Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55531 |
| ensemblid | ENSG00000110675.13 |
| hgncid | 25334 |
| symbol | ELMOD1 |
| name | ELMO domain containing 1 |
| refseq_nuc | NM_018712.4 |
| refseq_prot | NP_061182.3 |
| ensembl_nuc | ENST00000265840.12 |
| ensembl_prot | ENSP00000265840.7 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 107591147 |
| end | 107666779 |
| strand | + |
| ver | v1.2 |
| region | chr11:107591147-107666779 |
| region5000 | chr11:107586147-107671779 |
| regionname0 | ELMOD1_chr11_107591147_107666779 |
| regionname5000 | ELMOD1_chr11_107586147_107671779 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 334 | 338 | 93 | 60 | 140 | 12 | 31 | 111 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | MKHFL others(329): Show |
chr11 | 107586147 | 107671779 |
| a0002 | 0/0 | 334 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | MKHFL others(329): Show |
chr11 | 107586147 | 107671779 |
| a0003 | 0/0 | 334 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | MKHFL others(329): Show |
chr11 | 107586147 | 107671779 |
| a0004 | 0/0 | 334 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | MKHFL others(329): Show |
chr11 | 107586147 | 107671779 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1002 | 204 | 28 | 52 | 87 | 12 | 23 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | ATGAA others(997): Show |
chr11 | 107586147 | 107671779 | ||
| a0001c0002 | 0/0 | 1002 | 133 | 64 | 8 | 53 | 0 | 8 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | ATGAA others(997): Show |
chr11 | 107586147 | 107671779 | ||
| a0001c0006 | 0/0 | 1002 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | ATGAA others(997): Show |
chr11 | 107586147 | 107671779 | ||
| a0002c0003 | 0/0 | 1002 | 2 | 0 | 0 | 2 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | ATGAA others(997): Show |
chr11 | 107586147 | 107671779 | ||
| a0003c0005 | 0/0 | 1002 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | ATGAA others(997): Show |
chr11 | 107586147 | 107671779 | ||
| a0004c0004 | 0/0 | 1002 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | ATGAA others(997): Show |
chr11 | 107586147 | 107671779 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2927 | 78 | 10 | 18 | 44 | 2 | 3 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2922): Show |
chr11 | 107586147 | 107671779 |
| a0001c0001t0002 | 0/0 | 2931 | 50 | 9 | 10 | 21 | 3 | 7 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2926): Show |
chr11 | 107586147 | 107671779 |
| a0001c0001t0003 | 0/0 | 2931 | 31 | 0 | 10 | 10 | 3 | 8 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2926): Show |
chr11 | 107586147 | 107671779 |
| a0001c0001t0005 | 0/0 | 2923 | 11 | 3 | 4 | 0 | 4 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2918): Show |
chr11 | 107586147 | 107671779 |
| a0001c0001t0008 | 0/0 | 2931 | 12 | 0 | 3 | 8 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2926): Show |
chr11 | 107586147 | 107671779 |
| a0001c0001t0009 | 0/0 | 2927 | 7 | 3 | 2 | 0 | 0 | 2 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2922): Show |
chr11 | 107586147 | 107671779 |
| a0001c0001t0010 | 0/0 | 2935 | 7 | 2 | 3 | 1 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2930): Show |
chr11 | 107586147 | 107671779 |
| a0001c0001t0013 | 1/0 | 2935 | 3 | 0 | 0 | 2 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2930): Show |
chr11 | 107586147 | 107671779 |
| a0001c0001t0021 | 0/0 | 2931 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2926): Show |
chr11 | 107586147 | 107671779 |
| a0001c0001t0024 | 0/0 | 2939 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2934): Show |
chr11 | 107586147 | 107671779 |
| a0001c0001t0025 | 0/0 | 2939 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2934): Show |
chr11 | 107586147 | 107671779 |
| a0001c0001t0026 | 0/0 | 2919 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2914): Show |
chr11 | 107586147 | 107671779 |
| a0001c0001t0028 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2930): Show |
chr11 | 107586147 | 107671779 |
| a0001c0002t0002 | 0/0 | 2931 | 13 | 12 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2926): Show |
chr11 | 107586147 | 107671779 |
| a0001c0002t0004 | 0/0 | 2931 | 27 | 26 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2926): Show |
chr11 | 107586147 | 107671779 |
| a0001c0002t0005 | 0/0 | 2923 | 15 | 2 | 2 | 5 | 0 | 6 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2918): Show |
chr11 | 107586147 | 107671779 |
| a0001c0002t0006 | 0/0 | 2931 | 22 | 0 | 0 | 21 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2926): Show |
chr11 | 107586147 | 107671779 |
| a0001c0002t0007 | 0/0 | 2931 | 18 | 0 | 3 | 14 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2926): Show |
chr11 | 107586147 | 107671779 |
| a0001c0002t0009 | 0/0 | 2927 | 5 | 5 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2922): Show |
chr11 | 107586147 | 107671779 |
| a0001c0002t0010 | 0/0 | 2935 | 4 | 4 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2930): Show |
chr11 | 107586147 | 107671779 |
| a0001c0002t0011 | 0/0 | 2935 | 10 | 0 | 0 | 10 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2930): Show |
chr11 | 107586147 | 107671779 |
| a0001c0002t0012 | 0/0 | 2919 | 4 | 4 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2914): Show |
chr11 | 107586147 | 107671779 |
| a0001c0002t0014 | 0/0 | 2927 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2922): Show |
chr11 | 107586147 | 107671779 |
| a0001c0002t0015 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2926): Show |
chr11 | 107586147 | 107671779 |
| a0001c0002t0016 | 0/0 | 2927 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2922): Show |
chr11 | 107586147 | 107671779 |
| a0001c0002t0017 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2926): Show |
chr11 | 107586147 | 107671779 |
| a0001c0002t0018 | 0/0 | 2907 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2902): Show |
chr11 | 107586147 | 107671779 |
| a0001c0002t0019 | 0/0 | 2915 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2910): Show |
chr11 | 107586147 | 107671779 |
| a0001c0002t0020 | 0/0 | 2923 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2918): Show |
chr11 | 107586147 | 107671779 |
| a0001c0002t0022 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2930): Show |
chr11 | 107586147 | 107671779 |
| a0001c0002t0027 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2926): Show |
chr11 | 107586147 | 107671779 |
| a0001c0002t0029 | 0/0 | 2927 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2922): Show |
chr11 | 107586147 | 107671779 |
| a0001c0002t0030 | 0/0 | 2943 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2938): Show |
chr11 | 107586147 | 107671779 |
| a0001c0002t0031 | 0/0 | 2935 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2930): Show |
chr11 | 107586147 | 107671779 |
| a0001c0002t0032 | 0/0 | 2923 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2918): Show |
chr11 | 107586147 | 107671779 |
| a0001c0002t0033 | 0/0 | 2927 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2922): Show |
chr11 | 107586147 | 107671779 |
| a0001c0002t0034 | 0/0 | 2923 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2918): Show |
chr11 | 107586147 | 107671779 |
| a0001c0006t0004 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2926): Show |
chr11 | 107586147 | 107671779 |
| a0002c0003t0001 | 0/0 | 2927 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2922): Show |
chr11 | 107586147 | 107671779 |
| a0002c0003t0008 | 0/0 | 2931 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2926): Show |
chr11 | 107586147 | 107671779 |
| a0003c0005t0002 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2926): Show |
chr11 | 107586147 | 107671779 |
| a0004c0004t0023 | 0/0 | 2939 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | GGTCG others(2934): Show |
chr11 | 107586147 | 107671779 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0201 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0003g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0005g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0005g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0005g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0005g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0005g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0005g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0005g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0005g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0008g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0008g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0008g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0008g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0008g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0008g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0008g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0008g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0008g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0008g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0008g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0008g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0009g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0009g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0009g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0009g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0009g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0009g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0009g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0010g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0010g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0010g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0010g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0010g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0010g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0010g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0013g0136 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0013g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0013g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0021g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0024g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0025g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0026g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0001t0028g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0004g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0004g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0004g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0005g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0005g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0005g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0005g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0005g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0005g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0005g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0005g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0005g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0005g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0006g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0006g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0006g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0006g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0006g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0006g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0006g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0006g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0006g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0006g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0006g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0006g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0006g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0006g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0006g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0006g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0006g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0006g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0006g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0006g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0006g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0006g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0007g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0007g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0007g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0007g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0007g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0007g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0007g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0007g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0007g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0007g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0007g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0007g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0007g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0007g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0007g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0007g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0007g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0007g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0009g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0009g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0009g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0009g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0009g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0010g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0010g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0010g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0010g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0011g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0011g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0011g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0011g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0011g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0011g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0011g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0011g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0011g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0011g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0012g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0012g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0012g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0012g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0014g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0015g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0016g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0017g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0018g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0019g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0020g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0022g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0027g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0029g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0030g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0031g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0032g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0033g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0002t0034g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0001c0006t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0002c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0002c0003t0008g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0003c0005t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| a0004c0004t0023g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0312 | EUR | GBR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0167 | EUR | GBR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0220 | EUR | FIN | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0221 | EUR | FIN | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG00408 | hp2 | a0001 | c0002 | t0011 | g0044 | EAS | CHS | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG00423 | hp1 | a0001 | c0002 | t0006 | g0069 | EAS | CHS | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG00544 | hp1 | a0001 | c0002 | t0007 | g0076 | EAS | CHS | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | CHS | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG00609 | hp1 | a0002 | c0003 | t0001 | g0190 | EAS | CHS | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG00609 | hp2 | a0001 | c0002 | t0005 | g0059 | EAS | CHS | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0173 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG00642 | hp1 | a0001 | c0001 | t0010 | g0301 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0306 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG00738 | hp2 | a0001 | c0002 | t0005 | g0289 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0100 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0128 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01070 | hp2 | a0001 | c0002 | t0004 | g0211 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0336 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0132 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01081 | hp2 | a0001 | c0001 | t0010 | g0321 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0195 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01099 | hp2 | a0001 | c0002 | t0005 | g0288 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01109 | hp2 | a0001 | c0001 | t0025 | g0143 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01167 | hp2 | a0001 | c0002 | t0007 | g0103 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0134 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01168 | hp2 | a0001 | c0002 | t0034 | g0163 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01169 | hp1 | a0001 | c0002 | t0007 | g0104 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0127 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0302 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01175 | hp2 | a0001 | c0001 | t0021 | g0161 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0137 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0274 | AMR | CLM | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | CLM | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0149 | AMR | CLM | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0095 | AMR | CLM | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0111 | AMR | CLM | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01346 | hp1 | a0001 | c0001 | t0008 | g0160 | AMR | CLM | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01358 | hp1 | a0001 | c0001 | t0005 | g0101 | AMR | CLM | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01358 | hp2 | a0001 | c0001 | t0008 | g0198 | AMR | CLM | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01433 | hp1 | a0001 | c0001 | t0009 | g0225 | AMR | CLM | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01496 | hp2 | a0001 | c0001 | t0010 | g0043 | AMR | CLM | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01515 | hp1 | a0001 | c0001 | t0005 | g0196 | EUR | IBS | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0117 | EUR | IBS | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01516 | hp2 | a0001 | c0001 | t0005 | g0165 | EUR | IBS | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01517 | hp2 | a0001 | c0001 | t0005 | g0164 | EUR | IBS | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | ACB | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0326 | AFR | ACB | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0311 | AFR | ACB | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01891 | hp2 | a0001 | c0002 | t0012 | g0142 | AFR | ACB | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0313 | AMR | PEL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0303 | AMR | PEL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | PEL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02015 | hp2 | a0001 | c0002 | t0011 | g0181 | EAS | KHV | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02055 | hp1 | a0003 | c0005 | t0002 | g0088 | AFR | ACB | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02055 | hp2 | a0001 | c0002 | t0004 | g0202 | AFR | ACB | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | KHV | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02074 | hp2 | a0001 | c0001 | t0013 | g0304 | EAS | KHV | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | KHV | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0295 | EAS | KHV | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02132 | hp1 | a0001 | c0001 | t0008 | g0334 | EAS | KHV | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02132 | hp2 | a0001 | c0001 | t0008 | g0192 | EAS | KHV | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | KHV | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02135 | hp2 | a0001 | c0001 | t0026 | g0234 | EAS | KHV | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02145 | hp1 | a0001 | c0002 | t0004 | g0273 | AFR | ACB | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02145 | hp2 | a0001 | c0002 | t0004 | g0141 | AFR | ACB | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PEL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02148 | hp2 | a0001 | c0001 | t0008 | g0284 | AMR | PEL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | CDX | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | CDX | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02257 | hp1 | a0001 | c0002 | t0004 | g0007 | AFR | ACB | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0115 | AFR | ACB | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0253 | AFR | ACB | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0261 | AFR | ACB | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02280 | hp1 | a0001 | c0002 | t0009 | g0317 | AFR | ACB | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0278 | AFR | ACB | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0123 | AMR | PEL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | PEL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0122 | AFR | ACB | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02451 | hp2 | a0001 | c0002 | t0033 | g0251 | AFR | ACB | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0286 | AFR | GWD | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02572 | hp2 | a0001 | c0002 | t0019 | g0318 | AFR | GWD | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0239 | SAS | PJL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02615 | hp1 | a0001 | c0002 | t0004 | g0327 | AFR | GWD | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02615 | hp2 | a0001 | c0002 | t0009 | g0264 | AFR | GWD | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02622 | hp1 | a0001 | c0001 | t0028 | g0256 | AFR | GWD | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | GWD | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0086 | AFR | GWD | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02630 | hp2 | a0001 | c0001 | t0009 | g0120 | AFR | GWD | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02647 | hp1 | a0001 | c0002 | t0004 | g0335 | AFR | GWD | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02647 | hp2 | a0001 | c0002 | t0004 | g0087 | AFR | GWD | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0330 | AFR | GWD | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02723 | hp1 | a0001 | c0002 | t0004 | g0282 | AFR | GWD | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02723 | hp2 | a0001 | c0002 | t0027 | g0268 | AFR | GWD | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02809 | hp1 | a0001 | c0002 | t0004 | g0249 | AFR | GWD | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02809 | hp2 | a0001 | c0002 | t0014 | g0281 | AFR | GWD | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02818 | hp1 | a0001 | c0002 | t0020 | g0006 | AFR | GWD | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02818 | hp2 | a0001 | c0002 | t0005 | g0325 | AFR | GWD | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0267 | AFR | GWD | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0124 | AFR | GWD | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02895 | hp2 | a0001 | c0002 | t0010 | g0316 | AFR | GWD | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02896 | hp1 | a0001 | c0002 | t0004 | g0204 | AFR | GWD | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02896 | hp2 | a0001 | c0002 | t0010 | g0329 | AFR | GWD | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | GWD | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02897 | hp2 | a0001 | c0002 | t0010 | g0324 | AFR | GWD | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02922 | hp1 | a0001 | c0002 | t0004 | g0279 | AFR | ESN | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02922 | hp2 | a0001 | c0002 | t0016 | g0269 | AFR | ESN | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02965 | hp1 | a0001 | c0002 | t0009 | g0259 | AFR | ESN | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02970 | hp1 | a0001 | c0002 | t0004 | g0287 | AFR | ESN | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0109 | AFR | ESN | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02976 | hp1 | a0001 | c0001 | t0009 | g0247 | AFR | ESN | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02976 | hp2 | a0001 | c0002 | t0004 | g0207 | AFR | ESN | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03017 | hp1 | a0001 | c0002 | t0005 | g0309 | SAS | PJL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03017 | hp2 | a0001 | c0002 | t0006 | g0175 | SAS | PJL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03041 | hp1 | a0001 | c0002 | t0015 | g0283 | AFR | GWD | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03041 | hp2 | a0001 | c0002 | t0004 | g0250 | AFR | GWD | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03098 | hp1 | a0001 | c0002 | t0004 | g0209 | AFR | MSL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03098 | hp2 | a0001 | c0002 | t0004 | g0277 | AFR | MSL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0328 | AFR | ESN | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03130 | hp2 | a0001 | c0002 | t0022 | g0291 | AFR | ESN | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03139 | hp1 | a0001 | c0002 | t0004 | g0252 | AFR | ESN | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0285 | AFR | ESN | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | ESN | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03195 | hp2 | a0001 | c0006 | t0004 | g0055 | AFR | ESN | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03209 | hp1 | a0001 | c0002 | t0002 | g0275 | AFR | MSL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | MSL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03225 | hp1 | a0001 | c0002 | t0017 | g0262 | AFR | MSL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03225 | hp2 | a0001 | c0001 | t0010 | g0140 | AFR | MSL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0307 | SAS | PJL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0108 | SAS | PJL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0121 | AFR | MSL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03453 | hp2 | a0001 | c0002 | t0032 | g0254 | AFR | MSL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03486 | hp2 | a0001 | c0002 | t0012 | g0091 | AFR | MSL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0235 | SAS | PJL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0188 | SAS | PJL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03491 | hp2 | a0001 | c0002 | t0005 | g0119 | SAS | PJL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03492 | hp2 | a0001 | c0002 | t0005 | g0113 | SAS | PJL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03516 | hp1 | a0001 | c0002 | t0012 | g0110 | AFR | ESN | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03516 | hp2 | a0001 | c0002 | t0004 | g0270 | AFR | ESN | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03540 | hp2 | a0001 | c0002 | t0004 | g0208 | AFR | GWD | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03579 | hp1 | a0001 | c0001 | t0009 | g0266 | AFR | MSL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03579 | hp2 | a0001 | c0002 | t0004 | g0210 | AFR | MSL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0226 | SAS | PJL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0223 | SAS | PJL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0135 | SAS | PJL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0305 | SAS | PJL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03704 | hp1 | a0001 | c0001 | t0009 | g0129 | SAS | PJL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03704 | hp2 | a0001 | c0002 | t0005 | g0298 | SAS | PJL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0331 | SAS | PJL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0310 | SAS | BEB | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0162 | SAS | BEB | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03834 | hp1 | a0001 | c0002 | t0005 | g0246 | SAS | BEB | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0200 | SAS | BEB | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03927 | hp1 | a0001 | c0002 | t0005 | g0090 | SAS | BEB | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03927 | hp2 | a0001 | c0002 | t0007 | g0170 | SAS | BEB | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG04115 | hp1 | a0001 | c0001 | t0008 | g0157 | SAS | STU | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG04115 | hp2 | a0001 | c0001 | t0009 | g0131 | SAS | STU | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG04199 | hp1 | a0001 | c0001 | t0010 | g0230 | SAS | STU | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0056 | SAS | STU | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG04204 | hp1 | a0001 | c0001 | t0024 | g0308 | SAS | STU | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG04204 | hp2 | a0004 | c0004 | t0023 | g0179 | SAS | STU | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18522 | hp1 | a0001 | c0002 | t0004 | g0206 | AFR | YRI | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | YRI | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18612 | hp1 | a0001 | c0002 | t0006 | g0054 | EAS | CHB | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | CHB | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18940 | hp1 | a0001 | c0002 | t0006 | g0020 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18942 | hp1 | a0001 | c0001 | t0008 | g0023 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18942 | hp2 | a0001 | c0002 | t0006 | g0112 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18944 | hp1 | a0001 | c0002 | t0007 | g0051 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18944 | hp2 | a0001 | c0002 | t0011 | g0016 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18946 | hp1 | a0001 | c0002 | t0007 | g0189 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18948 | hp1 | a0001 | c0001 | t0010 | g0018 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18949 | hp1 | a0001 | c0002 | t0007 | g0217 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18952 | hp2 | a0001 | c0002 | t0007 | g0008 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18954 | hp1 | a0001 | c0001 | t0008 | g0060 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18954 | hp2 | a0002 | c0003 | t0008 | g0015 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18959 | hp1 | a0001 | c0002 | t0006 | g0033 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18960 | hp1 | a0001 | c0002 | t0006 | g0194 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18960 | hp2 | a0001 | c0002 | t0007 | g0099 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18961 | hp1 | a0001 | c0002 | t0006 | g0050 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18961 | hp2 | a0001 | c0002 | t0005 | g0169 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18964 | hp2 | a0001 | c0001 | t0008 | g0081 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18965 | hp1 | a0001 | c0002 | t0011 | g0182 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18965 | hp2 | a0001 | c0002 | t0007 | g0026 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18966 | hp2 | a0001 | c0002 | t0006 | g0152 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18968 | hp1 | a0001 | c0002 | t0011 | g0293 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18968 | hp2 | a0001 | c0002 | t0006 | g0047 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18969 | hp1 | a0001 | c0002 | t0006 | g0011 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18974 | hp2 | a0001 | c0002 | t0011 | g0025 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18983 | hp2 | a0001 | c0002 | t0011 | g0037 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18985 | hp2 | a0001 | c0002 | t0007 | g0258 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18988 | hp1 | a0001 | c0002 | t0006 | g0009 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18988 | hp2 | a0001 | c0002 | t0031 | g0070 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18994 | hp1 | a0001 | c0002 | t0005 | g0001 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18994 | hp2 | a0001 | c0002 | t0006 | g0036 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18998 | hp1 | a0001 | c0002 | t0006 | g0297 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18998 | hp2 | a0001 | c0002 | t0007 | g0042 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18999 | hp1 | a0001 | c0002 | t0007 | g0094 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18999 | hp2 | a0001 | c0002 | t0030 | g0151 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19000 | hp1 | a0001 | c0002 | t0005 | g0118 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19000 | hp2 | a0001 | c0002 | t0029 | g0034 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19001 | hp2 | a0001 | c0002 | t0006 | g0062 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19002 | hp1 | a0001 | c0002 | t0006 | g0029 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19011 | hp2 | a0001 | c0002 | t0007 | g0227 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19012 | hp1 | a0001 | c0002 | t0011 | g0046 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0292 | AFR | LWK | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19030 | hp2 | a0001 | c0002 | t0012 | g0205 | AFR | LWK | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19043 | hp1 | a0001 | c0002 | t0004 | g0203 | AFR | LWK | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19043 | hp2 | a0001 | c0002 | t0010 | g0271 | AFR | LWK | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19055 | hp1 | a0001 | c0002 | t0006 | g0077 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19058 | hp1 | a0001 | c0002 | t0007 | g0041 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19065 | hp1 | a0001 | c0002 | t0011 | g0024 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19065 | hp2 | a0001 | c0001 | t0008 | g0180 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19066 | hp2 | a0001 | c0002 | t0011 | g0064 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19070 | hp1 | a0001 | c0002 | t0006 | g0257 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19074 | hp1 | a0001 | c0002 | t0005 | g0001 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19074 | hp2 | a0001 | c0002 | t0007 | g0183 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19076 | hp2 | a0001 | c0002 | t0006 | g0155 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19077 | hp1 | a0001 | c0001 | t0013 | g0177 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19079 | hp2 | a0001 | c0002 | t0006 | g0035 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19081 | hp1 | a0001 | c0002 | t0006 | g0017 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19085 | hp1 | a0001 | c0002 | t0006 | g0012 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19091 | hp2 | a0001 | c0001 | t0008 | g0031 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19240 | hp1 | a0001 | c0002 | t0004 | g0255 | AFR | YRI | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA19240 | hp2 | a0001 | c0002 | t0004 | g0280 | AFR | YRI | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0166 | EUR | TSI | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0224 | EUR | TSI | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01123 | hp1 | a0001 | c0001 | t0009 | g0248 | AMR | CLM | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG01123 | hp2 | a0001 | c0002 | t0007 | g0045 | AMR | CLM | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0263 | AFR | ACB | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02486 | hp1 | a0001 | c0002 | t0005 | g0145 | AFR | ACB | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02486 | hp2 | a0001 | c0002 | t0018 | g0272 | AFR | ACB | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02559 | hp1 | a0001 | c0001 | t0010 | g0133 | AFR | ACB | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG02559 | hp2 | a0001 | c0002 | t0009 | g0144 | AFR | ACB | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03471 | hp1 | a0001 | c0002 | t0009 | g0265 | AFR | MSL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG03471 | hp2 | a0001 | c0002 | t0004 | g0114 | AFR | MSL | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0276 | AFR | USA | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | USA | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18955 | hp1 | a0001 | c0002 | t0007 | g0049 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA18955 | hp2 | a0001 | c0001 | t0008 | g0138 | EAS | JPT | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA20300 | hp1 | a0001 | c0002 | t0004 | g0213 | AFR | USA | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | USA | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0201 | REF | REF | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0013 | g0136 | REF | REF | ELMOD1_chr11_107586147_107671779 | ELMOD1 | chr11 | 107586147 | 107671779 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:107630702 | A | T | 1 | a0003 | 1 | HG02055.hp1 | missense_variant&splice_region_variant | MODERATE | c.166A>T | p.Thr56Ser | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 4/12 | 514/2935 | 166/1005 | 56/334 | chr11 | 107630702 | |||
| chr11:107654204 | G | T | 1 | a0002 | 2 | HG00609.hp1 NA18954.hp2 |
missense_variant | MODERATE | c.680G>T | p.Arg227Met | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/12 | 1028/2935 | 680/1005 | 227/334 | chr11 | 107654204 | |||
| chr11:107665040 | A | G | 1 | a0004 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.848A>G | p.Glu283Gly | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 12/12 | 1196/2935 | 848/1005 | 283/334 | chr11 | 107665040 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:107630499 | A | C | 1 | a0001c0006 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.100A>C | p.Arg34Arg | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 3/12 | 448/2935 | 100/1005 | 34/334 | chr11 | 107630499 | |||
| chr11:107665032 | G | A | 2 | a0001c0002 a0001c0006 |
134 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(131): Show |
synonymous_variant | LOW | c.840G>A | p.Leu280Leu | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 12/12 | 1188/2935 | 840/1005 | 280/334 | chr11 | 107665032 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:107591177 | T | A | 2 | a0001c0002t0014 a0001c0002t0015 |
2 | HG02809.hp2 HG03041.hp1 |
5_prime_UTR_variant | MODIFIER | c.-318T>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/12 | 27013 | chr11 | 107591177 | ||||||
| chr11:107591292 | G | C | 1 | a0001c0002t0016 | 1 | HG02922.hp2 | 5_prime_UTR_variant | MODIFIER | c.-203G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/12 | 26898 | chr11 | 107591292 | ||||||
| chr11:107591304 | C | T | 1 | a0001c0002t0034 | 1 | HG01168.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-191C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/12 | chr11 | 107591304 | |||||||
| chr11:107665667 | A | G | 10 | a0001c0002t0004 a0001c0002t0006 a0001c0002t0007 others(7): Show |
83 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*470A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 12/12 | 470 | chr11 | 107665667 | ||||||
| chr11:107665703 | C | A | 2 | a0001c0002t0016 a0001c0002t0017 |
2 | HG02922.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*506C>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 12/12 | 506 | chr11 | 107665703 | ||||||
| chr11:107665722 | G | T | 1 | a0001c0001t0028 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*525G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 12/12 | 525 | chr11 | 107665722 | ||||||
| chr11:107665762 | A | G | 2 | a0001c0002t0015 a0001c0002t0027 |
2 | HG02723.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*565A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 12/12 | 565 | chr11 | 107665762 | ||||||
| chr11:107665798 | T | A | 6 | a0001c0002t0006 a0001c0002t0007 a0001c0002t0011 others(3): Show |
53 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*601T>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 12/12 | 601 | chr11 | 107665798 | ||||||
| chr11:107665854 | C | T | 2 | a0001c0002t0015 a0001c0002t0027 |
2 | HG02723.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*657C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 12/12 | 657 | chr11 | 107665854 | ||||||
| chr11:107665962 | A | AAAAT | 3 | a0001c0001t0024 a0001c0001t0025 a0004c0004t0023 |
3 | HG01109.hp2 HG04204.hp1 HG04204.hp2 |
3_prime_UTR_variant | MODIFIER | c.*817_*820dupTAAA | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 12/12 | 821 | INFO_REALIGN_3_PRIME | chr11 | 107665962 | |||||
| chr11:107665962 | AAAAT | A | 15 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0008 others(12): Show |
181 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(178): Show |
3_prime_UTR_variant | MODIFIER | c.*817_*820delTAAA | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 12/12 | 817 | INFO_REALIGN_3_PRIME | chr11 | 107665962 | |||||
| chr11:107665962 | AAAATAAA others(1): Show |
A | 8 | a0001c0001t0001 a0001c0001t0009 a0001c0002t0009 others(5): Show |
94 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*813_*820delTAAATA others(2): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 12/12 | 813 | INFO_REALIGN_3_PRIME | chr11 | 107665962 | |||||
| chr11:107665962 | AAAATAAA others(5): Show |
A | 5 | a0001c0001t0005 a0001c0002t0005 a0001c0002t0020 others(2): Show |
29 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*809_*820delTAAATA others(6): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 12/12 | 809 | INFO_REALIGN_3_PRIME | chr11 | 107665962 | |||||
| chr11:107665962 | AAAATAAA others(9): Show |
A | 2 | a0001c0001t0026 a0001c0002t0012 |
5 | HG01891.hp2 HG02135.hp2 HG03486.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*805_*820delTAAATA others(10): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 12/12 | 805 | INFO_REALIGN_3_PRIME | chr11 | 107665962 | |||||
| chr11:107665962 | AAAATAAA others(13): Show |
A | 1 | a0001c0002t0019 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*801_*820delTAAATA others(14): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 12/12 | 801 | INFO_REALIGN_3_PRIME | chr11 | 107665962 | |||||
| chr11:107665962 | AAAATAAA others(21): Show |
A | 1 | a0001c0002t0018 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*793_*820delTAAATA others(22): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 12/12 | 793 | INFO_REALIGN_3_PRIME | chr11 | 107665962 | |||||
| chr11:107665973 | A | T | 2 | a0001c0001t0008 a0002c0003t0008 |
13 | HG01346.hp1 HG01358.hp2 HG02132.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*776A>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 12/12 | 776 | chr11 | 107665973 | ||||||
| chr11:107665977 | A | T | 2 | a0001c0001t0001 a0002c0003t0001 |
78 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*780A>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 12/12 | 780 | chr11 | 107665977 | ||||||
| chr11:107665985 | A | T | 1 | a0001c0001t0026 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*788A>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 12/12 | 788 | chr11 | 107665985 | ||||||
| chr11:107666131 | A | G | 38 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(35): Show |
305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*934A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 12/12 | 934 | chr11 | 107666131 | ||||||
| chr11:107666206 | C | T | 1 | a0001c0001t0025 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1009C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 12/12 | 1009 | chr11 | 107666206 | ||||||
| chr11:107666357 | G | GCTTGGGG others(5): Show |
1 | a0001c0002t0030 | 1 | NA18999.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1161_*1172dupCTTG others(8): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 12/12 | 1173 | INFO_REALIGN_3_PRIME | chr11 | 107666357 | |||||
| chr11:107666437 | T | C | 3 | a0001c0002t0007 a0001c0002t0029 a0001c0002t0031 |
20 | HG00544.hp1 HG01123.hp2 HG01167.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1240T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 12/12 | 1240 | chr11 | 107666437 | ||||||
| chr11:107666487 | C | T | 1 | a0001c0001t0021 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1290C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 12/12 | 1290 | chr11 | 107666487 | ||||||
| chr11:107666553 | A | G | 1 | a0001c0002t0020 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1356A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 12/12 | 1356 | chr11 | 107666553 | ||||||
| chr11:107666681 | T | C | 1 | a0001c0002t0022 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1484T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 12/12 | 1484 | chr11 | 107666681 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:107591681 | T | A | 1 | a0001c0002t0020g0006 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-86+272T>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107591681 | |||||||
| chr11:107591796 | G | C | 49 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(46): Show |
49 | HG00408.hp2 HG00558.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.-86+387G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107591796 | |||||||
| chr11:107591819 | C | T | 1 | a0001c0006t0004g0055 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-86+410C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107591819 | |||||||
| chr11:107591927 | G | T | 2 | a0001c0001t0001g0336 a0001c0001t0001g0337 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-86+518G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107591927 | |||||||
| chr11:107591937 | C | G | 1 | a0001c0002t0004g0335 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-86+528C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107591937 | |||||||
| chr11:107591939 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-86+530G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107591939 | |||||||
| chr11:107592019 | A | C | 3 | a0001c0001t0001g0332 a0001c0001t0002g0333 a0001c0001t0008g0334 |
3 | HG02074.hp1 HG02132.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.-86+610A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107592019 | |||||||
| chr11:107592152 | A | C | 251 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(248): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.-86+743A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107592152 | |||||||
| chr11:107592169 | G | A | 64 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0001g0146 others(61): Show |
65 | HG00099.hp2 HG00609.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.-86+760G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107592169 | |||||||
| chr11:107592216 | G | A | 62 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(59): Show |
63 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.-86+807G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107592216 | |||||||
| chr11:107592389 | A | C | 1 | a0001c0001t0003g0331 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-86+980A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107592389 | |||||||
| chr11:107592428 | C | T | 12 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0322 others(9): Show |
12 | HG01081.hp2 HG01884.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.-86+1019C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107592428 | |||||||
| chr11:107592433 | A | G | 47 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(44): Show |
47 | HG00408.hp2 HG00558.hp1 HG01123.hp2 others(44): Show |
intron_variant | MODIFIER | c.-86+1024A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107592433 | |||||||
| chr11:107592536 | C | G | 1 | a0001c0001t0008g0138 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-86+1127C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107592536 | |||||||
| chr11:107592603 | G | T | 1 | a0001c0002t0017g0262 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-86+1194G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107592603 | |||||||
| chr11:107592785 | T | C | 61 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(58): Show |
62 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.-86+1376T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107592785 | |||||||
| chr11:107593022 | A | G | 1 | a0001c0002t0009g0259 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-86+1613A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107593022 | |||||||
| chr11:107593111 | C | T | 1 | a0001c0002t0006g0054 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-86+1702C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107593111 | |||||||
| chr11:107593119 | C | T | 60 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(57): Show |
61 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-86+1710C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107593119 | |||||||
| chr11:107593121 | T | C | 1 | a0001c0002t0020g0006 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-86+1712T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107593121 | |||||||
| chr11:107593160 | G | C | 1 | a0001c0001t0003g0331 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-86+1751G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107593160 | |||||||
| chr11:107593161 | G | C | 1 | a0001c0002t0020g0006 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-86+1752G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107593161 | |||||||
| chr11:107593184 | T | C | 12 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0322 others(9): Show |
12 | HG01081.hp2 HG01884.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.-86+1775T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107593184 | |||||||
| chr11:107593210 | T | G | 256 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(253): Show |
259 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.-86+1801T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107593210 | |||||||
| chr11:107593328 | A | G | 1 | a0001c0002t0020g0006 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-86+1919A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107593328 | |||||||
| chr11:107593448 | T | C | 1 | a0001c0001t0003g0057 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-86+2039T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107593448 | |||||||
| chr11:107593452 | G | A | 61 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(58): Show |
62 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.-86+2043G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107593452 | |||||||
| chr11:107593509 | T | C | 1 | a0001c0002t0020g0006 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-86+2100T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107593509 | |||||||
| chr11:107593521 | C | G | 1 | a0001c0002t0010g0316 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-86+2112C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107593521 | |||||||
| chr11:107593533 | C | T | 6 | a0001c0001t0001g0312 a0001c0001t0001g0314 a0001c0001t0001g0315 others(3): Show |
6 | HG00099.hp1 HG00642.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.-86+2124C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107593533 | |||||||
| chr11:107593630 | G | A | 1 | a0001c0002t0007g0008 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-86+2221G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107593630 | |||||||
| chr11:107593660 | G | T | 253 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(250): Show |
256 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.-86+2251G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107593660 | |||||||
| chr11:107593913 | A | G | 7 | a0001c0002t0002g0326 a0001c0002t0002g0328 a0001c0002t0002g0330 others(4): Show |
7 | HG01884.hp2 HG02615.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-86+2504A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107593913 | |||||||
| chr11:107593946 | T | C | 3 | a0001c0001t0002g0267 a0001c0001t0009g0266 a0001c0002t0027g0268 |
3 | HG02723.hp2 HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-86+2537T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107593946 | |||||||
| chr11:107593975 | G | A | 1 | a0001c0002t0016g0269 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-86+2566G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107593975 | |||||||
| chr11:107594074 | G | A | 1 | a0001c0002t0006g0009 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-86+2665G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107594074 | |||||||
| chr11:107594149 | A | C | 12 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0322 others(9): Show |
12 | HG01081.hp2 HG01884.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.-86+2740A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107594149 | |||||||
| chr11:107594209 | C | T | 2 | a0001c0001t0002g0311 a0001c0002t0016g0269 |
2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-86+2800C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107594209 | |||||||
| chr11:107594229 | G | A | 12 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0322 others(9): Show |
12 | HG01081.hp2 HG01884.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.-86+2820G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107594229 | |||||||
| chr11:107594275 | G | GA | 45 | a0001c0001t0001g0004 a0001c0001t0001g0058 a0001c0001t0001g0061 others(42): Show |
46 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.-86+2878dupA | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107594275 | ||||||
| chr11:107594280 | A | G | 1 | a0001c0002t0020g0006 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-86+2871A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107594280 | |||||||
| chr11:107594287 | A | G | 1 | a0001c0002t0020g0006 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-86+2878A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107594287 | |||||||
| chr11:107594454 | G | A | 67 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(64): Show |
67 | HG00408.hp2 HG00558.hp1 HG01123.hp2 others(64): Show |
intron_variant | MODIFIER | c.-86+3045G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107594454 | |||||||
| chr11:107594671 | T | C | 1 | a0001c0002t0020g0006 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-86+3262T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107594671 | |||||||
| chr11:107594794 | T | G | 1 | a0001c0001t0001g0010 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-86+3385T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107594794 | |||||||
| chr11:107594846 | T | G | 1 | a0001c0001t0001g0058 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-86+3437T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107594846 | |||||||
| chr11:107594873 | T | C | 60 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(57): Show |
61 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-86+3464T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107594873 | |||||||
| chr11:107594996 | A | G | 2 | a0001c0001t0003g0331 a0001c0002t0020g0006 |
2 | HG02818.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-86+3587A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107594996 | |||||||
| chr11:107595123 | G | A | 1 | a0001c0001t0002g0147 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-86+3714G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107595123 | |||||||
| chr11:107595146 | T | C | 61 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(58): Show |
62 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.-86+3737T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107595146 | |||||||
| chr11:107595153 | G | GT | 9 | a0001c0001t0001g0146 a0001c0001t0001g0260 a0001c0001t0002g0263 others(6): Show |
9 | HG01109.hp2 HG02109.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-86+3757dupT | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107595153 | ||||||
| chr11:107595153 | GT | G | 250 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(247): Show |
253 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.-86+3757delT | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107595153 | ||||||
| chr11:107595511 | C | T | 60 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(57): Show |
61 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-86+4102C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107595511 | |||||||
| chr11:107595737 | T | C | 60 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(57): Show |
61 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-86+4328T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107595737 | |||||||
| chr11:107595846 | T | G | 252 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(249): Show |
255 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.-86+4437T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107595846 | |||||||
| chr11:107595867 | T | C | 13 | a0001c0001t0002g0212 a0001c0002t0004g0202 a0001c0002t0004g0203 others(10): Show |
13 | HG01070.hp2 HG01243.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-86+4458T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107595867 | |||||||
| chr11:107595994 | G | A | 1 | a0001c0002t0004g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-86+4585G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107595994 | |||||||
| chr11:107596052 | G | T | 252 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(249): Show |
255 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.-86+4643G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107596052 | |||||||
| chr11:107596130 | A | G | 60 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(57): Show |
61 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-86+4721A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107596130 | |||||||
| chr11:107596166 | T | G | 1 | a0001c0002t0020g0006 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-86+4757T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107596166 | |||||||
| chr11:107596552 | G | A | 63 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(60): Show |
64 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.-86+5143G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107596552 | |||||||
| chr11:107597040 | A | G | 1 | a0001c0001t0003g0200 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-86+5631A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107597040 | |||||||
| chr11:107597377 | G | A | 88 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(85): Show |
89 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.-86+5968G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107597377 | |||||||
| chr11:107597692 | C | CATAA | 60 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(57): Show |
61 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-86+6283_-86+6284i others(6): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107597692 | |||||||
| chr11:107597775 | A | T | 2 | a0001c0002t0006g0257 a0001c0002t0007g0258 |
2 | NA18985.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-86+6366A>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107597775 | |||||||
| chr11:107597955 | A | T | 19 | a0001c0001t0002g0311 a0001c0001t0008g0284 a0001c0002t0002g0274 others(16): Show |
19 | HG01255.hp2 HG01891.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-86+6546A>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107597955 | |||||||
| chr11:107597969 | T | C | 1 | a0001c0002t0005g0059 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-86+6560T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107597969 | |||||||
| chr11:107598053 | A | G | 1 | a0001c0001t0003g0331 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-86+6644A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107598053 | |||||||
| chr11:107598059 | T | C | 1 | a0001c0001t0003g0331 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-86+6650T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107598059 | |||||||
| chr11:107598223 | C | T | 1 | a0001c0001t0002g0126 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-86+6814C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107598223 | |||||||
| chr11:107598333 | G | A | 1 | a0001c0001t0005g0086 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-86+6924G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107598333 | |||||||
| chr11:107598362 | G | C | 2 | a0001c0002t0004g0270 a0001c0002t0010g0271 |
2 | HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-86+6953G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107598362 | |||||||
| chr11:107598502 | G | A | 1 | a0001c0002t0018g0272 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-86+7093G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107598502 | |||||||
| chr11:107598610 | G | C | 68 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(65): Show |
69 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.-86+7201G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107598610 | |||||||
| chr11:107598643 | T | A | 60 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(57): Show |
61 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-86+7234T>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107598643 | |||||||
| chr11:107598888 | T | G | 1 | a0001c0001t0001g0290 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-86+7479T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107598888 | |||||||
| chr11:107598922 | T | C | 1 | a0001c0001t0008g0060 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-86+7513T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107598922 | |||||||
| chr11:107598937 | G | A | 1 | a0001c0002t0004g0087 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-86+7528G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107598937 | |||||||
| chr11:107599032 | G | C | 68 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(65): Show |
69 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.-86+7623G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107599032 | |||||||
| chr11:107599114 | G | A | 6 | a0001c0002t0002g0274 a0001c0002t0002g0275 a0001c0002t0002g0276 others(3): Show |
