Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 348654 |
| ensemblid | ENSG00000178295.15 |
| hgncid | 26881 |
| symbol | GEN1 |
| name | GEN1 Holliday junction 5' flap endonuclease |
| refseq_nuc | NM_001130009.3 |
| refseq_prot | NP_001123481.3 |
| ensembl_nuc | ENST00000381254.7 |
| ensembl_prot | ENSP00000370653.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 17754138 |
| end | 17788946 |
| strand | + |
| ver | v1.2 |
| region | chr2:17754138-17788946 |
| region5000 | chr2:17749138-17793946 |
| regionname0 | GEN1_chr2_17754138_17788946 |
| regionname5000 | GEN1_chr2_17749138_17793946 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 908 | 134 | 8 | 22 | 76 | 8 | 20 | 58 | GEN1_chr2_17749138_17793946 | GEN1 | MGVND others(903): Show |
chr2 | 17749138 | 17793946 |
| a0002 | 0/0 | 908 | 49 | 19 | 14 | 5 | 7 | 4 | 4 | GEN1_chr2_17749138_17793946 | GEN1 | MGVND others(903): Show |
chr2 | 17749138 | 17793946 |
| a0003 | 0/0 | 908 | 38 | 21 | 6 | 7 | 2 | 2 | 6 | GEN1_chr2_17749138_17793946 | GEN1 | MGVND others(903): Show |
chr2 | 17749138 | 17793946 |
| a0004 | 0/0 | 839 | 30 | 2 | 8 | 17 | 1 | 2 | 10 | GEN1_chr2_17749138_17793946 | GEN1 | MGVND others(834): Show |
chr2 | 17749138 | 17793946 |
| a0005 | 0/0 | 908 | 16 | 0 | 1 | 15 | 0 | 0 | 14 | GEN1_chr2_17749138_17793946 | GEN1 | MGVND others(903): Show |
chr2 | 17749138 | 17793946 |
| a0006 | 0/0 | 908 | 13 | 13 | 0 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | MGVND others(903): Show |
chr2 | 17749138 | 17793946 |
| a0007 | 0/0 | 908 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | MGVND others(903): Show |
chr2 | 17749138 | 17793946 |
| a0008 | 0/0 | 908 | 7 | 0 | 4 | 0 | 0 | 3 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | MGVND others(903): Show |
chr2 | 17749138 | 17793946 |
| a0009 | 0/0 | 908 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | MGVND others(903): Show |
chr2 | 17749138 | 17793946 |
| a0010 | 0/0 | 908 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | MGVND others(903): Show |
chr2 | 17749138 | 17793946 |
| a0011 | 0/0 | 908 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | MGVND others(903): Show |
chr2 | 17749138 | 17793946 |
| a0012 | 0/0 | 908 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | MGVND others(903): Show |
chr2 | 17749138 | 17793946 |
| a0013 | 0/0 | 908 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | MGVND others(903): Show |
chr2 | 17749138 | 17793946 |
| a0014 | 0/0 | 908 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | MGVND others(903): Show |
chr2 | 17749138 | 17793946 |
| a0015 | 0/0 | 908 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | MGVND others(903): Show |
chr2 | 17749138 | 17793946 |
| a0016 | 0/0 | 908 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | MGVND others(903): Show |
chr2 | 17749138 | 17793946 |
| a0017 | 0/0 | 908 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | MGVND others(903): Show |
chr2 | 17749138 | 17793946 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2724 | 131 | 6 | 22 | 76 | 8 | 19 | GEN1_chr2_17749138_17793946 | GEN1 | ATGGG others(2719): Show |
chr2 | 17749138 | 17793946 | ||
| a0001c0012 | 0/0 | 2724 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | ATGGG others(2719): Show |
chr2 | 17749138 | 17793946 | ||
| a0001c0020 | 0/0 | 2724 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | ATGGG others(2719): Show |
chr2 | 17749138 | 17793946 | ||
| a0002c0002 | 0/0 | 2724 | 49 | 19 | 14 | 5 | 7 | 4 | GEN1_chr2_17749138_17793946 | GEN1 | ATGGG others(2719): Show |
chr2 | 17749138 | 17793946 | ||
| a0003c0003 | 0/0 | 2724 | 37 | 21 | 6 | 7 | 1 | 2 | GEN1_chr2_17749138_17793946 | GEN1 | ATGGG others(2719): Show |
chr2 | 17749138 | 17793946 | ||
| a0003c0019 | 0/0 | 2724 | 1 | 0 | 0 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | ATGGG others(2719): Show |
chr2 | 17749138 | 17793946 | ||
| a0004c0004 | 0/0 | 2719 | 30 | 2 | 8 | 17 | 1 | 2 | GEN1_chr2_17749138_17793946 | GEN1 | ATGGG others(2714): Show |
chr2 | 17749138 | 17793946 | ||
| a0005c0005 | 0/0 | 2724 | 16 | 0 | 1 | 15 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | ATGGG others(2719): Show |
chr2 | 17749138 | 17793946 | ||
| a0006c0006 | 0/0 | 2724 | 13 | 13 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | ATGGG others(2719): Show |
chr2 | 17749138 | 17793946 | ||
| a0007c0007 | 0/0 | 2724 | 9 | 9 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | ATGGG others(2719): Show |
chr2 | 17749138 | 17793946 | ||
| a0008c0009 | 0/0 | 2724 | 6 | 0 | 3 | 0 | 0 | 3 | GEN1_chr2_17749138_17793946 | GEN1 | ATGGG others(2719): Show |
chr2 | 17749138 | 17793946 | ||
| a0008c0018 | 0/0 | 2724 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | ATGGG others(2719): Show |
chr2 | 17749138 | 17793946 | ||
| a0009c0008 | 0/0 | 2724 | 7 | 6 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | ATGGG others(2719): Show |
chr2 | 17749138 | 17793946 | ||
| a0010c0010 | 0/0 | 2724 | 6 | 6 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | ATGGG others(2719): Show |
chr2 | 17749138 | 17793946 | ||
| a0011c0011 | 0/0 | 2724 | 3 | 0 | 0 | 0 | 0 | 3 | GEN1_chr2_17749138_17793946 | GEN1 | ATGGG others(2719): Show |
chr2 | 17749138 | 17793946 | ||
| a0012c0021 | 0/0 | 2724 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | ATGGG others(2719): Show |
chr2 | 17749138 | 17793946 | ||
| a0013c0015 | 0/0 | 2724 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | ATGGG others(2719): Show |
chr2 | 17749138 | 17793946 | ||
| a0014c0016 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | ATGGG others(2719): Show |
chr2 | 17749138 | 17793946 | ||
| a0015c0013 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | ATGGG others(2719): Show |
chr2 | 17749138 | 17793946 | ||
| a0016c0014 | 0/0 | 2724 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | ATGGG others(2719): Show |
chr2 | 17749138 | 17793946 | ||
| a0017c0017 | 0/0 | 2724 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | ATGGG others(2719): Show |
chr2 | 17749138 | 17793946 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 9958 | 100 | 4 | 22 | 54 | 4 | 16 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0001c0001t0004 | 0/0 | 9958 | 14 | 0 | 0 | 14 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0001c0001t0009 | 0/0 | 9958 | 5 | 1 | 0 | 0 | 3 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0001c0001t0013 | 0/0 | 9958 | 3 | 1 | 0 | 0 | 1 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0001c0001t0028 | 0/0 | 9958 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0001c0001t0029 | 0/0 | 9958 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0001c0001t0032 | 0/0 | 9958 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0001c0001t0033 | 0/0 | 9958 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0001c0001t0034 | 0/0 | 9958 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0001c0001t0035 | 0/0 | 9958 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0001c0001t0041 | 0/0 | 9958 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0001c0001t0049 | 0/0 | 9958 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0001c0001t0051 | 0/0 | 9958 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0001c0012t0018 | 0/0 | 9958 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0001c0020t0001 | 0/0 | 9958 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0002c0002t0002 | 0/0 | 9957 | 37 | 11 | 12 | 3 | 7 | 4 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9952): Show |
chr2 | 17749138 | 17793946 |
| a0002c0002t0007 | 0/0 | 9957 | 6 | 6 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9952): Show |
chr2 | 17749138 | 17793946 |
| a0002c0002t0022 | 0/0 | 9957 | 2 | 0 | 0 | 2 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9952): Show |
chr2 | 17749138 | 17793946 |
| a0002c0002t0039 | 0/0 | 9957 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9952): Show |
chr2 | 17749138 | 17793946 |
| a0002c0002t0040 | 0/0 | 9957 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9952): Show |
chr2 | 17749138 | 17793946 |
| a0002c0002t0042 | 0/0 | 9957 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9952): Show |
chr2 | 17749138 | 17793946 |
| a0002c0002t0043 | 0/0 | 9957 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9952): Show |
chr2 | 17749138 | 17793946 |
| a0003c0003t0003 | 0/0 | 9958 | 18 | 14 | 3 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0003c0003t0006 | 0/0 | 9958 | 8 | 3 | 0 | 4 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0003c0003t0014 | 0/0 | 9958 | 3 | 0 | 0 | 3 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0003c0003t0020 | 0/0 | 9958 | 2 | 0 | 2 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0003c0003t0044 | 0/0 | 9958 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0003c0003t0045 | 0/0 | 9958 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0003c0003t0046 | 0/0 | 9958 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0003c0003t0047 | 0/0 | 9958 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0003c0003t0048 | 0/0 | 9958 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0003c0003t0050 | 0/0 | 9958 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0003c0019t0003 | 0/0 | 9958 | 1 | 0 | 0 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0004c0004t0001 | 0/0 | 9953 | 27 | 2 | 6 | 16 | 1 | 2 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9948): Show |
chr2 | 17749138 | 17793946 |
| a0004c0004t0023 | 0/0 | 9953 | 2 | 0 | 2 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9948): Show |
chr2 | 17749138 | 17793946 |
| a0004c0004t0036 | 0/0 | 9953 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9948): Show |
chr2 | 17749138 | 17793946 |
| a0005c0005t0005 | 0/0 | 9953 | 12 | 0 | 0 | 12 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9948): Show |
chr2 | 17749138 | 17793946 |
| a0005c0005t0008 | 0/0 | 9953 | 2 | 0 | 0 | 2 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9948): Show |
chr2 | 17749138 | 17793946 |
| a0005c0005t0025 | 0/0 | 9953 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9948): Show |
chr2 | 17749138 | 17793946 |
| a0005c0005t0027 | 0/0 | 9953 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9948): Show |
chr2 | 17749138 | 17793946 |
| a0006c0006t0008 | 0/0 | 9953 | 3 | 3 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9948): Show |
chr2 | 17749138 | 17793946 |
| a0006c0006t0010 | 0/0 | 9953 | 4 | 4 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9948): Show |
chr2 | 17749138 | 17793946 |
| a0006c0006t0011 | 0/0 | 9953 | 4 | 4 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9948): Show |
chr2 | 17749138 | 17793946 |
| a0006c0006t0024 | 0/0 | 9953 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9948): Show |
chr2 | 17749138 | 17793946 |
| a0006c0006t0026 | 0/0 | 9953 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9948): Show |
chr2 | 17749138 | 17793946 |
| a0007c0007t0002 | 0/0 | 9957 | 5 | 5 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9952): Show |
chr2 | 17749138 | 17793946 |
| a0007c0007t0017 | 0/0 | 9957 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9952): Show |
chr2 | 17749138 | 17793946 |
| a0007c0007t0030 | 0/0 | 9252 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9247): Show |
chr2 | 17749138 | 17793946 |
| a0007c0007t0031 | 0/0 | 9957 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9952): Show |
chr2 | 17749138 | 17793946 |
| a0008c0009t0003 | 0/0 | 9958 | 2 | 0 | 1 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0008c0009t0019 | 0/0 | 9958 | 2 | 0 | 0 | 0 | 0 | 2 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0008c0009t0021 | 0/0 | 9958 | 2 | 0 | 2 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0008c0018t0003 | 0/0 | 9958 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0009c0008t0002 | 0/0 | 9957 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9952): Show |
chr2 | 17749138 | 17793946 |
| a0009c0008t0012 | 0/0 | 9957 | 3 | 2 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9952): Show |
chr2 | 17749138 | 17793946 |
| a0009c0008t0016 | 0/0 | 9957 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9952): Show |
chr2 | 17749138 | 17793946 |
| a0009c0008t0038 | 0/0 | 9957 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9952): Show |
chr2 | 17749138 | 17793946 |
| a0010c0010t0002 | 0/0 | 9957 | 6 | 6 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9952): Show |
chr2 | 17749138 | 17793946 |
| a0011c0011t0015 | 0/0 | 9958 | 3 | 0 | 0 | 0 | 0 | 3 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0012c0021t0002 | 0/0 | 9957 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9952): Show |
chr2 | 17749138 | 17793946 |
| a0013c0015t0037 | 0/0 | 9957 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9952): Show |
chr2 | 17749138 | 17793946 |
| a0014c0016t0001 | 0/0 | 9958 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0015c0013t0012 | 0/0 | 9957 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9952): Show |
chr2 | 17749138 | 17793946 |
| a0016c0014t0001 | 0/0 | 9958 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| a0017c0017t0001 | 0/0 | 9958 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | GCTGG others(9953): Show |
chr2 | 17749138 | 17793946 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 19 | 0 | 7 | 12 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0002 | 0/0 | 14 | 0 | 3 | 6 | 2 | 3 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0004g0001 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0009g0011 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0009g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0009g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0013g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0013g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0013g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0028g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0029g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0032g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0033g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0034g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0035g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0041g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0049g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0001t0051g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0012t0018g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0001c0020t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0002c0002t0002g0004 | 0/0 | 4 | 1 | 1 | 1 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0002c0002t0002g0008 | 0/0 | 5 | 0 | 2 | 0 | 2 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0002c0002t0002g0009 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0002c0002t0002g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0002c0002t0002g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0002c0002t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0002c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0002c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0002c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0002c0002t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0002c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0002c0002t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0002c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0002c0002t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0002c0002t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0002c0002t0007g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0002c0002t0007g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0002c0002t0007g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0002c0002t0022g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0002c0002t0039g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0002c0002t0040g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0002c0002t0042g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0002c0002t0043g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0003c0003t0003g0006 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0003c0003t0003g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0003c0003t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0003c0003t0003g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0003c0003t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0003c0003t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0003c0003t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0003c0003t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0003c0003t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0003c0003t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0003c0003t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0003c0003t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0003c0003t0006g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0003c0003t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0003c0003t0006g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0003c0003t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0003c0003t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0003c0003t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0003c0003t0006g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0003c0003t0014g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0003c0003t0014g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0003c0003t0014g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0003c0003t0020g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0003c0003t0044g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0003c0003t0045g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0003c0003t0046g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0003c0003t0047g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0003c0003t0048g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0003c0003t0050g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0003c0019t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0004c0004t0001g0005 | 0/0 | 8 | 1 | 2 | 4 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0004c0004t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0004c0004t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0004c0004t0001g0041 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0004c0004t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0004c0004t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0004c0004t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0004c0004t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0004c0004t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0004c0004t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0004c0004t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0004c0004t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0004c0004t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0004c0004t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0004c0004t0023g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0004c0004t0023g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0004c0004t0036g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0005c0005t0005g0003 