Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1666 |
| ensemblid | ENSG00000104325.7 |
| hgncid | 2753 |
| symbol | DECR1 |
| name | 2,4-dienoyl-CoA reductase 1 |
| refseq_nuc | NM_001359.2 |
| refseq_prot | NP_001350.1 |
| ensembl_nuc | ENST00000220764.7 |
| ensembl_prot | ENSP00000220764.2 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 90001477 |
| end | 90053633 |
| strand | + |
| ver | v1.2 |
| region | chr8:90001477-90053633 |
| region5000 | chr8:89996477-90058633 |
| regionname0 | DECR1_chr8_90001477_90053633 |
| regionname5000 | DECR1_chr8_89996477_90058633 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 335 | 375 | 86 | 64 | 169 | 14 | 40 | 127 | DECR1_chr8_89996477_90058633 | DECR1 | MKLPA others(330): Show |
chr8 | 89996477 | 90058633 |
| a0002 | 0/0 | 335 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | MKLPA others(330): Show |
chr8 | 89996477 | 90058633 |
| a0003 | 0/0 | 335 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | MKLPA others(330): Show |
chr8 | 89996477 | 90058633 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1005 | 375 | 86 | 64 | 169 | 14 | 40 | DECR1_chr8_89996477_90058633 | DECR1 | ATGAA others(1000): Show |
chr8 | 89996477 | 90058633 | ||
| a0002c0002 | 0/0 | 1005 | 2 | 0 | 0 | 0 | 0 | 2 | DECR1_chr8_89996477_90058633 | DECR1 | ATGAA others(1000): Show |
chr8 | 89996477 | 90058633 | ||
| a0003c0003 | 0/0 | 1005 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | ATGAA others(1000): Show |
chr8 | 89996477 | 90058633 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2760 | 163 | 36 | 29 | 77 | 3 | 18 | DECR1_chr8_89996477_90058633 | DECR1 | GTTCT others(2755): Show |
chr8 | 89996477 | 90058633 |
| a0001c0001t0002 | 1/1 | 2760 | 113 | 13 | 21 | 52 | 6 | 19 | DECR1_chr8_89996477_90058633 | DECR1 | GTTCT others(2755): Show |
chr8 | 89996477 | 90058633 |
| a0001c0001t0003 | 0/0 | 2759 | 43 | 0 | 6 | 33 | 1 | 3 | DECR1_chr8_89996477_90058633 | DECR1 | GTTCT others(2754): Show |
chr8 | 89996477 | 90058633 |
| a0001c0001t0004 | 0/0 | 2761 | 29 | 25 | 2 | 2 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | GTTCT others(2756): Show |
chr8 | 89996477 | 90058633 |
| a0001c0001t0005 | 0/0 | 2759 | 6 | 3 | 0 | 3 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | GTTCT others(2754): Show |
chr8 | 89996477 | 90058633 |
| a0001c0001t0006 | 0/0 | 2760 | 5 | 4 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | GTTCT others(2755): Show |
chr8 | 89996477 | 90058633 |
| a0001c0001t0007 | 0/0 | 2761 | 3 | 1 | 1 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | GTTCT others(2756): Show |
chr8 | 89996477 | 90058633 |
| a0001c0001t0008 | 0/0 | 2760 | 3 | 0 | 1 | 0 | 2 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | GTTCT others(2755): Show |
chr8 | 89996477 | 90058633 |
| a0001c0001t0009 | 0/0 | 2761 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | GTTCT others(2756): Show |
chr8 | 89996477 | 90058633 |
| a0001c0001t0010 | 0/0 | 2760 | 1 | 0 | 0 | 0 | 1 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | GTTCT others(2755): Show |
chr8 | 89996477 | 90058633 |
| a0001c0001t0011 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | GTTCT others(2755): Show |
chr8 | 89996477 | 90058633 |
| a0001c0001t0012 | 0/0 | 2760 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | GTTCT others(2755): Show |
chr8 | 89996477 | 90058633 |
| a0001c0001t0013 | 0/0 | 2760 | 1 | 0 | 0 | 0 | 1 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | GTTCT others(2755): Show |
chr8 | 89996477 | 90058633 |
| a0001c0001t0014 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | GTTCT others(2755): Show |
chr8 | 89996477 | 90058633 |
| a0001c0001t0015 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | GTTCT others(2755): Show |
chr8 | 89996477 | 90058633 |
| a0001c0001t0016 | 0/0 | 2760 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | GTTCT others(2755): Show |
chr8 | 89996477 | 90058633 |
| a0001c0001t0017 | 0/0 | 2759 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | GTTCT others(2754): Show |
chr8 | 89996477 | 90058633 |
| a0002c0002t0002 | 0/0 | 2760 | 2 | 0 | 0 | 0 | 0 | 2 | DECR1_chr8_89996477_90058633 | DECR1 | GTTCT others(2755): Show |
chr8 | 89996477 | 90058633 |
| a0003c0003t0002 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | GTTCT others(2755): Show |
chr8 | 89996477 | 90058633 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 10 | 1 | 0 | 9 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0004 | 0/0 | 9 | 0 | 3 | 6 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 0 | 2 | 0 | 4 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0007 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0009 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0010 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0001 | 1/0 | 22 | 1 | 4 | 14 | 1 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0003 | 0/0 | 9 | 1 | 2 | 5 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0011 | 0/0 | 5 | 0 | 0 | 0 | 0 | 5 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0146 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0003g0005 | 0/0 | 9 | 0 | 3 | 6 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0003g0008 | 0/0 | 8 | 0 | 2 | 3 | 1 | 2 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0003g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0003g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0003g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0004g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0004g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0004g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0004g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0005g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0006g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0006g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0007g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0007g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0007g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0008g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0008g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0008g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0009g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0010g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0011g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0012g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0013g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0014g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0015g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0016g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0001c0001t0017g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0002c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0002c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| a0003c0003t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0015 | EUR | GBR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG00099 | hp2 | a0001 | c0001 | t0008 | g0073 | EUR | GBR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0148 | EUR | GBR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG00140 | hp2 | a0001 | c0001 | t0010 | g0109 | EUR | GBR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0008 | EUR | FIN | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | FIN | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0031 | EUR | FIN | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG00597 | hp1 | a0001 | c0001 | t0005 | g0165 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG00741 | hp2 | a0001 | c0001 | t0016 | g0006 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0196 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01081 | hp2 | a0001 | c0001 | t0006 | g0021 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01175 | hp2 | a0001 | c0001 | t0007 | g0151 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0039 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01346 | hp1 | a0001 | c0001 | t0017 | g0015 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0031 | EUR | IBS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0233 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01891 | hp2 | a0001 | c0001 | t0015 | g0205 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01934 | hp1 | a0001 | c0001 | t0008 | g0006 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01934 | hp2 | a0001 | c0001 | t0012 | g0145 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0037 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0211 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | CDX | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CDX | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CDX | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CDX | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0224 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0222 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0044 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0137 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0198 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0113 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0218 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0220 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0234 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0199 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0201 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0044 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0197 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0223 | AFR | ESN | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03041 | hp1 | a0001 | c0001 | t0009 | g0043 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0229 | AFR | MSL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0039 | AFR | ESN | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03130 | hp2 | a0001 | c0001 | t0009 | g0043 | AFR | ESN | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0225 | AFR | ESN | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0112 | AFR | ESN | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ESN | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0227 | AFR | MSL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0195 | AFR | MSL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0210 | AFR | MSL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0054 | AFR | MSL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0141 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | STU | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | STU | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0143 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0168 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | BEB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | BEB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0152 | SAS | BEB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0014 | SAS | BEB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0185 | SAS | STU | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0159 | SAS | STU | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | STU | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0135 | SAS | STU | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0021 | AFR | YRI | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18522 | hp2 | a0001 | c0001 | t0007 | g0001 | AFR | YRI | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | CHB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | CHB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | CHB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0232 | AFR | YRI | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | YRI | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18982 | hp1 | a0001 | c0001 | t0005 | g0072 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18990 | hp2 | a0003 | c0003 | t0002 | g0003 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18993 | hp2 | a0001 | c0001 | t0007 | g0018 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0228 | AFR | LWK | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | LWK | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0221 | AFR | LWK | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | LWK | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19057 | hp2 | a0001 | c0001 | t0014 | g0105 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19062 | hp2 | a0001 | c0001 | t0005 | g0071 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0193 | AFR | YRI | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | YRI | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ASW | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ASW | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA20752 | hp1 | a0001 | c0001 | t0008 | g0080 | EUR | TSI | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA20752 | hp2 | a0001 | c0001 | t0013 | g0140 | EUR | TSI | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0161 | EUR | TSI | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | TSI | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0011 | SAS | GIH | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | GIH | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0231 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0021 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | MSL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | MSL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | USA | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0206 | AFR | USA | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | LWK | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| NA21309 | hp2 | a0001 | c0001 | t0011 | g0118 | AFR | LWK | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0146 | REF | REF | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0001 | REF | REF | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:90042781 | C | T | 1 | a0002 | 2 | HG04184.hp2 NA20905.hp1 |
missense_variant | MODERATE | c.719C>T | p.Pro240Leu | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/10 | 735/2760 | 719/1008 | 240/335 | chr8 | 90042781 | |||
| chr8:90044993 | G | A | 1 | a0003 | 1 | NA18990.hp2 | missense_variant&splice_region_variant | MODERATE | c.883G>A | p.Ala295Thr | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/10 | 899/2760 | 883/1008 | 295/335 | chr8 | 90044993 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:90051898 | G | A | 1 | a0001c0001t0010 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 10/10 | 1 | chr8 | 90051898 | ||||||
