Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3638 |
| ensemblid | ENSG00000186480.13 |
| hgncid | 6083 |
| symbol | INSIG1 |
| name | insulin induced gene 1 |
| refseq_nuc | NM_005542.6 |
| refseq_prot | NP_005533.2 |
| ensembl_nuc | ENST00000340368.9 |
| ensembl_prot | ENSP00000344741.4 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 155297878 |
| end | 155310235 |
| strand | + |
| ver | v1.2 |
| region | chr7:155297878-155310235 |
| region5000 | chr7:155292878-155315235 |
| regionname0 | INSIG1_chr7_155297878_155310235 |
| regionname5000 | INSIG1_chr7_155292878_155315235 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 277 | 441 | 96 | 76 | 215 | 18 | 34 | 173 | INSIG1_chr7_155292878_155315235 | INSIG1 | MPRLH others(272): Show |
chr7 | 155292878 | 155315235 |
| a0002 | 0/0 | 277 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | MPRLH others(272): Show |
chr7 | 155292878 | 155315235 |
| a0003 | 0/0 | 277 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | MPRLH others(272): Show |
chr7 | 155292878 | 155315235 |
| a0004 | 0/0 | 277 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | MPRLH others(272): Show |
chr7 | 155292878 | 155315235 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 831 | 432 | 90 | 73 | 215 | 18 | 34 | INSIG1_chr7_155292878_155315235 | INSIG1 | ATGCC others(826): Show |
chr7 | 155292878 | 155315235 | ||
| a0001c0002 | 0/0 | 831 | 8 | 5 | 3 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | ATGCC others(826): Show |
chr7 | 155292878 | 155315235 | ||
| a0001c0004 | 0/0 | 831 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | ATGCC others(826): Show |
chr7 | 155292878 | 155315235 | ||
| a0002c0006 | 0/0 | 831 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | ATGCC others(826): Show |
chr7 | 155292878 | 155315235 | ||
| a0003c0003 | 0/0 | 831 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | ATGCC others(826): Show |
chr7 | 155292878 | 155315235 | ||
| a0004c0005 | 0/0 | 831 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | ATGCC others(826): Show |
chr7 | 155292878 | 155315235 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2908 | 310 | 56 | 66 | 149 | 16 | 22 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2903): Show |
chr7 | 155292878 | 155315235 |
| a0001c0001t0002 | 0/0 | 2909 | 40 | 9 | 2 | 22 | 1 | 6 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2904): Show |
chr7 | 155292878 | 155315235 |
| a0001c0001t0003 | 0/0 | 2908 | 31 | 2 | 0 | 28 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2903): Show |
chr7 | 155292878 | 155315235 |
| a0001c0001t0004 | 0/0 | 2908 | 11 | 0 | 0 | 11 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2903): Show |
chr7 | 155292878 | 155315235 |
| a0001c0001t0005 | 0/0 | 2908 | 8 | 8 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2903): Show |
chr7 | 155292878 | 155315235 |
| a0001c0001t0006 | 0/0 | 2906 | 3 | 3 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2901): Show |
chr7 | 155292878 | 155315235 |
| a0001c0001t0007 | 0/0 | 2908 | 4 | 4 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2903): Show |
chr7 | 155292878 | 155315235 |
| a0001c0001t0008 | 0/1 | 2908 | 4 | 0 | 1 | 0 | 1 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2903): Show |
chr7 | 155292878 | 155315235 |
| a0001c0001t0009 | 0/0 | 2908 | 3 | 2 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2903): Show |
chr7 | 155292878 | 155315235 |
| a0001c0001t0011 | 0/0 | 2909 | 2 | 0 | 0 | 0 | 0 | 2 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2904): Show |
chr7 | 155292878 | 155315235 |
| a0001c0001t0012 | 0/0 | 2908 | 2 | 1 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2903): Show |
chr7 | 155292878 | 155315235 |
| a0001c0001t0014 | 0/0 | 2908 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2903): Show |
chr7 | 155292878 | 155315235 |
| a0001c0001t0015 | 0/0 | 2908 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2903): Show |
chr7 | 155292878 | 155315235 |
| a0001c0001t0016 | 0/0 | 2908 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2903): Show |
chr7 | 155292878 | 155315235 |
| a0001c0001t0017 | 0/0 | 2908 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2903): Show |
chr7 | 155292878 | 155315235 |
| a0001c0001t0018 | 0/0 | 2908 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2903): Show |
chr7 | 155292878 | 155315235 |
| a0001c0001t0019 | 0/0 | 2908 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2903): Show |
chr7 | 155292878 | 155315235 |
| a0001c0001t0020 | 0/0 | 2984 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2979): Show |
chr7 | 155292878 | 155315235 |
| a0001c0001t0021 | 0/0 | 2908 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2903): Show |
chr7 | 155292878 | 155315235 |
| a0001c0001t0022 | 0/0 | 2908 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2903): Show |
chr7 | 155292878 | 155315235 |
| a0001c0001t0023 | 0/0 | 2908 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2903): Show |
chr7 | 155292878 | 155315235 |
| a0001c0001t0024 | 0/0 | 2908 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2903): Show |
chr7 | 155292878 | 155315235 |
| a0001c0001t0025 | 0/0 | 2908 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2903): Show |
chr7 | 155292878 | 155315235 |
| a0001c0001t0026 | 0/0 | 2908 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2903): Show |
chr7 | 155292878 | 155315235 |
| a0001c0001t0027 | 0/0 | 2908 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2903): Show |
chr7 | 155292878 | 155315235 |
| a0001c0002t0001 | 0/0 | 2908 | 3 | 1 | 2 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2903): Show |
chr7 | 155292878 | 155315235 |
| a0001c0002t0006 | 0/0 | 2906 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2901): Show |
chr7 | 155292878 | 155315235 |
| a0001c0002t0010 | 0/0 | 2902 | 3 | 2 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2897): Show |
chr7 | 155292878 | 155315235 |
| a0001c0002t0013 | 0/0 | 2908 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2903): Show |
chr7 | 155292878 | 155315235 |
| a0001c0004t0002 | 0/0 | 2909 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2904): Show |
chr7 | 155292878 | 155315235 |
| a0002c0006t0001 | 0/0 | 2908 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2903): Show |
chr7 | 155292878 | 155315235 |
| a0003c0003t0001 | 0/0 | 2908 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2903): Show |
chr7 | 155292878 | 155315235 |
| a0004c0005t0003 | 0/0 | 2908 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | GCGGC others(2903): Show |
