Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79603 |
| ensemblid | ENSG00000090661.12 |
| hgncid | 23747 |
| symbol | CERS4 |
| name | ceramide synthase 4 |
| refseq_nuc | NM_024552.3 |
| refseq_prot | NP_078828.2 |
| ensembl_nuc | ENST00000251363.10 |
| ensembl_prot | ENSP00000251363.5 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 8209370 |
| end | 8262421 |
| strand | + |
| ver | v1.2 |
| region | chr19:8209370-8262421 |
| region5000 | chr19:8204370-8267421 |
| regionname0 | CERS4_chr19_8209370_8262421 |
| regionname5000 | CERS4_chr19_8204370_8267421 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 394 | 274 | 42 | 60 | 125 | 14 | 33 | 97 | CERS4_chr19_8204370_8267421 | CERS4 | MLSSF others(389): Show |
chr19 | 8204370 | 8267421 |
| a0002 | 0/0 | 394 | 56 | 24 | 3 | 26 | 0 | 3 | 20 | CERS4_chr19_8204370_8267421 | CERS4 | MLSSF others(389): Show |
chr19 | 8204370 | 8267421 |
| a0003 | 1/1 | 394 | 54 | 21 | 4 | 18 | 2 | 7 | 11 | CERS4_chr19_8204370_8267421 | CERS4 | MLSSF others(389): Show |
chr19 | 8204370 | 8267421 |
| a0004 | 0/0 | 394 | 26 | 6 | 8 | 7 | 0 | 5 | 4 | CERS4_chr19_8204370_8267421 | CERS4 | MLSSF others(389): Show |
chr19 | 8204370 | 8267421 |
| a0005 | 0/0 | 394 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | MLSSF others(389): Show |
chr19 | 8204370 | 8267421 |
| a0006 | 0/0 | 394 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | MLSSF others(389): Show |
chr19 | 8204370 | 8267421 |
| a0007 | 0/0 | 394 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | MLSSF others(389): Show |
chr19 | 8204370 | 8267421 |
| a0008 | 0/0 | 394 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | MLSSF others(389): Show |
chr19 | 8204370 | 8267421 |
| a0009 | 0/0 | 394 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | MLSSF others(389): Show |
chr19 | 8204370 | 8267421 |
| a0010 | 0/0 | 394 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | MLSSF others(389): Show |
chr19 | 8204370 | 8267421 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1182 | 168 | 30 | 27 | 77 | 7 | 27 | CERS4_chr19_8204370_8267421 | CERS4 | ATGCT others(1177): Show |
chr19 | 8204370 | 8267421 | ||
| a0001c0002 | 0/0 | 1182 | 72 | 3 | 24 | 32 | 7 | 6 | CERS4_chr19_8204370_8267421 | CERS4 | ATGCT others(1177): Show |
chr19 | 8204370 | 8267421 | ||
| a0001c0006 | 0/0 | 1182 | 20 | 0 | 7 | 13 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | ATGCT others(1177): Show |
chr19 | 8204370 | 8267421 | ||
| a0001c0008 | 0/0 | 1182 | 9 | 5 | 2 | 2 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | ATGCT others(1177): Show |
chr19 | 8204370 | 8267421 | ||
| a0001c0012 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | ATGCT others(1177): Show |
chr19 | 8204370 | 8267421 | ||
| a0001c0015 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | ATGCT others(1177): Show |
chr19 | 8204370 | 8267421 | ||
| a0001c0019 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | ATGCT others(1177): Show |
chr19 | 8204370 | 8267421 | ||
| a0001c0021 | 0/0 | 1182 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | ATGCT others(1177): Show |
chr19 | 8204370 | 8267421 | ||
| a0001c0025 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | ATGCT others(1177): Show |
chr19 | 8204370 | 8267421 | ||
| a0002c0003 | 0/0 | 1182 | 54 | 23 | 3 | 26 | 0 | 2 | CERS4_chr19_8204370_8267421 | CERS4 | ATGCT others(1177): Show |
chr19 | 8204370 | 8267421 | ||
| a0002c0013 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | ATGCT others(1177): Show |
chr19 | 8204370 | 8267421 | ||
| a0002c0023 | 0/0 | 1182 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | ATGCT others(1177): Show |
chr19 | 8204370 | 8267421 | ||
| a0003c0004 | 1/1 | 1182 | 37 | 9 | 2 | 18 | 1 | 5 | CERS4_chr19_8204370_8267421 | CERS4 | ATGCT others(1177): Show |
chr19 | 8204370 | 8267421 | ||
| a0003c0007 | 0/0 | 1182 | 15 | 11 | 1 | 0 | 1 | 2 | CERS4_chr19_8204370_8267421 | CERS4 | ATGCT others(1177): Show |
chr19 | 8204370 | 8267421 | ||
| a0003c0014 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | ATGCT others(1177): Show |
chr19 | 8204370 | 8267421 | ||
| a0003c0020 | 0/0 | 1182 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | ATGCT others(1177): Show |
chr19 | 8204370 | 8267421 | ||
| a0004c0005 | 0/0 | 1182 | 20 | 3 | 8 | 4 | 0 | 5 | CERS4_chr19_8204370_8267421 | CERS4 | ATGCT others(1177): Show |
chr19 | 8204370 | 8267421 | ||
| a0004c0009 | 0/0 | 1182 | 5 | 3 | 0 | 2 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | ATGCT others(1177): Show |
chr19 | 8204370 | 8267421 | ||
| a0004c0018 | 0/0 | 1182 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | ATGCT others(1177): Show |
chr19 | 8204370 | 8267421 | ||
| a0005c0010 | 0/0 | 1182 | 2 | 2 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | ATGCT others(1177): Show |
chr19 | 8204370 | 8267421 | ||
| a0006c0011 | 0/0 | 1182 | 2 | 2 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | ATGCT others(1177): Show |
chr19 | 8204370 | 8267421 | ||
| a0007c0017 | 0/0 | 1182 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | ATGCT others(1177): Show |
chr19 | 8204370 | 8267421 | ||
| a0008c0024 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | ATGCT others(1177): Show |
chr19 | 8204370 | 8267421 | ||
| a0009c0016 | 0/0 | 1182 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | ATGCT others(1177): Show |
chr19 | 8204370 | 8267421 | ||
| a0010c0022 | 0/0 | 1182 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | ATGCT others(1177): Show |
chr19 | 8204370 | 8267421 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1779 | 7 | 4 | 0 | 0 | 0 | 3 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0001c0001t0002 | 0/0 | 1779 | 73 | 8 | 12 | 39 | 2 | 12 | CERS4_chr19_8204370_8267421 | CERS4 | AGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0001c0001t0003 | 0/0 | 1779 | 67 | 13 | 10 | 30 | 4 | 10 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0001c0001t0004 | 0/0 | 1779 | 7 | 0 | 0 | 7 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | AGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0001c0001t0005 | 0/0 | 1779 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0001c0001t0006 | 0/0 | 1779 | 5 | 0 | 2 | 0 | 1 | 2 | CERS4_chr19_8204370_8267421 | CERS4 | AGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0001c0001t0007 | 0/0 | 1779 | 2 | 2 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | AGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0001c0001t0008 | 0/0 | 1779 | 2 | 1 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0001c0001t0010 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0001c0001t0012 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | AGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0001c0001t0016 | 0/0 | 1779 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0001c0001t0017 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0001c0002t0001 | 0/0 | 1779 | 14 | 2 | 6 | 5 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0001c0002t0002 | 0/0 | 1779 | 5 | 0 | 2 | 2 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | AGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0001c0002t0003 | 0/0 | 1779 | 3 | 0 | 0 | 1 | 0 | 2 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0001c0002t0004 | 0/0 | 1779 | 9 | 1 | 0 | 7 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | AGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0001c0002t0005 | 0/0 | 1779 | 23 | 0 | 11 | 6 | 4 | 2 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0001c0002t0006 | 0/0 | 1779 | 17 | 0 | 5 | 11 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | AGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0001c0002t0014 | 0/0 | 1779 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0001c0006t0005 | 0/0 | 1779 | 10 | 0 | 6 | 4 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0001c0006t0006 | 0/0 | 1779 | 9 | 0 | 1 | 8 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | AGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0001c0006t0013 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | AGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0001c0008t0001 | 0/0 | 1779 | 4 | 3 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0001c0008t0003 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0001c0008t0004 | 0/0 | 1779 | 2 | 2 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | AGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0001c0008t0005 | 0/0 | 1779 | 2 | 0 | 2 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0001c0012t0002 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | AGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0001c0015t0001 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0001c0019t0002 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | AGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0001c0021t0005 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0001c0025t0001 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0002c0003t0001 | 0/0 | 1779 | 25 | 16 | 1 | 6 | 0 | 2 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0002c0003t0002 | 0/0 | 1779 | 5 | 0 | 0 | 5 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | AGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0002c0003t0004 | 0/0 | 1779 | 21 | 4 | 2 | 15 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | AGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0002c0003t0008 | 0/0 | 1779 | 3 | 3 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0002c0013t0001 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0002c0023t0003 | 0/0 | 1779 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0003c0004t0001 | 0/1 | 1779 | 29 | 5 | 2 | 16 | 1 | 4 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0003c0004t0004 | 1/0 | 1779 | 7 | 4 | 0 | 1 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | AGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0003c0004t0009 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | AGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0003c0007t0001 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0003c0007t0003 | 0/0 | 1779 | 3 | 3 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0003c0007t0004 | 0/0 | 1779 | 4 | 0 | 1 | 0 | 1 | 2 | CERS4_chr19_8204370_8267421 | CERS4 | AGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0003c0007t0009 | 0/0 | 1779 | 4 | 4 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | AGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0003c0007t0010 | 0/0 | 1779 | 3 | 3 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0003c0014t0001 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0003c0020t0001 | 0/0 | 1779 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0004c0005t0007 | 0/0 | 1779 | 8 | 1 | 5 | 0 | 0 | 2 | CERS4_chr19_8204370_8267421 | CERS4 | AGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0004c0005t0008 | 0/0 | 1779 | 10 | 2 | 3 | 2 | 0 | 3 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0004c0005t0011 | 0/0 | 1779 | 2 | 0 | 0 | 2 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | AGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0004c0009t0007 | 0/0 | 1779 | 5 | 3 | 0 | 2 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | AGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0004c0018t0007 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | AGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0005c0010t0001 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0005c0010t0015 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0006c0011t0007 | 0/0 | 1779 | 2 | 2 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | AGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0007c0017t0003 | 0/0 | 1779 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0008c0024t0008 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | GGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0009c0016t0006 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | AGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| a0010c0022t0004 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | AGGAG others(1774): Show |
chr19 | 8204370 | 8267421 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0001g0407 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0001g0408 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0002g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0391 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0003g0397 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0004g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0004g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0006g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0006g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0006g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0006g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0006g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0007g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0007g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0008g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0008g0398 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0010g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0012g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0016g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0001t0017g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0001g0396 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0001g0412 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0002g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0003g0416 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0003g0417 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0004g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0004g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0004g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0004g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0393 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0413 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0005g0414 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0006g0381 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0002t0014g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0005g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0005g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0005g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0005g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0005g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0005g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0005g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0005g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0006g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0006g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0006g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0006g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0006g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0006g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0006g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0006g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0006g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0006t0013g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0008t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0008t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0008t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0008t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0008t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0008t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0008t0004g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0008t0005g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0008t0005g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0012t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0015t0001g0409 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0019t0002g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0021t0005g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0001c0025t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0392 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0399 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0400 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0401 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0404 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0405 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0001g0411 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0004g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0008g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0008g0395 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0003t0008g0403 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0013t0001g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0002c0023t0003g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0101 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0402 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0001g0410 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0004g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0004g0351 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0004t0009g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0007t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0007t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0007t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0007t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0007t0004g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0007t0004g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0007t0004g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0007t0004g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0007t0009g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0007t0009g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0007t0009g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0007t0009g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0007t0010g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0007t0010g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0007t0010g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0014t0001g0406 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0003c0020t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0007g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0007g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0007g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0007g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0007g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0007g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0007g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0007g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0008g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0008g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0008g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0008g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0008g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0008g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0008g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0008g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0008g0394 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0008g0415 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0011g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0005t0011g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0009t0007g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0009t0007g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0009t0007g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0009t0007g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0009t0007g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0004c0018t0007g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0005c0010t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0005c0010t0015g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0006c0011t0007g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0006c0011t0007g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0007c0017t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0008c0024t0008g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0009c0016t0006g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| a0010c0022t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0006 | g0381 | EUR | GBR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00099 | hp2 | a0001 | c0002 | t0005 | g0072 | EUR | GBR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00140 | hp1 | a0001 | c0001 | t0006 | g0215 | EUR | GBR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00140 | hp2 | a0003 | c0004 | t0001 | g0065 | EUR | GBR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0068 | EUR | FIN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0161 | EUR | FIN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00323 | hp1 | a0001 | c0002 | t0005 | g0102 | EUR | FIN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0297 | EUR | FIN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00408 | hp1 | a0002 | c0003 | t0004 | g0244 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00408 | hp2 | a0002 | c0003 | t0004 | g0298 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00423 | hp1 | a0002 | c0003 | t0004 | g0325 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0356 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00438 | hp2 | a0003 | c0004 | t0001 | g0146 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00544 | hp1 | a0003 | c0004 | t0001 | g0196 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0353 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00558 | hp1 | a0004 | c0005 | t0011 | g0300 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00558 | hp2 | a0001 | c0006 | t0013 | g0261 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0134 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00621 | hp2 | a0002 | c0003 | t0001 | g0159 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00639 | hp1 | a0001 | c0006 | t0005 | g0189 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00639 | hp2 | a0001 | c0002 | t0005 | g0081 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0248 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00642 | hp2 | a0001 | c0002 | t0006 | g0242 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00673 | hp1 | a0001 | c0008 | t0003 | g0245 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00673 | hp2 | a0001 | c0006 | t0005 | g0181 | EAS | CHS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00733 | hp1 | a0001 | c0001 | t0006 | g0221 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0042 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0341 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00735 | hp2 | a0001 | c0002 | t0005 | g0059 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00738 | hp1 | a0004 | c0005 | t0007 | g0379 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0374 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00741 | hp1 | a0004 | c0005 | t0008 | g0104 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG00741 | hp2 | a0004 | c0005 | t0008 | g0094 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01069 | hp1 | a0001 | c0002 | t0005 | g0414 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01069 | hp2 | a0001 | c0006 | t0005 | g0185 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0074 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0344 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0412 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01071 | hp2 | a0001 | c0002 | t0005 | g0078 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0099 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01074 | hp2 | a0001 | c0002 | t0005 | g0073 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01081 | hp1 | a0002 | c0003 | t0004 | g0355 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01081 | hp2 | a0003 | c0007 | t0004 | g0294 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01099 | hp1 | a0001 | c0002 | t0005 | g0080 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01099 | hp2 | a0001 | c0006 | t0005 | g0202 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01106 | hp1 | a0007 | c0017 | t0003 | g0158 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0290 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01109 | hp1 | a0001 | c0008 | t0005 | g0034 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01109 | hp2 | a0003 | c0004 | t0001 | g0054 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0100 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0219 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0098 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0157 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01175 | hp1 | a0001 | c0002 | t0006 | g0234 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0095 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01243 | hp2 | a0001 | c0002 | t0006 | g0293 | AMR | PUR | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01255 | hp1 | a0003 | c0020 | t0001 | g0079 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01258 | hp1 | a0004 | c0005 | t0008 | g0188 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0291 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01261 | hp1 | a0001 | c0006 | t0005 | g0193 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01261 | hp2 | a0001 | c0001 | t0008 | g0398 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01346 | hp1 | a0001 | c0002 | t0006 | g0236 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01346 | hp2 | a0001 | c0001 | t0006 | g0373 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01358 | hp1 | a0001 | c0002 | t0006 | g0275 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01358 | hp2 | a0001 | c0002 | t0005 | g0071 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0357 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0070 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0096 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01433 | hp2 | a0003 | c0004 | t0001 | g0041 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0174 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01496 | hp2 | a0004 | c0005 | t0007 | g0287 | AMR | CLM | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0089 | EUR | IBS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01515 | hp2 | a0001 | c0002 | t0005 | g0053 | EUR | IBS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0345 | EUR | IBS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0090 | EUR | IBS | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01891 | hp1 | a0002 | c0003 | t0001 | g0392 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01891 | hp2 | a0002 | c0003 | t0001 | g0055 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0172 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01928 | hp2 | a0001 | c0006 | t0005 | g0150 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01934 | hp1 | a0002 | c0003 | t0001 | g0401 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01934 | hp2 | a0001 | c0002 | t0005 | g0045 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0142 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0380 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01952 | hp2 | a0001 | c0002 | t0005 | g0393 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0176 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01975 | hp2 | a0001 | c0002 | t0005 | g0067 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0282 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01978 | hp2 | a0001 | c0002 | t0005 | g0039 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01981 | hp1 | a0002 | c0003 | t0004 | g0288 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01981 | hp2 | a0001 | c0006 | t0005 | g0190 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0173 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG01993 | hp2 | a0001 | c0006 | t0006 | g0299 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0175 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02004 | hp2 | a0004 | c0005 | t0007 | g0289 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02015 | hp2 | a0001 | c0006 | t0005 | g0088 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02027 | hp2 | a0003 | c0004 | t0009 | g0328 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02040 | hp1 | a0002 | c0003 | t0001 | g0103 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02055 | hp1 | a0001 | c0008 | t0001 | g0183 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02055 | hp2 | a0003 | c0007 | t0010 | g0006 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02071 | hp1 | a0002 | c0003 | t0001 | g0152 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02071 | hp2 | a0001 | c0006 | t0006 | g0263 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0340 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02080 | hp2 | a0001 | c0002 | t0005 | g0038 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02083 | hp1 | a0004 | c0005 | t0008 | g0394 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0352 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02129 | hp2 | a0003 | c0004 | t0001 | g0029 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02132 | hp2 | a0003 | c0004 | t0001 | g0009 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02135 | hp1 | a0003 | c0004 | t0001 | g0021 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0327 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0396 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0105 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02148 | hp1 | a0001 | c0008 | t0005 | g0075 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02148 | hp2 | a0004 | c0005 | t0007 | g0212 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02155 | hp1 | a0003 | c0004 | t0001 | g0014 | EAS | CDX | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | CDX | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02257 | hp2 | a0003 | c0007 | t0009 | g0335 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02258 | hp1 | a0003 | c0007 | t0001 | g0037 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02258 | hp2 | a0003 | c0014 | t0001 | g0406 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0186 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02273 | hp2 | a0004 | c0005 | t0007 | g0283 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02280 | hp1 | a0001 | c0012 | t0002 | g0140 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02280 | hp2 | a0002 | c0013 | t0001 | g0385 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0360 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02300 | hp2 | a0001 | c0001 | t0016 | g0093 | AMR | PEL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02451 | hp1 | a0003 | c0004 | t0001 | g0402 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02451 | hp2 | a0004 | c0005 | t0008 | g0204 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02523 | hp1 | a0004 | c0005 | t0008 | g0155 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | KHV | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02572 | hp1 | a0001 | c0001 | t0017 | g0386 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02572 | hp2 | a0002 | c0003 | t0001 | g0400 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02602 | hp1 | a0001 | c0002 | t0004 | g0004 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02602 | hp2 | a0001 | c0002 | t0005 | g0056 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02615 | hp1 | a0001 | c0008 | t0001 | g0051 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0109 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02622 | hp1 | a0004 | c0009 | t0007 | g0284 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02622 | hp2 | a0002 | c0003 | t0001 | g0113 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0408 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02630 | hp2 | a0003 | c0004 | t0004 | g0272 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02647 | hp1 | a0003 | c0004 | t0001 | g0388 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02647 | hp2 | a0001 | c0025 | t0001 | g0116 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0319 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0292 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0082 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0121 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0066 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02723 | hp1 | a0002 | c0003 | t0001 | g0405 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02735 | hp1 | a0004 | c0005 | t0008 | g0415 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0050 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0110 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02809 | hp2 | a0002 | c0003 | t0001 | g0411 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02818 | hp1 | a0001 | c0008 | t0004 | g0277 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0112 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02886 | hp1 | a0002 | c0003 | t0001 | g0061 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02886 | hp2 | a0005 | c0010 | t0001 | g0091 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02895 | hp1 | a0003 | c0004 | t0001 | g0106 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02895 | hp2 | a0002 | c0003 | t0004 | g0377 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02896 | hp1 | a0002 | c0003 | t0001 | g0043 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0378 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02897 | hp1 | a0002 | c0003 | t0004 | g0271 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02897 | hp2 | a0002 | c0003 | t0001 | g0062 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02922 | hp1 | a0003 | c0007 | t0003 | g0127 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02922 | hp2 | a0003 | c0004 | t0004 | g0270 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02965 | hp1 | a0006 | c0011 | t0007 | g0285 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02965 | hp2 | a0001 | c0008 | t0004 | g0359 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02970 | hp1 | a0004 | c0009 | t0007 | g0331 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02970 | hp2 | a0006 | c0011 | t0007 | g0280 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02976 | hp1 | a0003 | c0007 | t0009 | g0382 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02976 | hp2 | a0001 | c0019 | t0002 | g0372 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03017 | hp1 | a0003 | c0004 | t0001 | g0076 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0199 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03041 | hp1 | a0002 | c0003 | t0001 | g0404 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03041 | hp2 | a0003 | c0007 | t0009 | g0120 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0389 | AFR | MSL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03098 | hp2 | a0005 | c0010 | t0015 | g0092 | AFR | MSL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03130 | hp1 | a0003 | c0007 | t0003 | g0126 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03130 | hp2 | a0001 | c0001 | t0008 | g0390 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03139 | hp1 | a0004 | c0005 | t0007 | g0002 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03139 | hp2 | a0004 | c0009 | t0007 | g0281 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03195 | hp2 | a0003 | c0007 | t0010 | g0032 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03209 | hp1 | a0001 | c0001 | t0012 | g0279 | AFR | MSL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03209 | hp2 | a0002 | c0003 | t0001 | g0040 | AFR | MSL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03225 | hp1 | a0002 | c0003 | t0008 | g0395 | AFR | MSL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0117 | AFR | MSL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03239 | hp1 | a0001 | c0001 | t0006 | g0364 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0348 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03453 | hp1 | a0003 | c0007 | t0009 | g0136 | AFR | MSL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | MSL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03486 | hp1 | a0002 | c0003 | t0004 | g0358 | AFR | MSL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03486 | hp2 | a0002 | c0003 | t0008 | g0403 | AFR | MSL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0046 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03491 | hp1 | a0002 | c0003 | t0001 | g0274 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0048 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03492 | hp1 | a0002 | c0003 | t0001 | g0211 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0217 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03516 | hp1 | a0002 | c0003 | t0001 | g0205 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | ESN | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03540 | hp1 | a0002 | c0003 | t0001 | g0399 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03540 | hp2 | a0001 | c0015 | t0001 | g0409 | AFR | GWD | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03579 | hp1 | a0008 | c0024 | t0008 | g0108 | AFR | MSL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03579 | hp2 | a0004 | c0005 | t0008 | g0058 | AFR | MSL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0225 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03669 | hp1 | a0001 | c0002 | t0005 | g0119 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03669 | hp2 | a0003 | c0007 | t0004 | g0278 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03688 | hp1 | a0004 | c0005 | t0008 | g0246 | SAS | STU | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03688 | hp2 | a0004 | c0005 | t0008 | g0052 | SAS | STU | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03704 | hp1 | a0001 | c0002 | t0003 | g0417 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03704 | hp2 | a0003 | c0007 | t0004 | g0323 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03710 | hp2 | a0003 | c0004 | t0004 | g0316 | SAS | PJL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0214 | SAS | BEB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03831 | hp2 | a0003 | c0004 | t0001 | g0085 | SAS | BEB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0049 | SAS | BEB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03834 | hp2 | a0001 | c0001 | t0006 | g0222 | SAS | BEB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03927 | hp1 | a0003 | c0004 | t0001 | g0077 | SAS | BEB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | BEB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03942 | hp1 | a0004 | c0005 | t0007 | g0124 | SAS | BEB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0035 | SAS | BEB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG04115 | hp1 | a0001 | c0002 | t0003 | g0416 | SAS | STU | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0047 | SAS | STU | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0334 | SAS | BEB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0276 | SAS | STU | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0332 | SAS | STU | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0315 | SAS | STU | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0156 | SAS | STU | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG04228 | hp1 | a0003 | c0004 | t0001 | g0201 | SAS | STU | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG04228 | hp2 | a0004 | c0005 | t0007 | g0286 | SAS | STU | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18522 | hp1 | a0003 | c0004 | t0001 | g0410 | AFR | YRI | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18522 | hp2 | a0002 | c0003 | t0008 | g0107 | AFR | YRI | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0376 | EAS | CHB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0346 | EAS | CHB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | CHB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18747 | hp2 | a0001 | c0002 | t0004 | g0237 | EAS | CHB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0111 | AFR | YRI | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0387 | AFR | YRI | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18939 | hp1 | a0003 | c0004 | t0001 | g0023 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18942 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18943 | hp1 | a0001 | c0006 | t0005 | g0177 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18943 | hp2 | a0002 | c0003 | t0004 | g0322 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18945 | hp1 | a0001 | c0002 | t0005 | g0087 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18946 | hp1 | a0009 | c0016 | t0006 | g0207 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0354 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18948 | hp1 | a0001 | c0006 | t0006 | g0269 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18948 | hp2 | a0002 | c0003 | t0001 | g0163 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18951 | hp1 | a0001 | c0002 | t0004 | g0329 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18954 | hp1 | a0001 | c0002 | t0006 | g0210 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18956 | hp2 | a0001 | c0002 | t0004 | g0368 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18957 | hp1 | a0003 | c0004 | t0001 | g0044 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18957 | hp2 | a0001 | c0002 | t0006 | g0232 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18959 | hp1 | a0001 | c0006 | t0006 | g0347 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18959 | hp2 | a0003 | c0004 | t0001 | g0017 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0131 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18960 | hp2 | a0001 | c0002 | t0006 | g0230 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0363 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0123 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18963 | hp1 | a0004 | c0005 | t0011 | g0302 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18964 | hp1 | a0002 | c0003 | t0002 | g0330 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18966 | hp1 | a0003 | c0004 | t0001 | g0164 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18969 | hp1 | a0001 | c0002 | t0004 | g0238 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18969 | hp2 | a0001 | c0002 | t0005 | g0063 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18970 | hp2 | a0002 | c0003 | t0004 | g0223 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0250 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18973 | hp2 | a0001 | c0006 | t0006 | g0266 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0384 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18974 | hp2 | a0001 | c0002 | t0006 | g0310 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18977 | hp1 | a0001 | c0002 | t0005 | g0194 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18979 | hp1 | a0003 | c0004 | t0001 | g0180 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18979 | hp2 | a0002 | c0003 | t0004 | g0303 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18980 | hp1 | a0003 | c0004 | t0004 | g0267 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18983 | hp1 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18984 | hp1 | a0001 | c0002 | t0005 | g0084 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18984 | hp2 | a0002 | c0003 | t0002 | g0258 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0336 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18985 | hp2 | a0001 | c0002 | t0005 | g0195 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18988 | hp1 | a0001 | c0002 | t0006 | g0337 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18988 | hp2 | a0001 | c0001 | t0010 | g0010 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0249 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18993 | hp1 | a0003 | c0004 | t0001 | g0027 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18993 | hp2 | a0001 | c0006 | t0006 | g0375 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0366 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18995 | hp1 | a0001 | c0002 | t0006 | g0229 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18997 | hp1 | a0001 | c0021 | t0005 | g0184 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18997 | hp2 | a0002 | c0003 | t0004 | g0208 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0369 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18999 | hp2 | a0002 | c0003 | t0004 | g0305 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19000 | hp1 | a0003 | c0004 | t0001 | g0145 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19000 | hp2 | a0001 | c0006 | t0006 | g0256 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19002 | hp2 | a0004 | c0018 | t0007 | g0311 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19004 | hp1 | a0002 | c0003 | t0004 | g0367 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19004 | hp2 | a0003 | c0004 | t0001 | g0019 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19007 | hp1 | a0001 | c0006 | t0005 | g0187 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19007 | hp2 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19010 | hp1 | a0001 | c0002 | t0006 | g0255 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19010 | hp2 | a0001 | c0002 | t0006 | g0209 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0361 | AFR | LWK | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19030 | hp2 | a0003 | c0004 | t0001 | g0060 | AFR | LWK | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19043 | hp1 | a0003 | c0004 | t0004 | g0273 | AFR | LWK | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19043 | hp2 | a0002 | c0003 | t0001 | g0182 | AFR | LWK | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19055 | hp1 | a0001 | c0002 | t0006 | g0306 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19056 | hp1 | a0004 | c0009 | t0007 | g0129 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19057 | hp2 | a0001 | c0006 | t0006 | g0227 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19059 | hp1 | a0001 | c0002 | t0006 | g0304 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19059 | hp2 | a0001 | c0001 | t0002 | g0383 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19064 | hp1 | a0002 | c0003 | t0001 | g0165 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19064 | hp2 | a0010 | c0022 | t0004 | g0220 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19065 | hp1 | a0002 | c0003 | t0004 | g0371 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19065 | hp2 | a0002 | c0003 | t0004 | g0326 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0365 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0370 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19068 | hp1 | a0002 | c0003 | t0001 | g0179 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0350 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19070 | hp1 | a0002 | c0003 | t0002 | g0260 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19074 | hp1 | a0003 | c0004 | t0001 | g0031 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19074 | hp2 | a0002 | c0003 | t0004 | g0224 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0254 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19078 | hp1 | a0002 | c0003 | t0004 | g0362 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19081 | hp1 | a0003 | c0004 | t0001 | g0166 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19081 | hp2 | a0001 | c0002 | t0006 | g0233 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0314 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19085 | hp2 | a0001 | c0002 | t0004 | g0231 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19087 | hp1 | a0004 | c0009 | t0007 | g0243 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19087 | hp2 | a0002 | c0003 | t0004 | g0268 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19088 | hp1 | a0001 | c0006 | t0006 | g0259 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19088 | hp2 | a0001 | c0002 | t0004 | g0308 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19091 | hp1 | a0001 | c0008 | t0001 | g0086 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19091 | hp2 | a0001 | c0002 | t0004 | g0307 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19240 | hp1 | a0001 | c0008 | t0001 | g0206 | AFR | YRI | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | YRI | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0407 | AFR | ASW | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0342 | AFR | ASW | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA20752 | hp1 | a0003 | c0007 | t0004 | g0295 | EUR | TSI | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA20752 | hp2 | a0001 | c0002 | t0005 | g0413 | EUR | TSI | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0083 | EUR | TSI | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA20805 | hp2 | a0001 | c0002 | t0014 | g0057 | EUR | TSI | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0122 | SAS | GIH | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA20905 | hp2 | a0002 | c0023 | t0003 | g0008 | SAS | GIH | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02109 | hp1 | a0003 | c0007 | t0003 | g0128 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0391 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02486 | hp1 | a0003 | c0004 | t0004 | g0247 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02486 | hp2 | a0002 | c0003 | t0001 | g0118 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0397 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG02559 | hp2 | a0003 | c0007 | t0010 | g0033 | AFR | ACB | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03471 | hp1 | a0002 | c0003 | t0001 | g0114 | AFR | MSL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0343 | AFR | MSL | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | USA | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| HG06807 | hp2 | a0002 | c0003 | t0004 | g0138 | AFR | USA | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18955 | hp1 | a0002 | c0003 | t0004 | g0228 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | USA | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0349 | AFR | USA | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0097 | AFR | LWK | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| NA21309 | hp2 | a0001 | c0002 | t0004 | g0226 | AFR | LWK | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| homoSapiens | chm13v2 | a0003 | c0004 | t0001 | g0101 | REF | REF | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| homoSapiens | grch38p0 | a0003 | c0004 | t0004 | g0351 | REF | REF | CERS4_chr19_8204370_8267421 | CERS4 | chr19 | 8204370 | 8267421 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:8254569 | G | A | 1 | a0005 | 2 | HG02886.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.244G>A | p.Ala82Thr | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/12 | 527/1780 | 244/1185 | 82/394 | chr19 | 8254569 | |||
| chr19:8255671 | G | A | 3 | a0002 a0008 a0010 |
58 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(55): Show |
missense_variant | MODERATE | c.356G>A | p.Arg119Gln | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 5/12 | 639/1780 | 356/1185 | 119/394 | chr19 | 8255671 | |||
| chr19:8256706 | G | A | 1 | a0010 | 1 | NA19064.hp2 | missense_variant | MODERATE | c.608G>A | p.Arg203His | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 8/12 | 891/1780 | 608/1185 | 203/394 | chr19 | 8256706 | |||
| chr19:8257001 | T | C | 1 | a0006 | 2 | HG02965.hp1 HG02970.hp2 |
missense_variant | MODERATE | c.665T>C | p.Phe222Ser | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/12 | 948/1780 | 665/1185 | 222/394 | chr19 | 8257001 | |||
| chr19:8261740 | G | A | 1 | a0009 | 1 | NA18946.hp1 | missense_variant | MODERATE | c.901G>A | p.Gly301Ser | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 11/12 | 1184/1780 | 901/1185 | 301/394 | chr19 | 8261740 | |||
| chr19:8261982 | C | T | 3 | a0004 a0006 a0008 |
29 | HG00558.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
missense_variant | MODERATE | c.1058C>T | p.Ala353Val | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 12/12 | 1341/1780 | 1058/1185 | 353/394 | chr19 | 8261982 | |||
| chr19:8262020 | G | A | 5 | a0001 a0002 a0005 others(2): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
missense_variant | MODERATE | c.1096G>A | p.Ala366Thr | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 12/12 | 1379/1780 | 1096/1185 | 366/394 | chr19 | 8262020 | |||
| chr19:8262060 | G | A | 3 | a0004 a0006 a0007 |
29 | HG00558.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
missense_variant | MODERATE | c.1136G>A | p.Arg379Gln | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 12/12 | 1419/1780 | 1136/1185 | 379/394 | chr19 | 8262060 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:8254571 | C | T | 5 | a0001c0025 a0002c0003 a0002c0023 others(2): Show |
58 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(55): Show |
synonymous_variant | LOW | c.246C>T | p.Ala82Ala | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/12 | 529/1780 | 246/1185 | 82/394 | chr19 | 8254571 | |||
| chr19:8255645 | G | A | 1 | a0001c0012 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.330G>A | p.Thr110Thr | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 5/12 | 613/1780 | 330/1185 | 110/394 | chr19 | 8255645 | |||
| chr19:8256286 | G | A | 1 | a0003c0014 | 1 | HG02258.hp2 | splice_region_variant&synonymous_variant | LOW | c.519G>A | p.Gln173Gln | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 7/12 | 802/1780 | 519/1185 | 173/394 | chr19 | 8256286 | |||
| chr19:8256678 | C | T | 2 | a0001c0006 a0001c0021 |
21 | HG00558.hp2 HG00639.hp1 HG00673.hp2 others(18): Show |
synonymous_variant | LOW | c.580C>T | p.Leu194Leu | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 8/12 | 863/1780 | 580/1185 | 194/394 | chr19 | 8256678 | |||
| chr19:8257053 | C | T | 8 | a0001c0008 a0001c0025 a0002c0003 others(5): Show |
89 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
synonymous_variant | LOW | c.717C>T | p.His239His | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/12 | 1000/1780 | 717/1185 | 239/394 | chr19 | 8257053 | |||
| chr19:8257062 | T | C | 8 | a0001c0001 a0001c0012 a0001c0015 others(5): Show |
194 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(191): Show |
synonymous_variant | LOW | c.726T>C | p.Ser242Ser | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/12 | 1009/1780 | 726/1185 | 242/394 | chr19 | 8257062 | |||
| chr19:8257923 | C | T | 1 | a0001c0015 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.786C>T | p.Asp262Asp | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/12 | 1069/1780 | 786/1185 | 262/394 | chr19 | 8257923 | |||
| chr19:8261724 | C | T | 1 | a0001c0019 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.885C>T | p.Asn295Asn | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 11/12 | 1168/1780 | 885/1185 | 295/394 | chr19 | 8261724 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:8209370 | A | G | 33 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(30): Show |
222 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(219): Show |
5_prime_UTR_variant | MODIFIER | c.-283A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/12 | 41707 | chr19 | 8209370 | ||||||
| chr19:8210798 | C | T | 1 | a0001c0006t0013 | 1 | HG00558.hp2 | 5_prime_UTR_variant | MODIFIER | c.-66C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/12 | 40279 | chr19 | 8210798 | ||||||
| chr19:8262115 | C | T | 10 | a0001c0001t0007 a0001c0001t0008 a0002c0003t0008 others(7): Show |
36 | HG00558.hp1 HG00738.hp1 HG00741.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*6C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 12/12 | 6 | chr19 | 8262115 | ||||||
| chr19:8262171 | A | G | 1 | a0004c0005t0011 | 2 | HG00558.hp1 NA18963.hp1 |
3_prime_UTR_variant | MODIFIER | c.*62A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 12/12 | 62 | chr19 | 8262171 | ||||||
| chr19:8262271 | C | T | 2 | a0001c0001t0012 a0001c0001t0017 |
2 | HG02572.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*162C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 12/12 | 162 | chr19 | 8262271 | ||||||
| chr19:8262277 | A | G | 29 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(26): Show |
210 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*168A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 12/12 | 168 | chr19 | 8262277 | ||||||
| chr19:8262312 | G | C | 11 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0016 others(8): Show |
71 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*203G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 12/12 | 203 | chr19 | 8262312 | ||||||
| chr19:8262348 | C | T | 1 | a0001c0006t0013 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*239C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 12/12 | 239 | chr19 | 8262348 | ||||||
| chr19:8262360 | G | A | 26 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(23): Show |
202 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(199): Show |
3_prime_UTR_variant | MODIFIER | c.*251G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 12/12 | 251 | chr19 | 8262360 | ||||||
| chr19:8262369 | G | T | 1 | a0001c0002t0014 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*260G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 12/12 | 260 | chr19 | 8262369 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:8209503 | G | A | 1 | a0004c0005t0007g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-159+9G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8209503 | |||||||
| chr19:8209604 | T | G | 1 | a0001c0001t0002g0003 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-159+110T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8209604 | |||||||
| chr19:8209666 | T | C | 1 | a0001c0002t0004g0004 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-159+172T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8209666 | |||||||
| chr19:8209687 | C | G | 3 | a0001c0002t0003g0416 a0001c0002t0003g0417 a0004c0005t0008g0415 |
3 | HG02735.hp1 HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-159+193C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8209687 | |||||||
| chr19:8209776 | C | T | 3 | a0001c0002t0001g0412 a0001c0002t0005g0413 a0001c0002t0005g0414 |
3 | HG01069.hp1 HG01071.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-159+282C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8209776 | |||||||
| chr19:8209800 | G | T | 17 | a0001c0001t0001g0407 a0001c0001t0001g0408 a0001c0001t0003g0397 others(14): Show |
17 | HG01261.hp2 HG01934.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-159+306G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8209800 | |||||||
| chr19:8209850 | G | T | 1 | a0004c0005t0008g0394 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-159+356G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8209850 | |||||||
| chr19:8209929 | T | A | 1 | a0001c0001t0003g0005 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-159+435T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8209929 | |||||||
| chr19:8209945 | C | T | 1 | a0001c0002t0005g0393 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-159+451C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8209945 | |||||||
| chr19:8210022 | C | CCAGGAAA others(16): Show |
138 | a0001c0001t0001g0115 a0001c0001t0001g0407 a0001c0001t0001g0408 others(135): Show |
138 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.-159+532_-159+533i others(25): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr19 | 8210022 | ||||||
| chr19:8210269 | G | A | 2 | a0001c0001t0007g0121 a0003c0007t0009g0120 |
2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-158-437G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8210269 | |||||||
| chr19:8210336 | G | A | 1 | a0001c0001t0003g0122 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-158-370G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8210336 | |||||||
| chr19:8210359 | T | C | 17 | a0001c0001t0001g0407 a0001c0001t0001g0408 a0001c0001t0003g0397 others(14): Show |
17 | HG01261.hp2 HG01934.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-158-347T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8210359 | |||||||
| chr19:8210393 | T | C | 1 | a0001c0002t0002g0123 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-158-313T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8210393 | |||||||
| chr19:8210559 | G | A | 1 | a0004c0005t0007g0124 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-158-147G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8210559 | |||||||
| chr19:8210562 | A | G | 3 | a0001c0001t0003g0391 a0001c0001t0008g0390 a0002c0003t0001g0392 |
3 | HG01891.hp1 HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-158-144A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8210562 | |||||||
| chr19:8210565 | G | T | 1 | a0001c0002t0005g0119 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-158-141G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8210565 | |||||||
| chr19:8210602 | ACTGGGGC others(31): Show |
A | 4 | a0001c0001t0001g0125 a0003c0007t0003g0126 a0003c0007t0003g0127 others(1): Show |
4 | HG02109.hp1 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-158-99_-158-62del others(38): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr19 | 8210602 | ||||||
| chr19:8210616 | G | C | 5 | a0001c0001t0003g0387 a0001c0001t0003g0389 a0001c0001t0017g0386 others(2): Show |
5 | HG02280.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-158-90G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8210616 | |||||||
| chr19:8210678 | C | A | 6 | a0001c0001t0002g0130 a0001c0001t0002g0132 a0001c0001t0002g0133 others(3): Show |
6 | HG00621.hp1 HG02015.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.-158-28C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 1/11 | chr19 | 8210678 | |||||||
| chr19:8210885 | G | C | 16 | a0001c0001t0001g0407 a0001c0001t0001g0408 a0001c0001t0003g0397 others(13): Show |
16 | HG01261.hp2 HG01934.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-2+23G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8210885 | |||||||
| chr19:8211009 | G | A | 7 | a0001c0001t0002g0135 a0001c0001t0002g0137 a0001c0001t0002g0139 others(4): Show |
7 | HG02280.hp1 HG02723.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2+147G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8211009 | |||||||
| chr19:8211018 | C | T | 9 | a0001c0001t0001g0125 a0001c0001t0003g0387 a0001c0001t0003g0389 others(6): Show |
9 | HG02109.hp1 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-2+156C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8211018 | |||||||
| chr19:8211070 | T | C | 47 | a0001c0001t0001g0407 a0001c0001t0001g0408 a0001c0001t0003g0005 others(44): Show |
47 | HG00609.hp1 HG01261.hp2 HG01934.hp1 others(44): Show |
intron_variant | MODIFIER | c.-2+208T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8211070 | |||||||
| chr19:8211142 | C | T | 14 | a0001c0001t0001g0115 a0001c0001t0003g0105 a0001c0001t0003g0109 others(11): Show |
14 | HG02145.hp2 HG02257.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-2+280C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8211142 | |||||||
| chr19:8211182 | G | A | 13 | a0001c0001t0003g0397 a0001c0001t0008g0398 a0001c0002t0001g0396 others(10): Show |
13 | HG01261.hp2 HG01934.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-2+320G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8211182 | |||||||
| chr19:8211196 | G | C | 125 | a0001c0001t0001g0125 a0001c0001t0001g0197 a0001c0001t0001g0198 others(122): Show |
125 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.-2+334G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8211196 | |||||||
| chr19:8211234 | CCTGT | C | 63 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 others(60): Show |
63 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.-2+373_-2+376delCT others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8211234 | |||||||
| chr19:8211280 | G | A | 4 | a0001c0001t0001g0407 a0001c0001t0001g0408 a0001c0015t0001g0409 others(1): Show |
4 | HG02630.hp1 HG03540.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+418G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8211280 | |||||||
| chr19:8211802 | G | A | 1 | a0003c0007t0010g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-2+940G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8211802 | |||||||
| chr19:8211890 | C | CA | 116 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 others(113): Show |
116 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.-2+1051dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8211890 | ||||||
| chr19:8211890 | C | CAA | 14 | a0001c0001t0001g0125 a0001c0001t0001g0407 a0001c0001t0001g0408 others(11): Show |
14 | HG00438.hp2 HG01943.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.-2+1050_-2+1051dup others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8211890 | ||||||
| chr19:8211890 | CA | C | 16 | a0001c0001t0002g0380 a0001c0001t0002g0383 a0001c0001t0002g0384 others(13): Show |
16 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-2+1051delA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8211890 | ||||||
| chr19:8211890 | CAA | C | 27 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0013 others(24): Show |
27 | HG00609.hp1 HG01891.hp1 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.-2+1050_-2+1051del others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8211890 | ||||||
| chr19:8212057 | G | T | 1 | a0001c0001t0002g0384 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-2+1195G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212057 | |||||||
| chr19:8212105 | A | C | 2 | a0001c0001t0002g0374 a0001c0001t0006g0373 |
2 | HG00738.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.-2+1243A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212105 | |||||||
| chr19:8212161 | C | T | 1 | a0001c0002t0002g0248 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-2+1299C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212161 | |||||||
| chr19:8212307 | G | A | 24 | a0001c0001t0002g0251 a0001c0001t0002g0252 a0001c0001t0002g0253 others(21): Show |
25 | HG00558.hp2 HG02071.hp2 HG02129.hp1 others(22): Show |
intron_variant | MODIFIER | c.-2+1445G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212307 | |||||||
| chr19:8212326 | G | A | 1 | a0001c0001t0003g0105 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-2+1464G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212326 | |||||||
| chr19:8212448 | A | T | 1 | a0001c0019t0002g0372 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-2+1586A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212448 | |||||||
| chr19:8212591 | C | T | 1 | a0001c0002t0003g0417 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-2+1729C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212591 | |||||||
| chr19:8212633 | A | T | 215 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(212): Show |
215 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.-2+1771A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212633 | |||||||
| chr19:8212640 | A | AT | 77 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 others(74): Show |
77 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.-2+1786dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8212640 | ||||||
| chr19:8212640 | A | T | 113 | a0001c0001t0001g0115 a0001c0001t0003g0005 a0001c0001t0003g0011 others(110): Show |
113 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.-2+1778A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212640 | |||||||
| chr19:8212642 | T | TA | 4 | a0001c0002t0003g0416 a0001c0002t0003g0417 a0003c0007t0010g0006 others(1): Show |
4 | HG02055.hp2 HG02735.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+1780_-2+1781ins others(1): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212642 | |||||||
| chr19:8212643 | T | A | 5 | a0001c0001t0001g0407 a0001c0001t0001g0408 a0001c0015t0001g0409 others(2): Show |
5 | HG02630.hp1 HG02976.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2+1781T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212643 | |||||||
| chr19:8212648 | T | A | 1 | a0001c0002t0001g0042 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-2+1786T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212648 | |||||||
| chr19:8212663 | A | T | 1 | a0002c0003t0004g0244 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-2+1801A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212663 | |||||||
| chr19:8212715 | T | G | 100 | a0001c0001t0001g0125 a0001c0001t0001g0197 a0001c0001t0001g0198 others(97): Show |
100 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.-2+1853T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212715 | |||||||
| chr19:8212732 | G | A | 115 | a0001c0001t0001g0115 a0001c0001t0003g0005 a0001c0001t0003g0011 others(112): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.-2+1870G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212732 | |||||||
| chr19:8212829 | A | G | 213 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(210): Show |
213 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.-2+1967A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212829 | |||||||
| chr19:8212830 | A | G | 2 | a0001c0001t0003g0148 a0002c0003t0001g0043 |
2 | HG02896.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.-2+1968A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212830 | |||||||
| chr19:8212849 | T | C | 100 | a0001c0001t0001g0125 a0001c0001t0001g0197 a0001c0001t0001g0198 others(97): Show |
100 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.-2+1987T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212849 | |||||||
| chr19:8212940 | G | A | 1 | a0001c0002t0005g0393 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-2+2078G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8212940 | |||||||
| chr19:8213319 | T | C | 1 | a0001c0006t0006g0269 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-2+2457T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8213319 | |||||||
| chr19:8213440 | A | G | 1 | a0001c0001t0003g0147 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-2+2578A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8213440 | |||||||
| chr19:8213478 | A | C | 7 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 others(4): Show |
7 | HG02683.hp2 HG03017.hp2 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2+2616A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8213478 | |||||||
| chr19:8213560 | A | G | 35 | a0001c0001t0003g0005 a0001c0001t0003g0011 a0001c0001t0003g0012 others(32): Show |
35 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.-2+2698A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8213560 | |||||||
| chr19:8213597 | T | C | 265 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0407 others(262): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.-2+2735T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8213597 | |||||||
| chr19:8213701 | C | T | 1 | a0002c0003t0001g0205 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-2+2839C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8213701 | |||||||
| chr19:8213708 | G | A | 64 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 others(61): Show |
64 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.-2+2846G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8213708 | |||||||
| chr19:8213731 | C | T | 65 | a0001c0001t0002g0003 a0001c0001t0002g0213 a0001c0001t0002g0214 others(62): Show |
65 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.-2+2869C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8213731 | |||||||
| chr19:8213737 | G | A | 1 | a0003c0007t0009g0382 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-2+2875G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8213737 | |||||||
| chr19:8213895 | G | C | 9 | a0001c0001t0001g0125 a0001c0001t0003g0387 a0001c0001t0003g0389 others(6): Show |
9 | HG02109.hp1 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-2+3033G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8213895 | |||||||
| chr19:8213920 | C | T | 1 | a0003c0007t0010g0033 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-2+3058C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8213920 | |||||||
| chr19:8214061 | G | GTC | 5 | a0001c0002t0001g0203 a0001c0002t0005g0194 a0001c0002t0005g0195 others(2): Show |
5 | HG00438.hp2 HG00544.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2+3200_-2+3201dup others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8214061 | ||||||
| chr19:8214062 | T | TCACA | 29 | a0001c0001t0003g0005 a0001c0001t0003g0011 a0001c0001t0003g0012 others(26): Show |
29 | HG00609.hp1 HG00741.hp1 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.-2+3212_-2+3215dup others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8214062 | ||||||
| chr19:8214062 | T | TCACACA | 5 | a0001c0002t0001g0042 a0001c0002t0001g0097 a0001c0002t0001g0098 others(2): Show |
5 | HG00733.hp2 HG01074.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2+3210_-2+3215dup others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8214062 | ||||||
| chr19:8214072 | A | G | 107 | a0001c0001t0002g0003 a0001c0001t0002g0213 a0001c0001t0002g0214 others(104): Show |
107 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.-2+3210A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8214072 | |||||||
| chr19:8214084 | G | A | 1 | a0001c0001t0002g0213 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-2+3222G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8214084 | |||||||
| chr19:8214159 | T | C | 34 | a0001c0001t0003g0005 a0001c0001t0003g0011 a0001c0001t0003g0012 others(31): Show |
34 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.-2+3297T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8214159 | |||||||
| chr19:8214164 | CTG | C | 88 | a0001c0001t0001g0115 a0001c0001t0001g0407 a0001c0001t0001g0408 others(85): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-2+3306_-2+3307del others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8214164 | ||||||
| chr19:8214236 | T | C | 1 | a0002c0003t0001g0399 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-2+3374T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8214236 | |||||||
| chr19:8214412 | C | T | 34 | a0001c0001t0003g0005 a0001c0001t0003g0011 a0001c0001t0003g0012 others(31): Show |
34 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.-2+3550C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8214412 | |||||||
| chr19:8214631 | G | A | 5 | a0001c0001t0003g0387 a0001c0001t0003g0389 a0001c0001t0017g0386 others(2): Show |
5 | HG02280.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2+3769G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8214631 | |||||||
| chr19:8214708 | C | A | 62 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 others(59): Show |
62 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.-2+3846C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8214708 | |||||||
| chr19:8214715 | TG | T | 32 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0013 others(29): Show |
32 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.-2+3857delG | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8214715 | ||||||
| chr19:8214773 | C | T | 5 | a0002c0003t0004g0271 a0002c0003t0004g0377 a0003c0004t0004g0270 others(2): Show |
5 | HG02630.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2+3911C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8214773 | |||||||
| chr19:8214818 | C | T | 3 | a0001c0001t0003g0397 a0001c0001t0008g0398 a0001c0002t0001g0396 |
3 | HG01261.hp2 HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-2+3956C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8214818 | |||||||
| chr19:8214938 | C | CGAGGGGG others(38): Show |
4 | a0001c0008t0001g0206 a0002c0003t0001g0205 a0003c0007t0010g0006 others(1): Show |
4 | HG02055.hp2 HG02451.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+4099_-2+4143dup others(45): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8214938 | ||||||
| chr19:8214942 | G | GGGGAGGA others(2): Show |
35 | a0001c0001t0001g0407 a0001c0001t0003g0011 a0001c0001t0003g0012 others(32): Show |
35 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.-2+4089_-2+4097dup others(9): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8214942 | ||||||
| chr19:8214961 | GGGAGGAG others(35): Show |
G | 84 | a0001c0001t0001g0115 a0001c0001t0003g0035 a0001c0001t0003g0036 others(81): Show |
84 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.-2+4133_-2+4174del others(42): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8214961 | ||||||
| chr19:8214975 | A | AAGGAAGA others(8): Show |
64 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 others(61): Show |
64 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.-2+4118_-2+4132dup others(15): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8214975 | ||||||
| chr19:8214989 | G | GGAGGAA | 33 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0013 others(30): Show |
33 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.-2+4132_-2+4133ins others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8214989 | ||||||
| chr19:8215037 | C | T | 1 | a0001c0001t0005g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-2+4175C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8215037 | |||||||
| chr19:8215223 | G | T | 1 | a0003c0007t0010g0006 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-2+4361G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8215223 | |||||||