| chr8:90051917 | T | C | 1 | a0001c0001t0011 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*20T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 10/10 | 20 | chr8 | 90051917 | ||||||
| chr8:90052092 | T | TA | 3 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0009 |
34 | HG01070.hp1 HG01175.hp2 HG01243.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*208dupA | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 10/10 | 209 | INFO_REALIGN_3_PRIME | chr8 | 90052092 | |||||
| chr8:90052092 | TA | T | 3 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0017 |
50 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*208delA | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 10/10 | 208 | INFO_REALIGN_3_PRIME | chr8 | 90052092 | |||||
| chr8:90052227 | C | G | 12 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(9): Show |
256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*330C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 10/10 | 330 | chr8 | 90052227 | ||||||
| chr8:90052273 | C | T | 1 | a0001c0001t0009 | 2 | HG03041.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*376C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 10/10 | 376 | chr8 | 90052273 | ||||||
| chr8:90052407 | A | G | 2 | a0001c0001t0010 a0001c0001t0016 |
2 | HG00140.hp2 HG00741.hp2 |
3_prime_UTR_variant | MODIFIER | c.*510A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 10/10 | 510 | chr8 | 90052407 | ||||||
| chr8:90052409 | G | A | 1 | a0001c0001t0006 | 5 | HG01081.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*512G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 10/10 | 512 | chr8 | 90052409 | ||||||
| chr8:90052517 | G | A | 1 | a0001c0001t0008 | 3 | HG00099.hp2 HG01934.hp1 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*620G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 10/10 | 620 | chr8 | 90052517 | ||||||
| chr8:90052844 | C | T | 2 | a0001c0001t0003 a0001c0001t0011 |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*947C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 10/10 | 947 | chr8 | 90052844 | ||||||
| chr8:90052919 | C | G | 1 | a0001c0001t0015 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1022C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 10/10 | 1022 | chr8 | 90052919 | ||||||
| chr8:90052935 | C | T | 1 | a0001c0001t0013 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1038C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 10/10 | 1038 | chr8 | 90052935 | ||||||
| chr8:90053035 | G | A | 1 | a0001c0001t0012 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1138G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 10/10 | 1138 | chr8 | 90053035 | ||||||
| chr8:90053347 | C | T | 1 | a0001c0001t0014 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1450C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 10/10 | 1450 | chr8 | 90053347 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:90001772 | C | T | 1 | a0001c0001t0001g0046 | 2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.69+211C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90001772 | |||||||
| chr8:90001926 | G | T | 20 | a0001c0001t0001g0226 a0001c0001t0001g0230 a0001c0001t0001g0235 others(17): Show |
24 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.69+365G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90001926 | |||||||
| chr8:90001932 | C | T | 1 | a0001c0001t0003g0219 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.69+371C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90001932 | |||||||
| chr8:90002028 | G | C | 1 | a0001c0001t0002g0047 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.69+467G>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90002028 | |||||||
| chr8:90002045 | A | T | 1 | a0001c0001t0002g0218 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.69+484A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90002045 | |||||||
| chr8:90002074 | G | A | 1 | a0001c0001t0004g0220 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.69+513G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90002074 | |||||||
| chr8:90002100 | G | A | 1 | a0001c0001t0004g0221 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.69+539G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90002100 | |||||||
| chr8:90002497 | G | C | 4 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(1): Show |
7 | HG01884.hp1 HG01891.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.69+936G>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90002497 | |||||||
| chr8:90002499 | AGCAATAA others(4): Show |
A | 4 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(1): Show |
7 | HG01884.hp1 HG01891.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.69+939_69+949delGC others(9): Show |
DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90002499 | |||||||
| chr8:90002511 | C | A | 4 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(1): Show |
7 | HG01884.hp1 HG01891.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.69+950C>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90002511 | |||||||
| chr8:90002814 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.69+1253A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90002814 | |||||||
| chr8:90002823 | A | C | 1 | a0001c0001t0001g0235 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.69+1262A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90002823 | |||||||
| chr8:90002901 | G | T | 7 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0212 others(4): Show |
9 | HG02055.hp1 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.69+1340G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90002901 | |||||||
| chr8:90003274 | T | G | 20 | a0001c0001t0001g0226 a0001c0001t0001g0230 a0001c0001t0001g0235 others(17): Show |
24 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.69+1713T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90003274 | |||||||
| chr8:90003289 | A | T | 3 | a0001c0001t0006g0021 a0001c0001t0006g0210 a0001c0001t0006g0211 |
5 | HG01081.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.69+1728A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90003289 | |||||||
| chr8:90003313 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.69+1752A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90003313 | |||||||
| chr8:90003315 | A | C | 9 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(6): Show |
9 | HG01261.hp2 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.69+1754A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90003315 | |||||||
| chr8:90003383 | ATATT | A | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | HG01261.hp2 HG02109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.69+1827_69+1830del others(4): Show |
DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 90003383 | ||||||
| chr8:90003442 | TA | T | 10 | a0001c0001t0001g0194 a0001c0001t0001g0200 a0001c0001t0004g0039 others(7): Show |
11 | HG01070.hp1 HG01109.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.69+1887delA | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 90003442 | ||||||
| chr8:90003541 | A | T | 1 | a0001c0001t0001g0192 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.69+1980A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90003541 | |||||||
| chr8:90003615 | A | G | 1 | a0001c0001t0003g0191 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.69+2054A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90003615 | |||||||
| chr8:90003673 | C | T | 1 | a0001c0001t0002g0020 | 3 | NA18946.hp2 NA19010.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.69+2112C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90003673 | |||||||
| chr8:90003707 | T | G | 1 | a0001c0001t0001g0202 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.69+2146T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90003707 | |||||||
| chr8:90003735 | A | T | 1 | a0001c0001t0001g0192 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.69+2174A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90003735 | |||||||
| chr8:90003765 | C | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG01261.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.69+2204C>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90003765 | |||||||
| chr8:90003851 | A | G | 3 | a0001c0001t0002g0019 a0001c0001t0002g0189 a0001c0001t0002g0190 |
5 | HG00609.hp1 HG02083.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.69+2290A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90003851 | |||||||
| chr8:90003853 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.69+2292C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90003853 | |||||||
| chr8:90003896 | G | A | 3 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0212 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.69+2335G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90003896 | |||||||
| chr8:90003981 | T | G | 1 | a0001c0001t0002g0048 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.69+2420T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90003981 | |||||||
| chr8:90004352 | GA | G | 8 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(5): Show |
8 | HG00673.hp2 HG01261.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.69+2805delA | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 90004352 | ||||||
| chr8:90004386 | T | C | 1 | a0001c0001t0002g0051 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.69+2825T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90004386 | |||||||
| chr8:90004528 | A | G | 28 | a0001c0001t0001g0184 a0001c0001t0002g0185 a0001c0001t0003g0005 others(25): Show |
46 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.69+2967A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90004528 | |||||||
| chr8:90004602 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.69+3041C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90004602 | |||||||
| chr8:90004652 | T | A | 1 | a0001c0001t0005g0165 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.69+3091T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90004652 | |||||||
| chr8:90005002 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.69+3441G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90005002 | |||||||
| chr8:90005003 | A | G | 1 | a0001c0001t0001g0192 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.69+3442A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90005003 | |||||||
| chr8:90005036 | A | G | 1 | a0001c0001t0001g0192 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.69+3475A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90005036 | |||||||
| chr8:90005037 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.69+3476G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90005037 | |||||||
| chr8:90005086 | A | G | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG01167.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.69+3525A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90005086 | |||||||
| chr8:90005238 | G | T | 1 | a0001c0001t0001g0192 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.69+3677G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90005238 | |||||||
| chr8:90005373 | T | C | 9 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(6): Show |
9 | HG01261.hp2 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.69+3812T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90005373 | |||||||
| chr8:90005382 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.69+3821G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90005382 | |||||||
| chr8:90005445 | C | T | 1 | a0001c0001t0002g0162 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.69+3884C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90005445 | |||||||
| chr8:90005517 | T | C | 172 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.69+3956T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90005517 | |||||||
| chr8:90005551 | A | G | 7 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0212 others(4): Show |
9 | HG02055.hp1 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.69+3990A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90005551 | |||||||
| chr8:90005612 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0053 |
3 | HG02723.hp1 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.69+4051G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90005612 | |||||||
| chr8:90005763 | C | A | 1 | a0001c0001t0001g0204 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.69+4202C>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90005763 | |||||||
| chr8:90005883 | G | GGGGTGTT others(29): Show |
1 | a0001c0001t0001g0208 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.69+4376_69+4411dup others(36): Show |
DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 90005883 | ||||||
| chr8:90005903 | C | T | 1 | a0001c0001t0002g0161 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.69+4342C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90005903 | |||||||
| chr8:90005986 | A | G | 4 | a0001c0001t0002g0015 a0001c0001t0002g0159 a0001c0001t0002g0160 others(1): Show |
6 | HG00099.hp1 HG01346.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.69+4425A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90005986 | |||||||
| chr8:90006052 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.69+4491C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006052 | |||||||
| chr8:90006081 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.69+4520C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006081 | |||||||
| chr8:90006082 | C | T | 5 | a0001c0001t0001g0029 a0001c0001t0001g0049 a0001c0001t0001g0050 others(2): Show |
6 | HG02818.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.69+4521C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006082 | |||||||
| chr8:90006260 | C | T | 1 | a0001c0001t0001g0192 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.69+4699C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006260 | |||||||
| chr8:90006261 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.69+4700T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006261 | |||||||