chr7 | 155292878 | 155315235 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 47 | 0 | 7 | 33 | 1 | 6 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0002 | 0/0 | 32 | 2 | 6 | 23 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0003 | 0/0 | 32 | 0 | 0 | 30 | 0 | 2 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0005 | 1/0 | 22 | 0 | 0 | 21 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0006 | 0/0 | 18 | 2 | 10 | 0 | 3 | 3 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0007 | 0/0 | 19 | 1 | 15 | 0 | 2 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0008 | 0/0 | 18 | 0 | 13 | 0 | 3 | 2 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0011 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0016 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 1 | 1 | 2 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0020 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0023 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0028 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0030 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0002g0004 | 0/0 | 26 | 4 | 2 | 15 | 1 | 4 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0002g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0003g0009 | 0/0 | 13 | 1 | 0 | 12 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0003g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0003g0015 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0003g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0004g0001 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0005g0010 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0007g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0008g0022 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0008g0023 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0009g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0009g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0011g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0012g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0014g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0015g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0016g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0017g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0018g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0019g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0020g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0021g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0022g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0023g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0024g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0025g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0026g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0001t0027g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0002t0001g0027 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0002t0006g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0002t0010g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0002t0010g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0002t0013g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0001c0004t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0002c0006t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0003c0003t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| a0004c0005t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | GBR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | GBR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | GBR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00280 | hp1 | a0001 | c0001 | t0008 | g0022 | EUR | FIN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00597 | hp1 | a0001 | c0001 | t0015 | g0002 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00673 | hp1 | a0002 | c0006 | t0001 | g0005 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | CHS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01099 | hp1 | a0001 | c0001 | t0008 | g0022 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01109 | hp2 | a0001 | c0001 | t0009 | g0104 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01361 | hp1 | a0001 | c0001 | t0023 | g0006 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | IBS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | IBS | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01891 | hp2 | a0001 | c0002 | t0010 | g0072 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01934 | hp1 | a0001 | c0001 | t0012 | g0002 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01952 | hp1 | a0001 | c0002 | t0010 | g0019 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02015 | hp2 | a0001 | c0001 | t0014 | g0002 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02135 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CDX | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | CDX | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02258 | hp1 | a0001 | c0001 | t0017 | g0056 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02273 | hp2 | a0001 | c0001 | t0019 | g0007 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02630 | hp1 | a0001 | c0004 | t0002 | g0091 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02647 | hp1 | a0001 | c0001 | t0012 | g0002 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02683 | hp1 | a0001 | c0001 | t0008 | g0022 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02717 | hp1 | a0001 | c0001 | t0009 | g0024 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02818 | hp2 | a0001 | c0001 | t0021 | g0076 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02965 | hp1 | a0001 | c0002 | t0010 | g0019 | AFR | ESN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02965 | hp2 | a0001 | c0001 | t0007 | g0014 | AFR | ESN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03139 | hp2 | a0001 | c0002 | t0006 | g0019 | AFR | ESN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0014 | AFR | ESN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03195 | hp2 | a0001 | c0001 | t0009 | g0024 | AFR | ESN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | MSL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03453 | hp1 | a0001 | c0002 | t0013 | g0019 | AFR | MSL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | MSL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03540 | hp1 | a0001 | c0001 | t0026 | g0006 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | STU | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0015 | SAS | BEB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03927 | hp2 | a0001 | c0001 | t0011 | g0004 | SAS | BEB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0100 | SAS | BEB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03942 | hp2 | a0001 | c0001 | t0018 | g0008 | SAS | BEB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | STU | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0094 | SAS | STU | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | YRI | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0043 | AFR | YRI | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | YRI | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | YRI | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18947 | hp2 | a0001 | c0001 | t0016 | g0111 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18962 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18987 | hp2 | a0004 | c0005 | t0003 | g0012 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18988 | hp1 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18989 | hp1 | a0001 | c0001 | t0020 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18997 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18998 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0014 | AFR | LWK | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | LWK | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0073 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19087 | hp2 | a0001 | c0001 | t0024 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | YRI | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ASW | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ASW | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | TSI | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | TSI | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | TSI | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA20905 | hp1 | a0001 | c0001 | t0011 | g0004 | SAS | GIH | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA20905 | hp2 | a0001 | c0001 | t0025 | g0026 | SAS | GIH | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0079 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02559 | hp1 | a0001 | c0001 | t0022 | g0124 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0044 | AFR | MSL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0045 | AFR | MSL | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | USA | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | USA | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA20300 | hp2 | a0001 | c0001 | t0027 | g0042 | AFR | USA | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| NA21309 | hp2 | a0001 | c0001 | t0007 | g0014 | AFR | LWK | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0008 | g0023 | REF | REF | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0005 | REF | REF | INSIG1_chr7_155292878_155315235 | INSIG1 | chr7 | 155292878 | 155315235 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:155298385 | G | A | 1 | a0003 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.100G>A | p.Val34Ile | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/6 | 209/2908 | 100/834 | 34/277 | chr7 | 155298385 | |||
| chr7:155298529 | C | T | 1 | a0002 | 1 | HG00673.hp1 | missense_variant | MODERATE | c.244C>T | p.His82Tyr | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/6 | 353/2908 | 244/834 | 82/277 | chr7 | 155298529 | |||
| chr7:155301671 | G | T | 1 | a0004 | 1 | NA18987.hp2 | missense_variant | MODERATE | c.518G>T | p.Gly173Val | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 3/6 | 627/2908 | 518/834 | 173/277 | chr7 | 155301671 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:155298621 | T | A | 1 | a0001c0004 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.336T>A | p.Thr112Thr | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/6 | 445/2908 | 336/834 | 112/277 | chr7 | 155298621 | |||
| chr7:155302843 | T | C | 1 | a0001c0002 | 8 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(5): Show |
synonymous_variant | LOW | c.801T>C | p.Ala267Ala | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/6 | 910/2908 | 801/834 | 267/277 | chr7 | 155302843 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:155297906 | T | C | 1 | a0001c0001t0004 | 11 | NA18941.hp1 NA18949.hp2 NA18954.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-81T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 1/6 | 380 | chr7 | 155297906 | ||||||
| chr7:155297925 | T | C | 1 | a0001c0001t0009 | 3 | HG01109.hp2 HG02717.hp1 HG03195.hp2 |
5_prime_UTR_variant | MODIFIER | c.-62T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 1/6 | 361 | chr7 | 155297925 | ||||||
| chr7:155298268 | C | T | 1 | a0001c0001t0027 | 1 | NA20300.hp2 | 5_prime_UTR_variant | MODIFIER | c.-18C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/6 | 18 | chr7 | 155298268 | ||||||
| chr7:155308359 | G | A | 4 | a0001c0001t0006 a0001c0002t0006 a0001c0002t0010 others(1): Show |
8 | HG01891.hp2 HG01952.hp1 HG02486.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*89G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 89 | chr7 | 155308359 | ||||||
| chr7:155308613 | A | C | 1 | a0001c0001t0026 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*343A>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 343 | chr7 | 155308613 | ||||||
| chr7:155308688 | G | A | 1 | a0001c0001t0007 | 4 | HG02965.hp2 HG03195.hp1 NA19030.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*418G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 418 | chr7 | 155308688 | ||||||
| chr7:155308712 | A | G | 1 | a0001c0001t0025 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*442A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 442 | chr7 | 155308712 | ||||||
| chr7:155308738 | T | TA | 3 | a0001c0001t0002 a0001c0001t0011 a0001c0004t0002 |
43 | HG01074.hp1 HG01361.hp2 HG02074.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*479dupA | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 480 | INFO_REALIGN_3_PRIME | chr7 | 155308738 | |||||
| chr7:155308739 | A | T | 1 | a0001c0001t0024 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*469A>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 469 | chr7 | 155308739 | ||||||
| chr7:155308745 | A | C | 1 | a0001c0001t0023 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*475A>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 475 | chr7 | 155308745 | ||||||
| chr7:155308748 | AAC | A | 3 | a0001c0001t0006 a0001c0002t0006 a0001c0002t0010 |
7 | HG01891.hp2 HG01952.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*480_*481delCA | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 480 | INFO_REALIGN_3_PRIME | chr7 | 155308748 | |||||
| chr7:155308751 | A | C | 3 | a0001c0001t0006 a0001c0002t0006 a0001c0002t0010 |
7 | HG01891.hp2 HG01952.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*481A>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 481 | chr7 | 155308751 | ||||||
| chr7:155308805 | G | A | 2 | a0001c0001t0014 a0001c0001t0015 |
2 | HG00597.hp1 HG02015.hp2 |
3_prime_UTR_variant | MODIFIER | c.*535G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 535 | chr7 | 155308805 | ||||||
| chr7:155308807 | C | T | 1 | a0001c0001t0022 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*537C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 537 | chr7 | 155308807 | ||||||
| chr7:155308828 | C | T | 2 | a0001c0001t0005 a0001c0001t0027 |
9 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*558C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 558 | chr7 | 155308828 | ||||||
| chr7:155308836 | C | T | 1 | a0001c0001t0021 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*566C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 566 | chr7 | 155308836 | ||||||
| chr7:155308859 | T | C | 3 | a0001c0001t0006 a0001c0002t0006 a0001c0002t0010 |
7 | HG01891.hp2 HG01952.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*589T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 589 | chr7 | 155308859 | ||||||
| chr7:155308909 | C | T | 1 | a0001c0001t0012 | 2 | HG01934.hp1 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*639C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 639 | chr7 | 155308909 | ||||||
| chr7:155308975 | G | A | 2 | a0001c0001t0003 a0004c0005t0003 |
32 | HG00673.hp2 HG02027.hp2 HG02074.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*705G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 705 | chr7 | 155308975 | ||||||
| chr7:155309001 | T | A | 3 | a0001c0001t0006 a0001c0002t0006 a0001c0002t0010 |
7 | HG01891.hp2 HG01952.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*731T>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 731 | chr7 | 155309001 | ||||||
| chr7:155309073 | A | AGCCAAAA others(69): Show |
1 | a0001c0001t0020 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*805_*880dupCCAAAA others(70): Show |
INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 881 | INFO_REALIGN_3_PRIME | chr7 | 155309073 | |||||
| chr7:155309078 | A | G | 1 | a0001c0001t0011 | 2 | HG03927.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*808A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 808 | chr7 | 155309078 | ||||||
| chr7:155309288 | AACTT | A | 1 | a0001c0002t0010 | 3 | HG01891.hp2 HG01952.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1019_*1022delACTT | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 1019 | chr7 | 155309288 | ||||||
