Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 26063 |
| ensemblid | ENSG00000242612.7 |
| hgncid | 2754 |
| symbol | DECR2 |
| name | 2,4-dienoyl-CoA reductase 2 |
| refseq_nuc | NM_020664.4 |
| refseq_prot | NP_065715.1 |
| ensembl_nuc | ENST00000219481.10 |
| ensembl_prot | ENSP00000219481.5 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 401885 |
| end | 412482 |
| strand | + |
| ver | v1.2 |
| region | chr16:401885-412482 |
| region5000 | chr16:396885-417482 |
| regionname0 | DECR2_chr16_401885_412482 |
| regionname5000 | DECR2_chr16_396885_417482 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 292 | 331 | 65 | 71 | 140 | 14 | 40 | 101 | DECR2_chr16_396885_417482 | DECR2 | MAQPP others(287): Show |
chr16 | 396885 | 417482 |
| a0002 | 0/0 | 148 | 27 | 19 | 1 | 7 | 0 | 0 | 7 | DECR2_chr16_396885_417482 | DECR2 | MAQPP others(143): Show |
chr16 | 396885 | 417482 |
| a0003 | 0/0 | 292 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | MAQPP others(287): Show |
chr16 | 396885 | 417482 |
| a0004 | 0/0 | 292 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | MAQPP others(287): Show |
chr16 | 396885 | 417482 |
| a0005 | 0/0 | 292 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | MAQPP others(287): Show |
chr16 | 396885 | 417482 |
| a0006 | 0/0 | 292 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | MAQPP others(287): Show |
chr16 | 396885 | 417482 |
| a0007 | 0/0 | 292 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | MAQPP others(287): Show |
chr16 | 396885 | 417482 |
| a0008 | 0/0 | 292 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DECR2_chr16_396885_417482 | DECR2 | MAQPP others(287): Show |
chr16 | 396885 | 417482 |
| a0009 | 0/0 | 292 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DECR2_chr16_396885_417482 | DECR2 | MAQPP others(287): Show |
chr16 | 396885 | 417482 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 876 | 324 | 62 | 70 | 138 | 14 | 39 | DECR2_chr16_396885_417482 | DECR2 | ATGGC others(871): Show |
chr16 | 396885 | 417482 | ||
| a0001c0004 | 0/0 | 876 | 2 | 0 | 0 | 2 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | ATGGC others(871): Show |
chr16 | 396885 | 417482 | ||
| a0001c0005 | 0/0 | 876 | 2 | 1 | 0 | 0 | 0 | 1 | DECR2_chr16_396885_417482 | DECR2 | ATGGC others(871): Show |
chr16 | 396885 | 417482 | ||
| a0001c0010 | 0/0 | 876 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | ATGGC others(871): Show |
chr16 | 396885 | 417482 | ||
| a0001c0013 | 0/0 | 876 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | ATGGC others(871): Show |
chr16 | 396885 | 417482 | ||
| a0001c0014 | 0/0 | 876 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | ATGGC others(871): Show |
chr16 | 396885 | 417482 | ||
| a0002c0002 | 0/0 | 860 | 26 | 18 | 1 | 7 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | ATGGC others(855): Show |
chr16 | 396885 | 417482 | ||
| a0002c0008 | 0/0 | 860 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | ATGGC others(855): Show |
chr16 | 396885 | 417482 | ||
| a0003c0003 | 0/0 | 876 | 3 | 3 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | ATGGC others(871): Show |
chr16 | 396885 | 417482 | ||
| a0004c0007 | 0/0 | 876 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | ATGGC others(871): Show |
chr16 | 396885 | 417482 | ||
| a0005c0011 | 0/0 | 876 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | ATGGC others(871): Show |
chr16 | 396885 | 417482 | ||
| a0006c0009 | 0/0 | 876 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | ATGGC others(871): Show |
chr16 | 396885 | 417482 | ||
| a0007c0015 | 0/0 | 876 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | ATGGC others(871): Show |
chr16 | 396885 | 417482 | ||
| a0008c0006 | 0/0 | 876 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | ATGGC others(871): Show |
chr16 | 396885 | 417482 | ||
| a0009c0012 | 0/0 | 876 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | ATGGC others(871): Show |
chr16 | 396885 | 417482 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1551 | 304 | 50 | 69 | 131 | 14 | 39 | DECR2_chr16_396885_417482 | DECR2 | GAGTT others(1546): Show |
chr16 | 396885 | 417482 |
| a0001c0001t0003 | 0/0 | 1551 | 7 | 0 | 0 | 7 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | GAGTT others(1546): Show |
chr16 | 396885 | 417482 |
| a0001c0001t0004 | 0/0 | 1551 | 4 | 4 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | GAGTT others(1546): Show |
chr16 | 396885 | 417482 |
| a0001c0001t0005 | 0/0 | 1525 | 3 | 3 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | GAGTT others(1520): Show |
chr16 | 396885 | 417482 |
| a0001c0001t0006 | 0/0 | 1547 | 3 | 2 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | GAGTT others(1542): Show |
chr16 | 396885 | 417482 |
| a0001c0001t0007 | 0/0 | 1551 | 2 | 2 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | GAGTT others(1546): Show |
chr16 | 396885 | 417482 |
| a0001c0001t0008 | 0/0 | 1551 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | GAGTT others(1546): Show |
chr16 | 396885 | 417482 |
| a0001c0004t0001 | 0/0 | 1551 | 2 | 0 | 0 | 2 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | GAGTT others(1546): Show |
chr16 | 396885 | 417482 |
| a0001c0005t0001 | 0/0 | 1551 | 1 | 0 | 0 | 0 | 0 | 1 | DECR2_chr16_396885_417482 | DECR2 | GAGTT others(1546): Show |
chr16 | 396885 | 417482 |
| a0001c0005t0002 | 0/0 | 1551 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | GAGTT others(1546): Show |
chr16 | 396885 | 417482 |
| a0001c0010t0001 | 0/0 | 1551 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | GAGTT others(1546): Show |
chr16 | 396885 | 417482 |
| a0001c0013t0002 | 0/0 | 1551 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | GAGTT others(1546): Show |
chr16 | 396885 | 417482 |
| a0001c0014t0001 | 0/0 | 1551 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | GAGTT others(1546): Show |
chr16 | 396885 | 417482 |
| a0002c0002t0001 | 0/0 | 1535 | 12 | 5 | 0 | 7 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | GAGTT others(1530): Show |
chr16 | 396885 | 417482 |
| a0002c0002t0002 | 0/0 | 1535 | 14 | 13 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | GAGTT others(1530): Show |
chr16 | 396885 | 417482 |
| a0002c0008t0002 | 0/0 | 1535 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | GAGTT others(1530): Show |
chr16 | 396885 | 417482 |
| a0003c0003t0001 | 0/0 | 1551 | 3 | 3 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | GAGTT others(1546): Show |
chr16 | 396885 | 417482 |
| a0004c0007t0001 | 0/0 | 1551 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | GAGTT others(1546): Show |
chr16 | 396885 | 417482 |
| a0005c0011t0001 | 0/0 | 1551 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | GAGTT others(1546): Show |
chr16 | 396885 | 417482 |
| a0006c0009t0001 | 0/0 | 1551 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | GAGTT others(1546): Show |
chr16 | 396885 | 417482 |
| a0007c0015t0001 | 0/0 | 1551 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | GAGTT others(1546): Show |
chr16 | 396885 | 417482 |
| a0008c0006t0001 | 0/0 | 1551 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | GAGTT others(1546): Show |
chr16 | 396885 | 417482 |
| a0009c0012t0001 | 0/0 | 1551 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | GAGTT others(1546): Show |
chr16 | 396885 | 417482 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 44 | 0 | 11 | 25 | 1 | 7 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0002 | 0/0 | 26 | 2 | 8 | 9 | 3 | 4 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0003 | 0/0 | 16 | 0 | 4 | 12 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0004 | 0/0 | 10 | 1 | 4 | 4 | 0 | 1 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0005 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0007 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0008 | 0/0 | 8 | 0 | 4 | 0 | 2 | 2 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 1 | 2 | 0 | 2 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0016 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0019 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0147 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0003g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0004g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0005g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0006g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0007g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0007g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0001t0008g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0004t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0004t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0005t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0005t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0010t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0013t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0001c0014t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0002c0002t0001g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0002c0002t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0002c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0002c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0002c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0002c0002t0002g0006 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0002c0002t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0002c0002t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0002c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0002c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0002c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0002c0008t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0003c0003t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0004c0007t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0005c0011t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0006c0009t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0007c0015t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0008c0006t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| a0009c0012t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | GBR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0052 | EUR | GBR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | FIN | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00438 | hp2 | a0004 | c0007 | t0001 | g0041 | EAS | CHS | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00738 | hp2 | a0001 | c0001 | t0006 | g0164 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01243 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01257 | hp1 | a0005 | c0011 | t0001 | g0019 | AMR | CLM | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01433 | hp2 | a0001 | c0010 | t0001 | g0020 | AMR | CLM | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0144 | EUR | IBS | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01975 | hp1 | a0006 | c0009 | t0001 | g0128 | AMR | PEL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CDX | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02257 | hp1 | a0003 | c0003 | t0001 | g0010 | AFR | ACB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02257 | hp2 | a0001 | c0005 | t0002 | g0059 | AFR | ACB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0054 | AFR | ACB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02280 | hp1 | a0002 | c0002 | t0002 | g0006 | AFR | ACB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02280 | hp2 | a0002 | c0002 | t0002 | g0057 | AFR | ACB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0161 | AFR | GWD | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0162 | AFR | GWD | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02647 | hp2 | a0002 | c0002 | t0002 | g0029 | AFR | GWD | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0044 | AFR | GWD | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02723 | hp2 | a0002 | c0002 | t0002 | g0006 | AFR | GWD | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0158 | AFR | GWD | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0165 | AFR | GWD | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02970 | hp1 | a0007 | c0015 | t0001 | g0150 | AFR | ESN | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0154 | AFR | ESN | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03041 | hp2 | a0001 | c0013 | t0002 | g0092 | AFR | GWD | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03130 | hp1 | a0003 | c0003 | t0001 | g0010 | AFR | ESN | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03130 | hp2 | a0001 | c0001 | t0008 | g0064 | AFR | ESN | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0006 | AFR | ESN | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03209 | hp1 | a0002 | c0002 | t0002 | g0029 | AFR | MSL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03453 | hp1 | a0002 | c0002 | t0002 | g0006 | AFR | MSL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0159 | AFR | MSL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03486 | hp1 | a0002 | c0002 | t0002 | g0006 | AFR | MSL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0163 | AFR | ESN | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03579 | hp1 | a0001 | c0001 | t0007 | g0114 | AFR | MSL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0155 | AFR | MSL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03654 | hp2 | a0001 | c0005 | t0001 | g0160 | SAS | PJL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | STU | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | BEB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | STU | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | STU | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | STU | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | STU | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18522 | hp2 | a0002 | c0002 | t0002 | g0006 | AFR | YRI | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | YRI | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18970 | hp2 | a0008 | c0006 | t0001 | g0002 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18999 | hp1 | a0009 | c0012 | t0001 | g0120 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0044 | AFR | LWK | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0043 | AFR | LWK | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19043 | hp2 | a0001 | c0014 | t0001 | g0121 | AFR | LWK | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19067 | hp1 | a0001 | c0004 | t0001 | g0100 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19070 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ASW | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0058 | AFR | ASW | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | TSI | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | TSI | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | TSI | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | GIH | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | GIH | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0166 | AFR | ACB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0156 | AFR | ACB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0006 | AFR | ACB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0113 | AFR | ACB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02559 | hp1 | a0003 | c0003 | t0001 | g0010 | AFR | ACB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| HG03471 | hp2 | a0002 | c0002 | t0002 | g0056 | AFR | MSL | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0043 | AFR | USA | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | USA | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| NA21309 | hp2 | a0002 | c0008 | t0002 | g0055 | AFR | LWK | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0147 | REF | REF | DECR2_chr16_396885_417482 | DECR2 | chr16 | 396885 | 417482 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:405003 | G | A | 1 | a0008 | 1 | NA18970.hp2 | missense_variant | MODERATE | c.128G>A | p.Arg43Gln | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 2/9 | 207/1551 | 128/879 | 43/292 | chr16 | 405003 | |||
| chr16:407428 | G | A | 1 | a0004 | 1 | HG00438.hp2 | missense_variant | MODERATE | c.205G>A | p.Ala69Thr | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/9 | 284/1551 | 205/879 | 69/292 | chr16 | 407428 | |||
| chr16:407459 | G | T | 1 | a0007 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.236G>T | p.Arg79Leu | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/9 | 315/1551 | 236/879 | 79/292 | chr16 | 407459 | |||
| chr16:410321 | G | A | 1 | a0003 | 3 | HG02257.hp1 HG02559.hp1 HG03130.hp1 |
missense_variant | MODERATE | c.416G>A | p.Ser139Asn | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/9 | 495/1551 | 416/879 | 139/292 | chr16 | 410321 | |||
| chr16:410358 | G | T | 1 | a0001 | 10 | HG00609.hp1 HG02015.hp2 HG02080.hp1 others(7): Show |
missense_variant | MODERATE | c.453G>T | p.Lys151Asn | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/9 | 532/1551 | 453/879 | 151/292 | chr16 | 410358 | |||
| chr16:410778 | G | A | 1 | a0006 | 1 | HG01975.hp1 | missense_variant | MODERATE | c.550G>A | p.Ala184Thr | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 6/9 | 629/1551 | 550/879 | 184/292 | chr16 | 410778 | |||
| chr16:411068 | G | A | 1 | a0002 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.653G>A | p.Arg218Gln | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 7/9 | 732/1551 | 653/879 | 218/292 | chr16 | 411068 | |||
| chr16:411445 | T | G | 1 | a0005 | 1 | HG01257.hp1 | missense_variant | MODERATE | c.746T>G | p.Val249Gly | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 8/9 | 825/1551 | 746/879 | 249/292 | chr16 | 411445 | |||
| chr16:411507 | G | T | 1 | a0009 | 1 | NA18999.hp1 | missense_variant | MODERATE | c.808G>T | p.Gly270Trp | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 8/9 | 887/1551 | 808/879 | 270/292 | chr16 | 411507 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:407544 | C | T | 1 | a0001c0014 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.321C>T | p.Ile107Ile | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/9 | 400/1551 | 321/879 | 107/292 | chr16 | 407544 | |||
| chr16:410274 | C | T | 3 | a0001c0005 a0001c0013 a0007c0015 |
4 | HG02257.hp2 HG02970.hp1 HG03041.hp2 others(1): Show |
synonymous_variant | LOW | c.369C>T | p.Gly123Gly | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/9 | 448/1551 | 369/879 | 123/292 | chr16 | 410274 | |||
| chr16:410708 | C | T | 1 | a0001c0004 | 2 | NA19067.hp1 NA19070.hp1 |
synonymous_variant | LOW | c.480C>T | p.Ile160Ile | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 6/9 | 559/1551 | 480/879 | 160/292 | chr16 | 410708 | |||
| chr16:410976 | G | A | 1 | a0001c0010 | 1 | HG01433.hp2 | synonymous_variant | LOW | c.561G>A | p.Ala187Ala | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 7/9 | 640/1551 | 561/879 | 187/292 | chr16 | 410976 | |||
| chr16:411045 | C | T | 1 | a0001c0013 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.630C>T | p.Pro210Pro | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 7/9 | 709/1551 | 630/879 | 210/292 | chr16 | 411045 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:412017 | G | A | 1 | a0001c0001t0008 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*128G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 9/9 | 439 | chr16 | 412017 | ||||||
| chr16:412089 | GCCAGGTG others(19): Show |
G | 1 | a0001c0001t0005 | 3 | HG02615.hp1 HG02630.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*219_*244delTCTGAG others(20): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 9/9 | 530 | INFO_REALIGN_3_PRIME | chr16 | 412089 | |||||
| chr16:412280 | G | A | 4 | a0001c0005t0002 a0001c0013t0002 a0002c0002t0002 others(1): Show |
17 | HG01243.hp2 HG02257.hp2 HG02258.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*391G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 9/9 | 702 | chr16 | 412280 | ||||||
| chr16:412285 | C | T | 1 | a0001c0001t0005 | 3 | HG02615.hp1 HG02630.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*396C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 9/9 | 707 | chr16 | 412285 | ||||||
| chr16:412338 | G | A | 1 | a0001c0001t0007 | 2 | HG02486.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*449G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 9/9 | 760 | chr16 | 412338 | ||||||
| chr16:412395 | A | G | 1 | a0001c0001t0004 | 4 | HG02976.hp2 HG03579.hp2 NA19043.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*506A>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 9/9 | 817 | chr16 | 412395 | ||||||
| chr16:412397 | G | T | 1 | a0001c0001t0003 | 7 | NA18945.hp2 NA18953.hp1 NA18962.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*508G>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 9/9 | 819 | chr16 | 412397 | ||||||
| chr16:412450 | AAAAG | A | 1 | a0001c0001t0006 | 3 | HG00738.hp2 HG02109.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*567_*570delAAGA | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 9/9 | 878 | INFO_REALIGN_3_PRIME | chr16 | 412450 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:402064 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80+21G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 402064 | |||||||
| chr16:402131 | C | G | 1 | a0001c0001t0006g0166 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.80+88C>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 402131 | |||||||
| chr16:402132 | G | C | 1 | a0001c0001t0006g0166 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.80+89G>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 402132 | |||||||
| chr16:402159 | CCTTT | C | 5 | a0001c0001t0005g0161 a0001c0001t0005g0162 a0001c0001t0005g0163 others(2): Show |
5 | HG00738.hp2 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.80+125_80+128delCT others(2): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 402159 | ||||||
| chr16:402160 | CTTTCTTT others(4): Show |
C | 1 | a0007c0015t0001g0150 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.80+132_80+142delCT others(9): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 402160 | ||||||
| chr16:402168 | C | T | 21 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0016 others(18): Show |
40 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.80+125C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 402168 | |||||||
| chr16:402171 | T | C | 21 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0016 others(18): Show |
40 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.80+128T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 402171 | |||||||
| chr16:402176 | TTTC | T | 21 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0016 others(18): Show |
40 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.80+136_80+138delCT others(1): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 402176 | ||||||
| chr16:402179 | C | CT | 14 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(11): Show |
15 | HG00408.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.80+149dupT | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 402179 | ||||||
| chr16:402247 | T | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0060 |
3 | HG01891.hp1 HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.80+204T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 402247 | |||||||
| chr16:402381 | G | C | 1 | a0001c0001t0001g0061 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.80+338G>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 402381 | |||||||
| chr16:402382 | C | G | 1 | a0001c0001t0001g0061 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.80+339C>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 402382 | |||||||
| chr16:402414 | C | T | 1 | a0001c0005t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.80+371C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 402414 | |||||||
| chr16:402565 | A | G | 1 | a0001c0005t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.80+522A>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 402565 | |||||||
| chr16:402618 | C | T | 6 | a0002c0002t0001g0014 a0002c0002t0001g0044 a0002c0002t0001g0156 others(3): Show |
11 | HG02109.hp2 HG02717.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.80+575C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 402618 | |||||||
| chr16:402632 | C | CT | 6 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(3): Show |
7 | HG02976.hp2 HG03579.hp2 HG04199.hp2 others(4): Show |
intron_variant | MODIFIER | c.80+601dupT | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 402632 | ||||||
| chr16:402737 | T | G | 1 | a0001c0005t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.80+694T>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 402737 | |||||||