| chr8:90006279 | T | A | 49 | a0001c0001t0001g0184 a0001c0001t0001g0194 a0001c0001t0001g0202 others(46): Show |
70 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.69+4718T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006279 | |||||||
| chr8:90006612 | A | G | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.69+5051A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006612 | |||||||
| chr8:90006614 | G | A | 1 | a0001c0001t0002g0122 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.69+5053G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006614 | |||||||
| chr8:90006756 | T | C | 2 | a0001c0001t0001g0194 a0001c0001t0004g0193 |
2 | HG01109.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.69+5195T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006756 | |||||||
| chr8:90006757 | A | G | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | NA18940.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.69+5196A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006757 | |||||||
| chr8:90006772 | C | T | 1 | a0001c0001t0004g0199 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.69+5211C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006772 | |||||||
| chr8:90006778 | A | G | 3 | a0001c0001t0001g0017 a0001c0001t0001g0114 a0001c0001t0001g0115 |
5 | NA18966.hp2 NA18986.hp1 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.69+5217A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006778 | |||||||
| chr8:90006819 | C | T | 172 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.69+5258C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006819 | |||||||
| chr8:90006823 | G | A | 93 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(90): Show |
150 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.69+5262G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006823 | |||||||
| chr8:90006830 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.69+5269A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006830 | |||||||
| chr8:90006832 | C | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(117): Show |
183 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.69+5271C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006832 | |||||||
| chr8:90007254 | C | G | 1 | a0001c0001t0002g0158 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.69+5693C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90007254 | |||||||
| chr8:90007401 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.69+5840A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90007401 | |||||||
| chr8:90007550 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0055 a0001c0001t0001g0056 others(1): Show |
7 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.69+5989G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90007550 | |||||||
| chr8:90007575 | G | C | 1 | a0001c0001t0001g0058 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.69+6014G>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90007575 | |||||||
| chr8:90007728 | A | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(90): Show |
150 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.69+6167A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90007728 | |||||||
| chr8:90007910 | G | A | 1 | a0001c0001t0002g0051 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.69+6349G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90007910 | |||||||
| chr8:90008185 | T | G | 20 | a0001c0001t0001g0226 a0001c0001t0001g0230 a0001c0001t0001g0235 others(17): Show |
24 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.69+6624T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90008185 | |||||||
| chr8:90008397 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.69+6836A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90008397 | |||||||
| chr8:90008510 | A | G | 3 | a0001c0001t0006g0021 a0001c0001t0006g0210 a0001c0001t0006g0211 |
5 | HG01081.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.69+6949A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90008510 | |||||||
| chr8:90008606 | A | C | 114 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(111): Show |
175 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.69+7045A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90008606 | |||||||
| chr8:90008631 | A | G | 1 | a0001c0001t0003g0183 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.69+7070A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90008631 | |||||||
| chr8:90008757 | G | T | 1 | a0001c0001t0010g0109 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.69+7196G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90008757 | |||||||
| chr8:90008956 | T | A | 1 | a0001c0001t0001g0202 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.69+7395T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90008956 | |||||||
| chr8:90009054 | T | C | 23 | a0001c0001t0001g0226 a0001c0001t0001g0230 a0001c0001t0001g0235 others(20): Show |
27 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.69+7493T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90009054 | |||||||
| chr8:90009069 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.69+7508G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90009069 | |||||||
| chr8:90009089 | T | C | 1 | a0001c0001t0001g0060 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.69+7528T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90009089 | |||||||
| chr8:90009175 | C | G | 110 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(107): Show |
169 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.69+7614C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90009175 | |||||||
| chr8:90009452 | A | G | 5 | a0001c0001t0001g0029 a0001c0001t0001g0049 a0001c0001t0001g0050 others(2): Show |
6 | HG02818.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.70-7672A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90009452 | |||||||
| chr8:90009502 | G | GT | 81 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(78): Show |
121 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.70-7610dupT | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 90009502 | ||||||
| chr8:90009514 | T | TA | 5 | a0001c0001t0001g0194 a0001c0001t0004g0039 a0001c0001t0004g0193 others(2): Show |
6 | HG01109.hp1 HG01243.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.70-7609dupA | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 90009514 | ||||||
| chr8:90009799 | A | T | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.70-7325A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90009799 | |||||||
| chr8:90009941 | G | A | 1 | a0001c0001t0004g0042 | 2 | HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.70-7183G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90009941 | |||||||
| chr8:90010125 | C | T | 5 | a0001c0001t0003g0038 a0001c0001t0003g0179 a0001c0001t0003g0180 others(2): Show |
6 | HG00544.hp1 NA18612.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.70-6999C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90010125 | |||||||
| chr8:90010234 | G | A | 3 | a0001c0001t0006g0021 a0001c0001t0006g0210 a0001c0001t0006g0211 |
5 | HG01081.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-6890G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90010234 | |||||||
| chr8:90010540 | G | T | 1 | a0001c0001t0001g0104 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.70-6584G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90010540 | |||||||
| chr8:90010548 | G | A | 2 | a0001c0001t0004g0222 a0001c0001t0004g0223 |
2 | HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.70-6576G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90010548 | |||||||
| chr8:90010639 | G | A | 55 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(52): Show |
89 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.70-6485G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90010639 | |||||||
| chr8:90010758 | T | C | 1 | a0001c0001t0003g0166 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.70-6366T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90010758 | |||||||
| chr8:90010816 | T | C | 27 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(24): Show |
43 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.70-6308T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90010816 | |||||||
| chr8:90010890 | T | C | 172 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.70-6234T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90010890 | |||||||
| chr8:90010893 | T | G | 1 | a0001c0001t0001g0121 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.70-6231T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90010893 | |||||||
| chr8:90010925 | G | C | 1 | a0001c0001t0001g0061 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.70-6199G>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90010925 | |||||||
| chr8:90011304 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.70-5820A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90011304 | |||||||
| chr8:90011314 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.70-5810A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90011314 | |||||||
| chr8:90011329 | T | C | 28 | a0001c0001t0001g0184 a0001c0001t0003g0005 a0001c0001t0003g0008 others(25): Show |
46 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.70-5795T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90011329 | |||||||
| chr8:90011399 | A | G | 22 | a0001c0001t0001g0226 a0001c0001t0001g0230 a0001c0001t0001g0235 others(19): Show |
26 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.70-5725A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90011399 | |||||||
| chr8:90011582 | C | T | 3 | a0001c0001t0004g0232 a0001c0001t0004g0233 a0001c0001t0004g0234 |
3 | HG01884.hp2 HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.70-5542C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90011582 | |||||||
| chr8:90011617 | T | G | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.70-5507T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90011617 | |||||||
| chr8:90011622 | A | G | 1 | a0001c0001t0002g0122 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.70-5502A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90011622 | |||||||
| chr8:90011784 | A | G | 1 | a0001c0001t0001g0046 | 2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.70-5340A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90011784 | |||||||
| chr8:90011850 | T | A | 1 | a0001c0001t0001g0217 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.70-5274T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90011850 | |||||||
| chr8:90012069 | G | C | 2 | a0001c0001t0005g0112 a0001c0001t0005g0113 |
2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.70-5055G>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90012069 | |||||||
| chr8:90012156 | CT | C | 7 | a0001c0001t0001g0025 a0001c0001t0001g0053 a0001c0001t0001g0062 others(4): Show |
8 | HG02723.hp1 HG02922.hp2 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-4954delT | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 90012156 | ||||||
| chr8:90012161 | T | C | 3 | a0001c0001t0001g0040 a0001c0001t0001g0213 a0001c0001t0001g0214 |
4 | HG02486.hp1 HG02630.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-4963T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90012161 | |||||||
| chr8:90012164 | T | A | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.70-4960T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90012164 | |||||||
| chr8:90012193 | C | T | 2 | a0001c0001t0003g0177 a0001c0001t0003g0178 |
2 | NA18977.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.70-4931C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90012193 | |||||||
| chr8:90012262 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.70-4862C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90012262 | |||||||
| chr8:90012277 | C | T | 1 | a0001c0001t0002g0024 | 2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.70-4847C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90012277 | |||||||
| chr8:90012314 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.70-4810G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90012314 | |||||||
| chr8:90012343 | G | C | 1 | a0001c0001t0001g0217 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.70-4781G>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90012343 | |||||||
| chr8:90012388 | G | T | 8 | a0001c0001t0001g0194 a0001c0001t0004g0039 a0001c0001t0004g0193 others(5): Show |
9 | HG01070.hp1 HG01109.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.70-4736G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90012388 | |||||||
| chr8:90012432 | T | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG01167.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.70-4692T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90012432 | |||||||
| chr8:90012585 | A | G | 1 | a0001c0001t0003g0182 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.70-4539A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90012585 | |||||||
| chr8:90012654 | C | G | 3 | a0001c0001t0001g0029 a0001c0001t0001g0119 a0001c0001t0001g0120 |
4 | HG02896.hp2 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-4470C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90012654 | |||||||
| chr8:90012879 | T | C | 27 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(24): Show |
45 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.70-4245T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90012879 | |||||||
| chr8:90012949 | G | T | 20 | a0001c0001t0001g0226 a0001c0001t0001g0230 a0001c0001t0001g0235 others(17): Show |
24 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.70-4175G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90012949 | |||||||
| chr8:90013018 | C | T | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.70-4106C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90013018 | |||||||
| chr8:90013299 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.70-3825T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90013299 | |||||||
| chr8:90013343 | T | A | 1 | a0001c0001t0015g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.70-3781T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90013343 | |||||||
| chr8:90013399 | G | GT | 72 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0028 others(69): Show |
