-101T>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 2/13 | chr2 | 53795832 | |||||||
| chr2:53795847 | A | T | 1 | a0002c0003t0007g0170 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.268-86A>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 2/13 | chr2 | 53795847 | |||||||
| chr2:53796024 | T | C | 8 | a0001c0001t0002g0011 a0001c0001t0002g0121 a0001c0001t0002g0142 others(5): Show |
11 | HG02559.hp1 HG02572.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.348+11T>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 3/13 | chr2 | 53796024 | |||||||
| chr2:53796088 | C | T | 2 | a0001c0002t0001g0207 a0001c0002t0001g0208 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.348+75C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 3/13 | chr2 | 53796088 | |||||||
| chr2:53796110 | GT | G | 173 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0017 others(170): Show |
227 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.348+108delT | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 53796110 | ||||||
| chr2:53796185 | C | T | 57 | a0001c0001t0001g0038 a0001c0001t0001g0171 a0001c0001t0001g0192 others(54): Show |
69 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.348+172C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 3/13 | chr2 | 53796185 | |||||||
| chr2:53796246 | G | GT | 6 | a0001c0001t0001g0049 a0001c0001t0001g0061 a0001c0001t0001g0068 others(3): Show |
6 | HG00733.hp2 HG01358.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.348+250dupT | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 53796246 | ||||||
| chr2:53796246 | GT | G | 168 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0018 others(165): Show |
223 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.348+250delT | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 53796246 | ||||||
| chr2:53796273 | C | A | 1 | a0001c0004t0002g0157 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.348+260C>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 3/13 | chr2 | 53796273 | |||||||
| chr2:53796301 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.348+288A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 3/13 | chr2 | 53796301 | |||||||
| chr2:53796529 | G | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0031 others(1): Show |
12 | HG00438.hp2 HG02027.hp1 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.348+516G>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 3/13 | chr2 | 53796529 | |||||||
| chr2:53796629 | A | T | 4 | a0001c0001t0001g0036 a0001c0001t0001g0159 a0001c0001t0001g0165 others(1): Show |
5 | HG01255.hp1 HG03041.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.348+616A>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 3/13 | chr2 | 53796629 | |||||||
| chr2:53796697 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0104 |
3 | NA19004.hp2 NA19009.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.348+684G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 3/13 | chr2 | 53796697 | |||||||
| chr2:53796774 | T | G | 1 | a0002c0003t0002g0129 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.349-741T>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 3/13 | chr2 | 53796774 | |||||||
| chr2:53796788 | G | C | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.349-727G>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 3/13 | chr2 | 53796788 | |||||||
| chr2:53796889 | C | CT | 80 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0036 others(77): Show |
100 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.349-606dupT | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 53796889 | ||||||
| chr2:53796889 | CT | C | 6 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0074 others(3): Show |
6 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-606delT | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 53796889 | ||||||
| chr2:53796894 | T | C | 2 | a0001c0001t0001g0017 a0001c0001t0001g0187 |
4 | HG02818.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.349-621T>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 3/13 | chr2 | 53796894 | |||||||
| chr2:53797028 | G | A | 179 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0017 others(176): Show |
235 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.349-487G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 3/13 | chr2 | 53797028 | |||||||
| chr2:53797054 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.349-461G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 3/13 | chr2 | 53797054 | |||||||
| chr2:53797158 | G | A | 49 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0042 others(46): Show |
63 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.349-357G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 3/13 | chr2 | 53797158 | |||||||
| chr2:53797190 | C | A | 1 | a0001c0001t0001g0044 | 2 | HG02155.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.349-325C>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 3/13 | chr2 | 53797190 | |||||||
| chr2:53797190 | C | G | 179 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0017 others(176): Show |
234 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.349-325C>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 3/13 | chr2 | 53797190 | |||||||
| chr2:53797427 | G | C | 3 | a0001c0002t0001g0107 a0001c0002t0001g0108 a0001c0002t0001g0109 |
3 | NA19055.hp1 NA19070.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.349-88G>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 3/13 | chr2 | 53797427 | |||||||
| chr2:53797489 | C | T | 144 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0017 others(141): Show |
182 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.349-26C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 3/13 | chr2 | 53797489 | |||||||
| chr2:53797820 | C | G | 36 | a0001c0001t0001g0194 a0001c0002t0001g0005 a0001c0002t0001g0020 others(33): Show |
44 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.490+25C>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 5/13 | chr2 | 53797820 | |||||||
| chr2:53797872 | A | AT | 35 | a0001c0001t0001g0062 a0001c0001t0002g0112 a0001c0001t0004g0226 others(32): Show |
51 | HG00408.hp2 HG00621.hp2 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.490+87dupT | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 53797872 | ||||||
| chr2:53797913 | T | C | 1 | a0002c0003t0002g0130 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.490+118T>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 5/13 | chr2 | 53797913 | |||||||