| chr7:155309455 | C | A | 1 | a0001c0001t0022 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1185C>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 1185 | chr7 | 155309455 | ||||||
| chr7:155309495 | T | C | 1 | a0001c0001t0016 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1225T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 1225 | chr7 | 155309495 | ||||||
| chr7:155309505 | G | A | 3 | a0001c0001t0006 a0001c0002t0006 a0001c0002t0010 |
7 | HG01891.hp2 HG01952.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1235G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 1235 | chr7 | 155309505 | ||||||
| chr7:155309756 | T | C | 1 | a0001c0001t0017 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1486T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 1486 | chr7 | 155309756 | ||||||
| chr7:155309791 | A | T | 1 | a0001c0001t0015 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1521A>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 1521 | chr7 | 155309791 | ||||||
| chr7:155309823 | A | G | 1 | a0001c0001t0008 | 3 | HG00280.hp1 HG01099.hp1 HG02683.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1553A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 1553 | chr7 | 155309823 | ||||||
| chr7:155309839 | T | C | 1 | a0001c0001t0020 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1569T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 1569 | chr7 | 155309839 | ||||||
| chr7:155309870 | T | A | 1 | a0001c0001t0018 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1600T>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 1600 | chr7 | 155309870 | ||||||
| chr7:155310111 | T | C | 1 | a0001c0001t0019 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1841T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 6/6 | 1841 | chr7 | 155310111 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:155297979 | A | T | 1 | a0001c0001t0001g0040 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-28+20A>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 1/5 | chr7 | 155297979 | |||||||
| chr7:155297979 | AG | A | 22 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0030 others(19): Show |
60 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.-28+24delG | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 155297979 | ||||||
| chr7:155297991 | C | G | 1 | a0001c0001t0001g0125 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-28+32C>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 1/5 | chr7 | 155297991 | |||||||
| chr7:155298065 | G | A | 2 | a0001c0001t0001g0109 a0001c0001t0001g0125 |
2 | HG00558.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.-28+106G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 1/5 | chr7 | 155298065 | |||||||
| chr7:155298120 | C | A | 1 | a0001c0001t0001g0041 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-27-139C>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 1/5 | chr7 | 155298120 | |||||||
| chr7:155298255 | C | A | 1 | a0001c0001t0001g0110 | 1 | NA18939.hp2 | splice_region_variant&intron_variant | LOW | c.-27-4C>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 1/5 | chr7 | 155298255 | |||||||
| chr7:155298852 | G | T | 5 | a0001c0001t0003g0012 a0001c0001t0003g0015 a0001c0001t0003g0038 others(2): Show |
14 | HG03834.hp2 NA18939.hp1 NA18949.hp1 others(11): Show |
intron_variant | MODIFIER | c.412+155G>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155298852 | |||||||
| chr7:155298896 | C | G | 1 | a0001c0001t0001g0029 | 3 | HG01891.hp1 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.412+199C>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155298896 | |||||||
| chr7:155298932 | A | G | 30 | a0001c0001t0001g0009 a0001c0001t0001g0037 a0001c0001t0001g0089 others(27): Show |
82 | HG00673.hp2 HG01074.hp1 HG01109.hp2 others(79): Show |
intron_variant | MODIFIER | c.412+235A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155298932 | |||||||
| chr7:155299146 | T | G | 1 | a0001c0001t0003g0108 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.412+449T>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155299146 | |||||||
| chr7:155299235 | C | T | 1 | a0001c0001t0003g0088 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.412+538C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155299235 | |||||||
| chr7:155299302 | G | C | 1 | a0001c0001t0016g0111 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.412+605G>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155299302 | |||||||
| chr7:155299357 | A | G | 1 | a0001c0001t0003g0088 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.412+660A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155299357 | |||||||
| chr7:155299539 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.412+842C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155299539 | |||||||
| chr7:155299595 | A | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0029 a0001c0001t0001g0086 others(1): Show |
9 | HG01884.hp1 HG01891.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.412+898A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155299595 | |||||||
| chr7:155299696 | G | T | 29 | a0001c0001t0001g0009 a0001c0001t0001g0037 a0001c0001t0001g0099 others(26): Show |
81 | HG00673.hp2 HG01074.hp1 HG01109.hp2 others(78): Show |
intron_variant | MODIFIER | c.412+999G>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155299696 | |||||||
| chr7:155299836 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.412+1139A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155299836 | |||||||
| chr7:155299869 | T | C | 31 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0023 others(28): Show |
79 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.412+1172T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155299869 | |||||||
| chr7:155299961 | C | G | 22 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0030 others(19): Show |
60 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.412+1264C>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155299961 | |||||||
| chr7:155299968 | G | C | 22 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0030 others(19): Show |
60 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.412+1271G>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155299968 | |||||||
| chr7:155300007 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.412+1310G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300007 | |||||||
| chr7:155300043 | A | T | 29 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(26): Show |
93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.412+1346A>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300043 | |||||||
| chr7:155300046 | C | A | 1 | a0001c0001t0001g0112 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.412+1349C>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300046 | |||||||
| chr7:155300090 | C | A | 21 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0030 others(18): Show |
59 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.412+1393C>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300090 | |||||||
| chr7:155300181 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.413-1385T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300181 | |||||||
| chr7:155300229 | G | C | 4 | a0001c0001t0001g0031 a0001c0001t0005g0010 a0001c0001t0005g0043 others(1): Show |
11 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.413-1337G>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300229 | |||||||
| chr7:155300244 | CTG | C | 6 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0005g0010 others(3): Show |