102 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.70-3702dupT | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 90013399 | ||||||
| chr8:90013399 | G | GTT | 20 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0016 others(17): Show |
32 | HG00642.hp2 HG00673.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.70-3703_70-3702dup others(2): Show |
DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 90013399 | ||||||
| chr8:90013399 | G | GTTTT | 16 | a0001c0001t0003g0008 a0001c0001t0003g0036 a0001c0001t0003g0037 others(13): Show |
26 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.70-3705_70-3702dup others(4): Show |
DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 90013399 | ||||||
| chr8:90013399 | G | GTTTTT | 8 | a0001c0001t0003g0005 a0001c0001t0003g0172 a0001c0001t0003g0173 others(5): Show |
16 | HG00438.hp1 HG01952.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.70-3706_70-3702dup others(5): Show |
DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 90013399 | ||||||
| chr8:90013399 | G | T | 1 | a0001c0001t0002g0156 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.70-3725G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90013399 | |||||||
| chr8:90013399 | GT | G | 11 | a0001c0001t0001g0063 a0001c0001t0001g0066 a0001c0001t0001g0067 others(8): Show |
13 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.70-3702delT | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 90013399 | ||||||
| chr8:90013399 | GTTTTTTT others(2): Show |
G | 5 | a0001c0001t0001g0025 a0001c0001t0001g0062 a0001c0001t0001g0207 others(2): Show |
6 | HG01891.hp2 HG02615.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.70-3710_70-3702del others(9): Show |
DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 90013399 | ||||||
| chr8:90013423 | G | T | 2 | a0001c0001t0002g0153 a0001c0001t0002g0154 |
2 | NA18940.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.70-3701G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90013423 | |||||||
| chr8:90013970 | A | G | 1 | a0001c0001t0002g0152 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.70-3154A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90013970 | |||||||
| chr8:90013996 | G | T | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.70-3128G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90013996 | |||||||
| chr8:90014137 | C | T | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.70-2987C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90014137 | |||||||
| chr8:90014236 | A | G | 1 | a0001c0001t0004g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.70-2888A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90014236 | |||||||
| chr8:90014299 | C | T | 11 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(8): Show |
25 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.70-2825C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90014299 | |||||||
| chr8:90014673 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.70-2451G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90014673 | |||||||
| chr8:90014921 | G | A | 1 | a0001c0001t0002g0126 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.70-2203G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90014921 | |||||||
| chr8:90015173 | A | T | 1 | a0001c0001t0001g0016 | 3 | HG02027.hp1 NA18975.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.70-1951A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90015173 | |||||||
| chr8:90015197 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.70-1927C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90015197 | |||||||
| chr8:90015521 | T | C | 1 | a0001c0001t0003g0168 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.70-1603T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90015521 | |||||||
| chr8:90015641 | C | A | 9 | a0001c0001t0001g0194 a0001c0001t0004g0039 a0001c0001t0004g0193 others(6): Show |
10 | HG01070.hp1 HG01109.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-1483C>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90015641 | |||||||
| chr8:90015661 | G | A | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | HG01261.hp2 HG02109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.70-1463G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90015661 | |||||||
| chr8:90015697 | A | G | 1 | a0001c0001t0004g0227 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.70-1427A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90015697 | |||||||
| chr8:90015902 | G | A | 20 | a0001c0001t0001g0226 a0001c0001t0001g0230 a0001c0001t0001g0235 others(17): Show |
24 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.70-1222G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90015902 | |||||||
| chr8:90015934 | T | G | 1 | a0001c0001t0001g0064 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.70-1190T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90015934 | |||||||
| chr8:90016046 | C | G | 35 | a0001c0001t0001g0194 a0001c0001t0001g0226 a0001c0001t0001g0230 others(32): Show |
42 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.70-1078C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90016046 | |||||||
| chr8:90016068 | G | T | 1 | a0001c0001t0001g0050 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.70-1056G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90016068 | |||||||
| chr8:90016131 | G | A | 90 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(87): Show |
131 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.70-993G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90016131 | |||||||
| chr8:90016166 | A | G | 77 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(74): Show |
118 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.70-958A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90016166 | |||||||
| chr8:90016393 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.70-731T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90016393 | |||||||
| chr8:90016403 | G | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG01167.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.70-721G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90016403 | |||||||
| chr8:90016473 | A | G | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.70-651A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90016473 | |||||||
| chr8:90016498 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.70-626G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90016498 | |||||||
| chr8:90016797 | T | C | 1 | a0001c0001t0002g0127 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.70-327T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90016797 | |||||||
| chr8:90017578 | T | C | 27 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(24): Show |
45 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.272+252T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 2/9 | chr8 | 90017578 | |||||||
| chr8:90018054 | T | G | 1 | a0001c0001t0001g0066 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.272+728T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 2/9 | chr8 | 90018054 | |||||||
| chr8:90018177 | C | G | 2 | a0001c0001t0005g0112 a0001c0001t0005g0113 |
2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.273-732C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 2/9 | chr8 | 90018177 | |||||||
| chr8:90018308 | G | A | 172 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.273-601G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 2/9 | chr8 | 90018308 | |||||||
| chr8:90018508 | AT | A | 82 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(79): Show |
125 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.273-397delT | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr8 | 90018508 | ||||||
| chr8:90018526 | A | G | 82 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(79): Show |
125 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.273-383A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 2/9 | chr8 | 90018526 | |||||||
| chr8:90018533 | GT | G | 28 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(25): Show |
44 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.273-368delT | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr8 | 90018533 | ||||||
| chr8:90018682 | A | G | 22 | a0001c0001t0001g0226 a0001c0001t0001g0230 a0001c0001t0001g0235 others(19): Show |
26 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.273-227A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 2/9 | chr8 | 90018682 | |||||||
| chr8:90018782 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.273-127T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 2/9 | chr8 | 90018782 | |||||||
| chr8:90018846 | G | A | 48 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(45): Show |
72 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.273-63G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 2/9 | chr8 | 90018846 | |||||||
| chr8:90019205 | G | A | 35 | a0001c0001t0001g0194 a0001c0001t0001g0226 a0001c0001t0001g0230 others(32): Show |
42 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.417+33G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90019205 | |||||||
| chr8:90019350 | G | A | 6 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0225 others(3): Show |
7 | HG02257.hp2 HG02922.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.417+178G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90019350 | |||||||
| chr8:90019352 | A | C | 2 | a0001c0001t0001g0055 a0001c0001t0001g0057 |
2 | HG00738.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.417+180A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90019352 | |||||||
| chr8:90019386 | G | A | 1 | a0001c0001t0001g0046 | 2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.417+214G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90019386 | |||||||
| chr8:90019490 | A | G | 2 | a0001c0001t0004g0233 a0001c0001t0004g0234 |
2 | HG01884.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.417+318A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90019490 | |||||||
| chr8:90019671 | G | A | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.417+499G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90019671 | |||||||
| chr8:90019705 | A | G | 90 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(87): Show |
131 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.417+533A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90019705 | |||||||
| chr8:90019734 | A | G | 8 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0049 others(5): Show |
10 | HG02055.hp1 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.417+562A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90019734 | |||||||
| chr8:90019825 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.417+653A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90019825 | |||||||
| chr8:90019930 | G | A | 1 | a0001c0001t0005g0206 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.417+758G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90019930 | |||||||
| chr8:90019960 | T | G | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.417+788T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90019960 | |||||||
| chr8:90020103 | G | C | 3 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0152 |
3 | HG01070.hp2 HG01071.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.418-806G>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90020103 | |||||||
| chr8:90020107 | G | A | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.418-802G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90020107 | |||||||
| chr8:90020206 | G | T | 1 | a0001c0001t0012g0145 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.418-703G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90020206 | |||||||
| chr8:90020308 | T | C | 1 | a0001c0001t0002g0130 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.418-601T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90020308 | |||||||
| chr8:90020348 | T | C | 90 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(87): Show |
131 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.418-561T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90020348 | |||||||
| chr8:90020492 | G | A | 4 | a0001c0001t0003g0036 a0001c0001t0003g0167 a0001c0001t0003g0172 others(1): Show |
5 | HG02132.hp1 NA19004.hp2 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.418-417G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90020492 | |||||||
| chr8:90020504 | T | G | 2 | a0001c0001t0005g0112 a0001c0001t0005g0113 |
2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.418-405T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90020504 | |||||||
| chr8:90020605 | C | G | 90 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(87): Show |
131 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.418-304C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90020605 | |||||||
| chr8:90020852 | A | G | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.418-57A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90020852 | |||||||
| chr8:90021235 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.565+179T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90021235 | |||||||
| chr8:90021361 | A | G | 31 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(28): Show |
49 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.565+305A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90021361 | |||||||
| chr8:90021511 | A | G | 11 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(8): Show |
25 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.565+455A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90021511 | |||||||
| chr8:90021518 | A | G | 31 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(28): Show |
49 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.565+462A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90021518 | |||||||
| chr8:90021760 | T | A | 1 | a0001c0001t0003g0183 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.565+704T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90021760 | |||||||
| chr8:90021854 | C | G | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.565+798C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90021854 | |||||||
| chr8:90022129 | T | C | 58 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(55): Show |
