Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9896 |
| ensemblid | ENSG00000112367.12 |
| hgncid | 16873 |
| symbol | FIG4 |
| name | FIG4 phosphoinositide 5-phosphatase |
| refseq_nuc | NM_014845.6 |
| refseq_prot | NP_055660.1 |
| ensembl_nuc | ENST00000230124.8 |
| ensembl_prot | ENSP00000230124.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 109691296 |
| end | 109825426 |
| strand | + |
| ver | v1.2 |
| region | chr6:109691296-109825426 |
| region5000 | chr6:109686296-109830426 |
| regionname0 | FIG4_chr6_109691296_109825426 |
| regionname5000 | FIG4_chr6_109686296_109830426 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 907 | 190 | 22 | 44 | 97 | 7 | 18 | 81 | FIG4_chr6_109686296_109830426 | FIG4 | MPTAA others(902): Show |
chr6 | 109686296 | 109830426 |
| a0002 | 0/0 | 907 | 127 | 66 | 14 | 32 | 3 | 12 | 21 | FIG4_chr6_109686296_109830426 | FIG4 | MPTAA others(902): Show |
chr6 | 109686296 | 109830426 |
| a0003 | 0/0 | 907 | 38 | 0 | 7 | 28 | 0 | 3 | 26 | FIG4_chr6_109686296_109830426 | FIG4 | MPTAA others(902): Show |
chr6 | 109686296 | 109830426 |
| a0004 | 0/0 | 907 | 11 | 0 | 1 | 5 | 0 | 5 | 4 | FIG4_chr6_109686296_109830426 | FIG4 | MPTAA others(902): Show |
chr6 | 109686296 | 109830426 |
| a0005 | 0/0 | 907 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | MPTAA others(902): Show |
chr6 | 109686296 | 109830426 |
| a0006 | 0/0 | 907 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | MPTAA others(902): Show |
chr6 | 109686296 | 109830426 |
| a0007 | 0/0 | 319 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | MPTAA others(314): Show |
chr6 | 109686296 | 109830426 |
| a0008 | 0/0 | 907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | MPTAA others(902): Show |
chr6 | 109686296 | 109830426 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2721 | 114 | 18 | 23 | 60 | 3 | 8 | FIG4_chr6_109686296_109830426 | FIG4 | ATGCC others(2716): Show |
chr6 | 109686296 | 109830426 | ||
| a0001c0003 | 0/0 | 2721 | 74 | 4 | 19 | 37 | 4 | 10 | FIG4_chr6_109686296_109830426 | FIG4 | ATGCC others(2716): Show |
chr6 | 109686296 | 109830426 | ||
| a0001c0010 | 0/0 | 2721 | 2 | 0 | 2 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | ATGCC others(2716): Show |
chr6 | 109686296 | 109830426 | ||
| a0002c0002 | 0/0 | 2721 | 83 | 56 | 6 | 16 | 1 | 4 | FIG4_chr6_109686296_109830426 | FIG4 | ATGCC others(2716): Show |
chr6 | 109686296 | 109830426 | ||
| a0002c0004 | 0/0 | 2721 | 38 | 6 | 8 | 14 | 2 | 8 | FIG4_chr6_109686296_109830426 | FIG4 | ATGCC others(2716): Show |
chr6 | 109686296 | 109830426 | ||
| a0002c0009 | 0/0 | 2721 | 3 | 3 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | ATGCC others(2716): Show |
chr6 | 109686296 | 109830426 | ||
| a0002c0012 | 0/0 | 2721 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | ATGCC others(2716): Show |
chr6 | 109686296 | 109830426 | ||
| a0002c0014 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | ATGCC others(2716): Show |
chr6 | 109686296 | 109830426 | ||
| a0002c0015 | 0/0 | 2721 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | ATGCC others(2716): Show |
chr6 | 109686296 | 109830426 | ||
| a0003c0005 | 0/0 | 2721 | 31 | 0 | 7 | 23 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | ATGCC others(2716): Show |
chr6 | 109686296 | 109830426 | ||
| a0003c0007 | 0/0 | 2721 | 5 | 0 | 0 | 3 | 0 | 2 | FIG4_chr6_109686296_109830426 | FIG4 | ATGCC others(2716): Show |
chr6 | 109686296 | 109830426 | ||
| a0003c0017 | 0/0 | 2721 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | ATGCC others(2716): Show |
chr6 | 109686296 | 109830426 | ||
| a0003c0018 | 0/0 | 2721 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | ATGCC others(2716): Show |
chr6 | 109686296 | 109830426 | ||
| a0004c0006 | 0/0 | 2721 | 6 | 0 | 0 | 4 | 0 | 2 | FIG4_chr6_109686296_109830426 | FIG4 | ATGCC others(2716): Show |
chr6 | 109686296 | 109830426 | ||
| a0004c0008 | 0/0 | 2721 | 5 | 0 | 1 | 1 | 0 | 3 | FIG4_chr6_109686296_109830426 | FIG4 | ATGCC others(2716): Show |
chr6 | 109686296 | 109830426 | ||
| a0005c0011 | 0/0 | 2721 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | ATGCC others(2716): Show |
chr6 | 109686296 | 109830426 | ||
| a0006c0016 | 0/0 | 2721 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | ATGCC others(2716): Show |
chr6 | 109686296 | 109830426 | ||
| a0007c0013 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | ATGCC others(2716): Show |
chr6 | 109686296 | 109830426 | ||
| a0008c0019 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | ATGCC others(2716): Show |
chr6 | 109686296 | 109830426 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 1/1 | 3025 | 83 | 13 | 23 | 34 | 3 | 8 | FIG4_chr6_109686296_109830426 | FIG4 | GATCA others(3020): Show |
chr6 | 109686296 | 109830426 |
| a0001c0001t0003 | 0/0 | 3025 | 31 | 5 | 0 | 26 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | GATCA others(3020): Show |
chr6 | 109686296 | 109830426 |
| a0001c0003t0001 | 0/0 | 3025 | 74 | 4 | 19 | 37 | 4 | 10 | FIG4_chr6_109686296_109830426 | FIG4 | GATCA others(3020): Show |
chr6 | 109686296 | 109830426 |
| a0001c0010t0002 | 0/0 | 3025 | 2 | 0 | 2 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | GATCA others(3020): Show |
chr6 | 109686296 | 109830426 |
| a0002c0002t0001 | 0/0 | 3025 | 21 | 0 | 4 | 14 | 1 | 2 | FIG4_chr6_109686296_109830426 | FIG4 | GATCA others(3020): Show |
chr6 | 109686296 | 109830426 |
| a0002c0002t0002 | 0/0 | 3025 | 33 | 31 | 0 | 2 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | GATCA others(3020): Show |
chr6 | 109686296 | 109830426 |
| a0002c0002t0003 | 0/0 | 3025 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | GATCA others(3020): Show |
chr6 | 109686296 | 109830426 |
| a0002c0002t0004 | 0/0 | 3025 | 25 | 21 | 2 | 0 | 0 | 2 | FIG4_chr6_109686296_109830426 | FIG4 | GATCA others(3020): Show |
chr6 | 109686296 | 109830426 |
| a0002c0002t0005 | 0/0 | 3025 | 3 | 3 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | GATCA others(3020): Show |
chr6 | 109686296 | 109830426 |
| a0002c0004t0001 | 0/0 | 3025 | 37 | 5 | 8 | 14 | 2 | 8 | FIG4_chr6_109686296_109830426 | FIG4 | GATCA others(3020): Show |
chr6 | 109686296 | 109830426 |
| a0002c0004t0004 | 0/0 | 3025 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | GATCA others(3020): Show |
chr6 | 109686296 | 109830426 |
| a0002c0009t0002 | 0/0 | 3025 | 3 | 3 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | GATCA others(3020): Show |
chr6 | 109686296 | 109830426 |
| a0002c0012t0001 | 0/0 | 3025 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | GATCA others(3020): Show |
chr6 | 109686296 | 109830426 |
| a0002c0014t0002 | 0/0 | 3025 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | GATCA others(3020): Show |
chr6 | 109686296 | 109830426 |
| a0002c0015t0001 | 0/0 | 3025 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | GATCA others(3020): Show |
chr6 | 109686296 | 109830426 |
| a0003c0005t0001 | 0/0 | 3025 | 31 | 0 | 7 | 23 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | GATCA others(3020): Show |
chr6 | 109686296 | 109830426 |
| a0003c0007t0001 | 0/0 | 3025 | 4 | 0 | 0 | 2 | 0 | 2 | FIG4_chr6_109686296_109830426 | FIG4 | GATCA others(3020): Show |
chr6 | 109686296 | 109830426 |
| a0003c0007t0002 | 0/0 | 3025 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | GATCA others(3020): Show |
chr6 | 109686296 | 109830426 |
| a0003c0017t0001 | 0/0 | 3025 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | GATCA others(3020): Show |
chr6 | 109686296 | 109830426 |
| a0003c0018t0001 | 0/0 | 3025 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | GATCA others(3020): Show |
chr6 | 109686296 | 109830426 |
| a0004c0006t0001 | 0/0 | 3025 | 6 | 0 | 0 | 4 | 0 | 2 | FIG4_chr6_109686296_109830426 | FIG4 | GATCA others(3020): Show |
chr6 | 109686296 | 109830426 |
| a0004c0008t0002 | 0/0 | 3025 | 5 | 0 | 1 | 1 | 0 | 3 | FIG4_chr6_109686296_109830426 | FIG4 | GATCA others(3020): Show |
chr6 | 109686296 | 109830426 |
| a0005c0011t0001 | 0/0 | 3025 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | GATCA others(3020): Show |
chr6 | 109686296 | 109830426 |
| a0006c0016t0001 | 0/0 | 3025 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | GATCA others(3020): Show |
chr6 | 109686296 | 109830426 |
| a0007c0013t0002 | 0/0 | 3025 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | GATCA others(3020): Show |
chr6 | 109686296 | 109830426 |
| a0008c0019t0006 | 0/0 | 3025 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | GATCA others(3020): Show |
chr6 | 109686296 | 109830426 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0058 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0239 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0001t0003g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0003t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0010t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0001c0010t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0002g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0004g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0002t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0004t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0009t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0009t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0009t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0012t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0014t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0002c0015t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0005t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0007t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0007t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0007t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0007t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0007t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0017t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0003c0018t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0004c0006t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0004c0006t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0004c0006t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0004c0006t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0004c0006t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0004c0006t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0004c0008t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0004c0008t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0004c0008t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0004c0008t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0004c0008t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0005c0011t0001g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0006c0016t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0007c0013t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| a0008c0019t0006g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0004 | t0001 | g0041 | EUR | GBR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0243 | EUR | GBR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0054 | EUR | FIN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0153 | EUR | FIN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00408 | hp1 | a0001 | c0003 | t0001 | g0040 | EAS | CHS | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00408 | hp2 | a0001 | c0003 | t0001 | g0265 | EAS | CHS | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | CHS | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00423 | hp2 | a0002 | c0004 | t0001 | g0066 | EAS | CHS | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | CHS | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | CHS | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | CHS | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0354 | EAS | CHS | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | CHS | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | CHS | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00639 | hp1 | a0003 | c0005 | t0001 | g0325 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00735 | hp2 | a0001 | c0003 | t0001 | g0281 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0276 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0173 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01069 | hp2 | a0001 | c0003 | t0001 | g0259 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0282 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01071 | hp2 | a0001 | c0003 | t0001 | g0258 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01081 | hp1 | a0002 | c0002 | t0004 | g0352 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0170 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0262 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0289 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01109 | hp2 | a0001 | c0003 | t0001 | g0280 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0227 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01175 | hp2 | a0003 | c0005 | t0001 | g0345 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0081 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01243 | hp2 | a0002 | c0002 | t0004 | g0207 | AMR | PUR | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01255 | hp2 | a0002 | c0004 | t0001 | g0128 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01256 | hp1 | a0001 | c0003 | t0001 | g0300 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01258 | hp1 | a0001 | c0010 | t0002 | g0030 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01258 | hp2 | a0001 | c0003 | t0001 | g0301 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01261 | hp1 | a0002 | c0004 | t0001 | g0220 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0268 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01346 | hp1 | a0002 | c0004 | t0001 | g0215 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01346 | hp2 | a0001 | c0003 | t0001 | g0302 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01358 | hp2 | a0003 | c0005 | t0001 | g0317 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01361 | hp1 | a0001 | c0003 | t0001 | g0303 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01361 | hp2 | a0002 | c0004 | t0001 | g0232 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01433 | hp1 | a0002 | c0004 | t0001 | g0174 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01433 | hp2 | a0001 | c0003 | t0001 | g0261 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01496 | hp1 | a0004 | c0008 | t0002 | g0315 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01496 | hp2 | a0001 | c0010 | t0002 | g0031 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0051 | EUR | IBS | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01515 | hp2 | a0001 | c0003 | t0001 | g0270 | EUR | IBS | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01517 | hp1 | a0001 | c0003 | t0001 | g0271 | EUR | IBS | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0304 | EUR | IBS | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01928 | hp1 | a0003 | c0005 | t0001 | g0326 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0078 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0132 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01934 | hp2 | a0002 | c0004 | t0001 | g0189 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0130 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01952 | hp1 | a0003 | c0005 | t0001 | g0316 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01952 | hp2 | a0005 | c0011 | t0001 | g0363 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0146 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01975 | hp2 | a0006 | c0016 | t0001 | g0080 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01978 | hp1 | a0001 | c0003 | t0001 | g0296 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01978 | hp2 | a0001 | c0003 | t0001 | g0177 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01993 | hp1 | a0001 | c0003 | t0001 | g0172 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02004 | hp2 | a0003 | c0005 | t0001 | g0312 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | KHV | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02015 | hp2 | a0001 | c0003 | t0001 | g0037 | EAS | KHV | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02056 | hp1 | a0002 | c0004 | t0001 | g0045 | EAS | KHV | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0025 | EAS | KHV | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02071 | hp1 | a0002 | c0004 | t0001 | g0032 | EAS | KHV | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02071 | hp2 | a0004 | c0008 | t0002 | g0310 | EAS | KHV | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02074 | hp1 | a0001 | c0003 | t0001 | g0263 | EAS | KHV | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02074 | hp2 | a0003 | c0005 | t0001 | g0329 | EAS | KHV | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02132 | hp1 | a0002 | c0004 | t0001 | g0043 | EAS | KHV | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02132 | hp2 | a0002 | c0012 | t0001 | g0137 | EAS | KHV | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | KHV | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | KHV | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02148 | hp1 | a0001 | c0003 | t0001 | g0077 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02148 | hp2 | a0002 | c0004 | t0001 | g0129 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02155 | hp1 | a0002 | c0004 | t0001 | g0044 | EAS | CDX | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02155 | hp2 | a0003 | c0005 | t0001 | g0006 | EAS | CDX | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02257 | hp1 | a0002 | c0002 | t0004 | g0208 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02257 | hp2 | a0002 | c0002 | t0002 | g0121 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0279 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02258 | hp2 | a0002 | c0002 | t0004 | g0229 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02280 | hp1 | a0002 | c0002 | t0004 | g0202 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02280 | hp2 | a0002 | c0002 | t0002 | g0013 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0147 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02300 | hp2 | a0003 | c0005 | t0001 | g0327 | AMR | PEL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02451 | hp1 | a0002 | c0002 | t0004 | g0200 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02451 | hp2 | a0002 | c0002 | t0004 | g0294 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02523 | hp1 | a0002 | c0004 | t0001 | g0055 | EAS | KHV | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02523 | hp2 | a0001 | c0003 | t0001 | g0274 | EAS | KHV | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0085 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02602 | hp1 | a0002 | c0004 | t0001 | g0248 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02602 | hp2 | a0001 | c0003 | t0001 | g0285 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02615 | hp1 | a0002 | c0002 | t0002 | g0298 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0361 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0362 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0299 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02647 | hp2 | a0002 | c0002 | t0002 | g0164 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02698 | hp1 | a0002 | c0002 | t0004 | g0186 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02698 | hp2 | a0002 | c0004 | t0001 | g0068 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02717 | hp1 | a0002 | c0002 | t0004 | g0196 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0257 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0226 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02735 | hp1 | a0001 | c0003 | t0001 | g0047 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02735 | hp2 | a0002 | c0004 | t0001 | g0231 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02738 | hp1 | a0001 | c0003 | t0001 | g0028 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0234 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02809 | hp1 | a0002 | c0002 | t0004 | g0228 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02809 | hp2 | a0002 | c0002 | t0002 | g0011 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0360 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02818 | hp2 | a0002 | c0002 | t0002 | g0225 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0116 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0087 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02895 | hp1 | a0002 | c0009 | t0002 | g0159 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02895 | hp2 | a0002 | c0002 | t0002 | g0358 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0155 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02896 | hp2 | a0002 | c0002 | t0004 | g0206 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02897 | hp1 | a0002 | c0009 | t0002 | g0157 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0156 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ESN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02922 | hp2 | a0002 | c0002 | t0004 | g0356 | AFR | ESN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02965 | hp1 | a0002 | c0004 | t0001 | g0205 | AFR | ESN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02965 | hp2 | a0002 | c0002 | t0004 | g0350 | AFR | ESN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02970 | hp1 | a0002 | c0002 | t0004 | g0204 | AFR | ESN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02970 | hp2 | a0002 | c0002 | t0002 | g0114 | AFR | ESN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0110 | AFR | ESN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | ESN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03017 | hp1 | a0003 | c0007 | t0001 | g0328 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03041 | hp1 | a0007 | c0013 | t0002 | g0222 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03041 | hp2 | a0008 | c0019 | t0006 | g0020 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03098 | hp1 | a0002 | c0002 | t0002 | g0118 | AFR | MSL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03098 | hp2 | a0002 | c0002 | t0004 | g0123 | AFR | MSL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03130 | hp1 | a0002 | c0002 | t0002 | g0359 | AFR | ESN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0009 | AFR | ESN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0275 | AFR | ESN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03139 | hp2 | a0002 | c0002 | t0002 | g0117 | AFR | ESN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03209 | hp1 | a0002 | c0002 | t0002 | g0210 | AFR | MSL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03209 | hp2 | a0002 | c0002 | t0004 | g0238 | AFR | MSL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03225 | hp1 | a0002 | c0002 | t0002 | g0086 | AFR | MSL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03225 | hp2 | a0002 | c0002 | t0002 | g0112 | AFR | MSL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03239 | hp1 | a0002 | c0004 | t0001 | g0065 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0347 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03453 | hp1 | a0002 | c0002 | t0005 | g0127 | AFR | MSL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03453 | hp2 | a0002 | c0002 | t0002 | g0016 | AFR | MSL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03486 | hp1 | a0002 | c0002 | t0004 | g0197 | AFR | MSL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03486 | hp2 | a0002 | c0002 | t0002 | g0115 | AFR | MSL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03490 | hp1 | a0001 | c0003 | t0001 | g0269 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03490 | hp2 | a0002 | c0004 | t0001 | g0091 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03516 | hp1 | a0002 | c0004 | t0001 | g0161 | AFR | ESN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03516 | hp2 | a0002 | c0002 | t0004 | g0353 | AFR | ESN | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0014 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03540 | hp2 | a0002 | c0002 | t0002 | g0119 | AFR | GWD | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03579 | hp1 | a0002 | c0004 | t0001 | g0160 | AFR | MSL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0012 | AFR | MSL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03654 | hp1 | a0002 | c0002 | t0004 | g0348 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03654 | hp2 | a0003 | c0005 | t0001 | g0311 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03704 | hp1 | a0002 | c0004 | t0001 | g0295 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03704 | hp2 | a0003 | c0007 | t0001 | g0313 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03710 | hp1 | a0001 | c0003 | t0001 | g0286 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03710 | hp2 | a0002 | c0004 | t0001 | g0076 | SAS | PJL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0349 | SAS | BEB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03831 | hp2 | a0001 | c0003 | t0001 | g0064 | SAS | BEB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03834 | hp1 | a0002 | c0004 | t0001 | g0242 | SAS | BEB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0075 | SAS | BEB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | BEB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03927 | hp2 | a0004 | c0006 | t0001 | g0308 | SAS | BEB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0154 | SAS | BEB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03942 | hp2 | a0004 | c0008 | t0002 | g0323 | SAS | BEB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | BEB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG04184 | hp2 | a0001 | c0003 | t0001 | g0288 | SAS | BEB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG04199 | hp1 | a0001 | c0003 | t0001 | g0251 | SAS | STU | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG04199 | hp2 | a0004 | c0008 | t0002 | g0309 | SAS | STU | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG04204 | hp1 | a0004 | c0008 | t0002 | g0322 | SAS | STU | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG04204 | hp2 | a0001 | c0003 | t0001 | g0089 | SAS | STU | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0233 | SAS | STU | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG04228 | hp2 | a0001 | c0003 | t0001 | g0035 | SAS | STU | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18522 | hp1 | a0002 | c0002 | t0004 | g0010 | AFR | YRI | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18522 | hp2 | a0002 | c0002 | t0002 | g0113 | AFR | YRI | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | CHB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | CHB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | CHB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18747 | hp2 | a0001 | c0003 | t0001 | g0252 | EAS | CHB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18906 | hp1 | a0002 | c0014 | t0002 | g0015 | AFR | YRI | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18906 | hp2 | a0002 | c0002 | t0005 | g0126 | AFR | YRI | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18940 | hp2 | a0003 | c0005 | t0001 | g0005 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18942 | hp2 | a0001 | c0003 | t0001 | g0284 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18943 | hp1 | a0003 | c0005 | t0001 | g0346 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18943 | hp2 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18946 | hp1 | a0002 | c0004 | t0001 | g0057 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18946 | hp2 | a0001 | c0003 | t0001 | g0287 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18947 | hp1 | a0003 | c0005 | t0001 | g0006 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18948 | hp2 | a0003 | c0005 | t0001 | g0250 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18949 | hp2 | a0001 | c0003 | t0001 | g0293 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18951 | hp2 | a0001 | c0003 | t0001 | g0264 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18952 | hp1 | a0003 | c0005 | t0001 | g0330 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18953 | hp2 | a0001 | c0003 | t0001 | g0165 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18956 | hp1 | a0001 | c0003 | t0001 | g0272 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18957 | hp2 | a0001 | c0003 | t0001 | g0273 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18959 | hp2 | a0003 | c0017 | t0001 | g0314 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18960 | hp1 | a0002 | c0004 | t0001 | g0256 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18961 | hp1 | a0001 | c0003 | t0001 | g0253 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18961 | hp2 | a0002 | c0004 | t0001 | g0071 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18962 | hp2 | a0004 | c0006 | t0001 | g0307 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18967 | hp1 | a0003 | c0005 | t0001 | g0334 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18968 | hp2 | a0003 | c0005 | t0001 | g0320 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18969 | hp1 | a0001 | c0003 | t0001 | g0319 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18970 | hp1 | a0003 | c0005 | t0001 | g0072 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0357 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18973 | hp2 | a0003 | c0005 | t0001 | g0341 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18974 | hp2 | a0001 | c0003 | t0001 | g0254 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18975 | hp1 | a0001 | c0003 | t0001 | g0297 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18975 | hp2 | a0001 | c0003 | t0001 | g0048 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18977 | hp2 | a0001 | c0003 | t0001 | g0024 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18978 | hp1 | a0002 | c0004 | t0001 | g0178 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18978 | hp2 | a0001 | c0003 | t0001 | g0266 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18980 | hp2 | a0001 | c0003 | t0001 | g0097 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18982 | hp1 | a0002 | c0004 | t0001 | g0067 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18982 | hp2 | a0003 | c0005 | t0001 | g0332 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18983 | hp1 | a0001 | c0003 | t0001 | g0171 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18983 | hp2 | a0003 | c0005 | t0001 | g0004 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18985 | hp1 | a0002 | c0004 | t0001 | g0070 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18986 | hp1 | a0003 | c0007 | t0001 | g0321 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18990 | hp2 | a0001 | c0003 | t0001 | g0188 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18994 | hp1 | a0001 | c0003 | t0001 | g0291 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18994 | hp2 | a0003 | c0005 | t0001 | g0339 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18995 | hp1 | a0003 | c0005 | t0001 | g0004 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18998 | hp1 | a0001 | c0003 | t0001 | g0018 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18999 | hp1 | a0003 | c0005 | t0001 | g0005 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19002 | hp1 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19002 | hp2 | a0001 | c0003 | t0001 | g0039 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19003 | hp1 | a0003 | c0005 | t0001 | g0333 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19005 | hp1 | a0001 | c0003 | t0001 | g0267 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19005 | hp2 | a0003 | c0005 | t0001 | g0249 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19007 | hp2 | a0002 | c0004 | t0001 | g0140 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19010 | hp2 | a0001 | c0003 | t0001 | g0176 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19012 | hp1 | a0002 | c0015 | t0001 | g0181 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19012 | hp2 | a0004 | c0006 | t0001 | g0306 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19043 | hp1 | a0002 | c0002 | t0005 | g0125 | AFR | LWK | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19043 | hp2 | a0002 | c0002 | t0004 | g0351 | AFR | LWK | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19055 | hp1 | a0002 | c0004 | t0001 | g0131 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19055 | hp2 | a0001 | c0003 | t0001 | g0166 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19056 | hp2 | a0001 | c0003 | t0001 | g0145 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19057 | hp1 | a0004 | c0006 | t0001 | g0340 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0150 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19063 | hp2 | a0003 | c0005 | t0001 | g0335 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19066 | hp2 | a0003 | c0005 | t0001 | g0338 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19075 | hp1 | a0001 | c0003 | t0001 | g0292 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19075 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19079 | hp1 | a0001 | c0003 | t0001 | g0038 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19079 | hp2 | a0003 | c0005 | t0001 | g0331 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19082 | hp1 | a0003 | c0007 | t0002 | g0344 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19084 | hp1 | a0001 | c0003 | t0001 | g0175 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19084 | hp2 | a0003 | c0005 | t0001 | g0336 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19085 | hp2 | a0003 | c0018 | t0001 | g0318 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19086 | hp2 | a0003 | c0005 | t0001 | g0342 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0139 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19088 | hp2 | a0001 | c0003 | t0001 | g0364 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19091 | hp1 | a0004 | c0006 | t0001 | g0337 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0111 | AFR | YRI | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA19240 | hp2 | a0002 | c0009 | t0002 | g0158 | AFR | YRI | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0073 | AFR | ASW | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | ASW | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA20752 | hp1 | a0002 | c0004 | t0001 | g0216 | EUR | TSI | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0260 | EUR | TSI | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0152 | SAS | GIH | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA20905 | hp2 | a0004 | c0006 | t0001 | g0324 | SAS | GIH | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01123 | hp1 | a0002 | c0004 | t0001 | g0219 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0283 | AMR | CLM | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0211 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0278 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02486 | hp2 | a0002 | c0002 | t0002 | g0088 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0017 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG02559 | hp2 | a0002 | c0002 | t0004 | g0201 | AFR | ACB | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03471 | hp1 | a0002 | c0004 | t0001 | g0199 | AFR | MSL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG03471 | hp2 | a0002 | c0002 | t0003 | g0209 | AFR | MSL | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG06807 | hp1 | a0002 | c0004 | t0001 | g0212 | AFR | USA | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| HG06807 | hp2 | a0002 | c0004 | t0004 | g0230 | AFR | USA | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18955 | hp1 | a0003 | c0007 | t0001 | g0343 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA20300 | hp1 | a0002 | c0002 | t0004 | g0305 | AFR | USA | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA20300 | hp2 | a0002 | c0002 | t0004 | g0355 | AFR | USA | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA21309 | hp1 | a0002 | c0002 | t0002 | g0120 | AFR | LWK | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| NA21309 | hp2 | a0002 | c0002 | t0004 | g0203 | AFR | LWK | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0239 | REF | REF | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0058 | REF | REF | FIG4_chr6_109686296_109830426 | FIG4 | chr6 | 109686296 | 109830426 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:109715133 | T | C | 1 | a0005 | 1 | HG01952.hp2 | missense_variant | MODERATE | c.122T>C | p.Ile41Thr | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 2/23 | 262/3025 | 122/2724 | 41/907 | chr6 | 109715133 | |||
| chr6:109741476 | A | G | 1 | a0008 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.808A>G | p.Thr270Ala | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 8/23 | 948/3025 | 808/2724 | 270/907 | chr6 | 109741476 | |||
| chr6:109743192 | C | A | 1 | a0007 | 1 | HG03041.hp1 | stop_gained | HIGH | c.959C>A | p.Ser320* | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 9/23 | 1099/3025 | 959/2724 | 320/907 | chr6 | 109743192 | |||
| chr6:109743725 | A | T | 2 | a0003 a0004 |
49 | HG00639.hp1 HG01175.hp2 HG01358.hp2 others(46): Show |
missense_variant | MODERATE | c.1090A>T | p.Met364Leu | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/23 | 1230/3025 | 1090/2724 | 364/907 | chr6 | 109743725 | |||
| chr6:109760380 | A | G | 1 | a0006 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.1268A>G | p.Lys423Arg | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 11/23 | 1408/3025 | 1268/2724 | 423/907 | chr6 | 109760380 | |||
| chr6:109786314 | T | C | 3 | a0002 a0003 a0006 |
166 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(163): Show |
missense_variant | MODERATE | c.1961T>C | p.Val654Ala | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/23 | 2101/3025 | 1961/2724 | 654/907 | chr6 | 109786314 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:109716531 | G | A | 1 | a0002c0012 | 1 | HG02132.hp2 | synonymous_variant | LOW | c.252G>A | p.Ser84Ser | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/23 | 392/3025 | 252/2724 | 84/907 | chr6 | 109716531 | |||
| chr6:109735199 | C | A | 1 | a0001c0010 | 2 | HG01258.hp1 HG01496.hp2 |
synonymous_variant | LOW | c.547C>A | p.Arg183Arg | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/23 | 687/3025 | 547/2724 | 183/907 | chr6 | 109735199 | |||
| chr6:109760354 | T | C | 1 | a0002c0009 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
synonymous_variant | LOW | c.1242T>C | p.Ile414Ile | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 11/23 | 1382/3025 | 1242/2724 | 414/907 | chr6 | 109760354 | |||
| chr6:109762181 | C | T | 1 | a0003c0018 | 1 | NA19085.hp2 | synonymous_variant | LOW | c.1362C>T | p.Tyr454Tyr | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 12/23 | 1502/3025 | 1362/2724 | 454/907 | chr6 | 109762181 | |||
| chr6:109766730 | T | C | 1 | a0002c0014 | 1 | NA18906.hp1 | splice_region_variant&synonymous_variant | LOW | c.1585T>C | p.Leu529Leu | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/23 | 1725/3025 | 1585/2724 | 529/907 | chr6 | 109766730 | |||
| chr6:109791418 | G | T | 2 | a0002c0015 a0003c0017 |
2 | NA18959.hp2 NA19012.hp1 |
synonymous_variant | LOW | c.2223G>T | p.Thr741Thr | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 20/23 | 2363/3025 | 2223/2724 | 741/907 | chr6 | 109791418 | |||
| chr6:109825100 | G | A | 8 | a0001c0003 a0002c0004 a0002c0015 others(5): Show |
153 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(150): Show |
synonymous_variant | LOW | c.2559G>A | p.Ser853Ser | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 23/23 | 2699/3025 | 2559/2724 | 853/907 | chr6 | 109825100 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:109691315 | G | A | 1 | a0002c0002t0005 | 3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
5_prime_UTR_variant | MODIFIER | c.-121G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/23 | 121 | chr6 | 109691315 | ||||||
| chr6:109691316 | C | T | 1 | a0002c0002t0005 | 3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
5_prime_UTR_variant | MODIFIER | c.-120C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/23 | 120 | chr6 | 109691316 | ||||||
| chr6:109825272 | C | T | 2 | a0001c0001t0003 a0002c0002t0003 |
32 | HG00438.hp1 HG00558.hp2 HG02615.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*7C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 23/23 | 7 | chr6 | 109825272 | ||||||
| chr6:109825279 | C | T | 1 | a0008c0019t0006 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 23/23 | 14 | chr6 | 109825279 | ||||||
| chr6:109825294 | G | A | 2 | a0002c0002t0004 a0002c0004t0004 |
26 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*29G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 23/23 | 29 | chr6 | 109825294 | ||||||
| chr6:109825385 | C | T | 12 | a0001c0003t0001 a0002c0002t0001 a0002c0004t0001 others(9): Show |
179 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*120C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 23/23 | 120 | chr6 | 109825385 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:109691550 | C | T | 1 | a0001c0003t0001g0364 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.66+49C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109691550 | |||||||
| chr6:109691626 | A | G | 1 | a0005c0011t0001g0363 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.66+125A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109691626 | |||||||
| chr6:109691974 | T | C | 2 | a0001c0003t0001g0007 a0001c0003t0001g0008 |
2 | NA18943.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.66+473T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109691974 | |||||||
| chr6:109692033 | A | G | 3 | a0001c0001t0003g0360 a0001c0001t0003g0361 a0001c0001t0003g0362 |
3 | HG02615.hp2 HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.66+532A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109692033 | |||||||
| chr6:109692163 | G | C | 4 | a0002c0002t0002g0009 a0002c0002t0002g0011 a0002c0002t0002g0012 others(1): Show |
4 | HG02809.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+662G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109692163 | |||||||
| chr6:109692307 | A | T | 2 | a0002c0002t0002g0358 a0002c0002t0002g0359 |
2 | HG02895.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.66+806A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109692307 | |||||||
| chr6:109692708 | T | TC | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+1210dupC | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109692708 | ||||||
| chr6:109692744 | C | T | 1 | a0001c0001t0002g0357 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.66+1243C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109692744 | |||||||
| chr6:109692963 | C | T | 2 | a0002c0002t0004g0355 a0002c0002t0004g0356 |
2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.66+1462C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109692963 | |||||||
| chr6:109693031 | A | G | 1 | a0002c0002t0001g0354 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.66+1530A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109693031 | |||||||
| chr6:109693039 | G | A | 1 | a0001c0003t0001g0018 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.66+1538G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109693039 | |||||||
| chr6:109693145 | T | TG | 268 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(265): Show |
272 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(269): Show |
intron_variant | MODIFIER | c.66+1646dupG | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109693145 | ||||||
| chr6:109693190 | G | C | 12 | a0002c0002t0002g0110 a0002c0002t0002g0111 a0002c0002t0002g0112 others(9): Show |
12 | HG02257.hp2 HG02886.hp1 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.66+1689G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109693190 | |||||||
| chr6:109693277 | G | A | 3 | a0001c0001t0003g0360 a0001c0001t0003g0361 a0001c0001t0003g0362 |
3 | HG02615.hp2 HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.66+1776G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109693277 | |||||||
| chr6:109693478 | G | A | 3 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0002c0002t0004g0123 |
3 | HG02622.hp2 HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.66+1977G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109693478 | |||||||
| chr6:109693492 | C | G | 2 | a0002c0002t0002g0016 a0002c0002t0002g0017 |
2 | HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.66+1991C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109693492 | |||||||
| chr6:109693679 | C | T | 268 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(265): Show |
272 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(269): Show |
intron_variant | MODIFIER | c.66+2178C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109693679 | |||||||
| chr6:109693704 | C | A | 3 | a0002c0002t0005g0125 a0002c0002t0005g0126 a0002c0002t0005g0127 |