| chr16:402764 | A | C | 1 | a0007c0015t0001g0150 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.80+721A>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 402764 | |||||||
| chr16:402795 | C | G | 1 | a0001c0001t0001g0149 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.80+752C>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 402795 | |||||||
| chr16:402799 | C | T | 3 | a0001c0001t0006g0164 a0001c0001t0006g0165 a0001c0001t0006g0166 |
3 | HG00738.hp2 HG02109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.80+756C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 402799 | |||||||
| chr16:402840 | C | G | 4 | a0001c0001t0004g0043 a0001c0001t0004g0154 a0001c0001t0004g0155 others(1): Show |
5 | HG02257.hp2 HG02976.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.80+797C>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 402840 | |||||||
| chr16:402841 | C | T | 1 | a0001c0005t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.80+798C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 402841 | |||||||
| chr16:403007 | T | G | 1 | a0001c0005t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.80+964T>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 403007 | |||||||
| chr16:403065 | T | G | 1 | a0001c0001t0001g0062 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.80+1022T>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 403065 | |||||||
| chr16:403073 | C | T | 4 | a0001c0001t0001g0148 a0001c0001t0006g0164 a0001c0001t0006g0165 others(1): Show |
4 | HG00738.hp2 HG02109.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.80+1030C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 403073 | |||||||
| chr16:403321 | A | C | 1 | a0002c0002t0002g0058 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.80+1278A>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 403321 | |||||||
| chr16:403499 | T | A | 3 | a0001c0005t0001g0160 a0002c0002t0001g0044 a0002c0002t0001g0156 |
4 | HG02109.hp2 HG02717.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.80+1456T>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 403499 | |||||||
| chr16:403665 | C | T | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG01516.hp1 NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.81-1291C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 403665 | |||||||
| chr16:403683 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.81-1273C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 403683 | |||||||
| chr16:403901 | T | G | 1 | a0001c0001t0001g0062 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.81-1055T>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 403901 | |||||||
| chr16:404063 | C | T | 1 | a0001c0005t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.81-893C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 404063 | |||||||
| chr16:404122 | T | G | 1 | a0001c0001t0006g0164 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.81-834T>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 404122 | |||||||
| chr16:404165 | T | C | 4 | a0001c0001t0001g0030 a0001c0001t0001g0060 a0001c0001t0006g0165 others(1): Show |
5 | HG01891.hp1 HG02109.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.81-791T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 404165 | |||||||
| chr16:404188 | T | A | 1 | a0001c0001t0001g0063 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.81-768T>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 404188 | |||||||
| chr16:404192 | T | A | 1 | a0001c0005t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.81-764T>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 404192 | |||||||
| chr16:404193 | A | T | 1 | a0001c0001t0001g0142 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.81-763A>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 404193 | |||||||
| chr16:404197 | A | T | 1 | a0001c0001t0001g0142 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.81-759A>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 404197 | |||||||
| chr16:404200 | TTAAA | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0060 a0001c0001t0006g0164 others(2): Show |
6 | HG00738.hp2 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.81-751_81-748delTA others(2): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | 404200 | ||||||
| chr16:404206 | A | T | 1 | a0001c0001t0001g0042 | 2 | HG00438.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.81-750A>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 404206 | |||||||
| chr16:404242 | T | C | 4 | a0001c0001t0004g0043 a0001c0001t0004g0154 a0001c0001t0004g0155 others(1): Show |
5 | HG02257.hp2 HG02976.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.81-714T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 404242 | |||||||
| chr16:404249 | A | T | 1 | a0001c0005t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.81-707A>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 404249 | |||||||
| chr16:404429 | G | A | 2 | a0002c0002t0001g0044 a0002c0002t0001g0156 |
3 | HG02109.hp2 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.81-527G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 404429 | |||||||
| chr16:404465 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.81-491C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 404465 | |||||||
| chr16:404505 | G | A | 1 | a0002c0002t0002g0058 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.81-451G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 404505 | |||||||
| chr16:404580 | G | A | 1 | a0001c0001t0008g0064 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.81-376G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 404580 | |||||||
| chr16:404652 | C | T | 2 | a0001c0001t0006g0165 a0001c0001t0006g0166 |
2 | HG02109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.81-304C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 404652 | |||||||
| chr16:404653 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.81-303G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 404653 | |||||||
| chr16:404721 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.81-235C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 404721 | |||||||
| chr16:404819 | G | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0066 a0001c0001t0001g0067 others(2): Show |
8 | HG02040.hp2 HG02165.hp1 NA18941.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-137G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 404819 | |||||||
| chr16:404904 | C | T | 1 | a0001c0001t0004g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.81-52C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 1/8 | chr16 | 404904 | |||||||
| chr16:405042 | CCCTTCCC others(4): Show |
C | 1 | a0001c0001t0001g0070 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.149+22_149+32delTC others(9): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 405042 | ||||||
| chr16:405163 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.149+139G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 2/8 | chr16 | 405163 | |||||||
| chr16:405212 | A | G | 1 | a0001c0005t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.149+188A>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 2/8 | chr16 | 405212 | |||||||
| chr16:405232 | G | A | 8 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0032 others(5): Show |
13 | HG02055.hp2 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.149+208G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 2/8 | chr16 | 405232 | |||||||
| chr16:405289 | G | A | 1 | a0001c0005t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.149+265G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 2/8 | chr16 | 405289 | |||||||
| chr16:405305 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.149+281G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 2/8 | chr16 | 405305 | |||||||
| chr16:405331 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.149+307G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 2/8 | chr16 | 405331 | |||||||
| chr16:405403 | T | G | 1 | a0001c0001t0001g0078 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.149+379T>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 2/8 | chr16 | 405403 | |||||||
| chr16:405404 | G | T | 1 | a0001c0001t0001g0078 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.149+380G>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 2/8 | chr16 | 405404 | |||||||
| chr16:405410 | A | G | 16 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0032 others(13): Show |
29 | HG01243.hp2 HG02055.hp2 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.149+386A>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 2/8 | chr16 | 405410 | |||||||
| chr16:405497 | G | C | 29 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(26): Show |
55 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.149+473G>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 2/8 | chr16 | 405497 | |||||||
| chr16:405646 | A | G | 50 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(47): Show |
125 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.149+622A>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 2/8 | chr16 | 405646 | |||||||
| chr16:405697 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.150-649C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 2/8 | chr16 | 405697 | |||||||
| chr16:405774 | G | C | 1 | a0001c0001t0001g0066 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.150-572G>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 2/8 | chr16 | 405774 | |||||||
| chr16:405826 | G | T | 1 | a0001c0001t0001g0078 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.150-520G>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 2/8 | chr16 | 405826 | |||||||
| chr16:405827 | T | G | 1 | a0001c0001t0001g0078 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.150-519T>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 2/8 | chr16 | 405827 | |||||||
| chr16:405828 | G | T | 1 | a0001c0001t0001g0078 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.150-518G>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 2/8 | chr16 | 405828 | |||||||
| chr16:405857 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.150-489T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 2/8 | chr16 | 405857 | |||||||
| chr16:405865 | C | T | 8 | a0001c0005t0001g0160 a0002c0002t0001g0014 a0002c0002t0001g0044 others(5): Show |
13 | HG02109.hp2 HG02717.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.150-481C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 2/8 | chr16 | 405865 | |||||||
| chr16:405866 | G | A | 1 | a0001c0013t0002g0092 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.150-480G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 2/8 | chr16 | 405866 | |||||||
| chr16:405897 | C | A | 1 | a0001c0001t0001g0046 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.150-449C>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 2/8 | chr16 | 405897 | |||||||
| chr16:405991 | A | G | 8 | a0001c0005t0001g0160 a0002c0002t0001g0014 a0002c0002t0001g0044 others(5): Show |
13 | HG02109.hp2 HG02717.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.150-355A>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 2/8 | chr16 | 405991 | |||||||
| chr16:406187 | G | C | 1 | a0001c0005t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.150-159G>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 2/8 | chr16 | 406187 | |||||||
| chr16:406255 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.150-91C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 2/8 | chr16 | 406255 | |||||||
| chr16:406291 | G | GC | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.150-51dupC | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr16 | 406291 | ||||||
| chr16:406295 | C | CCT | 8 | a0001c0005t0001g0160 a0002c0002t0001g0014 a0002c0002t0001g0044 others(5): Show |
13 | HG02109.hp2 HG02717.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.150-51_150-50insCT | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 2/8 | chr16 | 406295 | |||||||
| chr16:406416 | T | G | 64 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(61): Show |
135 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.201+19T>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 3/8 | chr16 | 406416 | |||||||
| chr16:406429 | G | A | 30 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(27): Show |