19 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.413-1321_413-1320d others(4): Show |
INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300244 | |||||||
| chr7:155300377 | G | A | 1 | a0001c0001t0006g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.413-1189G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300377 | |||||||
| chr7:155300392 | C | G | 1 | a0001c0001t0004g0073 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.413-1174C>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300392 | |||||||
| chr7:155300432 | C | CTG | 28 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0030 others(25): Show |
69 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.413-1134_413-1133i others(4): Show |
INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300432 | |||||||
| chr7:155300436 | A | AT | 28 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0030 others(25): Show |
69 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.413-1124dupT | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr7 | 155300436 | ||||||
| chr7:155300495 | T | G | 86 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(83): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.413-1071T>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300495 | |||||||
| chr7:155300511 | A | G | 5 | a0001c0002t0001g0027 a0001c0002t0006g0019 a0001c0002t0010g0019 others(2): Show |
8 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.413-1055A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300511 | |||||||
| chr7:155300515 | C | G | 98 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(95): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.413-1051C>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300515 | |||||||
| chr7:155300608 | C | G | 1 | a0001c0001t0001g0071 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.413-958C>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300608 | |||||||
| chr7:155300701 | G | A | 29 | a0001c0001t0001g0009 a0001c0001t0001g0037 a0001c0001t0001g0099 others(26): Show |
81 | HG00673.hp2 HG01074.hp1 HG01109.hp2 others(78): Show |
intron_variant | MODIFIER | c.413-865G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300701 | |||||||
| chr7:155300730 | A | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0070 |
3 | NA18973.hp1 NA19007.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.413-836A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300730 | |||||||
| chr7:155300778 | A | T | 2 | a0001c0001t0003g0088 a0001c0001t0022g0124 |
2 | HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.413-788A>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300778 | |||||||
| chr7:155300863 | T | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0074 |
5 | HG02109.hp2 HG02451.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.413-703T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300863 | |||||||
| chr7:155300872 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.413-694C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300872 | |||||||
| chr7:155300916 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.413-650C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300916 | |||||||
| chr7:155300924 | G | A | 56 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0016 others(53): Show |
150 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.413-642G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155300924 | |||||||
| chr7:155301008 | C | T | 76 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(73): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.413-558C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155301008 | |||||||
| chr7:155301029 | C | T | 17 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0020 others(14): Show |
44 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.413-537C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155301029 | |||||||
| chr7:155301069 | C | T | 1 | a0001c0001t0003g0088 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.413-497C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155301069 | |||||||
| chr7:155301332 | C | T | 76 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(73): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.413-234C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155301332 | |||||||
| chr7:155301364 | TA | T | 5 | a0001c0001t0001g0031 a0001c0001t0001g0068 a0001c0001t0005g0010 others(2): Show |
12 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.413-196delA | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr7 | 155301364 | ||||||
| chr7:155301377 | C | T | 76 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(73): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.413-189C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155301377 | |||||||
| chr7:155301544 | A | G | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG02572.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.413-22A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 2/5 | chr7 | 155301544 | |||||||
| chr7:155301756 | T | G | 1 | a0001c0001t0003g0088 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.537+66T>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 3/5 | chr7 | 155301756 | |||||||
| chr7:155301864 | T | C | 39 | a0001c0001t0001g0009 a0001c0001t0001g0031 a0001c0001t0001g0037 others(36): Show |
101 | HG00673.hp2 HG01074.hp1 HG01109.hp2 others(98): Show |
intron_variant | MODIFIER | c.537+174T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 3/5 | chr7 | 155301864 | |||||||
| chr7:155301904 | T | A | 1 | a0001c0001t0004g0049 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.537+214T>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 3/5 | chr7 | 155301904 | |||||||
| chr7:155301925 | T | TTA | 3 | a0001c0001t0001g0014 a0001c0001t0001g0086 a0001c0001t0007g0014 |
6 | HG01884.hp1 HG02257.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.537+243_537+244dup others(2): Show |
INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 155301925 | ||||||
| chr7:155301933 | A | T | 1 | a0001c0001t0006g0079 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.537+243A>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 3/5 | chr7 | 155301933 | |||||||
| chr7:155301940 | A | AAT | 98 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(95): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.537+258_537+259dup others(2): Show |
INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 155301940 | ||||||
| chr7:155301955 | T | C | 29 | a0001c0001t0001g0009 a0001c0001t0001g0037 a0001c0001t0001g0099 others(26): Show |
81 | HG00673.hp2 HG01074.hp1 HG01109.hp2 others(78): Show |
intron_variant | MODIFIER | c.537+265T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 3/5 | chr7 | 155301955 | |||||||
| chr7:155302116 | T | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(138): Show |
418 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(415): Show |
intron_variant | MODIFIER | c.538-135T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 3/5 | chr7 | 155302116 | |||||||
| chr7:155302125 | G | C | 4 | a0001c0001t0001g0024 a0001c0001t0001g0047 a0001c0001t0001g0048 others(1): Show |
5 | HG02109.hp1 HG02717.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.538-126G>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 3/5 | chr7 | 155302125 | |||||||
| chr7:155302149 | G | A | 4 | a0001c0001t0001g0024 a0001c0001t0001g0047 a0001c0001t0001g0048 others(1): Show |