| chr19:8215298 | G | A | 1 | a0001c0001t0002g0003 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-2+4436G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8215298 | |||||||
| chr19:8215346 | G | A | 1 | a0001c0002t0005g0045 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-2+4484G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8215346 | |||||||
| chr19:8215377 | G | A | 89 | a0001c0001t0001g0115 a0001c0001t0003g0035 a0001c0001t0003g0036 others(86): Show |
89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.-2+4515G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8215377 | |||||||
| chr19:8215405 | G | C | 33 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0013 others(30): Show |
33 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.-2+4543G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8215405 | |||||||
| chr19:8215478 | C | CA | 15 | a0001c0001t0001g0197 a0001c0001t0002g0251 a0001c0001t0003g0149 others(12): Show |
15 | HG00733.hp2 HG00741.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.-2+4629dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8215478 | ||||||
| chr19:8215478 | C | CAA | 26 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0013 others(23): Show |
26 | HG00609.hp1 HG02040.hp2 HG02129.hp2 others(23): Show |
intron_variant | MODIFIER | c.-2+4628_-2+4629dup others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8215478 | ||||||
| chr19:8215487 | AAAAAC | A | 7 | a0002c0003t0001g0400 a0002c0003t0001g0401 a0002c0003t0001g0411 others(4): Show |
7 | HG01934.hp1 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2+4630_-2+4634del others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8215487 | ||||||
| chr19:8215516 | T | C | 1 | a0001c0006t0005g0150 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-2+4654T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8215516 | |||||||
| chr19:8215577 | C | G | 3 | a0001c0008t0001g0206 a0002c0003t0001g0205 a0004c0005t0008g0204 |
3 | HG02451.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-2+4715C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8215577 | |||||||
| chr19:8215596 | C | G | 3 | a0001c0002t0006g0381 a0003c0007t0004g0294 a0003c0007t0004g0295 |
3 | HG00099.hp1 HG01081.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-2+4734C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8215596 | |||||||
| chr19:8215737 | C | G | 105 | a0001c0001t0001g0115 a0001c0001t0001g0407 a0001c0001t0001g0408 others(102): Show |
105 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.-2+4875C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8215737 | |||||||
| chr19:8215939 | C | T | 1 | a0001c0002t0006g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-2+5077C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8215939 | |||||||
| chr19:8216056 | C | A | 1 | a0001c0001t0008g0390 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-2+5194C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8216056 | |||||||
| chr19:8216091 | T | C | 64 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 others(61): Show |
64 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.-2+5229T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8216091 | |||||||
| chr19:8216103 | G | C | 1 | a0004c0005t0008g0415 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-2+5241G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8216103 | |||||||
| chr19:8216148 | G | A | 1 | a0001c0019t0002g0372 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-2+5286G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8216148 | |||||||
| chr19:8216239 | C | T | 1 | a0004c0005t0007g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-2+5377C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8216239 | |||||||
| chr19:8216251 | C | T | 1 | a0002c0003t0001g0405 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-2+5389C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8216251 | |||||||
| chr19:8216358 | G | A | 3 | a0002c0003t0001g0400 a0002c0003t0001g0401 a0002c0003t0001g0411 |
3 | HG01934.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-2+5496G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8216358 | |||||||
| chr19:8216380 | G | GA | 12 | a0001c0001t0001g0125 a0001c0001t0002g0296 a0001c0001t0003g0387 others(9): Show |
12 | HG02109.hp1 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2+5533dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8216380 | ||||||
| chr19:8216549 | G | A | 12 | a0001c0001t0001g0115 a0001c0001t0003g0105 a0001c0001t0003g0109 others(9): Show |
12 | HG02145.hp2 HG02257.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2+5687G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8216549 | |||||||
| chr19:8216611 | G | GA | 6 | a0001c0001t0003g0035 a0001c0001t0003g0046 a0001c0001t0003g0047 others(3): Show |
6 | HG02735.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2+5757dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8216611 | ||||||
| chr19:8216622 | A | T | 1 | a0002c0003t0004g0228 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-2+5760A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8216622 | |||||||
| chr19:8216685 | G | GAAATTTC others(29): Show |
1 | a0002c0003t0004g0228 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-2+5825_-2+5860dup others(36): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8216685 | ||||||
| chr19:8216751 | G | A | 324 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(321): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.-2+5889G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8216751 | |||||||
| chr19:8216760 | G | T | 64 | a0001c0001t0002g0003 a0001c0001t0002g0213 a0001c0001t0002g0214 others(61): Show |
64 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.-2+5898G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8216760 | |||||||
| chr19:8216821 | C | T | 4 | a0001c0001t0002g0369 a0001c0001t0002g0370 a0001c0002t0004g0368 others(1): Show |
4 | NA18956.hp2 NA18999.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+5959C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8216821 | |||||||
| chr19:8217115 | T | C | 33 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0013 others(30): Show |
33 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.-2+6253T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8217115 | |||||||
| chr19:8217280 | G | A | 1 | a0004c0005t0008g0415 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-2+6418G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8217280 | |||||||
| chr19:8217394 | A | T | 33 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0013 others(30): Show |
33 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.-2+6532A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8217394 | |||||||
| chr19:8217433 | A | G | 1 | a0001c0019t0002g0372 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-2+6571A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8217433 | |||||||
| chr19:8217437 | C | T | 89 | a0001c0001t0001g0115 a0001c0001t0003g0035 a0001c0001t0003g0036 others(86): Show |
89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.-2+6575C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8217437 | |||||||
| chr19:8217537 | G | GT | 33 | a0001c0001t0001g0200 a0001c0001t0001g0407 a0001c0001t0001g0408 others(30): Show |
33 | HG00438.hp2 HG00642.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-2+6692dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8217537 | ||||||
| chr19:8217537 | GT | G | 6 | a0001c0001t0002g0296 a0001c0001t0003g0046 a0001c0008t0001g0051 others(3): Show |
6 | HG02615.hp1 HG02896.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+6692delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8217537 | ||||||
| chr19:8217606 | G | A | 3 | a0001c0001t0003g0148 a0001c0001t0003g0149 a0001c0001t0003g0151 |
3 | NA18944.hp2 NA18955.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.-2+6744G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8217606 | |||||||
| chr19:8217625 | C | T | 12 | a0002c0003t0001g0399 a0002c0003t0001g0400 a0002c0003t0001g0401 others(9): Show |
12 | HG01934.hp1 HG02258.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2+6763C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8217625 | |||||||
| chr19:8217739 | C | G | 11 | a0001c0001t0003g0144 a0001c0001t0003g0186 a0001c0001t0003g0191 others(8): Show |
11 | HG00639.hp1 HG01069.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.-2+6877C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8217739 | |||||||
| chr19:8217755 | T | C | 2 | a0001c0001t0002g0252 a0001c0001t0004g0376 |
2 | NA18612.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.-2+6893T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8217755 | |||||||
| chr19:8217758 | C | T | 1 | a0003c0004t0001g0410 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-2+6896C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8217758 | |||||||
| chr19:8217784 | G | A | 35 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0013 others(32): Show |
35 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.-2+6922G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8217784 | |||||||
| chr19:8217861 | C | T | 1 | a0003c0004t0001g0410 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-2+6999C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8217861 | |||||||
| chr19:8217912 | A | G | 3 | a0001c0008t0001g0206 a0002c0003t0001g0205 a0004c0005t0008g0204 |
3 | HG02451.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-2+7050A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8217912 | |||||||
| chr19:8218029 | A | G | 45 | a0001c0001t0001g0115 a0001c0001t0003g0011 a0001c0001t0003g0012 others(42): Show |
45 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.-2+7167A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8218029 | |||||||
| chr19:8218161 | C | T | 3 | a0001c0001t0002g0241 a0001c0001t0002g0365 a0002c0003t0004g0367 |
3 | NA19004.hp1 NA19057.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.-2+7299C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8218161 | |||||||
| chr19:8218246 | T | A | 3 | a0001c0008t0001g0206 a0002c0003t0001g0205 a0004c0005t0008g0204 |
3 | HG02451.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-2+7384T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8218246 | |||||||
| chr19:8218264 | C | A | 1 | a0004c0005t0007g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-2+7402C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8218264 | |||||||
| chr19:8218556 | G | A | 1 | a0002c0003t0001g0152 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-2+7694G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8218556 | |||||||
| chr19:8218650 | CAG | C | 3 | a0001c0008t0001g0206 a0002c0003t0001g0205 a0004c0005t0008g0204 |
3 | HG02451.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-2+7791_-2+7792del others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8218650 | ||||||
| chr19:8218721 | A | G | 2 | a0001c0001t0016g0093 a0003c0004t0004g0247 |
2 | HG02300.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-2+7859A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8218721 | |||||||
| chr19:8218732 | A | G | 8 | a0001c0001t0001g0125 a0001c0001t0003g0387 a0001c0001t0017g0386 others(5): Show |
8 | HG02109.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2+7870A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8218732 | |||||||
| chr19:8218750 | A | G | 3 | a0001c0002t0003g0416 a0001c0002t0003g0417 a0004c0005t0008g0415 |
3 | HG02735.hp1 HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-2+7888A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8218750 | |||||||
| chr19:8218766 | T | C | 2 | a0003c0007t0009g0136 a0003c0007t0010g0006 |
2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-2+7904T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8218766 | |||||||
| chr19:8218935 | C | A | 224 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(221): Show |
224 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-2+8073C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8218935 | |||||||
| chr19:8219148 | C | T | 8 | a0001c0001t0001g0125 a0001c0001t0003g0387 a0001c0001t0017g0386 others(5): Show |
8 | HG02109.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2+8286C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8219148 | |||||||
| chr19:8219218 | G | A | 63 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 others(60): Show |
63 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.-2+8356G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8219218 | |||||||
| chr19:8219462 | C | T | 257 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0407 others(254): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.-2+8600C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8219462 | |||||||
| chr19:8219529 | G | A | 12 | a0001c0001t0001g0115 a0001c0001t0003g0105 a0001c0001t0003g0109 others(9): Show |
12 | HG02145.hp2 HG02257.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2+8667G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8219529 | |||||||
| chr19:8219534 | G | C | 1 | a0001c0001t0002g0214 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-2+8672G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8219534 | |||||||
| chr19:8219550 | C | T | 2 | a0001c0001t0002g0141 a0001c0012t0002g0140 |
2 | HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-2+8688C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8219550 | |||||||
| chr19:8219587 | C | T | 2 | a0001c0019t0002g0372 a0003c0007t0009g0382 |
2 | HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-2+8725C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8219587 | |||||||
| chr19:8219662 | C | CA | 94 | a0001c0001t0001g0115 a0001c0001t0001g0408 a0001c0001t0003g0035 others(91): Show |
94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.-2+8807dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8219662 | ||||||
| chr19:8219814 | T | C | 13 | a0002c0003t0001g0399 a0002c0003t0001g0400 a0002c0003t0001g0401 others(10): Show |
13 | HG01934.hp1 HG02258.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-2+8952T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8219814 | |||||||
| chr19:8219874 | T | G | 1 | a0001c0002t0001g0153 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-2+9012T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8219874 | |||||||
| chr19:8219924 | A | C | 6 | a0001c0001t0003g0391 a0001c0001t0008g0390 a0002c0003t0001g0392 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+9062A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8219924 | |||||||
| chr19:8219987 | T | TA | 72 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 others(69): Show |
72 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.-2+9137dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8219987 | ||||||
| chr19:8219987 | T | TAA | 244 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0407 others(241): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.-2+9136_-2+9137dup others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8219987 | ||||||
| chr19:8219987 | T | TAAA | 6 | a0001c0001t0003g0036 a0001c0002t0003g0416 a0001c0002t0003g0417 others(3): Show |
6 | HG02735.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2+9135_-2+9137dup others(3): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8219987 | ||||||
| chr19:8220119 | C | T | 21 | a0001c0001t0001g0125 a0001c0001t0001g0407 a0001c0001t0003g0387 others(18): Show |
21 | HG01934.hp1 HG02055.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.-2+9257C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220119 | |||||||
| chr19:8220129 | C | T | 2 | a0001c0001t0002g0363 a0001c0001t0006g0364 |
2 | HG03239.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.-2+9267C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220129 | |||||||
| chr19:8220139 | C | T | 57 | a0001c0001t0003g0035 a0001c0001t0003g0036 a0001c0001t0003g0046 others(54): Show |
57 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.-2+9277C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220139 | |||||||
| chr19:8220141 | C | T | 1 | a0001c0006t0006g0266 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-2+9279C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220141 | |||||||
| chr19:8220202 | T | C | 1 | a0004c0005t0007g0289 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-2+9340T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220202 | |||||||
| chr19:8220244 | A | C | 1 | a0003c0014t0001g0406 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-2+9382A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220244 | |||||||
| chr19:8220286 | A | G | 1 | a0001c0002t0005g0045 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-2+9424A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220286 | |||||||
| chr19:8220373 | C | T | 2 | a0001c0001t0001g0197 a0001c0001t0001g0200 |
2 | HG02683.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-2+9511C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220373 | |||||||
| chr19:8220418 | C | T | 1 | a0001c0002t0004g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-2+9556C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220418 | |||||||
| chr19:8220511 | G | A | 55 | a0001c0001t0003g0142 a0001c0001t0003g0143 a0001c0001t0003g0144 others(52): Show |
55 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.-2+9649G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220511 | |||||||
| chr19:8220557 | G | A | 1 | a0001c0001t0002g0297 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-2+9695G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220557 | |||||||
| chr19:8220600 | C | T | 3 | a0001c0002t0006g0209 a0001c0002t0006g0210 a0009c0016t0006g0207 |
3 | NA18946.hp1 NA18954.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.-2+9738C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220600 | |||||||
| chr19:8220723 | G | A | 91 | a0001c0001t0001g0115 a0001c0001t0003g0035 a0001c0001t0003g0036 others(88): Show |
91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.-2+9861G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220723 | |||||||
| chr19:8220743 | C | T | 6 | a0001c0001t0003g0391 a0001c0001t0008g0390 a0002c0003t0001g0392 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+9881C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220743 | |||||||
| chr19:8220815 | GTGTTTTT others(5): Show |
G | 1 | a0001c0001t0006g0215 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-2+9966_-2+9977del others(12): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8220815 | ||||||
| chr19:8220817 | G | GT | 99 | a0001c0001t0001g0115 a0001c0001t0002g0137 a0001c0001t0002g0213 others(96): Show |
99 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.-2+9966dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8220817 | ||||||
| chr19:8220818 | T | G | 19 | a0001c0001t0001g0125 a0001c0001t0001g0407 a0001c0001t0003g0387 others(16): Show |
19 | HG01934.hp1 HG02109.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.-2+9956T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220818 | |||||||
| chr19:8220826 | T | G | 21 | a0001c0001t0001g0125 a0001c0001t0001g0407 a0001c0001t0003g0387 others(18): Show |
21 | HG01934.hp1 HG02055.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.-2+9964T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220826 | |||||||
| chr19:8220829 | G | T | 2 | a0001c0001t0007g0378 a0001c0002t0004g0004 |
2 | HG02602.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-2+9967G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220829 | |||||||
| chr19:8220846 | G | C | 70 | a0001c0001t0003g0035 a0001c0001t0003g0036 a0001c0001t0003g0046 others(67): Show |
70 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.-2+9984G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220846 | |||||||
| chr19:8220914 | T | C | 1 | a0001c0002t0006g0275 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-2+10052T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220914 | |||||||
| chr19:8220956 | G | C | 6 | a0001c0001t0003g0154 a0001c0002t0001g0203 a0001c0002t0005g0194 others(3): Show |
6 | HG00438.hp2 HG00544.hp1 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+10094G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220956 | |||||||
| chr19:8220975 | C | T | 3 | a0002c0003t0001g0043 a0002c0003t0001g0061 a0002c0003t0001g0062 |
3 | HG02886.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-2+10113C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8220975 | |||||||
| chr19:8221010 | A | G | 253 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0407 others(250): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-2+10148A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221010 | |||||||
| chr19:8221015 | C | T | 16 | a0001c0001t0003g0391 a0001c0001t0008g0390 a0002c0003t0001g0392 others(13): Show |
16 | HG01891.hp1 HG01934.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.-2+10153C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221015 | |||||||
| chr19:8221105 | G | A | 1 | a0003c0007t0009g0120 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-2+10243G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221105 | |||||||
| chr19:8221130 | A | AT | 17 | a0001c0001t0002g0133 a0001c0001t0002g0225 a0001c0001t0002g0265 others(14): Show |
17 | HG00621.hp1 HG00673.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.-2+10285dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8221130 | ||||||
| chr19:8221130 | AT | A | 61 | a0001c0001t0001g0407 a0001c0001t0001g0408 a0001c0001t0002g0241 others(58): Show |
61 | HG00408.hp2 HG00609.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.-2+10285delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8221130 | ||||||
| chr19:8221305 | T | G | 1 | a0001c0006t0006g0299 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-2+10443T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221305 | |||||||
| chr19:8221380 | G | T | 1 | a0001c0002t0002g0360 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-2+10518G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221380 | |||||||
| chr19:8221436 | G | T | 1 | a0001c0001t0008g0390 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-2+10574G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221436 | |||||||
| chr19:8221551 | AT | A | 36 | a0001c0001t0001g0408 a0001c0001t0002g0241 a0001c0001t0003g0011 others(33): Show |
36 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-2+10701delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8221551 | ||||||
| chr19:8221709 | A | G | 3 | a0001c0008t0001g0206 a0002c0003t0001g0205 a0004c0005t0008g0204 |
3 | HG02451.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-2+10847A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221709 | |||||||
| chr19:8221713 | T | G | 6 | a0001c0002t0001g0042 a0001c0002t0001g0097 a0001c0002t0001g0098 others(3): Show |
6 | HG00733.hp2 HG00741.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+10851T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221713 | |||||||
| chr19:8221752 | A | T | 1 | a0004c0005t0007g0287 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-2+10890A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221752 | |||||||
| chr19:8221870 | ATG | A | 10 | a0001c0001t0003g0387 a0001c0001t0017g0386 a0002c0003t0001g0400 others(7): Show |
10 | HG01934.hp1 HG02258.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2+11010_-2+11011d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8221870 | ||||||
| chr19:8221872 | G | GT | 34 | a0001c0001t0002g0133 a0001c0001t0002g0135 a0001c0001t0002g0139 others(31): Show |
34 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.-2+11037dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8221872 | ||||||
| chr19:8221872 | G | GTT | 68 | a0001c0001t0002g0137 a0001c0001t0002g0216 a0001c0001t0002g0217 others(65): Show |
68 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.-2+11036_-2+11037d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8221872 | ||||||
| chr19:8221872 | G | GTTT | 105 | a0001c0001t0001g0197 a0001c0001t0002g0214 a0001c0001t0002g0218 others(102): Show |
105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.-2+11035_-2+11037d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8221872 | ||||||
| chr19:8221872 | G | GTTTT | 59 | a0001c0001t0001g0198 a0001c0001t0001g0200 a0001c0001t0003g0035 others(56): Show |
59 | HG00438.hp2 HG00621.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.-2+11034_-2+11037d others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8221872 | ||||||
| chr19:8221872 | G | GTTTTT | 12 | a0001c0001t0001g0115 a0001c0001t0003g0047 a0001c0001t0003g0162 others(9): Show |
12 | HG00735.hp2 HG01109.hp2 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2+11033_-2+11037d others(7): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8221872 | ||||||
| chr19:8221872 | G | T | 4 | a0001c0001t0001g0125 a0003c0007t0003g0126 a0003c0007t0003g0127 others(1): Show |
4 | HG02109.hp1 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+11010G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221872 | |||||||
| chr19:8221872 | GT | G | 6 | a0001c0001t0002g0342 a0001c0001t0008g0390 a0001c0006t0013g0261 others(3): Show |
6 | HG00558.hp2 HG02451.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2+11037delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8221872 | ||||||
| chr19:8221872 | GTTTTTTT others(4): Show |
G | 2 | a0001c0008t0001g0206 a0004c0005t0008g0204 |
2 | HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-2+11027_-2+11037d others(13): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8221872 | ||||||
| chr19:8221872 | GTTTTTTT others(5): Show |
G | 2 | a0001c0002t0001g0020 a0002c0003t0001g0205 |
2 | HG00609.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-2+11026_-2+11037d others(14): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8221872 | ||||||
| chr19:8221878 | T | A | 4 | a0001c0001t0001g0125 a0003c0007t0003g0126 a0003c0007t0003g0127 others(1): Show |
4 | HG02109.hp1 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+11016T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221878 | |||||||
| chr19:8221879 | T | A | 1 | a0002c0013t0001g0385 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-2+11017T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221879 | |||||||
| chr19:8221880 | T | A | 10 | a0001c0001t0003g0387 a0001c0001t0017g0386 a0002c0003t0001g0400 others(7): Show |
10 | HG01934.hp1 HG02258.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2+11018T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221880 | |||||||
| chr19:8221881 | T | A | 3 | a0001c0001t0001g0407 a0003c0007t0009g0136 a0003c0007t0010g0006 |
3 | HG02055.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-2+11019T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221881 | |||||||
| chr19:8221882 | T | A | 4 | a0001c0001t0001g0125 a0003c0007t0003g0126 a0003c0007t0003g0127 others(1): Show |
4 | HG02109.hp1 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+11020T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221882 | |||||||
| chr19:8221883 | T | A | 1 | a0002c0013t0001g0385 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-2+11021T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221883 | |||||||
| chr19:8221884 | T | A | 5 | a0001c0001t0003g0387 a0001c0001t0017g0386 a0003c0004t0001g0388 others(2): Show |
5 | HG02055.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2+11022T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221884 | |||||||
| chr19:8221884 | T | G | 4 | a0001c0001t0001g0408 a0001c0002t0003g0416 a0001c0002t0003g0417 others(1): Show |
4 | HG02630.hp1 HG03704.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+11022T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221884 | |||||||
| chr19:8221884 | T | TTG | 6 | a0001c0002t0001g0042 a0001c0002t0001g0097 a0001c0002t0001g0098 others(3): Show |
6 | HG00733.hp2 HG00741.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+11023_-2+11024i others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8221884 | ||||||
| chr19:8221884 | T | TTTG | 17 | a0001c0001t0002g0241 a0001c0001t0003g0011 a0001c0001t0003g0012 others(14): Show |
17 | HG02040.hp2 HG02132.hp2 HG02155.hp1 others(14): Show |
intron_variant | MODIFIER | c.-2+11024_-2+11025i others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8221884 | ||||||
| chr19:8221885 | T | A | 1 | a0001c0001t0001g0407 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-2+11023T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221885 | |||||||
| chr19:8221886 | T | A | 11 | a0001c0001t0001g0125 a0002c0003t0001g0400 a0002c0003t0001g0401 others(8): Show |
11 | HG01934.hp1 HG02109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-2+11024T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221886 | |||||||
| chr19:8221889 | T | G | 1 | a0003c0004t0001g0044 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-2+11027T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221889 | |||||||
| chr19:8221945 | G | C | 1 | a0003c0004t0001g0402 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-2+11083G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8221945 | |||||||
| chr19:8222025 | T | C | 1 | a0001c0001t0003g0156 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-2+11163T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8222025 | |||||||
| chr19:8222034 | T | C | 308 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(305): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.-2+11172T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8222034 | |||||||
| chr19:8222037 | C | T | 8 | a0001c0001t0001g0125 a0001c0001t0003g0387 a0001c0001t0017g0386 others(5): Show |
8 | HG02109.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2+11175C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8222037 | |||||||
| chr19:8222186 | A | T | 1 | a0004c0005t0008g0104 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-2+11324A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8222186 | |||||||
| chr19:8222272 | G | A | 6 | a0002c0003t0004g0271 a0002c0003t0004g0377 a0002c0003t0008g0395 others(3): Show |
6 | HG02630.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+11410G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8222272 | |||||||
| chr19:8222351 | T | A | 2 | a0001c0019t0002g0372 a0003c0007t0009g0382 |
2 | HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-2+11489T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8222351 | |||||||
| chr19:8222624 | G | A | 1 | a0004c0005t0011g0300 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-2+11762G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8222624 | |||||||
| chr19:8222726 | G | C | 1 | a0001c0001t0003g0064 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-2+11864G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8222726 | |||||||
| chr19:8222769 | A | G | 3 | a0002c0003t0001g0040 a0005c0010t0001g0091 a0005c0010t0015g0092 |
3 | HG02886.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-2+11907A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8222769 | |||||||
| chr19:8223028 | A | G | 2 | a0001c0001t0001g0408 a0001c0015t0001g0409 |
2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-2+12166A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223028 | |||||||
| chr19:8223053 | G | C | 1 | a0001c0001t0004g0254 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-2+12191G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223053 | |||||||
| chr19:8223054 | C | T | 1 | a0001c0001t0004g0254 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-2+12192C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223054 | |||||||
| chr19:8223055 | T | G | 1 | a0001c0001t0004g0254 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-2+12193T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223055 | |||||||
| chr19:8223190 | G | A | 6 | a0001c0001t0003g0391 a0001c0001t0008g0390 a0002c0003t0001g0392 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+12328G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223190 | |||||||
| chr19:8223333 | G | A | 7 | a0001c0002t0004g0231 a0001c0002t0006g0229 a0001c0002t0006g0230 others(4): Show |
7 | NA18957.hp2 NA18960.hp2 NA18988.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2+12471G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223333 | |||||||
| chr19:8223414 | C | T | 314 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(311): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.-2+12552C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223414 | |||||||
| chr19:8223492 | G | A | 2 | a0003c0007t0009g0136 a0003c0007t0010g0006 |
2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-2+12630G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223492 | |||||||
| chr19:8223510 | T | C | 1 | a0001c0001t0003g0157 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-2+12648T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223510 | |||||||
| chr19:8223651 | C | T | 55 | a0001c0001t0003g0142 a0001c0001t0003g0143 a0001c0001t0003g0144 others(52): Show |
55 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.-2+12789C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223651 | |||||||
| chr19:8223658 | C | T | 309 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(306): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.-2+12796C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223658 | |||||||
| chr19:8223659 | G | A | 2 | a0001c0001t0003g0066 a0003c0004t0001g0065 |
2 | HG00140.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-2+12797G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223659 | |||||||
| chr19:8223728 | G | T | 1 | a0002c0003t0004g0228 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-2+12866G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223728 | |||||||
| chr19:8223873 | C | T | 309 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(306): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.-2+13011C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223873 | |||||||
| chr19:8223911 | C | T | 3 | a0001c0002t0006g0381 a0003c0007t0004g0294 a0003c0007t0004g0295 |
3 | HG00099.hp1 HG01081.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-2+13049C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223911 | |||||||
| chr19:8223972 | C | G | 55 | a0001c0001t0003g0142 a0001c0001t0003g0143 a0001c0001t0003g0144 others(52): Show |
55 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.-2+13110C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8223972 | |||||||
| chr19:8224104 | T | TA | 47 | a0001c0001t0001g0125 a0001c0001t0002g0235 a0001c0001t0002g0257 others(44): Show |
47 | HG00280.hp2 HG00621.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.-2+13264dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8224104 | ||||||
| chr19:8224104 | T | TAA | 24 | a0001c0001t0001g0408 a0001c0001t0002g0241 a0001c0001t0003g0011 others(21): Show |
24 | HG00609.hp1 HG00741.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.-2+13263_-2+13264d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8224104 | ||||||
| chr19:8224104 | TA | T | 7 | a0001c0001t0002g0264 a0001c0001t0002g0334 a0001c0001t0002g0366 others(4): Show |
7 | HG02818.hp1 HG02895.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2+13264delA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8224104 | ||||||
| chr19:8224104 | TAAAAAAA others(3): Show |
T | 1 | a0002c0003t0004g0367 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-2+13255_-2+13264d others(12): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8224104 | ||||||
| chr19:8224124 | AAAG | A | 21 | a0001c0001t0001g0115 a0001c0001t0001g0197 a0001c0001t0001g0198 others(18): Show |
21 | HG00280.hp1 HG01891.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.-2+13263_-2+13265d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224124 | |||||||
| chr19:8224125 | AAG | A | 58 | a0001c0001t0001g0200 a0001c0001t0003g0035 a0001c0001t0003g0036 others(55): Show |
58 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.-2+13264_-2+13265d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224125 | |||||||
| chr19:8224126 | AG | A | 10 | a0001c0001t0003g0069 a0001c0001t0005g0095 a0001c0001t0016g0093 others(7): Show |
10 | HG01175.hp2 HG01358.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2+13266delG | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8224126 | ||||||
| chr19:8224179 | C | T | 3 | a0001c0008t0001g0206 a0002c0003t0001g0205 a0004c0005t0008g0204 |
3 | HG02451.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-2+13317C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224179 | |||||||
| chr19:8224184 | G | A | 1 | a0001c0001t0003g0005 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-2+13322G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224184 | |||||||
| chr19:8224264 | G | A | 34 | a0001c0001t0001g0408 a0001c0001t0002g0241 a0001c0001t0003g0011 others(31): Show |
34 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.-2+13402G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224264 | |||||||
| chr19:8224276 | A | G | 1 | a0001c0002t0005g0059 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-2+13414A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224276 | |||||||
| chr19:8224277 | C | G | 1 | a0001c0002t0005g0059 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-2+13415C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224277 | |||||||
| chr19:8224278 | G | A | 3 | a0002c0003t0001g0400 a0003c0007t0009g0136 a0003c0007t0010g0006 |
3 | HG02055.hp2 HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-2+13416G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224278 | |||||||
| chr19:8224280 | G | A | 1 | a0001c0002t0005g0059 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-2+13418G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224280 | |||||||
| chr19:8224282 | T | C | 1 | a0001c0002t0005g0059 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-2+13420T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224282 | |||||||
| chr19:8224323 | C | T | 35 | a0001c0001t0001g0408 a0001c0001t0002g0241 a0001c0001t0003g0011 others(32): Show |
35 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.-2+13461C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224323 | |||||||
| chr19:8224406 | C | CA | 23 | a0001c0001t0001g0200 a0001c0001t0002g0133 a0001c0001t0002g0139 others(20): Show |
23 | HG00280.hp1 HG01175.hp1 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.-2+13563dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8224406 | ||||||
| chr19:8224406 | CA | C | 183 | a0001c0001t0001g0407 a0001c0001t0001g0408 a0001c0001t0002g0137 others(180): Show |
183 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.-2+13563delA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8224406 | ||||||
| chr19:8224406 | CAAAAA | C | 6 | a0001c0002t0001g0042 a0001c0002t0001g0097 a0001c0002t0001g0098 others(3): Show |
6 | HG00733.hp2 HG00741.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+13559_-2+13563d others(7): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8224406 | ||||||