6 | HG01255.hp2 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-86+7705G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107599114 | |||||||
| chr11:107599202 | A | G | 1 | a0001c0002t0004g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-86+7793A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107599202 | |||||||
| chr11:107599246 | C | G | 1 | a0001c0002t0004g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-86+7837C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107599246 | |||||||
| chr11:107599336 | G | C | 1 | a0003c0005t0002g0088 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-86+7927G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107599336 | |||||||
| chr11:107599349 | GCTCAA | G | 103 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0063 others(100): Show |
105 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.-86+7944_-86+7948d others(7): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107599349 | ||||||
| chr11:107599358 | G | A | 2 | a0001c0002t0004g0279 a0001c0002t0004g0280 |
2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-86+7949G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107599358 | |||||||
| chr11:107599383 | A | G | 68 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(65): Show |
69 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.-86+7974A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107599383 | |||||||
| chr11:107599453 | G | C | 9 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(6): Show |
9 | NA18612.hp1 NA18944.hp2 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.-86+8044G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107599453 | |||||||
| chr11:107599575 | C | T | 60 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(57): Show |
61 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-86+8166C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107599575 | |||||||
| chr11:107599581 | C | A | 330 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(327): Show |
334 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.-86+8172C>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107599581 | |||||||
| chr11:107599585 | T | C | 154 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(151): Show |
156 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.-86+8176T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107599585 | |||||||
| chr11:107599608 | G | A | 7 | a0001c0001t0002g0267 a0001c0001t0009g0266 a0001c0002t0005g0288 others(4): Show |
7 | HG00738.hp2 HG01099.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-86+8199G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107599608 | |||||||
| chr11:107599648 | G | A | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG00738.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.-86+8239G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107599648 | |||||||
| chr11:107599728 | C | T | 61 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(58): Show |
62 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.-86+8319C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107599728 | |||||||
| chr11:107599740 | C | CAAAAAAA | 10 | a0001c0002t0002g0274 a0001c0002t0002g0275 a0001c0002t0002g0276 others(7): Show |
10 | HG01255.hp2 HG02280.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-86+8336_-86+8342d others(9): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107599740 | ||||||
| chr11:107599740 | C | CAAAAAAA others(1): Show |
154 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(151): Show |
156 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.-86+8335_-86+8342d others(10): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107599740 | ||||||
| chr11:107599740 | C | CAAAAAAA others(2): Show |
9 | a0001c0001t0001g0019 a0001c0001t0001g0061 a0001c0001t0002g0089 others(6): Show |
9 | HG01433.hp2 HG01981.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.-86+8334_-86+8342d others(11): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107599740 | ||||||
| chr11:107599740 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0010g0018 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-86+8333_-86+8342d others(12): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107599740 | ||||||
| chr11:107599748 | A | AAAAAAAA others(1): Show |
12 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0322 others(9): Show |
12 | HG01081.hp2 HG01884.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.-86+8342_-86+8343i others(10): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107599748 | ||||||
| chr11:107599752 | G | A | 69 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(66): Show |
70 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.-86+8343G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107599752 | |||||||
| chr11:107599755 | A | AAAAAAAA others(6): Show |
1 | a0001c0002t0020g0006 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-86+8350_-86+8351i others(15): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107599755 | ||||||
| chr11:107599755 | A | AAAAAAAA others(3): Show |
6 | a0001c0001t0002g0267 a0001c0001t0009g0266 a0001c0002t0005g0288 others(3): Show |
6 | HG00738.hp2 HG01099.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-86+8350_-86+8351i others(12): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107599755 | ||||||
| chr11:107599755 | A | AAAAAAAG others(8): Show |
3 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0001c0002t0007g0217 |
3 | HG01934.hp1 NA18949.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-86+8350_-86+8351i others(17): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107599755 | ||||||
| chr11:107599755 | A | AAAAAAGA others(7): Show |
33 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0219 others(30): Show |
34 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.-86+8350_-86+8351i others(16): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107599755 | ||||||
| chr11:107599755 | A | AAAAAGAA others(6): Show |
25 | a0001c0001t0002g0212 a0001c0001t0002g0253 a0001c0001t0003g0331 others(22): Show |
25 | HG01070.hp2 HG01123.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.-86+8355_-86+8356i others(15): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107599755 | ||||||
| chr11:107599765 | G | GA | 6 | a0001c0001t0001g0021 a0001c0001t0001g0063 a0001c0001t0001g0139 others(3): Show |
6 | HG01981.hp2 HG02109.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-86+8370dupA | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107599765 | ||||||
| chr11:107599765 | GA | G | 8 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0322 others(5): Show |
8 | HG01081.hp2 HG02280.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-86+8370delA | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107599765 | ||||||
| chr11:107599777 | A | C | 1 | a0001c0002t0004g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-86+8368A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107599777 | |||||||
| chr11:107599779 | A | G | 13 | a0001c0001t0002g0212 a0001c0002t0004g0202 a0001c0002t0004g0203 others(10): Show |
13 | HG01070.hp2 HG01243.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-86+8370A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107599779 | |||||||
| chr11:107599795 | A | G | 60 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(57): Show |
61 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-86+8386A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107599795 | |||||||
| chr11:107599813 | A | G | 8 | a0001c0001t0001g0218 a0001c0001t0001g0241 a0001c0001t0001g0242 others(5): Show |
8 | NA18959.hp2 NA18969.hp2 NA18985.hp2 others(5): Show |
intron_variant | MODIFIER | c.-86+8404A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107599813 | |||||||
| chr11:107599877 | C | A | 1 | a0001c0001t0003g0092 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-86+8468C>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107599877 | |||||||
| chr11:107599983 | A | C | 88 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(85): Show |
89 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.-86+8574A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107599983 | |||||||
| chr11:107600007 | C | T | 3 | a0001c0002t0009g0317 a0001c0002t0012g0142 a0001c0002t0019g0318 |
3 | HG01891.hp2 HG02280.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-86+8598C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107600007 | |||||||
| chr11:107600119 | A | G | 1 | a0001c0001t0002g0005 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-86+8710A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107600119 | |||||||
| chr11:107600190 | A | G | 68 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(65): Show |
69 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.-86+8781A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107600190 | |||||||
| chr11:107600274 | A | C | 2 | a0001c0001t0001g0322 a0001c0001t0001g0323 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-86+8865A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107600274 | |||||||
| chr11:107600293 | C | CT | 243 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(240): Show |
246 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.-86+8891dupT | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107600293 | ||||||
| chr11:107600317 | T | A | 1 | a0001c0006t0004g0055 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-86+8908T>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107600317 | |||||||
| chr11:107600372 | A | G | 2 | a0001c0001t0002g0307 a0001c0001t0024g0308 |
2 | HG03239.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-86+8963A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107600372 | |||||||
| chr11:107600554 | G | A | 2 | a0001c0001t0002g0022 a0001c0001t0008g0023 |
2 | NA18942.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-86+9145G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107600554 | |||||||
| chr11:107600879 | C | CT | 56 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(53): Show |
57 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.-86+9483dupT | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107600879 | ||||||
| chr11:107600879 | CT | C | 6 | a0001c0001t0001g0150 a0001c0001t0003g0149 a0001c0001t0005g0134 others(3): Show |
6 | HG01168.hp1 HG01255.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.-86+9483delT | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107600879 | ||||||
| chr11:107601014 | A | C | 6 | a0001c0001t0001g0146 a0001c0001t0001g0260 a0001c0001t0005g0261 others(3): Show |
6 | HG01109.hp2 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-86+9605A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107601014 | |||||||
| chr11:107601060 | T | A | 3 | a0001c0001t0001g0154 a0001c0001t0003g0153 a0001c0002t0006g0152 |
3 | HG00621.hp2 NA18966.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.-86+9651T>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107601060 | |||||||
| chr11:107601257 | C | T | 60 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(57): Show |
61 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-86+9848C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107601257 | |||||||
| chr11:107601331 | CT | C | 8 | a0001c0001t0002g0267 a0001c0001t0003g0331 a0001c0001t0009g0266 others(5): Show |
8 | HG00738.hp2 HG01099.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-86+9931delT | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107601331 | ||||||
| chr11:107601331 | CTT | C | 60 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(57): Show |
61 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-86+9930_-86+9931d others(4): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107601331 | ||||||
| chr11:107601369 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0139 |
3 | HG02109.hp1 HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-86+9960G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107601369 | |||||||
| chr11:107601416 | C | CT | 80 | a0001c0001t0001g0098 a0001c0001t0001g0116 a0001c0001t0001g0125 others(77): Show |
82 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.-86+10024dupT | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107601416 | ||||||
| chr11:107601561 | A | G | 68 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(65): Show |
69 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.-86+10152A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107601561 | |||||||
| chr11:107601702 | C | T | 1 | a0001c0002t0004g0213 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-86+10293C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107601702 | |||||||
| chr11:107601954 | C | T | 2 | a0001c0002t0004g0279 a0001c0002t0004g0280 |
2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-86+10545C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107601954 | |||||||
| chr11:107602007 | C | T | 88 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(85): Show |
89 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.-86+10598C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107602007 | |||||||
| chr11:107602130 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-86+10721G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107602130 | |||||||
| chr11:107602162 | G | A | 1 | a0001c0002t0004g0335 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-86+10753G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107602162 | |||||||
| chr11:107602183 | G | A | 1 | a0001c0001t0002g0220 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-86+10774G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107602183 | |||||||
| chr11:107602228 | C | T | 1 | a0001c0002t0004g0335 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-86+10819C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107602228 | |||||||
| chr11:107602245 | T | G | 1 | a0001c0001t0003g0095 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-86+10836T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107602245 | |||||||
| chr11:107602262 | G | C | 136 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(133): Show |
137 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.-86+10853G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107602262 | |||||||
| chr11:107602322 | G | T | 1 | a0001c0002t0020g0006 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-86+10913G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107602322 | |||||||
| chr11:107602390 | T | G | 60 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(57): Show |
61 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-86+10981T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107602390 | |||||||
| chr11:107602673 | G | A | 5 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0322 others(2): Show |
5 | HG01081.hp2 HG02622.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-86+11264G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107602673 | |||||||
| chr11:107602688 | T | A | 5 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0322 others(2): Show |
5 | HG01081.hp2 HG02622.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-86+11279T>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107602688 | |||||||
| chr11:107602726 | C | CT | 147 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(144): Show |
149 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.-86+11329dupT | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107602726 | ||||||
| chr11:107602726 | C | CTT | 7 | a0001c0001t0001g0053 a0001c0001t0001g0061 a0001c0001t0001g0084 others(4): Show |
7 | HG00735.hp2 HG01433.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-86+11328_-86+1132 others(6): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107602726 | ||||||
| chr11:107602817 | C | A | 2 | a0001c0002t0005g0288 a0001c0002t0005g0289 |
2 | HG00738.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.-86+11408C>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107602817 | |||||||
| chr11:107602876 | C | CTG | 254 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(251): Show |
257 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.-86+11468_-86+1146 others(6): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107602876 | ||||||
| chr11:107602876 | C | G | 1 | a0001c0001t0002g0306 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-86+11467C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107602876 | |||||||
| chr11:107602893 | T | C | 3 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0010g0321 |
3 | HG01081.hp2 HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-86+11484T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107602893 | |||||||
| chr11:107602939 | T | C | 1 | a0001c0001t0003g0149 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-86+11530T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107602939 | |||||||
| chr11:107603110 | C | G | 1 | a0001c0002t0002g0330 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-86+11701C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107603110 | |||||||
| chr11:107603209 | G | A | 2 | a0001c0002t0004g0279 a0001c0002t0004g0280 |
2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-86+11800G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107603209 | |||||||
| chr11:107603255 | C | G | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG00738.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.-86+11846C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107603255 | |||||||
| chr11:107603362 | A | G | 50 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(47): Show |
50 | HG00408.hp2 HG00558.hp1 HG01123.hp2 others(47): Show |
intron_variant | MODIFIER | c.-86+11953A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107603362 | |||||||
| chr11:107603434 | G | A | 1 | a0001c0002t0004g0335 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-86+12025G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107603434 | |||||||
| chr11:107603570 | A | C | 1 | a0001c0001t0003g0331 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-86+12161A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107603570 | |||||||
| chr11:107603772 | G | A | 3 | a0001c0002t0009g0317 a0001c0002t0012g0142 a0001c0002t0019g0318 |
3 | HG01891.hp2 HG02280.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-86+12363G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107603772 | |||||||
| chr11:107603850 | C | T | 1 | a0001c0001t0002g0305 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-86+12441C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107603850 | |||||||
| chr11:107603866 | A | G | 2 | a0001c0001t0001g0240 a0001c0001t0002g0239 |
2 | HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-86+12457A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107603866 | |||||||
| chr11:107603876 | TA | T | 62 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(59): Show |
63 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.-86+12480delA | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107603876 | ||||||
| chr11:107604069 | A | G | 106 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0063 others(103): Show |
108 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.-86+12660A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107604069 | |||||||
| chr11:107604092 | GTACT | G | 60 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(57): Show |
61 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-86+12688_-86+1269 others(8): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107604092 | ||||||
| chr11:107604233 | G | T | 1 | a0001c0002t0004g0277 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-86+12824G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107604233 | |||||||
| chr11:107604302 | A | C | 2 | a0001c0002t0002g0121 a0001c0002t0002g0122 |
2 | HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-86+12893A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107604302 | |||||||
| chr11:107604427 | C | T | 15 | a0001c0001t0008g0284 a0001c0002t0002g0274 a0001c0002t0002g0275 others(12): Show |
15 | HG01255.hp2 HG02145.hp1 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.-86+13018C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107604427 | |||||||
| chr11:107604451 | C | T | 1 | a0001c0002t0004g0335 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-86+13042C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107604451 | |||||||
| chr11:107604455 | C | T | 1 | a0001c0002t0004g0007 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-86+13046C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107604455 | |||||||
| chr11:107604499 | T | C | 1 | a0001c0001t0003g0331 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-86+13090T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107604499 | |||||||
| chr11:107604517 | G | A | 2 | a0001c0002t0004g0279 a0001c0002t0004g0280 |
2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-86+13108G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107604517 | |||||||
| chr11:107604543 | T | G | 2 | a0001c0002t0004g0279 a0001c0002t0004g0280 |
2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-86+13134T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107604543 | |||||||
| chr11:107604645 | T | C | 154 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(151): Show |
156 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.-86+13236T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107604645 | |||||||
| chr11:107604829 | G | A | 1 | a0001c0001t0002g0096 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-85-13276G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107604829 | |||||||
| chr11:107604836 | C | T | 1 | a0001c0001t0002g0096 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-85-13269C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107604836 | |||||||
| chr11:107605112 | G | A | 49 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(46): Show |
50 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.-85-12993G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107605112 | |||||||
| chr11:107605122 | G | A | 1 | a0001c0002t0011g0025 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-85-12983G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107605122 | |||||||
| chr11:107605191 | C | CT | 12 | a0001c0001t0001g0053 a0001c0001t0001g0199 a0001c0001t0001g0237 others(9): Show |
12 | HG00544.hp2 HG01243.hp2 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.-85-12895dupT | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107605191 | ||||||
| chr11:107605191 | CT | C | 9 | a0001c0001t0001g0027 a0001c0001t0001g0319 a0001c0001t0003g0128 others(6): Show |
9 | HG00558.hp1 HG01070.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.-85-12895delT | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107605191 | ||||||
| chr11:107605259 | G | A | 72 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(69): Show |
72 | HG00408.hp2 HG00558.hp1 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.-85-12846G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107605259 | |||||||
| chr11:107605273 | C | T | 1 | a0001c0002t0010g0316 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-85-12832C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107605273 | |||||||
| chr11:107605274 | G | A | 2 | a0001c0002t0004g0270 a0001c0002t0010g0271 |
2 | HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-85-12831G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107605274 | |||||||
| chr11:107605382 | G | A | 1 | a0001c0002t0010g0316 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-85-12723G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107605382 | |||||||
| chr11:107605438 | T | G | 1 | a0001c0002t0006g0012 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-85-12667T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107605438 | |||||||
| chr11:107605579 | C | T | 5 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0322 others(2): Show |
5 | HG01081.hp2 HG02622.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-85-12526C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107605579 | |||||||
| chr11:107605596 | A | G | 1 | a0001c0001t0001g0310 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-85-12509A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107605596 | |||||||
| chr11:107605960 | A | G | 1 | a0001c0002t0020g0006 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-85-12145A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107605960 | |||||||
| chr11:107606066 | C | T | 1 | a0001c0001t0013g0304 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-85-12039C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107606066 | |||||||
| chr11:107606169 | A | G | 24 | a0001c0001t0002g0267 a0001c0001t0002g0311 a0001c0001t0008g0284 others(21): Show |
24 | HG00738.hp2 HG01099.hp2 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.-85-11936A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107606169 | |||||||
| chr11:107606353 | C | T | 1 | a0001c0001t0003g0331 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-85-11752C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107606353 | |||||||
| chr11:107606368 | C | A | 3 | a0001c0001t0001g0098 a0001c0001t0002g0097 a0001c0002t0007g0099 |
3 | NA18943.hp2 NA18960.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-85-11737C>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107606368 | |||||||
| chr11:107606607 | G | T | 1 | a0001c0002t0010g0316 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-85-11498G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107606607 | |||||||
| chr11:107606691 | C | T | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | NA18983.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-85-11414C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107606691 | |||||||
| chr11:107606692 | G | A | 6 | a0001c0001t0002g0089 a0001c0001t0002g0100 a0001c0001t0002g0102 others(3): Show |
6 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.-85-11413G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107606692 | |||||||
| chr11:107606825 | A | C | 2 | a0001c0001t0001g0240 a0001c0001t0002g0239 |
2 | HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-85-11280A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107606825 | |||||||
| chr11:107606835 | A | G | 2 | a0001c0001t0002g0311 a0001c0002t0016g0269 |
2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-85-11270A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107606835 | |||||||
| chr11:107607110 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-85-10995G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107607110 | |||||||
| chr11:107607239 | C | T | 1 | a0001c0001t0001g0236 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-85-10866C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107607239 | |||||||
| chr11:107607430 | C | T | 1 | a0001c0001t0009g0120 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-85-10675C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107607430 | |||||||
| chr11:107607446 | A | T | 3 | a0001c0001t0001g0154 a0001c0001t0003g0153 a0001c0002t0006g0152 |
3 | HG00621.hp2 NA18966.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.-85-10659A>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107607446 | |||||||
| chr11:107607636 | G | A | 1 | a0001c0001t0002g0263 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-85-10469G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107607636 | |||||||
| chr11:107607656 | A | AAAAC | 4 | a0001c0001t0002g0130 a0001c0001t0008g0157 a0001c0001t0009g0129 others(1): Show |
4 | HG01884.hp1 HG03704.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.-85-10422_-85-1041 others(8): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107607656 | ||||||
| chr11:107607656 | AAAAC | A | 61 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(58): Show |
62 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.-85-10422_-85-1041 others(8): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107607656 | ||||||
| chr11:107607656 | AAAACAAA others(5): Show |
A | 34 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0322 others(31): Show |
34 | HG01081.hp2 HG01255.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.-85-10430_-85-1041 others(16): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107607656 | ||||||
| chr11:107607860 | G | C | 273 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(270): Show |
277 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.-85-10245G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107607860 | |||||||
| chr11:107607977 | T | G | 153 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(150): Show |
155 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.-85-10128T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107607977 | |||||||
| chr11:107608018 | TA | T | 25 | a0001c0001t0001g0154 a0001c0001t0002g0311 a0001c0001t0003g0153 others(22): Show |
25 | HG00621.hp2 HG01255.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.-85-10072delA | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107608018 | ||||||
| chr11:107608034 | GAAAAAAA others(1): Show |
G | 7 | a0001c0001t0002g0253 a0001c0001t0028g0256 a0001c0002t0004g0250 others(4): Show |
7 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-85-10068_-85-1006 others(12): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107608034 | ||||||
| chr11:107608095 | G | A | 1 | a0001c0001t0002g0097 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-85-10010G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107608095 | |||||||
| chr11:107608147 | G | T | 101 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0063 others(98): Show |
103 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.-85-9958G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107608147 | |||||||
| chr11:107608222 | G | A | 11 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0003g0065 others(8): Show |
11 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(8): Show |
intron_variant | MODIFIER | c.-85-9883G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107608222 | |||||||
| chr11:107608223 | C | A | 11 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0003g0065 others(8): Show |
11 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(8): Show |
intron_variant | MODIFIER | c.-85-9882C>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107608223 | |||||||
| chr11:107608249 | G | C | 1 | a0001c0002t0004g0007 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-85-9856G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107608249 | |||||||
| chr11:107608293 | A | G | 1 | a0001c0002t0004g0007 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-85-9812A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107608293 | |||||||
| chr11:107608356 | T | TA | 236 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(233): Show |
239 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.-85-9740dupA | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107608356 | ||||||
| chr11:107608356 | T | TAA | 16 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0322 others(13): Show |
16 | HG01081.hp2 HG01884.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.-85-9741_-85-9740d others(4): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107608356 | ||||||
| chr11:107608583 | A | G | 1 | a0001c0001t0003g0331 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-85-9522A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107608583 | |||||||
| chr11:107608752 | T | G | 254 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(251): Show |
257 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.-85-9353T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107608752 | |||||||
| chr11:107608919 | A | G | 61 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(58): Show |