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0005c0005t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0005c0005t0008g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0005c0005t0025g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0005c0005t0027g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0006c0006t0008g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0006c0006t0008g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0006c0006t0010g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0006c0006t0010g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0006c0006t0011g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0006c0006t0011g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0006c0006t0011g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0006c0006t0024g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0006c0006t0026g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0007c0007t0002g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0007c0007t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0007c0007t0017g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0007c0007t0017g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0007c0007t0030g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0007c0007t0031g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0008c0009t0003g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0008c0009t0019g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0008c0009t0021g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0008c0018t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0009c0008t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0009c0008t0012g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0009c0008t0012g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0009c0008t0016g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0009c0008t0038g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0010c0010t0002g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0010c0010t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0010c0010t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0010c0010t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0011c0011t0015g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0011c0011t0015g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0012c0021t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0013c0015t0037g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0014c0016t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0015c0013t0012g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0016c0014t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| a0017c0017t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0169 | EUR | GBR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG00099 | hp2 | a0001 | c0001 | t0009 | g0011 | EUR | GBR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG00140 | hp1 | a0003 | c0019 | t0003 | g0060 | EUR | GBR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0078 | EUR | GBR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG00280 | hp1 | a0001 | c0001 | t0009 | g0011 | EUR | FIN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0008 | EUR | FIN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0154 | EUR | FIN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0004 | EUR | FIN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG00408 | hp1 | a0004 | c0004 | t0001 | g0012 | EAS | CHS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG00423 | hp1 | a0004 | c0004 | t0001 | g0157 | EAS | CHS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG00423 | hp2 | a0001 | c0001 | t0032 | g0001 | EAS | CHS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG00438 | hp2 | a0004 | c0004 | t0001 | g0012 | EAS | CHS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG00558 | hp1 | a0004 | c0004 | t0001 | g0167 | EAS | CHS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG00621 | hp1 | a0004 | c0004 | t0001 | g0005 | EAS | CHS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG00621 | hp2 | a0005 | c0005 | t0008 | g0003 | EAS | CHS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG00639 | hp1 | a0003 | c0003 | t0020 | g0017 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG00639 | hp2 | a0005 | c0005 | t0027 | g0003 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG00642 | hp1 | a0004 | c0004 | t0023 | g0118 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG00642 | hp2 | a0002 | c0002 | t0042 | g0073 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG00735 | hp1 | a0012 | c0021 | t0002 | g0071 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG00735 | hp2 | a0004 | c0004 | t0001 | g0005 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG00738 | hp1 | a0004 | c0004 | t0001 | g0041 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0084 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG00741 | hp1 | a0004 | c0004 | t0001 | g0168 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01069 | hp1 | a0008 | c0009 | t0021 | g0027 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01069 | hp2 | a0013 | c0015 | t0037 | g0100 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01070 | hp2 | a0008 | c0018 | t0003 | g0050 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01071 | hp2 | a0008 | c0009 | t0021 | g0027 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01074 | hp1 | a0004 | c0004 | t0001 | g0005 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01074 | hp2 | a0003 | c0003 | t0020 | g0017 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0072 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01106 | hp1 | a0004 | c0004 | t0001 | g0040 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01109 | hp2 | a0009 | c0008 | t0012 | g0037 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0077 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01175 | hp2 | a0004 | c0004 | t0023 | g0122 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01192 | hp1 | a0004 | c0004 | t0001 | g0040 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01192 | hp2 | a0002 | c0002 | t0039 | g0036 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01243 | hp1 | a0003 | c0003 | t0003 | g0006 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01256 | hp1 | a0002 | c0002 | t0002 | g0036 | AMR | CLM | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01261 | hp1 | a0003 | c0003 | t0003 | g0029 | AMR | CLM | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | CLM | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | CLM | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01433 | hp1 | a0008 | c0009 | t0003 | g0026 | AMR | CLM | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01433 | hp2 | a0002 | c0002 | t0002 | g0016 | AMR | CLM | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01496 | hp1 | a0003 | c0003 | t0046 | g0049 | AMR | CLM | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0025 | EUR | IBS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0008 | EUR | IBS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01516 | hp1 | a0002 | c0002 | t0002 | g0016 | EUR | IBS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0025 | EUR | IBS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01884 | hp1 | a0003 | c0003 | t0006 | g0059 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01884 | hp2 | a0003 | c0003 | t0045 | g0006 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01891 | hp1 | a0002 | c0002 | t0002 | g0033 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01891 | hp2 | a0003 | c0003 | t0003 | g0013 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01934 | hp1 | a0003 | c0003 | t0003 | g0052 | AMR | PEL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PEL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PEL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02015 | hp1 | a0004 | c0004 | t0001 | g0005 | EAS | KHV | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02027 | hp1 | a0001 | c0001 | t0028 | g0162 | EAS | KHV | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02055 | hp1 | a0002 | c0002 | t0007 | g0015 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0115 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02056 | hp2 | a0003 | c0003 | t0006 | g0030 | EAS | KHV | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02145 | hp1 | a0003 | c0003 | t0003 | g0090 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02145 | hp2 | a0003 | c0003 | t0006 | g0056 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CDX | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CDX | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0068 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02257 | hp2 | a0006 | c0006 | t0010 | g0177 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02258 | hp1 | a0004 | c0004 | t0001 | g0005 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02258 | hp2 | a0009 | c0008 | t0016 | g0038 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02280 | hp1 | a0002 | c0002 | t0002 | g0066 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02280 | hp2 | a0006 | c0006 | t0010 | g0023 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0016 | AMR | PEL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02451 | hp1 | a0006 | c0006 | t0026 | g0093 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02451 | hp2 | a0003 | c0003 | t0003 | g0006 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02572 | hp1 | a0001 | c0012 | t0018 | g0024 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02572 | hp2 | a0014 | c0016 | t0001 | g0119 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02602 | hp2 | a0004 | c0004 | t0001 | g0158 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02615 | hp1 | a0007 | c0007 | t0002 | g0010 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02615 | hp2 | a0006 | c0006 | t0024 | g0175 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02622 | hp1 | a0007 | c0007 | t0031 | g0087 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02622 | hp2 | a0002 | c0002 | t0002 | g0070 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02630 | hp1 | a0006 | c0006 | t0010 | g0023 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02630 | hp2 | a0007 | c0007 | t0002 | g0010 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02717 | hp2 | a0010 | c0010 | t0002 | g0004 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02723 | hp1 | a0002 | c0002 | t0002 | g0076 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02723 | hp2 | a0007 | c0007 | t0002 | g0032 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02738 | hp1 | a0001 | c0001 | t0009 | g0116 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02809 | hp1 | a0007 | c0007 | t0002 | g0010 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02809 | hp2 | a0003 | c0003 | t0003 | g0047 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02886 | hp1 | a0009 | c0008 | t0038 | g0045 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02886 | hp2 | a0015 | c0013 | t0012 | g0085 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02896 | hp1 | a0002 | c0002 | t0002 | g0033 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02896 | hp2 | a0006 | c0006 | t0008 | g0039 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02922 | hp1 | a0009 | c0008 | t0016 | g0038 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02922 | hp2 | a0003 | c0003 | t0003 | g0006 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02965 | hp1 | a0009 | c0008 | t0012 | g0086 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02965 | hp2 | a0006 | c0006 | t0011 | g0174 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02970 | hp1 | a0006 | c0006 | t0011 | g0044 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02970 | hp2 | a0002 | c0002 | t0007 | g0015 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02976 | hp1 | a0003 | c0003 | t0003 | g0006 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02976 | hp2 | a0010 | c0010 | t0002 | g0004 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03041 | hp1 | a0010 | c0010 | t0002 | g0080 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03041 | hp2 | a0002 | c0002 | t0007 | g0014 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03098 | hp1 | a0002 | c0002 | t0002 | g0004 | AFR | MSL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03098 | hp2 | a0006 | c0006 | t0008 | g0094 | AFR | MSL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03130 | hp1 | a0003 | c0003 | t0048 | g0006 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03130 | hp2 | a0007 | c0007 | t0017 | g0089 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03139 | hp1 | a0003 | c0003 | t0003 | g0013 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03139 | hp2 | a0002 | c0002 | t0007 | g0015 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03195 | hp1 | a0003 | c0003 | t0003 | g0013 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03195 | hp2 | a0006 | c0006 | t0010 | g0023 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03209 | hp1 | a0002 | c0002 | t0007 | g0014 | AFR | MSL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0067 | AFR | MSL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03225 | hp1 | a0001 | c0012 | t0018 | g0024 | AFR | MSL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0048 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03239 | hp2 | a0008 | c0009 | t0019 | g0028 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03453 | hp1 | a0010 | c0010 | t0002 | g0081 | AFR | MSL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03492 | hp1 | a0001 | c0001 | t0013 | g0011 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03516 | hp1 | a0003 | c0003 | t0050 | g0055 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03516 | hp2 | a0002 | c0002 | t0007 | g0065 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0069 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03540 | hp2 | a0007 | c0007 | t0017 | g0088 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03579 | hp1 | a0003 | c0003 | t0003 | g0029 | AFR | MSL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0075 | AFR | MSL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0009 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03654 | hp2 | a0016 | c0014 | t0001 | g0001 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03669 | hp1 | a0011 | c0011 | t0015 | g0064 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03669 | hp2 | a0004 | c0004 | t0001 | g0005 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | STU | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03688 | hp2 | a0001 | c0020 | t0001 | g0002 | SAS | STU | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03704 | hp1 | a0008 | c0009 | t0003 | g0026 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03710 | hp1 | a0008 | c0009 | t0019 | g0028 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03831 | hp1 | a0001 | c0001 | t0041 | g0001 | SAS | BEB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0008 | SAS | BEB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03834 | hp2 | a0017 | c0017 | t0001 | g0001 | SAS | BEB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG04199 | hp1 | a0011 | c0011 | t0015 | g0031 | SAS | STU | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | STU | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG04204 | hp1 | a0011 | c0011 | t0015 | g0031 | SAS | STU | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG04204 | hp2 | a0003 | c0003 | t0047 | g0063 | SAS | STU | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0079 | SAS | STU | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18522 | hp1 | a0009 | c0008 | t0012 | g0037 | AFR | YRI | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18522 | hp2 | a0010 | c0010 | t0002 | g0004 | AFR | YRI | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18612 | hp2 | a0004 | c0004 | t0001 | g0012 | EAS | CHB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | CHB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18906 | hp1 | a0006 | c0006 | t0011 | g0044 | AFR | YRI | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18906 | hp2 | a0003 | c0003 | t0003 | g0046 | AFR | YRI | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18939 | hp1 | a0004 | c0004 | t0001 | g0166 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18945 | hp1 | a0004 | c0004 | t0001 | g0012 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18945 | hp2 | a0005 | c0005 | t0005 | g0003 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18946 | hp1 | a0001 | c0001 | t0051 | g0149 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18946 | hp2 | a0005 | c0005 | t0025 | g0092 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18952 | hp2 | a0004 | c0004 | t0001 | g0156 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18954 | hp2 | a0004 | c0004 | t0001 | g0005 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18957 | hp1 | a0005 | c0005 | t0005 | g0003 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18959 | hp1 | a0003 | c0003 | t0014 | g0097 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18964 | hp2 | a0004 | c0004 | t0001 | g0042 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18967 | hp1 | a0001 | c0001 | t0034 | g0153 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18967 | hp2 | a0003 | c0003 | t0014 | g0099 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18968 | hp1 | a0001 | c0001 | t0035 | g0124 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18968 | hp2 | a0005 | c0005 | t0005 | g0003 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18970 | hp2 | a0004 | c0004 | t0001 | g0042 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18971 | hp2 | a0005 | c0005 | t0005 | g0003 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18972 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18977 | hp2 | a0005 | c0005 | t0008 | g0003 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18978 | hp1 | a0003 | c0003 | t0006 | g0030 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18979 | hp1 | a0005 | c0005 | t0005 | g0003 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18980 | hp1 | a0001 | c0001 | t0004 | g0120 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18982 | hp2 | a0004 | c0004 | t0001 | g0005 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18984 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18984 | hp2 | a0005 | c0005 | t0005 | g0003 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18986 | hp1 | a0001 | c0001 | t0033 | g0126 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18989 | hp1 | a0003 | c0003 | t0014 | g0098 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18992 | hp2 | a0005 | c0005 | t0005 | g0003 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18993 | hp1 | a0001 | c0001 | t0029 | g0130 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18993 | hp2 | a0004 | c0004 | t0001 | g0043 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18997 | hp1 | a0001 | c0001 | t0049 | g0117 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18997 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19001 | hp1 | a0005 | c0005 | t0005 | g0091 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19004 | hp2 | a0003 | c0003 | t0006 | g0058 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19006 | hp1 | a0005 | c0005 | t0005 | g0003 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19010 | hp2 | a0004 | c0004 | t0036 | g0043 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19012 | hp1 | a0005 | c0005 | t0005 | g0003 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19012 | hp2 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19030 | hp1 | a0003 | c0003 | t0006 | g0061 | AFR | LWK | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19030 | hp2 | a0006 | c0006 | t0011 | g0176 | AFR | LWK | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19043 | hp1 | a0006 | c0006 | t0008 | g0039 | AFR | LWK | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19043 | hp2 | a0003 | c0003 | t0044 | g0095 | AFR | LWK | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19057 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0147 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19060 | hp2 | a0004 | c0004 | t0001 | g0160 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19064 | hp1 | a0005 | c0005 | t0005 | g0003 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19067 | hp1 | a0002 | c0002 | t0022 | g0034 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19067 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19070 | hp2 | a0005 | c0005 | t0005 | g0003 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19076 | hp1 | a0003 | c0003 | t0006 | g0057 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0148 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19077 | hp2 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19089 | hp1 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19240 | hp1 | a0002 | c0002 | t0043 | g0014 | AFR | YRI | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA19240 | hp2 | a0010 | c0010 | t0002 | g0082 | AFR | YRI | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA20129 | hp1 | a0003 | c0003 | t0003 | g0017 | AFR | ASW | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA20129 | hp2 | a0007 | c0007 | t0030 | g0010 | AFR | ASW | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA20752 | hp1 | a0001 | c0001 | t0009 | g0011 | EUR | TSI | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA20752 | hp2 | a0003 | c0003 | t0006 | g0062 | EUR | TSI | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA20805 | hp1 | a0004 | c0004 | t0001 | g0041 | EUR | TSI | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA20805 | hp2 | a0001 | c0001 | t0013 | g0165 | EUR | TSI | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA20905 | hp1 | a0003 | c0003 | t0003 | g0054 | SAS | GIH | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | GIH | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02486 | hp1 | a0003 | c0003 | t0003 | g0051 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02486 | hp2 | a0009 | c0008 | t0002 | g0083 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0074 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG02559 | hp2 | a0007 | c0007 | t0002 | g0032 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03471 | hp1 | a0003 | c0003 | t0003 | g0053 | AFR | MSL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG03471 | hp2 | a0002 | c0002 | t0040 | g0004 | AFR | MSL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG06807 | hp1 | a0004 | c0004 | t0001 | g0159 | AFR | USA | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| HG06807 | hp2 | a0003 | c0003 | t0003 | g0096 | AFR | USA | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18955 | hp1 | a0002 | c0002 | t0022 | g0034 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA21309 | hp1 | a0001 | c0001 | t0013 | g0114 | AFR | LWK | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | LWK | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:17760083 | G | A | 1 | a0015 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.140G>A | p.Ser47Asn | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/14 | 363/9957 | 140/2727 | 47/908 | chr2 | 17760083 | |||