| chr2:53797936 | C | T | 1 | a0001c0001t0002g0123 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.490+141C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 5/13 | chr2 | 53797936 | |||||||
| chr2:53798023 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0187 |
4 | HG02818.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.490+228C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 5/13 | chr2 | 53798023 | |||||||
| chr2:53798055 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.490+260C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 5/13 | chr2 | 53798055 | |||||||
| chr2:53798064 | A | G | 183 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0017 others(180): Show |
239 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.490+269A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 5/13 | chr2 | 53798064 | |||||||
| chr2:53798067 | C | T | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.490+272C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 5/13 | chr2 | 53798067 | |||||||
| chr2:53798121 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0199 |
3 | HG02258.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.490+326G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 5/13 | chr2 | 53798121 | |||||||
| chr2:53798126 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.490+331C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 5/13 | chr2 | 53798126 | |||||||
| chr2:53798152 | A | G | 182 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0017 others(179): Show |
238 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.490+357A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 5/13 | chr2 | 53798152 | |||||||
| chr2:53798177 | A | C | 1 | a0001c0001t0001g0193 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.490+382A>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 5/13 | chr2 | 53798177 | |||||||
| chr2:53798478 | C | G | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.491-569C>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 5/13 | chr2 | 53798478 | |||||||
| chr2:53798570 | A | C | 5 | a0001c0001t0001g0036 a0001c0001t0001g0159 a0001c0001t0001g0164 others(2): Show |
6 | HG01255.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.491-477A>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 5/13 | chr2 | 53798570 | |||||||
| chr2:53799232 | T | C | 1 | a0001c0001t0001g0260 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.525+151T>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 6/13 | chr2 | 53799232 | |||||||
| chr2:53799260 | T | C | 6 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0100 others(3): Show |
8 | HG01109.hp2 HG01884.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.525+179T>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 6/13 | chr2 | 53799260 | |||||||
| chr2:53799430 | G | A | 3 | a0001c0002t0001g0020 a0001c0002t0001g0047 a0001c0002t0001g0179 |
4 | HG02809.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+349G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 6/13 | chr2 | 53799430 | |||||||
| chr2:53799733 | A | G | 1 | a0002c0003t0002g0137 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.525+652A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 6/13 | chr2 | 53799733 | |||||||
| chr2:53799933 | A | C | 1 | a0001c0001t0001g0250 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.525+852A>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 6/13 | chr2 | 53799933 | |||||||
| chr2:53800175 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.525+1094A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 6/13 | chr2 | 53800175 | |||||||
| chr2:53800511 | A | G | 3 | a0001c0004t0002g0156 a0001c0004t0002g0157 a0001c0004t0002g0158 |
3 | HG02572.hp2 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.526-886A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 6/13 | chr2 | 53800511 | |||||||
| chr2:53800600 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.526-797A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 6/13 | chr2 | 53800600 | |||||||
| chr2:53800648 | T | C | 1 | a0001c0002t0001g0177 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.526-749T>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 6/13 | chr2 | 53800648 | |||||||
| chr2:53800650 | A | C | 1 | a0001c0002t0001g0177 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.526-747A>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 6/13 | chr2 | 53800650 | |||||||
| chr2:53800651 | C | T | 1 | a0001c0002t0001g0177 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.526-746C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 6/13 | chr2 | 53800651 | |||||||
| chr2:53800655 | G | C | 1 | a0001c0002t0001g0177 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.526-742G>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 6/13 | chr2 | 53800655 | |||||||
| chr2:53800656 | C | G | 1 | a0001c0002t0001g0177 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.526-741C>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 6/13 | chr2 | 53800656 | |||||||
| chr2:53800658 | T | G | 1 | a0001c0002t0001g0177 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.526-739T>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 6/13 | chr2 | 53800658 | |||||||
| chr2:53800660 | T | G | 1 | a0001c0002t0001g0177 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.526-737T>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 6/13 | chr2 | 53800660 | |||||||
| chr2:53800661 | T | G | 1 | a0001c0002t0001g0177 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.526-736T>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 6/13 | chr2 | 53800661 | |||||||
| chr2:53800663 | A | T | 1 | a0001c0002t0001g0177 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.526-734A>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 6/13 | chr2 | 53800663 | |||||||
| chr2:53800708 | G | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0017 others(128): Show |
165 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.526-689G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 6/13 | chr2 | 53800708 | |||||||
| chr2:53800790 | C | G | 1 | a0001c0001t0001g0263 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.526-607C>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 6/13 | chr2 | 53800790 | |||||||
| chr2:53800820 | G | A | 2 | a0001c0002t0001g0180 a0001c0002t0001g0181 |