62 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.-85-9186A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107608919 | |||||||
| chr11:107608926 | G | A | 254 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(251): Show |
257 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.-85-9179G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107608926 | |||||||
| chr11:107609295 | G | C | 1 | a0001c0001t0003g0162 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-85-8810G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107609295 | |||||||
| chr11:107609570 | C | T | 1 | a0001c0002t0004g0335 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-85-8535C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107609570 | |||||||
| chr11:107609718 | CAA | C | 4 | a0001c0001t0008g0284 a0001c0002t0004g0282 a0001c0002t0014g0281 others(1): Show |
4 | HG02148.hp2 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-8386_-85-8385d others(4): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107609718 | |||||||
| chr11:107609807 | C | T | 5 | a0001c0002t0006g0011 a0001c0002t0006g0012 a0001c0002t0006g0017 others(2): Show |
5 | NA18612.hp1 NA18944.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.-85-8298C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107609807 | |||||||
| chr11:107610006 | A | G | 12 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0322 others(9): Show |
12 | HG01081.hp2 HG01884.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.-85-8099A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107610006 | |||||||
| chr11:107610099 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-85-8006A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107610099 | |||||||
| chr11:107610521 | G | A | 1 | a0003c0005t0002g0088 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-85-7584G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107610521 | |||||||
| chr11:107610547 | T | C | 1 | a0001c0002t0004g0282 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-85-7558T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107610547 | |||||||
| chr11:107610587 | C | T | 1 | a0001c0002t0020g0006 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-85-7518C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107610587 | |||||||
| chr11:107610595 | A | G | 251 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(248): Show |
254 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.-85-7510A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107610595 | |||||||
| chr11:107610661 | T | TA | 9 | a0001c0001t0001g0028 a0001c0001t0001g0082 a0001c0001t0001g0148 others(6): Show |
9 | HG01981.hp2 HG02074.hp1 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.-85-7425dupA | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107610661 | ||||||
| chr11:107610661 | TA | T | 8 | a0001c0001t0001g0027 a0001c0001t0001g0337 a0001c0001t0002g0191 others(5): Show |
8 | HG00558.hp1 HG00609.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.-85-7425delA | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107610661 | ||||||
| chr11:107610725 | G | A | 34 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0322 others(31): Show |
34 | HG01081.hp2 HG01255.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.-85-7380G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107610725 | |||||||
| chr11:107610731 | A | C | 1 | a0001c0002t0007g0189 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-85-7374A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107610731 | |||||||
| chr11:107610792 | C | T | 151 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(148): Show |
153 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.-85-7313C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107610792 | |||||||
| chr11:107610974 | G | C | 2 | a0001c0002t0004g0279 a0001c0002t0004g0280 |
2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-85-7131G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107610974 | |||||||
| chr11:107610998 | C | CA | 88 | a0001c0001t0001g0125 a0001c0001t0001g0214 a0001c0001t0001g0215 others(85): Show |
89 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.-85-7088dupA | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107610998 | ||||||
| chr11:107610998 | C | CAA | 75 | a0001c0001t0001g0098 a0001c0001t0001g0116 a0001c0001t0001g0290 others(72): Show |
76 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.-85-7089_-85-7088d others(4): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107610998 | ||||||
| chr11:107610998 | C | CAAA | 37 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0063 others(34): Show |
38 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.-85-7090_-85-7088d others(5): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107610998 | ||||||
| chr11:107611013 | A | AAG | 43 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(40): Show |
43 | HG00408.hp2 HG00558.hp1 HG01123.hp2 others(40): Show |
intron_variant | MODIFIER | c.-85-7091_-85-7090i others(4): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107611013 | ||||||
| chr11:107611133 | C | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0139 |
3 | HG02109.hp1 HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-85-6972C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107611133 | |||||||
| chr11:107611155 | A | G | 2 | a0001c0001t0002g0311 a0001c0002t0016g0269 |
2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-85-6950A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107611155 | |||||||
| chr11:107611466 | C | T | 1 | a0001c0001t0003g0117 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-85-6639C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107611466 | |||||||
| chr11:107611475 | C | T | 5 | a0001c0001t0001g0146 a0001c0001t0008g0284 a0001c0002t0004g0282 others(2): Show |
5 | HG02148.hp2 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-85-6630C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107611475 | |||||||
| chr11:107611485 | G | A | 267 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(264): Show |
270 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.-85-6620G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107611485 | |||||||
| chr11:107611486 | G | C | 267 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(264): Show |
270 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.-85-6619G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107611486 | |||||||
| chr11:107611516 | C | A | 1 | a0001c0001t0001g0296 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-85-6589C>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107611516 | |||||||
| chr11:107611625 | A | T | 2 | a0001c0002t0009g0317 a0001c0002t0019g0318 |
2 | HG02280.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-85-6480A>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107611625 | |||||||
| chr11:107611697 | T | A | 2 | a0001c0001t0010g0140 a0001c0002t0004g0141 |
2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-85-6408T>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107611697 | |||||||
| chr11:107611704 | C | CA | 11 | a0001c0001t0001g0158 a0001c0001t0002g0311 a0001c0001t0003g0162 others(8): Show |
11 | HG00741.hp2 HG01109.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.-85-6377dupA | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107611704 | ||||||
| chr11:107611704 | CA | C | 162 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(159): Show |
164 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.-85-6377delA | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107611704 | ||||||
| chr11:107611704 | CAA | C | 63 | a0001c0001t0001g0116 a0001c0001t0001g0214 a0001c0001t0001g0215 others(60): Show |
64 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.-85-6378_-85-6377d others(4): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107611704 | ||||||
| chr11:107611864 | A | G | 1 | a0001c0006t0004g0055 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-85-6241A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107611864 | |||||||
| chr11:107611870 | G | A | 1 | a0001c0006t0004g0055 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-85-6235G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107611870 | |||||||
| chr11:107611950 | A | G | 1 | a0001c0001t0013g0304 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-85-6155A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107611950 | |||||||
| chr11:107612040 | T | C | 1 | a0001c0001t0008g0192 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-85-6065T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107612040 | |||||||
| chr11:107612045 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-85-6060C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107612045 | |||||||
| chr11:107612287 | T | C | 1 | a0001c0001t0002g0107 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-85-5818T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107612287 | |||||||
| chr11:107612590 | A | G | 34 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0322 others(31): Show |
34 | HG01081.hp2 HG01255.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.-85-5515A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107612590 | |||||||
| chr11:107612591 | G | C | 48 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(45): Show |
48 | HG00408.hp2 HG00558.hp1 HG01123.hp2 others(45): Show |
intron_variant | MODIFIER | c.-85-5514G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107612591 | |||||||
| chr11:107612743 | C | T | 150 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(147): Show |
152 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.-85-5362C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107612743 | |||||||
| chr11:107612803 | T | C | 1 | a0001c0001t0005g0086 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-85-5302T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107612803 | |||||||
| chr11:107612972 | G | C | 1 | a0001c0001t0002g0073 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-85-5133G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107612972 | |||||||
| chr11:107613243 | A | G | 1 | a0001c0002t0032g0254 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-85-4862A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107613243 | |||||||
| chr11:107613302 | C | G | 5 | a0001c0001t0002g0267 a0001c0001t0009g0266 a0001c0002t0005g0288 others(2): Show |
5 | HG00738.hp2 HG01099.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-85-4803C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107613302 | |||||||
| chr11:107613451 | A | G | 1 | a0001c0002t0020g0006 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-85-4654A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107613451 | |||||||
| chr11:107613486 | G | A | 1 | a0001c0006t0004g0055 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-85-4619G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107613486 | |||||||
| chr11:107613519 | GT | G | 9 | a0001c0001t0001g0221 a0001c0001t0001g0240 a0001c0001t0002g0005 others(6): Show |
10 | HG00280.hp2 HG01069.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.-85-4584delT | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107613519 | ||||||
| chr11:107613532 | A | G | 1 | a0001c0001t0002g0107 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-85-4573A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107613532 | |||||||
| chr11:107613599 | C | T | 2 | a0001c0001t0002g0311 a0001c0002t0016g0269 |
2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-85-4506C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107613599 | |||||||
| chr11:107613787 | A | G | 2 | a0001c0001t0003g0128 a0001c0001t0003g0132 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-85-4318A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107613787 | |||||||
| chr11:107613940 | A | G | 1 | a0001c0001t0002g0220 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-85-4165A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107613940 | |||||||
| chr11:107613980 | A | C | 5 | a0001c0001t0001g0184 a0001c0002t0006g0194 a0001c0002t0007g0183 others(2): Show |
5 | HG02015.hp2 NA18940.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.-85-4125A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107613980 | |||||||
| chr11:107614061 | T | C | 1 | a0001c0001t0003g0065 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-85-4044T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107614061 | |||||||
| chr11:107614172 | A | G | 34 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0322 others(31): Show |
34 | HG01081.hp2 HG01255.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.-85-3933A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107614172 | |||||||
| chr11:107614209 | T | G | 6 | a0001c0001t0002g0267 a0001c0001t0009g0266 a0001c0002t0005g0288 others(3): Show |
6 | HG00738.hp2 HG01099.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85-3896T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107614209 | |||||||
| chr11:107614273 | T | C | 15 | a0001c0001t0008g0284 a0001c0002t0002g0274 a0001c0002t0002g0275 others(12): Show |
15 | HG01255.hp2 HG02145.hp1 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.-85-3832T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107614273 | |||||||
| chr11:107614366 | G | A | 1 | a0001c0001t0003g0295 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-85-3739G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107614366 | |||||||
| chr11:107614417 | C | G | 1 | a0001c0002t0018g0272 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-85-3688C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107614417 | |||||||
| chr11:107614431 | C | T | 6 | a0001c0001t0002g0267 a0001c0001t0009g0266 a0001c0002t0005g0288 others(3): Show |
6 | HG00738.hp2 HG01099.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85-3674C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107614431 | |||||||
| chr11:107614434 | G | A | 1 | a0001c0001t0003g0108 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-85-3671G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107614434 | |||||||
| chr11:107614584 | G | A | 1 | a0001c0001t0002g0226 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-85-3521G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107614584 | |||||||
| chr11:107614587 | T | C | 225 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(222): Show |
228 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.-85-3518T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107614587 | |||||||
| chr11:107614685 | G | T | 17 | a0001c0001t0008g0284 a0001c0002t0002g0274 a0001c0002t0002g0275 others(14): Show |
17 | HG01255.hp2 HG02145.hp1 HG02148.hp2 others(14): Show |
intron_variant | MODIFIER | c.-85-3420G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107614685 | |||||||
| chr11:107614758 | G | A | 3 | a0001c0001t0002g0166 a0001c0001t0005g0164 a0001c0001t0005g0165 |
3 | HG01516.hp2 HG01517.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-85-3347G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107614758 | |||||||
| chr11:107614789 | G | A | 237 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(234): Show |
240 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.-85-3316G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107614789 | |||||||
| chr11:107614821 | G | A | 1 | a0001c0002t0034g0163 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-85-3284G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107614821 | |||||||
| chr11:107614838 | G | A | 241 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(238): Show |
244 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.-85-3267G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107614838 | |||||||
| chr11:107614940 | T | G | 1 | a0001c0001t0003g0032 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-85-3165T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107614940 | |||||||
| chr11:107614962 | C | A | 1 | a0001c0002t0004g0007 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-85-3143C>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107614962 | |||||||
| chr11:107615007 | C | G | 235 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(232): Show |
238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.-85-3098C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107615007 | |||||||
| chr11:107615229 | C | CT | 42 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0001g0146 others(39): Show |
43 | HG00621.hp2 HG00738.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.-85-2851dupT | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107615229 | ||||||
| chr11:107615229 | C | CTT | 115 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0066 others(112): Show |
118 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.-85-2852_-85-2851d others(4): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107615229 | ||||||
| chr11:107615229 | C | CTTT | 35 | a0001c0001t0001g0063 a0001c0001t0001g0080 a0001c0001t0001g0233 others(32): Show |
35 | HG00642.hp2 HG01070.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.-85-2853_-85-2851d others(5): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107615229 | ||||||
| chr11:107615229 | CT | C | 54 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(51): Show |
54 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.-85-2851delT | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107615229 | ||||||
| chr11:107615229 | CTT | C | 12 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0322 others(9): Show |
12 | HG01081.hp2 HG01884.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.-85-2852_-85-2851d others(4): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107615229 | ||||||
| chr11:107615260 | G | A | 236 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(233): Show |
239 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.-85-2845G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107615260 | |||||||
| chr11:107615305 | G | A | 58 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(55): Show |
59 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.-85-2800G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107615305 | |||||||
| chr11:107615310 | A | G | 6 | a0001c0001t0002g0267 a0001c0001t0009g0266 a0001c0002t0005g0288 others(3): Show |
6 | HG00738.hp2 HG01099.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85-2795A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107615310 | |||||||
| chr11:107615330 | G | A | 235 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(232): Show |
238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.-85-2775G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107615330 | |||||||
| chr11:107615361 | A | G | 236 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(233): Show |
239 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.-85-2744A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107615361 | |||||||
| chr11:107615398 | G | A | 1 | a0001c0002t0004g0282 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-85-2707G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107615398 | |||||||
| chr11:107615423 | C | T | 1 | a0001c0002t0027g0268 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-85-2682C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107615423 | |||||||
| chr11:107615695 | G | T | 2 | a0001c0001t0003g0128 a0001c0001t0003g0132 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-85-2410G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107615695 | |||||||
| chr11:107615832 | G | A | 1 | a0001c0001t0001g0010 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-85-2273G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107615832 | |||||||
| chr11:107615872 | A | G | 237 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(234): Show |
240 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.-85-2233A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107615872 | |||||||
| chr11:107615898 | G | C | 237 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(234): Show |
240 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.-85-2207G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107615898 | |||||||
| chr11:107615926 | T | C | 1 | a0001c0001t0002g0226 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-85-2179T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107615926 | |||||||
| chr11:107615985 | CT | C | 64 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0001g0146 others(61): Show |
66 | HG00099.hp2 HG00609.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.-85-2092delT | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107615985 | ||||||
| chr11:107615985 | CTTTTTTT | C | 19 | a0001c0001t0001g0021 a0001c0001t0001g0219 a0001c0001t0001g0232 others(16): Show |
19 | HG00544.hp2 HG02135.hp2 HG02602.hp1 others(16): Show |
intron_variant | MODIFIER | c.-85-2098_-85-2092d others(9): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107615985 | ||||||
| chr11:107615985 | CTTTTTTT others(1): Show |
C | 202 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(199): Show |
205 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.-85-2099_-85-2092d others(10): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107615985 | ||||||
| chr11:107615985 | CTTTTTTT others(2): Show |
C | 18 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0322 others(15): Show |
18 | HG00738.hp2 HG01081.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.-85-2100_-85-2092d others(11): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107615985 | ||||||
| chr11:107616045 | G | C | 1 | a0001c0001t0003g0331 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-85-2060G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107616045 | |||||||
| chr11:107616154 | C | G | 1 | a0001c0001t0002g0056 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-85-1951C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107616154 | |||||||
| chr11:107616256 | A | G | 1 | a0001c0001t0002g0048 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-85-1849A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107616256 | |||||||
| chr11:107616334 | C | G | 49 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(46): Show |
49 | HG00408.hp2 HG00558.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.-85-1771C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107616334 | |||||||
| chr11:107616441 | G | A | 1 | a0001c0002t0006g0012 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-85-1664G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107616441 | |||||||
| chr11:107616498 | T | C | 274 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(271): Show |
278 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.-85-1607T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107616498 | |||||||
| chr11:107616596 | C | T | 71 | a0001c0001t0001g0058 a0001c0001t0001g0098 a0001c0001t0001g0116 others(68): Show |
73 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-85-1509C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107616596 | |||||||
| chr11:107616603 | G | A | 104 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0063 others(101): Show |
106 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.-85-1502G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107616603 | |||||||
| chr11:107616658 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-85-1447C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107616658 | |||||||
| chr11:107616704 | GGCTAC | G | 3 | a0001c0002t0004g0270 a0001c0002t0010g0271 a0001c0002t0018g0272 |
3 | HG02486.hp2 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-85-1399_-85-1395d others(7): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 107616704 | ||||||
| chr11:107616811 | G | A | 2 | a0001c0002t0002g0285 a0001c0002t0002g0286 |
2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-85-1294G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107616811 | |||||||
| chr11:107617202 | C | T | 1 | a0001c0001t0010g0301 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-85-903C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107617202 | |||||||
| chr11:107617203 | G | A | 2 | a0001c0001t0002g0191 a0001c0001t0005g0086 |
2 | HG02630.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-85-902G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107617203 | |||||||
| chr11:107617314 | G | A | 1 | a0001c0001t0003g0331 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-85-791G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107617314 | |||||||
| chr11:107617701 | G | A | 1 | a0001c0006t0004g0055 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-85-404G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107617701 | |||||||
| chr11:107617775 | T | C | 2 | a0001c0001t0001g0061 a0001c0001t0001g0084 |
2 | HG00735.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-85-330T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107617775 | |||||||
| chr11:107617851 | C | T | 252 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(249): Show |
255 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.-85-254C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107617851 | |||||||
| chr11:107617999 | C | A | 1 | a0001c0001t0002g0074 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-85-106C>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 1/11 | chr11 | 107617999 | |||||||
| chr11:107618219 | G | A | 6 | a0001c0001t0001g0146 a0001c0001t0001g0260 a0001c0001t0005g0261 others(3): Show |
6 | HG01109.hp2 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.17+13G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107618219 | |||||||
| chr11:107618308 | G | A | 1 | a0001c0001t0002g0220 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.17+102G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107618308 | |||||||
| chr11:107618390 | G | A | 12 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0322 others(9): Show |
12 | HG01081.hp2 HG01884.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.17+184G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107618390 | |||||||
| chr11:107618496 | C | T | 1 | a0001c0001t0001g0300 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.17+290C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107618496 | |||||||
| chr11:107618910 | A | T | 1 | a0001c0002t0009g0259 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.17+704A>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107618910 | |||||||
| chr11:107618924 | G | T | 12 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0322 others(9): Show |
12 | HG01081.hp2 HG01884.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.17+718G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107618924 | |||||||
| chr11:107618936 | G | A | 51 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(48): Show |
52 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.17+730G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107618936 | |||||||
| chr11:107618966 | G | A | 3 | a0001c0001t0003g0331 a0001c0002t0004g0335 a0001c0006t0004g0055 |
3 | HG02647.hp1 HG03195.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.17+760G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107618966 | |||||||
| chr11:107618980 | C | G | 1 | a0001c0001t0002g0292 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.17+774C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107618980 | |||||||
| chr11:107619003 | A | C | 1 | a0001c0001t0002g0292 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.17+797A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107619003 | |||||||
| chr11:107619076 | T | A | 1 | a0001c0001t0003g0032 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.17+870T>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107619076 | |||||||
| chr11:107619143 | T | G | 1 | a0001c0002t0010g0271 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.17+937T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107619143 | |||||||
| chr11:107619278 | G | A | 1 | a0001c0001t0003g0200 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.17+1072G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107619278 | |||||||
| chr11:107619326 | A | G | 1 | a0001c0001t0002g0302 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.17+1120A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107619326 | |||||||
| chr11:107619597 | G | C | 49 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(46): Show |
49 | HG00408.hp2 HG00558.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.17+1391G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107619597 | |||||||
| chr11:107619646 | T | C | 2 | a0001c0001t0002g0267 a0001c0002t0027g0268 |
2 | HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.17+1440T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107619646 | |||||||
| chr11:107619664 | C | A | 3 | a0001c0002t0004g0270 a0001c0002t0010g0271 a0001c0002t0018g0272 |
3 | HG02486.hp2 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.17+1458C>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107619664 | |||||||
| chr11:107619825 | A | G | 1 | a0001c0001t0003g0072 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.17+1619A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107619825 | |||||||
| chr11:107619897 | ATTAT | A | 12 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0322 others(9): Show |
12 | HG01081.hp2 HG01884.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.17+1696_17+1699del others(4): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 107619897 | ||||||
| chr11:107620057 | C | T | 1 | a0001c0002t0005g0090 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.17+1851C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107620057 | |||||||
| chr11:107620110 | C | G | 1 | a0001c0001t0009g0225 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.17+1904C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107620110 | |||||||
| chr11:107620138 | C | T | 2 | a0001c0002t0006g0033 a0001c0002t0006g0047 |
2 | NA18959.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.17+1932C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107620138 | |||||||
| chr11:107620162 | G | A | 1 | a0001c0001t0002g0030 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.17+1956G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107620162 | |||||||
| chr11:107620475 | A | G | 59 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(56): Show |
60 | HG00408.hp2 HG00558.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.17+2269A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107620475 | |||||||
| chr11:107620506 | A | G | 3 | a0001c0001t0002g0267 a0001c0001t0009g0266 a0001c0002t0027g0268 |
3 | HG02723.hp2 HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.17+2300A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107620506 | |||||||
| chr11:107620610 | G | A | 2 | a0001c0002t0007g0217 a0001c0002t0007g0227 |
2 | NA18949.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.17+2404G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107620610 | |||||||
| chr11:107620731 | G | A | 3 | a0001c0001t0008g0284 a0001c0002t0004g0282 a0001c0002t0015g0283 |
3 | HG02148.hp2 HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.17+2525G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107620731 | |||||||
| chr11:107620732 | C | T | 1 | a0001c0002t0004g0335 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.17+2526C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107620732 | |||||||
| chr11:107620806 | G | T | 1 | a0001c0001t0008g0023 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.17+2600G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107620806 | |||||||
| chr11:107620857 | C | T | 43 | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0027 others(40): Show |