3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.66+2203C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109693704 | |||||||
| chr6:109693890 | A | G | 116 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(113): Show |
119 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(116): Show |
intron_variant | MODIFIER | c.66+2389A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109693890 | |||||||
| chr6:109693898 | GGTTTT | G | 103 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(100): Show |
104 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.66+2418_66+2422del others(5): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109693898 | ||||||
| chr6:109693898 | GGTTTTGT others(3): Show |
G | 4 | a0001c0001t0003g0244 a0001c0001t0003g0245 a0001c0001t0003g0246 others(1): Show |
4 | NA18939.hp1 NA18940.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+2413_66+2422del others(10): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109693898 | ||||||
| chr6:109693998 | T | TA | 45 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(42): Show |
45 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.66+2504dupA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109693998 | ||||||
| chr6:109694006 | CAA | C | 9 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(6): Show |
9 | HG02280.hp2 HG02559.hp1 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.66+2509_66+2510del others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109694006 | ||||||
| chr6:109694052 | T | G | 3 | a0002c0002t0005g0125 a0002c0002t0005g0126 a0002c0002t0005g0127 |
3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.66+2551T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109694052 | |||||||
| chr6:109694120 | A | G | 101 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(98): Show |
104 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(101): Show |
intron_variant | MODIFIER | c.66+2619A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109694120 | |||||||
| chr6:109694361 | T | C | 3 | a0001c0003t0001g0291 a0001c0003t0001g0292 a0001c0003t0001g0293 |
3 | NA18949.hp2 NA18994.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.66+2860T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109694361 | |||||||
| chr6:109694458 | G | A | 3 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0008c0019t0006g0020 |
3 | HG02145.hp2 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.66+2957G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109694458 | |||||||
| chr6:109694672 | T | C | 116 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(113): Show |
119 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(116): Show |
intron_variant | MODIFIER | c.66+3171T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109694672 | |||||||
| chr6:109694828 | T | C | 1 | a0002c0004t0001g0248 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.66+3327T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109694828 | |||||||
| chr6:109694943 | C | A | 33 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0360 others(30): Show |
33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.66+3442C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109694943 | |||||||
| chr6:109695409 | T | C | 33 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0360 others(30): Show |
33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.66+3908T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109695409 | |||||||
| chr6:109695453 | A | G | 30 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0217 others(27): Show |
30 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.66+3952A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109695453 | |||||||
| chr6:109695458 | G | A | 1 | a0002c0002t0001g0354 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.66+3957G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109695458 | |||||||
| chr6:109695527 | G | A | 9 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(6): Show |
9 | HG02280.hp2 HG02559.hp1 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.66+4026G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109695527 | |||||||
| chr6:109695560 | A | G | 3 | a0002c0002t0005g0125 a0002c0002t0005g0126 a0002c0002t0005g0127 |
3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.66+4059A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109695560 | |||||||
| chr6:109695579 | T | TAC | 96 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(93): Show |
97 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.66+4098_66+4099dup others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109695579 | ||||||
| chr6:109695579 | T | TACAC | 30 | a0001c0003t0001g0319 a0001c0003t0001g0364 a0002c0004t0001g0161 others(27): Show |
31 | HG00639.hp1 HG01358.hp2 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.66+4096_66+4099dup others(4): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109695579 | ||||||
| chr6:109695579 | T | TACACACA others(19): Show |
1 | a0002c0004t0001g0129 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.66+4099_66+4100ins others(26): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109695579 | ||||||
| chr6:109695579 | TAC | T | 13 | a0002c0002t0002g0110 a0002c0002t0002g0111 a0002c0002t0002g0112 others(10): Show |
13 | HG02257.hp2 HG02886.hp1 HG02970.hp2 others(10): Show |
intron_variant | MODIFIER | c.66+4098_66+4099del others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109695579 | ||||||
| chr6:109695581 | C | CACACACA others(15): Show |
2 | a0002c0002t0001g0153 a0002c0002t0001g0154 |
2 | HG00323.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.66+4099_66+4100ins others(22): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109695581 | ||||||
| chr6:109695583 | C | CACACACA others(15): Show |
2 | a0002c0002t0001g0354 a0002c0004t0001g0128 |
2 | HG00544.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.66+4099_66+4100ins others(22): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109695583 | ||||||
| chr6:109695583 | C | CACACACA others(13): Show |
23 | a0001c0003t0001g0145 a0002c0002t0001g0130 a0002c0002t0001g0132 others(20): Show |
23 | HG01934.hp1 HG01943.hp1 HG01975.hp1 others(20): Show |
intron_variant | MODIFIER | c.66+4099_66+4100ins others(20): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109695583 | ||||||
| chr6:109695587 | C | CACACACA others(9): Show |
1 | a0001c0001t0003g0362 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.66+4099_66+4100ins others(16): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109695587 | ||||||
| chr6:109695589 | C | CACACACA others(7): Show |
2 | a0001c0001t0003g0360 a0001c0001t0003g0361 |
2 | HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.66+4099_66+4100ins others(14): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109695589 | ||||||
| chr6:109695595 | C | CACACACA others(3): Show |
1 | a0003c0005t0001g0345 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.66+4099_66+4100ins others(10): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109695595 | ||||||
| chr6:109695599 | C | CACACACA others(3): Show |
1 | a0004c0006t0001g0306 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.66+4099_66+4100ins others(10): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109695599 | ||||||
| chr6:109695599 | C | CACACAG | 15 | a0003c0005t0001g0005 a0003c0005t0001g0006 a0003c0005t0001g0332 others(12): Show |
17 | HG02155.hp2 NA18940.hp2 NA18947.hp1 others(14): Show |
intron_variant | MODIFIER | c.66+4099_66+4100ins others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109695599 | ||||||
| chr6:109695601 | G | C | 51 | a0001c0001t0003g0360 a0001c0001t0003g0361 a0001c0001t0003g0362 others(48): Show |
53 | HG00323.hp2 HG00544.hp2 HG01175.hp2 others(50): Show |
intron_variant | MODIFIER | c.66+4100G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109695601 | |||||||
| chr6:109695601 | G | GAC | 9 | a0001c0001t0002g0104 a0001c0001t0002g0105 a0001c0001t0002g0106 others(6): Show |
9 | HG03453.hp1 NA18906.hp2 NA18967.hp2 others(6): Show |
intron_variant | MODIFIER | c.66+4122_66+4123dup others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109695601 | ||||||
| chr6:109695601 | G | GACACACA others(5): Show |
2 | a0001c0001t0003g0155 a0001c0001t0003g0156 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.66+4112_66+4123dup others(12): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109695601 | ||||||
| chr6:109695601 | GAC | G | 3 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0003t0001g0024 |
3 | HG00544.hp1 NA18612.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.66+4122_66+4123del others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109695601 | ||||||
| chr6:109695653 | G | A | 1 | a0001c0001t0003g0162 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.66+4152G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109695653 | |||||||
| chr6:109695680 | C | G | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.66+4179C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109695680 | |||||||
| chr6:109695705 | G | A | 268 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(265): Show |
272 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(269): Show |
intron_variant | MODIFIER | c.66+4204G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109695705 | |||||||
| chr6:109695880 | A | G | 1 | a0001c0001t0002g0290 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.66+4379A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109695880 | |||||||
| chr6:109696356 | T | G | 1 | a0001c0003t0001g0025 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.66+4855T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109696356 | |||||||
| chr6:109696359 | G | A | 1 | a0001c0001t0003g0026 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.66+4858G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109696359 | |||||||
| chr6:109696392 | A | G | 235 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(232): Show |
239 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(236): Show |
intron_variant | MODIFIER | c.66+4891A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109696392 | |||||||
| chr6:109696397 | C | T | 1 | a0002c0002t0004g0353 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.66+4896C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109696397 | |||||||
| chr6:109696432 | A | G | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.66+4931A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109696432 | |||||||
| chr6:109696464 | G | A | 1 | a0002c0004t0001g0295 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.66+4963G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109696464 | |||||||
| chr6:109696683 | C | T | 1 | a0001c0001t0002g0289 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.66+5182C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109696683 | |||||||
| chr6:109696696 | A | G | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+5195A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109696696 | |||||||
| chr6:109696701 | A | G | 2 | a0001c0001t0003g0155 a0001c0001t0003g0156 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.66+5200A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109696701 | |||||||
| chr6:109696974 | C | T | 1 | a0001c0003t0001g0288 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.66+5473C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109696974 | |||||||
| chr6:109697128 | G | C | 1 | a0002c0002t0001g0130 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.66+5627G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109697128 | |||||||
| chr6:109697146 | T | C | 268 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(265): Show |
272 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(269): Show |
intron_variant | MODIFIER | c.66+5645T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109697146 | |||||||
| chr6:109697261 | C | CA | 30 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0002g0104 others(27): Show |
30 | HG00544.hp1 HG00735.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.66+5778dupA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109697261 | ||||||
| chr6:109697261 | C | CAA | 6 | a0001c0003t0001g0296 a0002c0004t0001g0295 a0002c0009t0002g0157 others(3): Show |
6 | HG01978.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+5777_66+5778dup others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109697261 | ||||||
| chr6:109697270 | A | G | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+5769A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109697270 | |||||||
| chr6:109697360 | G | A | 1 | a0002c0004t0001g0248 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.66+5859G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109697360 | |||||||
| chr6:109697391 | T | C | 4 | a0002c0002t0002g0009 a0002c0002t0002g0011 a0002c0002t0002g0012 others(1): Show |
4 | HG02809.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+5890T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109697391 | |||||||
| chr6:109697394 | A | G | 2 | a0001c0001t0002g0103 a0005c0011t0001g0363 |
2 | HG00741.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.66+5893A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109697394 | |||||||
| chr6:109697661 | C | T | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.66+6160C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109697661 | |||||||
| chr6:109697704 | A | G | 1 | a0001c0003t0001g0243 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.66+6203A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109697704 | |||||||
| chr6:109697889 | AT | A | 180 | a0001c0001t0002g0029 a0001c0001t0002g0198 a0001c0001t0002g0213 others(177): Show |
183 | HG00099.hp2 HG00408.hp2 HG00639.hp1 others(180): Show |
intron_variant | MODIFIER | c.66+6403delT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109697889 | ||||||
| chr6:109697889 | ATT | A | 53 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0003g0003 others(50): Show |
54 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.66+6402_66+6403del others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109697889 | ||||||
| chr6:109697951 | C | A | 33 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0360 others(30): Show |
33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.66+6450C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109697951 | |||||||
| chr6:109698130 | C | T | 4 | a0002c0002t0005g0125 a0002c0002t0005g0126 a0002c0002t0005g0127 others(1): Show |
4 | HG03453.hp1 HG03579.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+6629C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109698130 | |||||||
| chr6:109698189 | G | GT | 45 | a0001c0001t0002g0102 a0001c0001t0003g0155 a0001c0001t0003g0156 others(42): Show |
45 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.66+6700dupT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109698189 | ||||||
| chr6:109698201 | T | A | 2 | a0002c0002t0004g0355 a0002c0002t0004g0356 |
2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.66+6700T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109698201 | |||||||
| chr6:109698405 | T | A | 2 | a0001c0010t0002g0030 a0001c0010t0002g0031 |
2 | HG01258.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.66+6904T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109698405 | |||||||
| chr6:109698432 | T | C | 1 | a0008c0019t0006g0020 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.66+6931T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109698432 | |||||||
| chr6:109698503 | T | C | 5 | a0001c0001t0002g0255 a0001c0003t0001g0252 a0001c0003t0001g0253 others(2): Show |
5 | HG02004.hp1 NA18747.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.66+7002T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109698503 | |||||||
| chr6:109698509 | A | G | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.66+7008A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109698509 | |||||||
| chr6:109698567 | C | T | 2 | a0002c0002t0001g0152 a0002c0002t0001g0154 |
2 | HG03942.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.66+7066C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109698567 | |||||||
| chr6:109698699 | A | G | 3 | a0002c0002t0005g0125 a0002c0002t0005g0126 a0002c0002t0005g0127 |
3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.66+7198A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109698699 | |||||||
| chr6:109698708 | G | A | 4 | a0001c0001t0002g0198 a0002c0002t0004g0196 a0002c0002t0004g0197 others(1): Show |
4 | HG02572.hp1 HG02717.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.66+7207G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109698708 | |||||||
| chr6:109698764 | A | C | 18 | a0001c0001t0002g0002 a0001c0001t0002g0029 a0001c0001t0002g0092 others(15): Show |
19 | HG00423.hp1 NA18747.hp1 NA18953.hp1 others(16): Show |
intron_variant | MODIFIER | c.66+7263A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109698764 | |||||||
| chr6:109698769 | C | T | 3 | a0003c0005t0001g0329 a0003c0005t0001g0330 a0003c0005t0001g0331 |
3 | HG02074.hp2 NA18952.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.66+7268C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109698769 | |||||||
| chr6:109698799 | T | C | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.66+7298T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109698799 | |||||||
| chr6:109699122 | A | G | 1 | a0002c0002t0003g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.66+7621A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699122 | |||||||
| chr6:109699169 | T | C | 1 | a0002c0004t0001g0032 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.66+7668T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699169 | |||||||
| chr6:109699460 | G | A | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+7959G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699460 | |||||||
| chr6:109699480 | C | T | 1 | a0002c0004t0001g0242 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.66+7979C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699480 | |||||||
| chr6:109699498 | GTTTTTTT others(8): Show |
G | 1 | a0001c0001t0002g0347 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.66+8005_66+8019del others(15): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109699498 | ||||||
| chr6:109699499 | T | G | 1 | a0001c0001t0002g0106 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.66+7998T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699499 | |||||||
| chr6:109699525 | C | T | 1 | a0003c0007t0002g0344 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.66+8024C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699525 | |||||||
| chr6:109699526 | G | A | 3 | a0002c0002t0005g0125 a0002c0002t0005g0126 a0002c0002t0005g0127 |
3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.66+8025G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699526 | |||||||
| chr6:109699571 | C | T | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+8070C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699571 | |||||||
| chr6:109699580 | G | A | 3 | a0001c0003t0001g0257 a0001c0003t0001g0258 a0001c0003t0001g0259 |
3 | HG01069.hp2 HG01071.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.66+8079G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699580 | |||||||
| chr6:109699590 | C | T | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+8089C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699590 | |||||||
| chr6:109699605 | T | C | 33 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0360 others(30): Show |
33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.66+8104T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699605 | |||||||
| chr6:109699684 | G | A | 1 | a0004c0008t0002g0310 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.66+8183G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699684 | |||||||
| chr6:109699720 | T | C | 3 | a0002c0002t0004g0200 a0002c0002t0004g0201 a0002c0002t0004g0202 |
3 | HG02280.hp1 HG02451.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.66+8219T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699720 | |||||||
| chr6:109699808 | A | T | 1 | a0008c0019t0006g0020 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.66+8307A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699808 | |||||||
| chr6:109699811 | T | C | 1 | a0001c0001t0003g0027 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.66+8310T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699811 | |||||||
| chr6:109699902 | G | A | 1 | a0002c0004t0001g0215 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.66+8401G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109699902 | |||||||
| chr6:109700114 | T | C | 235 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(232): Show |
239 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(236): Show |
intron_variant | MODIFIER | c.66+8613T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109700114 | |||||||
| chr6:109700162 | A | C | 1 | a0002c0004t0001g0199 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.66+8661A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109700162 | |||||||
| chr6:109700242 | A | G | 33 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0360 others(30): Show |
33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.66+8741A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109700242 | |||||||
| chr6:109700272 | T | G | 33 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0360 others(30): Show |
33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.66+8771T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109700272 | |||||||
| chr6:109700320 | A | G | 1 | a0002c0004t0001g0091 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.66+8819A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109700320 | |||||||
| chr6:109700407 | C | T | 2 | a0001c0001t0002g0090 a0001c0003t0001g0089 |
2 | HG04184.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.66+8906C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109700407 | |||||||
| chr6:109700737 | G | A | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+9236G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109700737 | |||||||
| chr6:109701043 | A | G | 1 | a0002c0002t0004g0208 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.66+9542A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109701043 | |||||||
| chr6:109701099 | G | A | 33 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0360 others(30): Show |
33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.66+9598G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109701099 | |||||||
| chr6:109701209 | C | T | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.66+9708C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109701209 | |||||||
| chr6:109701265 | A | G | 2 | a0001c0001t0003g0194 a0001c0001t0003g0195 |
2 | NA18990.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.66+9764A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109701265 | |||||||
| chr6:109701496 | A | G | 33 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0360 others(30): Show |
33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.66+9995A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109701496 | |||||||
| chr6:109701793 | TG | T | 3 | a0002c0002t0005g0125 a0002c0002t0005g0126 a0002c0002t0005g0127 |
3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.66+10293delG | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109701793 | |||||||
| chr6:109701827 | G | A | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.66+10326G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109701827 | |||||||
| chr6:109701947 | C | A | 4 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(1): Show |
4 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+10446C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109701947 | |||||||
| chr6:109701955 | T | A | 1 | a0001c0003t0001g0018 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.66+10454T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109701955 | |||||||
| chr6:109702006 | G | A | 1 | a0002c0002t0004g0200 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.66+10505G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109702006 | |||||||
| chr6:109702019 | A | G | 2 | a0002c0002t0002g0013 a0002c0002t0002g0014 |
2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.66+10518A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109702019 | |||||||
| chr6:109702119 | T | C | 3 | a0001c0003t0001g0260 a0001c0003t0001g0261 a0001c0003t0001g0262 |
3 | HG01099.hp1 HG01433.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.66+10618T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109702119 | |||||||
| chr6:109702470 | C | T | 275 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0122 others(272): Show |
279 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(276): Show |
intron_variant | MODIFIER | c.66+10969C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109702470 | |||||||
| chr6:109702628 | A | G | 3 | a0002c0002t0005g0125 a0002c0002t0005g0126 a0002c0002t0005g0127 |
3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.66+11127A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109702628 | |||||||
| chr6:109702672 | A | ATTC | 275 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0122 others(272): Show |
279 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(276): Show |
intron_variant | MODIFIER | c.66+11174_66+11176d others(5): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109702672 | ||||||
| chr6:109702814 | C | T | 3 | a0001c0001t0003g0360 a0001c0001t0003g0361 a0001c0001t0003g0362 |
3 | HG02615.hp2 HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.66+11313C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109702814 | |||||||
| chr6:109702908 | G | C | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.66+11407G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109702908 | |||||||
| chr6:109702914 | A | G | 1 | a0003c0007t0001g0328 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.66+11413A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109702914 | |||||||
| chr6:109702973 | T | C | 4 | a0001c0001t0002g0347 a0001c0001t0002g0349 a0002c0002t0004g0348 others(1): Show |
4 | HG02965.hp2 HG03239.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.66+11472T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109702973 | |||||||
| chr6:109703099 | A | AT | 101 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(98): Show |
104 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(101): Show |
intron_variant | MODIFIER | c.66+11608dupT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109703099 | ||||||
| chr6:109703113 | C | A | 47 | a0001c0003t0001g0319 a0001c0003t0001g0364 a0003c0005t0001g0004 others(44): Show |
50 | HG00639.hp1 HG01175.hp2 HG01358.hp2 others(47): Show |
intron_variant | MODIFIER | c.66+11612C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109703113 | |||||||
| chr6:109703263 | A | G | 48 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(45): Show |
48 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.66+11762A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109703263 | |||||||
| chr6:109703618 | T | A | 3 | a0002c0002t0005g0125 a0002c0002t0005g0126 a0002c0002t0005g0127 |
3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.67-11460T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109703618 | |||||||
| chr6:109703725 | A | G | 1 | a0001c0001t0002g0101 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.67-11353A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109703725 | |||||||
| chr6:109703752 | C | T | 1 | a0001c0001t0002g0241 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.67-11326C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109703752 | |||||||
| chr6:109703755 | T | G | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.67-11323T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109703755 | |||||||
| chr6:109703756 | C | A | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.67-11322C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109703756 | |||||||
| chr6:109703759 | T | C | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.67-11319T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109703759 | |||||||
| chr6:109704415 | G | A | 9 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(6): Show |
9 | HG02280.hp2 HG02559.hp1 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.67-10663G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109704415 | |||||||
| chr6:109704476 | C | G | 4 | a0002c0002t0002g0085 a0002c0002t0002g0086 a0002c0002t0002g0087 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-10602C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109704476 | |||||||
| chr6:109704651 | G | C | 59 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0003g0003 others(56): Show |
60 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.67-10427G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109704651 | |||||||
| chr6:109704675 | C | CA | 8 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0022 others(5): Show |
8 | HG00544.hp1 HG01106.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.67-10380dupA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109704675 | ||||||
| chr6:109704675 | CA | C | 213 | a0001c0001t0002g0083 a0001c0001t0002g0084 a0001c0001t0002g0100 others(210): Show |
217 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.67-10380delA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109704675 | ||||||
| chr6:109704675 | CAA | C | 16 | a0001c0001t0002g0240 a0001c0001t0003g0190 a0001c0003t0001g0259 others(13): Show |
16 | HG00639.hp2 HG01069.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.67-10381_67-10380d others(4): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109704675 | ||||||
| chr6:109704702 | G | A | 4 | a0002c0002t0002g0009 a0002c0002t0002g0011 a0002c0002t0002g0012 others(1): Show |
4 | HG02809.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-10376G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109704702 | |||||||
| chr6:109704759 | A | T | 3 | a0003c0005t0001g0325 a0003c0005t0001g0326 a0003c0005t0001g0327 |
3 | HG00639.hp1 HG01928.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.67-10319A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109704759 | |||||||
| chr6:109704760 | A | T | 3 | a0003c0005t0001g0325 a0003c0005t0001g0326 a0003c0005t0001g0327 |
3 | HG00639.hp1 HG01928.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.67-10318A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109704760 | |||||||
| chr6:109704776 | G | A | 1 | a0002c0002t0002g0110 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.67-10302G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109704776 | |||||||
| chr6:109705156 | G | A | 7 | a0001c0001t0002g0347 a0001c0001t0002g0349 a0002c0002t0004g0348 others(4): Show |
7 | HG01081.hp1 HG02965.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-9922G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109705156 | |||||||
| chr6:109705369 | C | T | 1 | a0002c0002t0002g0121 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.67-9709C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109705369 | |||||||
| chr6:109705394 | G | T | 2 | a0001c0001t0003g0155 a0001c0001t0003g0156 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.67-9684G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109705394 | |||||||
| chr6:109705456 | T | C | 3 | a0002c0002t0005g0125 a0002c0002t0005g0126 a0002c0002t0005g0127 |
3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.67-9622T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109705456 | |||||||
| chr6:109705657 | A | G | 4 | a0002c0002t0002g0085 a0002c0002t0002g0086 a0002c0002t0002g0087 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-9421A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109705657 | |||||||
| chr6:109705769 | A | G | 1 | a0002c0002t0004g0200 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.67-9309A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109705769 | |||||||
| chr6:109705865 | A | G | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-9213A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109705865 | |||||||
| chr6:109705950 | T | C | 4 | a0002c0002t0005g0125 a0002c0002t0005g0126 a0002c0002t0005g0127 others(1): Show |
4 | HG03453.hp1 HG03579.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-9128T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109705950 | |||||||
| chr6:109706059 | T | C | 268 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(265): Show |
272 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(269): Show |
intron_variant | MODIFIER | c.67-9019T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109706059 | |||||||
| chr6:109706088 | A | G | 9 | a0001c0001t0002g0001 a0001c0001t0002g0078 a0001c0001t0002g0079 others(6): Show |
10 | HG01243.hp1 HG01258.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.67-8990A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109706088 | |||||||
| chr6:109706464 | T | A | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.67-8614T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109706464 | |||||||
| chr6:109706482 | C | T | 1 | a0002c0004t0001g0076 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.67-8596C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109706482 | |||||||
| chr6:109706514 | G | A | 116 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(113): Show |
119 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(116): Show |
intron_variant | MODIFIER | c.67-8564G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109706514 | |||||||
| chr6:109706632 | C | T | 1 | a0002c0004t0001g0212 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.67-8446C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109706632 | |||||||
| chr6:109706740 | G | T | 116 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(113): Show |
119 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(116): Show |
intron_variant | MODIFIER | c.67-8338G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109706740 | |||||||
| chr6:109706873 | G | C | 48 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(45): Show |
48 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.67-8205G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109706873 | |||||||
| chr6:109706902 | C | T | 275 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0122 others(272): Show |
279 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(276): Show |
intron_variant | MODIFIER | c.67-8176C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109706902 | |||||||
| chr6:109707108 | A | T | 33 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0360 others(30): Show |
33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.67-7970A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707108 | |||||||
| chr6:109707154 | T | A | 68 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0003g0003 others(65): Show |
69 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.67-7924T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707154 | |||||||
| chr6:109707281 | A | G | 59 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0003g0003 others(56): Show |
60 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.67-7797A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707281 | |||||||
| chr6:109707289 | A | ATG | 14 | a0002c0002t0002g0009 a0002c0002t0002g0011 a0002c0002t0002g0012 others(11): Show |
14 | HG01081.hp1 HG02280.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.67-7788_67-7787ins others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109707289 | ||||||
| chr6:109707291 | A | ATATG | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.67-7786_67-7785ins others(4): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109707291 | ||||||
| chr6:109707291 | A | ATG | 14 | a0001c0001t0002g0299 a0001c0001t0002g0304 a0001c0003t0001g0291 others(11): Show |
14 | HG01256.hp1 HG01258.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.67-7771_67-7770dup others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109707291 | ||||||
| chr6:109707291 | A | ATGTG | 58 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0003g0003 others(55): Show |
59 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.67-7773_67-7770dup others(4): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109707291 | ||||||
| chr6:109707291 | A | ATGTGTG | 34 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0360 others(31): Show |
34 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.67-7775_67-7770dup others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109707291 | ||||||
| chr6:109707291 | A | G | 110 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(107): Show |
113 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(110): Show |
intron_variant | MODIFIER | c.67-7787A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707291 | |||||||
| chr6:109707293 | G | A | 48 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(45): Show |
48 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.67-7785G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707293 | |||||||
| chr6:109707331 | G | GTA | 59 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0003g0003 others(56): Show |
60 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.67-7738_67-7737dup others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109707331 | ||||||
| chr6:109707346 | T | C | 5 | a0001c0003t0001g0263 a0001c0003t0001g0264 a0001c0003t0001g0265 others(2): Show |
5 | HG00408.hp2 HG02074.hp1 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-7732T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707346 | |||||||
| chr6:109707362 | CGT | C | 224 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(221): Show |
228 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(225): Show |
intron_variant | MODIFIER | c.67-7713_67-7712del others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109707362 | ||||||
| chr6:109707363 | GTGTA | G | 39 | a0001c0001t0002g0282 a0001c0001t0002g0283 a0001c0001t0003g0155 others(36): Show |
39 | HG00323.hp2 HG00544.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.67-7713_67-7710del others(4): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109707363 | ||||||
| chr6:109707365 | G | A | 3 | a0002c0002t0002g0210 a0002c0002t0004g0203 a0002c0002t0004g0204 |
3 | HG02970.hp1 HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.67-7713G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707365 | |||||||
| chr6:109707372 | T | TATACATA others(21): Show |
2 | a0002c0002t0004g0203 a0002c0002t0004g0204 |
2 | HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.67-7703_67-7702ins others(28): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109707372 | ||||||
| chr6:109707387 | A | C | 2 | a0002c0002t0004g0203 a0002c0002t0004g0204 |
2 | HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.67-7691A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707387 | |||||||
| chr6:109707410 | T | C | 13 | a0001c0001t0002g0299 a0001c0001t0002g0304 a0001c0003t0001g0291 others(10): Show |
13 | HG01256.hp1 HG01258.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.67-7668T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707410 | |||||||
| chr6:109707538 | G | A | 1 | a0002c0002t0004g0201 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.67-7540G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707538 | |||||||
| chr6:109707578 | C | T | 4 | a0004c0006t0001g0324 a0004c0008t0002g0309 a0004c0008t0002g0322 others(1): Show |
4 | HG03942.hp2 HG04199.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-7500C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707578 | |||||||
| chr6:109707610 | T | C | 275 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0122 others(272): Show |
279 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(276): Show |
intron_variant | MODIFIER | c.67-7468T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707610 | |||||||
| chr6:109707721 | T | A | 1 | a0001c0003t0001g0035 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.67-7357T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707721 | |||||||
| chr6:109707759 | G | A | 59 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0003g0003 others(56): Show |
60 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.67-7319G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707759 | |||||||
| chr6:109707763 | A | G | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.67-7315A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707763 | |||||||
| chr6:109707817 | A | T | 1 | a0002c0014t0002g0015 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.67-7261A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109707817 | |||||||
| chr6:109707992 | C | CT | 49 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(46): Show |
49 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.67-7072dupT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109707992 | ||||||
| chr6:109708281 | C | T | 1 | a0001c0001t0002g0214 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.67-6797C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109708281 | |||||||
| chr6:109708439 | G | T | 1 | a0002c0002t0002g0210 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.67-6639G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109708439 | |||||||
| chr6:109708527 | C | T | 54 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(51): Show |
54 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.67-6551C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109708527 | |||||||
| chr6:109708822 | G | A | 4 | a0002c0002t0002g0009 a0002c0002t0002g0011 a0002c0002t0002g0012 others(1): Show |
4 | HG02809.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-6256G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109708822 | |||||||
| chr6:109708858 | A | G | 1 | a0003c0007t0001g0321 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.67-6220A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109708858 | |||||||
| chr6:109708880 | C | A | 268 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(265): Show |
272 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(269): Show |
intron_variant | MODIFIER | c.67-6198C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109708880 | |||||||
| chr6:109709225 | T | C | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.67-5853T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109709225 | |||||||
| chr6:109709314 | G | A | 1 | a0003c0005t0001g0311 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.67-5764G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109709314 | |||||||
| chr6:109709376 | A | G | 59 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0003g0003 others(56): Show |
60 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.67-5702A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109709376 | |||||||
| chr6:109709769 | G | T | 12 | a0002c0002t0002g0110 a0002c0002t0002g0111 a0002c0002t0002g0112 others(9): Show |
12 | HG02257.hp2 HG02886.hp1 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.67-5309G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109709769 | |||||||
| chr6:109709887 | G | T | 2 | a0001c0001t0003g0155 a0001c0001t0003g0156 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.67-5191G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109709887 | |||||||
| chr6:109710007 | G | A | 2 | a0002c0002t0002g0210 a0002c0004t0001g0212 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.67-5071G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109710007 | |||||||
| chr6:109710074 | T | G | 1 | a0001c0003t0001g0291 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.67-5004T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109710074 | |||||||
| chr6:109710079 | T | C | 1 | a0001c0003t0001g0028 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.67-4999T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109710079 | |||||||
| chr6:109710118 | A | T | 268 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(265): Show |
272 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(269): Show |
intron_variant | MODIFIER | c.67-4960A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109710118 | |||||||
| chr6:109710382 | T | C | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-4696T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109710382 | |||||||
| chr6:109710571 | A | G | 1 | a0001c0001t0002g0241 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.67-4507A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109710571 | |||||||
| chr6:109710709 | C | T | 2 | a0001c0001t0002g0074 a0001c0001t0002g0075 |
2 | HG03834.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.67-4369C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109710709 | |||||||
| chr6:109710742 | C | A | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.67-4336C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109710742 | |||||||
| chr6:109710744 | A | T | 3 | a0001c0003t0001g0279 a0001c0003t0001g0280 a0001c0003t0001g0281 |