| chr2:17761508 | T | A | 14 | a0001 a0003 a0004 others(11): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
missense_variant | MODERATE | c.274T>A | p.Ser92Thr | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/14 | 497/9957 | 274/2727 | 92/908 | chr2 | 17761508 | |||
| chr2:17764938 | G | C | 1 | a0012 | 1 | HG00735.hp1 | missense_variant | MODERATE | c.390G>C | p.Gln130His | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/14 | 613/9957 | 390/2727 | 130/908 | chr2 | 17764938 | |||
| chr2:17764976 | A | G | 3 | a0003 a0008 a0011 |
48 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(45): Show |
missense_variant | MODERATE | c.428A>G | p.Asn143Ser | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/14 | 651/9957 | 428/2727 | 143/908 | chr2 | 17764976 | |||
| chr2:17766619 | G | A | 1 | a0008 | 7 | HG01069.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
missense_variant | MODERATE | c.566G>A | p.Ser189Asn | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/14 | 789/9957 | 566/2727 | 189/908 | chr2 | 17766619 | |||
| chr2:17766660 | A | G | 2 | a0005 a0006 |
29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
missense_variant | MODERATE | c.607A>G | p.Ile203Val | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/14 | 830/9957 | 607/2727 | 203/908 | chr2 | 17766660 | |||
| chr2:17772672 | T | C | 1 | a0016 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.841T>C | p.Cys281Arg | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 8/14 | 1064/9957 | 841/2727 | 281/908 | chr2 | 17772672 | |||
| chr2:17772760 | G | A | 15 | a0001 a0002 a0003 others(12): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
missense_variant | MODERATE | c.929G>A | p.Ser310Asn | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 8/14 | 1152/9957 | 929/2727 | 310/908 | chr2 | 17772760 | |||
| chr2:17773130 | G | A | 1 | a0011 | 3 | HG03669.hp1 HG04199.hp1 HG04204.hp1 |
missense_variant&splice_region_variant | MODERATE | c.988G>A | p.Glu330Lys | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 9/14 | 1211/9957 | 988/2727 | 330/908 | chr2 | 17773130 | |||
| chr2:17781251 | C | T | 11 | a0001 a0003 a0004 others(8): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
missense_variant | MODERATE | c.2039C>T | p.Thr680Ile | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2262/9957 | 2039/2727 | 680/908 | chr2 | 17781251 | |||
| chr2:17781647 | A | G | 1 | a0013 | 1 | HG01069.hp2 | missense_variant | MODERATE | c.2435A>G | p.Lys812Arg | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2658/9957 | 2435/2727 | 812/908 | chr2 | 17781647 | |||
| chr2:17781661 | A | G | 1 | a0007 | 9 | HG02559.hp2 HG02615.hp1 HG02622.hp1 others(6): Show |
missense_variant | MODERATE | c.2449A>G | p.Thr817Ala | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2672/9957 | 2449/2727 | 817/908 | chr2 | 17781661 | |||
| chr2:17781726 | CAAGTT | C | 1 | a0004 | 30 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(27): Show |
frameshift_variant | HIGH | c.2515_2519delAAGTT | p.Lys839fs | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2738/9957 | 2515/2727 | 839/908 | chr2 | 17781726 | |||
| chr2:17781831 | T | G | 1 | a0005 | 16 | HG00621.hp2 HG00639.hp2 NA18945.hp2 others(13): Show |
missense_variant | MODERATE | c.2619T>G | p.Ser873Arg | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2842/9957 | 2619/2727 | 873/908 | chr2 | 17781831 | |||
| chr2:17781864 | A | C | 1 | a0014 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.2652A>C | p.Glu884Asp | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2875/9957 | 2652/2727 | 884/908 | chr2 | 17781864 | |||
| chr2:17788241 | AGCAAAGC others(5698): Show |
A | 1 | a0007 | 1 | NA20129.hp2 | splice_region_variant | LOW | c.*6303_*12007del | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | chr2 | 17788241 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:17764974 | C | T | 1 | a0001c0020 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.426C>T | p.Leu142Leu | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/14 | 649/9957 | 426/2727 | 142/908 | chr2 | 17764974 | |||
| chr2:17780054 | A | G | 2 | a0005c0005 a0006c0006 |
29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
synonymous_variant | LOW | c.1341A>G | p.Ala447Ala | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 13/14 | 1564/9957 | 1341/2727 | 447/908 | chr2 | 17780054 | |||
| chr2:17780850 | T | A | 1 | a0003c0019 | 1 | HG00140.hp1 | synonymous_variant | LOW | c.1638T>A | p.Ser546Ser | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 1861/9957 | 1638/2727 | 546/908 | chr2 | 17780850 | |||
| chr2:17781183 | A | G | 6 | a0001c0001 a0001c0020 a0004c0004 others(3): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
synonymous_variant | LOW | c.1971A>G | p.Glu657Glu | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2194/9957 | 1971/2727 | 657/908 | chr2 | 17781183 | |||
| chr2:17781657 | C | T | 1 | a0008c0018 | 1 | HG01070.hp2 | synonymous_variant | LOW | c.2445C>T | p.Tyr815Tyr | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2668/9957 | 2445/2727 | 815/908 | chr2 | 17781657 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:17754185 | C | T | 1 | a0001c0001t0051 | 1 | NA18946.hp1 | 5_prime_UTR_variant | MODIFIER | c.-176C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/14 | 5759 | chr2 | 17754185 | ||||||
| chr2:17754227 | CT | C | 9 | a0005c0005t0005 a0005c0005t0008 a0005c0005t0025 others(6): Show |
29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
5_prime_UTR_variant | MODIFIER | c.-123delT | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/14 | 5706 | INFO_REALIGN_3_PRIME | chr2 | 17754227 | |||||
| chr2:17754228 | T | C | 4 | a0003c0003t0006 a0003c0003t0014 a0003c0003t0044 others(1): Show |
13 | HG01884.hp1 HG02056.hp2 HG02145.hp2 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-133T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/14 | 5716 | chr2 | 17754228 | ||||||
| chr2:17759932 | A | G | 1 | a0003c0003t0050 | 1 | HG03516.hp1 | 5_prime_UTR_variant | MODIFIER | c.-12A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/14 | 12 | chr2 | 17759932 | ||||||
| chr2:17782044 | C | G | 1 | a0004c0004t0023 | 2 | HG00642.hp1 HG01175.hp2 |
3_prime_UTR_variant | MODIFIER | c.*105C>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 105 | chr2 | 17782044 | ||||||
| chr2:17782220 | A | G | 1 | a0011c0011t0015 | 3 | HG03669.hp1 HG04199.hp1 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*281A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 281 | chr2 | 17782220 | ||||||
| chr2:17782526 | C | T | 1 | a0002c0002t0022 | 2 | NA18955.hp1 NA19067.hp1 |
3_prime_UTR_variant | MODIFIER | c.*587C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 587 | chr2 | 17782526 | ||||||
| chr2:17783001 | A | T | 1 | a0001c0001t0049 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1062A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 1062 | chr2 | 17783001 | ||||||
| chr2:17783072 | T | G | 10 | a0001c0001t0028 a0005c0005t0005 a0005c0005t0008 others(7): Show |
30 | HG00621.hp2 HG00639.hp2 HG02027.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1133T>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 1133 | chr2 | 17783072 | ||||||
| chr2:17783093 | T | C | 3 | a0009c0008t0012 a0009c0008t0016 a0015c0013t0012 |
6 | HG01109.hp2 HG02258.hp2 HG02886.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1154T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 1154 | chr2 | 17783093 | ||||||
| chr2:17783099 | C | T | 9 | a0005c0005t0005 a0005c0005t0008 a0005c0005t0025 others(6): Show |
29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1160C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 1160 | chr2 | 17783099 | ||||||
| chr2:17783296 | C | T | 1 | a0003c0003t0014 | 3 | NA18959.hp1 NA18967.hp2 NA18989.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1357C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 1357 | chr2 | 17783296 | ||||||
| chr2:17783648 | A | G | 1 | a0003c0003t0048 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1709A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 1709 | chr2 | 17783648 | ||||||
| chr2:17783730 | A | G | 6 | a0005c0005t0005 a0005c0005t0008 a0005c0005t0025 others(3): Show |
20 | HG00621.hp2 HG00639.hp2 HG02451.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1791A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 1791 | chr2 | 17783730 | ||||||
| chr2:17784383 | C | T | 1 | a0003c0003t0047 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2444C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2444 | chr2 | 17784383 | ||||||
| chr2:17784432 | C | T | 16 | a0003c0003t0003 a0003c0003t0006 a0003c0003t0014 others(13): Show |
48 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*2493C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2493 | chr2 | 17784432 | ||||||
| chr2:17784488 | T | C | 1 | a0001c0001t0029 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2549T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2549 | chr2 | 17784488 | ||||||
| chr2:17784522 | G | A | 2 | a0007c0007t0030 a0007c0007t0031 |
2 | HG02622.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2583G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2583 | chr2 | 17784522 | ||||||
| chr2:17784553 | A | G | 12 | a0003c0003t0003 a0003c0003t0020 a0003c0003t0045 others(9): Show |
35 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*2614A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2614 | chr2 | 17784553 | ||||||
| chr2:17784584 | G | A | 1 | a0006c0006t0024 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2645G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2645 | chr2 | 17784584 | ||||||
| chr2:17784656 | C | G | 9 | a0005c0005t0005 a0005c0005t0008 a0005c0005t0025 others(6): Show |
29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2717C>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2717 | chr2 | 17784656 | ||||||
| chr2:17784664 | G | A | 19 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(16): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*2725G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2725 | chr2 | 17784664 | ||||||
| chr2:17784673 | T | G | 1 | a0013c0015t0037 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2734T>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2734 | chr2 | 17784673 | ||||||
| chr2:17784677 | A | G | 3 | a0002c0002t0007 a0002c0002t0042 a0002c0002t0043 |
8 | HG00642.hp2 HG02055.hp1 HG02970.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2738A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2738 | chr2 | 17784677 | ||||||
| chr2:17784691 | CAGAG | C | 9 | a0005c0005t0005 a0005c0005t0008 a0005c0005t0025 others(6): Show |
29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2756_*2759delGAGA | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2756 | INFO_REALIGN_3_PRIME | chr2 | 17784691 | |||||
| chr2:17784890 | A | G | 47 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(44): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*2951A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2951 | chr2 | 17784890 | ||||||
| chr2:17784934 | G | A | 1 | a0001c0001t0032 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2995G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2995 | chr2 | 17784934 | ||||||
| chr2:17784982 | A | T | 2 | a0006c0006t0010 a0006c0006t0011 |
8 | HG02257.hp2 HG02280.hp2 HG02630.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3043A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3043 | chr2 | 17784982 | ||||||
| chr2:17784987 | C | T | 1 | a0003c0003t0046 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3048C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3048 | chr2 | 17784987 | ||||||
| chr2:17785154 | T | G | 47 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(44): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*3215T>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3215 | chr2 | 17785154 | ||||||
| chr2:17785208 | G | A | 1 | a0007c0007t0017 | 2 | HG03130.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3269G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3269 | chr2 | 17785208 | ||||||
| chr2:17785226 | A | G | 1 | a0006c0006t0011 | 4 | HG02965.hp2 HG02970.hp1 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3287A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3287 | chr2 | 17785226 | ||||||
| chr2:17785307 | T | C | 1 | a0009c0008t0038 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3368T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3368 | chr2 | 17785307 | ||||||
| chr2:17785464 | T | C | 2 | a0005c0005t0005 a0005c0005t0025 |
13 | NA18945.hp2 NA18946.hp2 NA18957.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3525T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3525 | chr2 | 17785464 | ||||||
| chr2:17785586 | A | AT | 46 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(43): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*3654dupT | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3655 | INFO_REALIGN_3_PRIME | chr2 | 17785586 | |||||
| chr2:17785752 | G | C | 1 | a0001c0001t0033 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3813G>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3813 | chr2 | 17785752 | ||||||
| chr2:17785763 | G | A | 1 | a0001c0012t0018 | 2 | HG02572.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3824G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3824 | chr2 | 17785763 | ||||||
| chr2:17785825 | C | T | 2 | a0002c0002t0007 a0002c0002t0043 |
7 | HG02055.hp1 HG02970.hp2 HG03041.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3886C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3886 | chr2 | 17785825 | ||||||
| chr2:17785839 | A | G | 1 | a0005c0005t0025 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3900A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3900 | chr2 | 17785839 | ||||||
| chr2:17785862 | T | G | 3 | a0006c0006t0010 a0006c0006t0011 a0006c0006t0024 |
9 | HG02257.hp2 HG02280.hp2 HG02615.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3923T>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3923 | chr2 | 17785862 | ||||||
| chr2:17785888 | C | A | 1 | a0008c0009t0019 | 2 | HG03239.hp2 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3949C>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3949 | chr2 | 17785888 | ||||||
| chr2:17785900 | A | T | 1 | a0013c0015t0037 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3961A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3961 | chr2 | 17785900 | ||||||
| chr2:17785919 | A | T | 6 | a0005c0005t0005 a0005c0005t0008 a0005c0005t0025 others(3): Show |
20 | HG00621.hp2 HG00639.hp2 HG02451.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*3980A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3980 | chr2 | 17785919 | ||||||
| chr2:17786014 | T | G | 21 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(18): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*4075T>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 4075 | chr2 | 17786014 | ||||||
| chr2:17786035 | A | G | 1 | a0003c0003t0045 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4096A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 4096 | chr2 | 17786035 | ||||||
| chr2:17786141 | A | G | 1 | a0004c0004t0036 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4202A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 4202 | chr2 | 17786141 | ||||||
| chr2:17786234 | C | T | 3 | a0001c0001t0004 a0001c0001t0035 a0001c0001t0051 |
16 | NA18946.hp1 NA18964.hp1 NA18968.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4295C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 4295 | chr2 | 17786234 | ||||||
| chr2:17786319 | A | G | 26 | a0001c0012t0018 a0003c0003t0003 a0003c0003t0006 others(23): Show |
79 | HG00140.hp1 HG00621.hp2 HG00639.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*4380A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 4380 | chr2 | 17786319 | ||||||
| chr2:17786532 | A | G | 1 | a0002c0002t0043 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4593A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 4593 | chr2 | 17786532 | ||||||
| chr2:17786569 | C | T | 17 | a0001c0012t0018 a0003c0003t0003 a0003c0003t0006 others(14): Show |
50 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*4630C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 4630 | chr2 | 17786569 | ||||||
| chr2:17786583 | A | G | 9 | a0005c0005t0005 a0005c0005t0008 a0005c0005t0025 others(6): Show |
29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*4644A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 4644 | chr2 | 17786583 | ||||||
| chr2:17786675 | C | T | 1 | a0013c0015t0037 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4736C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 4736 | chr2 | 17786675 | ||||||
| chr2:17786803 | G | A | 1 | a0001c0012t0018 | 2 | HG02572.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4864G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 4864 | chr2 | 17786803 | ||||||
| chr2:17786948 | C | A | 16 | a0003c0003t0003 a0003c0003t0006 a0003c0003t0014 others(13): Show |