| chr19:8224415 | A | T | 1 | a0001c0001t0003g0191 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-2+13553A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224415 | |||||||
| chr19:8224423 | A | T | 5 | a0001c0001t0003g0391 a0001c0001t0008g0390 a0002c0003t0008g0107 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2+13561A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224423 | |||||||
| chr19:8224588 | T | C | 2 | a0001c0006t0005g0185 a0001c0006t0005g0202 |
2 | HG01069.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.-2+13726T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224588 | |||||||
| chr19:8224635 | C | A | 351 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(348): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.-2+13773C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224635 | |||||||
| chr19:8224767 | G | A | 1 | a0002c0003t0004g0208 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-2+13905G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224767 | |||||||
| chr19:8224786 | G | T | 1 | a0001c0002t0001g0396 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-2+13924G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224786 | |||||||
| chr19:8224796 | C | T | 5 | a0004c0005t0007g0212 a0004c0005t0007g0286 a0004c0005t0007g0379 others(2): Show |
5 | HG00738.hp1 HG01106.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2+13934C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224796 | |||||||
| chr19:8224976 | C | T | 1 | a0004c0005t0008g0204 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-2+14114C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8224976 | |||||||
| chr19:8225018 | G | A | 1 | a0004c0005t0008g0058 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-2+14156G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8225018 | |||||||
| chr19:8225070 | G | C | 1 | a0001c0002t0001g0097 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-2+14208G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8225070 | |||||||
| chr19:8225204 | G | A | 5 | a0001c0001t0003g0391 a0001c0001t0008g0390 a0002c0003t0008g0107 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2+14342G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8225204 | |||||||
| chr19:8225417 | CT | C | 227 | a0001c0001t0001g0125 a0001c0001t0001g0197 a0001c0001t0001g0198 others(224): Show |
228 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.-2+14575delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8225417 | ||||||
| chr19:8225417 | CTT | C | 11 | a0001c0001t0003g0048 a0001c0002t0003g0416 a0001c0002t0003g0417 others(8): Show |
11 | HG00323.hp1 HG02132.hp2 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.-2+14574_-2+14575d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8225417 | ||||||
| chr19:8225473 | G | A | 2 | a0001c0001t0001g0197 a0001c0001t0001g0200 |
2 | HG02683.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-2+14611G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8225473 | |||||||
| chr19:8225509 | C | T | 4 | a0002c0003t0001g0399 a0002c0003t0001g0404 a0002c0003t0004g0138 others(1): Show |
4 | HG03041.hp1 HG03540.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+14647C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8225509 | |||||||
| chr19:8225536 | G | T | 2 | a0001c0001t0003g0105 a0008c0024t0008g0108 |
2 | HG02145.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-2+14674G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8225536 | |||||||
| chr19:8225654 | C | A | 1 | a0001c0001t0002g0336 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-2+14792C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8225654 | |||||||
| chr19:8225719 | C | T | 3 | a0001c0008t0001g0206 a0002c0003t0001g0205 a0004c0005t0008g0204 |
3 | HG02451.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-2+14857C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8225719 | |||||||
| chr19:8225852 | CT | C | 127 | a0001c0001t0001g0115 a0001c0001t0001g0197 a0001c0001t0001g0198 others(124): Show |
128 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.-2+14991delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8225852 | |||||||
| chr19:8225921 | C | T | 1 | a0005c0010t0015g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-2+15059C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8225921 | |||||||
| chr19:8225935 | C | T | 1 | a0001c0001t0003g0066 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-2+15073C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8225935 | |||||||
| chr19:8225938 | G | A | 2 | a0002c0003t0001g0165 a0003c0004t0001g0164 |
2 | NA18966.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.-2+15076G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8225938 | |||||||
| chr19:8225994 | A | G | 346 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(343): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.-2+15132A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8225994 | |||||||
| chr19:8226025 | G | A | 346 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(343): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.-2+15163G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8226025 | |||||||
| chr19:8226093 | A | T | 31 | a0001c0001t0002g0241 a0001c0001t0003g0011 a0001c0001t0003g0012 others(28): Show |
31 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.-2+15231A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8226093 | |||||||
| chr19:8226248 | T | C | 3 | a0001c0002t0005g0053 a0001c0002t0005g0059 a0004c0005t0008g0052 |
3 | HG00735.hp2 HG01515.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-2+15386T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8226248 | |||||||
| chr19:8226264 | G | A | 1 | a0001c0001t0010g0010 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-2+15402G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8226264 | |||||||
| chr19:8226312 | G | T | 1 | a0001c0001t0003g0191 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-2+15450G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8226312 | |||||||
| chr19:8226450 | G | C | 2 | a0003c0007t0009g0136 a0003c0007t0010g0006 |
2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-2+15588G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8226450 | |||||||
| chr19:8226731 | G | A | 1 | a0001c0001t0002g0341 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-2+15869G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8226731 | |||||||
| chr19:8226768 | G | A | 1 | a0003c0004t0001g0166 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-2+15906G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8226768 | |||||||
| chr19:8226769 | G | A | 1 | a0002c0003t0004g0298 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-2+15907G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8226769 | |||||||
| chr19:8226769 | GATTGCCT others(24): Show |
G | 1 | a0001c0001t0003g0191 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-2+15908_-2+15938d others(33): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8226769 | |||||||
| chr19:8226788 | T | G | 345 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(342): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.-2+15926T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8226788 | |||||||
| chr19:8226871 | G | A | 4 | a0001c0001t0002g0369 a0001c0001t0002g0370 a0001c0002t0004g0368 others(1): Show |
4 | NA18956.hp2 NA18999.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+16009G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8226871 | |||||||
| chr19:8226879 | A | T | 37 | a0001c0001t0001g0408 a0001c0001t0002g0241 a0001c0001t0003g0011 others(34): Show |
37 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.-2+16017A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8226879 | |||||||
| chr19:8227130 | A | G | 1 | a0001c0008t0004g0359 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-2+16268A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8227130 | |||||||
| chr19:8227142 | G | A | 3 | a0001c0008t0001g0206 a0002c0003t0001g0205 a0004c0005t0008g0204 |
3 | HG02451.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-2+16280G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8227142 | |||||||
| chr19:8227162 | G | T | 1 | a0002c0003t0001g0404 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-2+16300G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8227162 | |||||||
| chr19:8227211 | A | G | 4 | a0001c0001t0002g0240 a0001c0001t0002g0291 a0001c0001t0002g0292 others(1): Show |
4 | HG01243.hp2 HG01258.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+16349A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8227211 | |||||||
| chr19:8227327 | G | A | 55 | a0001c0001t0003g0142 a0001c0001t0003g0143 a0001c0001t0003g0144 others(52): Show |
55 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.-2+16465G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8227327 | |||||||
| chr19:8227581 | A | T | 3 | a0001c0002t0005g0087 a0001c0006t0005g0088 a0002c0003t0001g0103 |
3 | HG02015.hp2 HG02040.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.-2+16719A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8227581 | |||||||
| chr19:8227637 | C | G | 156 | a0001c0001t0002g0137 a0001c0001t0002g0213 a0001c0001t0002g0214 others(153): Show |
156 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.-2+16775C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8227637 | |||||||
| chr19:8227729 | A | G | 1 | a0002c0003t0004g0228 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-2+16867A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8227729 | |||||||
| chr19:8227771 | G | A | 3 | a0001c0002t0002g0123 a0001c0002t0004g0307 a0001c0002t0004g0308 |
3 | NA18962.hp2 NA19088.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-2+16909G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8227771 | |||||||
| chr19:8227978 | C | T | 3 | a0002c0003t0001g0040 a0005c0010t0001g0091 a0005c0010t0015g0092 |
3 | HG02886.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-2+17116C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8227978 | |||||||
| chr19:8227989 | G | A | 2 | a0001c0001t0002g0216 a0001c0001t0002g0217 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-2+17127G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8227989 | |||||||
| chr19:8228060 | C | T | 1 | a0006c0011t0007g0285 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-2+17198C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8228060 | |||||||
| chr19:8228175 | G | A | 6 | a0001c0001t0001g0408 a0001c0002t0003g0416 a0001c0002t0003g0417 others(3): Show |
6 | HG02055.hp2 HG02630.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+17313G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8228175 | |||||||
| chr19:8228178 | C | T | 4 | a0002c0003t0001g0399 a0002c0003t0001g0404 a0002c0003t0004g0138 others(1): Show |
4 | HG03041.hp1 HG03540.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+17316C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8228178 | |||||||
| chr19:8228216 | G | C | 345 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(342): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.-2+17354G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8228216 | |||||||
| chr19:8228368 | A | G | 1 | a0003c0004t0001g0009 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-2+17506A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8228368 | |||||||
| chr19:8228397 | G | A | 2 | a0003c0007t0009g0136 a0003c0007t0010g0006 |
2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-2+17535G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8228397 | |||||||
| chr19:8228401 | A | G | 2 | a0003c0007t0009g0136 a0003c0007t0010g0006 |
2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-2+17539A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8228401 | |||||||
| chr19:8228565 | C | T | 126 | a0001c0001t0001g0115 a0001c0001t0001g0197 a0001c0001t0001g0198 others(123): Show |
127 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.-2+17703C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8228565 | |||||||
| chr19:8228567 | C | T | 3 | a0001c0008t0001g0206 a0002c0003t0001g0205 a0004c0005t0008g0204 |
3 | HG02451.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-2+17705C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8228567 | |||||||
| chr19:8228685 | A | T | 3 | a0002c0003t0004g0223 a0002c0003t0004g0224 a0002c0003t0004g0228 |
3 | NA18955.hp1 NA18970.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-2+17823A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8228685 | |||||||
| chr19:8228689 | T | G | 1 | a0004c0009t0007g0331 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-2+17827T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8228689 | |||||||
| chr19:8228724 | T | TA | 179 | a0001c0001t0001g0125 a0001c0001t0001g0407 a0001c0001t0001g0408 others(176): Show |
179 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.-2+17871dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8228724 | ||||||
| chr19:8228724 | T | TAA | 164 | a0001c0001t0001g0115 a0001c0001t0001g0197 a0001c0001t0001g0198 others(161): Show |
165 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-2+17870_-2+17871d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8228724 | ||||||
| chr19:8228724 | T | TAAA | 6 | a0001c0001t0003g0022 a0002c0003t0001g0399 a0002c0003t0001g0404 others(3): Show |
6 | HG03041.hp1 HG03540.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2+17869_-2+17871d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8228724 | ||||||
| chr19:8228980 | C | T | 3 | a0001c0008t0001g0206 a0002c0003t0001g0205 a0004c0005t0008g0204 |
3 | HG02451.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-2+18118C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8228980 | |||||||
| chr19:8229020 | T | TA | 7 | a0001c0001t0002g0218 a0001c0001t0002g0265 a0001c0001t0003g0157 others(4): Show |
7 | HG01169.hp2 HG01255.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2+18173dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8229020 | ||||||
| chr19:8229020 | TA | T | 7 | a0001c0001t0001g0408 a0001c0001t0002g0132 a0001c0002t0003g0417 others(4): Show |
7 | HG02055.hp2 HG02630.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2+18173delA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8229020 | ||||||
| chr19:8229080 | C | T | 55 | a0001c0001t0003g0142 a0001c0001t0003g0143 a0001c0001t0003g0144 others(52): Show |
55 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.-2+18218C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8229080 | |||||||
| chr19:8229142 | T | C | 4 | a0001c0001t0002g0309 a0001c0001t0002g0333 a0001c0002t0006g0304 others(1): Show |
4 | HG00609.hp2 NA18974.hp2 NA19059.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+18280T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8229142 | |||||||
| chr19:8229320 | C | T | 4 | a0001c0001t0001g0125 a0003c0007t0003g0126 a0003c0007t0003g0127 others(1): Show |
4 | HG02109.hp1 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+18458C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8229320 | |||||||
| chr19:8229395 | TTTCTTCT others(5): Show |
T | 1 | a0001c0001t0003g0191 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-2+18536_-2+18547d others(14): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8229395 | ||||||
| chr19:8229395 | TTTCTTCT others(19): Show |
T | 1 | a0003c0007t0010g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-2+18548_-2+18573d others(28): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8229395 | ||||||
| chr19:8229404 | CTTCTTTC others(6): Show |
C | 154 | a0001c0001t0002g0137 a0001c0001t0002g0213 a0001c0001t0002g0214 others(151): Show |
154 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.-2+18545_-2+18557d others(15): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8229404 | ||||||
| chr19:8229405 | TTCTTTCT others(9): Show |
T | 133 | a0001c0001t0001g0115 a0001c0001t0001g0197 a0001c0001t0001g0198 others(130): Show |
134 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-2+18545_-2+18560d others(18): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8229405 | ||||||
| chr19:8229405 | TTCTTTCT others(15): Show |
T | 17 | a0001c0001t0001g0125 a0001c0001t0003g0387 a0001c0001t0017g0386 others(14): Show |
17 | HG01934.hp1 HG02109.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-2+18545_-2+18566d others(24): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8229405 | ||||||
| chr19:8229417 | T | C | 1 | a0001c0001t0003g0191 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-2+18555T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8229417 | |||||||
| chr19:8229418 | TTTC | T | 37 | a0001c0001t0001g0407 a0001c0001t0002g0241 a0001c0001t0003g0011 others(34): Show |
37 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.-2+18572_-2+18574d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8229418 | ||||||
| chr19:8229436 | C | A | 130 | a0001c0001t0001g0115 a0001c0001t0001g0197 a0001c0001t0001g0198 others(127): Show |
131 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.-2+18574C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8229436 | |||||||
| chr19:8229908 | T | C | 1 | a0004c0018t0007g0311 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-2+19046T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8229908 | |||||||
| chr19:8229942 | C | T | 1 | a0002c0003t0001g0399 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-2+19080C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8229942 | |||||||
| chr19:8229973 | G | A | 2 | a0001c0019t0002g0372 a0003c0007t0009g0382 |
2 | HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-2+19111G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8229973 | |||||||
| chr19:8230057 | A | C | 5 | a0001c0001t0001g0115 a0001c0025t0001g0116 a0002c0003t0001g0113 others(2): Show |
5 | HG02257.hp1 HG02486.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2+19195A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8230057 | |||||||
| chr19:8230179 | CCTTTTTT others(3): Show |
C | 1 | a0003c0007t0009g0335 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-2+19337_-2+19346d others(12): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8230179 | ||||||
| chr19:8230214 | G | A | 6 | a0001c0001t0001g0408 a0001c0002t0003g0416 a0001c0002t0003g0417 others(3): Show |
6 | HG02055.hp2 HG02630.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+19352G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8230214 | |||||||
| chr19:8230236 | A | G | 6 | a0001c0001t0001g0408 a0001c0002t0003g0416 a0001c0002t0003g0417 others(3): Show |
6 | HG02055.hp2 HG02630.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+19374A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8230236 | |||||||
| chr19:8230252 | A | G | 354 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(351): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.-2+19390A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8230252 | |||||||
| chr19:8230281 | C | G | 1 | a0003c0007t0010g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-2+19419C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8230281 | |||||||
| chr19:8230401 | G | A | 6 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 others(3): Show |
6 | HG01070.hp2 HG01517.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2+19539G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8230401 | |||||||
| chr19:8230420 | A | C | 354 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(351): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.-2+19558A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8230420 | |||||||
| chr19:8230490 | A | G | 6 | a0001c0001t0003g0035 a0001c0001t0003g0046 a0001c0001t0003g0047 others(3): Show |
6 | HG02735.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2+19628A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8230490 | |||||||
| chr19:8230852 | G | A | 1 | a0001c0001t0003g0066 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-2+19990G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8230852 | |||||||
| chr19:8230990 | C | G | 1 | a0001c0001t0002g0257 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-1-20086C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8230990 | |||||||
| chr19:8230996 | C | T | 3 | a0001c0008t0001g0206 a0002c0003t0001g0205 a0004c0005t0008g0204 |
3 | HG02451.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-1-20080C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8230996 | |||||||
| chr19:8231022 | TAG | T | 5 | a0001c0001t0003g0391 a0001c0001t0008g0390 a0002c0003t0008g0107 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-20050_-1-20049d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231022 | ||||||
| chr19:8231028 | C | T | 3 | a0001c0001t0001g0408 a0001c0015t0001g0409 a0003c0007t0009g0335 |
3 | HG02257.hp2 HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-1-20048C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8231028 | |||||||
| chr19:8231094 | G | C | 354 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(351): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.-1-19982G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8231094 | |||||||
| chr19:8231207 | A | G | 1 | a0001c0001t0003g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-1-19869A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8231207 | |||||||
| chr19:8231475 | T | C | 1 | a0003c0007t0010g0033 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-1-19601T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8231475 | |||||||
| chr19:8231536 | C | T | 4 | a0001c0001t0001g0408 a0001c0002t0003g0416 a0001c0002t0003g0417 others(1): Show |
4 | HG02630.hp1 HG03540.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-19540C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8231536 | |||||||
| chr19:8231630 | G | T | 1 | a0003c0007t0009g0382 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-1-19446G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8231630 | |||||||
| chr19:8231746 | G | A | 6 | a0001c0001t0001g0408 a0001c0002t0003g0416 a0001c0002t0003g0417 others(3): Show |
6 | HG02055.hp2 HG02630.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-19330G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8231746 | |||||||
| chr19:8231746 | G | T | 3 | a0002c0003t0001g0399 a0002c0003t0001g0404 a0002c0003t0004g0138 |
3 | HG03041.hp1 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-1-19330G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8231746 | |||||||
| chr19:8231788 | G | A | 2 | a0001c0001t0002g0312 a0001c0001t0002g0313 |
2 | NA18950.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.-1-19288G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8231788 | |||||||
| chr19:8231803 | T | C | 354 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(351): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.-1-19273T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8231803 | |||||||
| chr19:8231851 | A | AT | 7 | a0001c0001t0002g0219 a0001c0001t0002g0296 a0001c0001t0002g0370 others(4): Show |
7 | HG00423.hp2 HG01168.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-19203dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | ||||||
| chr19:8231851 | A | ATT | 122 | a0001c0001t0002g0137 a0001c0001t0002g0213 a0001c0001t0002g0214 others(119): Show |
122 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-1-19204_-1-19203d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | ||||||
| chr19:8231851 | A | ATTT | 28 | a0001c0001t0002g0282 a0001c0001t0002g0301 a0001c0001t0002g0327 others(25): Show |
28 | HG00621.hp2 HG00673.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.-1-19205_-1-19203d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | ||||||
| chr19:8231851 | A | ATTTTTTT others(3): Show |
1 | a0001c0002t0006g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-1-19212_-1-19203d others(12): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | ||||||
| chr19:8231851 | A | ATTTTTTT others(7): Show |
3 | a0001c0001t0002g0003 a0001c0019t0002g0372 a0003c0007t0009g0382 |
3 | HG02976.hp1 HG02976.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-1-19216_-1-19203d others(16): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | ||||||
| chr19:8231851 | A | ATTTTTTT others(8): Show |
2 | a0003c0004t0001g0106 a0003c0014t0001g0406 |
2 | HG02258.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-1-19217_-1-19203d others(17): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | ||||||
| chr19:8231851 | A | ATTTTTTT others(9): Show |
9 | a0001c0001t0003g0387 a0001c0001t0017g0386 a0002c0003t0001g0400 others(6): Show |
9 | HG01934.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1-19218_-1-19203d others(18): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | ||||||
| chr19:8231851 | A | ATTTTTTT others(10): Show |
3 | a0001c0001t0001g0125 a0002c0003t0001g0405 a0003c0004t0001g0388 |
3 | HG02647.hp1 HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-1-19219_-1-19203d others(19): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | ||||||
| chr19:8231851 | A | ATTTTTTT others(11): Show |
1 | a0004c0009t0007g0331 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-1-19220_-1-19203d others(20): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | ||||||
| chr19:8231851 | A | ATTTTTTT others(17): Show |
1 | a0001c0001t0002g0240 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-1-19203_-1-19202i others(26): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | ||||||
| chr19:8231851 | A | ATTTTTTT others(18): Show |
1 | a0003c0007t0009g0136 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-1-19203_-1-19202i others(27): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | ||||||
| chr19:8231851 | A | ATTTTTTT others(23): Show |
2 | a0001c0001t0002g0357 a0001c0008t0004g0359 |
2 | HG01361.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-1-19203_-1-19202i others(32): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | ||||||
| chr19:8231851 | A | ATTTTTTT others(24): Show |
3 | a0001c0001t0002g0135 a0001c0001t0002g0235 a0001c0001t0002g0341 |
3 | HG00735.hp1 HG01243.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-1-19203_-1-19202i others(33): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | ||||||
| chr19:8231851 | A | ATTTTTTT others(25): Show |
3 | a0001c0001t0002g0141 a0001c0001t0002g0239 a0001c0012t0002g0140 |
3 | HG01952.hp1 HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-1-19203_-1-19202i others(34): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | ||||||
| chr19:8231851 | A | ATTTTTTT others(26): Show |
2 | a0001c0001t0002g0139 a0003c0007t0010g0006 |
2 | HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-1-19203_-1-19202i others(35): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | ||||||
| chr19:8231851 | A | ATTTTTTT others(30): Show |
1 | a0002c0003t0004g0358 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-1-19203_-1-19202i others(39): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | ||||||
| chr19:8231851 | A | ATTTTTTT others(31): Show |
1 | a0001c0001t0002g0291 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-1-19203_-1-19202i others(40): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | ||||||
| chr19:8231851 | A | ATTTTTTT others(32): Show |
1 | a0001c0001t0002g0292 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-1-19203_-1-19202i others(41): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | ||||||
| chr19:8231851 | A | ATTTTTTT others(34): Show |
1 | a0001c0001t0003g0089 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-1-19203_-1-19202i others(43): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | ||||||
| chr19:8231851 | A | ATTTTTTT others(35): Show |
1 | a0001c0001t0003g0090 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-1-19203_-1-19202i others(44): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | ||||||
| chr19:8231851 | AT | A | 14 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0002g0346 others(11): Show |
14 | HG02040.hp2 HG02132.hp2 HG02300.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1-19203delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | ||||||
| chr19:8231851 | ATT | A | 31 | a0001c0001t0001g0198 a0001c0001t0002g0241 a0001c0001t0002g0265 others(28): Show |
31 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.-1-19204_-1-19203d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | ||||||
| chr19:8231851 | ATTT | A | 127 | a0001c0001t0001g0115 a0001c0001t0002g0251 a0001c0001t0002g0252 others(124): Show |
128 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.-1-19205_-1-19203d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8231851 | ||||||
| chr19:8231937 | C | T | 3 | a0001c0001t0002g0324 a0001c0001t0002g0336 a0002c0003t0004g0325 |
3 | HG00423.hp1 NA18941.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.-1-19139C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8231937 | |||||||
| chr19:8232031 | T | C | 4 | a0001c0001t0001g0408 a0001c0002t0003g0416 a0001c0002t0003g0417 others(1): Show |
4 | HG02630.hp1 HG03540.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-19045T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8232031 | |||||||
| chr19:8232066 | G | A | 2 | a0003c0007t0009g0136 a0003c0007t0010g0006 |
2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-1-19010G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8232066 | |||||||
| chr19:8232119 | G | A | 2 | a0001c0001t0002g0374 a0001c0001t0006g0373 |
2 | HG00738.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.-1-18957G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8232119 | |||||||
| chr19:8232121 | C | CA | 3 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0225 |
3 | HG03490.hp2 HG03492.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.-1-18954dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8232121 | ||||||
| chr19:8232234 | G | A | 1 | a0003c0007t0009g0382 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-1-18842G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8232234 | |||||||
| chr19:8232288 | C | G | 5 | a0001c0001t0003g0391 a0001c0001t0008g0390 a0002c0003t0008g0107 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-18788C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8232288 | |||||||
| chr19:8232471 | T | C | 3 | a0001c0008t0001g0206 a0002c0003t0001g0205 a0004c0005t0008g0204 |
3 | HG02451.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-1-18605T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8232471 | |||||||
| chr19:8232481 | G | A | 3 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0361 |
3 | HG03471.hp2 NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-1-18595G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8232481 | |||||||
| chr19:8232723 | C | CT | 21 | a0001c0001t0002g0133 a0001c0001t0002g0332 a0001c0001t0002g0366 others(18): Show |
21 | HG01978.hp2 HG02055.hp2 HG02071.hp1 others(18): Show |
intron_variant | MODIFIER | c.-1-18338dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8232723 | ||||||
| chr19:8232723 | CT | C | 178 | a0001c0001t0002g0137 a0001c0001t0002g0213 a0001c0001t0002g0214 others(175): Show |
178 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.-1-18338delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8232723 | ||||||
| chr19:8232745 | C | T | 136 | a0001c0001t0001g0115 a0001c0001t0001g0197 a0001c0001t0001g0198 others(133): Show |
137 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.-1-18331C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8232745 | |||||||
| chr19:8232866 | G | A | 148 | a0001c0001t0002g0137 a0001c0001t0002g0213 a0001c0001t0002g0214 others(145): Show |
148 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.-1-18210G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8232866 | |||||||
| chr19:8232885 | G | A | 4 | a0001c0001t0002g0369 a0001c0001t0002g0370 a0001c0002t0004g0368 others(1): Show |
4 | NA18956.hp2 NA18999.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-18191G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8232885 | |||||||
| chr19:8232889 | A | AT | 23 | a0001c0001t0002g0133 a0001c0001t0002g0218 a0001c0001t0002g0324 others(20): Show |
23 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.-1-18161dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8232889 | ||||||
| chr19:8232889 | AT | A | 178 | a0001c0001t0001g0200 a0001c0001t0001g0407 a0001c0001t0001g0408 others(175): Show |
179 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.-1-18161delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8232889 | ||||||
| chr19:8232889 | ATT | A | 28 | a0001c0001t0001g0115 a0001c0001t0001g0197 a0001c0001t0001g0198 others(25): Show |
28 | HG01109.hp1 HG01109.hp2 HG01515.hp2 others(25): Show |
intron_variant | MODIFIER | c.-1-18162_-1-18161d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8232889 | ||||||
| chr19:8232889 | ATTT | A | 7 | a0001c0001t0007g0121 a0002c0003t0001g0062 a0002c0003t0004g0271 others(4): Show |
7 | HG02630.hp2 HG02717.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-18163_-1-18161d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8232889 | ||||||
| chr19:8232889 | ATTTTTTT others(4): Show |
A | 5 | a0001c0001t0003g0391 a0001c0001t0008g0390 a0002c0003t0008g0107 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-18171_-1-18161d others(13): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8232889 | ||||||
| chr19:8232889 | ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0010g0010 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-1-18173_-1-18161d others(15): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8232889 | ||||||
| chr19:8232938 | A | G | 2 | a0002c0003t0001g0165 a0003c0004t0001g0164 |
2 | NA18966.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.-1-18138A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8232938 | |||||||
| chr19:8233013 | C | T | 4 | a0002c0003t0001g0399 a0002c0003t0001g0404 a0002c0003t0004g0138 others(1): Show |
4 | HG03041.hp1 HG03540.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-18063C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233013 | |||||||
| chr19:8233072 | G | T | 3 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 |
3 | HG02683.hp2 HG03654.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-1-18004G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233072 | |||||||
| chr19:8233166 | C | G | 1 | a0001c0001t0004g0249 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-1-17910C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233166 | |||||||
| chr19:8233181 | T | G | 2 | a0006c0011t0007g0280 a0006c0011t0007g0285 |
2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-1-17895T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233181 | |||||||
| chr19:8233229 | G | A | 13 | a0001c0001t0001g0115 a0001c0001t0003g0105 a0001c0001t0003g0109 others(10): Show |
13 | HG01891.hp1 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1-17847G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233229 | |||||||
| chr19:8233290 | C | T | 1 | a0001c0006t0005g0150 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-1-17786C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233290 | |||||||
| chr19:8233322 | C | T | 1 | a0001c0002t0003g0417 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-1-17754C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233322 | |||||||
| chr19:8233342 | T | C | 2 | a0003c0007t0009g0136 a0003c0007t0010g0006 |
2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-1-17734T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233342 | |||||||
| chr19:8233355 | C | T | 5 | a0001c0001t0003g0391 a0001c0001t0008g0390 a0002c0003t0008g0107 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-17721C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233355 | |||||||
| chr19:8233419 | G | A | 351 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(348): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.-1-17657G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233419 | |||||||
| chr19:8233456 | C | A | 1 | a0001c0001t0004g0254 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-1-17620C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233456 | |||||||
| chr19:8233497 | T | A | 1 | a0001c0001t0002g0348 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-1-17579T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233497 | |||||||
| chr19:8233506 | T | C | 2 | a0001c0001t0001g0408 a0001c0015t0001g0409 |
2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-1-17570T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233506 | |||||||
| chr19:8233527 | G | A | 196 | a0001c0001t0001g0115 a0001c0001t0001g0197 a0001c0001t0001g0198 others(193): Show |
197 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-1-17549G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233527 | |||||||
| chr19:8233734 | C | T | 196 | a0001c0001t0001g0115 a0001c0001t0001g0197 a0001c0001t0001g0198 others(193): Show |
197 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-1-17342C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233734 | |||||||
| chr19:8233738 | C | T | 1 | a0001c0001t0012g0279 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-1-17338C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233738 | |||||||
| chr19:8233739 | G | A | 1 | a0004c0005t0008g0246 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-1-17337G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233739 | |||||||
| chr19:8233821 | C | T | 33 | a0001c0001t0002g0241 a0001c0001t0003g0011 a0001c0001t0003g0012 others(30): Show |
33 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.-1-17255C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233821 | |||||||
| chr19:8233882 | T | G | 5 | a0001c0001t0003g0391 a0001c0001t0008g0390 a0002c0003t0008g0107 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-17194T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233882 | |||||||
| chr19:8233883 | G | T | 1 | a0001c0001t0003g0122 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-1-17193G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8233883 | |||||||
| chr19:8234077 | C | T | 18 | a0001c0001t0001g0125 a0001c0001t0001g0407 a0001c0001t0003g0387 others(15): Show |
18 | HG01934.hp1 HG02071.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-1-16999C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8234077 | |||||||
| chr19:8234133 | C | T | 1 | a0003c0007t0010g0033 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-1-16943C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8234133 | |||||||
| chr19:8234263 | G | A | 2 | a0001c0001t0012g0279 a0003c0007t0009g0335 |
2 | HG02257.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-1-16813G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8234263 | |||||||
| chr19:8234284 | C | T | 189 | a0001c0001t0001g0115 a0001c0001t0001g0197 a0001c0001t0001g0198 others(186): Show |