5 | HG02109.hp1 HG02717.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.538-102G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 3/5 | chr7 | 155302149 | |||||||
| chr7:155302196 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0086 a0001c0001t0007g0014 |
6 | HG01884.hp1 HG02257.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.538-55G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 3/5 | chr7 | 155302196 | |||||||
| chr7:155302215 | A | T | 21 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0030 others(18): Show |
59 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.538-36A>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 3/5 | chr7 | 155302215 | |||||||
| chr7:155302438 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.704+21A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 4/5 | chr7 | 155302438 | |||||||
| chr7:155302462 | C | T | 13 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(10): Show |
56 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(53): Show |
intron_variant | MODIFIER | c.704+45C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 4/5 | chr7 | 155302462 | |||||||
| chr7:155302555 | A | T | 1 | a0001c0001t0002g0107 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.704+138A>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 4/5 | chr7 | 155302555 | |||||||
| chr7:155302632 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.705-115C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 4/5 | chr7 | 155302632 | |||||||
| chr7:155302674 | A | C | 1 | a0001c0001t0001g0106 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.705-73A>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 4/5 | chr7 | 155302674 | |||||||
| chr7:155302882 | C | T | 38 | a0001c0001t0001g0009 a0001c0001t0001g0031 a0001c0001t0001g0037 others(35): Show |
100 | HG00673.hp2 HG01074.hp1 HG01109.hp2 others(97): Show |
intron_variant | MODIFIER | c.804+36C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155302882 | |||||||
| chr7:155302883 | G | T | 11 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(8): Show |
30 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.804+37G>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155302883 | |||||||
| chr7:155303340 | G | A | 7 | a0001c0001t0001g0006 a0001c0001t0001g0075 a0001c0001t0001g0077 others(4): Show |
24 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.804+494G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155303340 | |||||||
| chr7:155303365 | T | C | 38 | a0001c0001t0001g0009 a0001c0001t0001g0031 a0001c0001t0001g0037 others(35): Show |
98 | HG00673.hp2 HG01074.hp1 HG01109.hp2 others(95): Show |
intron_variant | MODIFIER | c.804+519T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155303365 | |||||||
| chr7:155303483 | G | C | 43 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(40): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.804+637G>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155303483 | |||||||
| chr7:155303541 | C | T | 1 | a0001c0001t0003g0105 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.804+695C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155303541 | |||||||
| chr7:155303542 | G | A | 7 | a0001c0001t0001g0006 a0001c0001t0001g0075 a0001c0001t0001g0077 others(4): Show |
24 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.804+696G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155303542 | |||||||
| chr7:155303576 | G | A | 4 | a0001c0001t0001g0031 a0001c0001t0005g0010 a0001c0001t0005g0043 others(1): Show |
11 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.804+730G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155303576 | |||||||
| chr7:155303660 | A | G | 1 | a0001c0001t0003g0088 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.804+814A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155303660 | |||||||
| chr7:155303726 | C | A | 37 | a0001c0001t0001g0009 a0001c0001t0001g0031 a0001c0001t0001g0037 others(34): Show |
97 | HG00673.hp2 HG01074.hp1 HG01361.hp2 others(94): Show |
intron_variant | MODIFIER | c.804+880C>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155303726 | |||||||
| chr7:155303742 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0008g0022 |
5 | HG00140.hp2 HG00280.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+896C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155303742 | |||||||
| chr7:155303976 | C | CT | 7 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0040 others(4): Show |
12 | HG00438.hp1 HG01123.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.804+1152dupT | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 155303976 | ||||||
| chr7:155303976 | CTT | C | 10 | a0001c0001t0001g0016 a0001c0001t0001g0023 a0001c0001t0001g0051 others(7): Show |
17 | HG00140.hp2 HG00280.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.804+1151_804+1152d others(4): Show |
INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 155303976 | ||||||
| chr7:155303976 | CTTT | C | 52 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(49): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.804+1150_804+1152d others(5): Show |
INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 155303976 | ||||||
| chr7:155303976 | CTTTT | C | 36 | a0001c0001t0001g0009 a0001c0001t0001g0031 a0001c0001t0001g0037 others(33): Show |
89 | HG00673.hp2 HG01074.hp1 HG01168.hp1 others(86): Show |
intron_variant | MODIFIER | c.804+1149_804+1152d others(6): Show |
INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 155303976 | ||||||
| chr7:155304083 | C | T | 4 | a0001c0001t0001g0031 a0001c0001t0005g0010 a0001c0001t0005g0043 others(1): Show |
11 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.804+1237C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155304083 | |||||||
| chr7:155304175 | G | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0086 a0001c0001t0007g0014 |
6 | HG01884.hp1 HG02257.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.804+1329G>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155304175 | |||||||
| chr7:155304214 | T | G | 5 | a0001c0001t0001g0031 a0001c0001t0005g0010 a0001c0001t0005g0043 others(2): Show |
12 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.804+1368T>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155304214 | |||||||
| chr7:155304234 | G | T | 1 | a0001c0001t0001g0060 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.804+1388G>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155304234 | |||||||
| chr7:155304389 | T | G | 28 | a0001c0001t0001g0009 a0001c0001t0001g0037 a0001c0001t0001g0099 others(25): Show |
80 | HG00673.hp2 HG01074.hp1 HG01361.hp2 others(77): Show |
intron_variant | MODIFIER | c.804+1543T>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155304389 | |||||||
| chr7:155304405 | G | A | 1 | a0001c0002t0001g0027 | 3 | HG01167.hp1 HG01169.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.804+1559G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155304405 | |||||||
| chr7:155304484 | A | T | 2 | a0001c0001t0006g0045 a0001c0001t0006g0079 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.804+1638A>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155304484 | |||||||
| chr7:155304567 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.804+1721G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155304567 | |||||||
| chr7:155304619 | A | C | 4 | a0001c0002t0006g0019 a0001c0002t0010g0019 a0001c0002t0010g0072 others(1): Show |
5 | HG01891.hp2 HG01952.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+1773A>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155304619 | |||||||