48 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*5009C>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5009 | chr2 | 17786948 | ||||||
| chr2:17787066 | T | C | 1 | a0009c0008t0016 | 2 | HG02258.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5127T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5127 | chr2 | 17787066 | ||||||
| chr2:17787081 | T | C | 1 | a0006c0006t0026 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5142T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5142 | chr2 | 17787081 | ||||||
| chr2:17787096 | T | G | 1 | a0009c0008t0038 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5157T>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5157 | chr2 | 17787096 | ||||||
| chr2:17787237 | C | T | 1 | a0001c0001t0009 | 5 | HG00099.hp2 HG00280.hp1 HG02055.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5298C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5298 | chr2 | 17787237 | ||||||
| chr2:17787266 | G | A | 9 | a0005c0005t0005 a0005c0005t0008 a0005c0005t0025 others(6): Show |
29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*5327G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5327 | chr2 | 17787266 | ||||||
| chr2:17787369 | C | A | 1 | a0002c0002t0040 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5430C>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5430 | chr2 | 17787369 | ||||||
| chr2:17787378 | G | A | 3 | a0009c0008t0012 a0009c0008t0016 a0015c0013t0012 |
6 | HG01109.hp2 HG02258.hp2 HG02886.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5439G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5439 | chr2 | 17787378 | ||||||
| chr2:17787421 | A | T | 1 | a0001c0012t0018 | 2 | HG02572.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5482A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5482 | chr2 | 17787421 | ||||||
| chr2:17787473 | T | C | 1 | a0003c0003t0044 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5534T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5534 | chr2 | 17787473 | ||||||
| chr2:17787559 | A | G | 1 | a0008c0009t0021 | 2 | HG01069.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5620A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5620 | chr2 | 17787559 | ||||||
| chr2:17787572 | C | T | 1 | a0001c0001t0034 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5633C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5633 | chr2 | 17787572 | ||||||
| chr2:17787617 | C | T | 9 | a0005c0005t0005 a0005c0005t0008 a0005c0005t0025 others(6): Show |
29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*5678C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5678 | chr2 | 17787617 | ||||||
| chr2:17787682 | G | C | 2 | a0007c0007t0030 a0007c0007t0031 |
2 | HG02622.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5743G>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5743 | chr2 | 17787682 | ||||||
| chr2:17787746 | A | G | 1 | a0003c0003t0020 | 2 | HG00639.hp1 HG01074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5807A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5807 | chr2 | 17787746 | ||||||
| chr2:17787757 | C | T | 1 | a0001c0001t0035 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5818C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5818 | chr2 | 17787757 | ||||||
| chr2:17787781 | G | A | 9 | a0005c0005t0005 a0005c0005t0008 a0005c0005t0025 others(6): Show |
29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*5842G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5842 | chr2 | 17787781 | ||||||
| chr2:17787848 | C | T | 3 | a0009c0008t0012 a0009c0008t0016 a0015c0013t0012 |
6 | HG01109.hp2 HG02258.hp2 HG02886.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5909C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5909 | chr2 | 17787848 | ||||||
| chr2:17788059 | G | A | 1 | a0009c0008t0038 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6120G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 6120 | chr2 | 17788059 | ||||||
| chr2:17788078 | C | T | 26 | a0001c0012t0018 a0003c0003t0003 a0003c0003t0006 others(23): Show |
79 | HG00140.hp1 HG00621.hp2 HG00639.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*6139C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 6139 | chr2 | 17788078 | ||||||
| chr2:17788157 | G | A | 2 | a0001c0001t0009 a0001c0001t0013 |
8 | HG00099.hp2 HG00280.hp1 HG02055.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*6218G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 6218 | chr2 | 17788157 | ||||||
| chr2:17788193 | C | T | 1 | a0005c0005t0027 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6254C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 6254 | chr2 | 17788193 | ||||||
| chr2:17788282 | C | T | 1 | a0011c0011t0015 | 3 | HG03669.hp1 HG04199.hp1 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6343C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 6343 | chr2 | 17788282 | ||||||
| chr2:17788675 | T | A | 1 | a0003c0003t0050 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6736T>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 6736 | chr2 | 17788675 | ||||||
| chr2:17788753 | G | C | 1 | a0001c0001t0001 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6814G>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 6814 | chr2 | 17788753 | ||||||
| chr2:17788791 | G | A | 1 | a0007c0007t0017 | 2 | HG03130.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6852G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 6852 | chr2 | 17788791 | ||||||
| chr2:17788909 | C | T | 1 | a0003c0003t0003 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6970C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 6970 | chr2 | 17788909 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:17754382 | G | T | 6 | a0006c0006t0010g0023 a0006c0006t0010g0177 a0006c0006t0011g0044 others(3): Show |
9 | HG02257.hp2 HG02280.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-16+37G>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17754382 | |||||||
| chr2:17754431 | T | C | 1 | a0009c0008t0038g0045 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-16+86T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17754431 | |||||||
| chr2:17754460 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-16+115A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17754460 | |||||||
| chr2:17754513 | T | C | 99 | a0001c0012t0018g0024 a0002c0002t0002g0004 a0002c0002t0002g0008 others(96): Show |
153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.-16+168T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17754513 | |||||||
| chr2:17754542 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-16+197C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17754542 | |||||||
| chr2:17754627 | G | C | 1 | a0001c0012t0018g0024 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-16+282G>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17754627 | |||||||
| chr2:17754629 | G | C | 3 | a0003c0003t0003g0013 a0003c0003t0003g0046 a0003c0003t0003g0047 |
5 | HG01891.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+284G>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17754629 | |||||||
| chr2:17754801 | C | T | 1 | a0001c0012t0018g0024 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-16+456C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17754801 | |||||||
| chr2:17754839 | C | T | 1 | a0013c0015t0037g0100 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-16+494C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17754839 | |||||||
| chr2:17754918 | T | C | 1 | a0003c0003t0003g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-16+573T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17754918 | |||||||
| chr2:17754924 | A | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG02074.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.-16+579A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17754924 | |||||||
| chr2:17754985 | C | T | 3 | a0003c0003t0014g0097 a0003c0003t0014g0098 a0003c0003t0014g0099 |
3 | NA18959.hp1 NA18967.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.-16+640C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17754985 | |||||||
| chr2:17755084 | CAA | C | 2 | a0003c0003t0003g0017 a0003c0003t0020g0017 |
3 | HG00639.hp1 HG01074.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-16+741_-16+742del others(2): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 17755084 | ||||||
| chr2:17755312 | G | T | 1 | a0001c0001t0001g0169 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-16+967G>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17755312 | |||||||
| chr2:17755514 | A | C | 1 | a0003c0003t0003g0096 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-16+1169A>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17755514 | |||||||
| chr2:17755875 | T | C | 1 | a0001c0012t0018g0024 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-16+1530T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17755875 | |||||||
| chr2:17755897 | T | G | 2 | a0002c0002t0002g0025 a0002c0002t0002g0048 |
3 | HG01515.hp1 HG01517.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-16+1552T>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17755897 | |||||||
| chr2:17755980 | A | T | 1 | a0003c0003t0044g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-16+1635A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17755980 | |||||||
| chr2:17755986 | A | G | 14 | a0005c0005t0005g0003 a0005c0005t0005g0091 a0005c0005t0008g0003 others(11): Show |
29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.-16+1641A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17755986 | |||||||
| chr2:17756016 | A | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(93): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-16+1671A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17756016 | |||||||
| chr2:17756097 | A | G | 1 | a0003c0003t0003g0090 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-16+1752A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17756097 | |||||||
| chr2:17756122 | G | A | 1 | a0009c0008t0038g0045 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-16+1777G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17756122 | |||||||
| chr2:17756147 | C | T | 14 | a0005c0005t0005g0003 a0005c0005t0005g0091 a0005c0005t0008g0003 others(11): Show |
29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.-16+1802C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17756147 | |||||||
| chr2:17756272 | C | G | 1 | a0004c0004t0001g0168 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-16+1927C>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17756272 | |||||||
| chr2:17756482 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-16+2137G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17756482 | |||||||
| chr2:17756502 | AC | A | 36 | a0003c0003t0003g0006 a0003c0003t0003g0013 a0003c0003t0003g0017 others(33): Show |
48 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.-16+2158delC | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17756502 | |||||||
| chr2:17756831 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-16+2486G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17756831 | |||||||
| chr2:17757008 | G | A | 1 | a0002c0002t0007g0065 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-16+2663G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17757008 | |||||||
| chr2:17757147 | C | T | 3 | a0004c0004t0001g0012 a0004c0004t0001g0166 a0004c0004t0001g0167 |
6 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-2782C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17757147 | |||||||
| chr2:17757234 | A | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(93): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-15-2695A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17757234 | |||||||
| chr2:17757246 | CT | C | 39 | a0001c0001t0001g0103 a0001c0012t0018g0024 a0003c0003t0003g0006 others(36): Show |
52 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.-15-2666delT | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 17757246 | ||||||
| chr2:17757387 | A | T | 1 | a0001c0001t0013g0165 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-15-2542A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17757387 | |||||||
| chr2:17757484 | A | G | 1 | a0009c0008t0038g0045 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-15-2445A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17757484 | |||||||
| chr2:17757540 | G | A | 1 | a0009c0008t0038g0045 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-15-2389G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17757540 | |||||||
| chr2:17757644 | A | T | 1 | a0001c0001t0001g0171 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-15-2285A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17757644 | |||||||
| chr2:17757729 | G | C | 1 | a0007c0007t0002g0032 | 2 | HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-15-2200G>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17757729 | |||||||
| chr2:17758269 | G | A | 21 | a0003c0003t0003g0006 a0003c0003t0003g0013 a0003c0003t0003g0017 others(18): Show |
31 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.-15-1660G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17758269 | |||||||
| chr2:17758468 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-15-1461T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17758468 | |||||||
| chr2:17758607 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-15-1322C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17758607 | |||||||
| chr2:17758817 | G | T | 8 | a0005c0005t0005g0003 a0005c0005t0005g0091 a0005c0005t0008g0003 others(5): Show |
20 | HG00621.hp2 HG00639.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.-15-1112G>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17758817 | |||||||
| chr2:17758819 | G | A | 14 | a0005c0005t0005g0003 a0005c0005t0005g0091 a0005c0005t0008g0003 others(11): Show |
29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.-15-1110G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17758819 | |||||||
| chr2:17758831 | G | A | 6 | a0002c0002t0002g0033 a0002c0002t0002g0066 a0002c0002t0002g0067 others(3): Show |
7 | HG01891.hp1 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-15-1098G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17758831 | |||||||
| chr2:17758831 | G | C | 20 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(17): Show |
42 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(39): Show |
intron_variant | MODIFIER | c.-15-1098G>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17758831 | |||||||
| chr2:17758839 | G | A | 1 | a0003c0003t0046g0049 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-15-1090G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17758839 | |||||||
| chr2:17758847 | C | T | 6 | a0001c0001t0009g0011 a0001c0001t0009g0115 a0001c0001t0009g0116 others(3): Show |
8 | HG00099.hp2 HG00280.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15-1082C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17758847 | |||||||
| chr2:17758869 | A | G | 1 | a0001c0001t0001g0022 | 3 | HG02717.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-15-1060A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17758869 | |||||||
| chr2:17758899 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-15-1030A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17758899 | |||||||
| chr2:17759129 | G | A | 1 | a0001c0001t0049g0117 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-15-800G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17759129 | |||||||
| chr2:17759159 | T | C | 14 | a0005c0005t0005g0003 a0005c0005t0005g0091 a0005c0005t0008g0003 others(11): Show |
29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.-15-770T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17759159 | |||||||
| chr2:17759386 | A | C | 36 | a0003c0003t0003g0006 a0003c0003t0003g0013 a0003c0003t0003g0017 others(33): Show |
48 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.-15-543A>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17759386 | |||||||
| chr2:17759430 | G | A | 1 | a0004c0004t0023g0118 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-15-499G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17759430 | |||||||
| chr2:17759524 | A | T | 1 | a0009c0008t0038g0045 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-15-405A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17759524 | |||||||
| chr2:17759530 | C | T | 14 | a0005c0005t0005g0003 a0005c0005t0005g0091 a0005c0005t0008g0003 others(11): Show |
29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.-15-399C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17759530 | |||||||
| chr2:17759644 | A | C | 1 | a0001c0001t0001g0113 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-15-285A>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17759644 | |||||||
| chr2:17759750 | A | G | 1 | a0001c0001t0028g0162 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-15-179A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17759750 | |||||||
| chr2:17759796 | C | T | 1 | a0002c0002t0002g0070 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-15-133C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17759796 | |||||||
| chr2:17759821 | A | G | 1 | a0001c0012t0018g0024 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-15-108A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17759821 | |||||||
| chr2:17760123 | C | G | 1 | a0001c0001t0001g0161 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.161+19C>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17760123 | |||||||
| chr2:17760156 | T | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(130): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.161+52T>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17760156 | |||||||
| chr2:17760302 | C | A | 1 | a0001c0001t0001g0022 | 3 | HG02717.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.161+198C>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17760302 | |||||||
| chr2:17760307 | A | G | 1 | a0002c0002t0002g0069 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.161+203A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17760307 | |||||||
| chr2:17760386 | A | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0112 |
4 | HG02738.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.161+282A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17760386 | |||||||
| chr2:17760447 | A | T | 1 | a0001c0001t0001g0111 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.161+343A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17760447 | |||||||
| chr2:17760629 | T | G | 1 | a0001c0012t0018g0024 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.161+525T>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17760629 | |||||||
| chr2:17760645 | C | T | 6 | a0006c0006t0010g0023 a0006c0006t0010g0177 a0006c0006t0011g0044 others(3): Show |
9 | HG02257.hp2 HG02280.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.161+541C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17760645 | |||||||
| chr2:17760650 | A | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(156): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.161+546A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17760650 | |||||||
| chr2:17760680 | G | A | 1 | a0014c0016t0001g0119 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.161+576G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17760680 | |||||||
| chr2:17760705 | A | G | 14 | a0005c0005t0005g0003 a0005c0005t0005g0091 a0005c0005t0008g0003 others(11): Show |
29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.161+601A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17760705 | |||||||
| chr2:17760921 | C | CA | 18 | a0001c0001t0001g0112 a0001c0001t0001g0121 a0001c0001t0001g0172 others(15): Show |