56 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.201+32G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 3/8 | chr16 | 406429 | |||||||
| chr16:406439 | G | C | 3 | a0001c0001t0006g0164 a0001c0001t0006g0165 a0001c0001t0006g0166 |
3 | HG00738.hp2 HG02109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.201+42G>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 3/8 | chr16 | 406439 | |||||||
| chr16:406483 | T | C | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(115): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.201+86T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 3/8 | chr16 | 406483 | |||||||
| chr16:406595 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.201+198T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 3/8 | chr16 | 406595 | |||||||
| chr16:406635 | C | G | 8 | a0001c0005t0001g0160 a0002c0002t0001g0014 a0002c0002t0001g0044 others(5): Show |
13 | HG02109.hp2 HG02717.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.201+238C>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 3/8 | chr16 | 406635 | |||||||
| chr16:406642 | T | C | 10 | a0001c0005t0001g0160 a0001c0013t0002g0092 a0002c0002t0001g0014 others(7): Show |
15 | HG02109.hp2 HG02717.hp2 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.201+245T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 3/8 | chr16 | 406642 | |||||||
| chr16:406701 | C | T | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(120): Show |
238 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.201+304C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 3/8 | chr16 | 406701 | |||||||
| chr16:406723 | T | C | 2 | a0001c0001t0001g0007 a0009c0012t0001g0120 |
9 | HG00423.hp2 HG00597.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.201+326T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 3/8 | chr16 | 406723 | |||||||
| chr16:406785 | CCACTGTG others(49): Show |
C | 63 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(60): Show |
134 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.201+444_201+499del others(56): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr16 | 406785 | ||||||
| chr16:406855 | C | T | 10 | a0001c0005t0001g0160 a0001c0013t0002g0092 a0002c0002t0001g0014 others(7): Show |
15 | HG02109.hp2 HG02717.hp2 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.201+458C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 3/8 | chr16 | 406855 | |||||||
| chr16:406977 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.202-448T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 3/8 | chr16 | 406977 | |||||||
| chr16:407007 | T | C | 10 | a0001c0005t0001g0160 a0001c0013t0002g0092 a0002c0002t0001g0014 others(7): Show |
15 | HG02109.hp2 HG02717.hp2 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.202-418T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 3/8 | chr16 | 407007 | |||||||
| chr16:407027 | T | G | 1 | a0001c0001t0001g0075 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.202-398T>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 3/8 | chr16 | 407027 | |||||||
| chr16:407071 | G | C | 1 | a0001c0001t0001g0079 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.202-354G>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 3/8 | chr16 | 407071 | |||||||
| chr16:407190 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.202-235C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 3/8 | chr16 | 407190 | |||||||
| chr16:407226 | G | A | 62 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(59): Show |
137 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.202-199G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 3/8 | chr16 | 407226 | |||||||
| chr16:407226 | G | T | 1 | a0001c0001t0001g0139 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.202-199G>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 3/8 | chr16 | 407226 | |||||||
| chr16:407268 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.202-157C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 3/8 | chr16 | 407268 | |||||||
| chr16:407293 | C | T | 2 | a0002c0002t0001g0158 a0002c0002t0001g0159 |
2 | HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.202-132C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 3/8 | chr16 | 407293 | |||||||
| chr16:407313 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.202-112C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 3/8 | chr16 | 407313 | |||||||
| chr16:407357 | G | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0047 a0001c0014t0001g0121 |
7 | HG01884.hp1 HG02258.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.202-68G>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 3/8 | chr16 | 407357 | |||||||
| chr16:407367 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.202-58G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 3/8 | chr16 | 407367 | |||||||
| chr16:407621 | C | T | 2 | a0001c0013t0002g0092 a0007c0015t0001g0150 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.337+61C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407621 | |||||||
| chr16:407627 | A | T | 1 | a0001c0001t0001g0137 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.337+67A>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407627 | |||||||
| chr16:407703 | C | T | 2 | a0001c0013t0002g0092 a0007c0015t0001g0150 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.337+143C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407703 | |||||||
| chr16:407746 | A | G | 1 | a0001c0005t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.337+186A>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407746 | |||||||
| chr16:407754 | C | G | 1 | a0001c0005t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.337+194C>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407754 | |||||||
| chr16:407768 | G | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(84): Show |
190 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.337+208G>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407768 | |||||||
| chr16:407769 | CCCCTGTC others(20): Show |
C | 2 | a0001c0001t0005g0162 a0001c0001t0005g0163 |
2 | HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.337+211_337+237del others(27): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 407769 | ||||||
| chr16:407771 | C | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(74): Show |
151 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.337+211C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407771 | |||||||
| chr16:407773 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.337+213T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407773 | |||||||
| chr16:407774 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.337+214G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407774 | |||||||
| chr16:407776 | C | A | 1 | a0001c0001t0001g0105 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.337+216C>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407776 | |||||||
| chr16:407777 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.337+217T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407777 | |||||||
| chr16:407778 | C | A | 1 | a0001c0001t0001g0105 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.337+218C>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407778 | |||||||
| chr16:407779 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.337+219C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407779 | |||||||
| chr16:407780 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.337+220G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407780 | |||||||
| chr16:407782 | G | T | 1 | a0001c0001t0001g0105 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.337+222G>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407782 | |||||||
| chr16:407783 | C | G | 1 | a0001c0001t0001g0105 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.337+223C>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407783 | |||||||
| chr16:407783 | CCTCTGTC others(6): Show |
C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(113): Show |
238 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.337+238_337+250del others(13): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 407783 | ||||||
| chr16:407784 | C | A | 1 | a0001c0001t0001g0105 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.337+224C>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407784 | |||||||
| chr16:407785 | T | C | 1 | a0001c0005t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.337+225T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407785 | |||||||
| chr16:407786 | C | G | 1 | a0001c0001t0001g0105 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.337+226C>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407786 | |||||||
| chr16:407788 | G | T | 1 | a0001c0001t0001g0105 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.337+228G>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407788 | |||||||
| chr16:407792 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.337+232C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407792 | |||||||
| chr16:407792 | CCGGGCTC others(20): Show |
C | 1 | a0001c0001t0001g0001 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.337+236_337+262del others(27): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 407792 | ||||||
| chr16:407793 | C | CGGCCGCA others(20): Show |
1 | a0001c0001t0005g0161 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.337+235_337+236ins others(27): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 407793 | ||||||
| chr16:407796 | G | C | 3 | a0001c0001t0001g0105 a0001c0001t0005g0161 a0001c0005t0001g0160 |
3 | HG02615.hp1 HG03654.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.337+236G>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407796 | |||||||
| chr16:407796 | G | GC | 48 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(45): Show |
116 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.337+237dupC | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 407796 | ||||||
| chr16:407796 | G | GCCTCTGT others(8): Show |
6 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(3): Show |
6 | HG00621.hp1 HG02602.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.337+237_337+238ins others(15): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 407796 | ||||||
| chr16:407798 | T | C | 1 | a0001c0005t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.337+238T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407798 | |||||||
| chr16:407811 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.337+251C>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407811 | |||||||
| chr16:407815 | G | C | 1 | a0001c0001t0005g0161 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.337+255G>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407815 | |||||||
| chr16:407819 | T | C | 1 | a0001c0001t0005g0161 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.337+259T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407819 | |||||||
| chr16:407825 | G | C | 2 | a0001c0001t0005g0161 a0001c0005t0001g0160 |
2 | HG02615.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.337+265G>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407825 | |||||||
| chr16:407827 | A | G | 1 | a0001c0005t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.337+267A>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407827 | |||||||
| chr16:407833 | G | T | 1 | a0001c0005t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.337+273G>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407833 | |||||||
| chr16:407846 | T | C | 2 | a0001c0001t0005g0161 a0001c0005t0001g0160 |
2 | HG02615.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.337+286T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407846 | |||||||
| chr16:407852 | T | C | 1 | a0001c0005t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.337+292T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407852 | |||||||
| chr16:407852 | T | TCTGTCTC others(19): Show |
1 | a0001c0001t0005g0161 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.337+302_337+303ins others(26): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 407852 | ||||||
| chr16:407865 | G | C | 2 | a0001c0001t0005g0161 a0001c0005t0001g0160 |
2 | HG02615.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.337+305G>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407865 | |||||||