2 | NA18970.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.526-577G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 6/13 | chr2 | 53800820 | |||||||
| chr2:53800860 | C | T | 6 | a0001c0001t0001g0007 a0001c0001t0001g0055 a0001c0001t0001g0088 others(3): Show |
10 | HG00733.hp2 HG00741.hp1 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.526-537C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 6/13 | chr2 | 53800860 | |||||||
| chr2:53801237 | A | G | 1 | a0001c0001t0002g0143 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.526-160A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 6/13 | chr2 | 53801237 | |||||||
| chr2:53801286 | T | A | 3 | a0001c0001t0001g0021 a0001c0001t0001g0029 a0001c0001t0001g0077 |
5 | HG00423.hp1 NA18612.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-111T>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 6/13 | chr2 | 53801286 | |||||||
| chr2:53801352 | C | T | 1 | a0003c0005t0001g0191 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.526-45C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 6/13 | chr2 | 53801352 | |||||||
| chr2:53801945 | A | G | 1 | a0002c0003t0002g0126 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.879+103A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53801945 | |||||||
| chr2:53802072 | G | C | 4 | a0001c0001t0002g0011 a0001c0001t0002g0121 a0001c0001t0002g0142 others(1): Show |
7 | HG02559.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.879+230G>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53802072 | |||||||
| chr2:53802260 | G | A | 47 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0042 others(44): Show |
61 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.879+418G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53802260 | |||||||
| chr2:53802283 | T | C | 1 | a0001c0001t0002g0147 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.879+441T>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53802283 | |||||||
| chr2:53802290 | C | T | 58 | a0001c0001t0001g0038 a0001c0001t0001g0171 a0001c0001t0001g0192 others(55): Show |
70 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.879+448C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53802290 | |||||||
| chr2:53802397 | C | G | 47 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0042 others(44): Show |
61 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.879+555C>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53802397 | |||||||
| chr2:53802707 | C | G | 1 | a0001c0001t0001g0249 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.879+865C>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53802707 | |||||||
| chr2:53802716 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.879+874A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53802716 | |||||||
| chr2:53802803 | C | T | 2 | a0001c0001t0001g0229 a0001c0001t0001g0248 |
2 | NA19011.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.879+961C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53802803 | |||||||
| chr2:53802904 | A | G | 4 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0187 others(1): Show |
7 | HG02258.hp2 HG02818.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.879+1062A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53802904 | |||||||
| chr2:53803033 | T | G | 33 | a0001c0001t0001g0014 a0001c0001t0001g0056 a0001c0001t0001g0093 others(30): Show |
42 | HG00738.hp1 HG01099.hp1 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.879+1191T>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53803033 | |||||||
| chr2:53803073 | G | A | 2 | a0001c0001t0002g0115 a0001c0001t0002g0116 |
2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.879+1231G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53803073 | |||||||
| chr2:53803338 | ATTCTC | A | 16 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0027 others(13): Show |
29 | HG00438.hp2 HG00558.hp2 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.879+1501_879+1505d others(7): Show |
ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 53803338 | ||||||
| chr2:53803381 | A | G | 54 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(51): Show |
71 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.879+1539A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53803381 | |||||||
| chr2:53803596 | CA | C | 128 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0017 others(125): Show |
162 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.879+1771delA | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 53803596 | ||||||
| chr2:53803598 | A | C | 1 | a0001c0002t0001g0206 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.879+1756A>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53803598 | |||||||
| chr2:53803627 | A | G | 1 | a0001c0001t0001g0032 | 2 | HG01109.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.879+1785A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53803627 | |||||||
| chr2:53803725 | G | A | 54 | a0001c0001t0001g0038 a0001c0001t0001g0171 a0001c0001t0001g0192 others(51): Show |
66 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.879+1883G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53803725 | |||||||
| chr2:53803790 | A | G | 265 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(262): Show |
368 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(365): Show |
intron_variant | MODIFIER | c.879+1948A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53803790 | |||||||
| chr2:53803894 | C | T | 1 | a0001c0001t0002g0128 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.879+2052C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53803894 | |||||||
| chr2:53803918 | C | T | 3 | a0001c0002t0001g0178 a0001c0002t0001g0201 a0001c0002t0001g0210 |
3 | HG00733.hp1 HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.879+2076C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53803918 | |||||||
| chr2:53803929 | G | C | 1 | a0001c0002t0001g0210 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.879+2087G>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53803929 | |||||||
| chr2:53804175 | T | C | 10 | a0001c0001t0001g0014 a0001c0001t0001g0056 a0001c0001t0001g0093 others(7): Show |
12 | HG00738.hp1 HG01167.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.879+2333T>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53804175 | |||||||
| chr2:53804195 | G | A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0187 others(1): Show |