23 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.162-459dupA | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 17760921 | ||||||
| chr2:17760963 | G | T | 17 | a0004c0004t0001g0005 a0004c0004t0001g0012 a0004c0004t0001g0040 others(14): Show |
30 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(27): Show |
intron_variant | MODIFIER | c.162-433G>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17760963 | |||||||
| chr2:17761011 | A | G | 1 | a0001c0001t0001g0022 | 3 | HG02717.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.162-385A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17761011 | |||||||
| chr2:17761037 | C | A | 6 | a0002c0002t0002g0072 a0002c0002t0007g0014 a0002c0002t0007g0015 others(3): Show |
9 | HG00642.hp2 HG01099.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.162-359C>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17761037 | |||||||
| chr2:17761172 | C | G | 1 | a0002c0002t0002g0084 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.162-224C>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17761172 | |||||||
| chr2:17761198 | C | G | 2 | a0002c0002t0002g0036 a0002c0002t0039g0036 |
2 | HG01192.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.162-198C>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17761198 | |||||||
| chr2:17761245 | A | G | 1 | a0009c0008t0002g0083 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.162-151A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17761245 | |||||||
| chr2:17761360 | T | A | 14 | a0005c0005t0005g0003 a0005c0005t0005g0091 a0005c0005t0008g0003 others(11): Show |
29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.162-36T>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17761360 | |||||||
| chr2:17761372 | G | A | 14 | a0005c0005t0005g0003 a0005c0005t0005g0091 a0005c0005t0008g0003 others(11): Show |
29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.162-24G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17761372 | |||||||
| chr2:17761589 | A | G | 14 | a0005c0005t0005g0003 a0005c0005t0005g0091 a0005c0005t0008g0003 others(11): Show |
29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
splice_region_variant&intron_variant | LOW | c.348+7A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17761589 | |||||||
| chr2:17761648 | T | A | 1 | a0003c0003t0006g0057 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.348+66T>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17761648 | |||||||
| chr2:17761661 | A | T | 1 | a0002c0002t0002g0070 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.348+79A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17761661 | |||||||
| chr2:17761698 | C | A | 14 | a0005c0005t0005g0003 a0005c0005t0005g0091 a0005c0005t0008g0003 others(11): Show |
29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.348+116C>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17761698 | |||||||
| chr2:17761748 | T | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(156): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.348+166T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17761748 | |||||||
| chr2:17761779 | T | G | 1 | a0009c0008t0038g0045 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.348+197T>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17761779 | |||||||
| chr2:17761868 | G | A | 2 | a0001c0001t0004g0123 a0001c0001t0035g0124 |
2 | NA18968.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.348+286G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17761868 | |||||||
| chr2:17761959 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.348+377A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17761959 | |||||||
| chr2:17761990 | T | C | 36 | a0003c0003t0003g0006 a0003c0003t0003g0013 a0003c0003t0003g0017 others(33): Show |
48 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.348+408T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17761990 | |||||||
| chr2:17762013 | A | G | 2 | a0011c0011t0015g0031 a0011c0011t0015g0064 |
3 | HG03669.hp1 HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.348+431A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17762013 | |||||||
| chr2:17762063 | G | A | 1 | a0001c0001t0004g0125 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.348+481G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17762063 | |||||||
| chr2:17762063 | G | C | 1 | a0001c0001t0033g0126 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.348+481G>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17762063 | |||||||
| chr2:17762106 | A | C | 14 | a0005c0005t0005g0003 a0005c0005t0005g0091 a0005c0005t0008g0003 others(11): Show |
29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.348+524A>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17762106 | |||||||
| chr2:17762173 | C | CT | 10 | a0001c0001t0001g0022 a0001c0001t0001g0121 a0005c0005t0005g0003 others(7): Show |
24 | HG00621.hp2 HG00639.hp2 HG02056.hp1 others(21): Show |
intron_variant | MODIFIER | c.348+601dupT | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 17762173 | ||||||
| chr2:17762203 | G | GT | 13 | a0001c0001t0001g0152 a0001c0001t0001g0154 a0001c0001t0001g0155 others(10): Show |
15 | HG00323.hp1 HG01109.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.348+637dupT | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 17762203 | ||||||
| chr2:17762203 | G | T | 1 | a0003c0003t0003g0090 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.348+621G>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17762203 | |||||||
| chr2:17762275 | C | T | 1 | a0008c0009t0019g0028 | 2 | HG03239.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.348+693C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17762275 | |||||||
| chr2:17762327 | G | A | 2 | a0011c0011t0015g0031 a0011c0011t0015g0064 |
3 | HG03669.hp1 HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.348+745G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17762327 | |||||||
| chr2:17762408 | T | C | 14 | a0005c0005t0005g0003 a0005c0005t0005g0091 a0005c0005t0008g0003 others(11): Show |
29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.348+826T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17762408 | |||||||
| chr2:17762466 | T | C | 14 | a0005c0005t0005g0003 a0005c0005t0005g0091 a0005c0005t0008g0003 others(11): Show |
29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.348+884T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17762466 | |||||||
| chr2:17762511 | T | C | 1 | a0003c0003t0006g0058 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.348+929T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17762511 | |||||||
| chr2:17762753 | T | C | 1 | a0013c0015t0037g0100 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.348+1171T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17762753 | |||||||
| chr2:17762880 | A | G | 1 | a0003c0003t0003g0054 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.348+1298A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17762880 | |||||||
| chr2:17763016 | C | T | 1 | a0003c0003t0003g0096 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.348+1434C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17763016 | |||||||
| chr2:17763036 | T | C | 14 | a0005c0005t0005g0003 a0005c0005t0005g0091 a0005c0005t0008g0003 others(11): Show |
29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.348+1454T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17763036 | |||||||
| chr2:17763059 | C | G | 1 | a0006c0006t0008g0094 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.348+1477C>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17763059 | |||||||
| chr2:17763088 | C | G | 5 | a0003c0003t0003g0013 a0003c0003t0003g0029 a0003c0003t0003g0046 others(2): Show |
8 | HG01261.hp1 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.348+1506C>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17763088 | |||||||
| chr2:17763313 | A | G | 1 | a0004c0004t0001g0160 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.349-1584A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17763313 | |||||||
| chr2:17763396 | A | G | 1 | a0008c0009t0021g0027 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.349-1501A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17763396 | |||||||
| chr2:17763580 | A | T | 51 | a0001c0012t0018g0024 a0003c0003t0003g0006 a0003c0003t0003g0013 others(48): Show |
79 | HG00140.hp1 HG00621.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.349-1317A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17763580 | |||||||
| chr2:17763932 | T | C | 14 | a0005c0005t0005g0003 a0005c0005t0005g0091 a0005c0005t0008g0003 others(11): Show |
29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.349-965T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17763932 | |||||||
| chr2:17764078 | A | G | 4 | a0002c0002t0002g0033 a0002c0002t0002g0068 a0002c0002t0002g0069 others(1): Show |
5 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.349-819A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17764078 | |||||||
| chr2:17764205 | G | A | 1 | a0002c0002t0002g0072 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.349-692G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17764205 | |||||||
| chr2:17764238 | A | C | 1 | a0001c0001t0001g0151 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.349-659A>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17764238 | |||||||
| chr2:17764278 | C | A | 1 | a0001c0001t0001g0127 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.349-619C>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17764278 | |||||||
| chr2:17764493 | T | G | 1 | a0001c0001t0001g0105 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.349-404T>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17764493 | |||||||
| chr2:17764512 | A | T | 1 | a0001c0001t0001g0150 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.349-385A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17764512 | |||||||
| chr2:17765111 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.525+38G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/13 | chr2 | 17765111 | |||||||
| chr2:17765180 | C | T | 9 | a0003c0003t0006g0030 a0003c0003t0006g0056 a0003c0003t0006g0057 others(6): Show |
10 | HG02056.hp2 HG02145.hp2 HG04204.hp2 others(7): Show |
intron_variant | MODIFIER | c.525+107C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/13 | chr2 | 17765180 | |||||||
| chr2:17765243 | T | C | 1 | a0001c0012t0018g0024 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.525+170T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/13 | chr2 | 17765243 | |||||||
| chr2:17765327 | G | A | 1 | a0011c0011t0015g0031 | 2 | HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.525+254G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/13 | chr2 | 17765327 | |||||||
| chr2:17765556 | G | A | 2 | a0005c0005t0005g0091 a0005c0005t0025g0092 |
2 | NA18946.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.525+483G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/13 | chr2 | 17765556 | |||||||
| chr2:17765885 | A | C | 1 | a0001c0001t0001g0109 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.526-694A>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/13 | chr2 | 17765885 | |||||||
| chr2:17765948 | A | AAT | 4 | a0002c0002t0002g0070 a0003c0003t0006g0059 a0011c0011t0015g0031 others(1): Show |
5 | HG01884.hp1 HG02622.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-614_526-613dup others(2): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 17765948 | ||||||
| chr2:17765948 | A | AATAT | 3 | a0002c0002t0002g0008 a0002c0002t0002g0025 a0002c0002t0002g0048 |
8 | HG00280.hp2 HG01168.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-616_526-613dup others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 17765948 | ||||||
| chr2:17765948 | AAT | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(118): Show |
210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.526-614_526-613del others(2): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 17765948 | ||||||
| chr2:17765989 | G | A | 3 | a0002c0002t0002g0074 a0002c0002t0002g0075 a0002c0002t0002g0076 |
3 | HG02559.hp1 HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.526-590G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/13 | chr2 | 17765989 | |||||||
| chr2:17766095 | A | G | 3 | a0003c0003t0003g0006 a0003c0003t0045g0006 a0003c0003t0048g0006 |
6 | HG01243.hp1 HG01884.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.526-484A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/13 | chr2 | 17766095 | |||||||
| chr2:17766191 | G | A | 1 | a0001c0012t0018g0024 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.526-388G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/13 | chr2 | 17766191 | |||||||
| chr2:17766356 | G | A | 36 | a0003c0003t0003g0006 a0003c0003t0003g0013 a0003c0003t0003g0017 others(33): Show |
48 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.526-223G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/13 | chr2 | 17766356 | |||||||
| chr2:17766410 | T | C | 1 | a0003c0019t0003g0060 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.526-169T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/13 | chr2 | 17766410 | |||||||
| chr2:17766481 | A | G | 14 | a0005c0005t0005g0003 a0005c0005t0005g0091 a0005c0005t0008g0003 others(11): Show |
29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.526-98A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/13 | chr2 | 17766481 | |||||||
| chr2:17766740 | C | T | 1 | a0002c0002t0002g0025 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.636+51C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17766740 | |||||||
| chr2:17766767 | A | G | 36 | a0003c0003t0003g0006 a0003c0003t0003g0013 a0003c0003t0003g0017 others(33): Show |
48 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.636+78A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17766767 | |||||||
| chr2:17766857 | G | A | 1 | a0003c0019t0003g0060 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.636+168G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17766857 | |||||||
| chr2:17766948 | A | G | 36 | a0003c0003t0003g0006 a0003c0003t0003g0013 a0003c0003t0003g0017 others(33): Show |
48 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.636+259A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17766948 | |||||||
| chr2:17767083 | C | G | 1 | a0001c0001t0009g0116 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.636+394C>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17767083 | |||||||
| chr2:17767152 | G | A | 1 | a0013c0015t0037g0100 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.636+463G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17767152 | |||||||
| chr2:17767247 | A | G | 1 | a0009c0008t0016g0038 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.636+558A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17767247 | |||||||
| chr2:17767382 | T | C | 37 | a0001c0012t0018g0024 a0003c0003t0003g0006 a0003c0003t0003g0013 others(34): Show |
50 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.636+693T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17767382 | |||||||
| chr2:17767449 | G | A | 1 | a0001c0012t0018g0024 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.636+760G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17767449 | |||||||
| chr2:17767685 | C | T | 37 | a0001c0012t0018g0024 a0003c0003t0003g0006 a0003c0003t0003g0013 others(34): Show |
50 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.636+996C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17767685 | |||||||
| chr2:17767753 | A | G | 1 | a0001c0001t0051g0149 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.637-985A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17767753 | |||||||
| chr2:17767968 | T | A | 1 | a0011c0011t0015g0031 | 2 | HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.637-770T>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17767968 | |||||||
| chr2:17768075 | T | A | 36 | a0003c0003t0003g0006 a0003c0003t0003g0013 a0003c0003t0003g0017 others(33): Show |
48 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.637-663T>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17768075 | |||||||
| chr2:17768085 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.637-653G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17768085 | |||||||
| chr2:17768093 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.637-645G>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17768093 | |||||||
| chr2:17768251 | T | A | 3 | a0007c0007t0002g0010 a0007c0007t0030g0010 a0007c0007t0031g0087 |
5 | HG02615.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.637-487T>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17768251 | |||||||
| chr2:17768450 | C | G | 1 | a0006c0006t0010g0177 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.637-288C>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17768450 | |||||||
| chr2:17768666 | G | A | 5 | a0003c0003t0050g0055 a0008c0009t0003g0026 a0008c0009t0019g0028 others(2): Show |
8 | HG01069.hp1 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.637-72G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17768666 | |||||||
| chr2:17768669 | C | A | 2 | a0001c0001t0001g0128 a0001c0001t0001g0152 |
2 | NA18978.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.637-69C>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17768669 | |||||||
| chr2:17768672 | TTAA | T | 37 | a0001c0012t0018g0024 a0003c0003t0003g0006 a0003c0003t0003g0013 others(34): Show |
50 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.637-63_637-61delAT others(1): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 17768672 | ||||||
| chr2:17768845 | A | G | 2 | a0001c0001t0004g0147 a0001c0001t0004g0148 |
2 | NA19060.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.710+34A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17768845 | |||||||
| chr2:17768928 | C | T | 1 | a0001c0012t0018g0024 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.710+117C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17768928 | |||||||
| chr2:17768934 | T | C | 1 | a0009c0008t0016g0038 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.710+123T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17768934 | |||||||
| chr2:17768961 | T | G | 1 | a0002c0002t0002g0068 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.710+150T>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17768961 | |||||||
| chr2:17768988 | G | A | 4 | a0002c0002t0007g0014 a0002c0002t0007g0015 a0002c0002t0007g0065 others(1): Show |
7 | HG02055.hp1 HG02970.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.710+177G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17768988 | |||||||
| chr2:17769015 | T | C | 36 | a0003c0003t0003g0006 a0003c0003t0003g0013 a0003c0003t0003g0017 others(33): Show |
48 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.710+204T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17769015 | |||||||
| chr2:17769080 | C | T | 2 | a0011c0011t0015g0031 a0011c0011t0015g0064 |
3 | HG03669.hp1 HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.710+269C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17769080 | |||||||
| chr2:17769553 | T | C | 5 | a0003c0003t0050g0055 a0008c0009t0003g0026 a0008c0009t0019g0028 others(2): Show |
8 | HG01069.hp1 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.710+742T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17769553 | |||||||
| chr2:17769584 | C | T | 3 | a0009c0008t0012g0037 a0009c0008t0012g0086 a0015c0013t0012g0085 |
4 | HG01109.hp2 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.710+773C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17769584 | |||||||
| chr2:17769812 | TTAA | T | 14 | a0005c0005t0005g0003 a0005c0005t0005g0091 a0005c0005t0008g0003 others(11): Show |