| chr16:407869 | C | G | 2 | a0001c0001t0005g0161 a0001c0005t0001g0160 |
2 | HG02615.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.337+309C>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407869 | |||||||
| chr16:407881 | A | G | 1 | a0001c0005t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.337+321A>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407881 | |||||||
| chr16:407889 | C | CCCCCTGT others(7): Show |
2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG02683.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.337+339_337+340ins others(14): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 407889 | ||||||
| chr16:407889 | C | G | 1 | a0001c0005t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.337+329C>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407889 | |||||||
| chr16:407900 | C | CGGGCCCC others(63): Show |
1 | a0007c0015t0001g0150 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.337+345_337+346ins others(70): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 407900 | ||||||
| chr16:407900 | C | CGGGCCCC others(91): Show |
1 | a0001c0013t0002g0092 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.337+345_337+346ins others(98): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 407900 | ||||||
| chr16:407903 | G | C | 1 | a0001c0005t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.337+343G>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407903 | |||||||
| chr16:407906 | T | C | 1 | a0001c0005t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.337+346T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407906 | |||||||
| chr16:407918 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.337+358C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407918 | |||||||
| chr16:407920 | C | CCTGTCTC others(219): Show |
1 | a0001c0005t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.337+360_337+361ins others(226): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407920 | |||||||
| chr16:407920 | CATCTCCG others(33): Show |
C | 1 | a0001c0001t0001g0053 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.337+361_337+400del others(40): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407920 | |||||||
| chr16:407921 | A | G | 1 | a0001c0005t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.337+361A>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407921 | |||||||
| chr16:407921 | ATCTCCGG others(35): Show |
A | 31 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0017 others(28): Show |
74 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.337+395_337+436del others(42): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 407921 | ||||||
| chr16:407927 | G | A | 4 | a0001c0001t0001g0025 a0001c0001t0001g0066 a0001c0001t0001g0101 others(1): Show |
5 | HG01109.hp2 HG01346.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.337+367G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407927 | |||||||
| chr16:407929 | C | CCCCCTGT others(7): Show |
1 | a0001c0001t0001g0065 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.337+381_337+394dup others(14): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 407929 | ||||||
| chr16:407940 | C | T | 1 | a0001c0005t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.337+380C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407940 | |||||||
| chr16:407943 | GCCCCTGT others(36): Show |
G | 1 | a0001c0001t0001g0066 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.337+387_337+429del others(43): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 407943 | ||||||
| chr16:407946 | C | T | 3 | a0001c0005t0001g0160 a0001c0013t0002g0092 a0007c0015t0001g0150 |
3 | HG02970.hp1 HG03041.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.337+386C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407946 | |||||||
| chr16:407954 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.337+394C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407954 | |||||||
| chr16:407955 | A | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(138): Show |
290 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(287): Show |
intron_variant | MODIFIER | c.337+395A>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407955 | |||||||
| chr16:407957 | G | C | 2 | a0001c0013t0002g0092 a0007c0015t0001g0150 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.337+397G>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407957 | |||||||
| chr16:407960 | T | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0026 others(4): Show |
7 | HG02630.hp2 HG02717.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.337+400T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407960 | |||||||
| chr16:407969 | G | A | 22 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0020 others(19): Show |
55 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.337+409G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407969 | |||||||
| chr16:407971 | C | CCCCCTGT others(7): Show |
12 | a0001c0001t0001g0032 a0001c0001t0001g0073 a0001c0001t0001g0074 others(9): Show |
13 | HG00738.hp2 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.337+428_337+441dup others(14): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 407971 | ||||||
| chr16:407971 | C | CCCCCTGT others(21): Show |
4 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0072 others(1): Show |
8 | HG02055.hp2 HG02145.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.337+414_337+441dup others(28): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 407971 | ||||||
| chr16:407971 | C | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0060 |
2 | HG00733.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.337+411C>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407971 | |||||||
| chr16:407985 | G | C | 1 | a0001c0005t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.337+425G>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407985 | |||||||
| chr16:407988 | C | CCTGTCTC others(7): Show |
1 | a0001c0001t0004g0043 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.337+439_337+452dup others(14): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 407988 | ||||||
| chr16:407988 | C | T | 3 | a0001c0013t0002g0092 a0002c0002t0001g0156 a0007c0015t0001g0150 |
3 | HG02109.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.337+428C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407988 | |||||||
| chr16:407990 | T | TGTCTCCG others(131): Show |
1 | a0001c0001t0001g0030 | 2 | HG01891.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.337+441_337+442ins others(138): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 407990 | ||||||
| chr16:407996 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.337+436C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407996 | |||||||
| chr16:407999 | G | C | 2 | a0001c0001t0001g0053 a0002c0002t0001g0156 |
2 | HG00733.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.337+439G>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 407999 | |||||||
| chr16:408002 | T | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(88): Show |
200 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.337+442T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408002 | |||||||
| chr16:408013 | C | CCCCCTGT others(7): Show |
23 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0016 others(20): Show |
54 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.337+470_337+483dup others(14): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408013 | ||||||
| chr16:408013 | C | CCCCCTGT others(35): Show |
2 | a0001c0001t0001g0019 a0005c0011t0001g0019 |
4 | HG00323.hp2 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.337+480_337+481ins others(42): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408013 | ||||||
| chr16:408013 | C | CCCCCTGT others(105): Show |
1 | a0001c0001t0001g0080 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.337+483_337+484ins others(112): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408013 | ||||||
| chr16:408013 | C | G | 15 | a0001c0001t0001g0030 a0001c0001t0001g0035 a0001c0001t0001g0053 others(12): Show |
25 | HG00733.hp1 HG01243.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.337+453C>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408013 | |||||||
| chr16:408016 | C | T | 7 | a0001c0001t0001g0030 a0002c0002t0002g0006 a0002c0002t0002g0029 others(4): Show |
16 | HG01243.hp2 HG01891.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.337+456C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408016 | |||||||
| chr16:408018 | T | TGTCTCCG others(75): Show |
1 | a0001c0001t0001g0060 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.337+469_337+470ins others(82): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408018 | ||||||
| chr16:408027 | G | C | 8 | a0001c0001t0001g0030 a0001c0001t0001g0094 a0002c0002t0002g0006 others(5): Show |
17 | HG01243.hp2 HG01891.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.337+467G>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408027 | |||||||
| chr16:408027 | G | GCCCCTGT others(21): Show |
3 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0103 |
6 | HG00544.hp1 HG02071.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.337+480_337+481ins others(28): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408027 | ||||||
| chr16:408027 | GCCCCTGT others(77): Show |
G | 2 | a0001c0001t0007g0113 a0001c0001t0007g0114 |
2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.337+470_337+553del others(84): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408027 | ||||||
| chr16:408030 | C | T | 4 | a0001c0001t0001g0060 a0001c0013t0002g0092 a0002c0002t0001g0156 others(1): Show |
4 | HG02109.hp2 HG02630.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.337+470C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408030 | |||||||
| chr16:408030 | CCTGTCTC others(77): Show |
C | 1 | a0001c0001t0001g0094 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.337+484_337+567del others(84): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408030 | ||||||
| chr16:408030 | CCTGTCTC others(133): Show |
C | 2 | a0001c0001t0001g0036 a0001c0004t0001g0100 |
3 | NA19056.hp1 NA19067.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.337+498_337+637del | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408030 | ||||||
| chr16:408039 | GGGCCTCT others(49): Show |
G | 3 | a0001c0001t0001g0095 a0001c0001t0001g0101 a0001c0001t0001g0102 |
3 | HG01346.hp2 HG02451.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.337+481_337+536del others(56): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408039 | ||||||
| chr16:408041 | G | C | 3 | a0001c0013t0002g0092 a0002c0002t0001g0156 a0007c0015t0001g0150 |
3 | HG02109.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.337+481G>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408041 | |||||||
| chr16:408041 | GCCTCTGT others(49): Show |
G | 1 | a0001c0001t0001g0025 | 2 | HG01109.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.337+484_337+539del others(56): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408041 | ||||||
| chr16:408044 | T | C | 50 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(47): Show |
88 | HG00140.hp1 HG00323.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.337+484T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408044 | |||||||
| chr16:408052 | C | T | 2 | a0001c0001t0006g0165 a0001c0001t0006g0166 |
2 | HG02109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.337+492C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408052 | |||||||
| chr16:408055 | C | CCCCATGT others(35): Show |
1 | a0001c0001t0001g0105 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.337+497_337+498ins others(42): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408055 | ||||||
| chr16:408055 | C | CCCCCTGT others(35): Show |
10 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(7): Show |
26 | HG00639.hp2 HG01106.hp1 HG01943.hp1 others(23): Show |
intron_variant | MODIFIER | c.337+497_337+498ins others(42): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408055 | ||||||
| chr16:408055 | C | CCCCCTGT others(21): Show |
2 | a0001c0001t0001g0005 a0001c0001t0001g0011 |
3 | HG02165.hp2 NA18944.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.337+497_337+498ins others(28): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408055 | ||||||