190 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.-1-16792C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8234284 | |||||||
| chr19:8234386 | C | G | 189 | a0001c0001t0001g0115 a0001c0001t0001g0197 a0001c0001t0001g0198 others(186): Show |
190 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.-1-16690C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8234386 | |||||||
| chr19:8234471 | A | G | 99 | a0001c0001t0002g0137 a0001c0001t0002g0213 a0001c0001t0002g0214 others(96): Show |
99 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.-1-16605A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8234471 | |||||||
| chr19:8234496 | T | A | 1 | a0001c0002t0001g0396 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-1-16580T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8234496 | |||||||
| chr19:8234542 | A | AT | 50 | a0001c0001t0001g0125 a0001c0001t0002g0133 a0001c0001t0002g0137 others(47): Show |
50 | HG00408.hp1 HG00423.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.-1-16506dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8234542 | ||||||
| chr19:8234542 | A | ATT | 9 | a0001c0001t0002g0135 a0001c0001t0002g0214 a0001c0001t0002g0338 others(6): Show |
9 | HG00733.hp2 HG01074.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-16507_-1-16506d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8234542 | ||||||
| chr19:8234542 | A | ATTT | 9 | a0001c0001t0002g0241 a0001c0001t0002g0252 a0001c0001t0003g0012 others(6): Show |
9 | HG00741.hp1 HG01168.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1-16508_-1-16506d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8234542 | ||||||
| chr19:8234542 | A | ATTTT | 12 | a0001c0001t0003g0022 a0001c0001t0003g0030 a0001c0002t0001g0020 others(9): Show |
12 | HG00609.hp1 HG02135.hp1 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.-1-16509_-1-16506d others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8234542 | ||||||
| chr19:8234542 | AT | A | 162 | a0001c0001t0001g0115 a0001c0001t0001g0197 a0001c0001t0001g0198 others(159): Show |
163 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.-1-16506delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8234542 | ||||||
| chr19:8234542 | ATT | A | 11 | a0001c0001t0001g0407 a0001c0001t0003g0050 a0001c0002t0001g0153 others(8): Show |
11 | HG01099.hp2 HG01515.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-16507_-1-16506d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8234542 | ||||||
| chr19:8234542 | ATTTTTTT others(5): Show |
A | 2 | a0001c0001t0002g0315 a0001c0001t0003g0156 |
2 | HG04204.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-1-16517_-1-16506d others(14): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8234542 | ||||||
| chr19:8234542 | ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0002g0349 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-1-16519_-1-16506d others(16): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8234542 | ||||||
| chr19:8234543 | T | C | 1 | a0003c0004t0001g0410 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-1-16533T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8234543 | |||||||
| chr19:8234571 | G | T | 1 | a0001c0001t0002g0003 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-1-16505G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8234571 | |||||||
| chr19:8234598 | GGCAGGAG others(49): Show |
G | 1 | a0002c0003t0001g0118 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-1-16474_-1-16419d others(58): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8234598 | ||||||
| chr19:8234623 | A | T | 1 | a0005c0010t0015g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-1-16453A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8234623 | |||||||
| chr19:8234670 | T | C | 189 | a0001c0001t0001g0115 a0001c0001t0001g0197 a0001c0001t0001g0198 others(186): Show |
190 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.-1-16406T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8234670 | |||||||
| chr19:8234720 | A | AT | 199 | a0001c0001t0001g0115 a0001c0001t0001g0197 a0001c0001t0001g0198 others(196): Show |
200 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.-1-16351dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8234720 | ||||||
| chr19:8234774 | G | C | 99 | a0001c0001t0002g0137 a0001c0001t0002g0213 a0001c0001t0002g0214 others(96): Show |
99 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.-1-16302G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8234774 | |||||||
| chr19:8234961 | G | A | 11 | a0001c0001t0003g0397 a0001c0001t0008g0398 a0001c0002t0001g0396 others(8): Show |
11 | HG01261.hp2 HG02145.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1-16115G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8234961 | |||||||
| chr19:8234995 | TTTTC | T | 4 | a0001c0001t0002g0282 a0001c0002t0006g0234 a0001c0002t0006g0236 others(1): Show |
4 | HG00642.hp2 HG01175.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-16065_-1-16062d others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8234995 | ||||||
| chr19:8235004 | TTTC | T | 3 | a0002c0003t0001g0040 a0005c0010t0001g0091 a0005c0010t0015g0092 |
3 | HG02886.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-1-16069_-1-16067d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8235004 | ||||||
| chr19:8235007 | C | CT | 13 | a0001c0001t0002g0341 a0001c0001t0003g0191 a0001c0001t0007g0121 others(10): Show |
13 | HG00735.hp1 HG02055.hp2 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1-16066dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8235007 | ||||||
| chr19:8235007 | C | CTT | 39 | a0001c0001t0001g0115 a0001c0001t0002g0241 a0001c0001t0002g0262 others(36): Show |
39 | HG00609.hp1 HG00733.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.-1-16067_-1-16066d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8235007 | ||||||
| chr19:8235007 | C | CTTT | 83 | a0001c0001t0002g0137 a0001c0001t0002g0213 a0001c0001t0002g0216 others(80): Show |
83 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.-1-16068_-1-16066d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8235007 | ||||||
| chr19:8235007 | C | CTTTT | 4 | a0001c0001t0002g0214 a0001c0001t0002g0252 a0001c0001t0002g0318 others(1): Show |
4 | HG00438.hp1 HG00642.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-16066_-1-16065i others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8235007 | ||||||
| chr19:8235010 | TC | T | 18 | a0001c0001t0001g0125 a0001c0001t0001g0408 a0001c0001t0003g0387 others(15): Show |
18 | HG02109.hp1 HG02109.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.-1-16065delC | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235010 | |||||||
| chr19:8235011 | C | T | 213 | a0001c0001t0001g0115 a0001c0001t0001g0197 a0001c0001t0001g0198 others(210): Show |
213 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.-1-16065C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235011 | |||||||
| chr19:8235011 | CT | C | 14 | a0001c0001t0002g0132 a0001c0001t0003g0066 a0001c0001t0003g0089 others(11): Show |
14 | HG01261.hp2 HG01515.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.-1-16051delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8235011 | ||||||
| chr19:8235026 | C | T | 3 | a0001c0001t0001g0408 a0001c0015t0001g0409 a0003c0007t0010g0033 |
3 | HG02559.hp2 HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-1-16050C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235026 | |||||||
| chr19:8235028 | G | A | 3 | a0001c0001t0001g0408 a0001c0015t0001g0409 a0003c0007t0010g0033 |
3 | HG02559.hp2 HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-1-16048G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235028 | |||||||
| chr19:8235039 | A | G | 330 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(327): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.-1-16037A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235039 | |||||||
| chr19:8235053 | G | GA | 5 | a0001c0001t0001g0408 a0001c0008t0001g0206 a0001c0015t0001g0409 others(2): Show |
5 | HG02451.hp2 HG02559.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-16022dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8235053 | ||||||
| chr19:8235054 | A | G | 2 | a0002c0003t0008g0395 a0003c0004t0004g0273 |
2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-1-16022A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235054 | |||||||
| chr19:8235061 | T | C | 2 | a0001c0008t0001g0206 a0004c0005t0008g0204 |
2 | HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-1-16015T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235061 | |||||||
| chr19:8235133 | C | T | 1 | a0001c0001t0003g0083 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-1-15943C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235133 | |||||||
| chr19:8235156 | A | G | 1 | a0001c0001t0003g0122 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-1-15920A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235156 | |||||||
| chr19:8235158 | A | G | 1 | a0001c0001t0003g0122 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-1-15918A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235158 | |||||||
| chr19:8235195 | A | G | 1 | a0003c0004t0004g0273 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-1-15881A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235195 | |||||||
| chr19:8235198 | G | A | 1 | a0001c0001t0003g0110 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-1-15878G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235198 | |||||||
| chr19:8235209 | A | G | 2 | a0001c0001t0012g0279 a0003c0007t0009g0335 |
2 | HG02257.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-1-15867A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235209 | |||||||
| chr19:8235214 | G | A | 17 | a0001c0001t0002g0219 a0001c0001t0003g0143 a0001c0001t0003g0162 others(14): Show |
17 | HG00140.hp1 HG01168.hp2 HG02976.hp1 others(14): Show |
intron_variant | MODIFIER | c.-1-15862G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235214 | |||||||
| chr19:8235228 | T | C | 8 | a0001c0001t0001g0125 a0001c0001t0003g0387 a0001c0001t0017g0386 others(5): Show |
8 | HG02109.hp1 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-15848T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235228 | |||||||
| chr19:8235286 | C | CG | 3 | a0001c0001t0002g0235 a0001c0001t0002g0290 a0001c0001t0017g0386 |
3 | HG01106.hp2 HG01243.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-1-15789dupG | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8235286 | ||||||
| chr19:8235291 | A | G | 1 | a0003c0007t0010g0033 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-1-15785A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235291 | |||||||
| chr19:8235293 | G | C | 1 | a0003c0007t0010g0033 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-1-15783G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235293 | |||||||
| chr19:8235313 | G | A | 354 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(351): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.-1-15763G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235313 | |||||||
| chr19:8235391 | G | A | 5 | a0001c0001t0003g0391 a0001c0001t0008g0390 a0002c0003t0008g0107 others(2): Show |
5 | HG02109.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-15685G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235391 | |||||||
| chr19:8235502 | A | G | 1 | a0002c0003t0004g0377 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-1-15574A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235502 | |||||||
| chr19:8235539 | G | A | 1 | a0002c0003t0001g0182 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-1-15537G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235539 | |||||||
| chr19:8235657 | G | A | 1 | a0004c0005t0007g0289 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-1-15419G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235657 | |||||||
| chr19:8235657 | G | T | 2 | a0001c0002t0003g0416 a0001c0002t0003g0417 |
2 | HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-1-15419G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235657 | |||||||
| chr19:8235661 | G | T | 1 | a0004c0005t0011g0302 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-1-15415G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235661 | |||||||
| chr19:8235724 | A | G | 1 | a0001c0001t0006g0364 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-1-15352A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235724 | |||||||
| chr19:8235730 | A | G | 1 | a0004c0005t0008g0204 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-1-15346A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235730 | |||||||
| chr19:8235762 | C | T | 4 | a0001c0001t0003g0387 a0001c0001t0017g0386 a0002c0013t0001g0385 others(1): Show |
4 | HG02280.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-15314C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235762 | |||||||
| chr19:8235895 | C | T | 1 | a0003c0004t0004g0267 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-1-15181C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235895 | |||||||
| chr19:8235921 | C | T | 161 | a0001c0001t0001g0115 a0001c0001t0001g0197 a0001c0001t0001g0198 others(158): Show |
162 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.-1-15155C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235921 | |||||||
| chr19:8235991 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-1-15085C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8235991 | |||||||
| chr19:8236151 | C | T | 5 | a0001c0001t0002g0349 a0001c0001t0002g0353 a0001c0001t0002g0380 others(2): Show |
5 | HG00423.hp2 HG00544.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-14925C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236151 | |||||||
| chr19:8236164 | C | T | 260 | a0001c0001t0001g0115 a0001c0001t0001g0197 a0001c0001t0001g0198 others(257): Show |
261 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.-1-14912C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236164 | |||||||
| chr19:8236321 | G | A | 1 | a0001c0001t0001g0407 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-1-14755G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236321 | |||||||
| chr19:8236387 | G | T | 2 | a0001c0001t0003g0171 a0001c0001t0003g0178 |
2 | NA18950.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.-1-14689G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236387 | |||||||
| chr19:8236467 | G | T | 7 | a0001c0001t0002g0137 a0001c0001t0003g0105 a0001c0001t0003g0109 others(4): Show |
7 | HG02145.hp2 HG02615.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1-14609G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236467 | |||||||
| chr19:8236471 | C | T | 3 | a0001c0001t0003g0068 a0001c0001t0003g0082 a0001c0006t0005g0189 |
3 | HG00280.hp1 HG00639.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.-1-14605C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236471 | |||||||
| chr19:8236526 | A | G | 1 | a0001c0001t0003g0391 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-1-14550A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236526 | |||||||
| chr19:8236576 | T | G | 19 | a0001c0001t0003g0397 a0001c0001t0008g0398 a0001c0002t0001g0396 others(16): Show |
19 | HG01261.hp2 HG02055.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1-14500T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236576 | |||||||
| chr19:8236582 | G | A | 19 | a0001c0001t0003g0397 a0001c0001t0008g0398 a0001c0002t0001g0396 others(16): Show |
19 | HG01261.hp2 HG02055.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1-14494G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236582 | |||||||
| chr19:8236605 | A | G | 19 | a0001c0001t0003g0397 a0001c0001t0008g0398 a0001c0002t0001g0396 others(16): Show |
19 | HG01261.hp2 HG02055.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1-14471A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236605 | |||||||
| chr19:8236641 | G | T | 19 | a0001c0001t0003g0397 a0001c0001t0008g0398 a0001c0002t0001g0396 others(16): Show |
19 | HG01261.hp2 HG02055.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1-14435G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236641 | |||||||
| chr19:8236680 | T | TAA | 6 | a0001c0001t0003g0397 a0001c0002t0001g0396 a0002c0003t0004g0271 others(3): Show |
6 | HG02145.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1-14376_-1-14375d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8236680 | ||||||
| chr19:8236680 | TAA | T | 57 | a0001c0001t0001g0125 a0001c0001t0002g0239 a0001c0001t0002g0297 others(54): Show |
57 | HG00323.hp2 HG00438.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.-1-14376_-1-14375d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8236680 | ||||||
| chr19:8236680 | TAAA | T | 14 | a0001c0001t0002g0137 a0001c0001t0003g0105 a0001c0001t0003g0109 others(11): Show |
14 | HG00280.hp2 HG00741.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.-1-14377_-1-14375d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8236680 | ||||||
| chr19:8236681 | A | T | 1 | a0001c0001t0003g0016 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-1-14395A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236681 | |||||||
| chr19:8236691 | AAAAAAAA others(4): Show |
A | 1 | a0001c0002t0005g0063 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-1-14381_-1-14371d others(13): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8236691 | ||||||
| chr19:8236694 | AAAAAAAA others(1): Show |
A | 11 | a0001c0002t0003g0416 a0001c0002t0006g0232 a0001c0006t0005g0187 others(8): Show |
11 | HG04115.hp1 HG04228.hp2 NA18948.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1-14378_-1-14371d others(10): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8236694 | ||||||
| chr19:8236695 | AAAAAAAG | A | 235 | a0001c0001t0001g0115 a0001c0001t0001g0197 a0001c0001t0001g0198 others(232): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.-1-14377_-1-14371d others(9): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8236695 | ||||||
| chr19:8236695 | AAAAAAAG others(4): Show |
A | 1 | a0003c0004t0009g0328 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-1-14377_-1-14367d others(13): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8236695 | ||||||
| chr19:8236696 | AAAAAAG | A | 9 | a0001c0001t0002g0214 a0001c0001t0002g0216 a0001c0001t0002g0217 others(6): Show |
9 | HG02071.hp1 HG02976.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1-14376_-1-14371d others(8): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8236696 | ||||||
| chr19:8236701 | AG | A | 7 | a0002c0003t0001g0113 a0002c0003t0008g0395 a0003c0004t0001g0106 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1-14374delG | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236701 | |||||||
| chr19:8236702 | G | A | 10 | a0001c0001t0003g0397 a0001c0001t0008g0398 a0001c0002t0001g0396 others(7): Show |
10 | HG01261.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1-14374G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236702 | |||||||
| chr19:8236732 | T | C | 1 | a0002c0003t0001g0040 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-1-14344T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236732 | |||||||
| chr19:8236819 | T | C | 65 | a0001c0001t0001g0407 a0001c0001t0001g0408 a0001c0001t0002g0213 others(62): Show |
65 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.-1-14257T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8236819 | |||||||
| chr19:8237002 | C | CA | 98 | a0001c0001t0002g0133 a0001c0001t0002g0214 a0001c0001t0002g0225 others(95): Show |
98 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.-1-14049dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8237002 | ||||||
| chr19:8237002 | C | CAA | 113 | a0001c0001t0001g0200 a0001c0001t0002g0241 a0001c0001t0002g0251 others(110): Show |
113 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.-1-14050_-1-14049d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8237002 | ||||||
| chr19:8237002 | C | CAAA | 81 | a0001c0001t0001g0115 a0001c0001t0001g0197 a0001c0001t0001g0198 others(78): Show |
82 | HG00140.hp2 HG00423.hp1 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.-1-14051_-1-14049d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8237002 | ||||||
| chr19:8237002 | C | CAAAA | 12 | a0001c0001t0002g0361 a0001c0001t0005g0095 a0001c0002t0005g0059 others(9): Show |
12 | HG00735.hp2 HG01175.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.-1-14052_-1-14049d others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8237002 | ||||||
| chr19:8237002 | CAA | C | 8 | a0001c0001t0008g0398 a0002c0003t0001g0113 a0002c0003t0008g0395 others(5): Show |
8 | HG01261.hp2 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1-14050_-1-14049d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8237002 | ||||||
| chr19:8237002 | CAAA | C | 9 | a0001c0001t0003g0397 a0001c0002t0001g0396 a0001c0002t0004g0226 others(6): Show |
9 | HG02145.hp1 HG02559.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1-14051_-1-14049d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8237002 | ||||||
| chr19:8237281 | G | A | 2 | a0003c0007t0009g0136 a0003c0007t0010g0006 |
2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-1-13795G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237281 | |||||||
| chr19:8237297 | C | A | 19 | a0001c0001t0003g0397 a0001c0001t0008g0398 a0001c0002t0001g0396 others(16): Show |
19 | HG01261.hp2 HG02055.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1-13779C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237297 | |||||||
| chr19:8237310 | G | A | 6 | a0001c0001t0002g0213 a0002c0003t0004g0223 a0002c0003t0004g0224 others(3): Show |
6 | HG00408.hp1 HG02523.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-13766G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237310 | |||||||
| chr19:8237530 | G | A | 59 | a0001c0001t0001g0407 a0001c0001t0001g0408 a0001c0001t0002g0214 others(56): Show |
59 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.-1-13546G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237530 | |||||||
| chr19:8237536 | A | G | 2 | a0001c0002t0005g0063 a0009c0016t0006g0207 |
2 | NA18946.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.-1-13540A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237536 | |||||||
| chr19:8237575 | G | T | 10 | a0001c0001t0003g0397 a0001c0001t0008g0398 a0001c0002t0001g0396 others(7): Show |
10 | HG01261.hp2 HG02145.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1-13501G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237575 | |||||||
| chr19:8237646 | T | C | 4 | a0001c0001t0002g0239 a0001c0001t0002g0297 a0001c0001t0002g0341 others(1): Show |
4 | HG00323.hp2 HG00735.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-13430T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237646 | |||||||
| chr19:8237719 | T | C | 4 | a0001c0001t0003g0011 a0001c0002t0005g0078 a0001c0002t0005g0413 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-13357T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237719 | |||||||
| chr19:8237744 | A | G | 3 | a0002c0003t0001g0040 a0005c0010t0001g0091 a0005c0010t0015g0092 |
3 | HG02886.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-1-13332A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237744 | |||||||
| chr19:8237768 | G | A | 4 | a0001c0001t0003g0387 a0001c0001t0017g0386 a0002c0013t0001g0385 others(1): Show |
4 | HG02280.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-13308G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237768 | |||||||
| chr19:8237778 | G | A | 4 | a0001c0001t0002g0239 a0001c0001t0002g0297 a0001c0001t0002g0341 others(1): Show |
4 | HG00323.hp2 HG00735.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-13298G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237778 | |||||||
| chr19:8237818 | A | T | 7 | a0001c0002t0014g0057 a0001c0006t0005g0181 a0002c0003t0001g0043 others(4): Show |
7 | HG00673.hp2 HG01891.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-13258A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237818 | |||||||
| chr19:8237821 | A | T | 159 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0216 others(156): Show |
159 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.-1-13255A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237821 | |||||||
| chr19:8237830 | G | A | 1 | a0002c0003t0001g0040 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-1-13246G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237830 | |||||||
| chr19:8237830 | G | T | 1 | a0001c0019t0002g0372 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-1-13246G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237830 | |||||||
| chr19:8237837 | C | T | 2 | a0001c0008t0003g0245 a0001c0019t0002g0372 |
2 | HG00673.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-1-13239C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237837 | |||||||
| chr19:8237848 | G | C | 168 | a0001c0001t0001g0125 a0001c0001t0002g0213 a0001c0001t0002g0214 others(165): Show |
168 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.-1-13228G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237848 | |||||||
| chr19:8237870 | T | C | 2 | a0001c0002t0002g0276 a0001c0002t0006g0275 |
2 | HG01358.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-1-13206T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237870 | |||||||
| chr19:8237915 | T | G | 4 | a0001c0002t0001g0042 a0001c0002t0001g0098 a0001c0002t0001g0099 others(1): Show |
4 | HG00733.hp2 HG01074.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-13161T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237915 | |||||||
| chr19:8237991 | G | A | 1 | a0001c0001t0001g0407 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-1-13085G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237991 | |||||||
| chr19:8237997 | A | T | 1 | a0001c0006t0006g0263 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-1-13079A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8237997 | |||||||
| chr19:8238043 | C | G | 3 | a0001c0001t0002g0218 a0001c0001t0006g0373 a0001c0002t0006g0242 |
3 | HG00642.hp2 HG01255.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.-1-13033C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8238043 | |||||||
| chr19:8238048 | A | C | 50 | a0001c0001t0002g0264 a0001c0001t0002g0317 a0001c0001t0002g0320 others(47): Show |
50 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.-1-13028A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8238048 | |||||||
| chr19:8238050 | T | C | 347 | a0001c0001t0001g0125 a0001c0001t0001g0197 a0001c0001t0001g0198 others(344): Show |
348 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.-1-13026T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8238050 | |||||||
| chr19:8238228 | C | G | 14 | a0001c0001t0007g0378 a0001c0001t0012g0279 a0001c0001t0017g0386 others(11): Show |
14 | HG02055.hp1 HG02572.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1-12848C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8238228 | |||||||
| chr19:8238289 | A | AGGGAGGG others(10): Show |
7 | a0001c0002t0004g0231 a0001c0002t0005g0063 a0001c0002t0006g0209 others(4): Show |
7 | NA18960.hp2 NA18969.hp2 NA18995.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-12778_-1-12762d others(19): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8238289 | ||||||
| chr19:8238315 | A | G | 192 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0408 others(189): Show |
192 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.-1-12761A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8238315 | |||||||
| chr19:8238469 | G | C | 1 | a0003c0004t0004g0272 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-1-12607G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8238469 | |||||||
| chr19:8238549 | T | A | 2 | a0006c0011t0007g0280 a0006c0011t0007g0285 |
2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-1-12527T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8238549 | |||||||
| chr19:8238612 | G | C | 4 | a0001c0001t0003g0036 a0001c0001t0003g0064 a0001c0002t0005g0084 others(1): Show |
4 | NA18970.hp1 NA18975.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-12464G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8238612 | |||||||
| chr19:8238708 | C | T | 2 | a0001c0001t0003g0387 a0003c0007t0010g0032 |
2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-1-12368C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8238708 | |||||||
| chr19:8238766 | C | T | 301 | a0001c0001t0001g0407 a0001c0001t0001g0408 a0001c0001t0002g0003 others(298): Show |
301 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.-1-12310C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8238766 | |||||||
| chr19:8238811 | C | T | 1 | a0003c0007t0010g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-1-12265C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8238811 | |||||||
| chr19:8238821 | G | A | 10 | a0001c0001t0003g0387 a0001c0002t0002g0276 a0001c0002t0003g0416 others(7): Show |
10 | HG02055.hp2 HG02559.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1-12255G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8238821 | |||||||
| chr19:8238840 | G | A | 3 | a0003c0007t0004g0278 a0003c0007t0004g0294 a0003c0007t0004g0295 |
3 | HG01081.hp2 HG03669.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-1-12236G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8238840 | |||||||
| chr19:8238895 | G | A | 1 | a0004c0005t0011g0302 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-1-12181G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8238895 | |||||||
| chr19:8239120 | G | T | 1 | a0001c0008t0001g0183 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-1-11956G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239120 | |||||||
| chr19:8239136 | T | G | 2 | a0001c0001t0001g0408 a0001c0015t0001g0409 |
2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-1-11940T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239136 | |||||||
| chr19:8239231 | G | A | 1 | a0001c0008t0001g0183 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-1-11845G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239231 | |||||||
| chr19:8239255 | C | T | 2 | a0001c0001t0001g0407 a0003c0004t0004g0316 |
2 | HG03710.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-1-11821C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239255 | |||||||
| chr19:8239292 | A | G | 321 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0407 others(318): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.-1-11784A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239292 | |||||||
| chr19:8239324 | G | A | 3 | a0001c0001t0001g0115 a0005c0010t0001g0091 a0005c0010t0015g0092 |
3 | HG02257.hp1 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-1-11752G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239324 | |||||||
| chr19:8239354 | G | A | 7 | a0001c0001t0003g0387 a0003c0007t0009g0120 a0003c0007t0009g0136 others(4): Show |
7 | HG02055.hp2 HG02559.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-11722G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239354 | |||||||
| chr19:8239355 | C | T | 3 | a0001c0002t0002g0276 a0001c0002t0003g0416 a0001c0002t0003g0417 |
3 | HG03704.hp1 HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-1-11721C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239355 | |||||||
| chr19:8239372 | C | T | 5 | a0001c0001t0002g0241 a0001c0001t0002g0251 a0001c0001t0002g0262 others(2): Show |
5 | HG02129.hp1 NA18951.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-11704C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239372 | |||||||
| chr19:8239394 | C | T | 136 | a0001c0001t0001g0408 a0001c0001t0002g0003 a0001c0001t0002g0130 others(133): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.-1-11682C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239394 | |||||||
| chr19:8239395 | G | A | 3 | a0003c0004t0001g0106 a0003c0004t0001g0402 a0003c0004t0004g0273 |
3 | HG02451.hp1 HG02895.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-1-11681G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239395 | |||||||
| chr19:8239409 | AAAG | A | 180 | a0001c0001t0001g0115 a0001c0001t0001g0407 a0001c0001t0001g0408 others(177): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.-1-11664_-1-11662d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8239409 | ||||||
| chr19:8239411 | AG | A | 125 | a0001c0001t0002g0132 a0001c0001t0002g0214 a0001c0001t0002g0216 others(122): Show |
125 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.-1-11664delG | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239411 | |||||||
| chr19:8239412 | G | A | 3 | a0001c0001t0002g0252 a0001c0001t0002g0361 a0004c0009t0007g0243 |
3 | NA19030.hp1 NA19055.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-1-11664G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239412 | |||||||
| chr19:8239418 | GA | G | 3 | a0001c0001t0002g0252 a0001c0001t0004g0131 a0001c0002t0004g0226 |
3 | NA18960.hp1 NA19055.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-1-11652delA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8239418 | ||||||
| chr19:8239422 | A | G | 1 | a0001c0002t0004g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-1-11654A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239422 | |||||||
| chr19:8239455 | C | T | 4 | a0001c0001t0007g0378 a0001c0001t0012g0279 a0001c0001t0017g0386 others(1): Show |
4 | HG02145.hp1 HG02572.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-11621C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239455 | |||||||
| chr19:8239537 | C | T | 7 | a0001c0001t0003g0387 a0003c0007t0009g0120 a0003c0007t0009g0136 others(4): Show |
7 | HG02055.hp2 HG02559.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-11539C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239537 | |||||||
| chr19:8239546 | G | A | 4 | a0001c0001t0003g0389 a0001c0002t0002g0276 a0001c0002t0003g0416 others(1): Show |
4 | HG03098.hp1 HG03704.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-11530G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239546 | |||||||
| chr19:8239546 | G | C | 4 | a0001c0001t0003g0391 a0001c0001t0007g0121 a0001c0001t0008g0390 others(1): Show |
4 | HG01261.hp2 HG02109.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-11530G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239546 | |||||||
| chr19:8239609 | C | T | 3 | a0001c0002t0002g0276 a0001c0002t0003g0416 a0001c0002t0003g0417 |
3 | HG03704.hp1 HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-1-11467C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239609 | |||||||
| chr19:8239748 | GT | G | 93 | a0001c0001t0002g0219 a0001c0001t0002g0257 a0001c0001t0003g0036 others(90): Show |
93 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.-1-11327delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239748 | |||||||
| chr19:8239875 | C | A | 2 | a0001c0001t0003g0025 a0001c0001t0003g0028 |
2 | NA18941.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.-1-11201C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239875 | |||||||
| chr19:8239923 | T | C | 7 | a0001c0001t0003g0387 a0003c0007t0009g0120 a0003c0007t0009g0136 others(4): Show |
7 | HG02055.hp2 HG02559.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-11153T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239923 | |||||||
| chr19:8239962 | C | A | 1 | a0001c0001t0007g0121 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-1-11114C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8239962 | |||||||
| chr19:8240176 | G | A | 2 | a0001c0001t0003g0068 a0001c0001t0003g0082 |
2 | HG00280.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.-1-10900G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8240176 | |||||||
| chr19:8240321 | G | C | 1 | a0001c0002t0005g0072 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-1-10755G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8240321 | |||||||
| chr19:8240350 | T | C | 3 | a0001c0002t0002g0276 a0001c0002t0003g0416 a0001c0002t0003g0417 |
3 | HG03704.hp1 HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-1-10726T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8240350 | |||||||
| chr19:8240379 | G | C | 1 | a0001c0006t0005g0181 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-1-10697G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8240379 | |||||||
| chr19:8240387 | A | G | 2 | a0001c0001t0003g0068 a0001c0001t0003g0082 |
2 | HG00280.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.-1-10689A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8240387 | |||||||
| chr19:8240412 | C | T | 1 | a0003c0007t0009g0335 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-1-10664C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8240412 | |||||||
| chr19:8240442 | A | C | 7 | a0001c0001t0001g0115 a0001c0001t0003g0391 a0001c0001t0007g0121 others(4): Show |
7 | HG01261.hp2 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-10634A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8240442 | |||||||
| chr19:8240502 | G | T | 7 | a0001c0001t0001g0115 a0001c0001t0003g0391 a0001c0001t0007g0121 others(4): Show |
7 | HG01261.hp2 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-10574G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8240502 | |||||||
| chr19:8240561 | C | T | 1 | a0001c0001t0002g0213 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-1-10515C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8240561 | |||||||
| chr19:8240562 | G | C | 1 | a0003c0007t0009g0335 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-1-10514G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8240562 | |||||||
| chr19:8240568 | G | A | 1 | a0001c0001t0002g0003 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-1-10508G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8240568 | |||||||
| chr19:8240585 | A | AGT | 8 | a0001c0001t0002g0282 a0001c0001t0003g0397 a0001c0002t0005g0072 others(5): Show |
8 | HG00099.hp2 HG01069.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1-10462_-1-10461d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240585 | ||||||
| chr19:8240585 | A | AGTGT | 118 | a0001c0001t0002g0132 a0001c0001t0002g0240 a0001c0001t0002g0252 others(115): Show |
118 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.-1-10464_-1-10461d others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240585 | ||||||
| chr19:8240585 | A | AGTGTGT | 17 | a0001c0001t0002g0219 a0001c0001t0002g0366 a0001c0001t0003g0016 others(14): Show |
17 | HG00140.hp2 HG00639.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.-1-10466_-1-10461d others(8): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240585 | ||||||
| chr19:8240585 | A | AGTGTGTG others(1): Show |
8 | a0001c0001t0002g0296 a0001c0001t0003g0162 a0003c0004t0001g0106 others(5): Show |
8 | HG02055.hp2 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1-10468_-1-10461d others(10): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240585 | ||||||
| chr19:8240585 | A | AGTGTGTG others(3): Show |