94 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.565+1073T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90022129 | |||||||
| chr8:90022207 | T | C | 3 | a0001c0001t0006g0021 a0001c0001t0006g0210 a0001c0001t0006g0211 |
5 | HG01081.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+1151T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90022207 | |||||||
| chr8:90022274 | T | C | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.565+1218T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90022274 | |||||||
| chr8:90022433 | T | C | 9 | a0001c0001t0001g0194 a0001c0001t0004g0039 a0001c0001t0004g0193 others(6): Show |
10 | HG01070.hp1 HG01109.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.565+1377T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90022433 | |||||||
| chr8:90022589 | C | T | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.565+1533C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90022589 | |||||||
| chr8:90022590 | G | A | 1 | a0001c0001t0009g0043 | 2 | HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.565+1534G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90022590 | |||||||
| chr8:90022647 | G | A | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.565+1591G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90022647 | |||||||
| chr8:90022895 | G | T | 1 | a0001c0001t0003g0168 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.565+1839G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90022895 | |||||||
| chr8:90023061 | A | T | 1 | a0001c0001t0001g0226 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.565+2005A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90023061 | |||||||
| chr8:90023318 | A | G | 1 | a0001c0001t0002g0152 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.565+2262A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90023318 | |||||||
| chr8:90023343 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.565+2287T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90023343 | |||||||
| chr8:90023387 | G | GT | 28 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(25): Show |
44 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.565+2340dupT | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr8 | 90023387 | ||||||
| chr8:90023676 | A | G | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.565+2620A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90023676 | |||||||
| chr8:90023685 | G | A | 90 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(87): Show |
131 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.565+2629G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90023685 | |||||||
| chr8:90024190 | G | A | 2 | a0001c0001t0006g0021 a0001c0001t0006g0210 |
4 | HG01081.hp2 HG02486.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+3134G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90024190 | |||||||
| chr8:90024250 | G | A | 2 | a0001c0001t0002g0131 a0001c0001t0002g0147 |
2 | NA18747.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.565+3194G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90024250 | |||||||
| chr8:90024403 | C | T | 1 | a0001c0001t0001g0046 | 2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.565+3347C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90024403 | |||||||
| chr8:90024467 | A | G | 2 | a0001c0001t0002g0035 a0001c0001t0002g0125 |
3 | HG02055.hp2 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.565+3411A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90024467 | |||||||
| chr8:90024647 | A | C | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.565+3591A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90024647 | |||||||
| chr8:90024738 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.565+3682T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90024738 | |||||||
| chr8:90024813 | G | C | 1 | a0001c0001t0001g0226 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.565+3757G>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90024813 | |||||||
| chr8:90024857 | G | T | 1 | a0001c0001t0001g0235 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.565+3801G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90024857 | |||||||
| chr8:90024916 | A | G | 48 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(45): Show |
72 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.565+3860A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90024916 | |||||||
| chr8:90025008 | G | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0082 |
3 | HG00735.hp2 HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.565+3952G>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90025008 | |||||||
| chr8:90025191 | T | A | 2 | a0001c0001t0003g0174 a0001c0001t0005g0071 |
2 | NA19062.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.565+4135T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90025191 | |||||||
| chr8:90025216 | G | A | 1 | a0001c0001t0004g0228 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.565+4160G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90025216 | |||||||
| chr8:90025387 | T | C | 2 | a0001c0001t0005g0112 a0001c0001t0005g0113 |
2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.565+4331T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90025387 | |||||||
| chr8:90025396 | A | G | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.565+4340A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90025396 | |||||||
| chr8:90025573 | T | A | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.565+4517T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90025573 | |||||||
| chr8:90025651 | A | G | 8 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0049 others(5): Show |
10 | HG02055.hp1 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+4595A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90025651 | |||||||
| chr8:90025682 | C | T | 1 | a0001c0001t0002g0143 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.565+4626C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90025682 | |||||||
| chr8:90025753 | A | C | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.565+4697A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90025753 | |||||||
| chr8:90025891 | G | A | 4 | a0001c0001t0005g0072 a0001c0001t0006g0021 a0001c0001t0006g0210 others(1): Show |
6 | HG01081.hp2 HG02145.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.565+4835G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90025891 | |||||||
| chr8:90025919 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.565+4863T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90025919 | |||||||
| chr8:90025936 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.565+4880G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90025936 | |||||||
| chr8:90025950 | G | A | 38 | a0001c0001t0001g0025 a0001c0001t0001g0053 a0001c0001t0001g0062 others(35): Show |
46 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.565+4894G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90025950 | |||||||
| chr8:90026021 | C | T | 1 | a0001c0001t0002g0142 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.565+4965C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90026021 | |||||||
| chr8:90026106 | G | T | 1 | a0001c0001t0004g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.565+5050G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90026106 | |||||||
| chr8:90026135 | C | T | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.565+5079C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90026135 | |||||||
| chr8:90026369 | G | A | 1 | a0001c0001t0008g0073 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.565+5313G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90026369 | |||||||
| chr8:90026427 | C | G | 1 | a0001c0001t0001g0111 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.565+5371C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90026427 | |||||||
| chr8:90026455 | G | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0074 a0001c0001t0001g0089 others(2): Show |
11 | HG00438.hp2 HG00673.hp1 NA18957.hp2 others(8): Show |
intron_variant | MODIFIER | c.565+5399G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90026455 | |||||||
| chr8:90026612 | C | G | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.565+5556C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90026612 | |||||||
| chr8:90026639 | A | G | 172 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.565+5583A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90026639 | |||||||
| chr8:90026939 | T | G | 2 | a0001c0001t0005g0112 a0001c0001t0005g0113 |
2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.565+5883T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90026939 | |||||||
| chr8:90027105 | G | C | 1 | a0001c0001t0015g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.565+6049G>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027105 | |||||||
| chr8:90027149 | G | A | 1 | a0001c0001t0001g0046 | 2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.565+6093G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027149 | |||||||
| chr8:90027302 | G | T | 2 | a0001c0001t0002g0153 a0001c0001t0002g0154 |
2 | NA18940.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.565+6246G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027302 | |||||||
| chr8:90027367 | G | A | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.565+6311G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027367 | |||||||
| chr8:90027575 | A | G | 2 | a0001c0001t0001g0235 a0001c0001t0002g0189 |
2 | HG02145.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.565+6519A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027575 | |||||||
| chr8:90027576 | T | G | 2 | a0001c0001t0001g0235 a0001c0001t0002g0189 |
2 | HG02145.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.565+6520T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027576 | |||||||
| chr8:90027577 | C | T | 2 | a0001c0001t0001g0235 a0001c0001t0002g0189 |
2 | HG02145.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.565+6521C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027577 | |||||||
| chr8:90027587 | C | G | 1 | a0001c0001t0001g0235 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.565+6531C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027587 | |||||||
| chr8:90027630 | T | A | 1 | a0001c0001t0001g0091 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.565+6574T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027630 | |||||||
| chr8:90027694 | A | C | 1 | a0001c0001t0001g0087 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.565+6638A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027694 | |||||||
| chr8:90027702 | C | T | 3 | a0001c0001t0006g0021 a0001c0001t0006g0210 a0001c0001t0006g0211 |
5 | HG01081.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+6646C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027702 | |||||||
| chr8:90027717 | C | T | 20 | a0001c0001t0001g0226 a0001c0001t0001g0230 a0001c0001t0001g0235 others(17): Show |
24 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.565+6661C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027717 | |||||||
| chr8:90027773 | T | A | 6 | a0001c0001t0001g0029 a0001c0001t0001g0050 a0001c0001t0001g0075 others(3): Show |
7 | HG02698.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.565+6717T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027773 | |||||||
| chr8:90027774 | T | A | 108 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(105): Show |
156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.565+6718T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027774 | |||||||
| chr8:90027775 | A | T | 27 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(24): Show |
45 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.565+6719A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027775 | |||||||
| chr8:90027846 | A | G | 3 | a0001c0001t0002g0141 a0001c0001t0002g0155 a0001c0001t0013g0140 |
3 | HG01433.hp1 HG03491.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.565+6790A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027846 | |||||||
| chr8:90027854 | G | T | 2 | a0001c0001t0002g0034 a0001c0001t0002g0158 |
3 | HG00741.hp1 HG01071.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.565+6798G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027854 | |||||||
| chr8:90027941 | A | G | 1 | a0001c0001t0004g0220 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+6885A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027941 | |||||||
| chr8:90028096 | T | G | 1 | a0001c0001t0004g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.565+7040T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90028096 | |||||||
| chr8:90028166 | C | T | 20 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(17): Show |
34 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.565+7110C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90028166 | |||||||
| chr8:90028349 | T | G | 1 | a0001c0001t0004g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.565+7293T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90028349 | |||||||
| chr8:90028385 | A | T | 1 | a0001c0001t0007g0151 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.565+7329A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90028385 | |||||||
| chr8:90028478 | G | A | 27 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(24): Show |
45 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.565+7422G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90028478 | |||||||
| chr8:90028638 | G | T | 1 | a0001c0001t0001g0062 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.565+7582G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90028638 | |||||||
| chr8:90028693 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.565+7637C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90028693 | |||||||
| chr8:90028725 | CT | C | 20 | a0001c0001t0001g0226 a0001c0001t0001g0230 a0001c0001t0001g0235 others(17): Show |
24 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.565+7676delT | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr8 | 90028725 | ||||||
| chr8:90028730 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.565+7674T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90028730 | |||||||
| chr8:90028880 | G | T | 5 | a0001c0001t0001g0025 a0001c0001t0001g0053 a0001c0001t0001g0062 others(2): Show |