43 | HG00408.hp2 HG00558.hp1 HG01123.hp2 others(40): Show |
intron_variant | MODIFIER | c.17+2651C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107620857 | |||||||
| chr11:107620880 | G | A | 225 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(222): Show |
228 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.17+2674G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107620880 | |||||||
| chr11:107621079 | C | T | 3 | a0001c0002t0004g0007 a0001c0002t0005g0288 a0001c0002t0005g0289 |
3 | HG00738.hp2 HG01099.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.17+2873C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107621079 | |||||||
| chr11:107621105 | A | G | 1 | a0001c0006t0004g0055 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.17+2899A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107621105 | |||||||
| chr11:107621174 | T | C | 1 | a0001c0006t0004g0055 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.17+2968T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107621174 | |||||||
| chr11:107621234 | C | T | 2 | a0001c0001t0010g0140 a0001c0002t0004g0141 |
2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.17+3028C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107621234 | |||||||
| chr11:107621461 | T | G | 1 | a0001c0002t0010g0271 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.17+3255T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107621461 | |||||||
| chr11:107621473 | G | T | 92 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(89): Show |
94 | HG00408.hp2 HG00558.hp1 HG00738.hp2 others(91): Show |
intron_variant | MODIFIER | c.17+3267G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107621473 | |||||||
| chr11:107621538 | G | A | 1 | a0001c0002t0016g0269 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.17+3332G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107621538 | |||||||
| chr11:107621574 | A | G | 1 | a0001c0002t0022g0291 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.17+3368A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107621574 | |||||||
| chr11:107621641 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.17+3435C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107621641 | |||||||
| chr11:107621666 | T | TTCTCATG others(41): Show |
111 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(108): Show |
112 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.17+3479_17+3480ins others(48): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 107621666 | ||||||
| chr11:107621666 | T | TTCTCATG others(41): Show |
1 | a0001c0001t0003g0108 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.17+3462_17+3509dup others(48): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 107621666 | ||||||
| chr11:107621668 | C | T | 1 | a0001c0002t0016g0269 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.17+3462C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107621668 | |||||||
| chr11:107621686 | T | C | 186 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(183): Show |
188 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.17+3480T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107621686 | |||||||
| chr11:107621686 | T | TACCCCAT others(41): Show |
4 | a0001c0001t0001g0314 a0001c0001t0002g0166 a0001c0002t0004g0282 others(1): Show |
4 | HG01256.hp1 HG02723.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.17+3509_17+3510ins others(48): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 107621686 | ||||||
| chr11:107621894 | G | A | 2 | a0001c0001t0003g0149 a0001c0001t0003g0195 |
2 | HG01099.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.17+3688G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107621894 | |||||||
| chr11:107621911 | C | T | 116 | a0001c0001t0001g0004 a0001c0001t0001g0058 a0001c0001t0001g0067 others(113): Show |
117 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.17+3705C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107621911 | |||||||
| chr11:107621957 | G | A | 1 | a0001c0002t0016g0269 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.17+3751G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107621957 | |||||||
| chr11:107621975 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.17+3769C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107621975 | |||||||
| chr11:107622020 | T | C | 1 | a0001c0002t0005g0118 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.17+3814T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107622020 | |||||||
| chr11:107622091 | C | A | 2 | a0001c0001t0003g0128 a0001c0001t0003g0132 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.17+3885C>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107622091 | |||||||
| chr11:107622098 | A | G | 289 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(286): Show |
293 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(290): Show |
intron_variant | MODIFIER | c.17+3892A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107622098 | |||||||
| chr11:107622133 | T | C | 3 | a0001c0002t0012g0142 a0001c0002t0016g0269 a0001c0002t0017g0262 |
3 | HG01891.hp2 HG02922.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.17+3927T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107622133 | |||||||
| chr11:107622234 | G | T | 5 | a0001c0002t0002g0109 a0001c0002t0002g0121 a0001c0002t0002g0122 others(2): Show |
5 | HG02451.hp1 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.17+4028G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107622234 | |||||||
| chr11:107622380 | C | G | 15 | a0001c0001t0001g0125 a0001c0001t0002g0253 a0001c0001t0005g0086 others(12): Show |
15 | HG01168.hp2 HG01255.hp2 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.17+4174C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107622380 | |||||||
| chr11:107622478 | A | T | 1 | a0001c0001t0002g0294 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.17+4272A>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107622478 | |||||||
| chr11:107622598 | A | G | 1 | a0001c0002t0015g0283 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.17+4392A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107622598 | |||||||
| chr11:107622687 | A | G | 12 | a0001c0001t0002g0096 a0001c0001t0002g0126 a0001c0001t0002g0212 others(9): Show |
12 | HG01123.hp1 HG01243.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.17+4481A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107622687 | |||||||
| chr11:107622695 | T | C | 4 | a0001c0002t0005g0288 a0001c0002t0005g0289 a0001c0002t0020g0006 others(1): Show |
4 | HG00738.hp2 HG01099.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.17+4489T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107622695 | |||||||
| chr11:107622890 | G | A | 167 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0058 others(164): Show |
170 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.17+4684G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107622890 | |||||||
| chr11:107623045 | T | C | 9 | a0001c0001t0002g0311 a0001c0002t0002g0326 a0001c0002t0002g0328 others(6): Show |
9 | HG01884.hp2 HG01891.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.17+4839T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107623045 | |||||||
| chr11:107623061 | G | C | 13 | a0001c0001t0002g0107 a0001c0001t0002g0299 a0001c0001t0003g0135 others(10): Show |
13 | HG01168.hp1 HG01169.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.17+4855G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107623061 | |||||||
| chr11:107623067 | T | C | 1 | a0001c0001t0001g0216 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.17+4861T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107623067 | |||||||
| chr11:107623069 | T | C | 1 | a0001c0001t0025g0143 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.17+4863T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107623069 | |||||||
| chr11:107623112 | C | T | 5 | a0001c0002t0004g0250 a0001c0002t0004g0252 a0001c0002t0004g0327 others(2): Show |
5 | HG02615.hp1 HG02809.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.17+4906C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107623112 | |||||||
| chr11:107623124 | G | C | 8 | a0001c0001t0002g0263 a0001c0002t0002g0285 a0001c0002t0002g0286 others(5): Show |
8 | HG02109.hp2 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.17+4918G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107623124 | |||||||
| chr11:107623125 | A | C | 8 | a0001c0001t0002g0263 a0001c0002t0002g0285 a0001c0002t0002g0286 others(5): Show |
8 | HG02109.hp2 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.17+4919A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107623125 | |||||||
| chr11:107623127 | T | C | 8 | a0001c0001t0002g0263 a0001c0002t0002g0285 a0001c0002t0002g0286 others(5): Show |
8 | HG02109.hp2 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.17+4921T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107623127 | |||||||
| chr11:107623309 | C | T | 4 | a0001c0002t0002g0274 a0001c0002t0002g0275 a0001c0002t0002g0276 others(1): Show |
4 | HG01255.hp2 HG02280.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.17+5103C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107623309 | |||||||
| chr11:107623368 | C | G | 2 | a0001c0002t0004g0141 a0001c0002t0004g0282 |
2 | HG02145.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.17+5162C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107623368 | |||||||
| chr11:107623478 | C | T | 234 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(231): Show |
238 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(235): Show |
intron_variant | MODIFIER | c.17+5272C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107623478 | |||||||
| chr11:107623479 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.17+5273G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107623479 | |||||||
| chr11:107623632 | A | G | 2 | a0001c0001t0001g0078 a0001c0002t0006g0077 |
2 | HG00423.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.17+5426A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107623632 | |||||||
| chr11:107623679 | G | T | 104 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0019 others(101): Show |
105 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.17+5473G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107623679 | |||||||
| chr11:107623762 | A | C | 18 | a0001c0001t0002g0212 a0001c0001t0002g0263 a0001c0001t0002g0267 others(15): Show |
18 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.17+5556A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107623762 | |||||||
| chr11:107623770 | C | T | 1 | a0001c0001t0028g0256 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.17+5564C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107623770 | |||||||
| chr11:107624016 | G | A | 1 | a0001c0002t0004g0270 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.17+5810G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107624016 | |||||||
| chr11:107624236 | T | C | 2 | a0001c0001t0002g0267 a0001c0001t0010g0140 |
2 | HG02886.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.17+6030T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107624236 | |||||||
| chr11:107624417 | G | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0002t0015g0283 |
4 | HG02109.hp1 HG02717.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.18-6000G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107624417 | |||||||
| chr11:107624486 | A | G | 1 | a0001c0002t0015g0283 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.18-5931A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107624486 | |||||||
| chr11:107624514 | T | G | 178 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(175): Show |
180 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.18-5903T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107624514 | |||||||
| chr11:107624520 | G | A | 2 | a0001c0001t0005g0086 a0001c0001t0005g0261 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.18-5897G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107624520 | |||||||
| chr11:107624522 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0061 |
2 | HG01433.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.18-5895G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107624522 | |||||||
| chr11:107624542 | A | G | 1 | a0001c0002t0004g0087 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.18-5875A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107624542 | |||||||
| chr11:107624618 | C | T | 1 | a0001c0002t0015g0283 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.18-5799C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107624618 | |||||||
| chr11:107625277 | C | T | 1 | a0001c0002t0029g0034 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.18-5140C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107625277 | |||||||
| chr11:107625282 | T | A | 1 | a0001c0001t0003g0111 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.18-5135T>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107625282 | |||||||
| chr11:107625305 | T | G | 1 | a0001c0002t0002g0330 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.18-5112T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107625305 | |||||||
| chr11:107625417 | A | G | 1 | a0001c0001t0002g0212 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.18-5000A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107625417 | |||||||
| chr11:107625471 | C | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0002g0263 others(1): Show |
5 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.18-4946C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107625471 | |||||||
| chr11:107625542 | C | T | 1 | a0001c0001t0008g0157 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.18-4875C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107625542 | |||||||
| chr11:107625581 | C | T | 9 | a0001c0002t0005g0059 a0001c0002t0005g0090 a0001c0002t0005g0169 others(6): Show |
9 | HG00609.hp2 HG00738.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.18-4836C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107625581 | |||||||
| chr11:107625582 | G | A | 4 | a0001c0002t0005g0145 a0001c0002t0012g0142 a0001c0002t0016g0269 others(1): Show |
4 | HG01891.hp2 HG02486.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.18-4835G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107625582 | |||||||
| chr11:107625951 | C | A | 1 | a0001c0001t0002g0166 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.18-4466C>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107625951 | |||||||
| chr11:107625987 | A | T | 1 | a0001c0001t0001g0218 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.18-4430A>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107625987 | |||||||
| chr11:107626125 | A | T | 1 | a0001c0002t0002g0109 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.18-4292A>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107626125 | |||||||
| chr11:107626195 | T | C | 2 | a0001c0001t0002g0107 a0001c0002t0004g0335 |
2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.18-4222T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107626195 | |||||||
| chr11:107626240 | A | G | 72 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0078 others(69): Show |
72 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.18-4177A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107626240 | |||||||
| chr11:107626314 | C | G | 29 | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0058 others(26): Show |
29 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.18-4103C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107626314 | |||||||
| chr11:107626376 | G | GA | 11 | a0001c0001t0001g0021 a0001c0001t0001g0332 a0001c0002t0005g0059 others(8): Show |
11 | HG00609.hp2 HG00738.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.18-4024dupA | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 107626376 | ||||||
| chr11:107626376 | G | GAAA | 15 | a0001c0001t0001g0146 a0001c0001t0001g0156 a0001c0001t0001g0260 others(12): Show |
15 | HG01243.hp1 HG02145.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.18-4026_18-4024dup others(3): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 107626376 | ||||||
| chr11:107626376 | GA | G | 11 | a0001c0001t0001g0322 a0001c0001t0003g0195 a0001c0001t0008g0157 others(8): Show |
11 | HG01099.hp1 HG01109.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.18-4024delA | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 107626376 | ||||||
| chr11:107626513 | TCTCC | T | 3 | a0001c0001t0001g0125 a0001c0001t0002g0212 a0001c0001t0002g0253 |
3 | HG01243.hp2 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.18-3900_18-3897del others(4): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 107626513 | ||||||
| chr11:107626610 | C | CTTCT | 18 | a0001c0001t0001g0125 a0001c0001t0002g0212 a0001c0001t0002g0253 others(15): Show |
18 | HG01243.hp2 HG01884.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.18-3795_18-3792dup others(4): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 107626610 | ||||||
| chr11:107626620 | T | C | 1 | a0001c0001t0001g0019 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.18-3797T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107626620 | |||||||
| chr11:107626621 | C | T | 1 | a0001c0001t0001g0019 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.18-3796C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107626621 | |||||||
| chr11:107626656 | TTTTC | T | 34 | a0001c0001t0001g0125 a0001c0001t0001g0146 a0001c0001t0001g0156 others(31): Show |
34 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.18-3744_18-3741del others(4): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 107626656 | ||||||
| chr11:107626660 | C | CTTTCCCT others(15): Show |
152 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(149): Show |
154 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.18-3753_18-3752ins others(22): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 107626660 | ||||||
| chr11:107626717 | A | G | 2 | a0001c0002t0010g0324 a0001c0002t0010g0329 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.18-3700A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107626717 | |||||||
| chr11:107626886 | G | A | 4 | a0001c0001t0002g0292 a0001c0001t0009g0247 a0001c0001t0009g0248 others(1): Show |
4 | HG01123.hp1 HG02976.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.18-3531G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107626886 | |||||||
| chr11:107626916 | G | T | 1 | a0001c0001t0001g0218 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.18-3501G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107626916 | |||||||
| chr11:107627048 | G | A | 207 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(204): Show |
210 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.18-3369G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107627048 | |||||||
| chr11:107627089 | G | A | 1 | a0001c0001t0002g0073 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.18-3328G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107627089 | |||||||
| chr11:107627143 | T | C | 26 | a0001c0001t0001g0197 a0001c0001t0002g0267 a0001c0001t0005g0086 others(23): Show |
26 | HG01168.hp1 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.18-3274T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107627143 | |||||||
| chr11:107627604 | G | A | 12 | a0001c0002t0005g0059 a0001c0002t0005g0090 a0001c0002t0005g0169 others(9): Show |
12 | HG00609.hp2 HG00738.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.18-2813G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107627604 | |||||||
| chr11:107627604 | G | T | 1 | a0001c0001t0002g0048 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.18-2813G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107627604 | |||||||
| chr11:107627637 | C | T | 73 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(70): Show |
73 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.18-2780C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107627637 | |||||||
| chr11:107627673 | T | G | 5 | a0001c0001t0002g0074 a0001c0002t0007g0217 a0001c0002t0007g0227 others(2): Show |
5 | NA18949.hp1 NA18952.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.18-2744T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107627673 | |||||||
| chr11:107627792 | G | A | 13 | a0001c0001t0002g0267 a0001c0001t0010g0140 a0001c0002t0002g0285 others(10): Show |
13 | HG01884.hp2 HG02280.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.18-2625G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107627792 | |||||||
| chr11:107627837 | A | G | 26 | a0001c0001t0001g0197 a0001c0001t0002g0267 a0001c0001t0005g0086 others(23): Show |
26 | HG01168.hp1 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.18-2580A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107627837 | |||||||
| chr11:107627840 | T | A | 199 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(196): Show |
202 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.18-2577T>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107627840 | |||||||
| chr11:107628086 | C | CT | 9 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0002t0005g0113 others(6): Show |
10 | HG01168.hp2 HG02109.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.18-2318dupT | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 107628086 | ||||||
| chr11:107628086 | CT | C | 6 | a0001c0001t0001g0078 a0001c0002t0006g0050 a0001c0002t0006g0077 others(3): Show |
6 | HG00423.hp2 NA18942.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.18-2318delT | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 107628086 | ||||||
| chr11:107628160 | T | A | 13 | a0001c0001t0002g0267 a0001c0001t0010g0140 a0001c0002t0002g0285 others(10): Show |
13 | HG01884.hp2 HG02280.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.18-2257T>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107628160 | |||||||
| chr11:107628162 | TTTTTG | T | 10 | a0001c0001t0001g0197 a0001c0001t0005g0086 a0001c0001t0005g0115 others(7): Show |
10 | HG01168.hp1 HG01169.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.18-2236_18-2232del others(5): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 107628162 | ||||||
| chr11:107628163 | TTTTG | T | 12 | a0001c0001t0002g0267 a0001c0001t0010g0140 a0001c0002t0002g0285 others(9): Show |
12 | HG01884.hp2 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.18-2250_18-2247del others(4): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 107628163 | ||||||
| chr11:107628206 | C | T | 23 | a0001c0001t0001g0197 a0001c0001t0002g0267 a0001c0001t0005g0086 others(20): Show |
23 | HG01168.hp1 HG01169.hp2 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.18-2211C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107628206 | |||||||
| chr11:107628220 | G | C | 1 | a0001c0002t0005g0145 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.18-2197G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107628220 | |||||||
| chr11:107628412 | G | A | 1 | a0001c0002t0005g0169 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.18-2005G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107628412 | |||||||
| chr11:107628457 | G | A | 3 | a0001c0002t0012g0142 a0001c0002t0016g0269 a0001c0002t0017g0262 |
3 | HG01891.hp2 HG02922.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.18-1960G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107628457 | |||||||
| chr11:107628605 | G | C | 2 | a0001c0001t0002g0107 a0001c0002t0004g0335 |
2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.18-1812G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107628605 | |||||||
| chr11:107628726 | G | T | 1 | a0001c0006t0004g0055 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.18-1691G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107628726 | |||||||
| chr11:107629027 | A | C | 2 | a0001c0001t0002g0263 a0001c0002t0004g0007 |
2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.18-1390A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107629027 | |||||||
| chr11:107629246 | T | C | 2 | a0001c0001t0025g0143 a0001c0001t0028g0256 |
2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.18-1171T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107629246 | |||||||
| chr11:107629300 | AG | A | 3 | a0001c0002t0005g0113 a0001c0002t0005g0119 a0001c0002t0034g0163 |
3 | HG01168.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.18-1116delG | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107629300 | |||||||
| chr11:107629515 | C | T | 2 | a0001c0002t0005g0169 a0001c0002t0006g0054 |
2 | NA18612.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.18-902C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107629515 | |||||||
| chr11:107630223 | T | C | 2 | a0001c0001t0025g0143 a0001c0001t0028g0256 |
2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.18-194T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 2/11 | chr11 | 107630223 | |||||||
| chr11:107630968 | C | T | 8 | a0001c0001t0003g0071 a0001c0001t0003g0072 a0001c0002t0006g0062 others(5): Show |
8 | HG00423.hp1 HG00558.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.192+240C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 4/11 | chr11 | 107630968 | |||||||
| chr11:107631050 | A | G | 10 | a0001c0001t0001g0197 a0001c0001t0005g0086 a0001c0001t0005g0115 others(7): Show |
10 | HG01168.hp1 HG01169.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.192+322A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 4/11 | chr11 | 107631050 | |||||||
| chr11:107631089 | A | G | 1 | a0001c0002t0015g0283 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.192+361A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 4/11 | chr11 | 107631089 | |||||||
| chr11:107631387 | A | C | 1 | a0001c0001t0001g0019 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.193-193A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 4/11 | chr11 | 107631387 | |||||||
| chr11:107631397 | A | AC | 32 | a0001c0001t0002g0048 a0001c0001t0002g0220 a0001c0001t0003g0003 others(29): Show |
33 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.193-172dupC | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 107631397 | ||||||
| chr11:107631397 | A | ACC | 42 | a0001c0001t0001g0176 a0001c0001t0001g0300 a0001c0001t0002g0056 others(39): Show |
43 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.193-173_193-172dup others(2): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 107631397 | ||||||
| chr11:107631397 | A | ACCC | 44 | a0001c0001t0001g0027 a0001c0001t0002g0263 a0001c0001t0002g0311 others(41): Show |
44 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.193-174_193-172dup others(3): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 107631397 | ||||||
| chr11:107631397 | AC | A | 65 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(62): Show |
65 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.193-172delC | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 107631397 | ||||||
| chr11:107631397 | ACCC | A | 99 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0063 others(96): Show |
102 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.193-174_193-172del others(3): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 107631397 | ||||||
| chr11:107631402 | C | A | 1 | a0001c0002t0009g0259 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.193-178C>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 4/11 | chr11 | 107631402 | |||||||
| chr11:107631406 | C | G | 1 | a0001c0001t0003g0095 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.193-174C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 4/11 | chr11 | 107631406 | |||||||
| chr11:107631454 | A | C | 6 | a0001c0002t0002g0285 a0001c0002t0002g0286 a0001c0002t0009g0259 others(3): Show |
6 | HG02280.hp1 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.193-126A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 4/11 | chr11 | 107631454 | |||||||
| chr11:107631521 | G | A | 12 | a0001c0002t0005g0059 a0001c0002t0005g0090 a0001c0002t0005g0169 others(9): Show |
12 | HG00609.hp2 HG00738.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.193-59G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 4/11 | chr11 | 107631521 | |||||||
| chr11:107631953 | A | G | 7 | a0001c0001t0002g0005 a0001c0001t0002g0222 a0001c0001t0002g0224 others(4): Show |
8 | HG01069.hp1 HG01433.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.290+276A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107631953 | |||||||
| chr11:107632145 | G | A | 19 | a0001c0001t0001g0197 a0001c0001t0002g0267 a0001c0001t0005g0086 others(16): Show |
19 | HG01168.hp1 HG01169.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.290+468G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107632145 | |||||||
| chr11:107632151 | T | C | 1 | a0001c0001t0002g0220 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.290+474T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107632151 | |||||||
| chr11:107632230 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.290+553C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107632230 | |||||||
| chr11:107632231 | G | A | 2 | a0001c0001t0025g0143 a0001c0001t0028g0256 |
2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.290+554G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107632231 | |||||||
| chr11:107632274 | A | T | 12 | a0001c0001t0001g0146 a0001c0001t0001g0156 a0001c0001t0001g0260 others(9): Show |
12 | HG01243.hp1 HG02451.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.290+597A>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107632274 | |||||||
| chr11:107632295 | C | T | 1 | a0001c0002t0006g0069 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.290+618C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107632295 | |||||||
| chr11:107632393 | G | C | 3 | a0001c0002t0004g0277 a0001c0002t0004g0279 a0001c0002t0004g0280 |
3 | HG02922.hp1 HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.290+716G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107632393 | |||||||
| chr11:107632395 | A | C | 3 | a0001c0002t0004g0277 a0001c0002t0004g0279 a0001c0002t0004g0280 |
3 | HG02922.hp1 HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.290+718A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107632395 | |||||||
| chr11:107632409 | C | G | 1 | a0001c0001t0001g0232 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.290+732C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107632409 | |||||||
| chr11:107632721 | C | T | 208 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(205): Show |
211 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.290+1044C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107632721 | |||||||
| chr11:107632745 | C | A | 8 | a0001c0001t0003g0071 a0001c0001t0003g0072 a0001c0002t0006g0062 others(5): Show |
8 | HG00423.hp1 HG00558.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.290+1068C>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107632745 | |||||||
| chr11:107632750 | G | A | 5 | a0001c0002t0002g0326 a0001c0002t0002g0328 a0001c0002t0005g0325 others(2): Show |
5 | HG01884.hp2 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.290+1073G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107632750 | |||||||
| chr11:107633045 | G | T | 12 | a0001c0001t0001g0146 a0001c0001t0001g0156 a0001c0001t0001g0260 others(9): Show |
12 | HG01243.hp1 HG02451.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.290+1368G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107633045 | |||||||
| chr11:107633163 | G | A | 7 | a0001c0002t0004g0114 a0001c0002t0004g0202 a0001c0002t0004g0250 others(4): Show |
7 | HG02055.hp2 HG02451.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.290+1486G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107633163 | |||||||