36 | a0001c0001t0001g0407 a0001c0001t0002g0312 a0001c0001t0002g0313 others(33): Show |
36 | HG00280.hp2 HG00408.hp1 HG01261.hp2 others(33): Show |
intron_variant | MODIFIER | c.-1-10470_-1-10461d others(12): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240585 | ||||||
| chr19:8240585 | A | AGTGTGTG others(5): Show |
56 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0218 others(53): Show |
56 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.-1-10472_-1-10461d others(14): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240585 | ||||||
| chr19:8240585 | A | AGTGTGTG others(7): Show |
14 | a0001c0001t0001g0115 a0001c0001t0002g0301 a0001c0001t0002g0317 others(11): Show |
14 | HG01943.hp1 HG01943.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1-10474_-1-10461d others(16): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240585 | ||||||
| chr19:8240585 | A | AGTGTGTG others(9): Show |
22 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0239 others(19): Show |
22 | HG00733.hp2 HG00735.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.-1-10476_-1-10461d others(18): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240585 | ||||||
| chr19:8240585 | A | AGTGTGTG others(11): Show |
14 | a0001c0001t0001g0125 a0001c0001t0001g0408 a0001c0001t0002g0130 others(11): Show |
14 | HG00323.hp2 HG00621.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1-10478_-1-10461d others(20): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240585 | ||||||
| chr19:8240585 | A | AGTGTGTG others(13): Show |
16 | a0001c0001t0002g0003 a0001c0001t0002g0133 a0001c0001t0002g0135 others(13): Show |
16 | HG01074.hp1 HG01168.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-1-10480_-1-10461d others(22): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240585 | ||||||
| chr19:8240585 | A | AGTGTGTG others(15): Show |
16 | a0001c0001t0002g0139 a0001c0001t0002g0264 a0001c0001t0002g0334 others(13): Show |
16 | HG00741.hp1 HG01169.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-1-10482_-1-10461d others(24): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240585 | ||||||
| chr19:8240585 | A | AGTGTGTG others(17): Show |
7 | a0001c0001t0003g0048 a0001c0001t0003g0186 a0001c0002t0002g0276 others(4): Show |
7 | HG02273.hp1 HG02965.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1-10484_-1-10461d others(26): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240585 | ||||||
| chr19:8240585 | A | AGTGTGTG others(19): Show |
2 | a0001c0002t0003g0416 a0001c0008t0004g0277 |
2 | HG02818.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-1-10486_-1-10461d others(28): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240585 | ||||||
| chr19:8240585 | AGTGTGTG others(5): Show |
A | 2 | a0001c0001t0003g0117 a0002c0003t0001g0392 |
2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-1-10472_-1-10461d others(14): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240585 | ||||||
| chr19:8240614 | G | GTGTGTGT others(12): Show |
1 | a0002c0013t0001g0385 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-1-10461_-1-10460i others(21): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240614 | ||||||
| chr19:8240719 | C | CA | 7 | a0001c0001t0003g0387 a0003c0007t0009g0120 a0003c0007t0009g0136 others(4): Show |
7 | HG02055.hp2 HG02559.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-10354dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8240719 | ||||||
| chr19:8240758 | A | G | 236 | a0001c0001t0001g0115 a0001c0001t0001g0407 a0001c0001t0001g0408 others(233): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.-1-10318A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8240758 | |||||||
| chr19:8240784 | G | A | 2 | a0001c0001t0002g0252 a0001c0001t0004g0250 |
2 | NA18971.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-1-10292G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8240784 | |||||||
| chr19:8241011 | G | A | 2 | a0001c0001t0002g0139 a0001c0001t0002g0141 |
2 | HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-1-10065G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8241011 | |||||||
| chr19:8241297 | A | G | 1 | a0001c0002t0004g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-1-9779A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8241297 | |||||||
| chr19:8241490 | T | A | 1 | a0001c0001t0002g0336 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-1-9586T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8241490 | |||||||
| chr19:8241631 | G | T | 1 | a0001c0001t0003g0110 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-1-9445G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8241631 | |||||||
| chr19:8241640 | C | T | 1 | a0002c0003t0001g0040 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-1-9436C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8241640 | |||||||
| chr19:8241796 | C | T | 6 | a0001c0002t0002g0248 a0001c0002t0002g0360 a0003c0007t0004g0278 others(3): Show |
6 | HG00642.hp1 HG01081.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-9280C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8241796 | |||||||
| chr19:8241798 | C | T | 1 | a0001c0001t0005g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-1-9278C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8241798 | |||||||
| chr19:8241890 | G | C | 8 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0012t0002g0140 others(5): Show |
8 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-9186G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8241890 | |||||||
| chr19:8241979 | T | G | 1 | a0001c0001t0003g0199 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-1-9097T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8241979 | |||||||
| chr19:8242057 | T | G | 8 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0012t0002g0140 others(5): Show |
8 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-9019T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8242057 | |||||||
| chr19:8242078 | C | T | 1 | a0002c0003t0004g0208 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-1-8998C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8242078 | |||||||
| chr19:8242138 | C | T | 9 | a0001c0001t0001g0125 a0001c0001t0002g0296 a0001c0001t0003g0144 others(6): Show |
9 | HG02109.hp1 HG02280.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-8938C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8242138 | |||||||
| chr19:8242272 | G | A | 1 | a0002c0003t0004g0138 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-1-8804G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8242272 | |||||||
| chr19:8242299 | T | C | 322 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 others(319): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.-1-8777T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8242299 | |||||||
| chr19:8242421 | A | G | 2 | a0001c0002t0006g0234 a0001c0002t0006g0236 |
2 | HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.-1-8655A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8242421 | |||||||
| chr19:8242752 | G | C | 1 | a0001c0001t0003g0035 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-1-8324G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8242752 | |||||||
| chr19:8242765 | T | C | 27 | a0001c0001t0002g0312 a0001c0001t0002g0313 a0001c0001t0002g0370 others(24): Show |
27 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.-1-8311T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8242765 | |||||||
| chr19:8242775 | G | A | 29 | a0001c0001t0003g0389 a0001c0002t0001g0042 a0001c0002t0001g0097 others(26): Show |
29 | HG00733.hp2 HG01074.hp1 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.-1-8301G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8242775 | |||||||
| chr19:8242810 | A | T | 324 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 others(321): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.-1-8266A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8242810 | |||||||
| chr19:8242908 | C | G | 1 | a0001c0001t0002g0321 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-1-8168C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8242908 | |||||||
| chr19:8242981 | GGTCT | G | 324 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 others(321): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.-1-8093_-1-8090del others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8242981 | ||||||
| chr19:8243165 | G | T | 8 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0012t0002g0140 others(5): Show |
8 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-7911G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8243165 | |||||||
| chr19:8243194 | TA | T | 62 | a0001c0001t0001g0198 a0001c0001t0002g0133 a0001c0001t0002g0214 others(59): Show |
62 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.-1-7853delA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8243194 | ||||||
| chr19:8243194 | TAA | T | 149 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0408 others(146): Show |
149 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.-1-7854_-1-7853del others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8243194 | ||||||
| chr19:8243194 | TAAA | T | 151 | a0001c0001t0002g0132 a0001c0001t0002g0135 a0001c0001t0002g0139 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.-1-7855_-1-7853del others(3): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8243194 | ||||||
| chr19:8243194 | TAAAA | T | 9 | a0001c0001t0001g0407 a0001c0002t0002g0123 a0001c0002t0004g0307 others(6): Show |
9 | HG00639.hp1 HG02040.hp1 NA18946.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-7856_-1-7853del others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8243194 | ||||||
| chr19:8243194 | TAAAAAAA others(5): Show |
T | 1 | a0001c0001t0008g0398 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-1-7864_-1-7853del others(12): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8243194 | ||||||
| chr19:8243194 | TAAAAAAA others(6): Show |
T | 3 | a0001c0001t0003g0391 a0001c0001t0007g0121 a0001c0001t0008g0390 |
3 | HG02109.hp2 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-1-7865_-1-7853del others(13): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8243194 | ||||||
| chr19:8243216 | AAAAAAAA others(1): Show |
A | 12 | a0001c0001t0001g0125 a0001c0012t0002g0140 a0003c0007t0003g0126 others(9): Show |
12 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-1-7858_-1-7851del others(8): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8243216 | ||||||
| chr19:8243327 | C | T | 7 | a0001c0002t0002g0248 a0001c0002t0002g0360 a0001c0019t0002g0372 others(4): Show |
7 | HG00642.hp1 HG01081.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-7749C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8243327 | |||||||
| chr19:8243428 | T | C | 109 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 others(106): Show |
109 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-1-7648T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8243428 | |||||||
| chr19:8243560 | C | T | 15 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0012t0002g0140 others(12): Show |
15 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-1-7516C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8243560 | |||||||
| chr19:8243562 | A | G | 352 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(349): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.-1-7514A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8243562 | |||||||
| chr19:8243629 | T | C | 4 | a0002c0003t0001g0118 a0002c0003t0004g0358 a0002c0003t0008g0107 others(1): Show |
4 | HG02486.hp2 HG03486.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-7447T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8243629 | |||||||
| chr19:8243647 | CT | C | 344 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(341): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.-1-7415delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8243647 | ||||||
| chr19:8243661 | T | C | 38 | a0001c0001t0001g0408 a0001c0001t0002g0003 a0001c0001t0002g0130 others(35): Show |
38 | HG00323.hp2 HG00621.hp1 HG01261.hp2 others(35): Show |
intron_variant | MODIFIER | c.-1-7415T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8243661 | |||||||
| chr19:8243729 | C | T | 3 | a0001c0001t0002g0309 a0001c0001t0002g0333 a0004c0005t0008g0155 |
3 | HG00609.hp2 HG02523.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-1-7347C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8243729 | |||||||
| chr19:8243848 | C | G | 4 | a0001c0001t0003g0391 a0001c0001t0007g0121 a0001c0001t0008g0390 others(1): Show |
4 | HG01261.hp2 HG02109.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-7228C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8243848 | |||||||
| chr19:8243904 | G | C | 1 | a0001c0001t0003g0389 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-1-7172G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8243904 | |||||||
| chr19:8244073 | C | T | 19 | a0001c0006t0005g0088 a0001c0008t0001g0086 a0001c0008t0005g0034 others(16): Show |
19 | HG00558.hp1 HG00738.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.-1-7003C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244073 | |||||||
| chr19:8244074 | G | A | 1 | a0001c0008t0001g0051 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-1-7002G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244074 | |||||||
| chr19:8244079 | C | T | 11 | a0001c0001t0003g0162 a0001c0002t0001g0020 a0003c0004t0001g0014 others(8): Show |
11 | HG00609.hp1 HG02129.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1-6997C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244079 | |||||||
| chr19:8244091 | T | C | 2 | a0005c0010t0001g0091 a0005c0010t0015g0092 |
2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-1-6985T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244091 | |||||||
| chr19:8244099 | T | G | 4 | a0001c0002t0002g0276 a0001c0002t0003g0416 a0001c0002t0003g0417 others(1): Show |
4 | HG01928.hp2 HG03704.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-6977T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244099 | |||||||
| chr19:8244166 | T | C | 339 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(336): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-1-6910T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244166 | |||||||
| chr19:8244308 | A | G | 1 | a0001c0002t0006g0275 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-1-6768A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244308 | |||||||
| chr19:8244321 | A | C | 5 | a0002c0003t0004g0271 a0002c0003t0004g0377 a0003c0004t0001g0410 others(2): Show |
5 | HG02630.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-6755A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244321 | |||||||
| chr19:8244358 | T | C | 323 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(320): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-1-6718T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244358 | |||||||
| chr19:8244359 | G | A | 1 | a0001c0012t0002g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-1-6717G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244359 | |||||||
| chr19:8244429 | A | G | 1 | a0001c0001t0002g0130 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-1-6647A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244429 | |||||||
| chr19:8244571 | G | A | 1 | a0001c0008t0004g0359 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-1-6505G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244571 | |||||||
| chr19:8244594 | A | T | 2 | a0001c0002t0006g0210 a0001c0002t0006g0255 |
2 | NA18954.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.-1-6482A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244594 | |||||||
| chr19:8244663 | C | T | 2 | a0003c0007t0003g0127 a0003c0007t0003g0128 |
2 | HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-1-6413C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244663 | |||||||
| chr19:8244671 | T | C | 14 | a0001c0001t0002g0240 a0001c0001t0002g0282 a0001c0001t0002g0290 others(11): Show |
14 | HG00280.hp1 HG01106.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-1-6405T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244671 | |||||||
| chr19:8244774 | G | A | 1 | a0002c0003t0001g0103 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-1-6302G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244774 | |||||||
| chr19:8244908 | G | A | 1 | a0002c0003t0008g0395 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-1-6168G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244908 | |||||||
| chr19:8244922 | A | G | 14 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0012t0002g0140 others(11): Show |
14 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1-6154A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244922 | |||||||
| chr19:8244960 | T | C | 339 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(336): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-1-6116T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8244960 | |||||||
| chr19:8245000 | C | T | 1 | a0003c0004t0001g0021 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-1-6076C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245000 | |||||||
| chr19:8245005 | G | A | 15 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0002g0336 others(12): Show |
15 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-1-6071G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245005 | |||||||
| chr19:8245039 | G | A | 1 | a0003c0007t0009g0335 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-1-6037G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245039 | |||||||
| chr19:8245094 | C | A | 336 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(333): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.-1-5982C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245094 | |||||||
| chr19:8245110 | T | TCAAAAAA others(20): Show |
5 | a0001c0001t0003g0049 a0001c0002t0006g0210 a0001c0002t0006g0304 others(2): Show |
5 | HG03834.hp1 NA18954.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-5958_-1-5957ins others(27): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245110 | ||||||
| chr19:8245111 | C | CA | 7 | a0001c0001t0003g0035 a0001c0001t0003g0047 a0001c0002t0002g0248 others(4): Show |
7 | HG00621.hp2 HG00642.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1-5941dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245111 | ||||||
| chr19:8245111 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0115 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-1-5951_-1-5941dup others(11): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245111 | ||||||
| chr19:8245111 | C | CAAAAAAA others(22): Show |
1 | a0001c0002t0006g0255 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-1-5958_-1-5957ins others(29): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245111 | ||||||
| chr19:8245111 | CA | C | 8 | a0001c0002t0001g0097 a0001c0002t0003g0416 a0001c0002t0003g0417 others(5): Show |
8 | HG01928.hp2 HG01981.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-5941delA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245111 | ||||||
| chr19:8245111 | CAA | C | 25 | a0001c0001t0003g0389 a0001c0002t0001g0042 a0001c0002t0001g0098 others(22): Show |
25 | HG00733.hp2 HG01074.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.-1-5942_-1-5941del others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245111 | ||||||
| chr19:8245112 | A | AAAAAAAC others(20): Show |
1 | a0001c0002t0006g0209 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-1-5958_-1-5957ins others(27): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245112 | ||||||
| chr19:8245112 | A | AAAAAAAC others(20): Show |
3 | a0001c0001t0007g0378 a0001c0006t0006g0256 a0001c0008t0001g0183 |
3 | HG02055.hp1 HG02896.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-1-5958_-1-5957ins others(27): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245112 | ||||||
| chr19:8245112 | A | AAAAAAAC others(19): Show |
87 | a0001c0001t0002g0257 a0001c0001t0003g0036 a0001c0001t0003g0046 others(84): Show |
87 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.-1-5958_-1-5957ins others(26): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245112 | ||||||
| chr19:8245113 | A | AAAAAACA others(18): Show |
1 | a0001c0002t0006g0232 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-1-5958_-1-5957ins others(25): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245113 | ||||||
| chr19:8245113 | A | AAAAACAA others(18): Show |
1 | a0004c0009t0007g0129 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-1-5959_-1-5958ins others(25): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245113 | ||||||
| chr19:8245114 | A | AAAACAAA others(17): Show |
42 | a0001c0001t0002g0132 a0001c0001t0002g0240 a0001c0001t0002g0252 others(39): Show |
42 | HG00280.hp1 HG00733.hp1 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.-1-5959_-1-5958ins others(24): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245114 | ||||||
| chr19:8245116 | A | AAACAAAA others(15): Show |
1 | a0001c0001t0002g0219 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-1-5958_-1-5957ins others(22): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245116 | ||||||
| chr19:8245116 | A | AAACAAAA others(14): Show |
1 | a0003c0007t0009g0335 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-1-5958_-1-5957ins others(21): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245116 | ||||||
| chr19:8245117 | A | AACAAAAA others(19): Show |
4 | a0001c0002t0001g0074 a0001c0002t0001g0412 a0001c0002t0005g0045 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-5958_-1-5957ins others(26): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245117 | ||||||
| chr19:8245118 | A | AAAAACAA others(13): Show |
2 | a0001c0001t0003g0117 a0002c0003t0001g0392 |
2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-1-5954_-1-5953ins others(20): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245118 | ||||||
| chr19:8245119 | A | C | 36 | a0001c0001t0001g0408 a0001c0001t0002g0003 a0001c0001t0002g0130 others(33): Show |
36 | HG00323.hp2 HG00621.hp1 HG01261.hp2 others(33): Show |
intron_variant | MODIFIER | c.-1-5957A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245119 | |||||||
| chr19:8245121 | A | AACAAAAC others(18): Show |
10 | a0001c0001t0002g0354 a0001c0001t0002g0370 a0001c0001t0003g0143 others(7): Show |
10 | HG02559.hp1 HG03942.hp1 NA18947.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1-5954_-1-5953ins others(25): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245121 | ||||||
| chr19:8245121 | A | C | 7 | a0001c0001t0003g0049 a0001c0002t0006g0210 a0001c0002t0006g0255 others(4): Show |
7 | HG03834.hp1 NA18954.hp1 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1-5955A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245121 | |||||||
| chr19:8245122 | A | AACAAAAC others(18): Show |
2 | a0001c0001t0002g0216 a0001c0001t0002g0217 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-1-5953_-1-5952ins others(25): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245122 | ||||||
| chr19:8245122 | A | AACAAACA others(13): Show |
2 | a0001c0001t0003g0083 a0003c0004t0004g0247 |
2 | HG02486.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-1-5953_-1-5952ins others(20): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245122 | ||||||
| chr19:8245122 | A | ACAAAACA others(17): Show |
126 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 others(123): Show |
126 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.-1-5954_-1-5953ins others(24): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245122 | |||||||
| chr19:8245122 | A | C | 137 | a0001c0001t0002g0132 a0001c0001t0002g0240 a0001c0001t0002g0252 others(134): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.-1-5954A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245122 | |||||||
| chr19:8245123 | A | C | 1 | a0001c0002t0006g0232 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-1-5953A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245123 | |||||||
| chr19:8245125 | A | C | 3 | a0003c0004t0001g0145 a0003c0004t0001g0164 a0003c0004t0001g0180 |
3 | NA18966.hp1 NA18979.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-1-5951A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245125 | |||||||
| chr19:8245126 | A | AACAAAAA others(18): Show |
31 | a0001c0001t0001g0408 a0001c0001t0002g0003 a0001c0001t0002g0130 others(28): Show |
31 | HG00323.hp2 HG00621.hp1 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.-1-5949_-1-5948ins others(25): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245126 | ||||||
| chr19:8245126 | A | AACAAAAA others(18): Show |
1 | a0001c0001t0002g0135 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-1-5949_-1-5948ins others(25): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245126 | ||||||
| chr19:8245126 | A | C | 8 | a0001c0001t0002g0219 a0001c0001t0002g0366 a0001c0001t0003g0117 others(5): Show |
8 | HG01168.hp2 HG01891.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-5950A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245126 | |||||||
| chr19:8245127 | A | AACAAAAA others(17): Show |
1 | a0001c0001t0003g0391 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-1-5948_-1-5947ins others(24): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245127 | ||||||
| chr19:8245127 | A | ACAAAAAA others(16): Show |
3 | a0001c0001t0007g0121 a0001c0001t0008g0390 a0001c0001t0008g0398 |
3 | HG01261.hp2 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-1-5949_-1-5948ins others(23): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245127 | |||||||
| chr19:8245129 | A | AAAAAAAA others(6): Show |
3 | a0001c0001t0001g0125 a0005c0010t0001g0091 a0005c0010t0015g0092 |
3 | HG02886.hp2 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-1-5941_-1-5940ins others(13): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245129 | ||||||
| chr19:8245129 | A | AAAAAAAA others(5): Show |
4 | a0001c0012t0002g0140 a0003c0007t0003g0126 a0003c0007t0003g0127 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-5941_-1-5940ins others(12): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245129 | ||||||
| chr19:8245129 | A | C | 3 | a0001c0001t0002g0296 a0001c0001t0003g0144 a0001c0001t0003g0191 |
3 | NA18942.hp1 NA18956.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-1-5947A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245129 | |||||||
| chr19:8245177 | C | A | 371 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(368): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.-1-5899C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245177 | |||||||
| chr19:8245217 | A | AT | 4 | a0001c0002t0002g0276 a0001c0002t0003g0416 a0001c0002t0003g0417 others(1): Show |
4 | HG01928.hp2 HG03704.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-5853dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245217 | ||||||
| chr19:8245346 | G | A | 1 | a0001c0001t0002g0219 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-1-5730G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245346 | |||||||
| chr19:8245365 | C | T | 14 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0012t0002g0140 others(11): Show |
14 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1-5711C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245365 | |||||||
| chr19:8245384 | A | G | 13 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0002t0002g0276 others(10): Show |
13 | HG01928.hp2 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1-5692A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245384 | |||||||
| chr19:8245424 | T | C | 3 | a0001c0006t0005g0088 a0004c0005t0011g0300 a0004c0005t0011g0302 |
3 | HG00558.hp1 HG02015.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.-1-5652T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245424 | |||||||
| chr19:8245472 | C | T | 1 | a0002c0003t0001g0205 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-1-5604C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245472 | |||||||
| chr19:8245596 | G | C | 5 | a0003c0007t0009g0120 a0003c0007t0009g0136 a0003c0007t0009g0382 others(2): Show |
5 | HG02055.hp2 HG02559.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-5480G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245596 | |||||||
| chr19:8245726 | G | A | 1 | a0001c0001t0005g0095 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-1-5350G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245726 | |||||||
| chr19:8245771 | C | T | 1 | a0002c0003t0001g0165 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-1-5305C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245771 | |||||||
| chr19:8245827 | A | G | 1 | a0004c0005t0008g0394 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-1-5249A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245827 | |||||||
| chr19:8245902 | C | CA | 74 | a0001c0001t0001g0408 a0001c0001t0002g0130 a0001c0001t0002g0133 others(71): Show |
74 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.-1-5149dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245902 | ||||||
| chr19:8245902 | C | CAA | 49 | a0001c0001t0002g0219 a0001c0001t0003g0046 a0001c0001t0003g0162 others(46): Show |
49 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.-1-5150_-1-5149dup others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245902 | ||||||
| chr19:8245902 | C | CAAA | 19 | a0001c0001t0001g0115 a0001c0002t0005g0038 a0001c0002t0005g0059 others(16): Show |
19 | HG00323.hp1 HG00735.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.-1-5151_-1-5149dup others(3): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245902 | ||||||
| chr19:8245902 | C | CAAAA | 7 | a0001c0002t0002g0276 a0001c0002t0003g0416 a0001c0002t0003g0417 others(4): Show |
7 | HG01891.hp2 HG01981.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-5152_-1-5149dup others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245902 | ||||||
| chr19:8245902 | CA | C | 6 | a0001c0001t0003g0391 a0001c0001t0007g0121 a0001c0001t0008g0390 others(3): Show |
6 | HG01261.hp2 HG02109.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-5149delA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245902 | ||||||
| chr19:8245902 | CAAA | C | 8 | a0001c0001t0002g0214 a0001c0001t0002g0235 a0001c0001t0002g0333 others(5): Show |
8 | HG01081.hp2 HG01243.hp1 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-5151_-1-5149del others(3): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245902 | ||||||
| chr19:8245902 | CAAAA | C | 78 | a0001c0001t0002g0213 a0001c0001t0002g0216 a0001c0001t0002g0217 others(75): Show |
78 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-1-5152_-1-5149del others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245902 | ||||||
| chr19:8245902 | CAAAAA | C | 14 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 others(11): Show |
14 | HG01109.hp2 HG02083.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-1-5153_-1-5149del others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245902 | ||||||
| chr19:8245902 | CAAAAAA | C | 88 | a0001c0001t0002g0132 a0001c0001t0002g0240 a0001c0001t0002g0252 others(85): Show |
88 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.-1-5154_-1-5149del others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245902 | ||||||
| chr19:8245902 | CAAAAAAA others(3): Show |
C | 1 | a0003c0004t0001g0106 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-1-5158_-1-5149del others(10): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8245902 | ||||||
| chr19:8245998 | T | C | 1 | a0001c0001t0002g0265 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-1-5078T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8245998 | |||||||
| chr19:8246006 | G | A | 6 | a0001c0002t0002g0248 a0001c0002t0002g0360 a0003c0007t0004g0278 others(3): Show |
6 | HG00642.hp1 HG01081.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-5070G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246006 | |||||||
| chr19:8246084 | AAAC | A | 9 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0002t0004g0226 others(6): Show |
9 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-4977_-1-4975del others(3): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8246084 | ||||||
| chr19:8246096 | C | CA | 33 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 others(30): Show |
33 | HG00558.hp1 HG00738.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.-1-4978dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8246096 | ||||||
| chr19:8246099 | C | A | 352 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(349): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.-1-4977C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246099 | |||||||
| chr19:8246136 | G | C | 87 | a0001c0001t0002g0219 a0001c0001t0002g0257 a0001c0001t0003g0036 others(84): Show |
87 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.-1-4940G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246136 | |||||||
| chr19:8246211 | G | A | 22 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 others(19): Show |
22 | HG00558.hp1 HG00738.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.-1-4865G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246211 | |||||||
| chr19:8246395 | C | CA | 6 | a0003c0007t0009g0120 a0003c0007t0009g0136 a0003c0007t0009g0382 others(3): Show |
6 | HG02055.hp2 HG02559.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-4676dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8246395 | ||||||
| chr19:8246454 | G | T | 1 | a0001c0001t0001g0407 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-1-4622G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246454 | |||||||
| chr19:8246476 | C | T | 6 | a0001c0002t0002g0248 a0001c0002t0002g0360 a0003c0007t0004g0278 others(3): Show |
6 | HG00642.hp1 HG01081.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-4600C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246476 | |||||||
| chr19:8246519 | T | C | 31 | a0001c0001t0001g0408 a0001c0001t0002g0003 a0001c0001t0002g0130 others(28): Show |
31 | HG00323.hp2 HG00621.hp1 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.-1-4557T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246519 | |||||||
| chr19:8246535 | A | G | 1 | a0001c0001t0002g0369 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-1-4541A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246535 | |||||||
| chr19:8246537 | A | G | 1 | a0001c0012t0002g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-1-4539A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246537 | |||||||
| chr19:8246612 | A | C | 2 | a0001c0001t0001g0408 a0001c0015t0001g0409 |
2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-1-4464A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246612 | |||||||
| chr19:8246628 | C | T | 39 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0408 others(36): Show |
39 | HG00323.hp2 HG00621.hp1 HG02015.hp1 others(36): Show |
intron_variant | MODIFIER | c.-1-4448C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246628 | |||||||
| chr19:8246663 | C | T | 1 | a0002c0003t0004g0305 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-1-4413C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246663 | |||||||
| chr19:8246743 | T | C | 370 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(367): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.-1-4333T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246743 | |||||||
| chr19:8246850 | G | T | 6 | a0001c0002t0001g0042 a0001c0002t0001g0097 a0001c0002t0001g0098 others(3): Show |
6 | HG00733.hp2 HG01074.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-4226G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246850 | |||||||
| chr19:8246856 | A | C | 34 | a0001c0001t0003g0397 a0001c0006t0005g0088 a0001c0008t0001g0051 others(31): Show |
34 | HG00558.hp1 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.-1-4220A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246856 | |||||||
| chr19:8246910 | A | G | 8 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0012t0002g0140 others(5): Show |
8 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-4166A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246910 | |||||||
| chr19:8246920 | C | T | 1 | a0001c0002t0006g0236 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-1-4156C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8246920 | |||||||
| chr19:8247128 | G | T | 133 | a0001c0001t0001g0115 a0001c0001t0001g0408 a0001c0001t0002g0003 others(130): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.-1-3948G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247128 | |||||||
| chr19:8247132 | C | T | 1 | a0001c0006t0006g0269 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-1-3944C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247132 | |||||||
| chr19:8247199 | T | C | 1 | a0001c0002t0005g0087 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-1-3877T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247199 | |||||||
| chr19:8247204 | C | T | 1 | a0003c0007t0009g0335 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-1-3872C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247204 | |||||||
| chr19:8247284 | C | T | 3 | a0001c0001t0003g0397 a0003c0004t0001g0054 a0003c0004t0001g0060 |
3 | HG01109.hp2 HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-1-3792C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247284 | |||||||
| chr19:8247296 | G | A | 2 | a0002c0003t0008g0403 a0003c0007t0010g0032 |
2 | HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-1-3780G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247296 | |||||||
| chr19:8247360 | G | A | 6 | a0003c0007t0009g0120 a0003c0007t0009g0136 a0003c0007t0009g0382 others(3): Show |
6 | HG02055.hp2 HG02559.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-3716G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247360 | |||||||
| chr19:8247362 | G | A | 5 | a0001c0001t0003g0391 a0001c0001t0007g0121 a0001c0001t0007g0378 others(2): Show |
5 | HG01261.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-3714G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247362 | |||||||
| chr19:8247563 | A | G | 4 | a0003c0007t0004g0278 a0003c0007t0004g0294 a0003c0007t0004g0295 others(1): Show |
4 | HG01081.hp2 HG03669.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-3513A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247563 | |||||||
| chr19:8247567 | G | A | 3 | a0001c0006t0005g0088 a0004c0005t0011g0300 a0004c0005t0011g0302 |
3 | HG00558.hp1 HG02015.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.-1-3509G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247567 | |||||||
| chr19:8247680 | A | G | 1 | a0001c0006t0005g0187 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-1-3396A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247680 | |||||||
| chr19:8247710 | T | C | 5 | a0001c0001t0003g0391 a0001c0001t0007g0121 a0001c0001t0007g0378 others(2): Show |