3 | HG00735.hp2 HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.67-4334A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109710744 | |||||||
| chr6:109710909 | T | TC | 57 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(54): Show |
57 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.67-4169_67-4168ins others(1): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109710909 | |||||||
| chr6:109710909 | T | TCA | 58 | a0001c0001t0002g0299 a0001c0001t0002g0304 a0001c0003t0001g0291 others(55): Show |
60 | HG00639.hp1 HG01175.hp2 HG01256.hp1 others(57): Show |
intron_variant | MODIFIER | c.67-4169_67-4168ins others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109710909 | |||||||
| chr6:109710909 | TA | T | 16 | a0002c0002t0001g0130 a0002c0002t0001g0149 a0002c0002t0002g0110 others(13): Show |
16 | HG01943.hp1 HG01952.hp2 HG02135.hp2 others(13): Show |
intron_variant | MODIFIER | c.67-4157delA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr6 | 109710909 | ||||||
| chr6:109710910 | A | C | 137 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(134): Show |
138 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.67-4168A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109710910 | |||||||
| chr6:109710910 | A | T | 4 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0002c0002t0002g0073 others(1): Show |
4 | HG02145.hp2 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-4168A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109710910 | |||||||
| chr6:109710911 | A | C | 15 | a0002c0002t0001g0130 a0002c0002t0001g0149 a0002c0002t0002g0110 others(12): Show |
15 | HG01943.hp1 HG02135.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.67-4167A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109710911 | |||||||
| chr6:109711025 | G | C | 48 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(45): Show |
48 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.67-4053G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109711025 | |||||||
| chr6:109711154 | C | T | 3 | a0002c0002t0005g0125 a0002c0002t0005g0126 a0002c0002t0005g0127 |
3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.67-3924C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109711154 | |||||||
| chr6:109711201 | C | T | 48 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(45): Show |
48 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.67-3877C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109711201 | |||||||
| chr6:109711227 | G | A | 1 | a0001c0003t0001g0267 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.67-3851G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109711227 | |||||||
| chr6:109711263 | G | A | 1 | a0001c0003t0001g0284 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.67-3815G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109711263 | |||||||
| chr6:109711377 | C | T | 152 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(149): Show |
153 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.67-3701C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109711377 | |||||||
| chr6:109711385 | C | G | 3 | a0002c0002t0005g0125 a0002c0002t0005g0126 a0002c0002t0005g0127 |
3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.67-3693C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109711385 | |||||||
| chr6:109711786 | G | A | 1 | a0002c0002t0002g0210 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.67-3292G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109711786 | |||||||
| chr6:109711833 | T | C | 1 | a0001c0003t0001g0297 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.67-3245T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109711833 | |||||||
| chr6:109712045 | G | C | 4 | a0004c0006t0001g0324 a0004c0008t0002g0309 a0004c0008t0002g0322 others(1): Show |
4 | HG03942.hp2 HG04199.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-3033G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109712045 | |||||||
| chr6:109712088 | T | C | 2 | a0001c0001t0002g0299 a0002c0002t0002g0298 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.67-2990T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109712088 | |||||||
| chr6:109712246 | C | G | 3 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0008c0019t0006g0020 |
3 | HG02145.hp2 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.67-2832C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109712246 | |||||||
| chr6:109712391 | G | A | 1 | a0001c0003t0001g0262 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.67-2687G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109712391 | |||||||
| chr6:109712525 | G | C | 50 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(47): Show |
50 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.67-2553G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109712525 | |||||||
| chr6:109712705 | A | G | 1 | a0001c0003t0001g0243 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.67-2373A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109712705 | |||||||
| chr6:109712824 | C | T | 1 | a0002c0004t0001g0091 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.67-2254C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109712824 | |||||||
| chr6:109713052 | C | T | 48 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(45): Show |
48 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.67-2026C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109713052 | |||||||
| chr6:109713188 | G | A | 54 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(51): Show |
54 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.67-1890G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109713188 | |||||||
| chr6:109713208 | G | A | 2 | a0002c0004t0001g0215 a0002c0004t0001g0216 |
2 | HG01346.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.67-1870G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109713208 | |||||||
| chr6:109713225 | C | T | 14 | a0001c0001t0002g0299 a0001c0001t0002g0304 a0001c0003t0001g0291 others(11): Show |
14 | HG01256.hp1 HG01258.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.67-1853C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109713225 | |||||||
| chr6:109713292 | G | T | 2 | a0001c0001t0003g0194 a0001c0001t0003g0195 |
2 | NA18990.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.67-1786G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109713292 | |||||||
| chr6:109713636 | C | T | 49 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(46): Show |
49 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.67-1442C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109713636 | |||||||
| chr6:109713752 | G | A | 1 | a0001c0001t0002g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.67-1326G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109713752 | |||||||
| chr6:109713795 | C | T | 59 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0003g0003 others(56): Show |
60 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.67-1283C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109713795 | |||||||
| chr6:109713855 | G | T | 1 | a0002c0004t0001g0129 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.67-1223G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109713855 | |||||||
| chr6:109713947 | C | T | 1 | a0002c0002t0004g0294 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.67-1131C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109713947 | |||||||
| chr6:109714045 | C | A | 1 | a0002c0002t0002g0358 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.67-1033C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109714045 | |||||||
| chr6:109714089 | G | T | 1 | a0002c0002t0002g0012 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.67-989G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109714089 | |||||||
| chr6:109714522 | A | G | 2 | a0001c0001t0003g0155 a0001c0001t0003g0156 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.67-556A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109714522 | |||||||
| chr6:109714672 | T | C | 59 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0003g0003 others(56): Show |
60 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.67-406T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109714672 | |||||||
| chr6:109714709 | C | T | 1 | a0001c0001t0002g0214 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.67-369C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109714709 | |||||||
| chr6:109714913 | T | C | 59 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0003g0003 others(56): Show |
60 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.67-165T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109714913 | |||||||
| chr6:109715071 | T | C | 14 | a0001c0001t0002g0299 a0001c0001t0002g0304 a0001c0003t0001g0291 others(11): Show |
14 | HG01256.hp1 HG01258.hp2 HG01346.hp2 others(11): Show |
splice_region_variant&intron_variant | LOW | c.67-7T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 1/22 | chr6 | 109715071 | |||||||
| chr6:109715276 | A | T | 47 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(44): Show |
47 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.165+100A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 2/22 | chr6 | 109715276 | |||||||
| chr6:109715404 | C | T | 4 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 others(1): Show |
4 | HG02071.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+228C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 2/22 | chr6 | 109715404 | |||||||
| chr6:109715426 | GAT | G | 16 | a0001c0001t0002g0002 a0001c0001t0002g0029 a0001c0001t0002g0036 others(13): Show |
17 | NA18747.hp1 NA18953.hp1 NA18967.hp2 others(14): Show |
intron_variant | MODIFIER | c.165+252_165+253del others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr6 | 109715426 | ||||||
| chr6:109715504 | C | T | 117 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(114): Show |
120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.165+328C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 2/22 | chr6 | 109715504 | |||||||
| chr6:109715560 | C | A | 117 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(114): Show |
120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.165+384C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 2/22 | chr6 | 109715560 | |||||||
| chr6:109715860 | G | A | 1 | a0002c0002t0003g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.166-585G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 2/22 | chr6 | 109715860 | |||||||
| chr6:109716196 | A | C | 1 | a0001c0001t0002g0096 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.166-249A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 2/22 | chr6 | 109716196 | |||||||
| chr6:109716719 | A | G | 3 | a0002c0002t0005g0125 a0002c0002t0005g0126 a0002c0002t0005g0127 |
3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.289+151A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109716719 | |||||||
| chr6:109716848 | A | G | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.289+280A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109716848 | |||||||
| chr6:109716899 | G | A | 273 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(270): Show |
277 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(274): Show |
intron_variant | MODIFIER | c.289+331G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109716899 | |||||||
| chr6:109716921 | G | A | 3 | a0002c0002t0002g0009 a0002c0002t0002g0011 a0002c0002t0004g0010 |
3 | HG02809.hp2 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.289+353G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109716921 | |||||||
| chr6:109717008 | C | CT | 137 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0122 others(134): Show |
138 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.289+457dupT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr6 | 109717008 | ||||||
| chr6:109717008 | C | CTT | 7 | a0001c0001t0002g0198 a0002c0002t0001g0130 a0002c0002t0005g0125 others(4): Show |
7 | HG01943.hp1 HG02572.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.289+456_289+457dup others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr6 | 109717008 | ||||||
| chr6:109717437 | A | G | 269 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(266): Show |
273 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(270): Show |
intron_variant | MODIFIER | c.289+869A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109717437 | |||||||
| chr6:109717719 | C | G | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.289+1151C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109717719 | |||||||
| chr6:109717762 | G | T | 1 | a0002c0004t0001g0189 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.289+1194G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109717762 | |||||||
| chr6:109717951 | C | T | 152 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(149): Show |
153 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.289+1383C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109717951 | |||||||
| chr6:109717958 | G | A | 1 | a0002c0014t0002g0015 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.289+1390G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109717958 | |||||||
| chr6:109718216 | A | G | 2 | a0002c0004t0001g0070 a0002c0004t0001g0071 |
2 | NA18961.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.289+1648A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109718216 | |||||||
| chr6:109718283 | C | T | 1 | a0001c0001t0002g0095 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.289+1715C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109718283 | |||||||
| chr6:109718537 | G | T | 60 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0003g0003 others(57): Show |
61 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.289+1969G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109718537 | |||||||
| chr6:109718639 | C | T | 56 | a0001c0001t0003g0003 a0001c0001t0003g0162 a0001c0001t0003g0163 others(53): Show |
57 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.289+2071C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109718639 | |||||||
| chr6:109718818 | A | G | 1 | a0002c0002t0004g0204 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.289+2250A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109718818 | |||||||
| chr6:109718912 | C | T | 3 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0004g0238 |
3 | HG02280.hp2 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.289+2344C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109718912 | |||||||
| chr6:109718920 | A | AT | 103 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(100): Show |
104 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.289+2368dupT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr6 | 109718920 | ||||||
| chr6:109718920 | AT | A | 54 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(51): Show |
54 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.289+2368delT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr6 | 109718920 | ||||||
| chr6:109718953 | G | A | 1 | a0001c0003t0001g0037 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.289+2385G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109718953 | |||||||
| chr6:109719323 | C | T | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.289+2755C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109719323 | |||||||
| chr6:109719532 | T | C | 1 | a0002c0002t0004g0196 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.289+2964T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109719532 | |||||||
| chr6:109719535 | C | T | 2 | a0001c0001t0002g0299 a0002c0002t0002g0298 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.289+2967C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109719535 | |||||||
| chr6:109719740 | T | C | 1 | a0001c0003t0001g0288 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.289+3172T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109719740 | |||||||
| chr6:109719931 | G | T | 1 | a0002c0004t0001g0189 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.289+3363G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109719931 | |||||||
| chr6:109720344 | A | T | 3 | a0002c0002t0005g0125 a0002c0002t0005g0126 a0002c0002t0005g0127 |
3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.289+3776A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109720344 | |||||||
| chr6:109720442 | T | C | 1 | a0002c0004t0001g0131 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.289+3874T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109720442 | |||||||
| chr6:109720448 | A | G | 1 | a0001c0001t0002g0124 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.289+3880A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109720448 | |||||||
| chr6:109720618 | A | G | 1 | a0002c0002t0004g0352 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.289+4050A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109720618 | |||||||
| chr6:109720638 | T | A | 1 | a0003c0005t0001g0332 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.289+4070T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109720638 | |||||||
| chr6:109720712 | T | G | 2 | a0002c0002t0004g0355 a0002c0002t0004g0356 |
2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.289+4144T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109720712 | |||||||
| chr6:109720819 | C | T | 1 | a0001c0003t0001g0281 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.289+4251C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109720819 | |||||||
| chr6:109720820 | G | A | 1 | a0004c0006t0001g0307 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.289+4252G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109720820 | |||||||
| chr6:109721054 | C | T | 1 | a0001c0003t0001g0278 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.289+4486C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109721054 | |||||||
| chr6:109721096 | G | A | 9 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0003t0001g0024 others(6): Show |
9 | HG00408.hp1 HG00544.hp1 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.289+4528G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109721096 | |||||||
| chr6:109721359 | G | C | 270 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(267): Show |
274 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(271): Show |
intron_variant | MODIFIER | c.289+4791G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109721359 | |||||||
| chr6:109721366 | C | T | 1 | a0001c0001t0003g0193 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.289+4798C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109721366 | |||||||
| chr6:109721577 | G | A | 65 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0221 others(62): Show |
66 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.289+5009G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109721577 | |||||||
| chr6:109721713 | A | G | 2 | a0002c0004t0001g0219 a0002c0004t0001g0220 |
2 | HG01123.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.289+5145A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109721713 | |||||||
| chr6:109722161 | T | C | 65 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0221 others(62): Show |
66 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.290-4948T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109722161 | |||||||
| chr6:109722396 | C | T | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.290-4713C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109722396 | |||||||
| chr6:109722480 | A | G | 1 | a0001c0003t0001g0188 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.290-4629A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109722480 | |||||||
| chr6:109722525 | G | GAC | 4 | a0002c0002t0002g0085 a0002c0002t0002g0086 a0002c0002t0002g0087 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-4572_290-4571d others(4): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr6 | 109722525 | ||||||
| chr6:109722610 | T | TTA | 4 | a0001c0003t0001g0300 a0001c0003t0001g0301 a0002c0002t0002g0298 others(1): Show |
4 | HG01256.hp1 HG01258.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.290-4483_290-4482d others(4): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr6 | 109722610 | ||||||
| chr6:109722702 | A | G | 1 | a0003c0005t0001g0327 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.290-4407A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109722702 | |||||||
| chr6:109722735 | AG | A | 117 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(114): Show |
120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.290-4371delG | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr6 | 109722735 | ||||||
| chr6:109722996 | CA | C | 270 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(267): Show |
274 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(271): Show |
intron_variant | MODIFIER | c.290-4111delA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr6 | 109722996 | ||||||
| chr6:109723059 | C | T | 1 | a0001c0001t0002g0069 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.290-4050C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109723059 | |||||||
| chr6:109723237 | G | A | 1 | a0002c0004t0001g0041 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.290-3872G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109723237 | |||||||
| chr6:109723808 | T | C | 1 | a0003c0005t0001g0345 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.290-3301T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109723808 | |||||||
| chr6:109724018 | G | A | 2 | a0002c0002t0002g0016 a0002c0002t0002g0017 |
2 | HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.290-3091G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109724018 | |||||||
| chr6:109724073 | C | T | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.290-3036C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109724073 | |||||||
| chr6:109724110 | C | T | 2 | a0001c0001t0002g0069 a0002c0004t0001g0068 |
2 | HG01169.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.290-2999C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109724110 | |||||||
| chr6:109724120 | G | A | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.290-2989G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109724120 | |||||||
| chr6:109724140 | C | T | 1 | a0001c0001t0003g0187 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.290-2969C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109724140 | |||||||
| chr6:109724278 | C | T | 3 | a0001c0001t0002g0198 a0002c0002t0004g0196 a0002c0004t0001g0199 |
3 | HG02572.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.290-2831C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109724278 | |||||||
| chr6:109724330 | C | T | 1 | a0003c0007t0001g0343 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.290-2779C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109724330 | |||||||
| chr6:109724364 | T | C | 4 | a0002c0002t0002g0009 a0002c0002t0002g0011 a0002c0002t0002g0012 others(1): Show |
4 | HG02809.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-2745T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109724364 | |||||||
| chr6:109724803 | T | TTG | 7 | a0001c0001t0003g0360 a0001c0001t0003g0361 a0001c0001t0003g0362 others(4): Show |
7 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.290-2278_290-2277d others(4): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr6 | 109724803 | ||||||
| chr6:109724803 | T | TTGTG | 14 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0002c0002t0002g0013 others(11): Show |
14 | HG02280.hp2 HG02559.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.290-2280_290-2277d others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr6 | 109724803 | ||||||
| chr6:109724803 | T | TTGTGTG | 4 | a0002c0002t0002g0088 a0002c0002t0005g0125 a0002c0002t0005g0126 others(1): Show |
4 | HG02486.hp2 HG03453.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-2282_290-2277d others(8): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr6 | 109724803 | ||||||
| chr6:109724803 | TTG | T | 50 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(47): Show |
50 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.290-2278_290-2277d others(4): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr6 | 109724803 | ||||||
| chr6:109724830 | T | TAC | 8 | a0001c0003t0001g0285 a0001c0003t0001g0296 a0001c0003t0001g0297 others(5): Show |
8 | HG01346.hp2 HG01361.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.290-2279_290-2278i others(4): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109724830 | |||||||
| chr6:109724831 | G | A | 112 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(109): Show |
114 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(111): Show |
intron_variant | MODIFIER | c.290-2278G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109724831 | |||||||
| chr6:109724832 | T | C | 103 | a0001c0001t0002g0255 a0001c0001t0002g0282 a0001c0001t0002g0283 others(100): Show |
105 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(102): Show |
intron_variant | MODIFIER | c.290-2277T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109724832 | |||||||
| chr6:109724834 | C | CAT | 12 | a0001c0003t0001g0018 a0001c0003t0001g0165 a0001c0003t0001g0166 others(9): Show |
13 | HG00741.hp1 HG01433.hp1 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.290-2260_290-2259d others(4): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr6 | 109724834 | ||||||
| chr6:109724834 | C | T | 112 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(109): Show |
114 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(111): Show |
intron_variant | MODIFIER | c.290-2275C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109724834 | |||||||
| chr6:109724944 | T | G | 42 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(39): Show |
42 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.290-2165T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109724944 | |||||||
| chr6:109724996 | A | G | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.290-2113A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109724996 | |||||||
| chr6:109725052 | G | A | 2 | a0002c0004t0001g0215 a0002c0004t0001g0216 |
2 | HG01346.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.290-2057G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109725052 | |||||||
| chr6:109725071 | GAATTA | G | 3 | a0001c0001t0002g0347 a0001c0001t0002g0349 a0002c0002t0004g0348 |
3 | HG03239.hp2 HG03654.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.290-2033_290-2029d others(7): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr6 | 109725071 | ||||||
| chr6:109725101 | A | T | 4 | a0001c0001t0002g0282 a0001c0001t0002g0283 a0002c0002t0001g0148 others(1): Show |
4 | HG01071.hp1 HG01123.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-2008A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109725101 | |||||||
| chr6:109725182 | A | G | 1 | a0002c0002t0004g0305 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.290-1927A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109725182 | |||||||
| chr6:109725197 | A | G | 2 | a0002c0002t0002g0086 a0002c0002t0002g0087 |
2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.290-1912A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109725197 | |||||||
| chr6:109725278 | G | C | 1 | a0002c0002t0001g0152 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.290-1831G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109725278 | |||||||
| chr6:109725279 | G | A | 1 | a0002c0002t0001g0152 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.290-1830G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109725279 | |||||||
| chr6:109725419 | C | A | 108 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0221 others(105): Show |
109 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.290-1690C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109725419 | |||||||
| chr6:109725487 | T | A | 3 | a0003c0005t0001g0329 a0003c0005t0001g0330 a0003c0005t0001g0331 |
3 | HG02074.hp2 NA18952.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.290-1622T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109725487 | |||||||
| chr6:109725681 | C | T | 3 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0008c0019t0006g0020 |
3 | HG02145.hp2 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.290-1428C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109725681 | |||||||
| chr6:109725692 | A | C | 2 | a0001c0001t0002g0098 a0001c0001t0002g0099 |
2 | HG00423.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.290-1417A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109725692 | |||||||
| chr6:109725737 | T | G | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.290-1372T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109725737 | |||||||
| chr6:109725919 | A | G | 4 | a0002c0002t0002g0085 a0002c0002t0002g0086 a0002c0002t0002g0087 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-1190A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109725919 | |||||||
| chr6:109725998 | A | C | 2 | a0002c0002t0004g0355 a0002c0002t0004g0356 |
2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.290-1111A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109725998 | |||||||
| chr6:109726021 | T | G | 1 | a0002c0004t0001g0131 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.290-1088T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109726021 | |||||||
| chr6:109726037 | C | T | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.290-1072C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109726037 | |||||||
| chr6:109726061 | G | C | 277 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0122 others(274): Show |
281 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(278): Show |
intron_variant | MODIFIER | c.290-1048G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109726061 | |||||||
| chr6:109726125 | TG | T | 117 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(114): Show |
120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.290-982delG | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr6 | 109726125 | ||||||
| chr6:109726127 | G | C | 117 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(114): Show |
120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.290-982G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109726127 | |||||||
| chr6:109726524 | C | A | 1 | a0002c0002t0002g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.290-585C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109726524 | |||||||
| chr6:109726563 | G | A | 1 | a0001c0003t0001g0252 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.290-546G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109726563 | |||||||
| chr6:109726625 | T | C | 42 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(39): Show |
42 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.290-484T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109726625 | |||||||
| chr6:109726642 | A | G | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.290-467A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109726642 | |||||||
| chr6:109726847 | G | A | 3 | a0003c0005t0001g0329 a0003c0005t0001g0330 a0003c0005t0001g0331 |
3 | HG02074.hp2 NA18952.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.290-262G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109726847 | |||||||
| chr6:109726962 | C | T | 270 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(267): Show |
274 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(271): Show |
intron_variant | MODIFIER | c.290-147C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109726962 | |||||||
| chr6:109727059 | G | A | 1 | a0002c0004t0001g0216 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.290-50G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 3/22 | chr6 | 109727059 | |||||||
| chr6:109727286 | C | CT | 269 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(266): Show |
273 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(270): Show |
intron_variant | MODIFIER | c.446+32dupT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr6 | 109727286 | ||||||
| chr6:109727648 | A | C | 1 | a0001c0001t0003g0169 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.446+383A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109727648 | |||||||
| chr6:109727930 | C | T | 1 | a0001c0003t0001g0037 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.446+665C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109727930 | |||||||
| chr6:109727977 | G | A | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.446+712G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109727977 | |||||||
| chr6:109728011 | A | T | 1 | a0002c0004t0001g0212 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.446+746A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109728011 | |||||||
| chr6:109728108 | C | T | 1 | a0008c0019t0006g0020 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.446+843C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109728108 | |||||||
| chr6:109728221 | T | C | 1 | a0001c0003t0001g0097 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.446+956T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109728221 | |||||||
| chr6:109728306 | T | C | 43 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0360 others(40): Show |
43 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(40): Show |
intron_variant | MODIFIER | c.446+1041T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109728306 | |||||||
| chr6:109728492 | G | A | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.446+1227G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109728492 | |||||||
| chr6:109728620 | G | A | 43 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0360 others(40): Show |
43 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(40): Show |
intron_variant | MODIFIER | c.446+1355G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109728620 | |||||||
| chr6:109728839 | G | A | 270 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(267): Show |
274 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(271): Show |
intron_variant | MODIFIER | c.446+1574G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109728839 | |||||||
| chr6:109728864 | A | T | 1 | a0002c0002t0002g0359 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.446+1599A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109728864 | |||||||
| chr6:109728901 | T | A | 1 | a0002c0002t0002g0210 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.446+1636T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109728901 | |||||||
| chr6:109729051 | T | C | 7 | a0001c0001t0002g0347 a0001c0001t0002g0349 a0002c0002t0004g0348 others(4): Show |
7 | HG01081.hp1 HG02965.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.446+1786T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109729051 | |||||||
| chr6:109729387 | T | C | 1 | a0001c0003t0001g0257 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.446+2122T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109729387 | |||||||
| chr6:109729765 | C | A | 1 | a0001c0001t0002g0122 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.446+2500C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109729765 | |||||||
| chr6:109729773 | CA | C | 196 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0221 others(193): Show |
200 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(197): Show |
intron_variant | MODIFIER | c.446+2524delA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr6 | 109729773 | ||||||
| chr6:109729777 | A | C | 2 | a0002c0002t0002g0358 a0002c0002t0002g0359 |
2 | HG02895.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.446+2512A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109729777 | |||||||
| chr6:109729792 | T | C | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.446+2527T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109729792 | |||||||
| chr6:109729821 | T | C | 1 | a0002c0002t0002g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.446+2556T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109729821 | |||||||
| chr6:109729938 | T | G | 210 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(207): Show |
214 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.446+2673T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109729938 | |||||||
| chr6:109730137 | C | T | 2 | a0002c0002t0002g0016 a0002c0002t0002g0017 |
2 | HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.447-2500C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109730137 | |||||||
| chr6:109730190 | A | G | 3 | a0001c0001t0002g0198 a0002c0002t0004g0196 a0002c0004t0001g0199 |
3 | HG02572.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.447-2447A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109730190 | |||||||
| chr6:109730309 | A | G | 1 | a0001c0003t0001g0319 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.447-2328A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109730309 | |||||||
| chr6:109730679 | G | T | 34 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0360 others(31): Show |
34 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.447-1958G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109730679 | |||||||
| chr6:109730756 | A | C | 1 | a0002c0002t0002g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.447-1881A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109730756 | |||||||
| chr6:109730801 | G | A | 2 | a0001c0003t0001g0038 a0001c0003t0001g0039 |
2 | NA19002.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.447-1836G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109730801 | |||||||
| chr6:109730827 | G | A | 42 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(39): Show |
42 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.447-1810G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109730827 | |||||||
| chr6:109730886 | T | TTTGCCTT others(16): Show |
2 | a0001c0001t0003g0155 a0001c0001t0003g0156 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.447-1748_447-1747i others(25): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr6 | 109730886 | ||||||
| chr6:109730893 | C | T | 12 | a0001c0001t0003g0003 a0001c0001t0003g0162 a0001c0001t0003g0168 others(9): Show |
13 | NA18939.hp1 NA18940.hp1 NA18956.hp2 others(10): Show |
intron_variant | MODIFIER | c.447-1744C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109730893 | |||||||
| chr6:109730907 | A | G | 3 | a0002c0002t0001g0130 a0002c0002t0001g0146 a0002c0002t0001g0147 |
3 | HG01943.hp1 HG01975.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.447-1730A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109730907 | |||||||
| chr6:109731067 | G | C | 46 | a0003c0005t0001g0004 a0003c0005t0001g0005 a0003c0005t0001g0006 others(43): Show |
49 | HG00639.hp1 HG01175.hp2 HG01358.hp2 others(46): Show |
intron_variant | MODIFIER | c.447-1570G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109731067 | |||||||
| chr6:109731312 | A | G | 60 | a0001c0001t0002g0299 a0001c0001t0002g0304 a0001c0003t0001g0291 others(57): Show |
63 | HG00639.hp1 HG01175.hp2 HG01256.hp1 others(60): Show |
intron_variant | MODIFIER | c.447-1325A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109731312 | |||||||
| chr6:109731323 | G | A | 1 | a0002c0002t0004g0294 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.447-1314G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109731323 | |||||||
| chr6:109731652 | A | G | 1 | a0003c0005t0001g0342 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.447-985A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109731652 | |||||||
| chr6:109731677 | G | T | 117 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(114): Show |
120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.447-960G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109731677 | |||||||
| chr6:109731775 | G | A | 1 | a0002c0002t0001g0152 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.447-862G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109731775 | |||||||
| chr6:109731870 | A | G | 4 | a0002c0002t0002g0085 a0002c0002t0002g0086 a0002c0002t0002g0087 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.447-767A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109731870 | |||||||
| chr6:109732047 | T | A | 53 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(50): Show |
53 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.447-590T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109732047 | |||||||
| chr6:109732073 | T | C | 150 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(147): Show |
151 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.447-564T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109732073 | |||||||
| chr6:109732253 | G | T | 46 | a0003c0005t0001g0004 a0003c0005t0001g0005 a0003c0005t0001g0006 others(43): Show |
49 | HG00639.hp1 HG01175.hp2 HG01358.hp2 others(46): Show |
intron_variant | MODIFIER | c.447-384G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109732253 | |||||||
| chr6:109732440 | A | G | 1 | a0001c0001t0002g0277 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.447-197A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109732440 | |||||||
| chr6:109732467 | A | G | 1 | a0002c0002t0004g0294 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.447-170A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109732467 | |||||||
| chr6:109732518 | T | G | 117 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(114): Show |
120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.447-119T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109732518 | |||||||
| chr6:109732544 | T | C | 10 | a0001c0003t0001g0018 a0001c0003t0001g0165 a0001c0003t0001g0166 others(7): Show |
10 | HG00741.hp1 HG01433.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.447-93T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | chr6 | 109732544 | |||||||
| chr6:109732621 | G | GT | 274 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0122 others(271): Show |
278 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(275): Show |
splice_acceptor_variant&intron_variant | HIGH | c.447-3dupT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr6 | 109732621 | ||||||
| chr6:109732748 | G | A | 3 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0002c0002t0002g0210 |
3 | HG02896.hp1 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.497+61G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109732748 | |||||||
| chr6:109732862 | A | T | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.497+175A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109732862 | |||||||
| chr6:109732911 | C | T | 1 | a0001c0001t0002g0103 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.497+224C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109732911 | |||||||
| chr6:109732914 | T | A | 34 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0360 others(31): Show |
34 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.497+227T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109732914 | |||||||
| chr6:109732933 | T | C | 34 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0360 others(31): Show |
34 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.497+246T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109732933 | |||||||
| chr6:109733283 | G | A | 150 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(147): Show |
151 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.497+596G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109733283 | |||||||
| chr6:109733321 | T | C | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.497+634T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109733321 | |||||||
| chr6:109733356 | G | A | 1 | a0003c0005t0001g0072 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.497+669G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109733356 | |||||||
| chr6:109733640 | A | G | 9 | a0001c0001t0002g0198 a0002c0002t0004g0196 a0002c0002t0004g0197 others(6): Show |
9 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.497+953A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109733640 | |||||||
| chr6:109733828 | CCTT | C | 3 | a0002c0002t0005g0125 a0002c0002t0005g0126 a0002c0002t0005g0127 |
3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.497+1149_497+1151d others(5): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr6 | 109733828 | ||||||
| chr6:109733949 | G | T | 1 | a0003c0005t0001g0326 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.498-1201G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109733949 | |||||||
| chr6:109734060 | A | T | 1 | a0002c0002t0002g0085 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.498-1090A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109734060 | |||||||
| chr6:109734110 | G | A | 60 | a0001c0001t0002g0299 a0001c0001t0002g0304 a0001c0003t0001g0291 others(57): Show |
63 | HG00639.hp1 HG01175.hp2 HG01256.hp1 others(60): Show |
intron_variant | MODIFIER | c.498-1040G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109734110 | |||||||
| chr6:109734500 | AC | A | 6 | a0001c0001t0002g0234 a0001c0001t0002g0235 a0001c0001t0002g0236 others(3): Show |