7 | HG02258.hp2 HG02818.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.879+2353G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53804195 | |||||||
| chr2:53804299 | C | T | 179 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0017 others(176): Show |
235 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.879+2457C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53804299 | |||||||
| chr2:53804331 | T | TGGCGCAA others(14): Show |
2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.879+2490_879+2510d others(23): Show |
ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 53804331 | ||||||
| chr2:53804345 | C | T | 4 | a0001c0001t0001g0243 a0001c0001t0001g0246 a0001c0001t0001g0247 others(1): Show |
4 | NA18941.hp2 NA18961.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.879+2503C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53804345 | |||||||
| chr2:53804417 | G | A | 3 | a0001c0004t0002g0156 a0001c0004t0002g0157 a0001c0004t0002g0158 |
3 | HG02572.hp2 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.879+2575G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53804417 | |||||||
| chr2:53804495 | C | T | 1 | a0001c0002t0001g0177 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.879+2653C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53804495 | |||||||
| chr2:53804710 | A | G | 50 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0042 others(47): Show |
64 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.879+2868A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53804710 | |||||||
| chr2:53804746 | G | A | 182 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0017 others(179): Show |
238 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.879+2904G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53804746 | |||||||
| chr2:53804784 | C | G | 1 | a0001c0002t0001g0174 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.879+2942C>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53804784 | |||||||
| chr2:53804818 | C | T | 2 | a0001c0001t0001g0078 a0001c0002t0001g0205 |
2 | HG04199.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.879+2976C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53804818 | |||||||
| chr2:53804900 | C | T | 1 | a0001c0002t0001g0214 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.879+3058C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53804900 | |||||||
| chr2:53804903 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.879+3061G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53804903 | |||||||
| chr2:53804989 | C | CT | 61 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0043 others(58): Show |
74 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.879+3170dupT | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 53804989 | ||||||
| chr2:53804989 | C | CTT | 7 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0197 others(4): Show |
8 | HG01069.hp2 HG01071.hp2 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.879+3169_879+3170d others(4): Show |
ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 53804989 | ||||||
| chr2:53804989 | CT | C | 16 | a0001c0001t0001g0013 a0001c0001t0001g0031 a0001c0001t0001g0059 others(13): Show |
23 | HG00323.hp1 HG00738.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.879+3170delT | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 53804989 | ||||||
| chr2:53805037 | C | G | 2 | a0001c0001t0002g0127 a0001c0001t0002g0146 |
2 | HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.879+3195C>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53805037 | |||||||
| chr2:53805075 | ACCTCCAA others(21): Show |
A | 1 | a0001c0001t0001g0196 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.880-3192_880-3165d others(30): Show |
ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 53805075 | ||||||
| chr2:53805231 | CA | C | 45 | a0001c0002t0001g0005 a0001c0002t0001g0008 a0001c0002t0001g0020 others(42): Show |
56 | HG00438.hp1 HG00558.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.880-3066delA | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 53805231 | ||||||
| chr2:53805243 | G | A | 1 | a0001c0001t0001g0017 | 3 | HG02818.hp2 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.880-3056G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53805243 | |||||||
| chr2:53805304 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.880-2995G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53805304 | |||||||
| chr2:53805503 | C | T | 3 | a0001c0002t0001g0176 a0001c0002t0001g0180 a0001c0002t0001g0181 |
3 | NA18970.hp1 NA18988.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.880-2796C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53805503 | |||||||
| chr2:53805628 | CAATAT | C | 4 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0187 others(1): Show |
7 | HG02258.hp2 HG02818.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.880-2669_880-2665d others(7): Show |
ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 53805628 | ||||||
| chr2:53805773 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.880-2526C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53805773 | |||||||
| chr2:53805796 | C | T | 5 | a0001c0001t0002g0011 a0001c0001t0002g0121 a0001c0001t0002g0142 others(2): Show |
8 | HG02559.hp1 HG02630.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.880-2503C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53805796 | |||||||
| chr2:53805848 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.880-2451G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53805848 | |||||||
| chr2:53806205 | A | C | 1 | a0002c0003t0006g0136 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.880-2094A>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53806205 | |||||||
| chr2:53806326 | A | G | 31 | a0001c0001t0001g0014 a0001c0001t0001g0056 a0001c0001t0001g0069 others(28): Show |
40 | HG00099.hp2 HG00738.hp1 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.880-1973A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53806326 | |||||||
| chr2:53806626 | G | A | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.880-1673G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53806626 | |||||||
| chr2:53806665 | C | T | 1 | a0004c0006t0002g0148 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.880-1634C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53806665 | |||||||
| chr2:53806851 | C | G | 146 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0017 others(143): Show |