5 | HG01261.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-3366T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247710 | |||||||
| chr19:8247728 | G | A | 40 | a0001c0001t0001g0408 a0001c0001t0002g0003 a0001c0001t0002g0130 others(37): Show |
40 | HG00323.hp2 HG00621.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.-1-3348G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247728 | |||||||
| chr19:8247732 | C | CT | 16 | a0001c0001t0002g0216 a0001c0001t0002g0327 a0001c0001t0002g0345 others(13): Show |
16 | HG00642.hp1 HG01517.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.-1-3325dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8247732 | ||||||
| chr19:8247732 | C | CTT | 184 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 others(181): Show |
184 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.-1-3326_-1-3325dup others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8247732 | ||||||
| chr19:8247732 | C | CTTT | 15 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0002g0132 others(12): Show |
15 | HG00544.hp2 HG02109.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-1-3327_-1-3325dup others(3): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8247732 | ||||||
| chr19:8247732 | CT | C | 42 | a0001c0001t0001g0408 a0001c0001t0002g0003 a0001c0001t0002g0130 others(39): Show |
42 | HG00621.hp1 HG01070.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.-1-3325delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8247732 | ||||||
| chr19:8247734 | T | C | 91 | a0001c0001t0002g0219 a0001c0001t0002g0257 a0001c0001t0003g0036 others(88): Show |
91 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.-1-3342T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247734 | |||||||
| chr19:8247735 | T | C | 2 | a0001c0002t0001g0074 a0003c0004t0001g0044 |
2 | HG01070.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.-1-3341T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247735 | |||||||
| chr19:8247735 | T | TTTTTTTT others(2782): Show |
1 | a0002c0003t0004g0358 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-1-3325_-1-3324ins others(2789): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8247735 | ||||||
| chr19:8247766 | C | T | 1 | a0001c0001t0002g0366 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-1-3310C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247766 | |||||||
| chr19:8247800 | T | C | 352 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(349): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.-1-3276T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247800 | |||||||
| chr19:8247881 | A | G | 11 | a0001c0002t0004g0226 a0003c0007t0004g0278 a0003c0007t0004g0294 others(8): Show |
11 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-3195A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247881 | |||||||
| chr19:8247895 | G | C | 91 | a0001c0001t0002g0219 a0001c0001t0002g0257 a0001c0001t0003g0036 others(88): Show |
91 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.-1-3181G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247895 | |||||||
| chr19:8247970 | A | G | 1 | a0001c0001t0002g0292 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-1-3106A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8247970 | |||||||
| chr19:8248032 | C | T | 1 | a0003c0007t0010g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-1-3044C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248032 | |||||||
| chr19:8248128 | C | T | 11 | a0001c0002t0004g0226 a0003c0007t0004g0278 a0003c0007t0004g0294 others(8): Show |
11 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-2948C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248128 | |||||||
| chr19:8248134 | G | A | 1 | a0002c0003t0008g0107 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-1-2942G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248134 | |||||||
| chr19:8248328 | C | T | 1 | a0001c0008t0001g0086 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-1-2748C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248328 | |||||||
| chr19:8248371 | G | A | 1 | a0002c0003t0001g0040 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-1-2705G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248371 | |||||||
| chr19:8248398 | G | A | 1 | a0002c0003t0001g0040 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-1-2678G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248398 | |||||||
| chr19:8248434 | A | C | 11 | a0001c0002t0004g0226 a0003c0007t0004g0278 a0003c0007t0004g0294 others(8): Show |
11 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-2642A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248434 | |||||||
| chr19:8248450 | C | T | 11 | a0001c0002t0004g0226 a0003c0007t0004g0278 a0003c0007t0004g0294 others(8): Show |
11 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-2626C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248450 | |||||||
| chr19:8248593 | GTGAA | G | 11 | a0001c0002t0004g0226 a0003c0007t0004g0278 a0003c0007t0004g0294 others(8): Show |
11 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-2480_-1-2477del others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8248593 | ||||||
| chr19:8248608 | G | A | 11 | a0001c0002t0004g0226 a0003c0007t0004g0278 a0003c0007t0004g0294 others(8): Show |
11 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-2468G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248608 | |||||||
| chr19:8248649 | T | G | 198 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 others(195): Show |
198 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.-1-2427T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248649 | |||||||
| chr19:8248689 | G | A | 198 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 others(195): Show |
198 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.-1-2387G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248689 | |||||||
| chr19:8248735 | A | G | 11 | a0001c0002t0004g0226 a0003c0007t0004g0278 a0003c0007t0004g0294 others(8): Show |
11 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-2341A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248735 | |||||||
| chr19:8248828 | TGATGGGT others(17): Show |
T | 27 | a0001c0001t0001g0408 a0001c0001t0002g0003 a0001c0001t0002g0130 others(24): Show |
27 | HG00323.hp2 HG00621.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.-1-2233_-1-2210del others(24): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8248828 | ||||||
| chr19:8248843 | C | T | 4 | a0001c0001t0002g0135 a0001c0001t0002g0139 a0001c0001t0002g0141 others(1): Show |
4 | HG02965.hp2 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-2233C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248843 | |||||||
| chr19:8248844 | A | G | 4 | a0001c0001t0002g0135 a0001c0001t0002g0139 a0001c0001t0002g0141 others(1): Show |
4 | HG02965.hp2 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-2232A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248844 | |||||||
| chr19:8248848 | C | G | 4 | a0001c0001t0002g0135 a0001c0001t0002g0139 a0001c0001t0002g0141 others(1): Show |
4 | HG02965.hp2 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-2228C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248848 | |||||||
| chr19:8248849 | T | G | 4 | a0001c0001t0002g0135 a0001c0001t0002g0139 a0001c0001t0002g0141 others(1): Show |
4 | HG02965.hp2 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-2227T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248849 | |||||||
| chr19:8248851 | T | G | 4 | a0001c0001t0002g0135 a0001c0001t0002g0139 a0001c0001t0002g0141 others(1): Show |
4 | HG02965.hp2 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-2225T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248851 | |||||||
| chr19:8248852 | G | GGTGGGCA others(322): Show |
4 | a0001c0001t0002g0135 a0001c0001t0002g0139 a0001c0001t0002g0141 others(1): Show |
4 | HG02965.hp2 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-2223_-1-2222ins others(329): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8248852 | ||||||
| chr19:8248862 | G | A | 1 | a0005c0010t0015g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-1-2214G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248862 | |||||||
| chr19:8248871 | T | TGGTGGGT others(74): Show |
10 | a0003c0007t0004g0278 a0003c0007t0004g0294 a0003c0007t0004g0295 others(7): Show |
10 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1-2196_-1-2195ins others(81): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8248871 | ||||||
| chr19:8248871 | T | TGGTGGGT others(78): Show |
1 | a0001c0002t0004g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-1-2196_-1-2195ins others(85): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8248871 | ||||||
| chr19:8248904 | T | G | 11 | a0001c0002t0004g0226 a0003c0007t0004g0278 a0003c0007t0004g0294 others(8): Show |
11 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-2172T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248904 | |||||||
| chr19:8248906 | T | C | 98 | a0001c0001t0002g0219 a0001c0001t0002g0257 a0001c0001t0003g0036 others(95): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.-1-2170T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248906 | |||||||
| chr19:8248977 | A | G | 11 | a0001c0002t0004g0226 a0003c0007t0004g0278 a0003c0007t0004g0294 others(8): Show |
11 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-2099A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8248977 | |||||||
| chr19:8248991 | TGATGGGT others(17): Show |
T | 11 | a0001c0002t0004g0226 a0003c0007t0004g0278 a0003c0007t0004g0294 others(8): Show |
11 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-2070_-1-2047del others(24): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8248991 | ||||||
| chr19:8249013 | TTGGA | T | 5 | a0001c0001t0003g0391 a0001c0001t0007g0121 a0001c0001t0007g0378 others(2): Show |
5 | HG01261.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-2059_-1-2056del others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8249013 | ||||||
| chr19:8249021 | G | A | 1 | a0001c0001t0006g0215 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-1-2055G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249021 | |||||||
| chr19:8249058 | GGAT | G | 31 | a0001c0001t0001g0408 a0001c0001t0002g0003 a0001c0001t0002g0130 others(28): Show |
31 | HG00323.hp2 HG00621.hp1 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.-1-2012_-1-2010del others(3): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8249058 | ||||||
| chr19:8249119 | A | G | 11 | a0001c0002t0004g0226 a0003c0007t0004g0278 a0003c0007t0004g0294 others(8): Show |
11 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-1957A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249119 | |||||||
| chr19:8249131 | AGTGGGTG others(32): Show |
A | 1 | a0008c0024t0008g0108 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-1-1911_-1-1873del others(39): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8249131 | ||||||
| chr19:8249150 | GGATGGGT others(47): Show |
G | 1 | a0001c0001t0003g0012 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-1-1875_-1-1822del others(54): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8249150 | ||||||
| chr19:8249168 | T | C | 2 | a0001c0001t0003g0117 a0002c0003t0001g0392 |
2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-1-1908T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249168 | |||||||
| chr19:8249175 | GTGGACAG others(17): Show |
G | 11 | a0001c0002t0004g0226 a0003c0007t0004g0278 a0003c0007t0004g0294 others(8): Show |
11 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-1895_-1-1872del others(24): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8249175 | ||||||
| chr19:8249206 | A | ATGGGTGG others(12): Show |
8 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0012t0002g0140 others(5): Show |
8 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-1861_-1-1843dup others(19): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8249206 | ||||||
| chr19:8249226 | T | G | 3 | a0002c0003t0001g0400 a0002c0003t0001g0401 a0002c0003t0001g0411 |
3 | HG01934.hp1 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-1-1850T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249226 | |||||||
| chr19:8249231 | G | A | 2 | a0001c0001t0004g0250 a0001c0001t0004g0352 |
2 | HG02083.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.-1-1845G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249231 | |||||||
| chr19:8249302 | C | T | 1 | a0002c0003t0001g0113 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-1-1774C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249302 | |||||||
| chr19:8249303 | G | A | 8 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0012t0002g0140 others(5): Show |
8 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-1773G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249303 | |||||||
| chr19:8249421 | G | A | 1 | a0001c0001t0003g0389 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-1-1655G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249421 | |||||||
| chr19:8249455 | A | C | 14 | a0001c0002t0004g0226 a0003c0007t0004g0278 a0003c0007t0004g0294 others(11): Show |
14 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-1-1621A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249455 | |||||||
| chr19:8249456 | G | C | 115 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0216 others(112): Show |
115 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.-1-1620G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249456 | |||||||
| chr19:8249582 | T | C | 5 | a0001c0002t0002g0248 a0001c0002t0002g0276 a0001c0002t0002g0360 others(2): Show |
5 | HG00642.hp1 HG02300.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-1494T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249582 | |||||||
| chr19:8249587 | A | AT | 84 | a0001c0001t0002g0219 a0001c0001t0002g0257 a0001c0001t0003g0036 others(81): Show |
84 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.-1-1467dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8249587 | ||||||
| chr19:8249587 | A | ATT | 14 | a0001c0001t0012g0279 a0001c0001t0017g0386 a0001c0002t0002g0248 others(11): Show |
14 | HG00642.hp1 HG01175.hp1 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.-1-1468_-1-1467dup others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8249587 | ||||||
| chr19:8249587 | A | ATTTT | 46 | a0001c0001t0001g0408 a0001c0001t0002g0132 a0001c0001t0002g0135 others(43): Show |
46 | HG00280.hp2 HG00423.hp2 HG02027.hp1 others(43): Show |
intron_variant | MODIFIER | c.-1-1470_-1-1467dup others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8249587 | ||||||
| chr19:8249587 | A | ATTTTT | 73 | a0001c0001t0001g0198 a0001c0001t0002g0003 a0001c0001t0002g0130 others(70): Show |
73 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.-1-1471_-1-1467dup others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8249587 | ||||||
| chr19:8249587 | A | ATTTTTT | 81 | a0001c0001t0001g0125 a0001c0001t0001g0197 a0001c0001t0002g0214 others(78): Show |
81 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.-1-1472_-1-1467dup others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8249587 | ||||||
| chr19:8249587 | A | ATTTTTTT | 29 | a0001c0001t0001g0200 a0001c0001t0002g0213 a0001c0001t0002g0216 others(26): Show |
29 | HG00438.hp1 HG00673.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.-1-1473_-1-1467dup others(7): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8249587 | ||||||
| chr19:8249587 | AT | A | 6 | a0001c0001t0003g0391 a0001c0001t0007g0121 a0001c0001t0007g0378 others(3): Show |
6 | HG01261.hp2 HG02109.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-1467delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8249587 | ||||||
| chr19:8249587 | ATTT | A | 7 | a0003c0007t0004g0278 a0003c0007t0004g0294 a0003c0007t0004g0295 others(4): Show |
7 | HG01081.hp2 HG02622.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-1469_-1-1467del others(3): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8249587 | ||||||
| chr19:8249587 | ATTTT | A | 7 | a0001c0002t0004g0226 a0003c0007t0009g0120 a0003c0007t0009g0136 others(4): Show |
7 | HG02055.hp2 HG02559.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-1470_-1-1467del others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8249587 | ||||||
| chr19:8249668 | T | C | 241 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 others(238): Show |
241 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.-1-1408T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249668 | |||||||
| chr19:8249735 | C | T | 5 | a0001c0001t0001g0125 a0001c0012t0002g0140 a0003c0007t0003g0126 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-1341C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249735 | |||||||
| chr19:8249778 | A | T | 3 | a0004c0009t0007g0281 a0004c0009t0007g0284 a0004c0009t0007g0331 |
3 | HG02622.hp1 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-1-1298A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249778 | |||||||
| chr19:8249783 | G | C | 1 | a0001c0008t0001g0183 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-1-1293G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249783 | |||||||
| chr19:8249864 | C | T | 14 | a0001c0002t0004g0226 a0003c0007t0004g0278 a0003c0007t0004g0294 others(11): Show |
14 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-1-1212C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249864 | |||||||
| chr19:8249885 | C | T | 194 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 others(191): Show |
194 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.-1-1191C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249885 | |||||||
| chr19:8249969 | G | A | 14 | a0001c0002t0004g0226 a0003c0007t0004g0278 a0003c0007t0004g0294 others(11): Show |
14 | HG01081.hp2 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-1-1107G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249969 | |||||||
| chr19:8249986 | C | T | 5 | a0001c0001t0001g0125 a0001c0012t0002g0140 a0003c0007t0003g0126 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-1090C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8249986 | |||||||
| chr19:8250000 | A | G | 8 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0012t0002g0140 others(5): Show |
8 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-1076A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8250000 | |||||||
| chr19:8250026 | G | A | 29 | a0001c0002t0001g0024 a0001c0002t0001g0153 a0001c0002t0001g0160 others(26): Show |
29 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.-1-1050G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8250026 | |||||||
| chr19:8250194 | C | CA | 15 | a0001c0002t0004g0226 a0003c0007t0004g0278 a0003c0007t0004g0294 others(12): Show |
15 | HG01081.hp2 HG02055.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-1-879dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 8250194 | ||||||
| chr19:8250270 | C | T | 8 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0012t0002g0140 others(5): Show |
8 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-806C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8250270 | |||||||
| chr19:8250362 | A | C | 1 | a0002c0003t0001g0103 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-1-714A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8250362 | |||||||
| chr19:8250377 | A | G | 1 | a0002c0013t0001g0385 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-1-699A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8250377 | |||||||
| chr19:8250442 | C | T | 5 | a0001c0002t0002g0248 a0001c0002t0002g0276 a0001c0002t0002g0360 others(2): Show |
5 | HG00642.hp1 HG02300.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-634C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8250442 | |||||||
| chr19:8250623 | A | G | 92 | a0001c0001t0002g0219 a0001c0001t0002g0257 a0001c0001t0003g0036 others(89): Show |
92 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.-1-453A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8250623 | |||||||
| chr19:8250690 | C | T | 1 | a0001c0001t0002g0235 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-1-386C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8250690 | |||||||
| chr19:8250703 | C | T | 5 | a0001c0002t0002g0248 a0001c0002t0002g0276 a0001c0002t0002g0360 others(2): Show |
5 | HG00642.hp1 HG02300.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-373C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8250703 | |||||||
| chr19:8250704 | C | T | 1 | a0002c0003t0004g0355 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-1-372C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8250704 | |||||||
| chr19:8250751 | G | A | 4 | a0001c0001t0001g0125 a0003c0007t0003g0126 a0003c0007t0003g0127 others(1): Show |
4 | HG02109.hp1 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-325G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8250751 | |||||||
| chr19:8250816 | A | G | 1 | a0001c0001t0002g0353 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-1-260A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8250816 | |||||||
| chr19:8250893 | G | A | 4 | a0001c0002t0001g0074 a0001c0002t0001g0412 a0001c0002t0005g0045 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-183G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8250893 | |||||||
| chr19:8250963 | A | G | 308 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 others(305): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.-1-113A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 2/11 | chr19 | 8250963 | |||||||
| chr19:8251326 | C | T | 2 | a0001c0001t0012g0279 a0001c0001t0017g0386 |
2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.173+77C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8251326 | |||||||
| chr19:8251368 | C | T | 6 | a0001c0002t0001g0042 a0001c0002t0001g0097 a0001c0002t0001g0098 others(3): Show |
6 | HG00733.hp2 HG01074.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.173+119C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8251368 | |||||||
| chr19:8251426 | T | C | 55 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(52): Show |
55 | HG00280.hp1 HG00733.hp1 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.173+177T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8251426 | |||||||
| chr19:8251549 | C | T | 6 | a0003c0007t0009g0120 a0003c0007t0009g0136 a0003c0007t0009g0382 others(3): Show |
6 | HG02055.hp2 HG02559.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.173+300C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8251549 | |||||||
| chr19:8251594 | TTGAGGTC others(15): Show |
T | 1 | a0001c0001t0002g0251 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.173+346_173+367del others(22): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8251594 | |||||||
| chr19:8251624 | C | G | 1 | a0001c0006t0006g0263 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.173+375C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8251624 | |||||||
| chr19:8251654 | A | G | 1 | a0001c0001t0002g0214 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.173+405A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8251654 | |||||||
| chr19:8251741 | T | C | 1 | a0001c0001t0002g0214 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.173+492T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8251741 | |||||||
| chr19:8251800 | T | TA | 200 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 others(197): Show |
200 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.173+564dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8251800 | ||||||
| chr19:8251813 | ATGTGAGC | A | 39 | a0001c0001t0001g0408 a0001c0001t0002g0003 a0001c0001t0002g0130 others(36): Show |
39 | HG00323.hp2 HG00621.hp1 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.173+567_173+573del others(7): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8251813 | ||||||
| chr19:8251844 | G | C | 1 | a0001c0002t0001g0396 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.173+595G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8251844 | |||||||
| chr19:8251881 | G | A | 29 | a0001c0002t0001g0024 a0001c0002t0001g0153 a0001c0002t0001g0160 others(26): Show |
29 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.173+632G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8251881 | |||||||
| chr19:8251928 | A | T | 1 | a0001c0002t0004g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.173+679A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8251928 | |||||||
| chr19:8251938 | G | T | 1 | a0001c0002t0004g0329 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.173+689G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8251938 | |||||||
| chr19:8252019 | G | A | 1 | a0001c0001t0006g0215 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.173+770G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8252019 | |||||||
| chr19:8252023 | T | C | 2 | a0001c0001t0012g0279 a0001c0001t0017g0386 |
2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.173+774T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8252023 | |||||||
| chr19:8252025 | G | C | 1 | a0001c0001t0003g0110 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.173+776G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8252025 | |||||||
| chr19:8252038 | G | A | 4 | a0001c0001t0007g0378 a0001c0001t0008g0390 a0001c0001t0008g0398 others(1): Show |
4 | HG01261.hp2 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.173+789G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8252038 | |||||||
| chr19:8252064 | T | TA | 107 | a0001c0001t0002g0003 a0001c0001t0002g0130 a0001c0001t0002g0133 others(104): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.173+828dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8252064 | ||||||
| chr19:8252064 | T | TAA | 17 | a0001c0001t0001g0408 a0001c0001t0002g0135 a0001c0001t0002g0137 others(14): Show |
17 | HG02109.hp2 HG02145.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.173+827_173+828dup others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8252064 | ||||||
| chr19:8252064 | TAA | T | 206 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(203): Show |
206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.173+827_173+828del others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8252064 | ||||||
| chr19:8252073 | A | T | 1 | a0001c0001t0004g0254 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.173+824A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8252073 | |||||||
| chr19:8252094 | G | C | 1 | a0004c0005t0011g0302 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.173+845G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8252094 | |||||||
| chr19:8252096 | T | C | 3 | a0001c0001t0002g0240 a0001c0001t0002g0291 a0001c0001t0002g0292 |
3 | HG01258.hp2 HG02698.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.173+847T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8252096 | |||||||
| chr19:8252106 | C | T | 2 | a0001c0001t0002g0290 a0001c0001t0003g0096 |
2 | HG01106.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.173+857C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8252106 | |||||||
| chr19:8252167 | A | G | 1 | a0001c0008t0001g0086 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.173+918A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8252167 | |||||||
| chr19:8252185 | G | A | 139 | a0001c0001t0001g0407 a0001c0001t0002g0213 a0001c0001t0002g0214 others(136): Show |
139 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.173+936G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8252185 | |||||||
| chr19:8252316 | G | A | 1 | a0001c0002t0001g0396 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.173+1067G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8252316 | |||||||
| chr19:8252352 | A | G | 253 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 others(250): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.173+1103A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8252352 | |||||||
| chr19:8252369 | T | TA | 381 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(378): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.173+1131dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8252369 | ||||||
| chr19:8252369 | T | TAA | 7 | a0001c0001t0002g0383 a0001c0001t0003g0064 a0001c0001t0003g0144 others(4): Show |
7 | HG00323.hp1 HG01952.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.173+1130_173+1131d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8252369 | ||||||
| chr19:8252369 | T | TAAA | 7 | a0003c0004t0001g0106 a0003c0004t0001g0388 a0003c0004t0001g0402 others(4): Show |
7 | HG02451.hp1 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.173+1129_173+1131d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8252369 | ||||||
| chr19:8252433 | G | C | 368 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(365): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.173+1184G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8252433 | |||||||
| chr19:8252442 | CT | C | 245 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(242): Show |
246 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.173+1207delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8252442 | ||||||
| chr19:8252442 | CTT | C | 20 | a0001c0001t0002g0344 a0001c0001t0003g0089 a0001c0001t0003g0090 others(17): Show |
20 | HG00558.hp1 HG00741.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.173+1206_173+1207d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8252442 | ||||||
| chr19:8252442 | CTTTT | C | 33 | a0001c0001t0001g0408 a0001c0001t0002g0003 a0001c0001t0002g0130 others(30): Show |
33 | HG00323.hp2 HG00621.hp1 HG02015.hp1 others(30): Show |
intron_variant | MODIFIER | c.173+1204_173+1207d others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8252442 | ||||||
| chr19:8252442 | CTTTTTT | C | 76 | a0001c0001t0002g0219 a0001c0001t0002g0257 a0001c0001t0003g0036 others(73): Show |
76 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.173+1202_173+1207d others(8): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8252442 | ||||||
| chr19:8252557 | G | C | 1 | a0001c0001t0003g0028 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.173+1308G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8252557 | |||||||
| chr19:8253022 | A | C | 1 | a0001c0001t0002g0365 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.174-1477A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8253022 | |||||||
| chr19:8253077 | C | T | 48 | a0001c0001t0002g0213 a0001c0001t0002g0225 a0001c0001t0002g0235 others(45): Show |
48 | HG00280.hp1 HG00438.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.174-1422C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8253077 | |||||||
| chr19:8253182 | G | A | 4 | a0002c0003t0004g0208 a0002c0003t0004g0303 a0002c0003t0004g0326 others(1): Show |
4 | NA18979.hp2 NA18997.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.174-1317G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8253182 | |||||||
| chr19:8253239 | G | GAT | 55 | a0001c0025t0001g0116 a0002c0003t0001g0040 a0002c0003t0001g0043 others(52): Show |
56 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.174-1259_174-1258d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8253239 | ||||||
| chr19:8253261 | A | T | 1 | a0001c0001t0003g0156 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.174-1238A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8253261 | |||||||
| chr19:8253292 | G | GA | 5 | a0001c0008t0004g0277 a0004c0005t0007g0002 a0004c0005t0008g0058 others(2): Show |
5 | HG02818.hp1 HG02965.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.174-1206dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8253292 | ||||||
| chr19:8253298 | C | T | 5 | a0001c0001t0003g0066 a0001c0001t0003g0109 a0001c0001t0003g0110 others(2): Show |
5 | HG02615.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.174-1201C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8253298 | |||||||
| chr19:8253325 | C | G | 1 | a0001c0001t0001g0407 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.174-1174C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8253325 | |||||||
| chr19:8253428 | TACAG | T | 7 | a0001c0001t0002g0241 a0001c0001t0002g0251 a0001c0001t0002g0262 others(4): Show |
7 | HG02129.hp1 NA18951.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.174-1067_174-1064d others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8253428 | ||||||
| chr19:8253449 | C | CT | 118 | a0001c0001t0001g0408 a0001c0001t0002g0133 a0001c0001t0002g0135 others(115): Show |
118 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.174-1028dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8253449 | ||||||
| chr19:8253449 | C | CTT | 13 | a0001c0001t0002g0139 a0001c0001t0002g0296 a0001c0001t0002g0327 others(10): Show |
13 | HG02135.hp2 HG02300.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.174-1029_174-1028d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8253449 | ||||||
| chr19:8253449 | C | CTTT | 6 | a0001c0001t0003g0066 a0001c0001t0003g0111 a0001c0001t0003g0112 others(3): Show |
6 | HG01081.hp2 HG02717.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.174-1030_174-1028d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8253449 | ||||||
| chr19:8253449 | CT | C | 33 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0002g0219 others(30): Show |
33 | HG00140.hp1 HG00733.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.174-1028delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8253449 | ||||||
| chr19:8253472 | G | T | 78 | a0001c0001t0002g0257 a0001c0001t0003g0028 a0001c0002t0001g0042 others(75): Show |
78 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.174-1027G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8253472 | |||||||
| chr19:8253626 | G | A | 69 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0003g0117 others(66): Show |
70 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.174-873G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8253626 | |||||||
| chr19:8253702 | T | A | 1 | a0001c0002t0004g0238 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.174-797T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8253702 | |||||||
| chr19:8253716 | G | A | 12 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0003g0117 others(9): Show |
12 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.174-783G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8253716 | |||||||
| chr19:8253716 | G | T | 79 | a0001c0001t0002g0257 a0001c0002t0001g0042 a0001c0002t0001g0074 others(76): Show |
79 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.174-783G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8253716 | |||||||
| chr19:8253802 | C | T | 29 | a0001c0001t0001g0408 a0001c0001t0002g0003 a0001c0001t0002g0130 others(26): Show |
29 | HG00323.hp2 HG00621.hp1 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.174-697C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8253802 | |||||||
| chr19:8253868 | A | G | 4 | a0004c0005t0007g0286 a0004c0005t0007g0379 a0004c0005t0008g0246 others(1): Show |
4 | HG00738.hp1 HG02735.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.174-631A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8253868 | |||||||
| chr19:8253995 | G | A | 166 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 others(163): Show |
166 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.174-504G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8253995 | |||||||
| chr19:8254049 | C | T | 1 | a0001c0001t0003g0049 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.174-450C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8254049 | |||||||
| chr19:8254075 | C | T | 55 | a0001c0025t0001g0116 a0002c0003t0001g0040 a0002c0003t0001g0043 others(52): Show |
56 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.174-424C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8254075 | |||||||
| chr19:8254141 | T | C | 29 | a0001c0001t0001g0408 a0001c0001t0002g0003 a0001c0001t0002g0130 others(26): Show |
29 | HG00323.hp2 HG00621.hp1 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.174-358T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8254141 | |||||||
| chr19:8254146 | C | T | 55 | a0001c0025t0001g0116 a0002c0003t0001g0040 a0002c0003t0001g0043 others(52): Show |
56 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.174-353C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8254146 | |||||||
| chr19:8254150 | G | A | 5 | a0001c0002t0002g0248 a0001c0002t0002g0276 a0001c0002t0002g0360 others(2): Show |
5 | HG00642.hp1 HG02300.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.174-349G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8254150 | |||||||
| chr19:8254183 | C | T | 6 | a0003c0007t0009g0120 a0003c0007t0009g0136 a0003c0007t0009g0382 others(3): Show |
6 | HG02055.hp2 HG02559.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.174-316C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8254183 | |||||||
| chr19:8254192 | G | A | 1 | a0001c0008t0001g0051 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.174-307G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8254192 | |||||||
| chr19:8254212 | A | G | 2 | a0001c0001t0003g0036 a0001c0001t0003g0064 |
2 | NA18970.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.174-287A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8254212 | |||||||
| chr19:8254220 | G | A | 12 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0003g0117 others(9): Show |
12 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.174-279G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8254220 | |||||||
| chr19:8254228 | C | G | 1 | a0002c0003t0004g0358 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.174-271C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8254228 | |||||||
| chr19:8254279 | C | A | 1 | a0006c0011t0007g0280 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.174-220C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8254279 | |||||||
| chr19:8254310 | A | C | 46 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 others(43): Show |
46 | HG00140.hp1 HG00733.hp1 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.174-189A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8254310 | |||||||
| chr19:8254322 | C | CA | 36 | a0001c0001t0002g0214 a0001c0001t0002g0309 a0001c0001t0002g0317 others(33): Show |
36 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.174-157dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8254322 | ||||||
| chr19:8254322 | C | CAA | 9 | a0001c0001t0002g0296 a0001c0001t0002g0333 a0001c0001t0003g0389 others(6): Show |
9 | HG01261.hp2 HG02717.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.174-158_174-157dup others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8254322 | ||||||
| chr19:8254322 | C | CAAAA | 24 | a0001c0001t0001g0408 a0001c0001t0002g0003 a0001c0001t0002g0130 others(21): Show |
24 | HG00323.hp2 HG00621.hp1 HG02015.hp1 others(21): Show |
intron_variant | MODIFIER | c.174-160_174-157dup others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8254322 | ||||||