6 | HG00099.hp2 HG00639.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.498-649delC | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109734500 | |||||||
| chr6:109734666 | T | C | 1 | a0002c0002t0002g0210 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.498-484T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109734666 | |||||||
| chr6:109734782 | G | A | 270 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(267): Show |
274 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(271): Show |
intron_variant | MODIFIER | c.498-368G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109734782 | |||||||
| chr6:109734860 | T | G | 1 | a0001c0001t0003g0190 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.498-290T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109734860 | |||||||
| chr6:109734867 | T | C | 1 | a0001c0001t0002g0042 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.498-283T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109734867 | |||||||
| chr6:109735012 | A | G | 2 | a0002c0004t0001g0215 a0002c0004t0001g0216 |
2 | HG01346.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.498-138A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109735012 | |||||||
| chr6:109735048 | G | A | 1 | a0001c0003t0001g0257 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.498-102G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109735048 | |||||||
| chr6:109735063 | T | C | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.498-87T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 5/22 | chr6 | 109735063 | |||||||
| chr6:109735653 | A | T | 1 | a0002c0002t0004g0305 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.646+355A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109735653 | |||||||
| chr6:109735800 | G | C | 1 | a0002c0002t0002g0086 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.646+502G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109735800 | |||||||
| chr6:109736016 | A | G | 270 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(267): Show |
274 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(271): Show |
intron_variant | MODIFIER | c.646+718A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109736016 | |||||||
| chr6:109736025 | G | A | 2 | a0001c0001t0002g0299 a0002c0002t0002g0298 |
2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.646+727G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109736025 | |||||||
| chr6:109736204 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0002g0021 |
2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.646+906G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109736204 | |||||||
| chr6:109736727 | T | C | 1 | a0001c0001t0002g0034 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.646+1429T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109736727 | |||||||
| chr6:109736860 | G | T | 1 | a0001c0003t0001g0097 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.647-1465G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109736860 | |||||||
| chr6:109737108 | G | A | 42 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(39): Show |
42 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.647-1217G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109737108 | |||||||
| chr6:109737153 | C | T | 1 | a0002c0004t0001g0067 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.647-1172C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109737153 | |||||||
| chr6:109737237 | T | G | 1 | a0001c0003t0001g0038 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.647-1088T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109737237 | |||||||
| chr6:109737486 | G | A | 1 | a0001c0003t0001g0293 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.647-839G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109737486 | |||||||
| chr6:109737680 | G | A | 3 | a0002c0002t0005g0125 a0002c0002t0005g0126 a0002c0002t0005g0127 |
3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.647-645G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109737680 | |||||||
| chr6:109737749 | C | T | 29 | a0001c0003t0001g0145 a0002c0002t0001g0130 a0002c0002t0001g0132 others(26): Show |
29 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.647-576C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109737749 | |||||||
| chr6:109737793 | A | G | 4 | a0002c0002t0002g0085 a0002c0002t0002g0086 a0002c0002t0002g0087 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.647-532A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109737793 | |||||||
| chr6:109737797 | G | A | 53 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(50): Show |
53 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.647-528G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109737797 | |||||||
| chr6:109737837 | C | T | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.647-488C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109737837 | |||||||
| chr6:109737974 | C | T | 1 | a0001c0001t0002g0109 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.647-351C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109737974 | |||||||
| chr6:109737986 | G | A | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.647-339G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109737986 | |||||||
| chr6:109738236 | T | C | 1 | a0001c0003t0001g0077 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.647-89T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109738236 | |||||||
| chr6:109738277 | C | T | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.647-48C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109738277 | |||||||
| chr6:109738307 | C | A | 117 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(114): Show |
120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.647-18C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 6/22 | chr6 | 109738307 | |||||||
| chr6:109738751 | G | A | 117 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(114): Show |
120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.775+298G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109738751 | |||||||
| chr6:109738766 | A | G | 6 | a0001c0001t0003g0191 a0001c0001t0003g0192 a0001c0001t0003g0193 others(3): Show |
6 | HG00558.hp2 NA18952.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.775+313A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109738766 | |||||||
| chr6:109738815 | G | A | 12 | a0002c0002t0002g0110 a0002c0002t0002g0111 a0002c0002t0002g0112 others(9): Show |
12 | HG02257.hp2 HG02886.hp1 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.775+362G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109738815 | |||||||
| chr6:109738833 | C | CAG | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.775+392_775+393dup others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr6 | 109738833 | ||||||
| chr6:109739246 | AC | A | 150 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(147): Show |
151 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.775+794delC | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109739246 | |||||||
| chr6:109739407 | C | T | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.775+954C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109739407 | |||||||
| chr6:109739433 | G | A | 6 | a0002c0004t0001g0032 a0002c0004t0001g0043 a0002c0004t0001g0044 others(3): Show |
6 | HG02056.hp1 HG02071.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.775+980G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109739433 | |||||||
| chr6:109739488 | G | A | 1 | a0002c0002t0002g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.775+1035G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109739488 | |||||||
| chr6:109739615 | C | T | 118 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(115): Show |
121 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(118): Show |
intron_variant | MODIFIER | c.775+1162C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109739615 | |||||||
| chr6:109739666 | C | T | 23 | a0001c0001t0002g0226 a0001c0003t0001g0018 a0001c0003t0001g0165 others(20): Show |
23 | HG01433.hp1 HG01934.hp2 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.775+1213C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109739666 | |||||||
| chr6:109739706 | T | C | 1 | a0001c0001t0002g0046 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.775+1253T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109739706 | |||||||
| chr6:109739877 | C | T | 46 | a0003c0005t0001g0004 a0003c0005t0001g0005 a0003c0005t0001g0006 others(43): Show |
49 | HG00639.hp1 HG01175.hp2 HG01358.hp2 others(46): Show |
intron_variant | MODIFIER | c.775+1424C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109739877 | |||||||
| chr6:109740253 | A | T | 1 | a0001c0003t0001g0276 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.776-1191A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109740253 | |||||||
| chr6:109740350 | C | T | 11 | a0001c0001t0002g0198 a0002c0002t0004g0196 a0002c0002t0004g0197 others(8): Show |
11 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.776-1094C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109740350 | |||||||
| chr6:109740413 | A | G | 2 | a0002c0002t0002g0013 a0002c0002t0002g0014 |
2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.776-1031A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109740413 | |||||||
| chr6:109740652 | G | C | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.776-792G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109740652 | |||||||
| chr6:109740708 | C | T | 41 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(38): Show |
41 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.776-736C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109740708 | |||||||
| chr6:109740878 | A | G | 12 | a0002c0002t0002g0110 a0002c0002t0002g0111 a0002c0002t0002g0112 others(9): Show |
12 | HG02257.hp2 HG02886.hp1 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.776-566A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109740878 | |||||||
| chr6:109740895 | A | T | 117 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(114): Show |
120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.776-549A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109740895 | |||||||
| chr6:109741020 | C | A | 270 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(267): Show |
274 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(271): Show |
intron_variant | MODIFIER | c.776-424C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109741020 | |||||||
| chr6:109741085 | G | C | 46 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(43): Show |
46 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.776-359G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109741085 | |||||||
| chr6:109741135 | G | C | 2 | a0001c0003t0001g0279 a0001c0003t0001g0280 |
2 | HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.776-309G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109741135 | |||||||
| chr6:109741149 | C | T | 1 | a0002c0004t0001g0256 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.776-295C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109741149 | |||||||
| chr6:109741174 | C | T | 6 | a0001c0001t0002g0221 a0001c0001t0002g0223 a0001c0001t0002g0224 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.776-270C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109741174 | |||||||
| chr6:109741348 | G | T | 33 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0360 others(30): Show |
33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.776-96G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 7/22 | chr6 | 109741348 | |||||||
| chr6:109741670 | T | G | 117 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(114): Show |
120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.876+126T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 8/22 | chr6 | 109741670 | |||||||
| chr6:109741784 | C | T | 2 | a0002c0002t0002g0086 a0002c0002t0002g0087 |
2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.876+240C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 8/22 | chr6 | 109741784 | |||||||
| chr6:109741825 | A | G | 15 | a0002c0002t0001g0130 a0002c0002t0001g0138 a0002c0002t0001g0141 others(12): Show |
15 | HG01943.hp1 HG01975.hp1 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.876+281A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 8/22 | chr6 | 109741825 | |||||||
| chr6:109741908 | G | A | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.876+364G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 8/22 | chr6 | 109741908 | |||||||
| chr6:109742426 | T | C | 16 | a0003c0005t0001g0005 a0003c0005t0001g0006 a0003c0005t0001g0332 others(13): Show |
18 | HG02155.hp2 NA18940.hp2 NA18947.hp1 others(15): Show |
intron_variant | MODIFIER | c.877-684T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 8/22 | chr6 | 109742426 | |||||||
| chr6:109742495 | G | T | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.877-615G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 8/22 | chr6 | 109742495 | |||||||
| chr6:109743052 | TATTTC | T | 41 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(38): Show |
41 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.877-54_877-50delTC others(3): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr6 | 109743052 | ||||||
| chr6:109743378 | G | A | 1 | a0001c0003t0001g0025 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1039+106G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 9/22 | chr6 | 109743378 | |||||||
| chr6:109743577 | T | G | 67 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0221 others(64): Show |
68 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.1040-98T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 9/22 | chr6 | 109743577 | |||||||
| chr6:109743846 | TAAC | T | 41 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(38): Show |
41 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.1137+77_1137+79del others(3): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109743846 | ||||||
| chr6:109743883 | G | A | 67 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0221 others(64): Show |
68 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.1137+111G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109743883 | |||||||
| chr6:109743984 | G | A | 1 | a0001c0003t0001g0264 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1137+212G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109743984 | |||||||
| chr6:109744165 | A | G | 1 | a0002c0002t0003g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1137+393A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109744165 | |||||||
| chr6:109744227 | G | T | 41 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(38): Show |
41 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.1137+455G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109744227 | |||||||
| chr6:109744443 | C | A | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1137+671C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109744443 | |||||||
| chr6:109744518 | C | G | 150 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(147): Show |
151 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.1137+746C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109744518 | |||||||
| chr6:109744811 | C | T | 1 | a0003c0005t0001g0341 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1137+1039C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109744811 | |||||||
| chr6:109744830 | C | T | 1 | a0001c0003t0001g0266 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1137+1058C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109744830 | |||||||
| chr6:109744835 | T | C | 154 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(151): Show |
155 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.1137+1063T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109744835 | |||||||
| chr6:109744907 | C | G | 39 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(36): Show |
39 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1137+1135C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109744907 | |||||||
| chr6:109744984 | C | T | 1 | a0002c0002t0004g0186 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1137+1212C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109744984 | |||||||
| chr6:109744995 | T | C | 18 | a0001c0001t0002g0002 a0001c0001t0002g0029 a0001c0001t0002g0036 others(15): Show |
19 | HG00423.hp1 NA18747.hp1 NA18953.hp1 others(16): Show |
intron_variant | MODIFIER | c.1137+1223T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109744995 | |||||||
| chr6:109745001 | A | G | 1 | a0002c0002t0002g0012 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1137+1229A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109745001 | |||||||
| chr6:109745249 | C | T | 3 | a0001c0001t0003g0360 a0001c0001t0003g0361 a0001c0001t0003g0362 |
3 | HG02615.hp2 HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1137+1477C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109745249 | |||||||
| chr6:109745369 | G | A | 1 | a0004c0008t0002g0323 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1137+1597G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109745369 | |||||||
| chr6:109745732 | G | A | 57 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(54): Show |
57 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.1137+1960G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109745732 | |||||||
| chr6:109745901 | C | T | 3 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0008c0019t0006g0020 |
3 | HG02145.hp2 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1137+2129C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109745901 | |||||||
| chr6:109746003 | A | G | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1137+2231A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109746003 | |||||||
| chr6:109746078 | A | G | 1 | a0002c0002t0004g0201 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1137+2306A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109746078 | |||||||
| chr6:109746202 | C | T | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1137+2430C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109746202 | |||||||
| chr6:109746216 | C | T | 4 | a0001c0003t0001g0296 a0001c0003t0001g0297 a0001c0003t0001g0302 others(1): Show |
4 | HG01346.hp2 HG01361.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1137+2444C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109746216 | |||||||
| chr6:109746279 | C | G | 3 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0008c0019t0006g0020 |
3 | HG02145.hp2 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1137+2507C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109746279 | |||||||
| chr6:109746301 | C | T | 33 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0360 others(30): Show |
33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1137+2529C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109746301 | |||||||
| chr6:109746419 | A | T | 3 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0008c0019t0006g0020 |
3 | HG02145.hp2 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1137+2647A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109746419 | |||||||
| chr6:109746489 | A | G | 3 | a0002c0002t0005g0125 a0002c0002t0005g0126 a0002c0002t0005g0127 |
3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1137+2717A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109746489 | |||||||
| chr6:109746569 | G | A | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1137+2797G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109746569 | |||||||
| chr6:109746570 | G | A | 60 | a0001c0001t0002g0299 a0001c0001t0002g0304 a0001c0003t0001g0291 others(57): Show |
63 | HG00639.hp1 HG01175.hp2 HG01256.hp1 others(60): Show |
intron_variant | MODIFIER | c.1137+2798G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109746570 | |||||||
| chr6:109746697 | C | G | 11 | a0001c0003t0001g0018 a0001c0003t0001g0097 a0001c0003t0001g0165 others(8): Show |
11 | HG00741.hp1 HG01433.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.1137+2925C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109746697 | |||||||
| chr6:109746881 | A | T | 1 | a0002c0002t0004g0206 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1137+3109A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109746881 | |||||||
| chr6:109746887 | G | A | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1137+3115G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109746887 | |||||||
| chr6:109746958 | C | T | 1 | a0002c0002t0002g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1137+3186C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109746958 | |||||||
| chr6:109747089 | G | A | 41 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(38): Show |
41 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.1137+3317G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109747089 | |||||||
| chr6:109747119 | C | T | 117 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(114): Show |
120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.1137+3347C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109747119 | |||||||
| chr6:109747147 | G | A | 4 | a0002c0002t0005g0125 a0002c0002t0005g0126 a0002c0002t0005g0127 others(1): Show |
4 | HG03453.hp1 HG03579.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1137+3375G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109747147 | |||||||
| chr6:109747411 | G | A | 117 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(114): Show |
120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.1137+3639G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109747411 | |||||||
| chr6:109747516 | A | G | 2 | a0002c0004t0001g0070 a0002c0004t0001g0071 |
2 | NA18961.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.1137+3744A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109747516 | |||||||
| chr6:109747583 | A | T | 154 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(151): Show |
155 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.1137+3811A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109747583 | |||||||
| chr6:109748147 | T | C | 46 | a0003c0005t0001g0004 a0003c0005t0001g0005 a0003c0005t0001g0006 others(43): Show |
49 | HG00639.hp1 HG01175.hp2 HG01358.hp2 others(46): Show |
intron_variant | MODIFIER | c.1137+4375T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109748147 | |||||||
| chr6:109748250 | T | C | 1 | a0003c0005t0001g0312 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1137+4478T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109748250 | |||||||
| chr6:109748267 | G | A | 270 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(267): Show |
274 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(271): Show |
intron_variant | MODIFIER | c.1137+4495G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109748267 | |||||||
| chr6:109748325 | G | T | 1 | a0001c0003t0001g0275 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1137+4553G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109748325 | |||||||
| chr6:109748354 | G | A | 1 | a0004c0006t0001g0307 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1137+4582G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109748354 | |||||||
| chr6:109748464 | A | C | 4 | a0002c0002t0002g0085 a0002c0002t0002g0086 a0002c0002t0002g0087 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1137+4692A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109748464 | |||||||
| chr6:109748501 | A | G | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1137+4729A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109748501 | |||||||
| chr6:109748756 | G | A | 1 | a0001c0003t0001g0035 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1137+4984G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109748756 | |||||||
| chr6:109748819 | G | A | 117 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(114): Show |
120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.1137+5047G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109748819 | |||||||
| chr6:109748875 | A | G | 1 | a0002c0002t0004g0352 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1137+5103A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109748875 | |||||||
| chr6:109748919 | C | T | 2 | a0002c0004t0001g0065 a0002c0004t0001g0066 |
2 | HG00423.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1137+5147C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109748919 | |||||||
| chr6:109748932 | G | A | 15 | a0001c0001t0002g0198 a0002c0002t0002g0164 a0002c0002t0004g0196 others(12): Show |
15 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1137+5160G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109748932 | |||||||
| chr6:109749026 | A | G | 4 | a0002c0002t0002g0009 a0002c0002t0002g0011 a0002c0002t0002g0012 others(1): Show |
4 | HG02809.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1137+5254A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109749026 | |||||||
| chr6:109749055 | C | CTG | 32 | a0001c0001t0002g0033 a0001c0001t0002g0054 a0001c0001t0002g0082 others(29): Show |
33 | HG00323.hp1 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1137+5331_1137+533 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749055 | ||||||
| chr6:109749055 | C | CTGTG | 39 | a0001c0001t0002g0002 a0001c0001t0002g0022 a0001c0001t0002g0029 others(36): Show |
40 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1137+5329_1137+533 others(8): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749055 | ||||||
| chr6:109749055 | C | CTGTGTG | 25 | a0001c0001t0002g0023 a0001c0001t0002g0046 a0001c0001t0002g0092 others(22): Show |
25 | HG00323.hp2 HG00438.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.1137+5327_1137+533 others(10): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749055 | ||||||
| chr6:109749055 | C | CTGTGTGT others(1): Show |
7 | a0001c0001t0002g0001 a0001c0001t0002g0304 a0001c0001t0003g0194 others(4): Show |
8 | HG01361.hp1 HG01517.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.1137+5325_1137+533 others(12): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749055 | ||||||
| chr6:109749055 | C | CTGTGTGT others(3): Show |
15 | a0001c0003t0001g0038 a0001c0003t0001g0292 a0001c0003t0001g0293 others(12): Show |
15 | HG00544.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1137+5323_1137+533 others(14): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749055 | ||||||
| chr6:109749055 | C | CTGTGTGT others(5): Show |
10 | a0001c0003t0001g0291 a0001c0003t0001g0302 a0002c0002t0001g0130 others(7): Show |
10 | HG01346.hp2 HG01943.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.1137+5321_1137+533 others(16): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749055 | ||||||
| chr6:109749055 | C | CTGTGTGT others(7): Show |
7 | a0002c0002t0001g0133 a0002c0002t0001g0134 a0002c0002t0001g0146 others(4): Show |
7 | HG01975.hp1 HG02015.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1137+5319_1137+533 others(18): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749055 | ||||||
| chr6:109749055 | C | CTGTGTGT others(9): Show |
3 | a0001c0003t0001g0297 a0002c0002t0001g0138 a0002c0002t0001g0149 |
3 | HG02135.hp2 NA18951.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.1137+5317_1137+533 others(20): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749055 | ||||||
| chr6:109749055 | CTG | C | 73 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0221 others(70): Show |
74 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.1137+5331_1137+533 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749055 | ||||||
| chr6:109749055 | CTGTG | C | 5 | a0002c0002t0002g0358 a0002c0002t0005g0125 a0002c0004t0001g0067 others(2): Show |
6 | HG02895.hp2 NA18982.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.1137+5329_1137+533 others(8): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749055 | ||||||
| chr6:109749055 | CTGTGTG | C | 16 | a0001c0001t0002g0213 a0001c0001t0002g0217 a0001c0001t0002g0227 others(13): Show |
16 | HG00735.hp1 HG01069.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.1137+5327_1137+533 others(10): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749055 | ||||||
| chr6:109749055 | CTGTGTGT others(1): Show |
C | 37 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0198 others(34): Show |
37 | HG00099.hp2 HG00639.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.1137+5325_1137+533 others(12): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749055 | ||||||
| chr6:109749055 | CTGTGTGT others(7): Show |
C | 1 | a0003c0005t0001g0333 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1137+5319_1137+533 others(18): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749055 | ||||||
| chr6:109749055 | CTGTGTGT others(21): Show |
C | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1137+5305_1137+533 others(32): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749055 | ||||||
| chr6:109749104 | T | TGTGTGTG others(4): Show |
1 | a0002c0004t0001g0128 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1137+5332_1137+533 others(15): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109749104 | |||||||
| chr6:109749178 | C | T | 1 | a0001c0003t0001g0035 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1137+5406C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109749178 | |||||||
| chr6:109749425 | T | G | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1137+5653T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109749425 | |||||||
| chr6:109749564 | A | G | 117 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(114): Show |
120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.1137+5792A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109749564 | |||||||
| chr6:109749588 | T | TAATAAAA others(3): Show |
11 | a0002c0002t0002g0085 a0002c0002t0002g0086 a0002c0002t0002g0087 others(8): Show |
11 | HG02258.hp2 HG02486.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1137+5839_1137+584 others(14): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749588 | ||||||
| chr6:109749588 | T | TAATAAAA others(8): Show |
103 | a0001c0001t0002g0198 a0001c0001t0002g0214 a0001c0001t0002g0217 others(100): Show |
106 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.1137+5834_1137+584 others(19): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749588 | ||||||
| chr6:109749588 | T | TAATAAAA others(13): Show |
114 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0213 others(111): Show |
115 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.1137+5829_1137+584 others(24): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749588 | ||||||
| chr6:109749588 | T | TAATAAAA others(18): Show |
32 | a0001c0001t0002g0289 a0001c0001t0002g0304 a0001c0003t0001g0018 others(29): Show |
32 | HG00408.hp2 HG00741.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.1137+5824_1137+584 others(29): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749588 | ||||||
| chr6:109749588 | T | TAATAAAA others(23): Show |
7 | a0001c0003t0001g0260 a0001c0003t0001g0261 a0001c0003t0001g0262 others(4): Show |
7 | HG00738.hp2 HG01099.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1137+5819_1137+584 others(34): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109749588 | ||||||
| chr6:109749723 | C | T | 1 | a0004c0008t0002g0323 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1137+5951C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109749723 | |||||||
| chr6:109749753 | A | G | 1 | a0003c0005t0001g0346 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1137+5981A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109749753 | |||||||
| chr6:109749766 | T | G | 109 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0221 others(106): Show |
110 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.1137+5994T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109749766 | |||||||
| chr6:109749783 | G | A | 33 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0360 others(30): Show |
33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1137+6011G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109749783 | |||||||
| chr6:109750116 | C | A | 109 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0221 others(106): Show |
110 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.1137+6344C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109750116 | |||||||
| chr6:109750159 | C | T | 4 | a0002c0002t0002g0085 a0002c0002t0002g0086 a0002c0002t0002g0087 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1137+6387C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109750159 | |||||||
| chr6:109750166 | C | A | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1137+6394C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109750166 | |||||||
| chr6:109750231 | A | G | 1 | a0003c0005t0001g0320 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1137+6459A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109750231 | |||||||
| chr6:109750327 | A | T | 1 | a0002c0004t0001g0071 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1137+6555A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109750327 | |||||||
| chr6:109750394 | G | A | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1137+6622G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109750394 | |||||||
| chr6:109750426 | G | T | 2 | a0001c0010t0002g0030 a0001c0010t0002g0031 |
2 | HG01258.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1137+6654G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109750426 | |||||||
| chr6:109750448 | G | A | 6 | a0001c0001t0003g0191 a0001c0001t0003g0192 a0001c0001t0003g0193 others(3): Show |
6 | HG00558.hp2 NA18952.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.1137+6676G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109750448 | |||||||
| chr6:109750509 | C | T | 1 | a0002c0002t0004g0356 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1137+6737C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109750509 | |||||||
| chr6:109750611 | C | T | 3 | a0001c0001t0002g0235 a0001c0001t0002g0236 a0001c0001t0002g0237 |
3 | HG01099.hp2 HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1137+6839C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109750611 | |||||||
| chr6:109750717 | A | G | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1137+6945A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109750717 | |||||||
| chr6:109750748 | A | C | 277 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0122 others(274): Show |
281 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(278): Show |
intron_variant | MODIFIER | c.1137+6976A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109750748 | |||||||
| chr6:109750909 | A | C | 1 | a0004c0008t0002g0310 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1137+7137A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109750909 | |||||||
| chr6:109751001 | C | T | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1137+7229C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109751001 | |||||||
| chr6:109751060 | A | G | 3 | a0002c0002t0002g0139 a0002c0002t0002g0150 a0002c0004t0001g0140 |
3 | NA19007.hp2 NA19063.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1137+7288A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109751060 | |||||||
| chr6:109751299 | T | G | 3 | a0001c0001t0003g0360 a0001c0001t0003g0361 a0001c0001t0003g0362 |
3 | HG02615.hp2 HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1137+7527T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109751299 | |||||||
| chr6:109751300 | G | A | 67 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0221 others(64): Show |
68 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.1137+7528G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109751300 | |||||||
| chr6:109751338 | G | A | 3 | a0002c0004t0001g0215 a0002c0004t0001g0216 a0002c0004t0001g0242 |
3 | HG01346.hp1 HG03834.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1137+7566G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109751338 | |||||||
| chr6:109751398 | G | A | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1137+7626G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109751398 | |||||||
| chr6:109751529 | G | A | 57 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(54): Show |
57 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.1137+7757G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109751529 | |||||||
| chr6:109751565 | C | T | 1 | a0002c0002t0004g0352 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1137+7793C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109751565 | |||||||
| chr6:109751706 | G | A | 1 | a0001c0003t0001g0165 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1137+7934G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109751706 | |||||||
| chr6:109751803 | CT | C | 274 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(271): Show |
278 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(275): Show |
intron_variant | MODIFIER | c.1137+8038delT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109751803 | ||||||
| chr6:109751960 | G | A | 2 | a0001c0003t0001g0260 a0001c0003t0001g0261 |
2 | HG01433.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1137+8188G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109751960 | |||||||
| chr6:109751994 | C | G | 1 | a0002c0002t0004g0352 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1137+8222C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109751994 | |||||||
| chr6:109752015 | A | T | 1 | a0001c0003t0001g0273 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1138-8235A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752015 | |||||||
| chr6:109752084 | C | T | 1 | a0004c0008t0002g0310 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1138-8166C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752084 | |||||||
| chr6:109752086 | G | T | 1 | a0002c0004t0001g0045 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1138-8164G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752086 | |||||||
| chr6:109752116 | A | G | 33 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0360 others(30): Show |
33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1138-8134A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752116 | |||||||
| chr6:109752246 | C | T | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1138-8004C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752246 | |||||||
| chr6:109752301 | G | A | 33 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0360 others(30): Show |
33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1138-7949G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752301 | |||||||
| chr6:109752317 | A | G | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1138-7933A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752317 | |||||||
| chr6:109752332 | G | A | 154 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(151): Show |
155 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.1138-7918G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752332 | |||||||
| chr6:109752335 | G | A | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1138-7915G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752335 | |||||||
| chr6:109752495 | T | C | 274 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(271): Show |
278 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(275): Show |
intron_variant | MODIFIER | c.1138-7755T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752495 | |||||||
| chr6:109752525 | G | A | 50 | a0002c0002t0002g0009 a0002c0002t0002g0011 a0002c0002t0002g0012 others(47): Show |
53 | HG00639.hp1 HG01175.hp2 HG01358.hp2 others(50): Show |
intron_variant | MODIFIER | c.1138-7725G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752525 | |||||||
| chr6:109752548 | G | A | 1 | a0002c0002t0004g0207 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1138-7702G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752548 | |||||||
| chr6:109752572 | C | T | 1 | a0004c0008t0002g0310 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1138-7678C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752572 | |||||||
| chr6:109752573 | G | A | 1 | a0002c0002t0002g0210 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1138-7677G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752573 | |||||||
| chr6:109752627 | T | G | 3 | a0002c0002t0005g0125 a0002c0002t0005g0126 a0002c0002t0005g0127 |
3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1138-7623T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752627 | |||||||
| chr6:109752634 | C | T | 13 | a0001c0001t0002g0289 a0001c0003t0001g0257 a0001c0003t0001g0258 others(10): Show |
13 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.1138-7616C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752634 | |||||||
| chr6:109752666 | T | G | 274 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(271): Show |
278 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(275): Show |
intron_variant | MODIFIER | c.1138-7584T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752666 | |||||||
| chr6:109752736 | T | A | 3 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0008c0019t0006g0020 |
3 | HG02145.hp2 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1138-7514T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752736 | |||||||
| chr6:109752896 | A | G | 2 | a0002c0002t0002g0013 a0002c0002t0002g0014 |
2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1138-7354A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752896 | |||||||
| chr6:109752993 | T | C | 12 | a0002c0002t0002g0110 a0002c0002t0002g0111 a0002c0002t0002g0112 others(9): Show |
12 | HG02257.hp2 HG02886.hp1 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.1138-7257T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109752993 | |||||||
| chr6:109753013 | G | C | 1 | a0001c0001t0002g0093 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1138-7237G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753013 | |||||||
| chr6:109753091 | A | G | 1 | a0002c0002t0004g0305 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1138-7159A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753091 | |||||||
| chr6:109753174 | C | G | 1 | a0001c0001t0002g0093 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1138-7076C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753174 | |||||||
| chr6:109753190 | C | T | 45 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(42): Show |
45 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.1138-7060C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753190 | |||||||
| chr6:109753193 | G | A | 33 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0360 others(30): Show |
33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1138-7057G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753193 | |||||||
| chr6:109753209 | C | T | 67 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0221 others(64): Show |
68 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.1138-7041C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753209 | |||||||
| chr6:109753255 | C | T | 2 | a0001c0001t0002g0098 a0001c0001t0002g0099 |
2 | HG00423.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.1138-6995C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753255 | |||||||
| chr6:109753262 | G | T | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1138-6988G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753262 | |||||||
| chr6:109753313 | G | C | 4 | a0002c0002t0002g0085 a0002c0002t0002g0086 a0002c0002t0002g0087 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1138-6937G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753313 | |||||||
| chr6:109753323 | C | A | 1 | a0001c0003t0001g0262 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1138-6927C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753323 | |||||||
| chr6:109753351 | T | G | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1138-6899T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753351 | |||||||
| chr6:109753411 | G | A | 3 | a0003c0005t0001g0249 a0003c0005t0001g0346 a0003c0017t0001g0314 |
3 | NA18943.hp1 NA18959.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1138-6839G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753411 | |||||||
| chr6:109753411 | G | C | 2 | a0002c0002t0002g0013 a0002c0002t0002g0014 |
2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1138-6839G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753411 | |||||||
| chr6:109753418 | T | C | 277 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0122 others(274): Show |
281 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(278): Show |
intron_variant | MODIFIER | c.1138-6832T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753418 | |||||||
| chr6:109753442 | A | G | 2 | a0001c0001t0002g0226 a0002c0002t0002g0225 |
2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1138-6808A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753442 | |||||||