| chr11:107633241 | C | T | 208 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(205): Show |
211 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.290+1564C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107633241 | |||||||
| chr11:107633290 | A | G | 5 | a0001c0002t0002g0326 a0001c0002t0002g0328 a0001c0002t0005g0325 others(2): Show |
5 | HG01884.hp2 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.290+1613A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107633290 | |||||||
| chr11:107633369 | T | C | 1 | a0001c0002t0027g0268 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.290+1692T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107633369 | |||||||
| chr11:107633519 | A | G | 208 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(205): Show |
211 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.290+1842A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107633519 | |||||||
| chr11:107633656 | C | T | 10 | a0001c0001t0001g0197 a0001c0001t0005g0086 a0001c0001t0005g0115 others(7): Show |
10 | HG01168.hp1 HG01169.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.290+1979C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107633656 | |||||||
| chr11:107633721 | G | A | 1 | a0001c0002t0002g0274 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.291-1915G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107633721 | |||||||
| chr11:107633965 | T | C | 8 | a0001c0001t0003g0071 a0001c0001t0003g0072 a0001c0002t0006g0062 others(5): Show |
8 | HG00423.hp1 HG00558.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.291-1671T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107633965 | |||||||
| chr11:107634066 | AT | A | 4 | a0001c0002t0005g0145 a0001c0002t0012g0142 a0001c0002t0016g0269 others(1): Show |
4 | HG01891.hp2 HG02486.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.291-1569delT | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107634066 | |||||||
| chr11:107634111 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.291-1525C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107634111 | |||||||
| chr11:107634611 | G | T | 1 | a0001c0006t0004g0055 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.291-1025G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107634611 | |||||||
| chr11:107634636 | G | C | 8 | a0001c0001t0002g0267 a0001c0001t0010g0140 a0001c0002t0002g0285 others(5): Show |
8 | HG02280.hp1 HG02572.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.291-1000G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107634636 | |||||||
| chr11:107634704 | G | A | 2 | a0001c0002t0012g0110 a0001c0002t0018g0272 |
2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.291-932G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107634704 | |||||||
| chr11:107634825 | C | T | 2 | a0001c0002t0004g0255 a0001c0002t0004g0287 |
2 | HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.291-811C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107634825 | |||||||
| chr11:107634918 | T | A | 14 | a0001c0001t0001g0146 a0001c0001t0001g0156 a0001c0001t0001g0260 others(11): Show |
14 | HG01243.hp1 HG02451.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.291-718T>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107634918 | |||||||
| chr11:107634974 | C | T | 1 | a0001c0001t0008g0060 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.291-662C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107634974 | |||||||
| chr11:107635000 | T | C | 1 | a0001c0001t0003g0068 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.291-636T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107635000 | |||||||
| chr11:107635191 | C | A | 75 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0063 others(72): Show |
78 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.291-445C>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107635191 | |||||||
| chr11:107635237 | T | C | 2 | a0001c0001t0003g0002 a0001c0001t0003g0111 |
3 | HG01255.hp1 HG01261.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.291-399T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107635237 | |||||||
| chr11:107635257 | A | G | 1 | a0001c0002t0004g0007 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.291-379A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107635257 | |||||||
| chr11:107635552 | T | A | 2 | a0001c0001t0005g0086 a0001c0001t0005g0261 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.291-84T>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107635552 | |||||||
| chr11:107635631 | C | T | 1 | a0001c0001t0001g0296 | 1 | NA18986.hp2 | splice_region_variant&intron_variant | LOW | c.291-5C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 5/11 | chr11 | 107635631 | |||||||
| chr11:107635823 | C | G | 1 | a0001c0002t0004g0114 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.420+58C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107635823 | |||||||
| chr11:107635823 | C | T | 5 | a0001c0002t0002g0326 a0001c0002t0002g0328 a0001c0002t0005g0325 others(2): Show |
5 | HG01884.hp2 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.420+58C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107635823 | |||||||
| chr11:107636007 | G | A | 1 | a0001c0002t0010g0316 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.420+242G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107636007 | |||||||
| chr11:107636111 | G | A | 19 | a0001c0001t0001g0197 a0001c0001t0002g0267 a0001c0001t0005g0086 others(16): Show |
19 | HG01168.hp1 HG01169.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.420+346G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107636111 | |||||||
| chr11:107636196 | A | G | 22 | a0001c0001t0001g0197 a0001c0001t0002g0267 a0001c0001t0005g0086 others(19): Show |
22 | HG01168.hp1 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.420+431A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107636196 | |||||||
| chr11:107636276 | T | C | 19 | a0001c0001t0001g0197 a0001c0001t0002g0267 a0001c0001t0005g0086 others(16): Show |
19 | HG01168.hp1 HG01169.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.420+511T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107636276 | |||||||
| chr11:107636531 | T | G | 1 | a0001c0002t0006g0112 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.420+766T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107636531 | |||||||
| chr11:107636532 | G | A | 4 | a0001c0001t0001g0237 a0001c0001t0002g0022 a0001c0001t0002g0030 others(1): Show |
4 | HG02056.hp1 NA18943.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.420+767G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107636532 | |||||||
| chr11:107636623 | G | A | 21 | a0001c0001t0001g0197 a0001c0001t0002g0267 a0001c0001t0005g0086 others(18): Show |
21 | HG01109.hp2 HG01168.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.420+858G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107636623 | |||||||
| chr11:107636625 | G | A | 73 | a0001c0001t0001g0019 a0001c0001t0001g0063 a0001c0001t0001g0125 others(70): Show |
75 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.420+860G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107636625 | |||||||
| chr11:107636655 | T | C | 12 | a0001c0002t0005g0059 a0001c0002t0005g0090 a0001c0002t0005g0169 others(9): Show |
12 | HG00609.hp2 HG00738.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.420+890T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107636655 | |||||||
| chr11:107637096 | C | T | 1 | a0001c0001t0003g0095 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.420+1331C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107637096 | |||||||
| chr11:107637125 | C | T | 1 | a0001c0006t0004g0055 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.420+1360C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107637125 | |||||||
| chr11:107637237 | A | G | 3 | a0001c0002t0005g0113 a0001c0002t0005g0119 a0001c0002t0034g0163 |
3 | HG01168.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.420+1472A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107637237 | |||||||
| chr11:107637306 | G | C | 5 | a0001c0002t0002g0326 a0001c0002t0002g0328 a0001c0002t0005g0325 others(2): Show |
5 | HG01884.hp2 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.420+1541G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107637306 | |||||||
| chr11:107637464 | G | A | 12 | a0001c0001t0001g0021 a0001c0001t0001g0066 a0001c0001t0001g0093 others(9): Show |
12 | HG00544.hp2 HG00621.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.420+1699G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107637464 | |||||||
| chr11:107637706 | C | CA | 70 | a0001c0001t0001g0027 a0001c0001t0001g0078 a0001c0001t0002g0074 others(67): Show |
70 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.420+1954dupA | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 107637706 | ||||||
| chr11:107637706 | CA | C | 74 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(71): Show |
74 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.420+1954delA | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 107637706 | ||||||
| chr11:107637734 | C | T | 1 | a0001c0002t0005g0145 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.420+1969C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107637734 | |||||||
| chr11:107637820 | G | C | 97 | a0001c0001t0001g0027 a0001c0001t0001g0078 a0001c0001t0001g0197 others(94): Show |
97 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.420+2055G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107637820 | |||||||
| chr11:107637916 | T | C | 1 | a0001c0002t0002g0121 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.420+2151T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107637916 | |||||||
| chr11:107637970 | G | A | 1 | a0001c0001t0010g0140 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.420+2205G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107637970 | |||||||
| chr11:107638036 | A | C | 1 | a0001c0002t0004g0141 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.420+2271A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107638036 | |||||||
| chr11:107638106 | C | T | 267 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(264): Show |
270 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.420+2341C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107638106 | |||||||
| chr11:107638183 | T | C | 14 | a0001c0001t0001g0146 a0001c0001t0001g0156 a0001c0001t0001g0260 others(11): Show |
14 | HG01243.hp1 HG02451.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.420+2418T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107638183 | |||||||
| chr11:107638194 | A | T | 4 | a0001c0002t0005g0145 a0001c0002t0012g0142 a0001c0002t0016g0269 others(1): Show |
4 | HG01891.hp2 HG02486.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.420+2429A>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107638194 | |||||||
| chr11:107638798 | C | T | 2 | a0001c0002t0006g0062 a0001c0002t0031g0070 |
2 | NA18988.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.420+3033C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107638798 | |||||||
| chr11:107638813 | G | A | 2 | a0001c0002t0004g0141 a0001c0002t0004g0282 |
2 | HG02145.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.420+3048G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107638813 | |||||||
| chr11:107639170 | A | G | 1 | a0001c0001t0002g0305 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.420+3405A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107639170 | |||||||
| chr11:107639252 | A | G | 75 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0063 others(72): Show |
78 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.420+3487A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107639252 | |||||||
| chr11:107639682 | A | G | 3 | a0001c0002t0012g0142 a0001c0002t0016g0269 a0001c0002t0017g0262 |
3 | HG01891.hp2 HG02922.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.420+3917A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107639682 | |||||||
| chr11:107639783 | A | G | 1 | a0001c0001t0001g0314 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.420+4018A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107639783 | |||||||
| chr11:107639803 | G | A | 287 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(284): Show |
290 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(287): Show |
intron_variant | MODIFIER | c.420+4038G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107639803 | |||||||
| chr11:107639832 | TGAGTGGA others(7): Show |
T | 1 | a0001c0002t0004g0273 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.420+4072_420+4085d others(16): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 107639832 | ||||||
| chr11:107640075 | C | G | 1 | a0001c0002t0004g0210 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.420+4310C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107640075 | |||||||
| chr11:107640135 | C | T | 3 | a0001c0002t0012g0142 a0001c0002t0016g0269 a0001c0002t0017g0262 |
3 | HG01891.hp2 HG02922.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.420+4370C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107640135 | |||||||
| chr11:107640263 | A | G | 1 | a0001c0001t0002g0311 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.420+4498A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107640263 | |||||||
| chr11:107640376 | A | G | 6 | a0001c0002t0002g0285 a0001c0002t0002g0286 a0001c0002t0009g0259 others(3): Show |
6 | HG02280.hp1 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.420+4611A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107640376 | |||||||
| chr11:107640377 | T | C | 1 | a0001c0001t0028g0256 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.420+4612T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107640377 | |||||||
| chr11:107640391 | A | G | 2 | a0001c0002t0010g0271 a0001c0002t0022g0291 |
2 | HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.420+4626A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107640391 | |||||||
| chr11:107640694 | T | A | 2 | a0001c0001t0025g0143 a0001c0001t0028g0256 |
2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.420+4929T>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107640694 | |||||||
| chr11:107640702 | T | C | 2 | a0001c0002t0012g0110 a0001c0002t0018g0272 |
2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.420+4937T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107640702 | |||||||
| chr11:107641160 | T | C | 209 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(206): Show |
212 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.420+5395T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107641160 | |||||||
| chr11:107641161 | G | A | 1 | a0001c0001t0003g0162 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.420+5396G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107641161 | |||||||
| chr11:107641172 | G | A | 1 | a0001c0002t0007g0170 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.420+5407G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107641172 | |||||||
| chr11:107641313 | A | G | 1 | a0001c0001t0003g0223 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.420+5548A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107641313 | |||||||
| chr11:107641317 | G | GTA | 11 | a0001c0001t0003g0223 a0001c0001t0008g0180 a0001c0002t0005g0059 others(8): Show |
11 | HG00609.hp2 HG00738.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.420+5568_420+5569d others(4): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 107641317 | ||||||
| chr11:107641317 | GTA | G | 114 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(111): Show |
115 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.420+5568_420+5569d others(4): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 107641317 | ||||||
| chr11:107641333 | A | C | 32 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0001g0197 others(29): Show |
33 | HG01168.hp1 HG01168.hp2 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.420+5568A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107641333 | |||||||
| chr11:107641335 | C | A | 2 | a0001c0001t0025g0143 a0001c0001t0028g0256 |
2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.420+5570C>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107641335 | |||||||
| chr11:107641369 | T | G | 3 | a0001c0002t0005g0288 a0001c0002t0005g0289 a0001c0002t0020g0006 |
3 | HG00738.hp2 HG01099.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.420+5604T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107641369 | |||||||
| chr11:107641645 | A | G | 1 | a0001c0001t0001g0290 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.421-5823A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107641645 | |||||||
| chr11:107641706 | T | C | 1 | a0001c0001t0002g0056 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.421-5762T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107641706 | |||||||
| chr11:107641939 | C | CT | 22 | a0001c0001t0001g0028 a0001c0001t0001g0176 a0001c0001t0002g0073 others(19): Show |
23 | HG01255.hp2 HG01358.hp1 HG01515.hp2 others(20): Show |
intron_variant | MODIFIER | c.421-5505dupT | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 107641939 | ||||||
| chr11:107641939 | CT | C | 110 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0053 others(107): Show |
112 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(109): Show |
intron_variant | MODIFIER | c.421-5505delT | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 107641939 | ||||||
| chr11:107641939 | CTT | C | 6 | a0001c0001t0001g0146 a0001c0001t0002g0052 a0001c0001t0003g0195 others(3): Show |
6 | HG00609.hp2 HG01099.hp1 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.421-5506_421-5505d others(4): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 107641939 | ||||||
| chr11:107641939 | CTTTTTTT | C | 22 | a0001c0001t0001g0197 a0001c0001t0002g0267 a0001c0001t0005g0086 others(19): Show |
22 | HG01168.hp2 HG01169.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.421-5511_421-5505d others(9): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 107641939 | ||||||
| chr11:107641983 | C | T | 1 | a0001c0002t0010g0316 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.421-5485C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107641983 | |||||||
| chr11:107642178 | A | G | 2 | a0001c0001t0025g0143 a0001c0001t0028g0256 |
2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.421-5290A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107642178 | |||||||
| chr11:107642390 | A | T | 2 | a0001c0002t0002g0121 a0001c0002t0002g0122 |
2 | HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.421-5078A>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107642390 | |||||||
| chr11:107642414 | G | T | 2 | a0001c0001t0001g0310 a0001c0001t0024g0308 |
2 | HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.421-5054G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107642414 | |||||||
| chr11:107642471 | C | G | 1 | a0001c0001t0028g0256 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.421-4997C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107642471 | |||||||
| chr11:107642526 | C | T | 1 | a0001c0001t0002g0048 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.421-4942C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107642526 | |||||||
| chr11:107642661 | A | G | 20 | a0001c0001t0001g0197 a0001c0001t0002g0267 a0001c0001t0005g0086 others(17): Show |
20 | HG01109.hp2 HG01168.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.421-4807A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107642661 | |||||||
| chr11:107642734 | A | T | 10 | a0001c0001t0001g0197 a0001c0001t0005g0086 a0001c0001t0005g0115 others(7): Show |
10 | HG01168.hp1 HG01169.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.421-4734A>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107642734 | |||||||
| chr11:107642852 | A | G | 1 | a0001c0001t0002g0191 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.421-4616A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107642852 | |||||||
| chr11:107642861 | T | G | 2 | a0001c0001t0025g0143 a0001c0001t0028g0256 |
2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.421-4607T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107642861 | |||||||
| chr11:107642874 | T | C | 1 | a0001c0001t0025g0143 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.421-4594T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107642874 | |||||||
| chr11:107643136 | G | A | 1 | a0001c0001t0002g0030 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.421-4332G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107643136 | |||||||
| chr11:107643199 | T | C | 2 | a0001c0001t0025g0143 a0001c0001t0028g0256 |
2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.421-4269T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107643199 | |||||||
| chr11:107643368 | G | GA | 75 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(72): Show |
75 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.421-4083dupA | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 107643368 | ||||||
| chr11:107643368 | GA | G | 22 | a0001c0001t0001g0197 a0001c0001t0002g0267 a0001c0001t0005g0086 others(19): Show |
22 | HG01109.hp2 HG01168.hp1 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.421-4083delA | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 107643368 | ||||||
| chr11:107643475 | G | A | 1 | a0001c0002t0010g0316 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.421-3993G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107643475 | |||||||
| chr11:107643587 | C | T | 1 | a0001c0001t0002g0005 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.421-3881C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107643587 | |||||||
| chr11:107643594 | T | C | 19 | a0001c0002t0005g0059 a0001c0002t0005g0090 a0001c0002t0005g0145 others(16): Show |
19 | HG00609.hp2 HG00738.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.421-3874T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107643594 | |||||||
| chr11:107643665 | A | G | 20 | a0001c0001t0001g0197 a0001c0001t0002g0267 a0001c0001t0005g0086 others(17): Show |
20 | HG01109.hp2 HG01168.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.421-3803A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107643665 | |||||||
| chr11:107643699 | T | C | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | NA18959.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.421-3769T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107643699 | |||||||
| chr11:107643765 | G | T | 39 | a0001c0001t0001g0019 a0001c0001t0001g0063 a0001c0001t0001g0237 others(36): Show |
40 | HG00609.hp1 HG01069.hp1 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.421-3703G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107643765 | |||||||
| chr11:107643786 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0002g0263 |
2 | HG02109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.421-3682G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107643786 | |||||||
| chr11:107644000 | C | T | 1 | a0001c0002t0011g0016 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.421-3468C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107644000 | |||||||
| chr11:107644066 | A | C | 10 | a0001c0002t0002g0109 a0001c0002t0002g0326 a0001c0002t0002g0328 others(7): Show |
10 | HG01884.hp2 HG02280.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.421-3402A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107644066 | |||||||
| chr11:107644121 | A | G | 1 | a0001c0001t0008g0023 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.421-3347A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107644121 | |||||||
| chr11:107644141 | C | T | 1 | a0001c0001t0003g0002 | 2 | HG01255.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.421-3327C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107644141 | |||||||
| chr11:107644292 | T | C | 2 | a0001c0002t0004g0279 a0001c0002t0004g0280 |
2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.421-3176T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107644292 | |||||||
| chr11:107644458 | G | GAT | 4 | a0001c0001t0002g0074 a0001c0001t0002g0220 a0001c0001t0010g0321 others(1): Show |
4 | HG00280.hp1 HG01081.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.421-2996_421-2995d others(4): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 107644458 | ||||||
| chr11:107644481 | T | G | 4 | a0001c0002t0006g0029 a0001c0002t0006g0033 a0001c0002t0006g0047 others(1): Show |
4 | NA18959.hp1 NA18968.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.421-2987T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107644481 | |||||||
| chr11:107644577 | C | T | 1 | a0001c0001t0025g0143 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.421-2891C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107644577 | |||||||
| chr11:107644748 | A | C | 1 | a0001c0002t0004g0213 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.421-2720A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107644748 | |||||||
| chr11:107644756 | A | G | 20 | a0001c0001t0001g0197 a0001c0001t0002g0267 a0001c0001t0005g0086 others(17): Show |
20 | HG01168.hp1 HG01168.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.421-2712A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107644756 | |||||||
| chr11:107644852 | A | G | 1 | a0002c0003t0008g0015 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.421-2616A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107644852 | |||||||
| chr11:107644907 | G | GGTTTTT | 12 | a0001c0001t0003g0065 a0001c0002t0002g0109 a0001c0002t0002g0326 others(9): Show |
12 | HG01884.hp2 HG02280.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.421-2529_421-2524d others(8): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 107644907 | ||||||
| chr11:107644907 | GGTTTTT | G | 14 | a0001c0001t0001g0146 a0001c0001t0001g0156 a0001c0001t0001g0260 others(11): Show |
14 | HG01109.hp2 HG01243.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.421-2529_421-2524d others(8): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 107644907 | ||||||
| chr11:107644907 | GGTTTTTG others(5): Show |
G | 6 | a0001c0002t0002g0121 a0001c0002t0002g0122 a0001c0002t0002g0124 others(3): Show |
6 | HG02451.hp1 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.421-2535_421-2524d others(14): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 107644907 | ||||||
| chr11:107644908 | G | GT | 72 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(69): Show |
72 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.421-2555dupT | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 107644908 | ||||||
| chr11:107644913 | TGTTTTTG | T | 14 | a0001c0001t0001g0197 a0001c0001t0005g0086 a0001c0001t0005g0115 others(11): Show |
14 | HG01168.hp1 HG01168.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.421-2554_421-2548d others(9): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107644913 | |||||||
| chr11:107644914 | G | T | 166 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(163): Show |
169 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.421-2554G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107644914 | |||||||
| chr11:107644920 | G | T | 14 | a0001c0001t0001g0146 a0001c0001t0001g0156 a0001c0001t0001g0260 others(11): Show |
14 | HG01109.hp2 HG01243.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.421-2548G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107644920 | |||||||
| chr11:107644926 | G | T | 6 | a0001c0002t0002g0121 a0001c0002t0002g0122 a0001c0002t0002g0124 others(3): Show |
6 | HG02451.hp1 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.421-2542G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107644926 | |||||||
| chr11:107645089 | A | AT | 108 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0027 others(105): Show |
108 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.421-2358dupT | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 107645089 | ||||||
| chr11:107645089 | A | ATT | 74 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0093 others(71): Show |
77 | HG00099.hp1 HG00621.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.421-2359_421-2358d others(4): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 107645089 | ||||||
| chr11:107645089 | A | ATTT | 15 | a0001c0001t0001g0019 a0001c0001t0001g0063 a0001c0001t0001g0214 others(12): Show |
15 | HG00609.hp1 HG00642.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.421-2360_421-2358d others(5): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 107645089 | ||||||
| chr11:107645089 | AT | A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0156 a0001c0001t0001g0260 others(6): Show |
9 | HG01070.hp1 HG01071.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.421-2358delT | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 107645089 | ||||||
| chr11:107645217 | G | A | 1 | a0001c0001t0002g0100 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.421-2251G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107645217 | |||||||
| chr11:107645289 | C | T | 2 | a0001c0002t0012g0142 a0001c0002t0017g0262 |
2 | HG01891.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.421-2179C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107645289 | |||||||
| chr11:107645383 | G | A | 3 | a0001c0002t0012g0142 a0001c0002t0016g0269 a0001c0002t0017g0262 |
3 | HG01891.hp2 HG02922.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.421-2085G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107645383 | |||||||
| chr11:107645410 | G | A | 2 | a0001c0001t0002g0267 a0001c0001t0010g0140 |
2 | HG02886.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.421-2058G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107645410 | |||||||
| chr11:107645575 | C | T | 16 | a0001c0002t0005g0059 a0001c0002t0005g0090 a0001c0002t0005g0145 others(13): Show |
16 | HG00609.hp2 HG00738.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.421-1893C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107645575 | |||||||
| chr11:107645731 | T | C | 76 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0063 others(73): Show |
79 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.421-1737T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107645731 | |||||||
| chr11:107645778 | G | C | 2 | a0001c0001t0025g0143 a0001c0001t0028g0256 |
2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.421-1690G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107645778 | |||||||
| chr11:107646074 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.421-1394A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107646074 | |||||||
| chr11:107646080 | A | T | 1 | a0001c0002t0005g0169 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.421-1388A>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107646080 | |||||||
| chr11:107646083 | G | T | 2 | a0001c0001t0025g0143 a0001c0001t0028g0256 |
2 | HG01109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.421-1385G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107646083 | |||||||
| chr11:107646177 | G | A | 1 | a0001c0001t0002g0126 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.421-1291G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107646177 | |||||||
| chr11:107646221 | C | CTT | 30 | a0001c0001t0001g0197 a0001c0001t0002g0267 a0001c0001t0005g0086 others(27): Show |
30 | HG01109.hp2 HG01168.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.421-1246_421-1245i others(4): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 107646221 | ||||||
| chr11:107646456 | C | T | 20 | a0001c0001t0001g0197 a0001c0001t0002g0267 a0001c0001t0005g0086 others(17): Show |
20 | HG01109.hp2 HG01168.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.421-1012C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107646456 | |||||||