| chr7:155304642 | G | A | 1 | a0001c0001t0003g0088 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.804+1796G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155304642 | |||||||
| chr7:155304659 | T | C | 1 | a0001c0001t0002g0090 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.804+1813T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155304659 | |||||||
| chr7:155304818 | T | A | 1 | a0001c0001t0001g0052 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.804+1972T>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155304818 | |||||||
| chr7:155304865 | C | T | 1 | a0001c0001t0003g0088 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.804+2019C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155304865 | |||||||
| chr7:155304876 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.804+2030G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155304876 | |||||||
| chr7:155304937 | A | G | 4 | a0001c0002t0006g0019 a0001c0002t0010g0019 a0001c0002t0010g0072 others(1): Show |
5 | HG01891.hp2 HG01952.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+2091A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155304937 | |||||||
| chr7:155304981 | C | CA | 11 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0061 others(8): Show |
17 | HG00408.hp1 HG01123.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.804+2151dupA | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 155304981 | ||||||
| chr7:155304981 | C | CAA | 61 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(58): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.804+2150_804+2151d others(4): Show |
INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 155304981 | ||||||
| chr7:155304981 | C | CAAA | 19 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0074 others(16): Show |
43 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.804+2149_804+2151d others(5): Show |
INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 155304981 | ||||||
| chr7:155305071 | G | A | 1 | a0001c0001t0003g0088 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.804+2225G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305071 | |||||||
| chr7:155305107 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.804+2261C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305107 | |||||||
| chr7:155305145 | C | CA | 33 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0024 others(30): Show |
73 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.804+2316dupA | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 155305145 | ||||||
| chr7:155305145 | C | CAA | 6 | a0001c0001t0001g0030 a0001c0001t0001g0047 a0001c0001t0001g0048 others(3): Show |
8 | HG01433.hp1 HG02109.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.804+2315_804+2316d others(4): Show |
INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 155305145 | ||||||
| chr7:155305157 | A | C | 1 | a0001c0001t0001g0023 | 2 | HG00140.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.804+2311A>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305157 | |||||||
| chr7:155305200 | G | A | 97 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(94): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.804+2354G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305200 | |||||||
| chr7:155305207 | T | C | 3 | a0001c0001t0005g0010 a0001c0001t0005g0043 a0001c0001t0027g0042 |
9 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.804+2361T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305207 | |||||||
| chr7:155305223 | C | G | 7 | a0001c0001t0001g0006 a0001c0001t0001g0075 a0001c0001t0001g0077 others(4): Show |
24 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.804+2377C>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305223 | |||||||
| chr7:155305256 | T | C | 4 | a0001c0002t0006g0019 a0001c0002t0010g0019 a0001c0002t0010g0072 others(1): Show |
5 | HG01891.hp2 HG01952.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+2410T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305256 | |||||||
| chr7:155305357 | G | A | 6 | a0001c0001t0006g0044 a0001c0001t0017g0056 a0001c0002t0006g0019 others(3): Show |
7 | HG01891.hp2 HG01952.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.804+2511G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305357 | |||||||
| chr7:155305462 | A | T | 3 | a0001c0001t0005g0010 a0001c0001t0005g0043 a0001c0001t0027g0042 |
9 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.804+2616A>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305462 | |||||||
| chr7:155305506 | A | G | 17 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(14): Show |
62 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(59): Show |
intron_variant | MODIFIER | c.804+2660A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305506 | |||||||
| chr7:155305512 | G | A | 2 | a0001c0001t0001g0057 a0001c0001t0001g0063 |
2 | HG02602.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.804+2666G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305512 | |||||||
| chr7:155305574 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.805-2667A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305574 | |||||||
| chr7:155305652 | A | G | 3 | a0001c0001t0005g0010 a0001c0001t0005g0043 a0001c0001t0027g0042 |
9 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.805-2589A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305652 | |||||||
| chr7:155305669 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.805-2572C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305669 | |||||||
| chr7:155305918 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0080 |
4 | HG01258.hp1 HG01261.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-2323G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305918 | |||||||
| chr7:155305933 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.805-2308C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305933 | |||||||
| chr7:155305977 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0008g0022 |
5 | HG00140.hp2 HG00280.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-2264T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155305977 | |||||||
| chr7:155306071 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.805-2170C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155306071 | |||||||
| chr7:155306095 | G | T | 5 | a0001c0001t0006g0044 a0001c0002t0006g0019 a0001c0002t0010g0019 others(2): Show |
6 | HG01891.hp2 HG01952.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.805-2146G>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155306095 | |||||||
| chr7:155306451 | T | C | 5 | a0001c0001t0006g0044 a0001c0002t0006g0019 a0001c0002t0010g0019 others(2): Show |
6 | HG01891.hp2 HG01952.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.805-1790T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155306451 | |||||||
| chr7:155306624 | G | A | 1 | a0001c0002t0001g0027 | 3 | HG01167.hp1 HG01169.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.805-1617G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155306624 | |||||||
| chr7:155306662 | T | A | 1 | a0001c0001t0001g0017 | 4 | NA18956.hp1 NA18957.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-1579T>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155306662 | |||||||
| chr7:155306671 | T | TAGAAACT others(21): Show |
1 | a0001c0001t0002g0098 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.805-1569_805-1542d others(30): Show |
INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 155306671 | ||||||
| chr7:155306767 | G | A | 5 | a0001c0001t0006g0044 a0001c0002t0006g0019 a0001c0002t0010g0019 others(2): Show |
6 | HG01891.hp2 HG01952.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.805-1474G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155306767 | |||||||
| chr7:155306775 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.805-1466C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155306775 | |||||||
| chr7:155306814 | AC | A | 12 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(9): Show |
31 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.805-1425delC | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 155306814 | ||||||
| chr7:155306857 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0017g0056 |
6 | HG02258.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.805-1384G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155306857 | |||||||
| chr7:155306928 | G | T | 14 | a0001c0001t0002g0004 a0001c0001t0002g0021 a0001c0001t0002g0090 others(11): Show |
43 | HG01074.hp1 HG01361.hp2 HG02074.hp1 others(40): Show |
intron_variant | MODIFIER | c.805-1313G>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155306928 | |||||||
| chr7:155306948 | G | A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0109 others(10): Show |
46 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.805-1293G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155306948 | |||||||
| chr7:155306987 | C | T | 1 | a0001c0001t0002g0101 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.805-1254C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155306987 | |||||||
| chr7:155306990 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.805-1251T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155306990 | |||||||
| chr7:155307002 | T | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0029 a0001c0001t0001g0086 others(2): Show |
12 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.805-1239T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307002 | |||||||
| chr7:155307011 | C | T | 1 | a0001c0001t0001g0037 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.805-1230C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307011 | |||||||
| chr7:155307154 | A | C | 7 | a0001c0001t0006g0044 a0001c0001t0006g0045 a0001c0001t0006g0079 others(4): Show |
8 | HG01891.hp2 HG01952.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.805-1087A>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307154 | |||||||
| chr7:155307399 | G | A | 3 | a0001c0001t0001g0055 a0001c0001t0001g0058 a0001c0001t0001g0085 |
3 | NA18967.hp1 NA18980.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.805-842G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307399 | |||||||
| chr7:155307420 | G | A | 7 | a0001c0001t0006g0044 a0001c0001t0006g0045 a0001c0001t0006g0079 others(4): Show |
8 | HG01891.hp2 HG01952.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.805-821G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307420 | |||||||
| chr7:155307432 | T | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0080 others(4): Show |
27 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.805-809T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307432 | |||||||
| chr7:155307466 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.805-775G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307466 | |||||||
| chr7:155307538 | T | G | 1 | a0001c0001t0002g0100 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.805-703T>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307538 | |||||||
| chr7:155307579 | A | C | 1 | a0001c0001t0001g0078 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.805-662A>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307579 | |||||||
| chr7:155307601 | T | C | 1 | a0001c0001t0001g0037 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.805-640T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307601 | |||||||
| chr7:155307636 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.805-605A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307636 | |||||||
| chr7:155307797 | A | T | 14 | a0001c0001t0002g0004 a0001c0001t0002g0021 a0001c0001t0002g0090 others(11): Show |
43 | HG01074.hp1 HG01361.hp2 HG02074.hp1 others(40): Show |
intron_variant | MODIFIER | c.805-444A>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307797 | |||||||
| chr7:155307810 | A | G | 1 | a0001c0001t0002g0097 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.805-431A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307810 | |||||||
| chr7:155307902 | A | G | 26 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0026 others(23): Show |
88 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.805-339A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307902 | |||||||
| chr7:155307927 | T | G | 46 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(43): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.805-314T>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307927 | |||||||
| chr7:155307940 | T | C | 46 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(43): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.805-301T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307940 | |||||||
| chr7:155307945 | C | T | 7 | a0001c0001t0001g0006 a0001c0001t0001g0075 a0001c0001t0001g0077 others(4): Show |
24 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.805-296C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307945 | |||||||
| chr7:155307946 | A | G | 67 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(64): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.805-295A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155307946 | |||||||
| chr7:155308050 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0099 |
3 | HG00408.hp2 NA18971.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.805-191G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155308050 | |||||||
| chr7:155308052 | T | C | 45 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(42): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.805-189T>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155308052 | |||||||
| chr7:155308053 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.805-188G>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155308053 | |||||||
| chr7:155308078 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.805-163C>T | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155308078 | |||||||
| chr7:155308082 | C | G | 1 | a0001c0001t0022g0124 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.805-159C>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155308082 | |||||||
| chr7:155308129 | C | A | 1 | a0001c0001t0005g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.805-112C>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155308129 | |||||||
| chr7:155308143 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.805-98A>G | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155308143 | |||||||
| chr7:155308145 | C | A | 37 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(34): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.805-96C>A | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155308145 | |||||||
| chr7:155308197 | G | C | 2 | a0001c0001t0001g0024 a0001c0001t0009g0024 |
3 | HG02717.hp1 HG03195.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.805-44G>C | INSIG1 | ENSG00000186480.13 | transcript | ENST00000340368.9 | protein_coding | 5/5 | chr7 | 155308197 |