184 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.880-1448C>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53806851 | |||||||
| chr2:53806973 | C | T | 1 | a0001c0001t0001g0038 | 2 | HG01081.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.880-1326C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53806973 | |||||||
| chr2:53806979 | T | C | 1 | a0001c0002t0001g0188 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.880-1320T>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53806979 | |||||||
| chr2:53807013 | C | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0050 a0001c0001t0001g0082 others(2): Show |
6 | NA18959.hp1 NA18969.hp2 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.880-1286C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53807013 | |||||||
| chr2:53807098 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0187 |
4 | HG02818.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.880-1201C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53807098 | |||||||
| chr2:53807114 | G | A | 36 | a0001c0001t0002g0112 a0002c0003t0001g0016 a0002c0003t0001g0167 others(33): Show |
54 | HG00408.hp2 HG00621.hp2 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.880-1185G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53807114 | |||||||
| chr2:53807262 | A | ATATC | 6 | a0001c0001t0001g0069 a0001c0001t0002g0010 a0001c0001t0002g0034 others(3): Show |
10 | HG00099.hp2 HG01099.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.880-1037_880-1036i others(6): Show |
ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53807262 | |||||||
| chr2:53807411 | C | CT | 195 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0014 others(192): Show |
256 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.880-880dupT | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 53807411 | ||||||
| chr2:53807431 | AGT | A | 34 | a0001c0001t0001g0014 a0001c0001t0001g0056 a0001c0001t0001g0069 others(31): Show |
43 | HG00099.hp2 HG00738.hp1 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.880-867_880-866del others(2): Show |
ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53807431 | |||||||
| chr2:53807465 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.880-834G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53807465 | |||||||
| chr2:53807627 | A | T | 1 | a0001c0001t0001g0086 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.880-672A>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53807627 | |||||||
| chr2:53807666 | A | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0199 |
3 | HG02258.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.880-633A>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53807666 | |||||||
| chr2:53807744 | G | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0017 others(83): Show |
112 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.880-555G>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53807744 | |||||||
| chr2:53807810 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.880-489C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53807810 | |||||||
| chr2:53807844 | A | AAAC | 27 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0056 others(24): Show |
35 | HG00099.hp2 HG00738.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.880-428_880-426dup others(3): Show |
ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 53807844 | ||||||
| chr2:53807844 | A | AAACAAC | 4 | a0001c0001t0002g0011 a0001c0001t0002g0121 a0001c0001t0002g0142 others(1): Show |
7 | HG02559.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.880-431_880-426dup others(6): Show |
ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 53807844 | ||||||
| chr2:53807844 | AAAC | A | 3 | a0001c0004t0002g0156 a0001c0004t0002g0157 a0001c0004t0002g0158 |
3 | HG02572.hp2 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.880-428_880-426del others(3): Show |
ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 53807844 | ||||||
| chr2:53807847 | C | A | 50 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0037 others(47): Show |
64 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.880-452C>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53807847 | |||||||
| chr2:53807871 | C | A | 1 | a0002c0003t0002g0041 | 2 | HG02080.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.880-428C>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53807871 | |||||||
| chr2:53807874 | A | C | 2 | a0002c0003t0002g0019 a0002c0003t0002g0118 |
3 | HG01515.hp2 HG01517.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.880-425A>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53807874 | |||||||
| chr2:53808114 | A | G | 36 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0056 others(33): Show |
46 | HG00099.hp2 HG00738.hp1 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.880-185A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53808114 | |||||||
| chr2:53808237 | A | G | 57 | a0001c0001t0001g0038 a0001c0001t0001g0110 a0001c0001t0001g0171 others(54): Show |
69 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.880-62A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53808237 | |||||||
| chr2:53808281 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0199 |
3 | HG02258.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.880-18G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 8/13 | chr2 | 53808281 | |||||||
| chr2:53808513 | G | A | 47 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0043 others(44): Show |
59 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.1041+53G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 9/13 | chr2 | 53808513 | |||||||
| chr2:53808525 | G | C | 1 | a0001c0001t0002g0116 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1041+65G>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 9/13 | chr2 | 53808525 | |||||||
| chr2:53808759 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1041+299T>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 9/13 | chr2 | 53808759 | |||||||
| chr2:53808854 | C | T | 2 | a0002c0003t0002g0135 a0002c0003t0002g0222 |
2 | HG01358.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1042-360C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 9/13 | chr2 | 53808854 | |||||||
| chr2:53809607 | G | A | 5 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0004t0002g0156 others(2): Show |