| chr16:408055 | C | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(104): Show |
227 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.337+495C>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408055 | |||||||
| chr16:408055 | CCCTCTGT others(7): Show |
C | 2 | a0002c0002t0001g0044 a0002c0002t0001g0157 |
3 | HG02717.hp2 NA19030.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.337+498_337+511del others(14): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408055 | ||||||
| chr16:408055 | CCCTCTGT others(119): Show |
C | 1 | a0001c0001t0001g0038 | 2 | HG02071.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.337+509_337+634del | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408055 | ||||||
| chr16:408058 | T | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(52): Show |
111 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.337+498T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408058 | |||||||
| chr16:408069 | G | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(87): Show |
214 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.337+509G>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408069 | |||||||
| chr16:408069 | G | GCCTCTGT others(157): Show |
7 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0032 others(4): Show |
12 | HG02055.hp2 HG02145.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.337+511_337+512ins others(164): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408069 | ||||||
| chr16:408072 | C | T | 20 | a0001c0001t0001g0028 a0001c0001t0001g0034 a0001c0001t0001g0052 others(17): Show |
30 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.337+512C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408072 | |||||||
| chr16:408074 | T | C | 2 | a0001c0001t0001g0003 a0001c0001t0001g0033 |
2 | NA18612.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.337+514T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408074 | |||||||
| chr16:408080 | C | T | 1 | a0002c0002t0002g0006 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.337+520C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408080 | |||||||
| chr16:408081 | GGGCCCCT others(7): Show |
G | 2 | a0001c0001t0003g0033 a0001c0001t0004g0043 |
2 | NA18984.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.337+523_337+536del others(14): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408081 | ||||||
| chr16:408083 | G | C | 18 | a0001c0001t0001g0028 a0001c0001t0001g0034 a0001c0001t0001g0052 others(15): Show |
24 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.337+523G>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408083 | |||||||
| chr16:408083 | GCCCCTGT others(21): Show |
G | 1 | a0001c0001t0001g0075 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.337+526_337+553del others(28): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408083 | ||||||
| chr16:408086 | C | T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(81): Show |
191 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.337+526C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408086 | |||||||
| chr16:408086 | CCTGTCTC others(49): Show |
C | 1 | a0001c0001t0001g0146 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.337+535_337+590del others(56): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408086 | ||||||
| chr16:408089 | G | A | 2 | a0001c0013t0002g0092 a0007c0015t0001g0150 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.337+529G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408089 | |||||||
| chr16:408095 | A | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(89): Show |
175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.337+535A>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408095 | |||||||
| chr16:408097 | C | G | 23 | a0001c0001t0001g0028 a0001c0001t0001g0034 a0001c0001t0001g0052 others(20): Show |
33 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.337+537C>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408097 | |||||||
| chr16:408100 | C | CCTGTCTC others(117): Show |
2 | a0001c0001t0006g0165 a0001c0001t0006g0166 |
2 | HG02109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.337+550_337+551ins others(124): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408100 | ||||||
| chr16:408100 | C | CCTGTCTC others(267): Show |
1 | a0001c0001t0006g0164 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.337+547_337+548ins others(274): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408100 | ||||||
| chr16:408100 | C | T | 15 | a0001c0001t0001g0028 a0001c0001t0001g0034 a0001c0001t0001g0052 others(12): Show |
25 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.337+540C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408100 | |||||||
| chr16:408109 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0008g0064 |
2 | HG03130.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.337+549G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408109 | |||||||
| chr16:408111 | A | C | 69 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(66): Show |
144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.337+551A>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408111 | |||||||
| chr16:408111 | A | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(94): Show |
212 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.337+551A>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408111 | |||||||
| chr16:408114 | T | C | 71 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(68): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.337+554T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408114 | |||||||
| chr16:408114 | T | TCTGTCTC others(7): Show |
1 | a0001c0001t0001g0060 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.337+562_337+563ins others(14): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408114 | ||||||
| chr16:408125 | G | C | 16 | a0001c0001t0001g0075 a0001c0001t0001g0090 a0001c0001t0005g0162 others(13): Show |
24 | HG00738.hp2 HG01243.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.337+565G>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408125 | |||||||
| chr16:408125 | G | GCCTCTGT others(7): Show |
2 | a0001c0001t0005g0161 a0001c0001t0005g0163 |
2 | HG02615.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.337+567_337+568ins others(14): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408125 | ||||||
| chr16:408128 | C | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(87): Show |
199 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.337+568C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408128 | |||||||
| chr16:408138 | GGCCTCTG others(9): Show |
G | 1 | a0001c0001t0001g0090 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.337+579_337+594del others(16): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408138 | |||||||
| chr16:408139 | G | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(79): Show |
189 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.337+579G>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408139 | |||||||
| chr16:408142 | T | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(85): Show |
196 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.337+582T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408142 | |||||||
| chr16:408142 | T | TCTGTCTC others(21): Show |
1 | a0001c0001t0001g0096 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.337+592_337+593ins others(28): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408142 | ||||||
| chr16:408150 | C | T | 2 | a0001c0013t0002g0092 a0007c0015t0001g0150 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.337+590C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408150 | |||||||
| chr16:408151 | G | A | 11 | a0001c0001t0001g0075 a0001c0001t0005g0161 a0001c0001t0005g0162 others(8): Show |
19 | HG01243.hp2 HG02258.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.337+591G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408151 | |||||||
| chr16:408153 | C | G | 3 | a0001c0013t0002g0092 a0002c0002t0001g0156 a0007c0015t0001g0150 |
3 | HG02109.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.337+593C>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408153 | |||||||
| chr16:408155 | C | T | 2 | a0001c0013t0002g0092 a0007c0015t0001g0150 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.337+595C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408155 | |||||||
| chr16:408156 | C | CCTGTCTC others(19): Show |
2 | a0001c0001t0001g0079 a0001c0001t0001g0089 |
2 | HG00323.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.337+606_337+607ins others(26): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408156 | ||||||
| chr16:408156 | C | CGTCTCCG others(5): Show |
2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.337+596_337+597ins others(12): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408156 | |||||||
| chr16:408156 | C | T | 3 | a0001c0013t0002g0092 a0002c0002t0001g0156 a0007c0015t0001g0150 |
3 | HG02109.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.337+596C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408156 | |||||||
| chr16:408156 | CCT | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(75): Show |
185 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.337+597_337+598del others(2): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408156 | |||||||
| chr16:408156 | CCTGTCTC others(7): Show |
C | 6 | a0002c0002t0001g0014 a0002c0002t0001g0044 a0002c0002t0001g0118 others(3): Show |
11 | HG02717.hp2 HG02809.hp2 HG03453.hp2 others(8): Show |
intron_variant | MODIFIER | c.337+621_337+634del others(14): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408156 | ||||||
| chr16:408158 | T | C | 1 | a0001c0001t0001g0090 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.337+598T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408158 | |||||||
| chr16:408158 | T | TGTCTCCG others(5): Show |
5 | a0001c0001t0001g0028 a0001c0001t0001g0034 a0001c0001t0001g0052 others(2): Show |
7 | HG00140.hp1 HG00639.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.337+606_337+607ins others(12): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408158 | ||||||
| chr16:408158 | T | TGTCTCCG others(461): Show |
1 | a0001c0001t0001g0087 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.337+606_337+607ins others(468): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408158 | ||||||
| chr16:408165 | G | A | 2 | a0001c0013t0002g0092 a0007c0015t0001g0150 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.337+605G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408165 | |||||||
| chr16:408166 | GGCCTCTG others(23): Show |
G | 1 | a0001c0001t0008g0064 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.337+607_337+636del others(30): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408166 | |||||||
| chr16:408167 | G | C | 4 | a0001c0005t0001g0160 a0001c0013t0002g0092 a0002c0002t0001g0156 others(1): Show |
4 | HG02109.hp2 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.337+607G>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408167 | |||||||
| chr16:408170 | T | C | 5 | a0001c0001t0001g0065 a0001c0005t0001g0160 a0001c0013t0002g0092 others(2): Show |
5 | HG02109.hp2 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.337+610T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408170 | |||||||
| chr16:408178 | C | T | 2 | a0001c0013t0002g0092 a0007c0015t0001g0150 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.337+618C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408178 | |||||||
| chr16:408181 | G | C | 6 | a0001c0001t0001g0036 a0001c0001t0001g0079 a0001c0001t0001g0085 others(3): Show |
7 | HG00323.hp1 HG02145.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.337+621G>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408181 | |||||||
| chr16:408184 | T | C | 7 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0079 others(4): Show |
9 | HG00323.hp1 HG02071.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.337+624T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408184 | |||||||
| chr16:408192 | C | T | 2 | a0001c0001t0006g0165 a0001c0001t0006g0166 |
2 | HG02109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.337+632C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408192 | |||||||
| chr16:408193 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.337+633G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408193 | |||||||