6 | HG01167.hp1 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.565+7824G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90028880 | |||||||
| chr8:90028920 | G | A | 11 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(8): Show |
25 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.565+7864G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90028920 | |||||||
| chr8:90028957 | C | T | 6 | a0001c0001t0004g0039 a0001c0001t0004g0195 a0001c0001t0004g0196 others(3): Show |
7 | HG01070.hp1 HG01243.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.566-7884C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90028957 | |||||||
| chr8:90029066 | T | A | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.566-7775T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90029066 | |||||||
| chr8:90029079 | AAG | A | 15 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(12): Show |
29 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.566-7760_566-7759d others(4): Show |
DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr8 | 90029079 | ||||||
| chr8:90029126 | A | G | 3 | a0001c0001t0006g0021 a0001c0001t0006g0210 a0001c0001t0006g0211 |
5 | HG01081.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.566-7715A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90029126 | |||||||
| chr8:90029511 | C | G | 10 | a0001c0001t0001g0194 a0001c0001t0004g0039 a0001c0001t0004g0054 others(7): Show |
11 | HG01070.hp1 HG01109.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.566-7330C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90029511 | |||||||
| chr8:90029591 | G | A | 1 | a0001c0001t0004g0220 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.566-7250G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90029591 | |||||||
| chr8:90029642 | A | T | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.566-7199A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90029642 | |||||||
| chr8:90029645 | A | T | 1 | a0001c0001t0002g0159 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.566-7196A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90029645 | |||||||
| chr8:90029708 | G | A | 1 | a0001c0001t0004g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.566-7133G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90029708 | |||||||
| chr8:90029739 | T | A | 1 | a0001c0001t0001g0217 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.566-7102T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90029739 | |||||||
| chr8:90029821 | C | T | 1 | a0001c0001t0005g0072 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.566-7020C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90029821 | |||||||
| chr8:90029823 | A | C | 1 | a0001c0001t0001g0049 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.566-7018A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90029823 | |||||||
| chr8:90029823 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.566-7018A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90029823 | |||||||
| chr8:90029998 | A | G | 2 | a0001c0001t0002g0033 a0001c0001t0002g0150 |
3 | NA18939.hp2 NA18952.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.566-6843A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90029998 | |||||||
| chr8:90030004 | G | A | 1 | a0001c0001t0004g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.566-6837G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90030004 | |||||||
| chr8:90030158 | A | G | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.566-6683A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90030158 | |||||||
| chr8:90030215 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.566-6626G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90030215 | |||||||
| chr8:90030319 | A | T | 1 | a0001c0001t0002g0154 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.566-6522A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90030319 | |||||||
| chr8:90030441 | C | T | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.566-6400C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90030441 | |||||||
| chr8:90030475 | T | G | 27 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(24): Show |
45 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.566-6366T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90030475 | |||||||
| chr8:90030599 | A | G | 3 | a0001c0001t0006g0021 a0001c0001t0006g0210 a0001c0001t0006g0211 |
5 | HG01081.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.566-6242A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90030599 | |||||||
| chr8:90030623 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0092 |
2 | NA18985.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.566-6218T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90030623 | |||||||
| chr8:90030913 | T | A | 1 | a0001c0001t0004g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.566-5928T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90030913 | |||||||
| chr8:90031088 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.566-5753T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90031088 | |||||||
| chr8:90031327 | C | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0093 |
2 | HG03831.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.566-5514C>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90031327 | |||||||
| chr8:90031414 | A | G | 172 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.566-5427A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90031414 | |||||||
| chr8:90031473 | G | C | 1 | a0001c0001t0001g0217 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.566-5368G>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90031473 | |||||||
| chr8:90031547 | G | A | 172 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.566-5294G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90031547 | |||||||
| chr8:90031822 | A | G | 1 | a0001c0001t0002g0162 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.566-5019A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90031822 | |||||||
| chr8:90031824 | A | G | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.566-5017A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90031824 | |||||||
| chr8:90031877 | G | A | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.566-4964G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90031877 | |||||||
| chr8:90031904 | A | T | 1 | a0001c0001t0001g0046 | 2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.566-4937A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90031904 | |||||||
| chr8:90032030 | T | A | 2 | a0001c0001t0005g0112 a0001c0001t0005g0113 |
2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.566-4811T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90032030 | |||||||
| chr8:90032053 | G | A | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.566-4788G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90032053 | |||||||
| chr8:90032162 | A | T | 3 | a0001c0001t0006g0021 a0001c0001t0006g0210 a0001c0001t0006g0211 |
5 | HG01081.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.566-4679A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90032162 | |||||||
| chr8:90032180 | C | T | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.566-4661C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90032180 | |||||||
| chr8:90032266 | A | G | 2 | a0001c0001t0002g0032 a0001c0001t0002g0139 |
3 | NA18943.hp2 NA18964.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.566-4575A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90032266 | |||||||
| chr8:90032444 | C | T | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.566-4397C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90032444 | |||||||
| chr8:90032600 | C | T | 1 | a0001c0001t0008g0080 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.566-4241C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90032600 | |||||||
| chr8:90032605 | A | G | 1 | a0001c0001t0006g0211 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.566-4236A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90032605 | |||||||
| chr8:90032643 | A | T | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.566-4198A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90032643 | |||||||
| chr8:90032849 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.566-3992C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90032849 | |||||||
| chr8:90032864 | T | A | 1 | a0001c0001t0001g0212 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.566-3977T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90032864 | |||||||
| chr8:90032910 | A | G | 9 | a0001c0001t0001g0194 a0001c0001t0004g0039 a0001c0001t0004g0193 others(6): Show |
10 | HG01070.hp1 HG01109.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.566-3931A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90032910 | |||||||
| chr8:90033038 | C | T | 2 | a0001c0001t0005g0112 a0001c0001t0005g0113 |
2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.566-3803C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90033038 | |||||||
| chr8:90033060 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.566-3781A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90033060 | |||||||
| chr8:90033513 | A | C | 2 | a0001c0001t0005g0112 a0001c0001t0005g0113 |
2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.566-3328A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90033513 | |||||||
| chr8:90033665 | A | C | 172 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.566-3176A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90033665 | |||||||
| chr8:90033667 | T | C | 172 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.566-3174T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90033667 | |||||||
| chr8:90034251 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.566-2590G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90034251 | |||||||
| chr8:90034257 | C | A | 4 | a0001c0001t0004g0196 a0001c0001t0004g0197 a0001c0001t0004g0198 others(1): Show |
4 | HG01070.hp1 HG02572.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-2584C>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90034257 | |||||||
| chr8:90034533 | C | T | 1 | a0001c0001t0002g0141 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.566-2308C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90034533 | |||||||
| chr8:90035107 | A | G | 11 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(8): Show |
25 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.566-1734A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90035107 | |||||||
| chr8:90035113 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566-1728A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90035113 | |||||||
| chr8:90035281 | C | T | 9 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0049 others(6): Show |
11 | HG02055.hp1 HG02486.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.566-1560C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90035281 | |||||||
| chr8:90035511 | G | T | 178 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(175): Show |
266 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.566-1330G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90035511 | |||||||
| chr8:90035659 | G | A | 20 | a0001c0001t0001g0226 a0001c0001t0001g0230 a0001c0001t0001g0235 others(17): Show |
24 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.566-1182G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90035659 | |||||||
| chr8:90035797 | T | C | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG01167.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.566-1044T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90035797 | |||||||
| chr8:90035886 | A | G | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG01167.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.566-955A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90035886 | |||||||
| chr8:90035931 | A | AT | 27 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(24): Show |
45 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.566-901dupT | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr8 | 90035931 | ||||||
| chr8:90036049 | A | G | 36 | a0001c0001t0001g0194 a0001c0001t0001g0216 a0001c0001t0001g0226 others(33): Show |
43 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.566-792A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90036049 | |||||||
| chr8:90036090 | A | G | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.566-751A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90036090 | |||||||
| chr8:90036138 | A | G | 2 | a0001c0001t0002g0138 a0001c0001t0002g0149 |
2 | HG02027.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.566-703A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90036138 | |||||||
| chr8:90036585 | G | A | 2 | a0001c0001t0002g0030 a0001c0001t0002g0126 |
3 | NA18948.hp2 NA18998.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.566-256G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90036585 | |||||||
| chr8:90036744 | C | A | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.566-97C>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90036744 | |||||||
| chr8:90037151 | G | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG01167.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.665+211G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90037151 | |||||||
| chr8:90037266 | T | G | 1 | a0001c0001t0001g0217 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.665+326T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90037266 | |||||||
| chr8:90037325 | C | G | 2 | a0001c0001t0003g0038 a0001c0001t0003g0182 |
3 | NA18939.hp1 NA18949.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.665+385C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90037325 | |||||||
| chr8:90037448 | C | CT | 27 | a0001c0001t0001g0097 a0001c0001t0003g0005 a0001c0001t0003g0008 others(24): Show |
45 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.665+524dupT | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 90037448 | ||||||
| chr8:90037511 | A | G | 2 | a0001c0001t0005g0112 a0001c0001t0005g0113 |
2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.665+571A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90037511 | |||||||
| chr8:90037603 | C | T | 5 | a0001c0001t0001g0026 a0001c0001t0001g0079 a0001c0001t0001g0081 others(2): Show |