5 | HG02572.hp2 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1101+334G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | chr2 | 53809607 | |||||||
| chr2:53809682 | G | A | 44 | a0001c0001t0001g0038 a0001c0001t0001g0171 a0001c0001t0001g0192 others(41): Show |
53 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.1101+409G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | chr2 | 53809682 | |||||||
| chr2:53809736 | G | C | 35 | a0002c0003t0001g0016 a0002c0003t0001g0167 a0002c0003t0001g0168 others(32): Show |
53 | HG00408.hp2 HG00621.hp2 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.1101+463G>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | chr2 | 53809736 | |||||||
| chr2:53809798 | G | A | 47 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0043 others(44): Show |
59 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.1101+525G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | chr2 | 53809798 | |||||||
| chr2:53809870 | A | G | 4 | a0001c0001t0002g0011 a0001c0001t0002g0121 a0001c0001t0002g0142 others(1): Show |
7 | HG02559.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1101+597A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | chr2 | 53809870 | |||||||
| chr2:53809882 | C | G | 4 | a0002c0003t0002g0035 a0002c0003t0002g0124 a0002c0003t0002g0125 others(1): Show |
5 | HG00621.hp2 HG02080.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.1101+609C>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | chr2 | 53809882 | |||||||
| chr2:53809882 | C | T | 31 | a0002c0003t0001g0016 a0002c0003t0001g0167 a0002c0003t0001g0168 others(28): Show |
48 | HG00408.hp2 HG01070.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.1101+609C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | chr2 | 53809882 | |||||||
| chr2:53809918 | G | A | 3 | a0001c0001t0001g0063 a0001c0001t0001g0076 a0001c0001t0001g0079 |
3 | HG01081.hp2 HG01099.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1101+645G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | chr2 | 53809918 | |||||||
| chr2:53809928 | A | G | 6 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0100 others(3): Show |
8 | HG01109.hp2 HG01884.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1101+655A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | chr2 | 53809928 | |||||||
| chr2:53810008 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0187 |
4 | HG02818.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1101+735G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | chr2 | 53810008 | |||||||
| chr2:53810096 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1101+823G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | chr2 | 53810096 | |||||||
| chr2:53810113 | T | C | 1 | a0001c0001t0001g0258 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1101+840T>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | chr2 | 53810113 | |||||||
| chr2:53810148 | A | C | 32 | a0001c0001t0001g0014 a0001c0001t0001g0056 a0001c0001t0001g0069 others(29): Show |
41 | HG00099.hp2 HG00738.hp1 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.1101+875A>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | chr2 | 53810148 | |||||||
| chr2:53810229 | G | T | 1 | a0001c0001t0001g0247 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1101+956G>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | chr2 | 53810229 | |||||||
| chr2:53810591 | G | T | 3 | a0001c0004t0002g0156 a0001c0004t0002g0157 a0001c0004t0002g0158 |
3 | HG02572.hp2 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1101+1318G>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | chr2 | 53810591 | |||||||
| chr2:53810921 | CTTAA | C | 57 | a0001c0001t0001g0038 a0001c0001t0001g0171 a0001c0001t0001g0192 others(54): Show |
69 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.1101+1653_1101+165 others(8): Show |
ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 53810921 | ||||||
| chr2:53810975 | T | G | 1 | a0001c0001t0001g0218 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1101+1702T>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | chr2 | 53810975 | |||||||
| chr2:53811245 | TTTAAG | T | 4 | a0001c0001t0002g0011 a0001c0001t0002g0121 a0001c0001t0002g0142 others(1): Show |
7 | HG02559.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1102-1701_1102-169 others(9): Show |
ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 53811245 | ||||||
| chr2:53811494 | ACCTGGAA others(15): Show |
A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0199 |
3 | HG02258.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1102-1454_1102-143 others(26): Show |
ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | chr2 | 53811494 | |||||||
| chr2:53811621 | T | C | 5 | a0001c0001t0002g0011 a0001c0001t0002g0121 a0001c0001t0002g0142 others(2): Show |
8 | HG02559.hp1 HG02630.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1102-1328T>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | chr2 | 53811621 | |||||||
| chr2:53811633 | TAAG | T | 3 | a0001c0001t0002g0127 a0001c0001t0002g0139 a0001c0001t0002g0146 |
3 | HG02109.hp1 HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1102-1312_1102-131 others(7): Show |
ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 53811633 | ||||||
| chr2:53811825 | A | G | 51 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0042 others(48): Show |
65 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.1102-1124A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | chr2 | 53811825 | |||||||
| chr2:53811912 | G | T | 1 | a0001c0001t0002g0147 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1102-1037G>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | chr2 | 53811912 | |||||||
| chr2:53811974 | A | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0187 |
4 | HG02818.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1102-975A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | chr2 | 53811974 | |||||||
| chr2:53812074 | C | T | 1 | a0001c0001t0002g0145 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1102-875C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | chr2 | 53812074 | |||||||
| chr2:53812104 | T | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0199 |
3 | HG02258.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1102-845T>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | chr2 | 53812104 | |||||||
| chr2:53812107 | T | C | 59 | a0001c0001t0001g0038 a0001c0001t0001g0110 a0001c0001t0001g0171 others(56): Show |