| chr16:408198 | C | CCTGTCTC others(21): Show |
1 | a0001c0001t0001g0065 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.337+648_337+649ins others(28): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408198 | ||||||
| chr16:408200 | T | C | 1 | a0001c0001t0008g0064 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.337+640T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408200 | |||||||
| chr16:408206 | C | T | 2 | a0001c0001t0007g0113 a0001c0001t0007g0114 |
2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.337+646C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408206 | |||||||
| chr16:408209 | C | G | 2 | a0001c0001t0008g0064 a0001c0005t0001g0160 |
2 | HG03130.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.337+649C>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408209 | |||||||
| chr16:408212 | C | T | 1 | a0001c0001t0008g0064 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.337+652C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408212 | |||||||
| chr16:408212 | CCT | C | 18 | a0001c0001t0001g0030 a0001c0001t0001g0060 a0001c0001t0001g0075 others(15): Show |
27 | HG00738.hp2 HG01243.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.337+653_337+654del others(2): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408212 | |||||||
| chr16:408220 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.337+660C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408220 | |||||||
| chr16:408223 | G | C | 2 | a0001c0001t0001g0065 a0001c0001t0001g0123 |
2 | HG04204.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.337+663G>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408223 | |||||||
| chr16:408226 | T | C | 3 | a0001c0001t0001g0065 a0001c0001t0001g0123 a0002c0002t0001g0157 |
3 | HG04204.hp2 NA18906.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.337+666T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408226 | |||||||
| chr16:408234 | C | CGGGCCTC others(21): Show |
1 | a0009c0012t0001g0120 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.337+695_337+722dup others(28): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408234 | ||||||
| chr16:408249 | G | A | 2 | a0001c0013t0002g0092 a0007c0015t0001g0150 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.337+689G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408249 | |||||||
| chr16:408251 | C | G | 1 | a0001c0005t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.337+691C>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408251 | |||||||
| chr16:408254 | C | T | 1 | a0001c0005t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.337+694C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408254 | |||||||
| chr16:408267 | C | T | 1 | a0001c0005t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.337+707C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408267 | |||||||
| chr16:408283 | A | G | 2 | a0001c0013t0002g0092 a0007c0015t0001g0150 |
2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.337+723A>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408283 | |||||||
| chr16:408288 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.337+728C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408288 | |||||||
| chr16:408311 | GTCTCTGG others(3): Show |
G | 2 | a0001c0001t0007g0113 a0001c0001t0007g0114 |
2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.337+755_337+764del others(10): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408311 | ||||||
| chr16:408319 | C | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(49): Show |
129 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.337+759C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408319 | |||||||
| chr16:408351 | T | C | 3 | a0001c0005t0001g0160 a0001c0013t0002g0092 a0007c0015t0001g0150 |
3 | HG02970.hp1 HG03041.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.337+791T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408351 | |||||||
| chr16:408372 | TGGCCCTC others(7): Show |
T | 1 | a0007c0015t0001g0150 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.337+817_337+830del others(14): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408372 | ||||||
| chr16:408387 | G | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(82): Show |
201 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.337+827G>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408387 | |||||||
| chr16:408522 | C | CT | 7 | a0001c0001t0001g0052 a0001c0001t0001g0069 a0001c0001t0001g0083 others(4): Show |
7 | HG00140.hp1 HG00597.hp1 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.337+976dupT | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408522 | ||||||
| chr16:408522 | CT | C | 18 | a0001c0001t0001g0149 a0001c0001t0004g0043 a0001c0001t0004g0154 others(15): Show |
32 | HG01243.hp2 HG01975.hp1 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.337+976delT | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408522 | ||||||
| chr16:408536 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.337+976T>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408536 | |||||||
| chr16:408556 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(104): Show |
225 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.337+996C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408556 | |||||||
| chr16:408570 | T | C | 7 | a0002c0002t0001g0014 a0002c0002t0001g0044 a0002c0002t0001g0118 others(4): Show |
12 | HG02109.hp2 HG02717.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.337+1010T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408570 | |||||||
| chr16:408645 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.337+1085C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408645 | |||||||
| chr16:408759 | T | C | 3 | a0001c0001t0005g0161 a0001c0001t0005g0162 a0001c0001t0005g0163 |
3 | HG02615.hp1 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.337+1199T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408759 | |||||||
| chr16:408834 | C | CT | 98 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(95): Show |
218 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.337+1289dupT | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408834 | ||||||
| chr16:408834 | C | CTT | 17 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0047 others(14): Show |
20 | HG00140.hp1 HG01071.hp1 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.337+1288_337+1289d others(4): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 408834 | ||||||
| chr16:408977 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.338-1266G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408977 | |||||||
| chr16:408981 | G | A | 1 | a0001c0001t0004g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.338-1262G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 408981 | |||||||
| chr16:409044 | C | T | 2 | a0001c0001t0007g0113 a0001c0001t0007g0114 |
2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.338-1199C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 409044 | |||||||
| chr16:409118 | C | T | 6 | a0001c0001t0005g0162 a0001c0001t0005g0163 a0001c0005t0001g0160 others(3): Show |
6 | HG02257.hp2 HG02630.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.338-1125C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 409118 | |||||||
| chr16:409162 | TATTTTTA others(3): Show |
T | 4 | a0001c0005t0001g0160 a0001c0005t0002g0059 a0001c0013t0002g0092 others(1): Show |
4 | HG02257.hp2 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.338-1071_338-1062d others(12): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | 409162 | ||||||
| chr16:409232 | C | T | 1 | a0007c0015t0001g0150 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.338-1011C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 409232 | |||||||
| chr16:409258 | G | A | 1 | a0001c0001t0003g0081 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.338-985G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 409258 | |||||||
| chr16:409312 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.338-931A>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 409312 | |||||||
| chr16:409319 | T | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0032 others(7): Show |
15 | HG02055.hp2 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.338-924T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 409319 | |||||||
| chr16:409365 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.338-878T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 409365 | |||||||
| chr16:409372 | A | G | 5 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0060 others(2): Show |
6 | HG00438.hp2 HG01891.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.338-871A>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 409372 | |||||||
| chr16:409406 | G | A | 2 | a0001c0005t0002g0059 a0001c0013t0002g0092 |
2 | HG02257.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.338-837G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 409406 | |||||||
| chr16:409422 | A | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(116): Show |
242 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.338-821A>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 409422 | |||||||
| chr16:409433 | G | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0032 others(7): Show |
15 | HG02055.hp2 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.338-810G>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 409433 | |||||||
| chr16:409450 | G | A | 6 | a0001c0001t0007g0113 a0001c0001t0007g0114 a0001c0005t0001g0160 others(3): Show |
6 | HG02257.hp2 HG02486.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.338-793G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 409450 | |||||||
| chr16:409452 | G | T | 1 | a0001c0001t0001g0049 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.338-791G>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 409452 | |||||||
| chr16:409462 | G | C | 16 | a0001c0001t0001g0030 a0001c0001t0001g0060 a0002c0002t0001g0014 others(13): Show |
30 | HG01243.hp2 HG01891.hp1 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.338-781G>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 409462 | |||||||
| chr16:409483 | A | T | 4 | a0001c0005t0001g0160 a0001c0005t0002g0059 a0001c0013t0002g0092 others(1): Show |
4 | HG02257.hp2 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.338-760A>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 409483 | |||||||
| chr16:409627 | C | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0050 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.338-616C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 409627 | |||||||
| chr16:409694 | T | C | 3 | a0001c0001t0004g0043 a0001c0001t0004g0154 a0001c0001t0004g0155 |
4 | HG02976.hp2 HG03579.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.338-549T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 409694 | |||||||
| chr16:409721 | G | A | 1 | a0001c0013t0002g0092 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.338-522G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 409721 | |||||||
| chr16:409800 | C | T | 6 | a0001c0001t0004g0043 a0001c0001t0004g0154 a0001c0001t0004g0155 others(3): Show |
7 | HG00738.hp2 HG02109.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.338-443C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 409800 | |||||||
| chr16:409829 | G | A | 1 | a0001c0005t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.338-414G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 409829 | |||||||
| chr16:409835 | G | A | 1 | a0001c0001t0001g0026 | 3 | HG02717.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.338-408G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 409835 | |||||||
| chr16:410123 | C | A | 2 | a0001c0001t0006g0165 a0001c0001t0006g0166 |
2 | HG02109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.338-120C>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 410123 | |||||||
| chr16:410124 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.338-119C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 4/8 | chr16 | 410124 | |||||||
| chr16:410351 | ATGAGAAG others(30): Show |
A | 14 | a0002c0002t0001g0014 a0002c0002t0001g0044 a0002c0002t0001g0118 others(11): Show |
27 | HG01243.hp2 HG02109.hp2 HG02258.hp2 others(24): Show |
intron_variant | MODIFIER | c.462+48_462+84delCG others(35): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 410351 | ||||||