29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.710+1003_710+1005d others(5): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | 17769812 | ||||||
| chr2:17769893 | C | T | 1 | a0011c0011t0015g0064 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.710+1082C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17769893 | |||||||
| chr2:17770125 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.711-1071A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17770125 | |||||||
| chr2:17770161 | G | A | 1 | a0003c0003t0044g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.711-1035G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17770161 | |||||||
| chr2:17770173 | T | A | 1 | a0004c0004t0001g0040 | 2 | HG01106.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.711-1023T>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17770173 | |||||||
| chr2:17770590 | G | C | 1 | a0002c0002t0002g0074 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.711-606G>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17770590 | |||||||
| chr2:17770660 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.711-536G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17770660 | |||||||
| chr2:17770794 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.711-402T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17770794 | |||||||
| chr2:17770877 | C | CA | 39 | a0003c0003t0003g0006 a0003c0003t0003g0013 a0003c0003t0003g0017 others(36): Show |
52 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.711-309dupA | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | 17770877 | ||||||
| chr2:17770897 | G | A | 5 | a0005c0005t0005g0003 a0005c0005t0005g0091 a0005c0005t0008g0003 others(2): Show |
16 | HG00621.hp2 HG00639.hp2 NA18945.hp2 others(13): Show |
intron_variant | MODIFIER | c.711-299G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17770897 | |||||||
| chr2:17770957 | A | G | 1 | a0013c0015t0037g0100 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.711-239A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17770957 | |||||||
| chr2:17771098 | G | A | 1 | a0009c0008t0016g0038 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.711-98G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17771098 | |||||||
| chr2:17771175 | A | T | 1 | a0001c0001t0001g0145 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.711-21A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17771175 | |||||||
| chr2:17771308 | G | T | 1 | a0001c0012t0018g0024 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.802+21G>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 7/13 | chr2 | 17771308 | |||||||
| chr2:17771511 | G | C | 2 | a0006c0006t0011g0044 a0006c0006t0011g0174 |
3 | HG02965.hp2 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.802+224G>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 7/13 | chr2 | 17771511 | |||||||
| chr2:17771691 | A | T | 1 | a0004c0004t0001g0040 | 2 | HG01106.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.802+404A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 7/13 | chr2 | 17771691 | |||||||
| chr2:17771766 | A | C | 3 | a0007c0007t0002g0010 a0007c0007t0030g0010 a0007c0007t0031g0087 |
5 | HG02615.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.802+479A>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 7/13 | chr2 | 17771766 | |||||||
| chr2:17771788 | T | TA | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(105): Show |
178 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.802+513dupA | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 17771788 | ||||||
| chr2:17771815 | C | T | 1 | a0013c0015t0037g0100 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.802+528C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 7/13 | chr2 | 17771815 | |||||||
| chr2:17772244 | A | G | 5 | a0005c0005t0005g0003 a0005c0005t0005g0091 a0005c0005t0008g0003 others(2): Show |
16 | HG00621.hp2 HG00639.hp2 NA18945.hp2 others(13): Show |
intron_variant | MODIFIER | c.803-390A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 7/13 | chr2 | 17772244 | |||||||
| chr2:17772293 | C | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(144): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.803-341C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 7/13 | chr2 | 17772293 | |||||||
| chr2:17772352 | G | A | 1 | a0004c0004t0001g0156 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.803-282G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 7/13 | chr2 | 17772352 | |||||||
| chr2:17772381 | A | T | 20 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(17): Show |
42 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(39): Show |
intron_variant | MODIFIER | c.803-253A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 7/13 | chr2 | 17772381 | |||||||
| chr2:17772583 | A | G | 7 | a0003c0003t0003g0053 a0003c0003t0046g0049 a0003c0003t0050g0055 others(4): Show |
10 | HG01069.hp1 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.803-51A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 7/13 | chr2 | 17772583 | |||||||
| chr2:17772873 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(150): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.953+89A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 8/13 | chr2 | 17772873 | |||||||
| chr2:17772978 | CTGTT | C | 3 | a0003c0003t0003g0006 a0003c0003t0045g0006 a0003c0003t0048g0006 |
6 | HG01243.hp1 HG01884.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.954-115_954-112del others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 17772978 | ||||||
| chr2:17772986 | G | A | 1 | a0007c0007t0017g0088 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.954-110G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 8/13 | chr2 | 17772986 | |||||||
| chr2:17773017 | G | A | 2 | a0002c0002t0002g0077 a0002c0002t0002g0078 |
2 | HG00140.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.954-79G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 8/13 | chr2 | 17773017 | |||||||
| chr2:17773154 | C | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(156): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.990+22C>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 9/13 | chr2 | 17773154 | |||||||
| chr2:17773359 | G | A | 1 | a0007c0007t0002g0032 | 2 | HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1071+60G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 10/13 | chr2 | 17773359 | |||||||
| chr2:17773380 | T | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(145): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1071+81T>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 10/13 | chr2 | 17773380 | |||||||
| chr2:17773625 | C | A | 6 | a0001c0001t0001g0019 a0001c0001t0001g0128 a0001c0001t0001g0129 others(3): Show |
8 | NA18612.hp1 NA18952.hp1 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.1071+326C>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 10/13 | chr2 | 17773625 | |||||||
| chr2:17773673 | G | A | 1 | a0006c0006t0024g0175 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1071+374G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 10/13 | chr2 | 17773673 | |||||||
| chr2:17773937 | T | C | 8 | a0003c0003t0003g0053 a0003c0003t0003g0054 a0003c0003t0046g0049 others(5): Show |
11 | HG01069.hp1 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.1072-334T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 10/13 | chr2 | 17773937 | |||||||
| chr2:17773985 | G | A | 12 | a0003c0003t0006g0030 a0003c0003t0006g0056 a0003c0003t0006g0057 others(9): Show |
13 | HG01884.hp1 HG02056.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1072-286G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 10/13 | chr2 | 17773985 | |||||||
| chr2:17773988 | G | A | 51 | a0001c0012t0018g0024 a0003c0003t0003g0006 a0003c0003t0003g0013 others(48): Show |
79 | HG00140.hp1 HG00621.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.1072-283G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 10/13 | chr2 | 17773988 | |||||||
| chr2:17774037 | G | A | 36 | a0003c0003t0003g0006 a0003c0003t0003g0013 a0003c0003t0003g0017 others(33): Show |
48 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.1072-234G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 10/13 | chr2 | 17774037 | |||||||
| chr2:17774060 | A | C | 1 | a0001c0001t0001g0131 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1072-211A>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 10/13 | chr2 | 17774060 | |||||||
| chr2:17774216 | G | A | 1 | a0003c0003t0003g0054 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1072-55G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 10/13 | chr2 | 17774216 | |||||||
| chr2:17774231 | G | A | 2 | a0003c0003t0014g0097 a0003c0003t0014g0099 |
2 | NA18959.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1072-40G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 10/13 | chr2 | 17774231 | |||||||
| chr2:17774427 | G | A | 6 | a0002c0002t0002g0072 a0002c0002t0007g0014 a0002c0002t0007g0015 others(3): Show |
9 | HG00642.hp2 HG01099.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1202+26G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17774427 | |||||||
| chr2:17774676 | G | T | 1 | a0004c0004t0001g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1202+275G>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17774676 | |||||||
| chr2:17774690 | G | A | 2 | a0004c0004t0023g0118 a0004c0004t0023g0122 |
2 | HG00642.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1202+289G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17774690 | |||||||
| chr2:17774690 | G | T | 1 | a0002c0002t0002g0025 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1202+289G>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17774690 | |||||||
| chr2:17775061 | C | T | 14 | a0005c0005t0005g0003 a0005c0005t0005g0091 a0005c0005t0008g0003 others(11): Show |
29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.1202+660C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17775061 | |||||||
| chr2:17775063 | T | A | 1 | a0002c0002t0002g0066 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1202+662T>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17775063 | |||||||
| chr2:17775078 | G | A | 3 | a0009c0008t0012g0037 a0009c0008t0012g0086 a0015c0013t0012g0085 |
4 | HG01109.hp2 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1202+677G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17775078 | |||||||
| chr2:17775225 | A | G | 1 | a0004c0004t0001g0158 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1202+824A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17775225 | |||||||
| chr2:17775439 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1202+1038A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17775439 | |||||||
| chr2:17775523 | A | G | 8 | a0005c0005t0005g0003 a0005c0005t0005g0091 a0005c0005t0008g0003 others(5): Show |
20 | HG00621.hp2 HG00639.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.1202+1122A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17775523 | |||||||
| chr2:17775615 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1202+1214A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17775615 | |||||||
| chr2:17775686 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1202+1285G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17775686 | |||||||
| chr2:17775905 | G | A | 14 | a0005c0005t0005g0003 a0005c0005t0005g0091 a0005c0005t0008g0003 others(11): Show |
29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.1202+1504G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17775905 | |||||||
| chr2:17775977 | G | A | 1 | a0003c0003t0006g0057 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1202+1576G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17775977 | |||||||
| chr2:17776084 | C | T | 1 | a0003c0003t0003g0053 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1202+1683C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17776084 | |||||||
| chr2:17776095 | G | A | 1 | a0013c0015t0037g0100 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1202+1694G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17776095 | |||||||
| chr2:17776115 | C | CA | 12 | a0001c0001t0009g0116 a0003c0003t0006g0057 a0007c0007t0002g0010 others(9): Show |
17 | HG01109.hp2 HG02258.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.1202+1735dupA | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 17776115 | ||||||
| chr2:17776115 | CA | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(107): Show |
173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1202+1735delA | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 17776115 | ||||||
| chr2:17776115 | CAA | C | 5 | a0001c0001t0001g0144 a0003c0003t0003g0017 a0003c0003t0014g0097 others(2): Show |
6 | HG00639.hp1 HG01070.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.1202+1734_1202+173 others(6): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 17776115 | ||||||
| chr2:17776199 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1202+1798C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17776199 | |||||||
| chr2:17776653 | G | A | 51 | a0001c0012t0018g0024 a0003c0003t0003g0006 a0003c0003t0003g0013 others(48): Show |
79 | HG00140.hp1 HG00621.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.1203-1349G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17776653 | |||||||
| chr2:17776670 | A | G | 2 | a0011c0011t0015g0031 a0011c0011t0015g0064 |
3 | HG03669.hp1 HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1203-1332A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17776670 | |||||||
| chr2:17776676 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0112 |
4 | HG02738.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1203-1326C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17776676 | |||||||
| chr2:17776853 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1203-1149C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17776853 | |||||||
| chr2:17776919 | A | T | 36 | a0003c0003t0003g0006 a0003c0003t0003g0013 a0003c0003t0003g0017 others(33): Show |
48 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.1203-1083A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17776919 | |||||||
| chr2:17776994 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(149): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1203-1008T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17776994 | |||||||
| chr2:17777327 | A | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0150 |
4 | HG02155.hp1 NA18944.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.1203-675A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17777327 | |||||||
| chr2:17777435 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1203-567A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17777435 | |||||||
| chr2:17777495 | G | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(73): Show |
123 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1203-507G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17777495 | |||||||
| chr2:17777657 | A | C | 1 | a0001c0012t0018g0024 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1203-345A>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17777657 | |||||||
| chr2:17777720 | C | T | 1 | a0002c0002t0002g0025 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1203-282C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17777720 | |||||||
| chr2:17777746 | C | A | 1 | a0002c0002t0002g0079 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1203-256C>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17777746 | |||||||
| chr2:17777832 | T | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(93): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.1203-170T>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17777832 | |||||||
| chr2:17778138 | G | GTA | 31 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0025 others(28): Show |
47 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.1264+90_1264+91dup others(2): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778138 | ||||||
| chr2:17778138 | GTA | G | 17 | a0001c0001t0001g0134 a0001c0012t0018g0024 a0003c0003t0006g0030 others(14): Show |
20 | HG00140.hp1 HG01884.hp1 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.1264+90_1264+91del others(2): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778138 | ||||||
| chr2:17778140 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1264+77A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778140 | |||||||
| chr2:17778153 | T | TAC | 8 | a0002c0002t0002g0009 a0002c0002t0002g0016 a0002c0002t0002g0077 others(5): Show |
15 | HG00735.hp1 HG01109.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.1264+100_1264+101d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778153 | ||||||
| chr2:17778153 | TAC | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(96): Show |
168 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.1264+100_1264+101d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778153 | ||||||
| chr2:17778155 | C | T | 4 | a0001c0001t0001g0109 a0001c0001t0001g0127 a0001c0001t0001g0132 others(1): Show |
5 | HG02258.hp2 HG02698.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1264+92C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778155 | |||||||
| chr2:17778174 | GTA | G | 22 | a0001c0001t0001g0135 a0001c0012t0018g0024 a0002c0002t0022g0034 others(19): Show |
40 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.1264+124_1264+125d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778174 | ||||||
| chr2:17778174 | GTATA | G | 3 | a0001c0001t0001g0146 a0001c0001t0004g0147 a0001c0001t0049g0117 |
3 | HG01243.hp2 NA18997.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1264+122_1264+125d others(6): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778174 | ||||||
| chr2:17778176 | A | G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(17): Show |
42 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(39): Show |
intron_variant | MODIFIER | c.1264+113A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778176 | |||||||
| chr2:17778185 | TATAC | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(67): Show |
117 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.1264+124_1264+127d others(6): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778185 | ||||||
| chr2:17778187 | T | C | 6 | a0002c0002t0002g0033 a0002c0002t0002g0066 a0002c0002t0002g0067 others(3): Show |
7 | HG01891.hp1 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1264+124T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778187 | |||||||
| chr2:17778187 | TAC | T | 4 | a0002c0002t0002g0009 a0009c0008t0012g0037 a0009c0008t0012g0086 others(1): Show |
5 | HG01109.hp1 HG01109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1264+134_1264+135d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778187 | ||||||
| chr2:17778189 | C | T | 2 | a0003c0003t0044g0095 a0003c0003t0046g0049 |
2 | HG01496.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1264+126C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778189 | |||||||
| chr2:17778197 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1264+134C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778197 | |||||||
| chr2:17778197 | CAT | C | 22 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(19): Show |
44 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.1264+139_1264+140d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778197 | ||||||
| chr2:17778199 | T | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(76): Show |
129 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.1264+136T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778199 | |||||||
| chr2:17778199 | T | G | 1 | a0001c0001t0001g0135 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1264+136T>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778199 | |||||||