71 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.1102-842T>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | chr2 | 53812107 | |||||||
| chr2:53812147 | C | T | 1 | a0001c0001t0002g0112 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1102-802C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | chr2 | 53812147 | |||||||
| chr2:53812428 | C | G | 79 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0018 others(76): Show |
102 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.1102-521C>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | chr2 | 53812428 | |||||||
| chr2:53812610 | G | A | 3 | a0002c0003t0002g0119 a0002c0003t0002g0131 a0002c0003t0002g0138 |
3 | HG01070.hp2 HG01109.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1102-339G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | chr2 | 53812610 | |||||||
| chr2:53812638 | A | G | 3 | a0001c0001t0002g0127 a0001c0001t0002g0139 a0001c0001t0002g0146 |
3 | HG02109.hp1 HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1102-311A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | chr2 | 53812638 | |||||||
| chr2:53812676 | C | T | 117 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0017 others(114): Show |
160 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1102-273C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | chr2 | 53812676 | |||||||
| chr2:53812876 | G | T | 1 | a0001c0001t0001g0066 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1102-73G>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | chr2 | 53812876 | |||||||
| chr2:53812946 | T | C | 2 | a0002c0003t0002g0223 a0002c0003t0002g0224 |
2 | NA18987.hp1 NA19078.hp2 |
splice_region_variant&intron_variant | LOW | c.1102-3T>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 10/13 | chr2 | 53812946 | |||||||
| chr2:53813111 | T | A | 2 | a0001c0001t0004g0226 a0001c0001t0004g0227 |
2 | HG02145.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1226+38T>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 11/13 | chr2 | 53813111 | |||||||
| chr2:53813174 | G | A | 1 | a0002c0003t0002g0132 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1226+101G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 11/13 | chr2 | 53813174 | |||||||
| chr2:53813267 | A | G | 84 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0017 others(81): Show |
109 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.1226+194A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 11/13 | chr2 | 53813267 | |||||||
| chr2:53813652 | A | C | 1 | a0001c0001t0001g0073 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1226+579A>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 11/13 | chr2 | 53813652 | |||||||
| chr2:53813950 | T | C | 2 | a0002c0003t0002g0019 a0002c0003t0002g0118 |
3 | HG01515.hp2 HG01517.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1227-593T>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 11/13 | chr2 | 53813950 | |||||||
| chr2:53814184 | C | T | 2 | a0002c0003t0002g0015 a0002c0003t0002g0154 |
4 | NA18944.hp1 NA18950.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.1227-359C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 11/13 | chr2 | 53814184 | |||||||
| chr2:53814221 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1227-322G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 11/13 | chr2 | 53814221 | |||||||
| chr2:53814333 | G | A | 3 | a0001c0004t0002g0156 a0001c0004t0002g0157 a0001c0004t0002g0158 |
3 | HG02572.hp2 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1227-210G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 11/13 | chr2 | 53814333 | |||||||
| chr2:53814383 | G | A | 1 | a0001c0002t0001g0212 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1227-160G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 11/13 | chr2 | 53814383 | |||||||
| chr2:53814846 | G | T | 146 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0017 others(143): Show |
184 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1305-14G>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 12/13 | chr2 | 53814846 | |||||||
| chr2:53814995 | C | CT | 51 | a0001c0001t0001g0027 a0001c0001t0001g0051 a0001c0001t0001g0061 others(48): Show |
68 | HG00408.hp2 HG00621.hp2 HG01070.hp2 others(65): Show |
intron_variant | MODIFIER | c.1380+81dupT | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 53814995 | ||||||
| chr2:53814995 | CT | C | 24 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0037 others(21): Show |
33 | HG00408.hp1 HG01069.hp1 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.1380+81delT | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 53814995 | ||||||
| chr2:53814995 | CTT | C | 44 | a0001c0002t0001g0005 a0001c0002t0001g0008 a0001c0002t0001g0020 others(41): Show |
55 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1380+80_1380+81del others(2): Show |
ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 53814995 | ||||||
| chr2:53814995 | CTTTTTTT others(3): Show |
C | 6 | a0001c0001t0001g0069 a0001c0001t0002g0010 a0001c0001t0002g0034 others(3): Show |
10 | HG00099.hp2 HG01099.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.1380+72_1380+81del others(10): Show |
ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 53814995 | ||||||
| chr2:53815009 | T | G | 10 | a0001c0001t0001g0014 a0001c0001t0001g0056 a0001c0001t0001g0093 others(7): Show |
12 | HG00738.hp1 HG01167.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1380+74T>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | chr2 | 53815009 | |||||||
| chr2:53815130 | C | T | 3 | a0001c0002t0001g0107 a0001c0002t0001g0108 a0001c0002t0001g0109 |
3 | NA19055.hp1 NA19070.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1380+195C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | chr2 | 53815130 | |||||||
| chr2:53815295 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0187 |
4 | HG02818.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1380+360C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | chr2 | 53815295 | |||||||
| chr2:53815302 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1380+367G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | chr2 | 53815302 | |||||||
| chr2:53815401 | T | C | 1 | a0001c0001t0001g0086 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1380+466T>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | chr2 | 53815401 | |||||||
| chr2:53815456 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0059 |