| chr16:410378 | CGTGCGCT others(67): Show |
C | 3 | a0001c0005t0002g0059 a0001c0013t0002g0092 a0007c0015t0001g0150 |
3 | HG02257.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.462+45_462+118delC others(73): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 410378 | ||||||
| chr16:410415 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0098 |
4 | HG01243.hp1 HG02602.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+48C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | chr16 | 410415 | |||||||
| chr16:410425 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.462+58G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | chr16 | 410425 | |||||||
| chr16:410446 | GTGCCT | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0098 |
4 | HG01243.hp1 HG02602.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+82_462+86delCC others(3): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 410446 | ||||||
| chr16:410455 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0098 |
4 | HG01243.hp1 HG02602.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+88G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | chr16 | 410455 | |||||||
| chr16:410456 | C | T | 1 | a0001c0005t0002g0059 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.462+89C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | chr16 | 410456 | |||||||
| chr16:410457 | G | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0098 |
4 | HG01243.hp1 HG02602.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+90G>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | chr16 | 410457 | |||||||
| chr16:410459 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0098 |
4 | HG01243.hp1 HG02602.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+92T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | chr16 | 410459 | |||||||
| chr16:410461 | T | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0098 |
4 | HG01243.hp1 HG02602.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+94T>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | chr16 | 410461 | |||||||
| chr16:410463 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0098 |
4 | HG01243.hp1 HG02602.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+96T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | chr16 | 410463 | |||||||
| chr16:410465 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0098 |
4 | HG01243.hp1 HG02602.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+98A>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | chr16 | 410465 | |||||||
| chr16:410466 | GAA | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0098 |
4 | HG01243.hp1 HG02602.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+100_462+101del others(2): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | chr16 | 410466 | |||||||
| chr16:410470 | T | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0098 |
4 | HG01243.hp1 HG02602.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+103T>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | chr16 | 410470 | |||||||
| chr16:410471 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0098 |
4 | HG01243.hp1 HG02602.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+104T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | chr16 | 410471 | |||||||
| chr16:410474 | T | TCC | 2 | a0001c0001t0001g0023 a0001c0001t0001g0098 |
4 | HG01243.hp1 HG02602.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+108_462+109dup others(2): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 410474 | ||||||
| chr16:410477 | G | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0098 |
4 | HG01243.hp1 HG02602.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+110G>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | chr16 | 410477 | |||||||
| chr16:410479 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0098 |
4 | HG01243.hp1 HG02602.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+112G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | chr16 | 410479 | |||||||
| chr16:410480 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0098 |
4 | HG01243.hp1 HG02602.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+113T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | chr16 | 410480 | |||||||
| chr16:410482 | G | GCC | 2 | a0001c0001t0001g0023 a0001c0001t0001g0098 |
4 | HG01243.hp1 HG02602.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+115_462+116ins others(2): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | chr16 | 410482 | |||||||
| chr16:410484 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0098 |
4 | HG01243.hp1 HG02602.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+117T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | chr16 | 410484 | |||||||
| chr16:410485 | G | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0098 |
4 | HG01243.hp1 HG02602.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+118G>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | chr16 | 410485 | |||||||
| chr16:410486 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0098 |
4 | HG01243.hp1 HG02602.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+119T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | chr16 | 410486 | |||||||
| chr16:410487 | A | C | 6 | a0001c0001t0007g0113 a0001c0001t0007g0114 a0001c0005t0001g0160 others(3): Show |
6 | HG02257.hp2 HG02486.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.462+120A>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | chr16 | 410487 | |||||||
| chr16:410487 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0098 |
4 | HG01243.hp1 HG02602.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+120A>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | chr16 | 410487 | |||||||
| chr16:410493 | A | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0098 |
4 | HG01243.hp1 HG02602.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+126A>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | chr16 | 410493 | |||||||
| chr16:410494 | G | GC | 2 | a0001c0001t0001g0023 a0001c0001t0001g0098 |
4 | HG01243.hp1 HG02602.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+128dupC | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 410494 | ||||||
| chr16:410496 | G | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0098 |
4 | HG01243.hp1 HG02602.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+129G>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | chr16 | 410496 | |||||||
| chr16:410497 | G | GGGGCCTT others(28): Show |
53 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(50): Show |
120 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.462+136_462+137ins others(35): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 410497 | ||||||
| chr16:410497 | G | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0098 |
4 | HG01243.hp1 HG02602.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+130G>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | chr16 | 410497 | |||||||
| chr16:410504 | C | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0067 others(2): Show |
13 | HG00423.hp2 HG00597.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.462+137C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | chr16 | 410504 | |||||||
| chr16:410508 | CTGACGGC others(28): Show |
C | 9 | a0001c0001t0004g0043 a0001c0001t0004g0154 a0001c0001t0004g0155 others(6): Show |
10 | HG02257.hp2 HG02486.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.463-148_463-114del others(35): Show |
DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | 410508 | ||||||
| chr16:410543 | A | C | 78 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(75): Show |
161 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.463-148A>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | chr16 | 410543 | |||||||
| chr16:410567 | T | C | 1 | a0001c0001t0001g0042 | 2 | HG00438.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.463-124T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | chr16 | 410567 | |||||||
| chr16:410578 | CT | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(83): Show |
194 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.463-112delT | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | chr16 | 410578 | |||||||
| chr16:410618 | A | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0051 a0001c0001t0007g0114 |
6 | HG00639.hp2 HG02572.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.463-73A>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | chr16 | 410618 | |||||||
| chr16:410659 | C | T | 6 | a0002c0002t0002g0006 a0002c0002t0002g0029 a0002c0002t0002g0054 others(3): Show |
14 | HG01243.hp2 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.463-32C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | chr16 | 410659 | |||||||
| chr16:410673 | G | A | 28 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(25): Show |
52 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.463-18G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 5/8 | chr16 | 410673 | |||||||
| chr16:410793 | A | AC | 27 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0018 others(24): Show |
43 | HG00408.hp1 HG00558.hp2 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.556+18dupC | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr16 | 410793 | ||||||
| chr16:410795 | C | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0125 |
5 | HG02895.hp2 HG02897.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.556+11C>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 6/8 | chr16 | 410795 | |||||||
| chr16:410796 | C | A | 7 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0032 others(4): Show |
12 | HG02055.hp2 HG02145.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.556+12C>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 6/8 | chr16 | 410796 | |||||||
| chr16:410830 | A | G | 14 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(11): Show |
35 | HG00544.hp1 HG01943.hp1 HG01981.hp1 others(32): Show |
intron_variant | MODIFIER | c.556+46A>G | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 6/8 | chr16 | 410830 | |||||||
| chr16:410837 | G | A | 1 | a0002c0002t0002g0056 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.556+53G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 6/8 | chr16 | 410837 | |||||||
| chr16:411332 | C | T | 1 | a0002c0002t0001g0157 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.662-29C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 7/8 | chr16 | 411332 | |||||||
| chr16:411624 | G | A | 1 | a0002c0002t0001g0118 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.879+46G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 8/8 | chr16 | 411624 | |||||||
| chr16:411660 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.879+82C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 8/8 | chr16 | 411660 | |||||||
| chr16:411697 | C | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(47): Show |
127 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.879+119C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 8/8 | chr16 | 411697 | |||||||
| chr16:411754 | C | T | 1 | a0001c0001t0007g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.*1-136C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 8/8 | chr16 | 411754 | |||||||
| chr16:411762 | T | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(115): Show |
241 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.*1-128T>C | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 8/8 | chr16 | 411762 | |||||||
| chr16:411780 | G | A | 1 | a0007c0015t0001g0150 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.*1-110G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 8/8 | chr16 | 411780 | |||||||
| chr16:411785 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.*1-105C>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 8/8 | chr16 | 411785 | |||||||
| chr16:411843 | G | T | 4 | a0001c0001t0001g0012 a0001c0001t0001g0078 a0001c0001t0001g0106 others(1): Show |
8 | NA18940.hp1 NA18950.hp1 NA18970.hp1 others(5): Show |
intron_variant | MODIFIER | c.*1-47G>T | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 8/8 | chr16 | 411843 | |||||||
| chr16:411863 | G | A | 1 | a0007c0015t0001g0150 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.*1-27G>A | DECR2 | ENSG00000242612.7 | transcript | ENST00000219481.10 | protein_coding | 8/8 | chr16 | 411863 |