| chr2:17778200 | A | G | 1 | a0001c0001t0001g0141 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1264+137A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778200 | |||||||
| chr2:17778202 | A | G | 5 | a0002c0002t0002g0066 a0002c0002t0007g0014 a0002c0002t0007g0015 others(2): Show |
8 | HG02055.hp1 HG02280.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1264+139A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778202 | |||||||
| chr2:17778204 | G | A | 1 | a0003c0003t0044g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1264+141G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778204 | |||||||
| chr2:17778206 | GTA | G | 36 | a0001c0012t0018g0024 a0003c0003t0003g0006 a0003c0003t0003g0013 others(33): Show |
49 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.1264+151_1264+152d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778206 | ||||||
| chr2:17778208 | A | G | 4 | a0001c0001t0013g0114 a0003c0003t0044g0095 a0003c0003t0047g0063 others(1): Show |
4 | HG00423.hp1 HG04204.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1264+145A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778208 | |||||||
| chr2:17778209 | T | C | 1 | a0002c0002t0002g0066 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1264+146T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778209 | |||||||
| chr2:17778212 | ATATG | A | 2 | a0002c0002t0007g0014 a0002c0002t0043g0014 |
3 | HG03041.hp2 HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1264+153_1264+156d others(6): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778212 | ||||||
| chr2:17778216 | G | A | 1 | a0003c0003t0046g0049 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1264+153G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778216 | |||||||
| chr2:17778219 | T | C | 1 | a0003c0003t0046g0049 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1264+156T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778219 | |||||||
| chr2:17778219 | TAC | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(53): Show |
88 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.1264+164_1264+165d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778219 | ||||||
| chr2:17778221 | C | T | 1 | a0002c0002t0002g0066 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1264+158C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778221 | |||||||
| chr2:17778227 | CAT | C | 4 | a0002c0002t0002g0016 a0002c0002t0002g0072 a0006c0006t0011g0176 others(1): Show |
6 | HG00735.hp1 HG01099.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1264+169_1264+170d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778227 | ||||||
| chr2:17778229 | T | C | 1 | a0002c0002t0002g0066 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1264+166T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778229 | |||||||
| chr2:17778229 | T | TATATGTG others(21): Show |
3 | a0009c0008t0012g0037 a0009c0008t0012g0086 a0015c0013t0012g0085 |
4 | HG01109.hp2 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264+190_1264+217d others(30): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778229 | ||||||
| chr2:17778232 | A | G | 1 | a0002c0002t0002g0066 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1264+169A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778232 | |||||||
| chr2:17778248 | GTATACAC others(23): Show |
G | 1 | a0001c0001t0029g0130 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1264+196_1264+225d others(32): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778248 | ||||||
| chr2:17778248 | GTATACAC others(111): Show |
G | 1 | a0003c0003t0003g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1264+196_1264+313d others(2): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778248 | ||||||
| chr2:17778248 | GTATACAC others(177): Show |
G | 1 | a0003c0003t0003g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1264+196_1264+379d others(2): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778248 | ||||||
| chr2:17778251 | T | C | 1 | a0001c0012t0018g0024 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1264+188T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778251 | |||||||
| chr2:17778251 | T | TAC | 14 | a0005c0005t0005g0003 a0005c0005t0005g0091 a0005c0005t0008g0003 others(11): Show |
29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.1264+194_1264+195d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778251 | ||||||
| chr2:17778251 | T | TACAC | 4 | a0001c0001t0001g0150 a0002c0002t0007g0014 a0002c0002t0043g0014 others(1): Show |
5 | HG01069.hp2 HG03041.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1264+192_1264+195d others(6): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778251 | ||||||
| chr2:17778253 | C | T | 1 | a0002c0002t0002g0066 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1264+190C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778253 | |||||||
| chr2:17778253 | CACACATA others(21): Show |
C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0106 |
4 | HG02027.hp2 NA18942.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.1264+196_1264+223d others(30): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778253 | ||||||
| chr2:17778255 | CACATATG others(77): Show |
C | 4 | a0003c0003t0003g0013 a0003c0003t0003g0029 a0003c0003t0003g0046 others(1): Show |
7 | HG01261.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1264+196_1264+279d others(86): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778255 | ||||||
| chr2:17778257 | C | CACAT | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(113): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.1264+195_1264+196i others(6): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778257 | ||||||
| chr2:17778257 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1264+194C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778257 | |||||||
| chr2:17778257 | CATATGTG others(3): Show |
C | 1 | a0001c0001t0035g0124 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1264+196_1264+205d others(12): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778257 | ||||||
| chr2:17778258 | A | ACG | 6 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0128 others(3): Show |
9 | HG03490.hp1 HG03492.hp2 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.1264+195_1264+196i others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778258 | |||||||
| chr2:17778259 | T | C | 3 | a0001c0001t0001g0020 a0002c0002t0002g0066 a0003c0019t0003g0060 |
3 | HG00140.hp1 HG02280.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1264+196T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778259 | |||||||
| chr2:17778260 | A | ATGTGTGT others(25): Show |
1 | a0010c0010t0002g0081 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1264+217_1264+218i others(34): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778260 | ||||||
| chr2:17778260 | A | ATGTGTGT others(25): Show |
2 | a0010c0010t0002g0004 a0010c0010t0002g0082 |
3 | HG02717.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1264+228_1264+259d others(34): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778260 | ||||||
| chr2:17778260 | A | G | 9 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0128 others(6): Show |
13 | HG01069.hp2 HG03041.hp2 HG03209.hp1 others(10): Show |
intron_variant | MODIFIER | c.1264+197A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778260 | |||||||
| chr2:17778261 | T | C | 1 | a0002c0002t0002g0066 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1264+198T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778261 | |||||||
| chr2:17778262 | G | A | 3 | a0001c0001t0001g0020 a0002c0002t0002g0066 a0003c0019t0003g0060 |
3 | HG00140.hp1 HG02280.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1264+199G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778262 | |||||||
| chr2:17778263 | T | C | 1 | a0002c0002t0002g0016 | 3 | HG01433.hp2 HG01516.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1264+200T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778263 | |||||||
| chr2:17778264 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1264+201G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778264 | |||||||
| chr2:17778264 | GTGTACAT others(77): Show |
G | 1 | a0003c0019t0003g0060 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1264+205_1264+288d others(86): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778264 | ||||||
| chr2:17778267 | TACATATA others(49): Show |
T | 1 | a0001c0001t0001g0020 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1264+205_1264+260d others(58): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778267 | |||||||
| chr2:17778276 | GTA | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(88): Show |
152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1264+218_1264+219d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778276 | ||||||
| chr2:17778279 | TATACACA others(87): Show |
T | 14 | a0005c0005t0005g0003 a0005c0005t0005g0091 a0005c0005t0008g0003 others(11): Show |
29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.1264+218_1264+311d others(96): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778279 | ||||||
| chr2:17778281 | T | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0107 others(35): Show |
47 | HG00408.hp2 HG00639.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.1264+218T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778281 | |||||||
| chr2:17778288 | ACATG | A | 3 | a0001c0001t0004g0147 a0001c0001t0004g0148 a0001c0001t0049g0117 |
3 | NA18997.hp1 NA19060.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1264+226_1264+229d others(6): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778288 | |||||||
| chr2:17778289 | C | T | 35 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(32): Show |
45 | HG00408.hp2 HG00639.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1264+226C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778289 | |||||||
| chr2:17778290 | A | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(81): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.1264+227A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778290 | |||||||
| chr2:17778291 | T | C | 1 | a0001c0001t0001g0019 | 2 | NA18612.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1264+228T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778291 | |||||||
| chr2:17778292 | G | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(28): Show |
40 | HG00408.hp2 HG00639.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.1264+229G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778292 | |||||||
| chr2:17778295 | TGTGTACA others(21): Show |
T | 3 | a0001c0001t0013g0165 a0001c0001t0034g0153 a0004c0004t0001g0156 |
3 | NA18952.hp2 NA18967.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1264+250_1264+277d others(30): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778295 | ||||||
| chr2:17778297 | TGTACATA others(19): Show |
T | 1 | a0001c0001t0001g0022 | 3 | HG02717.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1264+237_1264+262d others(28): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778297 | ||||||
| chr2:17778300 | ACATATAT others(17): Show |
A | 2 | a0001c0001t0001g0132 a0001c0001t0004g0001 |
2 | HG02698.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1264+238_1264+261d others(26): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778300 | |||||||
| chr2:17778308 | GTA | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(65): Show |
116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.1264+250_1264+251d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778308 | ||||||
| chr2:17778308 | GTATATAC others(53): Show |
G | 12 | a0003c0003t0006g0030 a0003c0003t0006g0056 a0003c0003t0006g0057 others(9): Show |
13 | HG01884.hp1 HG02056.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1264+248_1264+307d others(62): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778308 | ||||||
| chr2:17778310 | ATATACAC others(19): Show |
A | 2 | a0001c0001t0001g0109 a0013c0015t0037g0100 |
2 | HG01069.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1264+260_1264+285d others(28): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778310 | ||||||
| chr2:17778311 | TATAC | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0101 |
4 | HG01993.hp1 HG01993.hp2 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264+250_1264+253d others(6): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778311 | ||||||
| chr2:17778311 | TATACACA others(53): Show |
T | 1 | a0003c0003t0003g0006 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1264+250_1264+309d others(62): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778311 | ||||||
| chr2:17778312 | A | G | 1 | a0007c0007t0017g0089 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1264+249A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778312 | |||||||
| chr2:17778313 | T | C | 32 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(29): Show |
46 | HG00408.hp2 HG00741.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.1264+250T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778313 | |||||||
| chr2:17778313 | TAC | T | 22 | a0002c0002t0002g0004 a0002c0002t0002g0009 a0002c0002t0002g0016 others(19): Show |
35 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1264+259_1264+260d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778313 | ||||||
| chr2:17778313 | TACACACA others(21): Show |
T | 5 | a0001c0001t0001g0019 a0001c0001t0001g0128 a0001c0001t0001g0131 others(2): Show |
6 | NA18612.hp1 NA18952.hp1 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.1264+258_1264+285d others(30): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778313 | ||||||
| chr2:17778317 | CACACACG others(7): Show |
C | 2 | a0003c0003t0045g0006 a0008c0018t0003g0050 |
2 | HG01070.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.1264+256_1264+269d others(16): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778317 | ||||||
| chr2:17778319 | C | CGT | 5 | a0001c0001t0001g0002 a0001c0001t0001g0105 a0001c0001t0001g0164 others(2): Show |
8 | HG00408.hp2 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1264+256_1264+257i others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778319 | |||||||
| chr2:17778319 | C | T | 4 | a0003c0003t0003g0006 a0003c0003t0003g0096 a0003c0003t0046g0049 others(1): Show |
6 | HG01243.hp1 HG01496.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1264+256C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778319 | |||||||
| chr2:17778319 | CACACGTG others(5): Show |
C | 7 | a0003c0003t0003g0053 a0003c0003t0050g0055 a0008c0009t0003g0026 others(4): Show |
11 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.1264+258_1264+269d others(14): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778319 | ||||||
| chr2:17778319 | CACACGTG others(53): Show |
C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0142 |
2 | NA19006.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1264+258_1264+317d others(62): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778319 | ||||||
| chr2:17778320 | A | ATG | 5 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0003c0003t0003g0006 others(2): Show |
7 | HG01243.hp1 HG02451.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1264+257_1264+258i others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778320 | |||||||
| chr2:17778320 | A | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(8): Show |
15 | HG00408.hp2 HG01070.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1264+257A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778320 | |||||||
| chr2:17778321 | C | CGT | 1 | a0001c0001t0001g0002 | 3 | HG00741.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1264+258_1264+259i others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778321 | |||||||
| chr2:17778321 | C | T | 22 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(19): Show |
28 | HG00408.hp2 HG01070.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.1264+258C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778321 | |||||||
| chr2:17778321 | CACGTGTA others(3): Show |
C | 3 | a0001c0012t0018g0024 a0003c0003t0003g0017 a0003c0003t0020g0017 |
5 | HG00639.hp1 HG01074.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1264+260_1264+269d others(12): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778321 | ||||||
| chr2:17778322 | A | ATG | 5 | a0001c0001t0004g0147 a0001c0001t0004g0148 a0001c0001t0049g0117 others(2): Show |
6 | HG01496.hp1 HG02258.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1264+259_1264+260i others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778322 | |||||||
| chr2:17778322 | A | G | 20 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(17): Show |
30 | HG00408.hp2 HG00741.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1264+259A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778322 | |||||||
| chr2:17778323 | C | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(107): Show |
182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1264+260C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778323 | |||||||
| chr2:17778324 | GTGTACAT others(17): Show |
G | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(66): Show |
118 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.1264+265_1264+288d others(26): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778324 | ||||||
| chr2:17778326 | GTACATAT others(15): Show |
G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0101 |
4 | HG01993.hp1 HG01993.hp2 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264+265_1264+286d others(24): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778326 | ||||||
| chr2:17778336 | GTATACAC others(5): Show |
G | 13 | a0001c0012t0018g0024 a0003c0003t0003g0017 a0003c0003t0003g0052 others(10): Show |
19 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.1264+275_1264+286d others(14): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778336 | ||||||
| chr2:17778336 | GTATACAC others(23): Show |
G | 3 | a0002c0002t0002g0009 a0002c0002t0002g0016 a0012c0021t0002g0071 |
7 | HG00735.hp1 HG01109.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.1264+287_1264+316d others(32): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778336 | ||||||
| chr2:17778339 | T | C | 3 | a0003c0003t0003g0006 a0003c0003t0003g0096 a0003c0003t0048g0006 |
5 | HG01243.hp1 HG02451.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1264+276T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778339 | |||||||
| chr2:17778339 | T | TATAC | 5 | a0007c0007t0002g0010 a0007c0007t0002g0032 a0007c0007t0017g0088 others(2): Show |
8 | HG02559.hp2 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1264+277_1264+278i others(6): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778339 | ||||||
| chr2:17778341 | C | T | 12 | a0001c0001t0001g0020 a0001c0001t0001g0107 a0001c0001t0001g0111 others(9): Show |
14 | HG01109.hp2 HG02074.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1264+278C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778341 | |||||||
| chr2:17778345 | C | T | 4 | a0003c0003t0003g0013 a0003c0003t0003g0029 a0003c0003t0003g0046 others(1): Show |
7 | HG01261.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1264+282C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778345 | |||||||
| chr2:17778347 | C | CAT | 23 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(20): Show |
35 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.1264+285_1264+286d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778347 | ||||||
| chr2:17778347 | C | CATGTGTA others(23): Show |
1 | a0002c0002t0043g0014 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1264+290_1264+291i others(32): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778347 | ||||||
| chr2:17778347 | C | CATGTGTG others(21): Show |
1 | a0010c0010t0002g0080 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1264+305_1264+306i others(30): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778347 | ||||||