| chr6:109753801 | CTT | C | 3 | a0002c0002t0004g0351 a0002c0002t0004g0352 a0002c0002t0004g0353 |
3 | HG01081.hp1 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1138-6447_1138-644 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109753801 | ||||||
| chr6:109753864 | A | G | 10 | a0001c0001t0003g0187 a0001c0001t0003g0191 a0001c0001t0003g0192 others(7): Show |
10 | HG00558.hp2 HG01081.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.1138-6386A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753864 | |||||||
| chr6:109753871 | C | G | 3 | a0001c0001t0003g0003 a0001c0001t0003g0162 a0001c0001t0003g0168 |
4 | NA18960.hp2 NA18968.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.1138-6379C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753871 | |||||||
| chr6:109753913 | G | T | 1 | a0002c0002t0001g0154 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1138-6337G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753913 | |||||||
| chr6:109753920 | A | G | 1 | a0001c0003t0001g0064 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1138-6330A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753920 | |||||||
| chr6:109753996 | G | T | 151 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(148): Show |
152 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.1138-6254G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109753996 | |||||||
| chr6:109754152 | G | A | 1 | a0002c0002t0002g0012 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1138-6098G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754152 | |||||||
| chr6:109754165 | C | G | 57 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(54): Show |
57 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.1138-6085C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754165 | |||||||
| chr6:109754271 | T | G | 1 | a0001c0003t0001g0288 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1138-5979T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754271 | |||||||
| chr6:109754312 | C | G | 2 | a0002c0002t0001g0152 a0002c0002t0001g0154 |
2 | HG03942.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1138-5938C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754312 | |||||||
| chr6:109754390 | G | T | 2 | a0001c0003t0001g0177 a0002c0004t0001g0189 |
2 | HG01934.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1138-5860G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754390 | |||||||
| chr6:109754463 | T | G | 33 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0360 others(30): Show |
33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1138-5787T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754463 | |||||||
| chr6:109754475 | A | C | 3 | a0001c0003t0001g0257 a0001c0003t0001g0258 a0001c0003t0001g0259 |
3 | HG01069.hp2 HG01071.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1138-5775A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754475 | |||||||
| chr6:109754491 | A | G | 2 | a0002c0002t0004g0351 a0002c0002t0004g0353 |
2 | HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1138-5759A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754491 | |||||||
| chr6:109754638 | G | C | 1 | a0002c0004t0001g0216 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1138-5612G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754638 | |||||||
| chr6:109754653 | C | T | 67 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0221 others(64): Show |
68 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.1138-5597C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754653 | |||||||
| chr6:109754672 | G | C | 45 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(42): Show |
45 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.1138-5578G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754672 | |||||||
| chr6:109754725 | C | T | 67 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0221 others(64): Show |
68 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.1138-5525C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754725 | |||||||
| chr6:109754787 | T | A | 3 | a0001c0001t0003g0360 a0001c0001t0003g0361 a0001c0001t0003g0362 |
3 | HG02615.hp2 HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1138-5463T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754787 | |||||||
| chr6:109754865 | G | A | 2 | a0002c0004t0001g0215 a0002c0004t0001g0216 |
2 | HG01346.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1138-5385G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754865 | |||||||
| chr6:109754945 | G | A | 4 | a0002c0002t0005g0125 a0002c0002t0005g0126 a0002c0002t0005g0127 others(1): Show |
4 | HG03453.hp1 HG03579.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1138-5305G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754945 | |||||||
| chr6:109754974 | T | G | 3 | a0002c0002t0001g0153 a0002c0004t0001g0215 a0002c0004t0001g0216 |
3 | HG00323.hp2 HG01346.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1138-5276T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109754974 | |||||||
| chr6:109755032 | G | T | 2 | a0001c0003t0001g0270 a0001c0003t0001g0271 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1138-5218G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109755032 | |||||||
| chr6:109755147 | C | T | 3 | a0001c0003t0001g0302 a0001c0003t0001g0319 a0001c0003t0001g0364 |
3 | HG01346.hp2 NA18969.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1138-5103C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109755147 | |||||||
| chr6:109755148 | G | A | 1 | a0001c0001t0002g0304 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1138-5102G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109755148 | |||||||
| chr6:109755191 | T | C | 2 | a0001c0003t0001g0038 a0001c0003t0001g0039 |
2 | NA19002.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1138-5059T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109755191 | |||||||
| chr6:109755195 | C | T | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1138-5055C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109755195 | |||||||
| chr6:109755268 | G | C | 1 | a0003c0005t0001g0311 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1138-4982G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109755268 | |||||||
| chr6:109755413 | G | A | 3 | a0002c0002t0005g0125 a0002c0002t0005g0126 a0002c0002t0005g0127 |
3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1138-4837G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109755413 | |||||||
| chr6:109755613 | T | G | 2 | a0001c0001t0002g0069 a0002c0004t0001g0068 |
2 | HG01169.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1138-4637T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109755613 | |||||||
| chr6:109755614 | G | A | 3 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0002c0002t0004g0123 |
3 | HG02622.hp2 HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1138-4636G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109755614 | |||||||
| chr6:109755661 | T | C | 2 | a0002c0002t0002g0358 a0002c0002t0002g0359 |
2 | HG02895.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1138-4589T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109755661 | |||||||
| chr6:109755729 | A | G | 1 | a0001c0001t0002g0213 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1138-4521A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109755729 | |||||||
| chr6:109755820 | C | T | 117 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(114): Show |
120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.1138-4430C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109755820 | |||||||
| chr6:109755878 | T | G | 2 | a0001c0001t0002g0098 a0001c0001t0002g0099 |
2 | HG00423.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.1138-4372T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109755878 | |||||||
| chr6:109755957 | G | A | 13 | a0001c0001t0002g0299 a0001c0001t0002g0304 a0001c0003t0001g0291 others(10): Show |
13 | HG01256.hp1 HG01258.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.1138-4293G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109755957 | |||||||
| chr6:109755994 | T | C | 45 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(42): Show |
45 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.1138-4256T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109755994 | |||||||
| chr6:109756003 | C | T | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1138-4247C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756003 | |||||||
| chr6:109756083 | C | T | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1138-4167C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756083 | |||||||
| chr6:109756118 | T | G | 274 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(271): Show |
278 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(275): Show |
intron_variant | MODIFIER | c.1138-4132T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756118 | |||||||
| chr6:109756167 | A | G | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1138-4083A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756167 | |||||||
| chr6:109756187 | T | C | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1138-4063T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756187 | |||||||
| chr6:109756188 | A | T | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1138-4062A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756188 | |||||||
| chr6:109756189 | C | G | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1138-4061C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756189 | |||||||
| chr6:109756264 | C | A | 1 | a0002c0004t0001g0295 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1138-3986C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756264 | |||||||
| chr6:109756305 | C | T | 46 | a0003c0005t0001g0004 a0003c0005t0001g0005 a0003c0005t0001g0006 others(43): Show |
49 | HG00639.hp1 HG01175.hp2 HG01358.hp2 others(46): Show |
intron_variant | MODIFIER | c.1138-3945C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756305 | |||||||
| chr6:109756306 | A | G | 4 | a0002c0002t0002g0085 a0002c0002t0002g0086 a0002c0002t0002g0087 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1138-3944A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756306 | |||||||
| chr6:109756340 | C | G | 1 | a0002c0004t0001g0295 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1138-3910C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756340 | |||||||
| chr6:109756449 | T | C | 4 | a0002c0002t0002g0085 a0002c0002t0002g0086 a0002c0002t0002g0087 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1138-3801T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756449 | |||||||
| chr6:109756474 | A | G | 4 | a0002c0002t0002g0085 a0002c0002t0002g0086 a0002c0002t0002g0087 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1138-3776A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756474 | |||||||
| chr6:109756475 | T | C | 4 | a0002c0002t0002g0085 a0002c0002t0002g0086 a0002c0002t0002g0087 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1138-3775T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756475 | |||||||
| chr6:109756668 | C | T | 1 | a0001c0001t0002g0233 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1138-3582C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756668 | |||||||
| chr6:109756669 | G | A | 19 | a0001c0001t0003g0003 a0001c0001t0003g0162 a0001c0001t0003g0163 others(16): Show |
20 | HG00438.hp1 HG03041.hp2 NA18939.hp1 others(17): Show |
intron_variant | MODIFIER | c.1138-3581G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756669 | |||||||
| chr6:109756766 | A | G | 3 | a0002c0002t0002g0139 a0002c0002t0002g0150 a0002c0004t0001g0140 |
3 | NA19007.hp2 NA19063.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1138-3484A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756766 | |||||||
| chr6:109756912 | G | A | 33 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0360 others(30): Show |
33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1138-3338G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756912 | |||||||
| chr6:109756958 | G | C | 2 | a0002c0002t0002g0086 a0002c0002t0002g0087 |
2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1138-3292G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756958 | |||||||
| chr6:109756959 | C | G | 4 | a0002c0002t0005g0125 a0002c0002t0005g0126 a0002c0002t0005g0127 others(1): Show |
4 | HG03453.hp1 HG03579.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1138-3291C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109756959 | |||||||
| chr6:109757021 | T | C | 3 | a0002c0002t0005g0125 a0002c0002t0005g0126 a0002c0002t0005g0127 |
3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1138-3229T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109757021 | |||||||
| chr6:109757026 | G | A | 41 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(38): Show |
41 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.1138-3224G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109757026 | |||||||
| chr6:109757067 | C | T | 2 | a0002c0004t0001g0128 a0002c0004t0001g0129 |
2 | HG01255.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1138-3183C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109757067 | |||||||
| chr6:109757072 | A | G | 4 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(1): Show |
4 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1138-3178A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109757072 | |||||||
| chr6:109757078 | G | C | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1138-3172G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109757078 | |||||||
| chr6:109757178 | GT | G | 41 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(38): Show |
41 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.1138-3067delT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109757178 | ||||||
| chr6:109757508 | A | T | 1 | a0001c0001t0003g0185 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1138-2742A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109757508 | |||||||
| chr6:109757634 | A | T | 1 | a0002c0014t0002g0015 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1138-2616A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109757634 | |||||||
| chr6:109757794 | T | G | 1 | a0002c0002t0004g0294 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1138-2456T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109757794 | |||||||
| chr6:109757832 | C | G | 3 | a0002c0002t0005g0125 a0002c0002t0005g0126 a0002c0002t0005g0127 |
3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1138-2418C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109757832 | |||||||
| chr6:109757908 | A | G | 117 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(114): Show |
120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.1138-2342A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109757908 | |||||||
| chr6:109757955 | AAG | A | 3 | a0001c0003t0001g0296 a0001c0003t0001g0302 a0001c0003t0001g0303 |
3 | HG01346.hp2 HG01361.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1138-2290_1138-228 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109757955 | ||||||
| chr6:109758261 | C | T | 270 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(267): Show |
274 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(271): Show |
intron_variant | MODIFIER | c.1138-1989C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109758261 | |||||||
| chr6:109758416 | A | C | 3 | a0003c0005t0001g0249 a0003c0005t0001g0346 a0003c0017t0001g0314 |
3 | NA18943.hp1 NA18959.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1138-1834A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109758416 | |||||||
| chr6:109758422 | T | TGG | 41 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(38): Show |
41 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.1138-1827_1138-182 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109758422 | ||||||
| chr6:109758524 | A | G | 4 | a0002c0002t0002g0085 a0002c0002t0002g0086 a0002c0002t0002g0087 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1138-1726A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109758524 | |||||||
| chr6:109758787 | G | A | 1 | a0001c0001t0002g0214 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1138-1463G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109758787 | |||||||
| chr6:109758915 | G | A | 1 | a0002c0002t0002g0014 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1138-1335G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109758915 | |||||||
| chr6:109759098 | G | T | 1 | a0001c0001t0002g0100 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1138-1152G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109759098 | |||||||
| chr6:109759194 | C | T | 6 | a0001c0001t0002g0060 a0001c0001t0002g0061 a0001c0001t0002g0062 others(3): Show |
6 | NA18947.hp2 NA18949.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.1138-1056C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109759194 | |||||||
| chr6:109759239 | A | G | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1138-1011A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109759239 | |||||||
| chr6:109759264 | C | T | 1 | a0002c0002t0002g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1138-986C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109759264 | |||||||
| chr6:109759268 | A | T | 3 | a0002c0002t0001g0143 a0002c0002t0001g0144 a0002c0002t0001g0148 |
3 | NA18955.hp2 NA18998.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1138-982A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109759268 | |||||||
| chr6:109759354 | T | C | 150 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(147): Show |
151 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.1138-896T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109759354 | |||||||
| chr6:109759417 | GA | G | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1138-824delA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr6 | 109759417 | ||||||
| chr6:109759426 | A | C | 28 | a0002c0002t0001g0130 a0002c0002t0001g0132 a0002c0002t0001g0133 others(25): Show |
28 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.1138-824A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109759426 | |||||||
| chr6:109759443 | T | A | 1 | a0002c0002t0004g0305 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1138-807T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109759443 | |||||||
| chr6:109759549 | C | T | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1138-701C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109759549 | |||||||
| chr6:109759565 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0002g0021 |
2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1138-685G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109759565 | |||||||
| chr6:109759799 | G | A | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1138-451G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109759799 | |||||||
| chr6:109759959 | G | A | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1138-291G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109759959 | |||||||
| chr6:109759966 | A | G | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1138-284A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109759966 | |||||||
| chr6:109759998 | G | A | 2 | a0004c0008t0002g0309 a0004c0008t0002g0322 |
2 | HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1138-252G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109759998 | |||||||
| chr6:109760075 | G | T | 15 | a0001c0001t0002g0198 a0002c0002t0002g0164 a0002c0002t0004g0196 others(12): Show |
15 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1138-175G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109760075 | |||||||
| chr6:109760135 | G | C | 1 | a0002c0004t0001g0055 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1138-115G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109760135 | |||||||
| chr6:109760205 | A | T | 1 | a0002c0004t0001g0295 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1138-45A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109760205 | |||||||
| chr6:109760228 | A | G | 1 | a0003c0005t0001g0345 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1138-22A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 10/22 | chr6 | 109760228 | |||||||
| chr6:109760415 | G | A | 109 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0221 others(106): Show |
110 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.1271+32G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 11/22 | chr6 | 109760415 | |||||||
| chr6:109760821 | C | T | 33 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0360 others(30): Show |
33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1271+438C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 11/22 | chr6 | 109760821 | |||||||
| chr6:109760879 | C | T | 1 | a0001c0001t0002g0233 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1271+496C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 11/22 | chr6 | 109760879 | |||||||
| chr6:109760919 | G | A | 46 | a0003c0005t0001g0004 a0003c0005t0001g0005 a0003c0005t0001g0006 others(43): Show |
49 | HG00639.hp1 HG01175.hp2 HG01358.hp2 others(46): Show |
intron_variant | MODIFIER | c.1271+536G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 11/22 | chr6 | 109760919 | |||||||
| chr6:109761361 | T | G | 1 | a0002c0002t0001g0133 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1272-730T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 11/22 | chr6 | 109761361 | |||||||
| chr6:109761736 | C | T | 6 | a0001c0001t0002g0221 a0001c0001t0002g0223 a0001c0001t0002g0224 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1272-355C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 11/22 | chr6 | 109761736 | |||||||
| chr6:109761853 | C | T | 41 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(38): Show |
41 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.1272-238C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 11/22 | chr6 | 109761853 | |||||||
| chr6:109762585 | A | G | 1 | a0002c0002t0004g0350 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1388+378A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 12/22 | chr6 | 109762585 | |||||||
| chr6:109762622 | G | A | 1 | a0002c0002t0004g0204 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1388+415G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 12/22 | chr6 | 109762622 | |||||||
| chr6:109762861 | A | G | 53 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(50): Show |
53 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1388+654A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 12/22 | chr6 | 109762861 | |||||||
| chr6:109762875 | C | T | 41 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(38): Show |
41 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.1388+668C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 12/22 | chr6 | 109762875 | |||||||
| chr6:109762876 | G | A | 1 | a0001c0001t0002g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1388+669G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 12/22 | chr6 | 109762876 | |||||||
| chr6:109762950 | G | A | 1 | a0002c0002t0004g0351 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1388+743G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 12/22 | chr6 | 109762950 | |||||||
| chr6:109763001 | G | T | 1 | a0008c0019t0006g0020 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1388+794G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 12/22 | chr6 | 109763001 | |||||||
| chr6:109763103 | C | G | 1 | a0004c0006t0001g0308 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1389-834C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 12/22 | chr6 | 109763103 | |||||||
| chr6:109763331 | G | A | 117 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(114): Show |
120 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.1389-606G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 12/22 | chr6 | 109763331 | |||||||
| chr6:109763402 | T | A | 151 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(148): Show |
152 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.1389-535T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 12/22 | chr6 | 109763402 | |||||||
| chr6:109763406 | TC | T | 151 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(148): Show |
152 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.1389-530delC | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 12/22 | chr6 | 109763406 | |||||||
| chr6:109763767 | A | G | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1389-170A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 12/22 | chr6 | 109763767 | |||||||
| chr6:109764036 | G | A | 9 | a0001c0001t0002g0277 a0001c0003t0001g0007 a0001c0003t0001g0008 others(6): Show |
9 | HG02602.hp1 HG04184.hp2 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1434+54G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | chr6 | 109764036 | |||||||
| chr6:109764054 | A | G | 68 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0221 others(65): Show |
69 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.1434+72A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | chr6 | 109764054 | |||||||
| chr6:109764140 | A | T | 1 | a0002c0002t0004g0353 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1434+158A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | chr6 | 109764140 | |||||||
| chr6:109764163 | G | T | 53 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(50): Show |
53 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1434+181G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | chr6 | 109764163 | |||||||
| chr6:109764211 | G | A | 1 | a0001c0001t0003g0362 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1434+229G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | chr6 | 109764211 | |||||||
| chr6:109764220 | T | C | 275 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(272): Show |
279 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(276): Show |
intron_variant | MODIFIER | c.1434+238T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | chr6 | 109764220 | |||||||
| chr6:109764235 | G | A | 1 | a0001c0003t0001g0025 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1434+253G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | chr6 | 109764235 | |||||||
| chr6:109764305 | G | A | 2 | a0001c0001t0003g0155 a0001c0001t0003g0156 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1434+323G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | chr6 | 109764305 | |||||||
| chr6:109764443 | GA | G | 221 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0221 others(218): Show |
225 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(222): Show |
intron_variant | MODIFIER | c.1434+475delA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr6 | 109764443 | ||||||
| chr6:109764719 | A | G | 3 | a0001c0003t0001g0025 a0001c0003t0001g0035 a0001c0003t0001g0037 |
3 | HG02015.hp2 HG02056.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1435-294A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | chr6 | 109764719 | |||||||
| chr6:109764723 | A | G | 1 | a0001c0001t0003g0179 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1435-290A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | chr6 | 109764723 | |||||||
| chr6:109764757 | T | C | 33 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0360 others(30): Show |
33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1435-256T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | chr6 | 109764757 | |||||||
| chr6:109764895 | T | TTTTTTG | 10 | a0001c0003t0001g0284 a0001c0003t0001g0285 a0001c0003t0001g0286 others(7): Show |
10 | HG01081.hp1 HG01175.hp2 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.1435-84_1435-79dup others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr6 | 109764895 | ||||||
| chr6:109764895 | T | TTTTTTGT others(5): Show |
50 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(47): Show |
50 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.1435-90_1435-79dup others(12): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr6 | 109764895 | ||||||
| chr6:109764895 | TTTTTTG | T | 67 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0221 others(64): Show |
68 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.1435-84_1435-79del others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr6 | 109764895 | ||||||
| chr6:109764895 | TTTTTTGT others(5): Show |
T | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1435-90_1435-79del others(12): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr6 | 109764895 | ||||||
| chr6:109764895 | TTTTTTGT others(11): Show |
T | 1 | a0001c0001t0003g0185 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1435-96_1435-79del others(18): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr6 | 109764895 | ||||||
| chr6:109766412 | T | C | 41 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(38): Show |
41 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.1584-317T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 14/22 | chr6 | 109766412 | |||||||
| chr6:109766414 | G | A | 68 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0221 others(65): Show |
69 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.1584-315G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 14/22 | chr6 | 109766414 | |||||||
| chr6:109766645 | T | A | 68 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0221 others(65): Show |
69 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.1584-84T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 14/22 | chr6 | 109766645 | |||||||
| chr6:109766699 | A | C | 4 | a0002c0002t0002g0009 a0002c0002t0002g0011 a0002c0002t0002g0012 others(1): Show |
4 | HG02809.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1584-30A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 14/22 | chr6 | 109766699 | |||||||
| chr6:109766916 | A | G | 1 | a0002c0004t0001g0091 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1750+21A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109766916 | |||||||
| chr6:109766950 | A | G | 1 | a0001c0001t0002g0290 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1750+55A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109766950 | |||||||
| chr6:109767116 | T | A | 1 | a0001c0001t0002g0074 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1750+221T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109767116 | |||||||
| chr6:109767247 | G | A | 1 | a0002c0002t0003g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1750+352G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109767247 | |||||||
| chr6:109767454 | G | T | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1750+559G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109767454 | |||||||
| chr6:109767525 | T | C | 1 | a0002c0004t0001g0067 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1750+630T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109767525 | |||||||
| chr6:109767596 | C | T | 15 | a0001c0001t0002g0198 a0002c0002t0002g0164 a0002c0002t0004g0196 others(12): Show |
15 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1750+701C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109767596 | |||||||
| chr6:109767636 | C | T | 6 | a0001c0001t0002g0221 a0001c0001t0002g0223 a0001c0001t0002g0224 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1750+741C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109767636 | |||||||
| chr6:109767707 | A | G | 1 | a0002c0002t0004g0186 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1750+812A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109767707 | |||||||
| chr6:109767842 | A | T | 1 | a0003c0007t0001g0328 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1750+947A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109767842 | |||||||
| chr6:109767850 | C | T | 47 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(44): Show |
47 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.1750+955C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109767850 | |||||||
| chr6:109767871 | C | T | 3 | a0002c0002t0005g0125 a0002c0002t0005g0126 a0002c0002t0005g0127 |
3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1750+976C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109767871 | |||||||
| chr6:109767939 | G | A | 3 | a0002c0002t0005g0125 a0002c0002t0005g0126 a0002c0002t0005g0127 |
3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1750+1044G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109767939 | |||||||
| chr6:109768389 | A | G | 1 | a0002c0002t0004g0197 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1750+1494A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109768389 | |||||||
| chr6:109768445 | G | A | 14 | a0001c0001t0002g0299 a0001c0001t0002g0304 a0001c0003t0001g0291 others(11): Show |
14 | HG01256.hp1 HG01258.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1750+1550G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109768445 | |||||||
| chr6:109768601 | C | T | 1 | a0001c0001t0002g0357 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1750+1706C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109768601 | |||||||
| chr6:109768732 | C | T | 6 | a0001c0003t0001g0145 a0001c0003t0001g0263 a0001c0003t0001g0264 others(3): Show |
6 | HG00408.hp2 HG02074.hp1 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.1750+1837C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109768732 | |||||||
| chr6:109768789 | A | C | 271 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(268): Show |
275 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(272): Show |
intron_variant | MODIFIER | c.1750+1894A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109768789 | |||||||
| chr6:109768846 | C | G | 60 | a0001c0001t0002g0299 a0001c0001t0002g0304 a0001c0003t0001g0291 others(57): Show |
63 | HG00639.hp1 HG01175.hp2 HG01256.hp1 others(60): Show |
intron_variant | MODIFIER | c.1750+1951C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109768846 | |||||||
| chr6:109768874 | T | G | 41 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(38): Show |
41 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.1750+1979T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109768874 | |||||||
| chr6:109768885 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1750+1990C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109768885 | |||||||
| chr6:109769087 | C | T | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1750+2192C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109769087 | |||||||
| chr6:109769107 | C | CT | 147 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(144): Show |
150 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(147): Show |
intron_variant | MODIFIER | c.1750+2226dupT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr6 | 109769107 | ||||||
| chr6:109769144 | A | C | 271 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(268): Show |
275 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(272): Show |
intron_variant | MODIFIER | c.1750+2249A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109769144 | |||||||
| chr6:109769793 | C | A | 1 | a0002c0002t0004g0207 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1750+2898C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109769793 | |||||||
| chr6:109769827 | C | G | 275 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(272): Show |
279 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(276): Show |
intron_variant | MODIFIER | c.1750+2932C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109769827 | |||||||
| chr6:109769861 | G | C | 95 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(92): Show |
95 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.1750+2966G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109769861 | |||||||
| chr6:109770007 | G | A | 11 | a0001c0001t0002g0304 a0001c0003t0001g0291 a0001c0003t0001g0292 others(8): Show |
11 | HG01256.hp1 HG01258.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.1750+3112G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109770007 | |||||||
| chr6:109770252 | C | T | 1 | a0003c0005t0001g0311 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1750+3357C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109770252 | |||||||
| chr6:109770347 | G | A | 2 | a0001c0001t0002g0083 a0001c0003t0001g0064 |
2 | HG03017.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1750+3452G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109770347 | |||||||
| chr6:109770359 | GTA | G | 3 | a0002c0002t0002g0016 a0002c0002t0002g0017 a0002c0014t0002g0015 |
3 | HG02559.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1750+3472_1750+347 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr6 | 109770359 | ||||||
| chr6:109770361 | A | G | 28 | a0001c0001t0003g0003 a0001c0001t0003g0162 a0001c0001t0003g0163 others(25): Show |
29 | HG00438.hp1 HG00558.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.1750+3466A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109770361 | |||||||
| chr6:109770416 | T | C | 1 | a0001c0003t0001g0145 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1750+3521T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109770416 | |||||||
| chr6:109770564 | T | A | 2 | a0002c0002t0001g0141 a0002c0002t0001g0142 |
2 | NA19004.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1750+3669T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109770564 | |||||||
| chr6:109770851 | G | T | 108 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(105): Show |
109 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.1750+3956G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109770851 | |||||||
| chr6:109770868 | G | A | 1 | a0002c0004t0001g0055 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1750+3973G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109770868 | |||||||
| chr6:109770901 | TC | T | 4 | a0002c0002t0002g0211 a0002c0009t0002g0157 a0002c0009t0002g0158 others(1): Show |
4 | HG02109.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1750+4009delC | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr6 | 109770901 | ||||||
| chr6:109771461 | C | CT | 106 | a0001c0001t0002g0019 a0001c0001t0002g0046 a0001c0001t0002g0063 others(103): Show |
109 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1750+4591dupT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr6 | 109771461 | ||||||
| chr6:109771461 | C | CTT | 64 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(61): Show |
64 | HG00738.hp2 HG01069.hp2 HG01071.hp1 others(61): Show |
intron_variant | MODIFIER | c.1750+4590_1750+459 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr6 | 109771461 | ||||||
| chr6:109771461 | C | CTTT | 10 | a0001c0001t0003g0362 a0001c0003t0001g0008 a0001c0003t0001g0251 others(7): Show |
10 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1750+4589_1750+459 others(7): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr6 | 109771461 | ||||||
| chr6:109771461 | CTT | C | 8 | a0001c0001t0002g0214 a0001c0001t0003g0162 a0001c0001t0003g0195 others(5): Show |
8 | HG01109.hp1 HG01243.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1750+4590_1750+459 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr6 | 109771461 | ||||||
| chr6:109771461 | CTTT | C | 98 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(95): Show |
99 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1750+4589_1750+459 others(7): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr6 | 109771461 | ||||||
| chr6:109771499 | C | T | 23 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0217 others(20): Show |
23 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.1750+4604C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109771499 | |||||||
| chr6:109771500 | G | C | 2 | a0003c0005t0001g0335 a0003c0005t0001g0336 |
2 | NA19063.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1750+4605G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109771500 | |||||||
| chr6:109771538 | G | T | 4 | a0002c0002t0002g0009 a0002c0002t0002g0011 a0002c0002t0002g0012 others(1): Show |
4 | HG02809.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1750+4643G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109771538 | |||||||
| chr6:109771559 | C | T | 33 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0360 others(30): Show |
33 | HG00323.hp2 HG00544.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1750+4664C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109771559 | |||||||
| chr6:109771593 | C | T | 67 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0221 others(64): Show |
68 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.1750+4698C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109771593 | |||||||
| chr6:109771697 | C | A | 203 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(200): Show |
204 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.1750+4802C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109771697 | |||||||
| chr6:109771716 | G | A | 1 | a0002c0002t0003g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1750+4821G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109771716 | |||||||
| chr6:109771974 | C | T | 1 | a0003c0017t0001g0314 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1751-4948C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109771974 | |||||||
| chr6:109772097 | A | G | 2 | a0001c0001t0002g0069 a0002c0004t0001g0068 |
2 | HG01169.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1751-4825A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109772097 | |||||||
| chr6:109772418 | G | A | 4 | a0002c0002t0002g0085 a0002c0002t0002g0086 a0002c0002t0002g0087 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1751-4504G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109772418 | |||||||
| chr6:109772494 | T | C | 3 | a0001c0003t0001g0257 a0001c0003t0001g0258 a0001c0003t0001g0259 |
3 | HG01069.hp2 HG01071.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1751-4428T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109772494 | |||||||
| chr6:109772645 | G | T | 41 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(38): Show |
41 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.1751-4277G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109772645 | |||||||
| chr6:109772652 | C | T | 1 | a0002c0002t0002g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1751-4270C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109772652 | |||||||
| chr6:109772681 | G | A | 60 | a0001c0001t0002g0299 a0001c0001t0002g0304 a0001c0003t0001g0291 others(57): Show |
63 | HG00639.hp1 HG01175.hp2 HG01256.hp1 others(60): Show |
intron_variant | MODIFIER | c.1751-4241G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109772681 | |||||||
| chr6:109772836 | G | A | 64 | a0001c0001t0002g0299 a0001c0001t0002g0304 a0001c0003t0001g0291 others(61): Show |
67 | HG00639.hp1 HG01175.hp2 HG01256.hp1 others(64): Show |
intron_variant | MODIFIER | c.1751-4086G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109772836 | |||||||
| chr6:109773356 | A | T | 1 | a0001c0003t0001g0064 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1751-3566A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109773356 | |||||||
| chr6:109773413 | A | T | 1 | a0003c0005t0001g0342 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1751-3509A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109773413 | |||||||
| chr6:109773423 | C | T | 95 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(92): Show |
95 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.1751-3499C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109773423 | |||||||
| chr6:109773520 | C | T | 1 | a0002c0015t0001g0181 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1751-3402C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109773520 | |||||||
| chr6:109773612 | C | T | 1 | a0001c0003t0001g0275 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1751-3310C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109773612 | |||||||
| chr6:109773624 | C | T | 3 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0008c0019t0006g0020 |
3 | HG02145.hp2 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1751-3298C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109773624 | |||||||
| chr6:109773880 | C | A | 1 | a0003c0005t0001g0339 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1751-3042C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109773880 | |||||||
| chr6:109773897 | C | T | 1 | a0002c0002t0002g0011 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1751-3025C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109773897 | |||||||
| chr6:109774460 | G | A | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1751-2462G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109774460 | |||||||
| chr6:109774526 | A | C | 2 | a0001c0001t0002g0069 a0002c0004t0001g0068 |
2 | HG01169.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1751-2396A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109774526 | |||||||
| chr6:109774542 | T | G | 4 | a0002c0002t0002g0085 a0002c0002t0002g0086 a0002c0002t0002g0087 others(1): Show |