6 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(3): Show |
intron_variant | MODIFIER | c.665+663C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90037603 | |||||||
| chr8:90037735 | C | T | 1 | a0001c0001t0002g0130 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.665+795C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90037735 | |||||||
| chr8:90037823 | A | C | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.665+883A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90037823 | |||||||
| chr8:90038049 | T | A | 4 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(1): Show |
7 | HG01884.hp1 HG01891.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.665+1109T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90038049 | |||||||
| chr8:90038052 | T | C | 1 | a0001c0001t0005g0112 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.665+1112T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90038052 | |||||||
| chr8:90038068 | A | G | 11 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(8): Show |
25 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.665+1128A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90038068 | |||||||
| chr8:90038128 | A | G | 1 | a0001c0001t0004g0231 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.665+1188A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90038128 | |||||||
| chr8:90038262 | A | T | 3 | a0001c0001t0006g0021 a0001c0001t0006g0210 a0001c0001t0006g0211 |
5 | HG01081.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.665+1322A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90038262 | |||||||
| chr8:90038454 | C | CT | 32 | a0001c0001t0001g0013 a0001c0001t0001g0055 a0001c0001t0001g0056 others(29): Show |
40 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.665+1535dupT | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 90038454 | ||||||
| chr8:90038454 | CT | C | 53 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0049 others(50): Show |
74 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.665+1535delT | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 90038454 | ||||||
| chr8:90038463 | T | C | 1 | a0001c0001t0004g0195 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.665+1523T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90038463 | |||||||
| chr8:90038536 | G | A | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.665+1596G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90038536 | |||||||
| chr8:90039104 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.665+2164T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90039104 | |||||||
| chr8:90039162 | A | G | 1 | a0001c0001t0003g0180 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.665+2222A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90039162 | |||||||
| chr8:90039199 | C | A | 1 | a0001c0001t0002g0133 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.665+2259C>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90039199 | |||||||
| chr8:90039234 | A | G | 1 | a0001c0001t0004g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.665+2294A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90039234 | |||||||
| chr8:90039268 | CTGAGACT others(8): Show |
C | 28 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(25): Show |
44 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.665+2330_665+2344d others(17): Show |
DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 90039268 | ||||||
| chr8:90039397 | T | A | 82 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(79): Show |
125 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.665+2457T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90039397 | |||||||
| chr8:90039400 | TC | T | 3 | a0001c0001t0001g0207 a0001c0001t0005g0206 a0001c0001t0015g0205 |
3 | HG01891.hp2 HG02615.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.665+2462delC | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 90039400 | ||||||
| chr8:90039624 | C | A | 9 | a0001c0001t0004g0042 a0001c0001t0004g0044 a0001c0001t0004g0221 others(6): Show |
11 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.665+2684C>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90039624 | |||||||
| chr8:90040016 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.666-2712G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90040016 | |||||||
| chr8:90040039 | G | GC | 3 | a0001c0001t0001g0207 a0001c0001t0005g0206 a0001c0001t0015g0205 |
3 | HG01891.hp2 HG02615.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.666-2689_666-2688i others(3): Show |
DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90040039 | |||||||
| chr8:90040040 | T | A | 3 | a0001c0001t0001g0207 a0001c0001t0005g0206 a0001c0001t0015g0205 |
3 | HG01891.hp2 HG02615.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.666-2688T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90040040 | |||||||
| chr8:90040447 | C | T | 2 | a0001c0001t0001g0070 a0001c0001t0002g0185 |
2 | HG00735.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.666-2281C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90040447 | |||||||
| chr8:90040463 | T | C | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.666-2265T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90040463 | |||||||
| chr8:90040484 | T | A | 1 | a0001c0001t0002g0134 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.666-2244T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90040484 | |||||||
| chr8:90040598 | A | T | 2 | a0001c0001t0002g0153 a0001c0001t0002g0154 |
2 | NA18940.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.666-2130A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90040598 | |||||||
| chr8:90040604 | C | T | 8 | a0001c0001t0001g0194 a0001c0001t0004g0039 a0001c0001t0004g0193 others(5): Show |
9 | HG01070.hp1 HG01109.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.666-2124C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90040604 | |||||||
| chr8:90040678 | G | A | 1 | a0001c0001t0001g0029 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.666-2050G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90040678 | |||||||
| chr8:90040712 | G | A | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.666-2016G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90040712 | |||||||
| chr8:90040782 | A | G | 174 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(171): Show |
261 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.666-1946A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90040782 | |||||||
| chr8:90040800 | A | C | 1 | a0001c0001t0001g0103 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.666-1928A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90040800 | |||||||
| chr8:90040888 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.666-1840G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90040888 | |||||||
| chr8:90040896 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.666-1832T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90040896 | |||||||
| chr8:90041025 | T | C | 10 | a0001c0001t0001g0194 a0001c0001t0004g0039 a0001c0001t0004g0054 others(7): Show |
11 | HG01070.hp1 HG01109.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.666-1703T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90041025 | |||||||
| chr8:90041261 | A | G | 4 | a0001c0001t0003g0037 a0001c0001t0003g0170 a0001c0001t0003g0171 others(1): Show |
5 | HG01943.hp1 NA18943.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.666-1467A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90041261 | |||||||
| chr8:90041369 | C | T | 1 | a0001c0001t0002g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.666-1359C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90041369 | |||||||
| chr8:90041569 | A | G | 1 | a0001c0001t0002g0143 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.666-1159A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90041569 | |||||||
| chr8:90041610 | G | A | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.666-1118G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90041610 | |||||||
| chr8:90041644 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.666-1084A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90041644 | |||||||
| chr8:90041747 | A | G | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.666-981A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90041747 | |||||||
| chr8:90041811 | G | A | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.666-917G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90041811 | |||||||
| chr8:90041882 | A | C | 1 | a0001c0001t0004g0232 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.666-846A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90041882 | |||||||
| chr8:90042319 | G | T | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.666-409G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90042319 | |||||||
| chr8:90042953 | G | A | 1 | a0001c0001t0002g0124 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.738+153G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90042953 | |||||||
| chr8:90042973 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.738+173C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90042973 | |||||||
| chr8:90043117 | A | G | 27 | a0001c0001t0001g0090 a0001c0001t0003g0005 a0001c0001t0003g0008 others(24): Show |
45 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.738+317A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90043117 | |||||||
| chr8:90043159 | A | T | 32 | a0001c0001t0001g0194 a0001c0001t0001g0226 a0001c0001t0001g0230 others(29): Show |
37 | HG01070.hp1 HG01109.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.738+359A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90043159 | |||||||
| chr8:90043183 | A | T | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.738+383A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90043183 | |||||||
| chr8:90043221 | A | T | 1 | a0001c0001t0003g0169 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.738+421A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90043221 | |||||||
| chr8:90043225 | G | A | 3 | a0001c0001t0002g0141 a0001c0001t0002g0155 a0001c0001t0013g0140 |
3 | HG01433.hp1 HG03491.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.738+425G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90043225 | |||||||
| chr8:90043241 | G | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(76): Show |
121 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.738+441G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90043241 | |||||||
| chr8:90043265 | A | G | 1 | a0001c0001t0001g0186 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.738+465A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90043265 | |||||||
| chr8:90043477 | A | C | 1 | a0001c0001t0004g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.738+677A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90043477 | |||||||
| chr8:90043622 | G | T | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.738+822G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90043622 | |||||||
| chr8:90043636 | T | TA | 178 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(175): Show |
266 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.738+841dupA | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr8 | 90043636 | ||||||
| chr8:90043687 | G | A | 83 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(80): Show |
126 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.738+887G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90043687 | |||||||
| chr8:90043757 | A | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0074 a0001c0001t0001g0089 others(2): Show |
11 | HG00438.hp2 HG00673.hp1 NA18957.hp2 others(8): Show |
intron_variant | MODIFIER | c.738+957A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90043757 | |||||||
| chr8:90043956 | A | G | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.739-893A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90043956 | |||||||
| chr8:90044205 | C | T | 27 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(24): Show |
45 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.739-644C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90044205 | |||||||
| chr8:90044393 | C | T | 27 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(24): Show |
43 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.739-456C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90044393 | |||||||
| chr8:90044495 | T | C | 2 | a0001c0001t0005g0112 a0001c0001t0005g0113 |
2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.739-354T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90044495 | |||||||
| chr8:90044582 | T | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0053 |
3 | HG02723.hp1 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.739-267T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90044582 | |||||||
| chr8:90044611 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.739-238G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90044611 | |||||||
| chr8:90045001 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG02630.hp2 | splice_region_variant&intron_variant | LOW | c.885+6C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90045001 | |||||||
| chr8:90045002 | GT | G | 4 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(1): Show |
7 | HG01884.hp1 HG01891.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.885+9delT | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 90045002 | ||||||
| chr8:90045160 | T | G | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.885+165T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90045160 | |||||||
| chr8:90045385 | C | T | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.885+390C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90045385 | |||||||
| chr8:90045392 | G | T | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0091 others(1): Show |
4 | HG01123.hp2 HG03654.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.885+397G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90045392 | |||||||
| chr8:90045679 | G | A | 2 | a0001c0001t0005g0112 a0001c0001t0005g0113 |
2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.885+684G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90045679 | |||||||
| chr8:90045899 | A | G | 54 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(51): Show |