| chr2:17778347 | C | T | 17 | a0001c0001t0001g0109 a0001c0001t0034g0153 a0003c0003t0003g0006 others(14): Show |
25 | HG01243.hp1 HG01261.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.1264+284C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778347 | |||||||
| chr2:17778348 | A | ATG | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(9): Show |
20 | HG00408.hp2 HG00741.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.1264+291_1264+292d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778348 | ||||||
| chr2:17778348 | A | G | 8 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0020 others(5): Show |
10 | HG01069.hp2 HG02717.hp1 HG03225.hp2 others(7): Show |
intron_variant | MODIFIER | c.1264+285A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778348 | |||||||
| chr2:17778349 | T | C | 5 | a0002c0002t0007g0014 a0009c0008t0012g0037 a0009c0008t0012g0086 others(2): Show |
8 | HG01109.hp2 HG02258.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1264+286T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778349 | |||||||
| chr2:17778350 | G | A | 1 | a0009c0008t0016g0038 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1264+287G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778350 | |||||||
| chr2:17778350 | G | ATGTGTAC others(25): Show |
1 | a0002c0002t0007g0014 | 2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1264+286_1264+287i others(34): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778350 | |||||||
| chr2:17778364 | GTA | G | 7 | a0002c0002t0002g0079 a0003c0003t0003g0013 a0003c0003t0003g0029 others(4): Show |
9 | HG01891.hp2 HG02145.hp1 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.1264+306_1264+307d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778364 | ||||||
| chr2:17778364 | GTATA | G | 4 | a0003c0003t0003g0017 a0003c0003t0020g0017 a0003c0003t0045g0006 others(1): Show |
5 | HG00639.hp1 HG01074.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.1264+304_1264+307d others(6): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778364 | ||||||
| chr2:17778367 | T | C | 1 | a0003c0019t0003g0060 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1264+304T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778367 | |||||||
| chr2:17778367 | TATAC | T | 9 | a0003c0003t0003g0029 a0003c0003t0003g0053 a0003c0003t0003g0054 others(6): Show |
12 | HG01069.hp1 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1264+306_1264+309d others(6): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778367 | ||||||
| chr2:17778368 | A | G | 1 | a0003c0003t0003g0006 | 3 | HG01243.hp1 HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1264+305A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778368 | |||||||
| chr2:17778369 | T | C | 3 | a0003c0019t0003g0060 a0011c0011t0015g0031 a0011c0011t0015g0064 |
3 | HG00140.hp1 HG03669.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1264+306T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778369 | |||||||
| chr2:17778369 | TAC | T | 4 | a0002c0002t0002g0072 a0002c0002t0002g0074 a0002c0002t0007g0015 others(1): Show |
6 | HG01099.hp2 HG02055.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1264+314_1264+315d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778369 | ||||||
| chr2:17778371 | C | CACGCACA others(21): Show |
1 | a0009c0008t0016g0038 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1264+310_1264+311i others(30): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778371 | ||||||
| chr2:17778371 | CACACACA others(25): Show |
C | 1 | a0002c0002t0042g0073 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1264+348_1264+379d others(34): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778371 | ||||||
| chr2:17778373 | C | CACATATG others(19): Show |
1 | a0007c0007t0030g0010 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1264+313_1264+314i others(28): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778373 | ||||||
| chr2:17778375 | CACAT | C | 17 | a0001c0001t0001g0020 a0001c0001t0001g0104 a0001c0001t0001g0107 others(14): Show |
21 | HG01975.hp1 HG02074.hp1 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.1264+314_1264+317d others(6): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778375 | ||||||
| chr2:17778375 | CACATAT | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(79): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.1264+314_1264+319d others(8): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778375 | ||||||
| chr2:17778377 | C | T | 2 | a0002c0002t0002g0035 a0003c0019t0003g0060 |
2 | HG00140.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1264+314C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778377 | |||||||
| chr2:17778379 | T | C | 19 | a0002c0002t0002g0008 a0003c0003t0003g0029 a0005c0005t0005g0003 others(16): Show |
35 | HG00621.hp2 HG00639.hp2 HG01261.hp1 others(32): Show |
intron_variant | MODIFIER | c.1264+316T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778379 | |||||||
| chr2:17778379 | T | TATGTGTG others(25): Show |
1 | a0009c0008t0012g0037 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1264+318_1264+319i others(34): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778379 | ||||||
| chr2:17778379 | T | TATGTGTG others(57): Show |
3 | a0009c0008t0012g0037 a0009c0008t0012g0086 a0015c0013t0012g0085 |
3 | HG02886.hp2 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1264+318_1264+319i others(66): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778379 | ||||||
| chr2:17778380 | A | G | 1 | a0003c0019t0003g0060 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1264+317A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778380 | |||||||
| chr2:17778381 | T | TATGTATA others(7): Show |
1 | a0001c0001t0001g0019 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1264+322_1264+323i others(16): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778381 | ||||||
| chr2:17778382 | A | G | 36 | a0001c0001t0001g0101 a0001c0001t0001g0150 a0002c0002t0002g0008 others(33): Show |
50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.1264+319A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778382 | |||||||
| chr2:17778390 | A | G | 3 | a0001c0001t0001g0001 a0001c0001t0001g0102 a0001c0001t0001g0173 |
3 | HG01106.hp2 HG01358.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1264+327A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778390 | |||||||
| chr2:17778394 | A | G | 8 | a0005c0005t0005g0003 a0005c0005t0005g0091 a0005c0005t0008g0003 others(5): Show |
20 | HG00621.hp2 HG00639.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.1264+331A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778394 | |||||||
| chr2:17778398 | GTA | G | 6 | a0001c0001t0001g0001 a0003c0003t0003g0013 a0003c0003t0003g0029 others(3): Show |
9 | HG01261.hp1 HG01891.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1264+340_1264+341d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778398 | ||||||
| chr2:17778400 | A | ATG | 3 | a0003c0003t0003g0006 a0003c0003t0045g0006 a0003c0003t0048g0006 |
6 | HG01243.hp1 HG01884.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1264+338_1264+339i others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778400 | ||||||
| chr2:17778403 | T | C | 9 | a0003c0003t0003g0006 a0003c0003t0003g0013 a0003c0003t0003g0029 others(6): Show |
15 | HG01243.hp1 HG01261.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1264+340T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778403 | |||||||
| chr2:17778403 | T | TAC | 52 | a0001c0012t0018g0024 a0002c0002t0002g0004 a0002c0002t0002g0009 others(49): Show |
73 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1264+346_1264+347d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778403 | ||||||
| chr2:17778403 | T | TACACACA others(25): Show |
1 | a0002c0002t0002g0008 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1264+350_1264+351i others(34): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778403 | ||||||
| chr2:17778409 | CAT | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(93): Show |
176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.1264+351_1264+352d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778409 | ||||||
| chr2:17778409 | CATATATG others(5): Show |
C | 13 | a0001c0001t0001g0020 a0001c0001t0001g0104 a0001c0001t0001g0107 others(10): Show |
15 | HG01975.hp1 HG02074.hp1 HG03831.hp2 others(12): Show |
intron_variant | MODIFIER | c.1264+348_1264+359d others(14): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778409 | ||||||
| chr2:17778411 | T | C | 13 | a0001c0001t0001g0001 a0003c0003t0003g0053 a0003c0003t0003g0054 others(10): Show |
18 | HG01069.hp1 HG01070.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.1264+348T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778411 | |||||||
| chr2:17778412 | A | G | 2 | a0003c0003t0003g0052 a0003c0003t0003g0096 |
2 | HG01934.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1264+349A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778412 | |||||||
| chr2:17778413 | T | C | 2 | a0003c0003t0003g0054 a0008c0009t0019g0028 |
2 | HG03710.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1264+350T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778413 | |||||||
| chr2:17778414 | A | G | 23 | a0001c0001t0001g0136 a0001c0001t0001g0145 a0003c0003t0003g0006 others(20): Show |
34 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.1264+351A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778414 | |||||||
| chr2:17778416 | GTGTGTAC others(9): Show |
G | 1 | a0003c0003t0003g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1264+355_1264+370d others(18): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778416 | ||||||
| chr2:17778419 | TGTACATA others(31): Show |
T | 2 | a0003c0003t0003g0052 a0003c0003t0003g0096 |
2 | HG01934.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1264+357_1264+394d others(40): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778419 | |||||||
| chr2:17778435 | TAC | T | 32 | a0003c0003t0003g0006 a0003c0003t0003g0013 a0003c0003t0003g0017 others(29): Show |
44 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.1264+380_1264+381d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778435 | ||||||
| chr2:17778437 | C | T | 1 | a0003c0003t0003g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1264+374C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778437 | |||||||
| chr2:17778439 | C | CACATATA others(7): Show |
1 | a0001c0001t0001g0007 | 6 | NA18942.hp2 NA18977.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.1264+379_1264+380i others(16): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778439 | ||||||
| chr2:17778439 | C | CACATATG others(9): Show |
1 | a0001c0001t0001g0022 | 3 | HG02717.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1264+379_1264+380i others(18): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778439 | ||||||
| chr2:17778443 | C | T | 28 | a0001c0001t0001g0020 a0001c0001t0001g0104 a0001c0001t0001g0107 others(25): Show |
46 | HG00621.hp2 HG00639.hp2 HG01975.hp1 others(43): Show |
intron_variant | MODIFIER | c.1264+380C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778443 | |||||||
| chr2:17778445 | T | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0009c0008t0012g0086 |
10 | HG02717.hp1 HG02965.hp1 HG03225.hp2 others(7): Show |
intron_variant | MODIFIER | c.1264+382T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778445 | |||||||
| chr2:17778445 | T | TATGTATA others(7): Show |
1 | a0001c0001t0001g0140 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1264+384_1264+385i others(16): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778445 | ||||||
| chr2:17778446 | A | G | 62 | a0001c0001t0001g0020 a0001c0001t0001g0104 a0001c0001t0001g0107 others(59): Show |
92 | HG00140.hp1 HG00621.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.1264+383A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778446 | |||||||
| chr2:17778450 | G | GTATATAC others(11): Show |
1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1264+388_1264+389i others(20): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778450 | ||||||
| chr2:17778452 | G | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(78): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.1264+389G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778452 | |||||||
| chr2:17778453 | TGTAC | T | 62 | a0001c0001t0001g0020 a0001c0001t0001g0104 a0001c0001t0001g0107 others(59): Show |
92 | HG00140.hp1 HG00621.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.1264+391_1264+394d others(6): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778453 | |||||||
| chr2:17778454 | G | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(75): Show |
138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.1264+391G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778454 | |||||||
| chr2:17778456 | A | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0140 |
10 | HG02717.hp1 HG03225.hp2 HG03453.hp2 others(7): Show |
intron_variant | MODIFIER | c.1264+393A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778456 | |||||||
| chr2:17778457 | C | CACACATA others(9): Show |
78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(75): Show |
138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.1264+395_1264+396i others(18): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778457 | ||||||
| chr2:17778457 | C | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0106 others(1): Show |
11 | HG02717.hp1 HG03225.hp2 HG03453.hp2 others(8): Show |
intron_variant | MODIFIER | c.1264+394C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778457 | |||||||
| chr2:17778458 | A | C | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1264+395A>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778458 | |||||||
| chr2:17778460 | A | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(142): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1264+397A>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778460 | |||||||
| chr2:17778461 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1264+398T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778461 | |||||||
| chr2:17778464 | G | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(143): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1264+401G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778464 | |||||||
| chr2:17778469 | T | C | 1 | a0001c0012t0018g0024 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1264+406T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778469 | |||||||
| chr2:17778588 | CTT | C | 36 | a0003c0003t0003g0006 a0003c0003t0003g0013 a0003c0003t0003g0017 others(33): Show |
48 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.1264+527_1264+528d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778588 | ||||||
| chr2:17778678 | A | G | 6 | a0001c0001t0009g0011 a0001c0001t0009g0115 a0001c0001t0009g0116 others(3): Show |
8 | HG00099.hp2 HG00280.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1264+615A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778678 | |||||||
| chr2:17778777 | CT | C | 51 | a0001c0012t0018g0024 a0003c0003t0003g0006 a0003c0003t0003g0013 others(48): Show |
79 | HG00140.hp1 HG00621.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.1264+725delT | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778777 | ||||||
| chr2:17778828 | A | ATTATTC | 8 | a0005c0005t0005g0003 a0005c0005t0005g0091 a0005c0005t0008g0003 others(5): Show |
20 | HG00621.hp2 HG00639.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.1264+771_1264+776d others(8): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778828 | ||||||
| chr2:17779013 | T | C | 1 | a0004c0004t0001g0166 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1264+950T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779013 | |||||||
| chr2:17779143 | G | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(93): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.1265-835G>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779143 | |||||||
| chr2:17779189 | C | T | 1 | a0004c0004t0001g0167 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1265-789C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779189 | |||||||
| chr2:17779194 | A | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(72): Show |
120 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1265-784A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779194 | |||||||
| chr2:17779453 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1265-525C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779453 | |||||||
| chr2:17779553 | C | G | 1 | a0013c0015t0037g0100 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1265-425C>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779553 | |||||||
| chr2:17779622 | A | G | 1 | a0004c0004t0001g0042 | 2 | NA18964.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.1265-356A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779622 | |||||||
| chr2:17779670 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1265-308C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779670 | |||||||
| chr2:17779682 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1265-296A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779682 | |||||||
| chr2:17779694 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1265-284C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779694 | |||||||
| chr2:17779709 | C | G | 2 | a0007c0007t0017g0088 a0007c0007t0017g0089 |
2 | HG03130.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1265-269C>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779709 | |||||||
| chr2:17779714 | G | T | 1 | a0001c0001t0001g0131 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1265-264G>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779714 | |||||||
| chr2:17779783 | A | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(156): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1265-195A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779783 | |||||||
| chr2:17779862 | C | T | 12 | a0003c0003t0006g0030 a0003c0003t0006g0056 a0003c0003t0006g0057 others(9): Show |
13 | HG01884.hp1 HG02056.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1265-116C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779862 | |||||||
| chr2:17779863 | G | A | 1 | a0003c0003t0003g0029 | 2 | HG01261.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1265-115G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779863 | |||||||
| chr2:17779920 | G | T | 2 | a0003c0003t0003g0053 a0003c0003t0046g0049 |
2 | HG01496.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1265-58G>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779920 | |||||||
| chr2:17780137 | G | A | 1 | a0010c0010t0002g0081 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1408+16G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 13/13 | chr2 | 17780137 | |||||||
| chr2:17780153 | A | C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0163 |
2 | NA18972.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1408+32A>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 13/13 | chr2 | 17780153 | |||||||
| chr2:17780334 | C | G | 8 | a0005c0005t0005g0003 a0005c0005t0005g0091 a0005c0005t0008g0003 others(5): Show |
20 | HG00621.hp2 HG00639.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.1408+213C>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 13/13 | chr2 | 17780334 | |||||||
| chr2:17780395 | G | A | 2 | a0002c0002t0002g0079 a0009c0008t0038g0045 |
2 | HG02886.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1409-226G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 13/13 | chr2 | 17780395 | |||||||
| chr2:17780524 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1409-97A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 13/13 | chr2 | 17780524 |