4 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1751-2380T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109774542 | |||||||
| chr6:109774624 | T | C | 1 | a0003c0005t0001g0072 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1751-2298T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109774624 | |||||||
| chr6:109774743 | G | A | 12 | a0002c0002t0002g0110 a0002c0002t0002g0111 a0002c0002t0002g0112 others(9): Show |
12 | HG02257.hp2 HG02886.hp1 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.1751-2179G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109774743 | |||||||
| chr6:109774799 | T | C | 1 | a0003c0005t0001g0320 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1751-2123T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109774799 | |||||||
| chr6:109774830 | C | G | 3 | a0002c0002t0005g0125 a0002c0002t0005g0126 a0002c0002t0005g0127 |
3 | HG03453.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1751-2092C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109774830 | |||||||
| chr6:109774850 | A | G | 275 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0198 others(272): Show |
279 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(276): Show |
intron_variant | MODIFIER | c.1751-2072A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109774850 | |||||||
| chr6:109774914 | G | A | 4 | a0002c0002t0002g0211 a0002c0009t0002g0157 a0002c0009t0002g0158 others(1): Show |
4 | HG02109.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1751-2008G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109774914 | |||||||
| chr6:109775517 | G | C | 8 | a0001c0001t0002g0221 a0001c0001t0002g0223 a0001c0001t0002g0224 others(5): Show |
8 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1751-1405G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109775517 | |||||||
| chr6:109775564 | C | T | 2 | a0001c0003t0001g0279 a0001c0003t0001g0280 |
2 | HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1751-1358C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109775564 | |||||||
| chr6:109775693 | T | C | 53 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(50): Show |
53 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1751-1229T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109775693 | |||||||
| chr6:109775700 | A | G | 14 | a0001c0001t0002g0299 a0001c0001t0002g0304 a0001c0003t0001g0291 others(11): Show |
14 | HG01256.hp1 HG01258.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1751-1222A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109775700 | |||||||
| chr6:109775759 | C | T | 2 | a0001c0003t0001g0300 a0001c0003t0001g0301 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1751-1163C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109775759 | |||||||
| chr6:109775876 | A | G | 6 | a0001c0001t0002g0198 a0002c0002t0004g0196 a0002c0002t0005g0125 others(3): Show |
6 | HG02572.hp1 HG02717.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1751-1046A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109775876 | |||||||
| chr6:109776039 | G | A | 1 | a0001c0001t0002g0214 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1751-883G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109776039 | |||||||
| chr6:109776060 | A | G | 1 | a0001c0003t0001g0272 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1751-862A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109776060 | |||||||
| chr6:109776179 | T | C | 1 | a0002c0002t0001g0151 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1751-743T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109776179 | |||||||
| chr6:109776214 | G | A | 5 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0360 others(2): Show |
5 | HG02615.hp2 HG02630.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1751-708G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109776214 | |||||||
| chr6:109776585 | A | T | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0016 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1751-337A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109776585 | |||||||
| chr6:109776588 | T | A | 10 | a0001c0001t0002g0221 a0001c0001t0002g0223 a0001c0001t0002g0224 others(7): Show |
10 | HG02109.hp2 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1751-334T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109776588 | |||||||
| chr6:109776612 | G | A | 1 | a0001c0001t0002g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1751-310G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109776612 | |||||||
| chr6:109776628 | A | G | 3 | a0002c0009t0002g0157 a0002c0009t0002g0158 a0002c0009t0002g0159 |
3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1751-294A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109776628 | |||||||
| chr6:109776670 | A | G | 1 | a0002c0002t0004g0229 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1751-252A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109776670 | |||||||
| chr6:109776806 | G | A | 1 | a0001c0001t0003g0167 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1751-116G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109776806 | |||||||
| chr6:109776847 | C | T | 1 | a0002c0002t0001g0136 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1751-75C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 15/22 | chr6 | 109776847 | |||||||
| chr6:109777184 | A | T | 1 | a0002c0002t0002g0119 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1889+124A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109777184 | |||||||
| chr6:109777362 | T | G | 1 | a0004c0006t0001g0308 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1889+302T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109777362 | |||||||
| chr6:109777670 | G | T | 42 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(39): Show |
42 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1889+610G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109777670 | |||||||
| chr6:109777707 | C | T | 4 | a0002c0002t0002g0009 a0002c0002t0002g0011 a0002c0002t0002g0012 others(1): Show |
4 | HG02809.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1889+647C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109777707 | |||||||
| chr6:109777723 | G | C | 1 | a0001c0001t0002g0213 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1889+663G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109777723 | |||||||
| chr6:109777938 | A | G | 1 | a0002c0002t0001g0354 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1889+878A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109777938 | |||||||
| chr6:109777947 | A | T | 1 | a0002c0002t0004g0206 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1889+887A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109777947 | |||||||
| chr6:109777994 | A | C | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1889+934A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109777994 | |||||||
| chr6:109778078 | C | G | 63 | a0001c0001t0002g0122 a0001c0001t0002g0124 a0001c0001t0002g0221 others(60): Show |
64 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.1889+1018C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778078 | |||||||
| chr6:109778163 | G | A | 2 | a0001c0003t0001g0252 a0002c0002t0004g0228 |
2 | HG02809.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1889+1103G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778163 | |||||||
| chr6:109778182 | C | T | 44 | a0001c0001t0002g0122 a0001c0001t0003g0003 a0001c0001t0003g0162 others(41): Show |
45 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.1889+1122C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778182 | |||||||
| chr6:109778183 | G | A | 40 | a0001c0001t0002g0198 a0001c0001t0002g0213 a0001c0001t0002g0214 others(37): Show |
40 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.1889+1123G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778183 | |||||||
| chr6:109778298 | T | TA | 69 | a0001c0001t0002g0255 a0001c0001t0002g0277 a0001c0001t0002g0282 others(66): Show |
69 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.1889+1252dupA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109778298 | ||||||
| chr6:109778363 | G | A | 13 | a0001c0001t0002g0198 a0002c0002t0002g0211 a0002c0002t0004g0196 others(10): Show |
13 | HG02109.hp1 HG02280.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1889+1303G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778363 | |||||||
| chr6:109778470 | C | CA | 284 | a0001c0001t0002g0056 a0001c0001t0002g0083 a0001c0001t0002g0095 others(281): Show |
288 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(285): Show |
intron_variant | MODIFIER | c.1889+1423dupA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109778470 | ||||||
| chr6:109778611 | T | G | 1 | a0001c0001t0002g0100 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1889+1551T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778611 | |||||||
| chr6:109778632 | T | C | 39 | a0001c0001t0002g0056 a0001c0001t0002g0213 a0001c0001t0002g0214 others(36): Show |
39 | HG00099.hp2 HG00423.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.1889+1572T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778632 | |||||||
| chr6:109778699 | C | T | 2 | a0001c0001t0002g0083 a0001c0003t0001g0064 |
2 | HG03017.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1889+1639C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778699 | |||||||
| chr6:109778715 | C | T | 1 | a0004c0006t0001g0340 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1889+1655C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778715 | |||||||
| chr6:109778744 | G | A | 20 | a0001c0003t0001g0276 a0002c0002t0001g0132 a0002c0002t0001g0134 others(17): Show |
20 | HG00544.hp2 HG00738.hp2 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.1889+1684G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778744 | |||||||
| chr6:109778755 | T | C | 5 | a0001c0001t0002g0034 a0001c0003t0001g0296 a0001c0003t0001g0297 others(2): Show |
5 | HG01106.hp2 HG01346.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.1889+1695T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778755 | |||||||
| chr6:109778790 | G | A | 322 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0019 others(319): Show |
328 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(325): Show |
intron_variant | MODIFIER | c.1889+1730G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778790 | |||||||
| chr6:109778809 | T | C | 99 | a0001c0001t0002g0001 a0001c0001t0002g0019 a0001c0001t0002g0021 others(96): Show |
101 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.1889+1749T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778809 | |||||||
| chr6:109778812 | G | A | 2 | a0002c0002t0002g0358 a0002c0002t0002g0359 |
2 | HG02895.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1889+1752G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778812 | |||||||
| chr6:109778813 | G | A | 357 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0019 others(354): Show |
363 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(360): Show |
intron_variant | MODIFIER | c.1889+1753G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778813 | |||||||
| chr6:109778815 | G | A | 46 | a0001c0001t0002g0049 a0001c0001t0002g0074 a0001c0001t0002g0105 others(43): Show |
46 | HG01255.hp1 HG01256.hp1 HG01258.hp2 others(43): Show |
intron_variant | MODIFIER | c.1889+1755G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778815 | |||||||
| chr6:109778820 | T | C | 12 | a0001c0003t0001g0274 a0002c0002t0002g0358 a0002c0002t0002g0359 others(9): Show |
12 | HG01081.hp1 HG01243.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.1889+1760T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778820 | |||||||
| chr6:109778830 | C | A | 8 | a0002c0002t0002g0086 a0002c0002t0002g0087 a0002c0002t0002g0358 others(5): Show |
8 | HG01255.hp2 HG02886.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1889+1770C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778830 | |||||||
| chr6:109778841 | T | C | 12 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0360 others(9): Show |
12 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1889+1781T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778841 | |||||||
| chr6:109778842 | G | C | 2 | a0002c0002t0002g0358 a0002c0002t0002g0359 |
2 | HG02895.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1889+1782G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778842 | |||||||
| chr6:109778846 | G | A | 2 | a0002c0002t0002g0358 a0002c0002t0002g0359 |
2 | HG02895.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1889+1786G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778846 | |||||||
| chr6:109778848 | C | T | 2 | a0002c0004t0001g0219 a0002c0004t0001g0220 |
2 | HG01123.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1889+1788C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778848 | |||||||
| chr6:109778850 | T | C | 2 | a0002c0002t0002g0358 a0002c0002t0002g0359 |
2 | HG02895.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1889+1790T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778850 | |||||||
| chr6:109778879 | G | A | 14 | a0001c0001t0002g0056 a0001c0001t0002g0213 a0001c0001t0002g0214 others(11): Show |
14 | HG00099.hp2 HG00735.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.1889+1819G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778879 | |||||||
| chr6:109778881 | G | C | 1 | a0002c0002t0002g0210 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1889+1821G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778881 | |||||||
| chr6:109778884 | C | T | 6 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0267 others(3): Show |
6 | HG03927.hp2 NA18943.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.1889+1824C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778884 | |||||||
| chr6:109778889 | G | A | 2 | a0001c0001t0002g0029 a0002c0002t0001g0218 |
2 | NA19010.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1889+1829G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778889 | |||||||
| chr6:109778891 | G | A | 1 | a0002c0004t0001g0205 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1889+1831G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778891 | |||||||
| chr6:109778896 | G | T | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1889+1836G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778896 | |||||||
| chr6:109778921 | T | C | 3 | a0003c0005t0001g0329 a0003c0005t0001g0330 a0003c0005t0001g0331 |
3 | HG02074.hp2 NA18952.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1889+1861T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778921 | |||||||
| chr6:109778999 | A | G | 77 | a0001c0001t0002g0104 a0001c0001t0003g0003 a0001c0001t0003g0026 others(74): Show |
79 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.1889+1939A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109778999 | |||||||
| chr6:109779023 | T | A | 2 | a0001c0001t0002g0019 a0001c0001t0002g0021 |
2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1889+1963T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109779023 | |||||||
| chr6:109779130 | C | G | 1 | a0003c0005t0001g0335 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1889+2070C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109779130 | |||||||
| chr6:109779140 | T | G | 1 | a0003c0005t0001g0335 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1889+2080T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109779140 | |||||||
| chr6:109779272 | A | G | 58 | a0001c0001t0002g0124 a0001c0001t0002g0221 a0001c0001t0002g0223 others(55): Show |
62 | HG00639.hp1 HG01175.hp2 HG01243.hp1 others(59): Show |
intron_variant | MODIFIER | c.1889+2212A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109779272 | |||||||
| chr6:109779521 | G | A | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1889+2461G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109779521 | |||||||
| chr6:109779834 | G | A | 2 | a0001c0001t0003g0179 a0004c0008t0002g0315 |
2 | HG01496.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.1889+2774G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109779834 | |||||||
| chr6:109780177 | G | C | 1 | a0002c0002t0002g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1889+3117G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109780177 | |||||||
| chr6:109780207 | G | A | 1 | a0005c0011t0001g0363 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1889+3147G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109780207 | |||||||
| chr6:109780220 | C | G | 1 | a0001c0003t0001g0269 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1889+3160C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109780220 | |||||||
| chr6:109780297 | T | C | 17 | a0001c0001t0003g0187 a0001c0003t0001g0028 a0001c0003t0001g0170 others(14): Show |
17 | HG01081.hp2 HG01256.hp1 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1889+3237T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109780297 | |||||||
| chr6:109780353 | C | T | 1 | a0001c0001t0002g0100 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1889+3293C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109780353 | |||||||
| chr6:109780593 | A | C | 3 | a0002c0002t0002g0016 a0002c0002t0002g0017 a0002c0014t0002g0015 |
3 | HG02559.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1889+3533A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109780593 | |||||||
| chr6:109780782 | A | G | 1 | a0002c0002t0004g0348 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1889+3722A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109780782 | |||||||
| chr6:109780955 | T | C | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1889+3895T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109780955 | |||||||
| chr6:109781107 | C | T | 3 | a0002c0002t0002g0016 a0002c0002t0002g0017 a0002c0014t0002g0015 |
3 | HG02559.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1890-3863C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109781107 | |||||||
| chr6:109781317 | C | T | 1 | a0001c0003t0001g0293 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1890-3653C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109781317 | |||||||
| chr6:109781331 | C | G | 1 | a0002c0002t0002g0359 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1890-3639C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109781331 | |||||||
| chr6:109781366 | T | C | 2 | a0003c0005t0001g0329 a0003c0005t0001g0330 |
2 | HG02074.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.1890-3604T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109781366 | |||||||
| chr6:109781398 | C | A | 109 | a0001c0001t0002g0050 a0001c0001t0002g0056 a0001c0001t0002g0213 others(106): Show |
109 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1890-3572C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109781398 | |||||||
| chr6:109781425 | A | G | 29 | a0001c0003t0001g0048 a0001c0003t0001g0145 a0001c0003t0001g0251 others(26): Show |
29 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.1890-3545A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109781425 | |||||||
| chr6:109781718 | A | G | 2 | a0002c0009t0002g0157 a0002c0009t0002g0159 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1890-3252A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109781718 | |||||||
| chr6:109781773 | C | CAGATTTT others(270): Show |
1 | a0001c0003t0001g0273 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(281): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(271): Show |
1 | a0001c0003t0001g0272 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(282): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(272): Show |
1 | a0001c0003t0001g0173 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(283): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(275): Show |
1 | a0001c0001t0002g0289 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(286): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(277): Show |
1 | a0001c0003t0001g0251 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(288): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(278): Show |
1 | a0001c0003t0001g0188 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(289): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(279): Show |
2 | a0001c0003t0001g0037 a0001c0003t0001g0175 |
2 | HG02015.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(290): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(280): Show |
8 | a0001c0001t0002g0217 a0001c0003t0001g0047 a0001c0003t0001g0258 others(5): Show |
8 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(291): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(281): Show |
4 | a0001c0003t0001g0048 a0001c0003t0001g0269 a0001c0003t0001g0278 others(1): Show |
4 | HG00735.hp2 HG02486.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(292): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(282): Show |
3 | a0001c0003t0001g0038 a0001c0003t0001g0165 a0001c0003t0001g0263 |
3 | HG02074.hp1 NA18953.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(293): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(283): Show |
2 | a0001c0003t0001g0039 a0001c0003t0001g0166 |
2 | NA19002.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(294): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(284): Show |
1 | a0001c0003t0001g0275 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(295): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(285): Show |
1 | a0001c0003t0001g0288 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(296): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(286): Show |
1 | a0001c0003t0001g0257 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(297): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(287): Show |
1 | a0004c0008t0002g0309 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(298): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(287): Show |
3 | a0001c0003t0001g0243 a0001c0003t0001g0253 a0004c0006t0001g0337 |
3 | HG00099.hp2 NA18961.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(298): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(288): Show |
1 | a0004c0008t0002g0322 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(299): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(288): Show |
2 | a0001c0003t0001g0007 a0001c0003t0001g0008 |
2 | NA18943.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(299): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(289): Show |
2 | a0001c0003t0001g0297 a0001c0003t0001g0302 |
2 | HG01346.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(300): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(290): Show |
4 | a0001c0001t0002g0304 a0001c0003t0001g0296 a0001c0003t0001g0303 others(1): Show |
4 | HG01361.hp1 HG01517.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(301): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(291): Show |
3 | a0002c0002t0002g0086 a0002c0002t0002g0087 a0008c0019t0006g0020 |
3 | HG02886.hp2 HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(302): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(292): Show |
1 | a0002c0002t0002g0085 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(303): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(293): Show |
1 | a0001c0001t0002g0241 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(304): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(294): Show |
2 | a0001c0001t0002g0227 a0004c0006t0001g0307 |
2 | HG01169.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(305): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(297): Show |
2 | a0001c0003t0001g0293 a0002c0002t0002g0013 |
2 | HG02280.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(308): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(298): Show |
8 | a0001c0003t0001g0170 a0001c0003t0001g0171 a0001c0003t0001g0172 others(5): Show |
8 | HG01081.hp2 HG01256.hp1 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(309): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(299): Show |
5 | a0001c0003t0001g0028 a0001c0003t0001g0176 a0001c0003t0001g0301 others(2): Show |
5 | HG01258.hp2 HG02738.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(310): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(300): Show |
8 | a0001c0003t0001g0145 a0001c0003t0001g0260 a0001c0003t0001g0262 others(5): Show |
8 | HG00738.hp2 HG01099.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(311): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(301): Show |
1 | a0001c0003t0001g0266 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(312): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(302): Show |
1 | a0001c0003t0001g0271 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(313): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(303): Show |
2 | a0001c0001t0002g0282 a0001c0001t0003g0187 |
2 | HG01071.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(314): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(304): Show |
3 | a0001c0001t0002g0240 a0001c0001t0002g0347 a0001c0003t0001g0285 |
3 | HG00639.hp2 HG02602.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(315): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(305): Show |
13 | a0001c0001t0002g0214 a0001c0001t0002g0234 a0001c0001t0002g0283 others(10): Show |
13 | HG00408.hp1 HG01109.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(316): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(306): Show |
3 | a0001c0001t0002g0050 a0001c0001t0002g0056 a0001c0003t0001g0265 |
3 | HG00408.hp2 HG01175.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(317): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(308): Show |
3 | a0001c0001t0002g0233 a0001c0003t0001g0064 a0001c0003t0001g0081 |
3 | HG01243.hp1 HG03831.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(319): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(309): Show |
3 | a0001c0001t0002g0235 a0001c0001t0002g0236 a0004c0006t0001g0340 |
3 | HG01099.hp2 NA19057.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(320): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(310): Show |
3 | a0001c0001t0002g0237 a0001c0003t0001g0025 a0001c0003t0001g0035 |
3 | HG02056.hp2 HG02145.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(321): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(311): Show |
4 | a0001c0003t0001g0097 a0001c0003t0001g0177 a0001c0003t0001g0252 others(1): Show |
4 | HG01978.hp2 HG02523.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.1890-3191_1890-319 others(322): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(313): Show |
1 | a0001c0001t0002g0213 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(324): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781773 | C | CAGATTTT others(315): Show |
1 | a0001c0001t0002g0277 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1890-3191_1890-319 others(326): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109781773 | ||||||
| chr6:109781800 | C | T | 28 | a0002c0002t0002g0011 a0002c0002t0003g0209 a0002c0002t0004g0010 others(25): Show |
28 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(25): Show |
intron_variant | MODIFIER | c.1890-3170C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109781800 | |||||||
| chr6:109782055 | C | T | 1 | a0001c0003t0001g0286 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1890-2915C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109782055 | |||||||
| chr6:109782078 | T | G | 6 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0085 others(3): Show |
6 | HG02280.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1890-2892T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109782078 | |||||||
| chr6:109782477 | G | C | 1 | a0004c0006t0001g0307 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1890-2493G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109782477 | |||||||
| chr6:109782565 | C | T | 1 | a0002c0012t0001g0137 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1890-2405C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109782565 | |||||||
| chr6:109782569 | T | A | 1 | a0001c0001t0002g0277 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1890-2401T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109782569 | |||||||
| chr6:109782599 | CT | C | 137 | a0001c0001t0002g0124 a0001c0001t0002g0221 a0001c0001t0002g0223 others(134): Show |
140 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1890-2368delT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr6 | 109782599 | ||||||
| chr6:109782633 | T | C | 30 | a0001c0001t0002g0104 a0001c0001t0003g0003 a0001c0001t0003g0026 others(27): Show |
31 | HG00438.hp1 HG00558.hp2 HG02615.hp2 others(28): Show |
intron_variant | MODIFIER | c.1890-2337T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109782633 | |||||||
| chr6:109782694 | A | T | 1 | a0004c0006t0001g0307 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1890-2276A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109782694 | |||||||
| chr6:109782884 | A | C | 1 | a0001c0003t0001g0262 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1890-2086A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109782884 | |||||||
| chr6:109782927 | C | T | 102 | a0001c0001t0002g0050 a0001c0001t0002g0056 a0001c0001t0002g0213 others(99): Show |
102 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.1890-2043C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109782927 | |||||||
| chr6:109782945 | T | C | 1 | a0001c0001t0002g0023 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1890-2025T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109782945 | |||||||
| chr6:109783006 | T | C | 2 | a0002c0002t0002g0016 a0002c0002t0002g0017 |
2 | HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1890-1964T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109783006 | |||||||
| chr6:109783095 | A | C | 1 | a0002c0002t0001g0152 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1890-1875A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109783095 | |||||||
| chr6:109783151 | G | A | 3 | a0002c0002t0002g0009 a0002c0002t0004g0294 a0002c0002t0005g0125 |
3 | HG02451.hp2 HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1890-1819G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109783151 | |||||||
| chr6:109783243 | G | A | 25 | a0002c0002t0002g0009 a0002c0002t0002g0012 a0002c0002t0002g0073 others(22): Show |
25 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(22): Show |
intron_variant | MODIFIER | c.1890-1727G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109783243 | |||||||
| chr6:109783500 | A | T | 29 | a0001c0001t0003g0003 a0001c0001t0003g0026 a0001c0001t0003g0027 others(26): Show |
30 | HG00438.hp1 HG00558.hp2 HG02615.hp2 others(27): Show |
intron_variant | MODIFIER | c.1890-1470A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109783500 | |||||||
| chr6:109783860 | T | A | 1 | a0002c0002t0004g0196 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1890-1110T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109783860 | |||||||
| chr6:109783894 | G | A | 29 | a0001c0001t0003g0003 a0001c0001t0003g0026 a0001c0001t0003g0027 others(26): Show |
30 | HG00438.hp1 HG00558.hp2 HG02615.hp2 others(27): Show |
intron_variant | MODIFIER | c.1890-1076G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109783894 | |||||||
| chr6:109784116 | A | G | 1 | a0004c0006t0001g0324 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1890-854A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109784116 | |||||||
| chr6:109784260 | G | T | 2 | a0002c0002t0002g0016 a0002c0002t0002g0017 |
2 | HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1890-710G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109784260 | |||||||
| chr6:109784266 | A | G | 13 | a0002c0002t0004g0010 a0002c0002t0004g0196 a0002c0002t0004g0197 others(10): Show |
13 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1890-704A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109784266 | |||||||
| chr6:109784412 | G | A | 1 | a0001c0003t0001g0028 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1890-558G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109784412 | |||||||
| chr6:109784551 | G | A | 3 | a0003c0005t0001g0332 a0003c0005t0001g0334 a0003c0007t0001g0343 |
3 | NA18955.hp1 NA18967.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.1890-419G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109784551 | |||||||
| chr6:109784869 | G | T | 25 | a0002c0002t0002g0009 a0002c0002t0002g0012 a0002c0002t0002g0073 others(22): Show |
25 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(22): Show |
intron_variant | MODIFIER | c.1890-101G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 16/22 | chr6 | 109784869 | |||||||
| chr6:109785031 | A | G | 111 | a0001c0001t0002g0050 a0001c0001t0002g0056 a0001c0001t0002g0124 others(108): Show |
111 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(108): Show |
splice_region_variant&intron_variant | LOW | c.1948+3A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109785031 | |||||||
| chr6:109785074 | C | A | 129 | a0002c0002t0001g0130 a0002c0002t0001g0132 a0002c0002t0001g0133 others(126): Show |
132 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.1948+46C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109785074 | |||||||
| chr6:109785084 | T | C | 2 | a0002c0002t0005g0126 a0002c0002t0005g0127 |
2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1948+56T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109785084 | |||||||
| chr6:109785119 | T | G | 1 | a0001c0001t0002g0103 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1948+91T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109785119 | |||||||
| chr6:109785356 | A | G | 1 | a0003c0005t0001g0345 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1948+328A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109785356 | |||||||
| chr6:109785380 | G | A | 41 | a0002c0004t0001g0128 a0002c0004t0001g0129 a0002c0004t0001g0174 others(38): Show |
44 | HG00639.hp1 HG01175.hp2 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.1948+352G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109785380 | |||||||
| chr6:109785399 | G | A | 19 | a0002c0002t0002g0012 a0002c0002t0002g0110 a0002c0002t0002g0111 others(16): Show |
19 | HG02257.hp2 HG02615.hp1 HG02647.hp2 others(16): Show |
intron_variant | MODIFIER | c.1948+371G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109785399 | |||||||
| chr6:109785498 | A | G | 1 | a0001c0003t0001g0268 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1948+470A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109785498 | |||||||
| chr6:109785538 | A | T | 163 | a0002c0002t0001g0130 a0002c0002t0001g0132 a0002c0002t0001g0133 others(160): Show |
166 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.1948+510A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109785538 | |||||||
| chr6:109785692 | C | T | 2 | a0002c0002t0002g0011 a0002c0009t0002g0158 |
2 | HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1949-610C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109785692 | |||||||
| chr6:109785707 | C | T | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1949-595C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109785707 | |||||||
| chr6:109785863 | T | C | 1 | a0002c0002t0002g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1949-439T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109785863 | |||||||
| chr6:109785911 | C | T | 3 | a0001c0003t0001g0260 a0001c0003t0001g0261 a0001c0003t0001g0262 |
3 | HG01099.hp1 HG01433.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1949-391C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109785911 | |||||||
| chr6:109785994 | G | A | 111 | a0001c0001t0002g0050 a0001c0001t0002g0056 a0001c0001t0002g0124 others(108): Show |
111 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.1949-308G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109785994 | |||||||
| chr6:109786075 | C | T | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1949-227C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109786075 | |||||||
| chr6:109786125 | A | C | 15 | a0001c0001t0003g0003 a0001c0001t0003g0162 a0001c0001t0003g0163 others(12): Show |
16 | HG00438.hp1 NA18939.hp1 NA18940.hp1 others(13): Show |
intron_variant | MODIFIER | c.1949-177A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109786125 | |||||||
| chr6:109786131 | C | T | 1 | a0002c0004t0001g0055 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1949-171C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109786131 | |||||||
| chr6:109786154 | A | G | 6 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0085 others(3): Show |
6 | HG02280.hp2 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1949-148A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109786154 | |||||||
| chr6:109786181 | G | A | 2 | a0002c0002t0005g0126 a0002c0002t0005g0127 |
2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1949-121G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 17/22 | chr6 | 109786181 | |||||||
| chr6:109786860 | G | C | 26 | a0002c0002t0003g0209 a0002c0002t0004g0010 a0002c0002t0004g0123 others(23): Show |
26 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.2096+411G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109786860 | |||||||
| chr6:109787146 | C | T | 2 | a0002c0002t0004g0010 a0002c0002t0004g0197 |
2 | HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2096+697C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109787146 | |||||||
| chr6:109787236 | A | G | 2 | a0001c0001t0002g0046 a0001c0001t0002g0357 |
2 | HG00438.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.2096+787A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109787236 | |||||||
| chr6:109787242 | A | G | 26 | a0002c0002t0003g0209 a0002c0002t0004g0010 a0002c0002t0004g0123 others(23): Show |
26 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.2096+793A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109787242 | |||||||
| chr6:109787299 | T | C | 29 | a0001c0001t0003g0003 a0001c0001t0003g0026 a0001c0001t0003g0027 others(26): Show |
30 | HG00438.hp1 HG00558.hp2 HG02615.hp2 others(27): Show |
intron_variant | MODIFIER | c.2096+850T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109787299 | |||||||
| chr6:109787359 | C | T | 29 | a0002c0004t0001g0032 a0002c0004t0001g0041 a0002c0004t0001g0043 others(26): Show |
29 | HG00099.hp1 HG00423.hp2 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.2096+910C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109787359 | |||||||
| chr6:109787421 | T | C | 2 | a0002c0002t0005g0126 a0002c0002t0005g0127 |
2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2096+972T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109787421 | |||||||
| chr6:109787423 | G | T | 1 | a0001c0001t0002g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2096+974G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109787423 | |||||||
| chr6:109787652 | G | T | 303 | a0001c0001t0002g0050 a0001c0001t0002g0056 a0001c0001t0002g0124 others(300): Show |
307 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(304): Show |
intron_variant | MODIFIER | c.2096+1203G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109787652 | |||||||
| chr6:109787884 | C | A | 1 | a0001c0001t0002g0299 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2096+1435C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109787884 | |||||||
| chr6:109787962 | A | G | 1 | a0002c0004t0001g0129 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2096+1513A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109787962 | |||||||
| chr6:109788239 | A | G | 1 | a0001c0003t0001g0288 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2097-1355A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109788239 | |||||||
| chr6:109788371 | G | A | 1 | a0002c0002t0004g0196 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2097-1223G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109788371 | |||||||
| chr6:109788576 | G | A | 22 | a0002c0002t0002g0009 a0002c0002t0002g0012 a0002c0002t0002g0110 others(19): Show |
22 | HG02257.hp2 HG02451.hp2 HG02615.hp1 others(19): Show |
intron_variant | MODIFIER | c.2097-1018G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109788576 | |||||||
| chr6:109788588 | C | T | 1 | a0001c0001t0002g0074 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2097-1006C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109788588 | |||||||
| chr6:109788664 | C | T | 3 | a0002c0002t0004g0351 a0002c0002t0004g0352 a0002c0002t0004g0353 |
3 | HG01081.hp1 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2097-930C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109788664 | |||||||
| chr6:109788673 | G | A | 2 | a0002c0002t0004g0294 a0002c0002t0005g0125 |
2 | HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2097-921G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109788673 | |||||||
| chr6:109789007 | T | C | 1 | a0001c0001t0003g0026 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2097-587T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109789007 | |||||||
| chr6:109789036 | G | A | 4 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0099 others(1): Show |
4 | HG00423.hp1 HG00544.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.2097-558G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109789036 | |||||||
| chr6:109789099 | A | G | 15 | a0001c0001t0003g0003 a0001c0001t0003g0162 a0001c0001t0003g0163 others(12): Show |
16 | HG00438.hp1 NA18939.hp1 NA18940.hp1 others(13): Show |
intron_variant | MODIFIER | c.2097-495A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109789099 | |||||||
| chr6:109789126 | T | C | 2 | a0002c0002t0002g0073 a0002c0002t0002g0211 |
2 | HG02109.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2097-468T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109789126 | |||||||
| chr6:109789222 | C | A | 1 | a0002c0002t0001g0146 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2097-372C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109789222 | |||||||
| chr6:109789351 | A | C | 304 | a0001c0001t0002g0050 a0001c0001t0002g0056 a0001c0001t0002g0104 others(301): Show |
308 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(305): Show |
intron_variant | MODIFIER | c.2097-243A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109789351 | |||||||
| chr6:109789377 | C | T | 29 | a0001c0001t0003g0003 a0001c0001t0003g0026 a0001c0001t0003g0027 others(26): Show |
30 | HG00438.hp1 HG00558.hp2 HG02615.hp2 others(27): Show |
intron_variant | MODIFIER | c.2097-217C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 18/22 | chr6 | 109789377 | |||||||
| chr6:109789740 | G | T | 103 | a0001c0001t0002g0050 a0001c0001t0002g0056 a0001c0001t0002g0213 others(100): Show |
103 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.2180+63G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 19/22 | chr6 | 109789740 | |||||||
| chr6:109789858 | T | C | 2 | a0001c0001t0003g0361 a0001c0001t0003g0362 |
2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2180+181T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 19/22 | chr6 | 109789858 | |||||||
| chr6:109790073 | T | A | 101 | a0002c0002t0001g0130 a0002c0002t0001g0132 a0002c0002t0001g0133 others(98): Show |
104 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.2180+396T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 19/22 | chr6 | 109790073 | |||||||
| chr6:109790810 | T | TC | 60 | a0002c0002t0001g0130 a0002c0002t0001g0132 a0002c0002t0001g0133 others(57): Show |
60 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.2181-560dupC | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr6 | 109790810 | ||||||
| chr6:109790814 | C | T | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2181-562C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 19/22 | chr6 | 109790814 | |||||||
| chr6:109790821 | A | G | 5 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0360 others(2): Show |
5 | HG02615.hp2 HG02630.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2181-555A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 19/22 | chr6 | 109790821 | |||||||
| chr6:109790831 | A | G | 1 | a0001c0001t0002g0124 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2181-545A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 19/22 | chr6 | 109790831 | |||||||
| chr6:109790912 | T | G | 8 | a0001c0001t0002g0124 a0001c0001t0002g0221 a0001c0001t0002g0223 others(5): Show |
8 | HG02109.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2181-464T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 19/22 | chr6 | 109790912 | |||||||
| chr6:109790973 | G | A | 14 | a0002c0002t0003g0209 a0002c0002t0004g0010 a0002c0002t0004g0196 others(11): Show |
14 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.2181-403G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 19/22 | chr6 | 109790973 | |||||||
| chr6:109791009 | T | A | 41 | a0002c0004t0001g0128 a0002c0004t0001g0129 a0002c0004t0001g0174 others(38): Show |
44 | HG00639.hp1 HG01175.hp2 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.2181-367T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 19/22 | chr6 | 109791009 | |||||||