3 | HG00280.hp1 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1380+521G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | chr2 | 53815456 | |||||||
| chr2:53815525 | A | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0187 |
4 | HG02818.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1380+590A>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | chr2 | 53815525 | |||||||
| chr2:53815665 | G | C | 47 | a0001c0002t0001g0005 a0001c0002t0001g0008 a0001c0002t0001g0020 others(44): Show |
58 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1380+730G>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | chr2 | 53815665 | |||||||
| chr2:53815815 | A | C | 2 | a0001c0001t0001g0017 a0001c0001t0001g0187 |
4 | HG02818.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1380+880A>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | chr2 | 53815815 | |||||||
| chr2:53815870 | A | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0187 |
4 | HG02818.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1380+935A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | chr2 | 53815870 | |||||||
| chr2:53816114 | G | T | 5 | a0001c0002t0001g0172 a0001c0002t0001g0177 a0001c0002t0001g0202 others(2): Show |
5 | HG00438.hp1 HG02074.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.1380+1179G>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | chr2 | 53816114 | |||||||
| chr2:53816252 | T | G | 1 | a0001c0001t0002g0123 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1380+1317T>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | chr2 | 53816252 | |||||||
| chr2:53816265 | G | GT | 9 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0058 others(6): Show |
9 | HG00738.hp2 HG01358.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1380+1349dupT | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 53816265 | ||||||
| chr2:53816265 | GT | G | 89 | a0001c0001t0001g0018 a0001c0001t0001g0038 a0001c0001t0001g0171 others(86): Show |
121 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1380+1349delT | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 53816265 | ||||||
| chr2:53816265 | GTT | G | 73 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0017 others(70): Show |
96 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.1380+1348_1380+134 others(6): Show |
ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 53816265 | ||||||
| chr2:53816369 | C | T | 1 | a0002c0003t0001g0169 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1380+1434C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | chr2 | 53816369 | |||||||
| chr2:53816459 | G | C | 1 | a0001c0001t0002g0123 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1381-1439G>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | chr2 | 53816459 | |||||||
| chr2:53816543 | A | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0187 |
4 | HG02818.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1381-1355A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | chr2 | 53816543 | |||||||
| chr2:53816585 | T | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0187 |
4 | HG02818.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1381-1313T>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | chr2 | 53816585 | |||||||
| chr2:53816847 | A | C | 1 | a0001c0001t0001g0080 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1381-1051A>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | chr2 | 53816847 | |||||||
| chr2:53817042 | G | C | 1 | a0002c0003t0002g0134 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1381-856G>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | chr2 | 53817042 | |||||||
| chr2:53817138 | AT | A | 174 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0018 others(171): Show |
228 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.1381-747delT | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | 53817138 | ||||||
| chr2:53817165 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1381-733G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | chr2 | 53817165 | |||||||
| chr2:53817210 | T | C | 4 | a0001c0001t0002g0011 a0001c0001t0002g0121 a0001c0001t0002g0142 others(1): Show |
7 | HG02559.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1381-688T>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | chr2 | 53817210 | |||||||
| chr2:53817335 | A | G | 48 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0042 others(45): Show |
62 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.1381-563A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | chr2 | 53817335 | |||||||
| chr2:53817357 | T | A | 1 | a0001c0001t0005g0090 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1381-541T>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | chr2 | 53817357 | |||||||
| chr2:53817358 | C | T | 1 | a0001c0001t0005g0090 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1381-540C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | chr2 | 53817358 | |||||||
| chr2:53817359 | T | C | 1 | a0001c0001t0005g0090 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1381-539T>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | chr2 | 53817359 | |||||||
| chr2:53817422 | C | T | 2 | a0001c0001t0002g0128 a0004c0006t0002g0148 |
2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1381-476C>T | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | chr2 | 53817422 | |||||||
| chr2:53817423 | G | A | 66 | a0001c0001t0001g0014 a0001c0001t0001g0056 a0001c0001t0001g0069 others(63): Show |
93 | HG00099.hp2 HG00408.hp2 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.1381-475G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | chr2 | 53817423 | |||||||
| chr2:53817430 | G | A | 3 | a0001c0001t0002g0127 a0001c0001t0002g0139 a0001c0001t0002g0146 |
3 | HG02109.hp1 HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1381-468G>A | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | chr2 | 53817430 | |||||||
| chr2:53817438 | T | C | 1 | a0001c0002t0001g0220 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1381-460T>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | chr2 | 53817438 | |||||||
| chr2:53817490 | T | C | 1 | a0001c0001t0005g0090 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1381-408T>C | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | chr2 | 53817490 | |||||||
| chr2:53817524 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1381-374A>G | ERLEC1 | ENSG00000068912.15 | transcript | ENST00000185150.9 | protein_coding | 13/13 | chr2 | 53817524 |