88 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.885+904A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90045899 | |||||||
| chr8:90046122 | C | A | 8 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0049 others(5): Show |
10 | HG02055.hp1 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.885+1127C>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90046122 | |||||||
| chr8:90046163 | C | T | 83 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(80): Show |
126 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.885+1168C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90046163 | |||||||
| chr8:90046179 | G | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(7): Show |
24 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.885+1184G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90046179 | |||||||
| chr8:90046255 | G | A | 1 | a0001c0001t0004g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.885+1260G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90046255 | |||||||
| chr8:90046279 | G | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0212 a0001c0001t0001g0215 |
4 | HG02055.hp1 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.885+1284G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90046279 | |||||||
| chr8:90046298 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.885+1303G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90046298 | |||||||
| chr8:90046773 | G | A | 27 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(24): Show |
43 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.885+1778G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90046773 | |||||||
| chr8:90046855 | T | C | 172 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.885+1860T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90046855 | |||||||
| chr8:90046898 | T | G | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.885+1903T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90046898 | |||||||
| chr8:90046902 | T | G | 22 | a0001c0001t0001g0226 a0001c0001t0001g0230 a0001c0001t0001g0235 others(19): Show |
26 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.885+1907T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90046902 | |||||||
| chr8:90046988 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.885+1993A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90046988 | |||||||
| chr8:90047019 | A | G | 172 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.885+2024A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90047019 | |||||||
| chr8:90047148 | C | T | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.885+2153C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90047148 | |||||||
| chr8:90047169 | T | A | 8 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0049 others(5): Show |
10 | HG02055.hp1 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.885+2174T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90047169 | |||||||
| chr8:90047316 | C | T | 22 | a0001c0001t0001g0226 a0001c0001t0001g0230 a0001c0001t0001g0235 others(19): Show |
26 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.885+2321C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90047316 | |||||||
| chr8:90047359 | CA | C | 9 | a0001c0001t0001g0194 a0001c0001t0004g0039 a0001c0001t0004g0193 others(6): Show |
10 | HG01070.hp1 HG01109.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.885+2373delA | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 90047359 | ||||||
| chr8:90047596 | C | T | 2 | a0001c0001t0001g0194 a0001c0001t0004g0193 |
2 | HG01109.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.885+2601C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90047596 | |||||||
| chr8:90047625 | C | G | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.885+2630C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90047625 | |||||||
| chr8:90047737 | T | C | 63 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(60): Show |
86 | HG00642.hp2 HG00673.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.885+2742T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90047737 | |||||||
| chr8:90048117 | T | G | 1 | a0001c0001t0002g0031 | 2 | HG00323.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.885+3122T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90048117 | |||||||
| chr8:90048208 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0095 |
3 | HG01496.hp1 HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.885+3213G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90048208 | |||||||
| chr8:90048267 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.885+3272A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90048267 | |||||||
| chr8:90048286 | T | C | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.885+3291T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90048286 | |||||||
| chr8:90048359 | C | T | 1 | a0001c0001t0002g0135 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.886-3318C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90048359 | |||||||
| chr8:90048385 | C | T | 10 | a0001c0001t0001g0194 a0001c0001t0004g0039 a0001c0001t0004g0054 others(7): Show |
11 | HG01070.hp1 HG01109.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.886-3292C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90048385 | |||||||
| chr8:90048527 | A | T | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.886-3150A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90048527 | |||||||
| chr8:90048697 | T | A | 1 | a0001c0001t0001g0062 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.886-2980T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90048697 | |||||||
| chr8:90048754 | C | G | 1 | a0001c0001t0001g0052 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.886-2923C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90048754 | |||||||
| chr8:90048842 | C | G | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.886-2835C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90048842 | |||||||
| chr8:90048843 | G | C | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.886-2834G>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90048843 | |||||||
| chr8:90048889 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.886-2788C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90048889 | |||||||
| chr8:90048974 | C | T | 6 | a0001c0001t0001g0025 a0001c0001t0001g0053 a0001c0001t0001g0062 others(3): Show |
7 | HG01167.hp1 HG01891.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.886-2703C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90048974 | |||||||
| chr8:90049031 | G | T | 1 | a0001c0001t0002g0136 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.886-2646G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049031 | |||||||
| chr8:90049253 | T | C | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.886-2424T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049253 | |||||||
| chr8:90049377 | C | T | 6 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0225 others(3): Show |
7 | HG02257.hp2 HG02922.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.886-2300C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049377 | |||||||
| chr8:90049446 | A | G | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.886-2231A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049446 | |||||||
| chr8:90049567 | A | G | 2 | a0001c0001t0005g0112 a0001c0001t0005g0113 |
2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.886-2110A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049567 | |||||||
| chr8:90049661 | A | G | 1 | a0001c0001t0004g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.886-2016A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049661 | |||||||
| chr8:90049710 | A | G | 99 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(96): Show |
143 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.886-1967A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049710 | |||||||
| chr8:90049742 | A | G | 1 | a0001c0001t0001g0046 | 2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.886-1935A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049742 | |||||||
| chr8:90049813 | C | CT | 8 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0049 others(5): Show |
10 | HG02055.hp1 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.886-1864_886-1863i others(3): Show |
DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049813 | |||||||
| chr8:90049814 | G | A | 1 | a0001c0001t0004g0233 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.886-1863G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049814 | |||||||
| chr8:90049837 | C | T | 6 | a0001c0001t0004g0039 a0001c0001t0004g0195 a0001c0001t0004g0196 others(3): Show |
7 | HG01070.hp1 HG01243.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.886-1840C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049837 | |||||||
| chr8:90049890 | G | A | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.886-1787G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049890 | |||||||
| chr8:90049914 | C | A | 1 | a0001c0001t0001g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.886-1763C>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049914 | |||||||
| chr8:90049918 | A | C | 28 | a0001c0001t0002g0011 a0001c0001t0002g0014 a0001c0001t0002g0015 others(25): Show |
38 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.886-1759A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049918 | |||||||
| chr8:90049928 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.886-1749A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049928 | |||||||
| chr8:90049982 | A | G | 20 | a0001c0001t0001g0226 a0001c0001t0001g0230 a0001c0001t0001g0235 others(17): Show |
24 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.886-1695A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049982 | |||||||
| chr8:90050008 | C | G | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.886-1669C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90050008 | |||||||
| chr8:90050143 | A | G | 1 | a0001c0001t0002g0023 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.886-1534A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90050143 | |||||||
| chr8:90050162 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.886-1515C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90050162 | |||||||
| chr8:90050274 | C | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0119 a0001c0001t0001g0120 |
4 | HG02896.hp2 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.886-1403C>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90050274 | |||||||
| chr8:90050289 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.886-1388G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90050289 | |||||||
| chr8:90050315 | T | A | 5 | a0001c0001t0001g0026 a0001c0001t0001g0079 a0001c0001t0001g0081 others(2): Show |
6 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(3): Show |
intron_variant | MODIFIER | c.886-1362T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90050315 | |||||||
| chr8:90050499 | G | T | 3 | a0001c0001t0006g0021 a0001c0001t0006g0210 a0001c0001t0006g0211 |
5 | HG01081.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.886-1178G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90050499 | |||||||
| chr8:90050566 | G | A | 27 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(24): Show |
45 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.886-1111G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90050566 | |||||||
| chr8:90050592 | A | C | 46 | a0001c0001t0001g0226 a0001c0001t0001g0230 a0001c0001t0001g0235 others(43): Show |
68 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.886-1085A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90050592 | |||||||
| chr8:90050683 | G | A | 5 | a0001c0001t0003g0038 a0001c0001t0003g0179 a0001c0001t0003g0180 others(2): Show |
6 | HG00544.hp1 NA18612.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.886-994G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90050683 | |||||||
| chr8:90051020 | G | A | 8 | a0001c0001t0001g0194 a0001c0001t0004g0039 a0001c0001t0004g0193 others(5): Show |
9 | HG01070.hp1 HG01109.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.886-657G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90051020 | |||||||
| chr8:90051022 | C | G | 83 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(80): Show |
126 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.886-655C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90051022 | |||||||
| chr8:90051174 | T | TA | 37 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(34): Show |
69 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.886-490dupA | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 90051174 | ||||||
| chr8:90051174 | TA | T | 11 | a0001c0001t0001g0186 a0001c0001t0001g0194 a0001c0001t0002g0123 others(8): Show |
12 | HG01109.hp1 HG01243.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.886-490delA | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 90051174 | ||||||
| chr8:90051376 | T | A | 30 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(27): Show |
48 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.886-301T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90051376 | |||||||
| chr8:90051389 | C | T | 26 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0036 others(23): Show |
44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.886-288C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90051389 | |||||||
| chr8:90051471 | A | G | 1 | a0001c0001t0003g0170 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.886-206A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90051471 | |||||||
| chr8:90051500 | A | C | 3 | a0001c0001t0006g0021 a0001c0001t0006g0210 a0001c0001t0006g0211 |
5 | HG01081.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.886-177A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90051500 | |||||||
| chr8:90051559 | G | T | 78 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(75): Show |
119 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.886-118G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90051559 | |||||||
| chr8:90051808 | G | C | 172 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.949-30G>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 9/9 | chr8 | 90051808 |