| chr11:107646504 | G | A | 1 | a0001c0002t0004g0206 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.421-964G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107646504 | |||||||
| chr11:107646563 | C | T | 2 | a0001c0002t0009g0259 a0001c0002t0010g0316 |
2 | HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.421-905C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107646563 | |||||||
| chr11:107646564 | G | T | 1 | a0001c0001t0013g0304 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.421-904G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107646564 | |||||||
| chr11:107646730 | G | A | 1 | a0001c0001t0003g0162 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.421-738G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107646730 | |||||||
| chr11:107646921 | T | C | 1 | a0001c0001t0005g0167 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.421-547T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107646921 | |||||||
| chr11:107646943 | A | AATCT | 69 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0061 others(66): Show |
71 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.421-483_421-480dup others(4): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 107646943 | ||||||
| chr11:107646943 | A | AATCTATC others(1): Show |
8 | a0001c0001t0002g0005 a0001c0001t0002g0096 a0001c0001t0002g0193 others(5): Show |
9 | HG00639.hp1 HG01099.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.421-487_421-480dup others(8): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 107646943 | ||||||
| chr11:107646943 | AATCT | A | 64 | a0001c0001t0001g0146 a0001c0001t0001g0241 a0001c0001t0001g0244 others(61): Show |
65 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.421-483_421-480del others(4): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 107646943 | ||||||
| chr11:107646943 | AATCTATC others(1): Show |
A | 92 | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0058 others(89): Show |
92 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.421-487_421-480del others(8): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 107646943 | ||||||
| chr11:107646943 | AATCTATC others(5): Show |
A | 1 | a0001c0002t0004g0277 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.421-491_421-480del others(12): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 107646943 | ||||||
| chr11:107646943 | AATCTATC others(9): Show |
A | 1 | a0001c0001t0001g0010 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.421-495_421-480del others(16): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 107646943 | ||||||
| chr11:107646949 | T | C | 1 | a0001c0002t0015g0283 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.421-519T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107646949 | |||||||
| chr11:107646954 | C | A | 1 | a0001c0001t0028g0256 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.421-514C>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107646954 | |||||||
| chr11:107646980 | A | G | 1 | a0001c0001t0003g0200 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.421-488A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107646980 | |||||||
| chr11:107647004 | T | C | 14 | a0001c0001t0001g0146 a0001c0001t0001g0156 a0001c0001t0001g0260 others(11): Show |
14 | HG01243.hp1 HG02451.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.421-464T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107647004 | |||||||
| chr11:107647292 | G | A | 76 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0063 others(73): Show |
79 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.421-176G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107647292 | |||||||
| chr11:107647461 | C | T | 1 | a0001c0002t0027g0268 | 1 | HG02723.hp2 | splice_region_variant&intron_variant | LOW | c.421-7C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 6/11 | chr11 | 107647461 | |||||||
| chr11:107647698 | C | A | 1 | a0001c0001t0002g0005 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.554+97C>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 7/11 | chr11 | 107647698 | |||||||
| chr11:107647701 | A | G | 1 | a0001c0001t0003g0003 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.554+100A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 7/11 | chr11 | 107647701 | |||||||
| chr11:107648102 | C | T | 208 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(205): Show |
211 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.554+501C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 7/11 | chr11 | 107648102 | |||||||
| chr11:107648147 | A | G | 1 | a0001c0001t0025g0143 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.554+546A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 7/11 | chr11 | 107648147 | |||||||
| chr11:107648240 | G | C | 76 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0063 others(73): Show |
79 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.554+639G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 7/11 | chr11 | 107648240 | |||||||
| chr11:107648597 | T | C | 1 | a0003c0005t0002g0088 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.554+996T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 7/11 | chr11 | 107648597 | |||||||
| chr11:107648721 | C | T | 20 | a0001c0001t0001g0197 a0001c0001t0002g0267 a0001c0001t0005g0086 others(17): Show |
20 | HG01109.hp2 HG01168.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.554+1120C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 7/11 | chr11 | 107648721 | |||||||
| chr11:107648764 | A | AT | 329 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(326): Show |
334 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.554+1175dupT | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 107648764 | ||||||
| chr11:107648797 | C | T | 34 | a0001c0001t0001g0146 a0001c0001t0001g0156 a0001c0001t0001g0197 others(31): Show |
34 | HG01109.hp2 HG01168.hp1 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.554+1196C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 7/11 | chr11 | 107648797 | |||||||
| chr11:107648984 | T | C | 10 | a0001c0002t0005g0059 a0001c0002t0005g0090 a0001c0002t0005g0145 others(7): Show |
10 | HG00609.hp2 HG00738.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.555-1351T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 7/11 | chr11 | 107648984 | |||||||
| chr11:107649077 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.555-1258T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 7/11 | chr11 | 107649077 | |||||||
| chr11:107649156 | A | G | 20 | a0001c0001t0001g0197 a0001c0001t0002g0267 a0001c0001t0005g0086 others(17): Show |
20 | HG01109.hp2 HG01168.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.555-1179A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 7/11 | chr11 | 107649156 | |||||||
| chr11:107649192 | T | C | 1 | a0001c0001t0002g0096 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.555-1143T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 7/11 | chr11 | 107649192 | |||||||
| chr11:107649218 | A | G | 10 | a0001c0002t0005g0059 a0001c0002t0005g0090 a0001c0002t0005g0145 others(7): Show |
10 | HG00609.hp2 HG00738.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.555-1117A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 7/11 | chr11 | 107649218 | |||||||
| chr11:107649516 | C | T | 1 | a0001c0001t0003g0200 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.555-819C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 7/11 | chr11 | 107649516 | |||||||
| chr11:107649562 | G | A | 1 | a0001c0001t0009g0225 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.555-773G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 7/11 | chr11 | 107649562 | |||||||
| chr11:107649694 | C | T | 2 | a0001c0001t0005g0127 a0001c0001t0005g0134 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.555-641C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 7/11 | chr11 | 107649694 | |||||||
| chr11:107649965 | A | G | 1 | a0001c0002t0009g0259 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.555-370A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 7/11 | chr11 | 107649965 | |||||||
| chr11:107650080 | G | C | 1 | a0001c0001t0001g0245 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.555-255G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 7/11 | chr11 | 107650080 | |||||||
| chr11:107650257 | C | T | 3 | a0001c0001t0001g0148 a0001c0001t0001g0232 a0001c0001t0001g0240 |
3 | HG01981.hp2 HG02602.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.555-78C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 7/11 | chr11 | 107650257 | |||||||
| chr11:107650287 | G | A | 3 | a0001c0001t0001g0150 a0001c0001t0001g0199 a0001c0001t0001g0236 |
3 | NA18947.hp1 NA18947.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.555-48G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 7/11 | chr11 | 107650287 | |||||||
| chr11:107650463 | C | T | 1 | a0001c0001t0001g0332 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.623+60C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 8/11 | chr11 | 107650463 | |||||||
| chr11:107650476 | C | G | 1 | a0001c0001t0002g0226 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.623+73C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 8/11 | chr11 | 107650476 | |||||||
| chr11:107650554 | T | C | 8 | a0001c0001t0002g0030 a0001c0001t0002g0089 a0001c0001t0002g0100 others(5): Show |
8 | HG00741.hp1 HG01496.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.623+151T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 8/11 | chr11 | 107650554 | |||||||
| chr11:107650912 | T | C | 2 | a0001c0002t0009g0144 a0001c0002t0012g0091 |
2 | HG02559.hp2 HG03486.hp2 |
splice_region_variant&intron_variant | LOW | c.647+4T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 9/11 | chr11 | 107650912 | |||||||
| chr11:107651133 | C | T | 2 | a0001c0001t0003g0128 a0001c0001t0003g0132 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.647+225C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 9/11 | chr11 | 107651133 | |||||||
| chr11:107651192 | C | T | 1 | a0001c0002t0007g0076 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.647+284C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 9/11 | chr11 | 107651192 | |||||||
| chr11:107651318 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0139 |
3 | HG02109.hp1 HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.647+410G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 9/11 | chr11 | 107651318 | |||||||
| chr11:107651364 | T | A | 2 | a0001c0002t0010g0271 a0001c0002t0022g0291 |
2 | HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.647+456T>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 9/11 | chr11 | 107651364 | |||||||
| chr11:107651571 | C | T | 6 | a0001c0002t0002g0109 a0001c0002t0002g0326 a0001c0002t0002g0328 others(3): Show |
6 | HG01884.hp2 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.647+663C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 9/11 | chr11 | 107651571 | |||||||
| chr11:107651620 | C | G | 4 | a0001c0001t0002g0267 a0001c0001t0010g0140 a0001c0002t0002g0285 others(1): Show |
4 | HG02572.hp1 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.647+712C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 9/11 | chr11 | 107651620 | |||||||
| chr11:107651636 | CT | C | 13 | a0001c0001t0001g0146 a0001c0001t0001g0156 a0001c0001t0001g0260 others(10): Show |
13 | HG01243.hp1 HG02451.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.647+731delT | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 107651636 | ||||||
| chr11:107652043 | C | T | 1 | a0001c0006t0004g0055 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.647+1135C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 9/11 | chr11 | 107652043 | |||||||
| chr11:107652413 | GTGTT | G | 3 | a0001c0001t0003g0003 a0001c0001t0005g0101 a0001c0001t0005g0167 |
4 | HG00099.hp2 HG01358.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.647+1511_647+1514d others(6): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 107652413 | ||||||
| chr11:107652664 | G | T | 1 | a0001c0001t0005g0137 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.648-1508G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 9/11 | chr11 | 107652664 | |||||||
| chr11:107652982 | C | A | 1 | a0001c0001t0008g0138 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.648-1190C>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 9/11 | chr11 | 107652982 | |||||||
| chr11:107653078 | G | A | 17 | a0001c0001t0025g0143 a0001c0002t0005g0059 a0001c0002t0005g0090 others(14): Show |
17 | HG00609.hp2 HG00738.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.648-1094G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 9/11 | chr11 | 107653078 | |||||||
| chr11:107653250 | T | A | 1 | a0001c0001t0008g0060 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.648-922T>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 9/11 | chr11 | 107653250 | |||||||
| chr11:107653335 | A | AAG | 14 | a0001c0001t0001g0197 a0001c0001t0002g0253 a0001c0001t0005g0086 others(11): Show |
14 | HG00099.hp2 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.648-813_648-812dup others(2): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 107653335 | ||||||
| chr11:107653335 | AAGAG | A | 63 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0021 others(60): Show |
63 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.648-815_648-812del others(4): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 107653335 | ||||||
| chr11:107653335 | AAGAGAGA others(5): Show |
A | 3 | a0001c0001t0003g0128 a0001c0001t0003g0132 a0001c0001t0003g0173 |
3 | HG00639.hp1 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.648-823_648-812del others(12): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 107653335 | ||||||
| chr11:107653584 | A | C | 88 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(85): Show |
88 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.648-588A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 9/11 | chr11 | 107653584 | |||||||
| chr11:107653599 | C | G | 24 | a0001c0001t0001g0116 a0001c0001t0001g0187 a0001c0001t0010g0140 others(21): Show |
24 | HG01070.hp2 HG02145.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.648-573C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 9/11 | chr11 | 107653599 | |||||||
| chr11:107653649 | C | G | 1 | a0001c0001t0028g0256 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.648-523C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 9/11 | chr11 | 107653649 | |||||||
| chr11:107653859 | C | T | 202 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0139 others(199): Show |
204 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.648-313C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 9/11 | chr11 | 107653859 | |||||||
| chr11:107653862 | G | A | 10 | a0001c0001t0001g0197 a0001c0001t0005g0101 a0001c0001t0005g0115 others(7): Show |
10 | HG00099.hp2 HG01168.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.648-310G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 9/11 | chr11 | 107653862 | |||||||
| chr11:107654242 | T | C | 3 | a0001c0001t0002g0306 a0001c0001t0010g0230 a0001c0001t0010g0301 |
3 | HG00642.hp1 HG00735.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.698+20T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | chr11 | 107654242 | |||||||
| chr11:107654301 | A | G | 1 | a0001c0001t0002g0226 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.698+79A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | chr11 | 107654301 | |||||||
| chr11:107654386 | T | C | 1 | a0001c0001t0002g0107 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.698+164T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | chr11 | 107654386 | |||||||
| chr11:107654410 | G | A | 1 | a0001c0001t0025g0143 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.698+188G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | chr11 | 107654410 | |||||||
| chr11:107654498 | G | A | 3 | a0001c0002t0012g0142 a0001c0002t0016g0269 a0001c0002t0017g0262 |
3 | HG01891.hp2 HG02922.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.698+276G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | chr11 | 107654498 | |||||||
| chr11:107654516 | T | G | 7 | a0001c0001t0002g0005 a0001c0001t0002g0222 a0001c0001t0002g0224 others(4): Show |
8 | HG01069.hp1 HG01433.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.698+294T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | chr11 | 107654516 | |||||||
| chr11:107654555 | G | C | 2 | a0001c0002t0010g0271 a0001c0002t0022g0291 |
2 | HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.698+333G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | chr11 | 107654555 | |||||||
| chr11:107654570 | C | T | 5 | a0001c0001t0001g0010 a0001c0001t0001g0058 a0001c0001t0001g0082 others(2): Show |
5 | NA18951.hp1 NA18962.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.698+348C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | chr11 | 107654570 | |||||||
| chr11:107654596 | C | T | 6 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0001g0146 others(3): Show |
7 | HG01243.hp1 HG02109.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.698+374C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | chr11 | 107654596 | |||||||
| chr11:107654658 | A | G | 1 | a0001c0001t0008g0334 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.698+436A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | chr11 | 107654658 | |||||||
| chr11:107654693 | T | C | 1 | a0001c0001t0002g0263 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.698+471T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | chr11 | 107654693 | |||||||
| chr11:107654716 | T | C | 73 | a0001c0001t0001g0125 a0001c0001t0002g0005 a0001c0001t0002g0022 others(70): Show |
74 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.698+494T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | chr11 | 107654716 | |||||||
| chr11:107654750 | C | T | 1 | a0001c0002t0006g0112 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.698+528C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | chr11 | 107654750 | |||||||
| chr11:107654762 | C | T | 7 | a0001c0001t0002g0096 a0001c0001t0002g0226 a0001c0001t0002g0306 others(4): Show |
7 | HG00642.hp1 HG00735.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.698+540C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | chr11 | 107654762 | |||||||
| chr11:107654768 | C | CA | 18 | a0001c0001t0001g0004 a0001c0001t0001g0080 a0001c0001t0001g0139 others(15): Show |
19 | HG00558.hp2 HG01109.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.698+565dupA | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 107654768 | ||||||
| chr11:107654768 | C | CAA | 14 | a0001c0001t0005g0086 a0001c0001t0005g0101 a0001c0001t0005g0115 others(11): Show |
14 | HG00099.hp2 HG01168.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.698+564_698+565dup others(2): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 107654768 | ||||||
| chr11:107654768 | CA | C | 8 | a0001c0001t0001g0019 a0001c0001t0001g0319 a0001c0001t0008g0081 others(5): Show |
8 | HG01169.hp1 HG02486.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.698+565delA | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 107654768 | ||||||
| chr11:107654828 | T | C | 1 | a0001c0002t0010g0316 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.698+606T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | chr11 | 107654828 | |||||||
| chr11:107654856 | T | A | 1 | a0001c0001t0001g0063 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.698+634T>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | chr11 | 107654856 | |||||||
| chr11:107654857 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.698+635A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | chr11 | 107654857 | |||||||
| chr11:107654858 | G | T | 1 | a0001c0001t0001g0063 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.698+636G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | chr11 | 107654858 | |||||||
| chr11:107654904 | G | T | 1 | a0001c0002t0005g0298 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.698+682G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | chr11 | 107654904 | |||||||
| chr11:107655037 | C | T | 12 | a0001c0002t0005g0001 a0001c0002t0005g0059 a0001c0002t0005g0090 others(9): Show |
13 | HG00609.hp2 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.698+815C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | chr11 | 107655037 | |||||||
| chr11:107655076 | C | A | 1 | a0001c0001t0001g0053 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.698+854C>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | chr11 | 107655076 | |||||||
| chr11:107655159 | C | CTG | 294 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(291): Show |
297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.699-770_699-769dup others(2): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 107655159 | ||||||
| chr11:107655256 | T | C | 7 | a0001c0002t0002g0109 a0001c0002t0002g0286 a0001c0002t0002g0326 others(4): Show |
7 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.699-677T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | chr11 | 107655256 | |||||||
| chr11:107655264 | T | G | 293 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(290): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.699-669T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | chr11 | 107655264 | |||||||
| chr11:107655342 | A | G | 3 | a0001c0002t0005g0113 a0001c0002t0005g0119 a0001c0002t0034g0163 |
3 | HG01168.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.699-591A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | chr11 | 107655342 | |||||||
| chr11:107655376 | C | T | 3 | a0001c0002t0012g0110 a0001c0002t0012g0205 a0001c0002t0018g0272 |
3 | HG02486.hp2 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.699-557C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | chr11 | 107655376 | |||||||
| chr11:107655423 | A | G | 1 | a0001c0001t0009g0120 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.699-510A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | chr11 | 107655423 | |||||||
| chr11:107655503 | C | T | 1 | a0001c0001t0008g0284 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.699-430C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | chr11 | 107655503 | |||||||
| chr11:107655561 | T | C | 1 | a0001c0001t0001g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.699-372T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | chr11 | 107655561 | |||||||
| chr11:107655573 | C | CTTT | 16 | a0001c0002t0002g0121 a0001c0002t0002g0122 a0001c0002t0002g0124 others(13): Show |
16 | HG02055.hp2 HG02280.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.699-347_699-345dup others(3): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 107655573 | ||||||
| chr11:107655573 | C | CTTTT | 11 | a0001c0002t0005g0001 a0001c0002t0005g0059 a0001c0002t0005g0118 others(8): Show |
12 | HG00609.hp2 HG00738.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.699-348_699-345dup others(4): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 107655573 | ||||||
| chr11:107655573 | C | CTTTTTTT others(1): Show |
55 | a0001c0001t0001g0125 a0001c0001t0002g0005 a0001c0001t0002g0022 others(52): Show |
56 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.699-352_699-345dup others(8): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 107655573 | ||||||
| chr11:107655573 | C | CTTTTTTT others(2): Show |
6 | a0001c0001t0002g0193 a0001c0001t0002g0253 a0001c0001t0009g0225 others(3): Show |
6 | HG01081.hp2 HG01433.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.699-353_699-345dup others(9): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 107655573 | ||||||
| chr11:107655573 | C | CTTTTTTT others(3): Show |
14 | a0001c0001t0005g0101 a0001c0001t0005g0115 a0001c0001t0005g0127 others(11): Show |
14 | HG00099.hp2 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.699-354_699-345dup others(10): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 107655573 | ||||||
| chr11:107655573 | C | CTTTTTTT others(4): Show |
8 | a0001c0001t0002g0263 a0001c0001t0005g0086 a0001c0002t0004g0114 others(5): Show |
8 | HG01169.hp1 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.699-355_699-345dup others(11): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 107655573 | ||||||
| chr11:107655573 | C | CTTTTTTT others(5): Show |
73 | a0001c0001t0001g0053 a0001c0001t0001g0063 a0001c0001t0001g0098 others(70): Show |
73 | HG00408.hp2 HG00423.hp1 HG01070.hp2 others(70): Show |
intron_variant | MODIFIER | c.699-356_699-345dup others(12): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 107655573 | ||||||
| chr11:107655573 | C | CTTTTTTT others(6): Show |
70 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(67): Show |
70 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.699-357_699-345dup others(13): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 107655573 | ||||||
| chr11:107655573 | C | CTTTTTTT others(7): Show |
17 | a0001c0001t0001g0021 a0001c0001t0001g0078 a0001c0001t0001g0158 others(14): Show |
17 | HG00280.hp2 HG00423.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.699-358_699-345dup others(14): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 107655573 | ||||||
| chr11:107655573 | C | CTTTTTTT others(8): Show |
2 | a0001c0001t0001g0084 a0001c0001t0001g0237 |
2 | HG00735.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.699-359_699-345dup others(15): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 107655573 | ||||||
| chr11:107655573 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0026g0234 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.699-345_699-344ins others(16): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 107655573 | ||||||
| chr11:107655649 | G | A | 1 | a0001c0001t0001g0310 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.699-284G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 10/11 | chr11 | 107655649 | |||||||
| chr11:107656258 | C | T | 1 | a0001c0001t0002g0226 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.832+192C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107656258 | |||||||
| chr11:107656319 | T | C | 1 | a0001c0001t0003g0068 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.832+253T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107656319 | |||||||
| chr11:107656420 | TTA | T | 138 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0001g0146 others(135): Show |
140 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.832+363_832+364del others(2): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr11 | 107656420 | ||||||
| chr11:107656436 | A | G | 1 | a0001c0001t0002g0299 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.832+370A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107656436 | |||||||
| chr11:107656487 | G | T | 128 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0001g0146 others(125): Show |
130 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.832+421G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107656487 | |||||||
| chr11:107656569 | C | A | 1 | a0001c0001t0001g0158 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.832+503C>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107656569 | |||||||
| chr11:107656611 | T | C | 138 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0001g0146 others(135): Show |
140 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.832+545T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107656611 | |||||||
| chr11:107656641 | T | C | 5 | a0001c0002t0004g0007 a0001c0002t0004g0204 a0001c0002t0004g0207 others(2): Show |
5 | HG02145.hp1 HG02257.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.832+575T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107656641 | |||||||
| chr11:107656775 | A | G | 296 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(293): Show |
299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.832+709A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107656775 | |||||||
| chr11:107656930 | G | A | 1 | a0001c0001t0009g0120 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.832+864G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107656930 | |||||||
| chr11:107656934 | C | T | 93 | a0001c0001t0002g0263 a0001c0001t0008g0031 a0001c0002t0002g0109 others(90): Show |
93 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.832+868C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107656934 | |||||||
| chr11:107657005 | T | C | 1 | a0001c0002t0006g0112 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.832+939T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107657005 | |||||||
| chr11:107657023 | A | C | 1 | a0001c0001t0003g0295 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.832+957A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107657023 | |||||||
| chr11:107657220 | T | A | 75 | a0001c0001t0001g0125 a0001c0001t0002g0005 a0001c0001t0002g0022 others(72): Show |
76 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.832+1154T>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107657220 | |||||||
| chr11:107657297 | A | C | 4 | a0001c0002t0010g0316 a0001c0002t0012g0110 a0001c0002t0012g0205 others(1): Show |
4 | HG02486.hp2 HG02895.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.832+1231A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107657297 | |||||||
| chr11:107657414 | C | T | 138 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0001g0146 others(135): Show |
140 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.832+1348C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107657414 | |||||||
| chr11:107657458 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.832+1392G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107657458 | |||||||
| chr11:107657459 | C | T | 2 | a0001c0001t0003g0032 a0001c0001t0003g0092 |
2 | HG02165.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.832+1393C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107657459 | |||||||
| chr11:107657460 | C | T | 1 | a0001c0002t0006g0033 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.832+1394C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107657460 | |||||||
| chr11:107657525 | C | T | 1 | a0001c0002t0007g0099 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.832+1459C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107657525 | |||||||
| chr11:107657629 | A | C | 138 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0001g0146 others(135): Show |
140 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.832+1563A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107657629 | |||||||
| chr11:107657677 | C | A | 1 | a0001c0001t0025g0143 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.832+1611C>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107657677 | |||||||
| chr11:107657759 | G | A | 80 | a0001c0001t0008g0031 a0001c0002t0004g0007 a0001c0002t0004g0087 others(77): Show |
80 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.832+1693G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107657759 | |||||||
| chr11:107657946 | T | C | 138 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0001g0146 others(135): Show |
140 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.832+1880T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107657946 | |||||||
| chr11:107658047 | CTA | C | 138 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0001g0146 others(135): Show |
140 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.832+1983_832+1984d others(4): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr11 | 107658047 | ||||||
| chr11:107658070 | G | A | 2 | a0001c0001t0005g0164 a0001c0001t0005g0165 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.832+2004G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107658070 | |||||||