| chr6:109791012 | C | T | 41 | a0002c0004t0001g0128 a0002c0004t0001g0129 a0002c0004t0001g0174 others(38): Show |
44 | HG00639.hp1 HG01175.hp2 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.2181-364C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 19/22 | chr6 | 109791012 | |||||||
| chr6:109791126 | T | A | 1 | a0001c0001t0003g0027 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2181-250T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 19/22 | chr6 | 109791126 | |||||||
| chr6:109791133 | C | T | 3 | a0001c0003t0001g0166 a0001c0003t0001g0173 a0001c0003t0001g0177 |
3 | HG00741.hp1 HG01978.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.2181-243C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 19/22 | chr6 | 109791133 | |||||||
| chr6:109791731 | A | C | 1 | a0002c0002t0002g0210 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2376+160A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 20/22 | chr6 | 109791731 | |||||||
| chr6:109791900 | G | A | 1 | a0002c0009t0002g0158 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2376+329G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 20/22 | chr6 | 109791900 | |||||||
| chr6:109792008 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2376+437C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 20/22 | chr6 | 109792008 | |||||||
| chr6:109792166 | A | C | 1 | a0003c0005t0001g0325 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2377-416A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 20/22 | chr6 | 109792166 | |||||||
| chr6:109792560 | CT | C | 42 | a0001c0001t0002g0282 a0001c0001t0002g0283 a0002c0004t0001g0128 others(39): Show |
45 | HG00639.hp1 HG01071.hp1 HG01123.hp2 others(42): Show |
intron_variant | MODIFIER | c.2377-10delT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr6 | 109792560 | ||||||
| chr6:109792562 | T | TC | 22 | a0002c0004t0001g0032 a0002c0004t0001g0041 a0002c0004t0001g0043 others(19): Show |
22 | HG00099.hp1 HG00423.hp2 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.2377-20_2377-19ins others(1): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 20/22 | chr6 | 109792562 | |||||||
| chr6:109792563 | T | C | 36 | a0002c0002t0001g0130 a0002c0002t0001g0132 a0002c0002t0001g0133 others(33): Show |
36 | HG00323.hp2 HG00544.hp2 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.2377-19T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 20/22 | chr6 | 109792563 | |||||||
| chr6:109792723 | C | T | 2 | a0002c0002t0004g0294 a0002c0002t0005g0125 |
2 | HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2459+59C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109792723 | |||||||
| chr6:109792736 | C | CT | 15 | a0001c0001t0002g0104 a0002c0004t0001g0032 a0002c0004t0001g0043 others(12): Show |
15 | HG00423.hp2 HG02056.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.2459+91dupT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109792736 | ||||||
| chr6:109792736 | CT | C | 192 | a0001c0001t0002g0050 a0001c0001t0002g0056 a0001c0001t0002g0060 others(189): Show |
193 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.2459+91delT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109792736 | ||||||
| chr6:109792736 | CTT | C | 40 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0227 others(37): Show |
40 | HG01081.hp1 HG01099.hp1 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.2459+90_2459+91del others(2): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109792736 | ||||||
| chr6:109792814 | C | T | 1 | a0002c0002t0002g0009 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2459+150C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109792814 | |||||||
| chr6:109792858 | T | C | 3 | a0002c0002t0002g0016 a0002c0002t0002g0017 a0002c0014t0002g0015 |
3 | HG02559.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2459+194T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109792858 | |||||||
| chr6:109793118 | A | AAATG | 4 | a0001c0003t0001g0254 a0001c0003t0001g0291 a0001c0003t0001g0292 others(1): Show |
4 | NA18949.hp2 NA18974.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.2459+455_2459+458d others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109793118 | ||||||
| chr6:109793277 | A | G | 1 | a0001c0003t0001g0081 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2459+613A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109793277 | |||||||
| chr6:109793296 | C | T | 1 | a0002c0002t0005g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2459+632C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109793296 | |||||||
| chr6:109793400 | T | G | 6 | a0002c0002t0002g0014 a0002c0002t0002g0085 a0002c0002t0002g0086 others(3): Show |
6 | HG02486.hp2 HG02572.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2459+736T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109793400 | |||||||
| chr6:109793457 | C | T | 22 | a0002c0002t0002g0009 a0002c0002t0002g0012 a0002c0002t0002g0110 others(19): Show |
22 | HG02257.hp2 HG02451.hp2 HG02615.hp1 others(19): Show |
intron_variant | MODIFIER | c.2459+793C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109793457 | |||||||
| chr6:109793465 | T | C | 2 | a0001c0001t0002g0224 a0007c0013t0002g0222 |
2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2459+801T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109793465 | |||||||
| chr6:109793473 | C | G | 37 | a0001c0001t0002g0124 a0001c0001t0002g0221 a0001c0001t0002g0223 others(34): Show |
38 | HG00438.hp1 HG00558.hp2 HG02109.hp2 others(35): Show |
intron_variant | MODIFIER | c.2459+809C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109793473 | |||||||
| chr6:109793518 | T | C | 15 | a0002c0002t0002g0012 a0002c0002t0002g0110 a0002c0002t0002g0111 others(12): Show |
15 | HG02257.hp2 HG02615.hp1 HG02818.hp2 others(12): Show |
intron_variant | MODIFIER | c.2459+854T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109793518 | |||||||
| chr6:109793625 | A | T | 1 | a0002c0002t0004g0305 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2459+961A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109793625 | |||||||
| chr6:109793669 | T | C | 1 | a0002c0002t0002g0017 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2459+1005T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109793669 | |||||||
| chr6:109793702 | G | C | 30 | a0001c0001t0002g0277 a0002c0002t0002g0009 a0002c0002t0002g0012 others(27): Show |
30 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(27): Show |
intron_variant | MODIFIER | c.2459+1038G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109793702 | |||||||
| chr6:109793703 | C | T | 30 | a0002c0002t0002g0014 a0002c0002t0002g0085 a0002c0002t0002g0086 others(27): Show |
30 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.2459+1039C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109793703 | |||||||
| chr6:109793933 | A | G | 1 | a0001c0001t0002g0277 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2459+1269A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109793933 | |||||||
| chr6:109793963 | T | C | 27 | a0002c0002t0003g0209 a0002c0002t0004g0010 a0002c0002t0004g0123 others(24): Show |
27 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.2459+1299T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109793963 | |||||||
| chr6:109794273 | C | T | 1 | a0001c0001t0002g0277 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2459+1609C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109794273 | |||||||
| chr6:109794396 | G | C | 1 | a0001c0001t0002g0074 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2459+1732G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109794396 | |||||||
| chr6:109794732 | C | T | 23 | a0002c0002t0002g0009 a0002c0002t0002g0012 a0002c0002t0002g0088 others(20): Show |
23 | HG02257.hp2 HG02451.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.2460-2033C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109794732 | |||||||
| chr6:109794986 | C | T | 3 | a0002c0002t0002g0016 a0002c0002t0002g0017 a0002c0014t0002g0015 |
3 | HG02559.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2460-1779C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109794986 | |||||||
| chr6:109794988 | C | T | 1 | a0002c0004t0001g0044 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2460-1777C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109794988 | |||||||
| chr6:109795038 | A | G | 3 | a0002c0002t0002g0073 a0002c0002t0002g0211 a0002c0004t0001g0160 |
3 | HG02109.hp1 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2460-1727A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795038 | |||||||
| chr6:109795094 | AGTTTTTT others(5): Show |
A | 7 | a0001c0001t0003g0163 a0001c0001t0003g0182 a0001c0001t0003g0184 others(4): Show |
7 | HG02818.hp1 NA18952.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.2460-1670_2460-165 others(16): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795094 | |||||||
| chr6:109795094 | AGTTTTTT others(6): Show |
A | 30 | a0001c0001t0002g0124 a0001c0001t0002g0221 a0001c0001t0002g0223 others(27): Show |
31 | HG00438.hp1 HG00558.hp2 HG02109.hp2 others(28): Show |
intron_variant | MODIFIER | c.2460-1670_2460-165 others(17): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795094 | |||||||
| chr6:109795095 | G | GT | 8 | a0001c0001t0002g0019 a0001c0001t0002g0046 a0001c0001t0002g0059 others(5): Show |
8 | HG00438.hp2 HG00738.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.2460-1630dupT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | ||||||
| chr6:109795095 | G | GTTT | 7 | a0001c0001t0002g0022 a0001c0001t0002g0034 a0001c0001t0002g0098 others(4): Show |
7 | HG00544.hp1 HG00639.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.2460-1632_2460-163 others(7): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | ||||||
| chr6:109795095 | G | GTTTTTTT others(3): Show |
2 | a0001c0001t0002g0052 a0001c0001t0002g0053 |
2 | HG00558.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.2460-1639_2460-163 others(14): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | ||||||
| chr6:109795095 | G | GTTTTTTT others(4): Show |
2 | a0001c0001t0002g0227 a0001c0001t0002g0241 |
2 | HG01169.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.2460-1640_2460-163 others(15): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | ||||||
| chr6:109795095 | G | GTTTTTTT others(6): Show |
1 | a0001c0001t0002g0042 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2460-1642_2460-163 others(17): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | ||||||
| chr6:109795095 | GT | G | 21 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0023 others(18): Show |
21 | HG02004.hp1 HG02280.hp2 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.2460-1630delT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | ||||||
| chr6:109795095 | GTTTTTTT others(3): Show |
G | 1 | a0002c0002t0002g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2460-1639_2460-163 others(14): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | ||||||
| chr6:109795095 | GTTTTTTT others(4): Show |
G | 6 | a0002c0002t0002g0116 a0002c0002t0002g0118 a0002c0002t0002g0121 others(3): Show |
6 | HG02257.hp2 HG02647.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2460-1640_2460-163 others(15): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | ||||||
| chr6:109795095 | GTTTTTTT others(5): Show |
G | 24 | a0002c0002t0001g0143 a0002c0002t0001g0149 a0002c0002t0001g0154 others(21): Show |
24 | HG01261.hp1 HG02135.hp2 HG02486.hp2 others(21): Show |
intron_variant | MODIFIER | c.2460-1641_2460-163 others(16): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | ||||||
| chr6:109795095 | GTTTTTTT others(6): Show |
G | 66 | a0001c0003t0001g0038 a0001c0003t0001g0064 a0001c0003t0001g0077 others(63): Show |
66 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.2460-1642_2460-163 others(17): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | ||||||
| chr6:109795095 | GTTTTTTT others(7): Show |
G | 71 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0018 others(68): Show |
71 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.2460-1643_2460-163 others(18): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | ||||||
| chr6:109795095 | GTTTTTTT others(8): Show |
G | 27 | a0001c0003t0001g0259 a0001c0003t0001g0285 a0002c0002t0003g0209 others(24): Show |
27 | HG01069.hp2 HG01081.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.2460-1644_2460-163 others(19): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | ||||||
| chr6:109795095 | GTTTTTTT others(9): Show |
G | 1 | a0001c0001t0002g0198 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2460-1645_2460-163 others(20): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | ||||||
| chr6:109795095 | GTTTTTTT others(10): Show |
G | 2 | a0001c0001t0002g0282 a0001c0001t0002g0283 |
2 | HG01071.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.2460-1646_2460-163 others(21): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | ||||||
| chr6:109795095 | GTTTTTTT others(13): Show |
G | 2 | a0002c0002t0002g0086 a0002c0002t0002g0087 |
2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2460-1649_2460-163 others(24): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | ||||||
| chr6:109795095 | GTTTTTTT others(15): Show |
G | 1 | a0001c0001t0002g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2460-1651_2460-163 others(26): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795095 | ||||||
| chr6:109795105 | T | TTG | 12 | a0002c0004t0001g0174 a0002c0004t0001g0178 a0003c0005t0001g0005 others(9): Show |
12 | HG00639.hp1 HG01175.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.2460-1659_2460-165 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795105 | ||||||
| chr6:109795106 | T | TG | 29 | a0002c0004t0001g0128 a0002c0004t0001g0129 a0002c0004t0001g0189 others(26): Show |
30 | HG01255.hp2 HG01358.hp2 HG01934.hp2 others(27): Show |
intron_variant | MODIFIER | c.2460-1659_2460-165 others(5): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795106 | |||||||
| chr6:109795113 | T | G | 1 | a0002c0014t0002g0015 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2460-1652T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795113 | |||||||
| chr6:109795118 | T | G | 2 | a0002c0009t0002g0157 a0002c0009t0002g0159 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2460-1647T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795118 | |||||||
| chr6:109795122 | T | G | 1 | a0003c0005t0001g0338 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2460-1643T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795122 | |||||||
| chr6:109795139 | A | G | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2460-1626A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795139 | |||||||
| chr6:109795162 | G | A | 1 | a0002c0004t0001g0041 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2460-1603G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795162 | |||||||
| chr6:109795225 | C | T | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2460-1540C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795225 | |||||||
| chr6:109795403 | T | A | 29 | a0002c0002t0001g0130 a0002c0002t0001g0132 a0002c0002t0001g0133 others(26): Show |
29 | HG00323.hp2 HG00544.hp2 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.2460-1362T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795403 | |||||||
| chr6:109795558 | AAAGGAAA others(1): Show |
A | 27 | a0002c0002t0003g0209 a0002c0002t0004g0010 a0002c0002t0004g0123 others(24): Show |
27 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.2460-1198_2460-119 others(12): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795558 | ||||||
| chr6:109795595 | C | CT | 15 | a0002c0002t0001g0134 a0002c0002t0002g0013 a0002c0002t0002g0014 others(12): Show |
15 | HG01261.hp1 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2460-1144dupT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795595 | ||||||
| chr6:109795595 | C | CTT | 86 | a0001c0001t0002g0021 a0001c0001t0002g0061 a0001c0001t0002g0093 others(83): Show |
86 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.2460-1145_2460-114 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795595 | ||||||
| chr6:109795595 | C | CTTT | 93 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0019 others(90): Show |
95 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.2460-1146_2460-114 others(7): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795595 | ||||||
| chr6:109795595 | C | CTTTT | 79 | a0001c0001t0002g0034 a0001c0001t0002g0050 a0001c0001t0002g0052 others(76): Show |
79 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.2460-1147_2460-114 others(8): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795595 | ||||||
| chr6:109795595 | C | CTTTTT | 12 | a0001c0001t0002g0107 a0001c0003t0001g0037 a0001c0003t0001g0064 others(9): Show |
12 | HG00735.hp2 HG02015.hp2 HG02148.hp1 others(9): Show |
intron_variant | MODIFIER | c.2460-1148_2460-114 others(9): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795595 | ||||||
| chr6:109795595 | CTTTT | C | 12 | a0001c0001t0003g0003 a0001c0001t0003g0163 a0001c0001t0003g0168 others(9): Show |
13 | HG00438.hp1 NA18939.hp1 NA18940.hp1 others(10): Show |
intron_variant | MODIFIER | c.2460-1147_2460-114 others(8): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795595 | ||||||
| chr6:109795595 | CTTTTTTT others(4): Show |
C | 38 | a0002c0004t0001g0128 a0002c0004t0001g0129 a0002c0004t0001g0174 others(35): Show |
41 | HG00639.hp1 HG01175.hp2 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.2460-1154_2460-114 others(15): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr6 | 109795595 | ||||||
| chr6:109795663 | A | G | 164 | a0001c0001t0002g0277 a0002c0002t0001g0130 a0002c0002t0001g0132 others(161): Show |
167 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.2460-1102A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795663 | |||||||
| chr6:109795769 | T | A | 27 | a0002c0002t0003g0209 a0002c0002t0004g0010 a0002c0002t0004g0123 others(24): Show |
27 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.2460-996T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795769 | |||||||
| chr6:109795803 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2460-962G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795803 | |||||||
| chr6:109795823 | G | A | 3 | a0002c0002t0002g0009 a0002c0002t0004g0294 a0002c0002t0005g0125 |
3 | HG02451.hp2 HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2460-942G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795823 | |||||||
| chr6:109795892 | C | T | 3 | a0002c0002t0002g0011 a0002c0002t0005g0126 a0002c0002t0005g0127 |
3 | HG02809.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2460-873C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795892 | |||||||
| chr6:109795893 | G | A | 1 | a0002c0002t0004g0294 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2460-872G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795893 | |||||||
| chr6:109795895 | G | A | 23 | a0002c0002t0002g0009 a0002c0002t0002g0012 a0002c0002t0002g0088 others(20): Show |
23 | HG02257.hp2 HG02451.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.2460-870G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795895 | |||||||
| chr6:109795919 | A | T | 27 | a0002c0002t0003g0209 a0002c0002t0004g0010 a0002c0002t0004g0123 others(24): Show |
27 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.2460-846A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795919 | |||||||
| chr6:109795967 | C | T | 80 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0018 others(77): Show |
80 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.2460-798C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109795967 | |||||||
| chr6:109796237 | G | T | 2 | a0001c0001t0002g0019 a0001c0001t0002g0021 |
2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2460-528G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109796237 | |||||||
| chr6:109796513 | A | G | 29 | a0002c0004t0001g0032 a0002c0004t0001g0041 a0002c0004t0001g0043 others(26): Show |
29 | HG00099.hp1 HG00423.hp2 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.2460-252A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109796513 | |||||||
| chr6:109796546 | A | G | 1 | a0001c0001t0003g0187 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2460-219A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109796546 | |||||||
| chr6:109796559 | A | G | 1 | a0002c0002t0002g0009 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2460-206A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109796559 | |||||||
| chr6:109796638 | C | T | 26 | a0002c0002t0003g0209 a0002c0002t0004g0010 a0002c0002t0004g0123 others(23): Show |
26 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.2460-127C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109796638 | |||||||
| chr6:109796727 | C | T | 3 | a0002c0002t0002g0011 a0002c0002t0005g0126 a0002c0002t0005g0127 |
3 | HG02809.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2460-38C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 21/22 | chr6 | 109796727 | |||||||
| chr6:109797009 | C | T | 30 | a0001c0001t0003g0003 a0001c0001t0003g0026 a0001c0001t0003g0027 others(27): Show |
31 | HG00438.hp1 HG00558.hp2 HG02615.hp2 others(28): Show |
intron_variant | MODIFIER | c.2546+158C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109797009 | |||||||
| chr6:109797236 | T | G | 41 | a0002c0004t0001g0128 a0002c0004t0001g0129 a0002c0004t0001g0174 others(38): Show |
44 | HG00639.hp1 HG01175.hp2 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.2546+385T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109797236 | |||||||
| chr6:109797282 | C | T | 1 | a0006c0016t0001g0080 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2546+431C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109797282 | |||||||
| chr6:109797383 | A | G | 283 | a0001c0001t0002g0104 a0001c0001t0002g0124 a0001c0001t0002g0221 others(280): Show |
287 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(284): Show |
intron_variant | MODIFIER | c.2546+532A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109797383 | |||||||
| chr6:109797472 | T | C | 2 | a0003c0007t0001g0321 a0003c0018t0001g0318 |
2 | NA18986.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2546+621T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109797472 | |||||||
| chr6:109797571 | C | G | 1 | a0008c0019t0006g0020 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2546+720C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109797571 | |||||||
| chr6:109797573 | G | A | 283 | a0001c0001t0002g0104 a0001c0001t0002g0124 a0001c0001t0002g0221 others(280): Show |
287 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(284): Show |
intron_variant | MODIFIER | c.2546+722G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109797573 | |||||||
| chr6:109797896 | C | CA | 11 | a0001c0001t0002g0019 a0001c0001t0002g0029 a0001c0001t0002g0052 others(8): Show |
11 | HG01928.hp2 HG02074.hp1 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.2546+1064dupA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109797896 | ||||||
| chr6:109797896 | CA | C | 103 | a0001c0001t0002g0083 a0001c0001t0002g0224 a0001c0003t0001g0165 others(100): Show |
106 | HG00323.hp2 HG00544.hp2 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.2546+1064delA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109797896 | ||||||
| chr6:109797915 | A | AG | 3 | a0002c0002t0003g0209 a0002c0002t0004g0123 a0002c0002t0004g0229 |
3 | HG02258.hp2 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2546+1064_2546+106 others(5): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109797915 | |||||||
| chr6:109797915 | A | G | 23 | a0002c0002t0004g0010 a0002c0002t0004g0186 a0002c0002t0004g0196 others(20): Show |
23 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.2546+1064A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109797915 | |||||||
| chr6:109798008 | G | A | 1 | a0002c0004t0001g0212 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2546+1157G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109798008 | |||||||
| chr6:109798395 | T | C | 1 | a0001c0003t0001g0262 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2546+1544T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109798395 | |||||||
| chr6:109798541 | T | A | 1 | a0001c0003t0001g0252 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2546+1690T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109798541 | |||||||
| chr6:109798611 | G | A | 3 | a0002c0002t0002g0011 a0002c0002t0005g0126 a0002c0002t0005g0127 |
3 | HG02809.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2546+1760G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109798611 | |||||||
| chr6:109798816 | CT | C | 16 | a0001c0003t0001g0145 a0002c0002t0003g0209 a0002c0002t0004g0010 others(13): Show |
16 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.2546+1975delT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109798816 | ||||||
| chr6:109798831 | G | A | 38 | a0002c0004t0001g0128 a0002c0004t0001g0129 a0002c0004t0001g0174 others(35): Show |
41 | HG00639.hp1 HG01175.hp2 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.2546+1980G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109798831 | |||||||
| chr6:109798842 | C | A | 3 | a0001c0003t0001g0028 a0001c0003t0001g0300 a0001c0003t0001g0301 |
3 | HG01256.hp1 HG01258.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.2546+1991C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109798842 | |||||||
| chr6:109798889 | A | G | 1 | a0003c0005t0001g0250 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2546+2038A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109798889 | |||||||
| chr6:109798924 | T | G | 1 | a0001c0001t0002g0056 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2546+2073T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109798924 | |||||||
| chr6:109798928 | T | G | 283 | a0001c0001t0002g0104 a0001c0001t0002g0124 a0001c0001t0002g0221 others(280): Show |
287 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(284): Show |
intron_variant | MODIFIER | c.2546+2077T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109798928 | |||||||
| chr6:109799064 | A | C | 58 | a0002c0002t0001g0130 a0002c0002t0001g0132 a0002c0002t0001g0133 others(55): Show |
58 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.2546+2213A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109799064 | |||||||
| chr6:109799088 | C | T | 2 | a0001c0003t0001g0285 a0001c0003t0001g0286 |
2 | HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.2546+2237C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109799088 | |||||||
| chr6:109799321 | A | G | 283 | a0001c0001t0002g0104 a0001c0001t0002g0124 a0001c0001t0002g0221 others(280): Show |
287 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(284): Show |
intron_variant | MODIFIER | c.2546+2470A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109799321 | |||||||
| chr6:109799363 | GGT | G | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0085 others(2): Show |
5 | HG02280.hp2 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2546+2524_2546+252 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109799363 | ||||||
| chr6:109799409 | T | C | 2 | a0002c0002t0002g0086 a0002c0002t0002g0087 |
2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2546+2558T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109799409 | |||||||
| chr6:109799427 | C | T | 41 | a0002c0004t0001g0128 a0002c0004t0001g0129 a0002c0004t0001g0174 others(38): Show |
44 | HG00639.hp1 HG01175.hp2 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.2546+2576C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109799427 | |||||||
| chr6:109799442 | A | G | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2546+2591A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109799442 | |||||||
| chr6:109800028 | A | G | 1 | a0002c0004t0004g0230 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2546+3177A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109800028 | |||||||
| chr6:109800161 | A | G | 3 | a0002c0002t0002g0016 a0002c0002t0002g0017 a0002c0014t0002g0015 |
3 | HG02559.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2546+3310A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109800161 | |||||||
| chr6:109800429 | T | G | 1 | a0001c0003t0001g0297 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2546+3578T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109800429 | |||||||
| chr6:109800552 | A | C | 1 | a0001c0001t0002g0277 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2546+3701A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109800552 | |||||||
| chr6:109800567 | G | A | 1 | a0002c0002t0002g0114 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2546+3716G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109800567 | |||||||
| chr6:109800635 | ACT | A | 21 | a0001c0003t0001g0018 a0001c0003t0001g0025 a0001c0003t0001g0035 others(18): Show |
21 | HG00408.hp1 HG00741.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.2546+3785_2546+378 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109800635 | |||||||
| chr6:109800671 | G | A | 1 | a0002c0004t0001g0068 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2546+3820G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109800671 | |||||||
| chr6:109800806 | C | T | 254 | a0001c0001t0002g0124 a0001c0001t0002g0221 a0001c0001t0002g0223 others(251): Show |
258 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.2546+3955C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109800806 | |||||||
| chr6:109801007 | A | G | 1 | a0001c0001t0002g0021 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2546+4156A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801007 | |||||||
| chr6:109801055 | A | C | 1 | a0002c0002t0003g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2546+4204A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801055 | |||||||
| chr6:109801098 | T | C | 1 | a0001c0003t0001g0035 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2546+4247T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801098 | |||||||
| chr6:109801147 | A | G | 2 | a0002c0009t0002g0157 a0002c0009t0002g0159 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2546+4296A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801147 | |||||||
| chr6:109801178 | T | C | 1 | a0001c0001t0002g0122 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2546+4327T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801178 | |||||||
| chr6:109801316 | G | A | 1 | a0001c0003t0001g0257 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2546+4465G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801316 | |||||||
| chr6:109801420 | C | T | 1 | a0002c0004t0001g0215 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2546+4569C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801420 | |||||||
| chr6:109801425 | A | G | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2546+4574A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801425 | |||||||
| chr6:109801437 | A | G | 1 | a0003c0005t0001g0249 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2546+4586A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801437 | |||||||
| chr6:109801455 | G | A | 1 | a0001c0003t0001g0037 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2546+4604G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801455 | |||||||
| chr6:109801534 | C | T | 1 | a0002c0002t0005g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2546+4683C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801534 | |||||||
| chr6:109801591 | A | G | 4 | a0002c0002t0004g0228 a0002c0002t0004g0229 a0002c0002t0004g0238 others(1): Show |
4 | HG02258.hp2 HG02809.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2546+4740A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801591 | |||||||
| chr6:109801599 | A | G | 1 | a0001c0003t0001g0040 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2546+4748A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801599 | |||||||
| chr6:109801649 | G | A | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0085 others(2): Show |
5 | HG02280.hp2 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2546+4798G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801649 | |||||||
| chr6:109801661 | C | T | 2 | a0002c0002t0002g0016 a0002c0002t0002g0017 |
2 | HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2546+4810C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801661 | |||||||
| chr6:109801760 | A | G | 1 | a0001c0001t0002g0277 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2546+4909A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801760 | |||||||
| chr6:109801882 | A | T | 1 | a0001c0001t0002g0226 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2546+5031A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109801882 | |||||||
| chr6:109802115 | G | A | 281 | a0001c0001t0002g0124 a0001c0001t0002g0221 a0001c0001t0002g0223 others(278): Show |
285 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(282): Show |
intron_variant | MODIFIER | c.2546+5264G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109802115 | |||||||
| chr6:109802246 | A | T | 1 | a0002c0004t0001g0295 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2546+5395A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109802246 | |||||||
| chr6:109802276 | C | T | 1 | a0003c0005t0001g0325 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2546+5425C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109802276 | |||||||
| chr6:109802485 | C | T | 29 | a0002c0002t0001g0130 a0002c0002t0001g0132 a0002c0002t0001g0133 others(26): Show |
29 | HG00323.hp2 HG00544.hp2 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.2546+5634C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109802485 | |||||||
| chr6:109802702 | T | C | 1 | a0001c0003t0001g0048 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2546+5851T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109802702 | |||||||
| chr6:109802731 | A | C | 41 | a0002c0004t0001g0128 a0002c0004t0001g0129 a0002c0004t0001g0174 others(38): Show |
44 | HG00639.hp1 HG01175.hp2 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.2546+5880A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109802731 | |||||||
| chr6:109803158 | T | G | 26 | a0002c0002t0003g0209 a0002c0002t0004g0010 a0002c0002t0004g0123 others(23): Show |
26 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.2546+6307T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109803158 | |||||||
| chr6:109803223 | G | A | 23 | a0002c0002t0002g0009 a0002c0002t0002g0012 a0002c0002t0002g0088 others(20): Show |
23 | HG02257.hp2 HG02451.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.2546+6372G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109803223 | |||||||
| chr6:109803303 | G | T | 1 | a0002c0002t0004g0356 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2546+6452G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109803303 | |||||||
| chr6:109803317 | G | A | 6 | a0001c0001t0002g0124 a0001c0001t0002g0221 a0001c0001t0002g0223 others(3): Show |
6 | HG02109.hp2 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2546+6466G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109803317 | |||||||
| chr6:109803325 | C | G | 87 | a0001c0001t0002g0124 a0001c0001t0002g0221 a0001c0001t0002g0223 others(84): Show |
87 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.2546+6474C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109803325 | |||||||
| chr6:109803330 | A | G | 7 | a0001c0001t0002g0124 a0001c0001t0002g0221 a0001c0001t0002g0223 others(4): Show |
7 | HG02109.hp2 HG02622.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2546+6479A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109803330 | |||||||
| chr6:109803528 | C | A | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2546+6677C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109803528 | |||||||
| chr6:109803621 | C | CT | 37 | a0001c0001t0002g0052 a0001c0003t0001g0007 a0001c0003t0001g0008 others(34): Show |
37 | HG00408.hp1 HG00741.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.2546+6780dupT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109803621 | ||||||
| chr6:109803621 | CT | C | 59 | a0001c0001t0002g0124 a0002c0002t0001g0130 a0002c0002t0001g0132 others(56): Show |
59 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.2546+6780delT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109803621 | ||||||
| chr6:109803768 | C | A | 2 | a0002c0002t0002g0016 a0002c0002t0002g0017 |
2 | HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2546+6917C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109803768 | |||||||
| chr6:109803775 | C | G | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2546+6924C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109803775 | |||||||
| chr6:109803808 | C | G | 2 | a0002c0002t0002g0073 a0002c0002t0002g0211 |
2 | HG02109.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2546+6957C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109803808 | |||||||
| chr6:109803989 | A | C | 41 | a0002c0004t0001g0128 a0002c0004t0001g0129 a0002c0004t0001g0174 others(38): Show |
44 | HG00639.hp1 HG01175.hp2 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.2546+7138A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109803989 | |||||||
| chr6:109804039 | G | A | 1 | a0002c0002t0004g0305 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2546+7188G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109804039 | |||||||
| chr6:109804162 | A | G | 1 | a0008c0019t0006g0020 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2546+7311A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109804162 | |||||||
| chr6:109804246 | C | T | 1 | a0001c0001t0003g0244 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2546+7395C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109804246 | |||||||
| chr6:109804392 | T | A | 3 | a0002c0002t0002g0016 a0002c0002t0002g0017 a0002c0014t0002g0015 |
3 | HG02559.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2546+7541T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109804392 | |||||||
| chr6:109804431 | T | A | 29 | a0002c0002t0001g0130 a0002c0002t0001g0132 a0002c0002t0001g0133 others(26): Show |
29 | HG00323.hp2 HG00544.hp2 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.2546+7580T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109804431 | |||||||
| chr6:109805190 | G | A | 2 | a0001c0003t0001g0285 a0001c0003t0001g0286 |
2 | HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.2546+8339G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109805190 | |||||||
| chr6:109805201 | A | G | 1 | a0001c0001t0003g0362 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2546+8350A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109805201 | |||||||
| chr6:109805230 | C | T | 3 | a0002c0002t0004g0351 a0002c0002t0004g0352 a0002c0002t0004g0353 |
3 | HG01081.hp1 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2546+8379C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109805230 | |||||||
| chr6:109805591 | A | G | 1 | a0002c0009t0002g0158 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2546+8740A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109805591 | |||||||
| chr6:109805628 | A | G | 27 | a0002c0002t0003g0209 a0002c0002t0004g0010 a0002c0002t0004g0123 others(24): Show |
27 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.2546+8777A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109805628 | |||||||
| chr6:109805728 | TA | T | 4 | a0001c0001t0003g0027 a0001c0001t0003g0187 a0001c0001t0003g0194 others(1): Show |
4 | NA18990.hp1 NA19009.hp2 NA19075.hp2 others(1): Show |
intron_variant | MODIFIER | c.2546+8879delA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109805728 | ||||||
| chr6:109806215 | G | T | 2 | a0001c0003t0001g0319 a0001c0003t0001g0364 |
2 | NA18969.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2546+9364G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109806215 | |||||||
| chr6:109806286 | C | G | 1 | a0003c0005t0001g0325 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2546+9435C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109806286 | |||||||
| chr6:109806469 | G | A | 1 | a0002c0002t0002g0009 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2546+9618G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109806469 | |||||||
| chr6:109806482 | A | AGT | 3 | a0002c0002t0001g0135 a0002c0002t0001g0218 a0002c0002t0002g0116 |
3 | HG02886.hp1 NA18612.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.2546+9645_2546+964 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109806482 | ||||||
| chr6:109806516 | A | G | 2 | a0001c0001t0002g0104 a0001c0001t0003g0192 |
2 | NA18977.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.2546+9665A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109806516 | |||||||
| chr6:109806599 | G | A | 1 | a0002c0002t0002g0359 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2546+9748G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109806599 | |||||||
| chr6:109806666 | A | G | 1 | a0001c0001t0003g0185 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2546+9815A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109806666 | |||||||
| chr6:109806754 | C | G | 88 | a0001c0001t0002g0124 a0001c0001t0002g0221 a0001c0001t0002g0223 others(85): Show |
88 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.2546+9903C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109806754 | |||||||
| chr6:109806787 | G | C | 27 | a0002c0002t0003g0209 a0002c0002t0004g0010 a0002c0002t0004g0123 others(24): Show |
27 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.2546+9936G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109806787 | |||||||
| chr6:109807126 | A | G | 3 | a0002c0002t0002g0016 a0002c0002t0002g0017 a0002c0014t0002g0015 |
3 | HG02559.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2546+10275A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109807126 | |||||||
| chr6:109807226 | A | G | 1 | a0002c0009t0002g0158 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2546+10375A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109807226 | |||||||
| chr6:109807278 | C | T | 30 | a0001c0001t0003g0003 a0001c0001t0003g0026 a0001c0001t0003g0027 others(27): Show |
31 | HG00438.hp1 HG00558.hp2 HG02615.hp2 others(28): Show |
intron_variant | MODIFIER | c.2546+10427C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109807278 | |||||||
| chr6:109807293 | A | G | 1 | a0002c0002t0004g0196 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2546+10442A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109807293 | |||||||
| chr6:109807329 | G | T | 1 | a0004c0006t0001g0307 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2546+10478G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109807329 | |||||||
| chr6:109807395 | C | T | 15 | a0002c0002t0002g0012 a0002c0002t0002g0110 a0002c0002t0002g0111 others(12): Show |
15 | HG02257.hp2 HG02615.hp1 HG02818.hp2 others(12): Show |
intron_variant | MODIFIER | c.2546+10544C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109807395 | |||||||
| chr6:109807425 | G | A | 1 | a0001c0003t0001g0025 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2546+10574G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109807425 | |||||||
| chr6:109807483 | G | A | 79 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0018 others(76): Show |
79 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.2546+10632G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109807483 | |||||||
| chr6:109807528 | T | C | 41 | a0002c0004t0001g0128 a0002c0004t0001g0129 a0002c0004t0001g0174 others(38): Show |
44 | HG00639.hp1 HG01175.hp2 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.2546+10677T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109807528 | |||||||
| chr6:109807546 | A | C | 1 | a0001c0001t0002g0277 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2546+10695A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109807546 | |||||||
| chr6:109807560 | C | G | 1 | a0001c0001t0002g0277 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2546+10709C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109807560 | |||||||
| chr6:109807882 | T | C | 1 | a0001c0001t0002g0042 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2546+11031T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109807882 | |||||||
| chr6:109808024 | A | G | 1 | a0001c0001t0003g0193 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2546+11173A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109808024 | |||||||
| chr6:109808130 | A | G | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2546+11279A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109808130 | |||||||
| chr6:109808310 | A | G | 1 | a0002c0002t0002g0009 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2546+11459A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109808310 | |||||||
| chr6:109808350 | C | CA | 58 | a0001c0001t0002g0002 a0001c0001t0002g0019 a0001c0001t0002g0029 others(55): Show |
59 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.2546+11523dupA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109808350 | ||||||