| chr19:8254322 | C | CAAAAA | 14 | a0001c0001t0002g0133 a0001c0001t0002g0137 a0001c0001t0002g0139 others(11): Show |
14 | HG00733.hp2 HG02074.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.174-161_174-157dup others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8254322 | ||||||
| chr19:8254322 | C | CAAAAAA | 6 | a0001c0001t0001g0125 a0001c0001t0002g0225 a0001c0002t0001g0097 others(3): Show |
6 | HG01074.hp1 HG01168.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.174-162_174-157dup others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8254322 | ||||||
| chr19:8254322 | C | CAAAAAAA others(1): Show |
77 | a0001c0001t0002g0213 a0001c0001t0002g0216 a0001c0001t0002g0217 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.174-164_174-157dup others(8): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8254322 | ||||||
| chr19:8254322 | C | CAAAAAAA others(2): Show |
68 | a0001c0001t0001g0197 a0001c0001t0002g0132 a0001c0001t0002g0257 others(65): Show |
68 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.174-165_174-157dup others(9): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8254322 | ||||||
| chr19:8254322 | C | CAAAAAAA others(3): Show |
50 | a0001c0001t0001g0198 a0001c0001t0001g0200 a0001c0001t0002g0219 others(47): Show |
50 | HG00558.hp1 HG00558.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.174-166_174-157dup others(10): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8254322 | ||||||
| chr19:8254322 | C | CAAAAAAA others(4): Show |
14 | a0001c0001t0002g0239 a0001c0001t0002g0344 a0001c0002t0002g0248 others(11): Show |
14 | HG00642.hp1 HG00741.hp2 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.174-167_174-157dup others(11): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8254322 | ||||||
| chr19:8254322 | C | CAAAAAAA others(5): Show |
3 | a0001c0002t0002g0276 a0001c0002t0003g0416 a0001c0002t0003g0417 |
3 | HG03704.hp1 HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.174-168_174-157dup others(12): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8254322 | ||||||
| chr19:8254322 | CA | C | 7 | a0001c0001t0001g0115 a0003c0007t0009g0120 a0003c0007t0009g0136 others(4): Show |
7 | HG02055.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.174-157delA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 8254322 | ||||||
| chr19:8254417 | C | T | 5 | a0001c0001t0003g0066 a0001c0001t0003g0109 a0001c0001t0003g0110 others(2): Show |
5 | HG02615.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.174-82C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8254417 | |||||||
| chr19:8254461 | T | A | 1 | a0001c0002t0001g0097 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.174-38T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 3/11 | chr19 | 8254461 | |||||||
| chr19:8254629 | C | T | 2 | a0002c0003t0004g0223 a0002c0003t0004g0224 |
2 | NA18970.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.291+13C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8254629 | |||||||
| chr19:8254638 | C | T | 29 | a0001c0001t0001g0408 a0001c0001t0002g0003 a0001c0001t0002g0130 others(26): Show |
29 | HG00323.hp2 HG00621.hp1 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.291+22C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8254638 | |||||||
| chr19:8254643 | C | T | 1 | a0001c0006t0006g0299 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.291+27C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8254643 | |||||||
| chr19:8254687 | C | T | 1 | a0001c0002t0004g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.291+71C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8254687 | |||||||
| chr19:8254763 | A | G | 1 | a0001c0012t0002g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.291+147A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8254763 | |||||||
| chr19:8254783 | A | AC | 11 | a0001c0001t0002g0296 a0001c0001t0002g0309 a0001c0001t0002g0318 others(8): Show |
11 | HG00438.hp1 HG00544.hp2 HG00609.hp2 others(8): Show |
intron_variant | MODIFIER | c.291+173dupC | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 8254783 | ||||||
| chr19:8254808 | C | T | 4 | a0001c0001t0003g0046 a0001c0001t0003g0048 a0001c0001t0003g0049 others(1): Show |
4 | HG02735.hp2 HG03490.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.291+192C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8254808 | |||||||
| chr19:8254845 | C | T | 8 | a0001c0001t0001g0115 a0001c0001t0003g0117 a0003c0007t0009g0120 others(5): Show |
8 | HG02055.hp2 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.291+229C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8254845 | |||||||
| chr19:8254875 | A | AC | 53 | a0001c0001t0002g0133 a0001c0001t0002g0214 a0001c0001t0002g0218 others(50): Show |
53 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.291+267dupC | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 8254875 | ||||||
| chr19:8254881 | C | G | 1 | a0002c0003t0001g0118 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.291+265C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8254881 | |||||||
| chr19:8254883 | C | G | 8 | a0001c0001t0003g0389 a0003c0007t0004g0278 a0003c0007t0004g0294 others(5): Show |
8 | HG01081.hp2 HG02622.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.291+267C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8254883 | |||||||
| chr19:8255029 | A | G | 362 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(359): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.291+413A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8255029 | |||||||
| chr19:8255132 | G | A | 1 | a0001c0001t0003g0117 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.292-475G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8255132 | |||||||
| chr19:8255204 | C | T | 4 | a0001c0001t0007g0121 a0001c0001t0007g0378 a0001c0001t0008g0390 others(1): Show |
4 | HG01261.hp2 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-403C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8255204 | |||||||
| chr19:8255303 | G | A | 1 | a0004c0005t0008g0104 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.292-304G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8255303 | |||||||
| chr19:8255315 | C | T | 112 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0216 others(109): Show |
112 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.292-292C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8255315 | |||||||
| chr19:8255332 | G | A | 1 | a0001c0002t0005g0045 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.292-275G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8255332 | |||||||
| chr19:8255378 | C | T | 1 | a0001c0001t0003g0015 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.292-229C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8255378 | |||||||
| chr19:8255384 | C | T | 13 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0003g0117 others(10): Show |
13 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.292-223C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8255384 | |||||||
| chr19:8255399 | A | T | 1 | a0002c0003t0004g0371 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.292-208A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | chr19 | 8255399 | |||||||
| chr19:8255594 | A | AC | 5 | a0001c0001t0003g0156 a0001c0006t0006g0256 a0001c0021t0005g0184 others(2): Show |
5 | HG02135.hp1 HG03209.hp2 HG04204.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.292-8dupC | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 8255594 | ||||||
| chr19:8255763 | G | A | 5 | a0001c0002t0002g0248 a0001c0002t0002g0360 a0001c0002t0003g0416 others(2): Show |
5 | HG00642.hp1 HG02300.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.410+38G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 5/11 | chr19 | 8255763 | |||||||
| chr19:8255772 | TGGGGCGG others(3): Show |
T | 72 | a0001c0002t0001g0042 a0001c0002t0001g0074 a0001c0002t0001g0097 others(69): Show |
72 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.411-46_411-37delGC others(8): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 8255772 | ||||||
| chr19:8255785 | G | T | 33 | a0001c0001t0001g0408 a0001c0001t0002g0003 a0001c0001t0002g0130 others(30): Show |
33 | HG00323.hp2 HG00621.hp1 HG02015.hp1 others(30): Show |
intron_variant | MODIFIER | c.411-37G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 5/11 | chr19 | 8255785 | |||||||
| chr19:8255947 | G | C | 2 | a0001c0006t0006g0259 a0001c0006t0006g0269 |
2 | NA18948.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.468+68G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 6/11 | chr19 | 8255947 | |||||||
| chr19:8255979 | A | C | 1 | a0001c0001t0003g0026 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.468+100A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 6/11 | chr19 | 8255979 | |||||||
| chr19:8255999 | C | A | 2 | a0001c0001t0002g0290 a0001c0001t0003g0096 |
2 | HG01106.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.468+120C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 6/11 | chr19 | 8255999 | |||||||
| chr19:8256006 | T | G | 78 | a0001c0001t0003g0066 a0001c0001t0003g0109 a0001c0001t0003g0110 others(75): Show |
78 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.468+127T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 6/11 | chr19 | 8256006 | |||||||
| chr19:8256015 | G | T | 1 | a0001c0001t0003g0005 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.468+136G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 6/11 | chr19 | 8256015 | |||||||
| chr19:8256017 | G | A | 1 | a0001c0001t0002g0334 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.468+138G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 6/11 | chr19 | 8256017 | |||||||
| chr19:8256081 | A | T | 1 | a0001c0001t0003g0028 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.469-155A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 6/11 | chr19 | 8256081 | |||||||
| chr19:8256096 | G | A | 13 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0003g0117 others(10): Show |
13 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.469-140G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 6/11 | chr19 | 8256096 | |||||||
| chr19:8256172 | C | T | 2 | a0005c0010t0001g0091 a0005c0010t0015g0092 |
2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.469-64C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 6/11 | chr19 | 8256172 | |||||||
| chr19:8256173 | G | A | 1 | a0001c0001t0001g0407 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.469-63G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 6/11 | chr19 | 8256173 | |||||||
| chr19:8256298 | A | T | 134 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0002g0132 others(131): Show |
134 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.519+12A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 7/11 | chr19 | 8256298 | |||||||
| chr19:8256444 | A | ACT | 304 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(301): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.519+159_519+160ins others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr19 | 8256444 | ||||||
| chr19:8256539 | C | T | 2 | a0001c0001t0002g0317 a0001c0001t0002g0320 |
2 | NA18973.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.520-79C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 7/11 | chr19 | 8256539 | |||||||
| chr19:8256569 | G | A | 1 | a0001c0001t0002g0253 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.520-49G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 7/11 | chr19 | 8256569 | |||||||
| chr19:8256571 | T | C | 1 | a0003c0007t0010g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.520-47T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 7/11 | chr19 | 8256571 | |||||||
| chr19:8256721 | A | T | 2 | a0001c0001t0002g0216 a0001c0001t0002g0217 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.612+11A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 8/11 | chr19 | 8256721 | |||||||
| chr19:8256750 | C | T | 1 | a0001c0001t0003g0117 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.612+40C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 8/11 | chr19 | 8256750 | |||||||
| chr19:8256774 | A | G | 1 | a0001c0001t0002g0350 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.612+64A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 8/11 | chr19 | 8256774 | |||||||
| chr19:8256829 | T | C | 2 | a0001c0001t0002g0348 a0001c0001t0003g0117 |
2 | HG03225.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.612+119T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 8/11 | chr19 | 8256829 | |||||||
| chr19:8256921 | C | T | 1 | a0001c0002t0005g0413 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.613-28C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 8/11 | chr19 | 8256921 | |||||||
| chr19:8257085 | C | T | 120 | a0001c0001t0002g0132 a0001c0001t0002g0213 a0001c0001t0002g0214 others(117): Show |
120 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(117): Show |
splice_region_variant&intron_variant | LOW | c.741+8C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257085 | |||||||
| chr19:8257176 | T | C | 89 | a0001c0001t0001g0408 a0001c0001t0002g0003 a0001c0001t0002g0130 others(86): Show |
90 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.741+99T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257176 | |||||||
| chr19:8257177 | G | A | 2 | a0002c0003t0001g0399 a0002c0003t0004g0138 |
2 | HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.741+100G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257177 | |||||||
| chr19:8257185 | A | G | 291 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(288): Show |
292 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(289): Show |
intron_variant | MODIFIER | c.741+108A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257185 | |||||||
| chr19:8257303 | C | T | 1 | a0004c0005t0008g0394 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.741+226C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257303 | |||||||
| chr19:8257318 | T | C | 2 | a0005c0010t0001g0091 a0005c0010t0015g0092 |
2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.741+241T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257318 | |||||||
| chr19:8257376 | G | A | 1 | a0002c0003t0001g0040 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.741+299G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257376 | |||||||
| chr19:8257440 | AT | A | 285 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(282): Show |
286 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.741+374delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 8257440 | ||||||
| chr19:8257457 | G | A | 13 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0003g0117 others(10): Show |
13 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.741+380G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257457 | |||||||
| chr19:8257588 | G | A | 1 | a0002c0003t0004g0325 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.742-291G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257588 | |||||||
| chr19:8257608 | G | C | 1 | a0001c0002t0004g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.742-271G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257608 | |||||||
| chr19:8257633 | T | C | 1 | a0001c0001t0001g0407 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.742-246T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257633 | |||||||
| chr19:8257677 | G | A | 10 | a0001c0002t0001g0042 a0001c0002t0001g0074 a0001c0002t0001g0097 others(7): Show |
10 | HG00733.hp2 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.742-202G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257677 | |||||||
| chr19:8257709 | C | T | 1 | a0001c0002t0005g0073 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.742-170C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257709 | |||||||
| chr19:8257710 | G | A | 234 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0002g0132 others(231): Show |
235 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.742-169G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257710 | |||||||
| chr19:8257768 | G | A | 1 | a0001c0001t0008g0398 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.742-111G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257768 | |||||||
| chr19:8257801 | T | A | 6 | a0001c0002t0002g0248 a0001c0002t0002g0276 a0001c0002t0002g0360 others(3): Show |
6 | HG00642.hp1 HG02300.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.742-78T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257801 | |||||||
| chr19:8257838 | G | A | 2 | a0001c0008t0001g0206 a0004c0005t0008g0204 |
2 | HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.742-41G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257838 | |||||||
| chr19:8257849 | G | T | 3 | a0001c0002t0006g0234 a0001c0002t0006g0236 a0001c0002t0006g0242 |
3 | HG00642.hp2 HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.742-30G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257849 | |||||||
| chr19:8257850 | A | T | 3 | a0001c0002t0006g0234 a0001c0002t0006g0236 a0001c0002t0006g0242 |
3 | HG00642.hp2 HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.742-29A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 9/11 | chr19 | 8257850 | |||||||
| chr19:8258013 | G | A | 2 | a0001c0001t0012g0279 a0001c0001t0017g0386 |
2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.848+28G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8258013 | |||||||
| chr19:8258156 | G | A | 1 | a0002c0003t0004g0288 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.848+171G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8258156 | |||||||
| chr19:8258173 | AATT | A | 5 | a0001c0001t0001g0125 a0003c0007t0001g0037 a0003c0007t0003g0126 others(2): Show |
5 | HG02109.hp1 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.848+196_848+198del others(3): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8258173 | ||||||
| chr19:8258311 | A | ATCCCGGC others(3): Show |
1 | a0001c0001t0002g0366 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.848+328_848+337dup others(10): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8258311 | ||||||
| chr19:8258408 | C | T | 2 | a0001c0001t0004g0250 a0001c0001t0004g0352 |
2 | HG02083.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.848+423C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8258408 | |||||||
| chr19:8258425 | C | G | 285 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(282): Show |
286 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.848+440C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8258425 | |||||||
| chr19:8258507 | C | T | 1 | a0001c0001t0003g0026 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.848+522C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8258507 | |||||||
| chr19:8258546 | T | C | 3 | a0002c0003t0001g0392 a0002c0003t0001g0404 a0002c0003t0004g0138 |
3 | HG01891.hp1 HG03041.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.848+561T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8258546 | |||||||
| chr19:8258619 | A | C | 365 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(362): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.848+634A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8258619 | |||||||
| chr19:8258677 | TATTAAAA | T | 8 | a0001c0002t0001g0042 a0001c0002t0001g0074 a0001c0002t0001g0097 others(5): Show |
8 | HG00733.hp2 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.848+704_848+710del others(7): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8258677 | ||||||
| chr19:8258699 | G | A | 1 | a0003c0004t0001g0402 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.848+714G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8258699 | |||||||
| chr19:8258702 | C | T | 1 | a0003c0004t0004g0270 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.848+717C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8258702 | |||||||
| chr19:8258865 | G | C | 12 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0003c0007t0003g0126 others(9): Show |
12 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.848+880G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8258865 | |||||||
| chr19:8258874 | C | T | 113 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(110): Show |
113 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.848+889C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8258874 | |||||||
| chr19:8258965 | C | G | 1 | a0002c0003t0004g0298 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.848+980C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8258965 | |||||||
| chr19:8259006 | C | T | 16 | a0001c0008t0004g0277 a0001c0008t0004g0359 a0002c0003t0001g0040 others(13): Show |
16 | HG01891.hp1 HG01981.hp1 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.848+1021C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259006 | |||||||
| chr19:8259026 | C | G | 3 | a0003c0004t0001g0145 a0003c0004t0001g0164 a0003c0004t0001g0180 |
3 | NA18966.hp1 NA18979.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.848+1041C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259026 | |||||||
| chr19:8259113 | G | A | 1 | a0008c0024t0008g0108 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.848+1128G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259113 | |||||||
| chr19:8259159 | G | A | 1 | a0001c0002t0006g0232 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.848+1174G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259159 | |||||||
| chr19:8259220 | G | A | 6 | a0001c0001t0003g0082 a0001c0002t0002g0248 a0001c0002t0002g0276 others(3): Show |
6 | HG00642.hp1 HG02300.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.848+1235G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259220 | |||||||
| chr19:8259231 | G | A | 2 | a0001c0001t0006g0222 a0008c0024t0008g0108 |
2 | HG03579.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.848+1246G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259231 | |||||||
| chr19:8259463 | C | T | 112 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(109): Show |
112 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.848+1478C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259463 | |||||||
| chr19:8259549 | A | C | 1 | a0003c0004t0001g0388 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.848+1564A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259549 | |||||||
| chr19:8259634 | C | G | 1 | a0002c0003t0008g0107 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.848+1649C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259634 | |||||||
| chr19:8259749 | G | C | 2 | a0001c0001t0003g0105 a0001c0001t0003g0391 |
2 | HG02109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.848+1764G>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259749 | |||||||
| chr19:8259764 | G | A | 16 | a0001c0008t0004g0277 a0001c0008t0004g0359 a0002c0003t0001g0040 others(13): Show |
16 | HG01891.hp1 HG01981.hp1 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.848+1779G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259764 | |||||||
| chr19:8259813 | G | A | 1 | a0001c0002t0001g0396 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.848+1828G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259813 | |||||||
| chr19:8259856 | G | A | 1 | a0001c0001t0002g0380 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.849-1832G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259856 | |||||||
| chr19:8259939 | C | G | 1 | a0001c0012t0002g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.849-1749C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259939 | |||||||
| chr19:8259940 | T | C | 95 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0002g0130 others(92): Show |
95 | HG00323.hp2 HG00558.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.849-1748T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259940 | |||||||
| chr19:8259941 | C | T | 95 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0002g0130 others(92): Show |
95 | HG00323.hp2 HG00558.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.849-1747C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259941 | |||||||
| chr19:8259952 | C | A | 65 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0002g0130 others(62): Show |
65 | HG00323.hp2 HG00621.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.849-1736C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259952 | |||||||
| chr19:8259957 | T | C | 1 | a0004c0009t0007g0129 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.849-1731T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259957 | |||||||
| chr19:8259959 | C | A | 1 | a0004c0009t0007g0129 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.849-1729C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259959 | |||||||
| chr19:8259960 | A | G | 1 | a0004c0009t0007g0129 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.849-1728A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259960 | |||||||
| chr19:8259971 | C | A | 1 | a0001c0002t0004g0237 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.849-1717C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259971 | |||||||
| chr19:8259976 | T | A | 1 | a0004c0009t0007g0129 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.849-1712T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8259976 | |||||||
| chr19:8260006 | A | AGATAAGG others(3): Show |
1 | a0004c0009t0007g0129 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.849-1682_849-1681i others(12): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260006 | |||||||
| chr19:8260009 | T | G | 133 | a0001c0001t0002g0003 a0001c0001t0002g0132 a0001c0001t0002g0213 others(130): Show |
134 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.849-1679T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260009 | |||||||
| chr19:8260020 | T | A | 1 | a0004c0009t0007g0129 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.849-1668T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260020 | |||||||
| chr19:8260021 | G | T | 1 | a0004c0009t0007g0129 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.849-1667G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260021 | |||||||
| chr19:8260111 | C | G | 183 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0002g0003 others(180): Show |
184 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.849-1577C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260111 | |||||||
| chr19:8260301 | TCTC | T | 65 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0002g0130 others(62): Show |
65 | HG00323.hp2 HG00621.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.849-1384_849-1382d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260301 | ||||||
| chr19:8260330 | A | G | 1 | a0001c0012t0002g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.849-1358A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260330 | |||||||
| chr19:8260369 | A | AT | 65 | a0001c0001t0005g0095 a0001c0001t0006g0215 a0001c0001t0006g0221 others(62): Show |
65 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(62): Show |
intron_variant | MODIFIER | c.849-1302dupT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260369 | ||||||
| chr19:8260369 | A | ATT | 9 | a0001c0002t0005g0038 a0001c0002t0005g0081 a0001c0002t0006g0229 others(6): Show |
9 | HG00639.hp2 HG00642.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.849-1303_849-1302d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260369 | ||||||
| chr19:8260369 | AT | A | 50 | a0001c0001t0001g0407 a0001c0001t0001g0408 a0001c0001t0002g0369 others(47): Show |
50 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.849-1302delT | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260369 | ||||||
| chr19:8260369 | ATT | A | 157 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 others(154): Show |
158 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(155): Show |
intron_variant | MODIFIER | c.849-1303_849-1302d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260369 | ||||||
| chr19:8260369 | ATTT | A | 24 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0002g0132 others(21): Show |
24 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.849-1304_849-1302d others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260369 | ||||||
| chr19:8260369 | ATTTT | A | 41 | a0001c0001t0002g0130 a0001c0001t0002g0133 a0001c0001t0002g0137 others(38): Show |
41 | HG00323.hp2 HG00621.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.849-1305_849-1302d others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260369 | ||||||
| chr19:8260533 | G | GA | 160 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(157): Show |
160 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.849-1145dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260533 | ||||||
| chr19:8260533 | G | GAA | 123 | a0001c0001t0001g0407 a0001c0001t0002g0003 a0001c0001t0002g0132 others(120): Show |
124 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.849-1146_849-1145d others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260533 | ||||||
| chr19:8260651 | TAAAG | T | 3 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0018 |
3 | HG02040.hp2 NA18747.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.849-1034_849-1031d others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260651 | ||||||
| chr19:8260675 | T | C | 3 | a0001c0002t0001g0098 a0001c0002t0001g0099 a0001c0002t0001g0100 |
3 | HG01074.hp1 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.849-1013T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260675 | |||||||
| chr19:8260681 | G | A | 1 | a0004c0009t0007g0331 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.849-1007G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260681 | |||||||
| chr19:8260699 | C | T | 1 | a0002c0003t0004g0298 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.849-989C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260699 | |||||||
| chr19:8260732 | T | A | 186 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0002g0003 others(183): Show |
187 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.849-956T>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260732 | |||||||
| chr19:8260752 | C | A | 1 | a0001c0006t0006g0375 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.849-936C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260752 | |||||||
| chr19:8260915 | C | T | 10 | a0001c0001t0002g0354 a0001c0001t0003g0143 a0001c0001t0003g0167 others(7): Show |
10 | HG00558.hp2 NA18947.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.849-773C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260915 | |||||||
| chr19:8260945 | C | T | 6 | a0001c0001t0003g0389 a0003c0007t0001g0037 a0003c0007t0004g0278 others(3): Show |
6 | HG01081.hp2 HG02258.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.849-743C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260945 | |||||||
| chr19:8260946 | A | G | 232 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0002g0003 others(229): Show |
233 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(230): Show |
intron_variant | MODIFIER | c.849-742A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260946 | |||||||
| chr19:8260950 | C | CA | 24 | a0001c0001t0004g0249 a0001c0002t0001g0160 a0001c0002t0004g0329 others(21): Show |
24 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.849-711dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260950 | ||||||
| chr19:8260950 | C | CAA | 12 | a0001c0002t0001g0042 a0001c0002t0001g0074 a0001c0002t0001g0097 others(9): Show |
12 | HG00408.hp2 HG00621.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.849-712_849-711dup others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260950 | ||||||
| chr19:8260950 | C | CAAAA | 15 | a0001c0002t0001g0396 a0001c0002t0004g0231 a0001c0002t0005g0056 others(12): Show |
15 | HG00642.hp2 HG01069.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.849-714_849-711dup others(4): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260950 | ||||||
| chr19:8260950 | C | CAAAAA | 24 | a0001c0001t0006g0215 a0001c0001t0006g0222 a0001c0001t0006g0364 others(21): Show |
24 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.849-715_849-711dup others(5): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260950 | ||||||
| chr19:8260950 | C | CAAAAAA | 19 | a0001c0001t0005g0095 a0001c0001t0006g0221 a0001c0002t0005g0038 others(16): Show |
19 | HG00099.hp2 HG00639.hp2 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.849-716_849-711dup others(6): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260950 | ||||||
| chr19:8260950 | C | CAAAAAAA | 10 | a0001c0001t0006g0373 a0001c0002t0005g0084 a0001c0002t0006g0337 others(7): Show |
10 | HG01346.hp2 HG02071.hp2 NA18943.hp1 others(7): Show |
intron_variant | MODIFIER | c.849-717_849-711dup others(7): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260950 | ||||||
| chr19:8260950 | CA | C | 19 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 others(16): Show |
19 | HG00280.hp2 HG00609.hp1 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.849-711delA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260950 | ||||||
| chr19:8260958 | A | AAAC | 11 | a0001c0001t0002g0265 a0001c0001t0002g0282 a0001c0001t0003g0035 others(8): Show |
11 | HG01891.hp1 HG01978.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.849-728_849-727ins others(3): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260958 | ||||||
| chr19:8260958 | A | AAC | 212 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0002g0003 others(209): Show |
213 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(210): Show |
intron_variant | MODIFIER | c.849-729_849-728ins others(2): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260958 | ||||||
| chr19:8260962 | A | C | 1 | a0004c0005t0007g0289 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.849-726A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260962 | |||||||
| chr19:8260966 | A | C | 2 | a0001c0001t0002g0327 a0001c0001t0003g0011 |
2 | HG02135.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.849-722A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260966 | |||||||
| chr19:8260967 | A | C | 228 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0002g0003 others(225): Show |
229 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(226): Show |
intron_variant | MODIFIER | c.849-721A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260967 | |||||||
| chr19:8260968 | AAAAAAAA others(3): Show |
A | 1 | a0008c0024t0008g0108 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.849-717_849-708del others(10): Show |
CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8260968 | ||||||
| chr19:8260971 | A | C | 2 | a0004c0005t0007g0289 a0004c0005t0008g0204 |
2 | HG02004.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.849-717A>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8260971 | |||||||
| chr19:8261052 | A | G | 1 | a0001c0002t0006g0381 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.849-636A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8261052 | |||||||
| chr19:8261122 | A | G | 1 | a0001c0001t0003g0068 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.849-566A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8261122 | |||||||
| chr19:8261183 | C | T | 99 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0200 others(96): Show |
99 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.849-505C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8261183 | |||||||
| chr19:8261191 | G | T | 16 | a0001c0008t0004g0277 a0001c0008t0004g0359 a0002c0003t0001g0040 others(13): Show |
16 | HG01891.hp1 HG01981.hp1 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.849-497G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8261191 | |||||||
| chr19:8261209 | T | TA | 114 | a0001c0001t0002g0003 a0001c0001t0002g0132 a0001c0001t0002g0213 others(111): Show |
115 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.849-478dupA | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 8261209 | ||||||
| chr19:8261253 | A | T | 199 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0002g0003 others(196): Show |
200 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.849-435A>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8261253 | |||||||
| chr19:8261262 | T | C | 7 | a0001c0001t0007g0121 a0001c0001t0007g0378 a0001c0001t0008g0390 others(4): Show |
7 | HG01261.hp2 HG02717.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.849-426T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8261262 | |||||||
| chr19:8261296 | C | A | 1 | a0001c0001t0008g0390 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.849-392C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8261296 | |||||||
| chr19:8261360 | A | G | 278 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0197 others(275): Show |
279 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(276): Show |
intron_variant | MODIFIER | c.849-328A>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8261360 | |||||||
| chr19:8261464 | G | A | 1 | a0003c0004t0001g0085 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.849-224G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8261464 | |||||||
| chr19:8261491 | G | T | 1 | a0001c0001t0002g0135 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.849-197G>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8261491 | |||||||
| chr19:8261625 | C | A | 1 | a0008c0024t0008g0108 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.849-63C>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8261625 | |||||||
| chr19:8261646 | G | A | 1 | a0001c0006t0006g0227 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.849-42G>A | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8261646 | |||||||
| chr19:8261665 | T | G | 3 | a0001c0001t0002g0315 a0001c0001t0012g0279 a0001c0001t0017g0386 |
3 | HG02572.hp1 HG03209.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.849-23T>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 10/11 | chr19 | 8261665 | |||||||
| chr19:8261857 | C | T | 2 | a0001c0002t0004g0226 a0008c0024t0008g0108 |
2 | HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1005+13C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 11/11 | chr19 | 8261857 | |||||||
| chr19:8261881 | C | T | 1 | a0001c0001t0003g0016 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1005+37C>T | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 11/11 | chr19 | 8261881 | |||||||
| chr19:8261888 | T | C | 9 | a0001c0002t0001g0042 a0001c0002t0001g0074 a0001c0002t0001g0097 others(6): Show |
9 | HG00733.hp2 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1006-42T>C | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 11/11 | chr19 | 8261888 | |||||||
| chr19:8261894 | C | G | 1 | a0008c0024t0008g0108 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1006-36C>G | CERS4 | ENSG00000090661.12 | transcript | ENST00000251363.10 | protein_coding | 11/11 | chr19 | 8261894 |