| chr11:107658092 | A | G | 1 | a0001c0001t0009g0129 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.832+2026A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107658092 | |||||||
| chr11:107658247 | T | C | 138 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0001g0146 others(135): Show |
140 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.832+2181T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107658247 | |||||||
| chr11:107658257 | C | T | 12 | a0001c0002t0005g0001 a0001c0002t0005g0059 a0001c0002t0005g0090 others(9): Show |
13 | HG00609.hp2 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.832+2191C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107658257 | |||||||
| chr11:107658293 | T | G | 11 | a0001c0001t0005g0086 a0001c0001t0005g0101 a0001c0001t0005g0115 others(8): Show |
11 | HG00099.hp2 HG01168.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.832+2227T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107658293 | |||||||
| chr11:107658803 | C | T | 1 | a0001c0002t0005g0298 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.832+2737C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107658803 | |||||||
| chr11:107658868 | G | A | 2 | a0001c0001t0003g0002 a0001c0001t0003g0111 |
3 | HG01255.hp1 HG01261.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.832+2802G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107658868 | |||||||
| chr11:107658996 | G | T | 4 | a0001c0002t0006g0009 a0001c0002t0006g0062 a0001c0002t0006g0155 others(1): Show |
4 | NA18988.hp1 NA18998.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.832+2930G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107658996 | |||||||
| chr11:107659108 | G | A | 158 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(155): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.832+3042G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107659108 | |||||||
| chr11:107659214 | G | A | 139 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0001g0146 others(136): Show |
141 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.832+3148G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107659214 | |||||||
| chr11:107659309 | A | G | 297 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(294): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.832+3243A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107659309 | |||||||
| chr11:107659411 | G | A | 158 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(155): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.832+3345G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107659411 | |||||||
| chr11:107659551 | A | G | 127 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0001g0146 others(124): Show |
128 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.832+3485A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107659551 | |||||||
| chr11:107659551 | A | T | 12 | a0001c0002t0005g0001 a0001c0002t0005g0059 a0001c0002t0005g0090 others(9): Show |
13 | HG00609.hp2 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.832+3485A>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107659551 | |||||||
| chr11:107659643 | TTGGG | T | 31 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0001g0146 others(28): Show |
32 | HG01243.hp1 HG01255.hp2 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.832+3597_832+3600d others(6): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr11 | 107659643 | ||||||
| chr11:107659651 | G | T | 7 | a0001c0002t0002g0285 a0001c0002t0009g0144 a0001c0002t0009g0259 others(4): Show |
7 | HG02280.hp1 HG02559.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.832+3585G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107659651 | |||||||
| chr11:107659655 | GTGGGTGG others(5): Show |
G | 1 | a0001c0001t0008g0138 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.832+3593_832+3604d others(14): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr11 | 107659655 | ||||||
| chr11:107659659 | GTGGGTGG others(1): Show |
G | 6 | a0001c0002t0002g0121 a0001c0002t0002g0122 a0001c0002t0002g0124 others(3): Show |
6 | HG02451.hp1 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.832+3597_832+3604d others(10): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr11 | 107659659 | ||||||
| chr11:107659663 | G | A | 102 | a0001c0001t0002g0263 a0001c0001t0008g0031 a0001c0002t0002g0109 others(99): Show |
103 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.832+3597G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107659663 | |||||||
| chr11:107659663 | G | GTGGA | 5 | a0001c0001t0001g0053 a0001c0001t0001g0319 a0001c0001t0002g0212 others(2): Show |
5 | HG01081.hp2 HG01243.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.832+3641_832+3644d others(6): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr11 | 107659663 | ||||||
| chr11:107659663 | GTGGA | G | 101 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(98): Show |
101 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.832+3641_832+3644d others(6): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr11 | 107659663 | ||||||
| chr11:107659667 | A | G | 4 | a0001c0001t0001g0084 a0001c0001t0001g0221 a0001c0001t0003g0188 others(1): Show |
4 | HG00280.hp2 HG00735.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.832+3601A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107659667 | |||||||
| chr11:107659703 | A | C | 7 | a0001c0002t0002g0109 a0001c0002t0002g0286 a0001c0002t0002g0328 others(4): Show |
7 | HG00408.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.832+3637A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107659703 | |||||||
| chr11:107659707 | A | C | 112 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0001g0146 others(109): Show |
113 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.832+3641A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107659707 | |||||||
| chr11:107659773 | C | A | 138 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0001g0146 others(135): Show |
140 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.832+3707C>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107659773 | |||||||
| chr11:107659789 | C | T | 5 | a0001c0002t0002g0121 a0001c0002t0002g0122 a0001c0002t0002g0124 others(2): Show |
5 | HG02451.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.832+3723C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107659789 | |||||||
| chr11:107659790 | G | A | 2 | a0001c0001t0001g0322 a0001c0001t0001g0323 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.832+3724G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107659790 | |||||||
| chr11:107659912 | A | G | 17 | a0001c0002t0002g0121 a0001c0002t0002g0122 a0001c0002t0002g0124 others(14): Show |
18 | HG00609.hp2 HG00738.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.832+3846A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107659912 | |||||||
| chr11:107659992 | C | T | 1 | a0001c0002t0005g0145 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.832+3926C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107659992 | |||||||
| chr11:107660061 | G | A | 12 | a0001c0001t0002g0263 a0001c0002t0002g0109 a0001c0002t0002g0286 others(9): Show |
12 | HG01884.hp2 HG02109.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.832+3995G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107660061 | |||||||
| chr11:107660066 | A | C | 1 | a0001c0002t0027g0268 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.832+4000A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107660066 | |||||||
| chr11:107660127 | A | C | 1 | a0001c0001t0002g0226 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.832+4061A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107660127 | |||||||
| chr11:107660204 | T | C | 9 | a0001c0002t0005g0113 a0001c0002t0005g0119 a0001c0002t0006g0029 others(6): Show |
9 | HG01168.hp2 HG03491.hp2 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.832+4138T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107660204 | |||||||
| chr11:107660338 | T | G | 1 | a0001c0001t0003g0295 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.832+4272T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107660338 | |||||||
| chr11:107660482 | C | G | 297 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(294): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.832+4416C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107660482 | |||||||
| chr11:107660555 | C | T | 1 | a0001c0001t0001g0296 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.833-4470C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107660555 | |||||||
| chr11:107660594 | C | T | 138 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0001g0146 others(135): Show |
140 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.833-4431C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107660594 | |||||||
| chr11:107660649 | G | A | 2 | a0001c0001t0001g0322 a0001c0001t0001g0323 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.833-4376G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107660649 | |||||||
| chr11:107660662 | A | G | 3 | a0001c0002t0012g0110 a0001c0002t0012g0205 a0001c0002t0018g0272 |
3 | HG02486.hp2 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.833-4363A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107660662 | |||||||
| chr11:107660704 | T | C | 18 | a0001c0002t0002g0121 a0001c0002t0002g0122 a0001c0002t0002g0124 others(15): Show |
19 | HG00609.hp2 HG00738.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.833-4321T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107660704 | |||||||
| chr11:107660706 | G | C | 82 | a0001c0001t0008g0031 a0001c0002t0004g0007 a0001c0002t0004g0087 others(79): Show |
82 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.833-4319G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107660706 | |||||||
| chr11:107660778 | G | C | 2 | a0001c0001t0005g0101 a0001c0001t0005g0167 |
2 | HG00099.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.833-4247G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107660778 | |||||||
| chr11:107660829 | C | T | 3 | a0001c0001t0001g0116 a0001c0001t0001g0176 a0001c0001t0001g0187 |
3 | HG02056.hp2 NA18974.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.833-4196C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107660829 | |||||||
| chr11:107660967 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.833-4058A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107660967 | |||||||
| chr11:107661033 | C | T | 297 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(294): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.833-3992C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107661033 | |||||||
| chr11:107661094 | C | G | 297 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(294): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.833-3931C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107661094 | |||||||
| chr11:107661112 | C | A | 297 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(294): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.833-3913C>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107661112 | |||||||
| chr11:107661124 | A | T | 1 | a0003c0005t0002g0088 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.833-3901A>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107661124 | |||||||
| chr11:107661191 | C | T | 139 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0001g0146 others(136): Show |
141 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.833-3834C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107661191 | |||||||
| chr11:107661200 | G | A | 139 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0001g0146 others(136): Show |
141 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.833-3825G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107661200 | |||||||
| chr11:107661345 | T | G | 1 | a0001c0002t0005g0325 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.833-3680T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107661345 | |||||||
| chr11:107661719 | T | A | 4 | a0001c0002t0010g0316 a0001c0002t0012g0110 a0001c0002t0012g0205 others(1): Show |
4 | HG02486.hp2 HG02895.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.833-3306T>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107661719 | |||||||
| chr11:107661986 | A | G | 4 | a0001c0002t0005g0113 a0001c0002t0005g0119 a0001c0002t0012g0091 others(1): Show |
4 | HG01168.hp2 HG03486.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.833-3039A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107661986 | |||||||
| chr11:107662111 | A | G | 139 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0001g0146 others(136): Show |
141 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.833-2914A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107662111 | |||||||
| chr11:107662245 | G | A | 127 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0001g0146 others(124): Show |
129 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.833-2780G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107662245 | |||||||
| chr11:107662478 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.833-2547C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107662478 | |||||||
| chr11:107662506 | AG | A | 139 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0001g0146 others(136): Show |
141 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.833-2517delG | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr11 | 107662506 | ||||||
| chr11:107662581 | G | A | 1 | a0001c0001t0008g0031 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.833-2444G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107662581 | |||||||
| chr11:107662598 | G | A | 1 | a0001c0002t0007g0094 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.833-2427G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107662598 | |||||||
| chr11:107662610 | C | CA | 140 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0139 others(137): Show |
142 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.833-2405dupA | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr11 | 107662610 | ||||||
| chr11:107662651 | G | T | 5 | a0001c0001t0001g0312 a0001c0001t0001g0336 a0001c0001t0001g0337 others(2): Show |
5 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.833-2374G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107662651 | |||||||
| chr11:107662716 | G | A | 82 | a0001c0001t0008g0031 a0001c0002t0004g0007 a0001c0002t0004g0087 others(79): Show |
82 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.833-2309G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107662716 | |||||||
| chr11:107662729 | A | C | 18 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0001g0146 others(15): Show |
19 | HG01168.hp2 HG01243.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.833-2296A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107662729 | |||||||
| chr11:107662899 | T | A | 75 | a0001c0001t0001g0125 a0001c0001t0002g0005 a0001c0001t0002g0022 others(72): Show |
76 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.833-2126T>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107662899 | |||||||
| chr11:107663005 | A | ACC | 76 | a0001c0001t0001g0125 a0001c0001t0002g0005 a0001c0001t0002g0022 others(73): Show |
77 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.833-2020_833-2019i others(4): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663005 | |||||||
| chr11:107663069 | C | A | 1 | a0001c0001t0003g0173 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.833-1956C>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663069 | |||||||
| chr11:107663074 | C | A | 298 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(295): Show |
301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.833-1951C>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663074 | |||||||
| chr11:107663082 | T | C | 1 | a0001c0006t0004g0055 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.833-1943T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663082 | |||||||
| chr11:107663213 | C | G | 2 | a0001c0002t0012g0205 a0001c0002t0018g0272 |
2 | HG02486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.833-1812C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663213 | |||||||
| chr11:107663427 | A | G | 298 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(295): Show |
301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.833-1598A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663427 | |||||||
| chr11:107663434 | C | T | 2 | a0001c0002t0004g0087 a0001c0002t0004g0203 |
2 | HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.833-1591C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663434 | |||||||
| chr11:107663460 | C | T | 132 | a0001c0002t0002g0109 a0001c0002t0002g0121 a0001c0002t0002g0122 others(129): Show |
133 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.833-1565C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663460 | |||||||
| chr11:107663462 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.833-1563T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663462 | |||||||
| chr11:107663496 | TA | T | 133 | a0001c0001t0002g0186 a0001c0002t0002g0109 a0001c0002t0002g0121 others(130): Show |
134 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.833-1517delA | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr11 | 107663496 | ||||||
| chr11:107663561 | C | G | 1 | a0001c0002t0002g0124 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.833-1464C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663561 | |||||||
| chr11:107663762 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1263G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663762 | |||||||
| chr11:107663765 | A | T | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1260A>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663765 | |||||||
| chr11:107663768 | A | C | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1257A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663768 | |||||||
| chr11:107663769 | G | T | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1256G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663769 | |||||||
| chr11:107663775 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1250C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663775 | |||||||
| chr11:107663776 | A | C | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1249A>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663776 | |||||||
| chr11:107663778 | A | T | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1247A>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663778 | |||||||
| chr11:107663802 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1223T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663802 | |||||||
| chr11:107663804 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1221G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663804 | |||||||
| chr11:107663810 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1215A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663810 | |||||||
| chr11:107663812 | T | A | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1213T>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663812 | |||||||
| chr11:107663820 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1205T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663820 | |||||||
| chr11:107663828 | T | G | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1197T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663828 | |||||||
| chr11:107663831 | C | G | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1194C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663831 | |||||||
| chr11:107663832 | T | G | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1193T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663832 | |||||||
| chr11:107663841 | T | A | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1184T>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663841 | |||||||
| chr11:107663848 | C | G | 1 | a0001c0001t0028g0256 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.833-1177C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663848 | |||||||
| chr11:107663854 | T | G | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1171T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663854 | |||||||
| chr11:107663864 | G | C | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1161G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663864 | |||||||
| chr11:107663865 | C | A | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1160C>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663865 | |||||||
| chr11:107663866 | A | T | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1159A>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663866 | |||||||
| chr11:107663874 | G | T | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1151G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663874 | |||||||
| chr11:107663876 | A | T | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1149A>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663876 | |||||||
| chr11:107663884 | G | T | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1141G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663884 | |||||||
| chr11:107663892 | A | T | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1133A>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663892 | |||||||
| chr11:107663904 | G | T | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1121G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663904 | |||||||
| chr11:107663911 | A | T | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1114A>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663911 | |||||||
| chr11:107663927 | T | G | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1098T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663927 | |||||||
| chr11:107663938 | T | G | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1087T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663938 | |||||||
| chr11:107663944 | G | T | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1081G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663944 | |||||||
| chr11:107663946 | T | A | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1079T>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663946 | |||||||
| chr11:107663948 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1077A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663948 | |||||||
| chr11:107663952 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1073A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663952 | |||||||
| chr11:107663955 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1070G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663955 | |||||||
| chr11:107663956 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1069A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663956 | |||||||
| chr11:107663957 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1068A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663957 | |||||||
| chr11:107663959 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1066A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663959 | |||||||
| chr11:107663960 | T | G | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1065T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663960 | |||||||
| chr11:107663961 | T | G | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1064T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663961 | |||||||
| chr11:107663964 | GCATAATC others(3): Show |
G | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1060_833-1051d others(12): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663964 | |||||||
| chr11:107663976 | T | G | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1049T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663976 | |||||||
| chr11:107663979 | T | G | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1046T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663979 | |||||||
| chr11:107663980 | T | A | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1045T>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663980 | |||||||
| chr11:107663983 | T | G | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1042T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663983 | |||||||
| chr11:107663986 | G | A | 12 | a0001c0002t0002g0121 a0001c0002t0002g0122 a0001c0002t0002g0124 others(9): Show |
12 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.833-1039G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663986 | |||||||
| chr11:107663986 | G | C | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1039G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663986 | |||||||
| chr11:107663987 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1038T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663987 | |||||||
| chr11:107663988 | C | A | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1037C>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663988 | |||||||
| chr11:107663997 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1028C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107663997 | |||||||
| chr11:107664005 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1020G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664005 | |||||||
| chr11:107664011 | G | T | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1014G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664011 | |||||||
| chr11:107664012 | G | T | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1013G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664012 | |||||||
| chr11:107664016 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1009C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664016 | |||||||
| chr11:107664022 | G | T | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1003G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664022 | |||||||
| chr11:107664024 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1001C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664024 | |||||||
| chr11:107664025 | A | T | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-1000A>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664025 | |||||||
| chr11:107664026 | C | A | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-999C>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664026 | |||||||
| chr11:107664032 | C | A | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-993C>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664032 | |||||||
| chr11:107664033 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-992T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664033 | |||||||
| chr11:107664034 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-991G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664034 | |||||||
| chr11:107664038 | T | G | 1 | a0001c0001t0028g0256 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.833-987T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664038 | |||||||
| chr11:107664042 | G | T | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-983G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664042 | |||||||
| chr11:107664043 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-982T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664043 | |||||||
| chr11:107664044 | G | T | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-981G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664044 | |||||||
| chr11:107664045 | G | T | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-980G>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664045 | |||||||
| chr11:107664053 | A | T | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-972A>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664053 | |||||||
| chr11:107664054 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-971C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664054 | |||||||
| chr11:107664055 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-970A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664055 | |||||||
| chr11:107664056 | G | C | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-969G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664056 | |||||||
| chr11:107664062 | T | G | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-963T>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664062 | |||||||
| chr11:107664065 | A | T | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-960A>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664065 | |||||||
| chr11:107664068 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.833-957C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664068 | |||||||
| chr11:107664091 | T | C | 82 | a0001c0002t0004g0007 a0001c0002t0004g0087 a0001c0002t0004g0114 others(79): Show |
82 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.833-934T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664091 | |||||||
| chr11:107664227 | T | A | 14 | a0001c0002t0002g0274 a0001c0002t0002g0275 a0001c0002t0002g0276 others(11): Show |
14 | HG01168.hp2 HG01255.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.833-798T>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664227 | |||||||
| chr11:107664252 | TA | T | 134 | a0001c0001t0001g0231 a0001c0002t0002g0109 a0001c0002t0002g0121 others(131): Show |
135 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.833-763delA | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr11 | 107664252 | ||||||
| chr11:107664268 | T | C | 83 | a0001c0002t0004g0007 a0001c0002t0004g0087 a0001c0002t0004g0114 others(80): Show |
83 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.833-757T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664268 | |||||||
| chr11:107664354 | T | C | 1 | a0001c0001t0002g0263 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.833-671T>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664354 | |||||||
| chr11:107664510 | G | A | 1 | a0001c0001t0028g0256 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.833-515G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664510 | |||||||
| chr11:107664592 | G | A | 1 | a0001c0001t0002g0306 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.833-433G>A | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664592 | |||||||
| chr11:107664647 | A | G | 133 | a0001c0002t0002g0109 a0001c0002t0002g0121 a0001c0002t0002g0122 others(130): Show |
134 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.833-378A>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664647 | |||||||
| chr11:107664671 | C | T | 133 | a0001c0002t0002g0109 a0001c0002t0002g0121 a0001c0002t0002g0122 others(130): Show |
134 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.833-354C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664671 | |||||||
| chr11:107664740 | C | T | 1 | a0004c0004t0023g0179 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.833-285C>T | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664740 | |||||||
| chr11:107664751 | CAA | C | 133 | a0001c0002t0002g0109 a0001c0002t0002g0121 a0001c0002t0002g0122 others(130): Show |
134 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.833-273_833-272del others(2): Show |
ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664751 | |||||||
| chr11:107664875 | C | G | 1 | a0001c0001t0001g0010 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.833-150C>G | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664875 | |||||||
| chr11:107664898 | G | C | 125 | a0001c0002t0002g0121 a0001c0002t0002g0122 a0001c0002t0002g0124 others(122): Show |
126 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.833-127G>C | ELMOD1 | ENSG00000110675.13 | transcript | ENST00000265840.12 | protein_coding | 11/11 | chr11 | 107664898 |