| chr6:109808350 | C | CAA | 7 | a0001c0001t0002g0107 a0002c0002t0001g0138 a0002c0002t0001g0218 others(4): Show |
7 | HG02056.hp1 HG02572.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.2546+11522_2546+11 others(8): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109808350 | ||||||
| chr6:109808350 | C | CAAA | 21 | a0002c0002t0001g0130 a0002c0002t0001g0132 a0002c0002t0001g0133 others(18): Show |
21 | HG00323.hp2 HG00544.hp2 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.2546+11521_2546+11 others(9): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109808350 | ||||||
| chr6:109808350 | CA | C | 69 | a0001c0001t0002g0054 a0001c0001t0002g0082 a0001c0001t0002g0299 others(66): Show |
72 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.2546+11523delA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109808350 | ||||||
| chr6:109808350 | CAA | C | 80 | a0001c0001t0002g0124 a0001c0001t0002g0221 a0001c0001t0002g0223 others(77): Show |
80 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.2546+11522_2546+11 others(8): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109808350 | ||||||
| chr6:109808374 | AG | A | 3 | a0002c0002t0001g0143 a0002c0002t0001g0144 a0002c0002t0001g0148 |
3 | NA18955.hp2 NA18998.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.2546+11524delG | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109808374 | |||||||
| chr6:109808375 | G | A | 26 | a0002c0002t0001g0130 a0002c0002t0001g0132 a0002c0002t0001g0133 others(23): Show |
26 | HG00323.hp2 HG00544.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.2546+11524G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109808375 | |||||||
| chr6:109808544 | G | A | 16 | a0002c0002t0001g0130 a0002c0002t0001g0138 a0002c0002t0001g0141 others(13): Show |
16 | HG01943.hp1 HG01975.hp1 HG02135.hp2 others(13): Show |
intron_variant | MODIFIER | c.2546+11693G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109808544 | |||||||
| chr6:109808763 | T | A | 1 | a0001c0001t0002g0277 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2546+11912T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109808763 | |||||||
| chr6:109808961 | A | G | 3 | a0002c0002t0002g0016 a0002c0002t0002g0017 a0002c0014t0002g0015 |
3 | HG02559.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2546+12110A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109808961 | |||||||
| chr6:109809085 | T | C | 68 | a0002c0002t0003g0209 a0002c0002t0004g0010 a0002c0002t0004g0123 others(65): Show |
71 | HG00639.hp1 HG01081.hp1 HG01175.hp2 others(68): Show |
intron_variant | MODIFIER | c.2546+12234T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109809085 | |||||||
| chr6:109809234 | C | T | 3 | a0002c0002t0002g0016 a0002c0002t0002g0017 a0002c0014t0002g0015 |
3 | HG02559.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2546+12383C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109809234 | |||||||
| chr6:109809328 | T | C | 41 | a0002c0004t0001g0128 a0002c0004t0001g0129 a0002c0004t0001g0174 others(38): Show |
44 | HG00639.hp1 HG01175.hp2 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.2546+12477T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109809328 | |||||||
| chr6:109809898 | G | A | 1 | a0001c0001t0002g0277 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2546+13047G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109809898 | |||||||
| chr6:109809938 | C | G | 68 | a0002c0002t0003g0209 a0002c0002t0004g0010 a0002c0002t0004g0123 others(65): Show |
71 | HG00639.hp1 HG01081.hp1 HG01175.hp2 others(68): Show |
intron_variant | MODIFIER | c.2546+13087C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109809938 | |||||||
| chr6:109810049 | C | T | 87 | a0001c0001t0002g0124 a0001c0001t0002g0221 a0001c0001t0002g0223 others(84): Show |
87 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.2546+13198C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109810049 | |||||||
| chr6:109810143 | G | C | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2546+13292G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109810143 | |||||||
| chr6:109810147 | G | A | 1 | a0001c0001t0002g0277 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2546+13296G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109810147 | |||||||
| chr6:109810272 | G | A | 1 | a0001c0001t0002g0283 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2546+13421G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109810272 | |||||||
| chr6:109810389 | T | C | 2 | a0001c0003t0001g0319 a0001c0003t0001g0364 |
2 | NA18969.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2546+13538T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109810389 | |||||||
| chr6:109810469 | G | A | 1 | a0001c0001t0002g0277 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2546+13618G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109810469 | |||||||
| chr6:109810592 | C | G | 10 | a0002c0002t0002g0111 a0002c0002t0002g0112 a0002c0002t0002g0113 others(7): Show |
10 | HG02257.hp2 HG02615.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2546+13741C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109810592 | |||||||
| chr6:109810785 | G | A | 68 | a0002c0002t0003g0209 a0002c0002t0004g0010 a0002c0002t0004g0123 others(65): Show |
71 | HG00639.hp1 HG01081.hp1 HG01175.hp2 others(68): Show |
intron_variant | MODIFIER | c.2546+13934G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109810785 | |||||||
| chr6:109810803 | G | A | 42 | a0002c0004t0001g0128 a0002c0004t0001g0129 a0002c0004t0001g0174 others(39): Show |
45 | HG00639.hp1 HG01175.hp2 HG01255.hp2 others(42): Show |
intron_variant | MODIFIER | c.2546+13952G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109810803 | |||||||
| chr6:109810821 | T | G | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0085 others(2): Show |
5 | HG02280.hp2 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2546+13970T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109810821 | |||||||
| chr6:109810898 | G | C | 1 | a0002c0002t0002g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2546+14047G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109810898 | |||||||
| chr6:109811070 | T | C | 1 | a0002c0002t0004g0186 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2547-14018T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109811070 | |||||||
| chr6:109811074 | G | T | 1 | a0002c0009t0002g0158 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2547-14014G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109811074 | |||||||
| chr6:109811106 | A | G | 2 | a0002c0009t0002g0157 a0002c0009t0002g0159 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2547-13982A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109811106 | |||||||
| chr6:109811154 | C | G | 1 | a0001c0001t0003g0026 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2547-13934C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109811154 | |||||||
| chr6:109811174 | G | A | 1 | a0001c0001t0002g0277 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2547-13914G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109811174 | |||||||
| chr6:109811347 | G | A | 1 | a0002c0009t0002g0158 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2547-13741G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109811347 | |||||||
| chr6:109811396 | A | G | 43 | a0002c0002t0002g0211 a0002c0002t0004g0305 a0002c0004t0001g0128 others(40): Show |
46 | HG00639.hp1 HG01175.hp2 HG01255.hp2 others(43): Show |
intron_variant | MODIFIER | c.2547-13692A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109811396 | |||||||
| chr6:109811668 | G | A | 74 | a0001c0003t0001g0007 a0001c0003t0001g0018 a0001c0003t0001g0025 others(71): Show |
74 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.2547-13420G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109811668 | |||||||
| chr6:109811792 | T | G | 1 | a0002c0004t0001g0178 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2547-13296T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109811792 | |||||||
| chr6:109812112 | G | A | 1 | a0002c0014t0002g0015 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2547-12976G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109812112 | |||||||
| chr6:109812291 | A | G | 1 | a0002c0002t0005g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2547-12797A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109812291 | |||||||
| chr6:109812364 | G | C | 1 | a0001c0001t0002g0289 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2547-12724G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109812364 | |||||||
| chr6:109812418 | G | A | 1 | a0001c0001t0002g0277 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2547-12670G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109812418 | |||||||
| chr6:109812501 | G | A | 194 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0033 others(191): Show |
197 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.2547-12587G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109812501 | |||||||
| chr6:109812539 | T | C | 1 | a0001c0003t0001g0024 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2547-12549T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109812539 | |||||||
| chr6:109812661 | T | C | 269 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0033 others(266): Show |
273 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(270): Show |
intron_variant | MODIFIER | c.2547-12427T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109812661 | |||||||
| chr6:109813051 | C | T | 5 | a0002c0002t0002g0011 a0002c0002t0002g0017 a0002c0002t0005g0126 others(2): Show |
5 | HG02559.hp1 HG02809.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.2547-12037C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109813051 | |||||||
| chr6:109813446 | G | T | 264 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0033 others(261): Show |
268 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.2547-11642G>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109813446 | |||||||
| chr6:109813577 | T | C | 1 | a0001c0001t0002g0042 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2547-11511T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109813577 | |||||||
| chr6:109813688 | G | A | 1 | a0001c0001t0002g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2547-11400G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109813688 | |||||||
| chr6:109813737 | G | A | 26 | a0002c0002t0004g0010 a0002c0002t0004g0123 a0002c0002t0004g0186 others(23): Show |
26 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.2547-11351G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109813737 | |||||||
| chr6:109813905 | C | T | 6 | a0001c0001t0003g0183 a0002c0002t0002g0013 a0002c0002t0002g0014 others(3): Show |
6 | HG02280.hp2 HG02572.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2547-11183C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109813905 | |||||||
| chr6:109813906 | G | A | 26 | a0002c0004t0001g0032 a0002c0004t0001g0041 a0002c0004t0001g0043 others(23): Show |
26 | HG00099.hp1 HG00423.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.2547-11182G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109813906 | |||||||
| chr6:109813945 | G | A | 26 | a0002c0002t0004g0010 a0002c0002t0004g0123 a0002c0002t0004g0186 others(23): Show |
26 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.2547-11143G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109813945 | |||||||
| chr6:109814178 | G | A | 5 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0033 others(2): Show |
5 | HG02145.hp2 HG02572.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2547-10910G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109814178 | |||||||
| chr6:109814261 | C | T | 2 | a0002c0002t0002g0117 a0002c0002t0002g0118 |
2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2547-10827C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109814261 | |||||||
| chr6:109814304 | A | G | 7 | a0001c0001t0002g0124 a0001c0001t0002g0221 a0001c0001t0002g0223 others(4): Show |
7 | HG02109.hp2 HG02622.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2547-10784A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109814304 | |||||||
| chr6:109814311 | T | A | 2 | a0002c0002t0002g0016 a0002c0009t0002g0158 |
2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2547-10777T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109814311 | |||||||
| chr6:109814313 | A | AT | 224 | a0001c0001t0002g0033 a0001c0001t0002g0198 a0001c0001t0002g0277 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.2547-10767dupT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109814313 | ||||||
| chr6:109814447 | A | AT | 23 | a0001c0001t0002g0002 a0001c0001t0002g0029 a0001c0001t0002g0036 others(20): Show |
24 | HG02004.hp1 HG02698.hp1 HG02965.hp2 others(21): Show |
intron_variant | MODIFIER | c.2547-10631dupT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109814447 | ||||||
| chr6:109814447 | AT | A | 226 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0033 others(223): Show |
230 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.2547-10631delT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109814447 | ||||||
| chr6:109814479 | A | G | 1 | a0002c0002t0004g0352 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2547-10609A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109814479 | |||||||
| chr6:109815210 | G | C | 1 | a0003c0005t0001g0316 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2547-9878G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109815210 | |||||||
| chr6:109815211 | C | T | 1 | a0003c0005t0001g0316 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2547-9877C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109815211 | |||||||
| chr6:109815226 | A | C | 262 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0033 others(259): Show |
266 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.2547-9862A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109815226 | |||||||
| chr6:109815311 | C | T | 1 | a0004c0006t0001g0340 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2547-9777C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109815311 | |||||||
| chr6:109815377 | C | T | 1 | a0002c0002t0004g0305 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2547-9711C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109815377 | |||||||
| chr6:109815393 | C | G | 8 | a0001c0001t0002g0124 a0001c0001t0002g0221 a0001c0001t0002g0223 others(5): Show |
8 | HG02109.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2547-9695C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109815393 | |||||||
| chr6:109815495 | G | GC | 51 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0033 others(48): Show |
52 | HG00438.hp1 HG00558.hp2 HG02109.hp1 others(49): Show |
intron_variant | MODIFIER | c.2547-9585dupC | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109815495 | ||||||
| chr6:109815496 | C | CT | 173 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0018 others(170): Show |
176 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.2547-9592_2547-959 others(5): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109815496 | |||||||
| chr6:109815668 | A | G | 1 | a0002c0002t0004g0305 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2547-9420A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109815668 | |||||||
| chr6:109815694 | C | T | 175 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0018 others(172): Show |
178 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.2547-9394C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109815694 | |||||||
| chr6:109815803 | C | CA | 22 | a0002c0004t0001g0041 a0002c0004t0001g0055 a0002c0004t0001g0057 others(19): Show |
22 | HG00099.hp1 HG00423.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.2547-9276dupA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109815803 | ||||||
| chr6:109815803 | C | CAA | 7 | a0002c0004t0001g0032 a0002c0004t0001g0043 a0002c0004t0001g0044 others(4): Show |
7 | HG02056.hp1 HG02071.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.2547-9277_2547-927 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109815803 | ||||||
| chr6:109815935 | A | G | 5 | a0002c0002t0002g0011 a0002c0002t0002g0017 a0002c0002t0005g0126 others(2): Show |
5 | HG02559.hp1 HG02809.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.2547-9153A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109815935 | |||||||
| chr6:109816109 | G | A | 236 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0033 others(233): Show |
240 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.2547-8979G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109816109 | |||||||
| chr6:109816228 | G | A | 175 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0018 others(172): Show |
178 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.2547-8860G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109816228 | |||||||
| chr6:109816366 | G | A | 1 | a0001c0001t0002g0096 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2547-8722G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109816366 | |||||||
| chr6:109816513 | C | T | 9 | a0001c0003t0001g0048 a0001c0003t0001g0145 a0001c0003t0001g0175 others(6): Show |
9 | HG00408.hp2 HG02074.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.2547-8575C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109816513 | |||||||
| chr6:109816590 | A | G | 3 | a0001c0003t0001g0166 a0001c0003t0001g0173 a0001c0003t0001g0177 |
3 | HG00741.hp1 HG01978.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.2547-8498A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109816590 | |||||||
| chr6:109816673 | A | G | 1 | a0002c0002t0004g0186 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2547-8415A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109816673 | |||||||
| chr6:109816778 | G | A | 26 | a0002c0002t0004g0010 a0002c0002t0004g0123 a0002c0002t0004g0186 others(23): Show |
26 | HG01081.hp1 HG01243.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.2547-8310G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109816778 | |||||||
| chr6:109816905 | C | G | 1 | a0002c0014t0002g0015 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2547-8183C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109816905 | |||||||
| chr6:109816918 | A | G | 8 | a0001c0001t0002g0124 a0001c0001t0002g0221 a0001c0001t0002g0223 others(5): Show |
8 | HG02109.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2547-8170A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109816918 | |||||||
| chr6:109816962 | C | T | 2 | a0002c0004t0001g0231 a0002c0004t0001g0232 |
2 | HG01361.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.2547-8126C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109816962 | |||||||
| chr6:109817063 | T | C | 2 | a0002c0004t0001g0231 a0002c0004t0001g0232 |
2 | HG01361.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.2547-8025T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109817063 | |||||||
| chr6:109817567 | G | A | 148 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0018 others(145): Show |
151 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.2547-7521G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109817567 | |||||||
| chr6:109817568 | TA | T | 115 | a0001c0001t0002g0198 a0001c0001t0002g0277 a0001c0003t0001g0007 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.2547-7505delA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109817568 | ||||||
| chr6:109817569 | A | T | 37 | a0002c0004t0001g0128 a0002c0004t0001g0129 a0002c0004t0001g0174 others(34): Show |
40 | HG00639.hp1 HG01255.hp2 HG01358.hp2 others(37): Show |
intron_variant | MODIFIER | c.2547-7519A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109817569 | |||||||
| chr6:109817570 | A | T | 1 | a0001c0003t0001g0266 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2547-7518A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109817570 | |||||||
| chr6:109817675 | C | T | 1 | a0002c0002t0002g0121 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2547-7413C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109817675 | |||||||
| chr6:109817816 | AG | A | 7 | a0001c0001t0002g0124 a0001c0001t0002g0221 a0001c0001t0002g0223 others(4): Show |
7 | HG02109.hp2 HG02622.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2547-7269delG | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109817816 | ||||||
| chr6:109817854 | G | A | 15 | a0002c0002t0002g0012 a0002c0002t0002g0110 a0002c0002t0002g0111 others(12): Show |
15 | HG02257.hp2 HG02615.hp1 HG02818.hp2 others(12): Show |
intron_variant | MODIFIER | c.2547-7234G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109817854 | |||||||
| chr6:109818202 | CT | C | 14 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0033 others(11): Show |
14 | HG01069.hp2 HG02145.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.2547-6871delT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109818202 | ||||||
| chr6:109818264 | G | A | 6 | a0001c0001t0003g0155 a0001c0001t0003g0156 a0001c0001t0003g0360 others(3): Show |
6 | HG02615.hp2 HG02630.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2547-6824G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109818264 | |||||||
| chr6:109818452 | G | A | 1 | a0002c0002t0004g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2547-6636G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109818452 | |||||||
| chr6:109818480 | A | C | 175 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0018 others(172): Show |
178 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.2547-6608A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109818480 | |||||||
| chr6:109818493 | C | T | 31 | a0001c0001t0003g0003 a0001c0001t0003g0026 a0001c0001t0003g0027 others(28): Show |
32 | HG00438.hp1 HG00558.hp2 HG02615.hp2 others(29): Show |
intron_variant | MODIFIER | c.2547-6595C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109818493 | |||||||
| chr6:109818496 | G | A | 9 | a0002c0002t0004g0010 a0002c0002t0004g0197 a0002c0002t0004g0200 others(6): Show |
9 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2547-6592G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109818496 | |||||||
| chr6:109818649 | T | C | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0085 others(2): Show |
5 | HG02280.hp2 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2547-6439T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109818649 | |||||||
| chr6:109818723 | C | T | 5 | a0002c0002t0002g0011 a0002c0002t0002g0017 a0002c0002t0005g0126 others(2): Show |
5 | HG02559.hp1 HG02809.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.2547-6365C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109818723 | |||||||
| chr6:109818773 | G | C | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2547-6315G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109818773 | |||||||
| chr6:109818872 | A | C | 6 | a0001c0001t0002g0060 a0001c0001t0002g0061 a0001c0001t0002g0062 others(3): Show |
6 | NA18947.hp2 NA18949.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.2547-6216A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109818872 | |||||||
| chr6:109819032 | T | C | 2 | a0001c0003t0001g0170 a0001c0003t0001g0172 |
2 | HG01081.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.2547-6056T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109819032 | |||||||
| chr6:109819043 | C | A | 5 | a0002c0004t0001g0041 a0002c0004t0001g0076 a0002c0004t0001g0091 others(2): Show |
5 | HG00099.hp1 HG02602.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.2547-6045C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109819043 | |||||||
| chr6:109819201 | A | G | 32 | a0001c0001t0002g0104 a0001c0001t0003g0003 a0001c0001t0003g0026 others(29): Show |
33 | HG00438.hp1 HG00558.hp2 HG02615.hp2 others(30): Show |
intron_variant | MODIFIER | c.2547-5887A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109819201 | |||||||
| chr6:109819291 | G | A | 2 | a0001c0001t0002g0282 a0001c0001t0002g0283 |
2 | HG01071.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.2547-5797G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109819291 | |||||||
| chr6:109819634 | A | G | 1 | a0001c0003t0001g0288 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2547-5454A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109819634 | |||||||
| chr6:109819823 | T | G | 1 | a0004c0008t0002g0315 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2547-5265T>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109819823 | |||||||
| chr6:109819988 | C | G | 11 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0033 others(8): Show |
11 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2547-5100C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109819988 | |||||||
| chr6:109820027 | G | C | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0085 others(2): Show |
5 | HG02280.hp2 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2547-5061G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109820027 | |||||||
| chr6:109820038 | G | A | 1 | a0001c0001t0002g0277 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2547-5050G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109820038 | |||||||
| chr6:109820086 | G | A | 1 | a0001c0001t0002g0277 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2547-5002G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109820086 | |||||||
| chr6:109820096 | G | A | 2 | a0002c0009t0002g0157 a0002c0009t0002g0159 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2547-4992G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109820096 | |||||||
| chr6:109820135 | A | C | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2547-4953A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109820135 | |||||||
| chr6:109820231 | A | G | 2 | a0001c0003t0001g0319 a0001c0003t0001g0364 |
2 | NA18969.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2547-4857A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109820231 | |||||||
| chr6:109820287 | A | T | 1 | a0002c0014t0002g0015 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2547-4801A>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109820287 | |||||||
| chr6:109820409 | C | T | 1 | a0004c0008t0002g0310 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2547-4679C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109820409 | |||||||
| chr6:109820488 | G | C | 213 | a0001c0001t0003g0003 a0001c0001t0003g0026 a0001c0001t0003g0027 others(210): Show |
217 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.2547-4600G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109820488 | |||||||
| chr6:109820501 | T | A | 1 | a0002c0002t0001g0136 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2547-4587T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109820501 | |||||||
| chr6:109820506 | G | A | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0085 others(2): Show |
5 | HG02280.hp2 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2547-4582G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109820506 | |||||||
| chr6:109820644 | G | A | 1 | a0002c0002t0004g0305 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2547-4444G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109820644 | |||||||
| chr6:109820711 | A | G | 2 | a0002c0002t0002g0115 a0002c0002t0002g0116 |
2 | HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2547-4377A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109820711 | |||||||
| chr6:109820834 | C | A | 1 | a0001c0001t0002g0241 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2547-4254C>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109820834 | |||||||
| chr6:109820908 | G | A | 26 | a0002c0004t0001g0032 a0002c0004t0001g0041 a0002c0004t0001g0043 others(23): Show |
26 | HG00099.hp1 HG00423.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.2547-4180G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109820908 | |||||||
| chr6:109821077 | A | C | 1 | a0001c0001t0002g0227 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2547-4011A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109821077 | |||||||
| chr6:109821092 | C | T | 2 | a0002c0004t0001g0128 a0002c0004t0001g0129 |
2 | HG01255.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.2547-3996C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109821092 | |||||||
| chr6:109821112 | C | T | 1 | a0001c0001t0002g0277 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2547-3976C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109821112 | |||||||
| chr6:109821362 | A | C | 1 | a0001c0001t0003g0167 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2547-3726A>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109821362 | |||||||
| chr6:109821417 | C | T | 1 | a0002c0004t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2547-3671C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109821417 | |||||||
| chr6:109821480 | G | C | 1 | a0001c0001t0002g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2547-3608G>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109821480 | |||||||
| chr6:109821507 | A | G | 5 | a0001c0003t0001g0008 a0001c0003t0001g0039 a0001c0003t0001g0267 others(2): Show |
5 | NA18943.hp2 NA18956.hp1 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.2547-3581A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109821507 | |||||||
| chr6:109821629 | G | A | 204 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0033 others(201): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.2547-3459G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109821629 | |||||||
| chr6:109821766 | C | T | 1 | a0001c0001t0003g0193 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2547-3322C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109821766 | |||||||
| chr6:109821769 | A | G | 194 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0033 others(191): Show |
197 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.2547-3319A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109821769 | |||||||
| chr6:109821784 | G | A | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2547-3304G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109821784 | |||||||
| chr6:109821901 | T | C | 1 | a0002c0002t0004g0208 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2547-3187T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109821901 | |||||||
| chr6:109822021 | T | C | 5 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0033 others(2): Show |
5 | HG02145.hp2 HG02572.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2547-3067T>C | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822021 | |||||||
| chr6:109822211 | A | G | 26 | a0001c0001t0002g0104 a0001c0001t0003g0003 a0001c0001t0003g0026 others(23): Show |
27 | HG00438.hp1 HG00558.hp2 NA18939.hp1 others(24): Show |
intron_variant | MODIFIER | c.2547-2877A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822211 | |||||||
| chr6:109822364 | TA | T | 177 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0018 others(174): Show |
180 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.2547-2718delA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822364 | ||||||
| chr6:109822755 | GT | G | 5 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0033 others(2): Show |
5 | HG02145.hp2 HG02572.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2547-2331delT | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822755 | ||||||
| chr6:109822763 | G | A | 263 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0033 others(260): Show |
267 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.2547-2325G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822763 | |||||||
| chr6:109822783 | GTATGTAT others(3): Show |
G | 10 | a0001c0003t0001g0064 a0002c0002t0001g0141 a0002c0002t0001g0142 others(7): Show |
10 | HG02071.hp1 HG02135.hp2 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.2547-2301_2547-229 others(14): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822783 | ||||||
| chr6:109822783 | GTATGTAT others(5): Show |
G | 21 | a0001c0003t0001g0028 a0002c0002t0001g0132 a0002c0002t0001g0133 others(18): Show |
21 | HG00323.hp2 HG00544.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.2547-2301_2547-229 others(16): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822783 | ||||||
| chr6:109822783 | GTATGTAT others(7): Show |
G | 31 | a0001c0003t0001g0170 a0001c0003t0001g0172 a0001c0003t0001g0173 others(28): Show |
32 | HG00639.hp1 HG00741.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.2547-2301_2547-228 others(18): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822783 | ||||||
| chr6:109822783 | GTATGTAT others(9): Show |
G | 97 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0018 others(94): Show |
97 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.2547-2301_2547-228 others(20): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822783 | ||||||
| chr6:109822783 | GTATGTAT others(11): Show |
G | 6 | a0001c0003t0001g0284 a0002c0002t0002g0011 a0002c0002t0002g0211 others(3): Show |
6 | HG02109.hp1 HG02809.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2547-2301_2547-228 others(22): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822783 | ||||||
| chr6:109822783 | GTATGTAT others(13): Show |
G | 5 | a0001c0001t0002g0277 a0002c0002t0002g0017 a0002c0002t0002g0086 others(2): Show |
5 | HG02559.hp1 HG02886.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2547-2301_2547-228 others(24): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822783 | ||||||
| chr6:109822783 | GTATGTAT others(15): Show |
G | 15 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0033 others(12): Show |
15 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.2547-2301_2547-228 others(26): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822783 | ||||||
| chr6:109822783 | GTATGTAT others(21): Show |
G | 12 | a0002c0004t0001g0256 a0003c0005t0001g0005 a0003c0005t0001g0006 others(9): Show |
14 | HG02155.hp2 NA18940.hp2 NA18947.hp1 others(11): Show |
intron_variant | MODIFIER | c.2547-2301_2547-227 others(32): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822783 | ||||||
| chr6:109822785 | A | G | 3 | a0001c0003t0001g0252 a0002c0002t0001g0130 a0002c0002t0001g0135 |
3 | HG01943.hp1 NA18612.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.2547-2303A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822785 | |||||||
| chr6:109822786 | TGTATATA others(6): Show |
T | 1 | a0002c0002t0001g0135 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2547-2301_2547-228 others(17): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822786 | |||||||
| chr6:109822787 | G | GTA | 29 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0036 others(26): Show |
31 | HG00741.hp2 HG01943.hp2 HG01993.hp2 others(28): Show |
intron_variant | MODIFIER | c.2547-2261_2547-226 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822787 | ||||||
| chr6:109822787 | G | GTATA | 10 | a0001c0001t0002g0090 a0001c0001t0002g0108 a0001c0001t0002g0234 others(7): Show |
10 | HG02738.hp2 HG03130.hp1 HG03130.hp2 others(7): Show |
intron_variant | MODIFIER | c.2547-2263_2547-226 others(8): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822787 | ||||||
| chr6:109822787 | G | GTATATA | 6 | a0001c0001t0002g0001 a0001c0001t0002g0094 a0001c0001t0002g0098 others(3): Show |
6 | HG00558.hp2 HG02300.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.2547-2265_2547-226 others(10): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822787 | ||||||
| chr6:109822787 | G | GTATATAT others(5): Show |
1 | a0002c0009t0002g0158 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2547-2271_2547-226 others(16): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822787 | ||||||
| chr6:109822787 | GTA | G | 49 | a0001c0001t0002g0022 a0001c0001t0002g0042 a0001c0001t0002g0046 others(46): Show |
49 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.2547-2261_2547-226 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822787 | ||||||
| chr6:109822787 | GTATA | G | 26 | a0001c0001t0002g0122 a0001c0001t0002g0214 a0001c0001t0002g0235 others(23): Show |
26 | HG01081.hp1 HG01109.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.2547-2263_2547-226 others(8): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822787 | ||||||
| chr6:109822787 | GTATATA | G | 6 | a0001c0001t0002g0034 a0002c0002t0002g0119 a0002c0002t0004g0186 others(3): Show |
6 | HG01106.hp2 HG02451.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2547-2265_2547-226 others(10): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822787 | ||||||
| chr6:109822787 | GTATATAT others(3): Show |
G | 1 | a0002c0002t0001g0130 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2547-2269_2547-226 others(14): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822787 | ||||||
| chr6:109822787 | GTATATAT others(9): Show |
G | 1 | a0001c0003t0001g0252 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2547-2275_2547-226 others(20): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822787 | ||||||
| chr6:109822789 | A | G | 1 | a0008c0019t0006g0020 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2547-2299A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822789 | |||||||
| chr6:109822791 | A | G | 2 | a0002c0002t0004g0204 a0002c0002t0004g0353 |
2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2547-2297A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822791 | |||||||
| chr6:109822793 | A | G | 5 | a0002c0002t0001g0152 a0002c0002t0004g0123 a0002c0002t0004g0202 others(2): Show |
5 | HG02257.hp1 HG02280.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2547-2295A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822793 | |||||||
| chr6:109822795 | A | G | 26 | a0001c0003t0001g0064 a0002c0002t0001g0141 a0002c0002t0001g0142 others(23): Show |
26 | HG01081.hp1 HG01243.hp2 HG02071.hp1 others(23): Show |
intron_variant | MODIFIER | c.2547-2293A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822795 | |||||||
| chr6:109822797 | A | G | 25 | a0001c0003t0001g0028 a0002c0002t0001g0132 a0002c0002t0001g0133 others(22): Show |
25 | HG00323.hp2 HG00544.hp2 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.2547-2291A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822797 | |||||||
| chr6:109822799 | A | G | 31 | a0001c0003t0001g0170 a0001c0003t0001g0172 a0001c0003t0001g0173 others(28): Show |
32 | HG00639.hp1 HG00741.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.2547-2289A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822799 | |||||||
| chr6:109822801 | A | G | 97 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0018 others(94): Show |
97 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.2547-2287A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822801 | |||||||
| chr6:109822803 | A | G | 6 | a0001c0003t0001g0284 a0002c0002t0002g0011 a0002c0002t0002g0211 others(3): Show |
6 | HG02109.hp1 HG02809.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2547-2285A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822803 | |||||||
| chr6:109822805 | A | G | 5 | a0001c0001t0002g0277 a0002c0002t0002g0017 a0002c0002t0002g0086 others(2): Show |
5 | HG02559.hp1 HG02886.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2547-2283A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822805 | |||||||
| chr6:109822807 | A | G | 8 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0033 others(5): Show |
8 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2547-2281A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822807 | |||||||
| chr6:109822813 | A | G | 12 | a0002c0004t0001g0256 a0003c0005t0001g0005 a0003c0005t0001g0006 others(9): Show |
14 | HG02155.hp2 NA18940.hp2 NA18947.hp1 others(11): Show |
intron_variant | MODIFIER | c.2547-2275A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822813 | |||||||
| chr6:109822829 | C | T | 1 | a0001c0001t0003g0027 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2547-2259C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822829 | |||||||
| chr6:109822885 | G | A | 1 | a0003c0005t0001g0339 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2547-2203G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822885 | |||||||
| chr6:109822912 | G | GTA | 36 | a0001c0001t0002g0347 a0001c0001t0002g0349 a0001c0001t0003g0003 others(33): Show |
38 | HG00438.hp1 HG00558.hp2 HG02615.hp2 others(35): Show |
intron_variant | MODIFIER | c.2547-2165_2547-216 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822912 | ||||||
| chr6:109822925 | C | T | 1 | a0002c0002t0004g0305 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2547-2163C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109822925 | |||||||
| chr6:109822931 | ATC | A | 5 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0033 others(2): Show |
5 | HG02145.hp2 HG02572.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2547-2154_2547-215 others(6): Show |
FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109822931 | ||||||
| chr6:109823024 | C | T | 1 | a0001c0001t0002g0033 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2547-2064C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109823024 | |||||||
| chr6:109823226 | G | A | 26 | a0002c0004t0001g0032 a0002c0004t0001g0041 a0002c0004t0001g0043 others(23): Show |
26 | HG00099.hp1 HG00423.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.2547-1862G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109823226 | |||||||
| chr6:109823291 | A | G | 1 | a0003c0005t0001g0250 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2547-1797A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109823291 | |||||||
| chr6:109823459 | G | A | 2 | a0002c0002t0002g0016 a0002c0009t0002g0158 |
2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2547-1629G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109823459 | |||||||
| chr6:109823605 | C | T | 31 | a0001c0001t0003g0003 a0001c0001t0003g0026 a0001c0001t0003g0027 others(28): Show |
32 | HG00438.hp1 HG00558.hp2 HG02615.hp2 others(29): Show |
intron_variant | MODIFIER | c.2547-1483C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109823605 | |||||||
| chr6:109823707 | C | G | 1 | a0008c0019t0006g0020 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2547-1381C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109823707 | |||||||
| chr6:109823816 | T | A | 1 | a0001c0001t0002g0357 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2547-1272T>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109823816 | |||||||
| chr6:109823821 | G | A | 26 | a0002c0004t0001g0032 a0002c0004t0001g0041 a0002c0004t0001g0043 others(23): Show |
26 | HG00099.hp1 HG00423.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.2547-1267G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109823821 | |||||||
| chr6:109823857 | G | A | 2 | a0002c0009t0002g0157 a0002c0009t0002g0159 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2547-1231G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109823857 | |||||||
| chr6:109823919 | C | G | 4 | a0002c0002t0002g0011 a0002c0002t0002g0017 a0002c0002t0005g0126 others(1): Show |
4 | HG02559.hp1 HG02809.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2547-1169C>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109823919 | |||||||
| chr6:109823984 | G | A | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2547-1104G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109823984 | |||||||
| chr6:109824097 | CA | C | 5 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0033 others(2): Show |
5 | HG02145.hp2 HG02572.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2547-989delA | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr6 | 109824097 | ||||||
| chr6:109824110 | G | A | 1 | a0001c0001t0002g0122 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2547-978G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109824110 | |||||||
| chr6:109824170 | G | A | 37 | a0002c0004t0001g0128 a0002c0004t0001g0129 a0002c0004t0001g0174 others(34): Show |
40 | HG00639.hp1 HG01255.hp2 HG01358.hp2 others(37): Show |
intron_variant | MODIFIER | c.2547-918G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109824170 | |||||||
| chr6:109824307 | G | A | 1 | a0003c0005t0001g0312 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2547-781G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109824307 | |||||||
| chr6:109824580 | G | A | 1 | a0002c0002t0002g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2547-508G>A | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109824580 | |||||||
| chr6:109824587 | C | T | 1 | a0001c0003t0001g0275 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2547-501C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109824587 | |||||||
| chr6:109824699 | A | G | 1 | a0002c0014t0002g0015 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2547-389A>G | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109824699 | |||||||
| chr6:109824817 | C | T | 1 | a0001c0003t0001g0089 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2547-271C>T | FIG4 | ENSG00000112367.12 | transcript | ENST00000230124.8 | protein_coding | 22/22 | chr6 | 109824817 |