Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51141 |
| ensemblid | ENSG00000125629.16 |
| hgncid | 20452 |
| symbol | INSIG2 |
| name | insulin induced gene 2 |
| refseq_nuc | NM_016133.4 |
| refseq_prot | NP_057217.2 |
| ensembl_nuc | ENST00000245787.9 |
| ensembl_prot | ENSP00000245787.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 118088471 |
| end | 118110997 |
| strand | + |
| ver | v1.2 |
| region | chr2:118088471-118110997 |
| region5000 | chr2:118083471-118115997 |
| regionname0 | INSIG2_chr2_118088471_118110997 |
| regionname5000 | INSIG2_chr2_118083471_118115997 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 225 | 437 | 96 | 80 | 199 | 16 | 44 | 151 | INSIG2_chr2_118083471_118115997 | INSIG2 | MAEGE others(220): Show |
chr2 | 118083471 | 118115997 |
| a0002 | 0/0 | 225 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | INSIG2_chr2_118083471_118115997 | INSIG2 | MAEGE others(220): Show |
chr2 | 118083471 | 118115997 |
| a0003 | 0/0 | 240 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | MAEGE others(235): Show |
chr2 | 118083471 | 118115997 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 675 | 425 | 85 | 80 | 199 | 16 | 43 | INSIG2_chr2_118083471_118115997 | INSIG2 | ATGGC others(670): Show |
chr2 | 118083471 | 118115997 | ||
| a0001c0002 | 0/0 | 675 | 10 | 10 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | ATGGC others(670): Show |
chr2 | 118083471 | 118115997 | ||
| a0001c0004 | 0/0 | 675 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | ATGGC others(670): Show |
chr2 | 118083471 | 118115997 | ||
| a0001c0005 | 0/0 | 675 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | ATGGC others(670): Show |
chr2 | 118083471 | 118115997 | ||
| a0002c0003 | 0/0 | 675 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | ATGGC others(670): Show |
chr2 | 118083471 | 118115997 | ||
| a0003c0006 | 0/0 | 720 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | ATGGC others(715): Show |
chr2 | 118083471 | 118115997 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3560 | 88 | 7 | 19 | 54 | 2 | 6 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3555): Show |
chr2 | 118083471 | 118115997 |
| a0001c0001t0002 | 0/0 | 3563 | 84 | 15 | 5 | 60 | 0 | 4 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3558): Show |
chr2 | 118083471 | 118115997 |
| a0001c0001t0003 | 0/0 | 3558 | 54 | 7 | 12 | 27 | 2 | 6 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3553): Show |
chr2 | 118083471 | 118115997 |
| a0001c0001t0004 | 0/0 | 3559 | 46 | 24 | 9 | 4 | 2 | 7 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3554): Show |
chr2 | 118083471 | 118115997 |
| a0001c0001t0005 | 0/0 | 3559 | 41 | 1 | 6 | 20 | 4 | 10 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3554): Show |
chr2 | 118083471 | 118115997 |
| a0001c0001t0006 | 1/0 | 3562 | 16 | 12 | 0 | 3 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3557): Show |
chr2 | 118083471 | 118115997 |
| a0001c0001t0007 | 0/0 | 3559 | 15 | 0 | 9 | 1 | 1 | 4 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3554): Show |
chr2 | 118083471 | 118115997 |
| a0001c0001t0008 | 0/0 | 3563 | 9 | 9 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3558): Show |
chr2 | 118083471 | 118115997 |
| a0001c0001t0009 | 0/0 | 3562 | 8 | 2 | 6 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3557): Show |
chr2 | 118083471 | 118115997 |
| a0001c0001t0010 | 0/0 | 3558 | 7 | 0 | 1 | 6 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3553): Show |
chr2 | 118083471 | 118115997 |
| a0001c0001t0011 | 0/0 | 3559 | 7 | 0 | 3 | 0 | 3 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3554): Show |
chr2 | 118083471 | 118115997 |
| a0001c0001t0012 | 0/0 | 3560 | 6 | 2 | 1 | 3 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3555): Show |
chr2 | 118083471 | 118115997 |
| a0001c0001t0013 | 0/0 | 3559 | 5 | 0 | 3 | 0 | 2 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3554): Show |
chr2 | 118083471 | 118115997 |
| a0001c0001t0014 | 0/0 | 3561 | 4 | 1 | 2 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3556): Show |
chr2 | 118083471 | 118115997 |
| a0001c0001t0015 | 0/0 | 3560 | 4 | 0 | 0 | 4 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3555): Show |
chr2 | 118083471 | 118115997 |
| a0001c0001t0016 | 0/0 | 3559 | 3 | 3 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3554): Show |
chr2 | 118083471 | 118115997 |
| a0001c0001t0017 | 0/0 | 3561 | 4 | 0 | 0 | 4 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3556): Show |
chr2 | 118083471 | 118115997 |
| a0001c0001t0018 | 0/0 | 3560 | 4 | 0 | 0 | 3 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3555): Show |
chr2 | 118083471 | 118115997 |
| a0001c0001t0019 | 0/0 | 3559 | 3 | 0 | 0 | 0 | 0 | 3 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3554): Show |
chr2 | 118083471 | 118115997 |
| a0001c0001t0020 | 0/0 | 3556 | 3 | 0 | 0 | 3 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3551): Show |
chr2 | 118083471 | 118115997 |
| a0001c0001t0021 | 0/0 | 3559 | 2 | 0 | 0 | 1 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3554): Show |
chr2 | 118083471 | 118115997 |
| a0001c0001t0022 | 0/0 | 3560 | 2 | 0 | 2 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3555): Show |
chr2 | 118083471 | 118115997 |
| a0001c0001t0023 | 0/0 | 3558 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3553): Show |
chr2 | 118083471 | 118115997 |
| a0001c0001t0024 | 0/0 | 3561 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3556): Show |
chr2 | 118083471 | 118115997 |
| a0001c0001t0025 | 0/0 | 3558 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3553): Show |
chr2 | 118083471 | 118115997 |
| a0001c0001t0026 | 0/0 | 3555 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3550): Show |
chr2 | 118083471 | 118115997 |
| a0001c0001t0027 | 0/0 | 3558 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3553): Show |
chr2 | 118083471 | 118115997 |
| a0001c0001t0028 | 0/0 | 3558 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3553): Show |
chr2 | 118083471 | 118115997 |
| a0001c0001t0029 | 0/0 | 3563 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3558): Show |
chr2 | 118083471 | 118115997 |
| a0001c0001t0030 | 0/0 | 3560 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3555): Show |
chr2 | 118083471 | 118115997 |
| a0001c0001t0031 | 0/1 | 3562 | 1 | 0 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3557): Show |
chr2 | 118083471 | 118115997 |
| a0001c0001t0033 | 0/0 | 3556 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3551): Show |
chr2 | 118083471 | 118115997 |
| a0001c0002t0004 | 0/0 | 3559 | 7 | 7 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3554): Show |
chr2 | 118083471 | 118115997 |
| a0001c0002t0012 | 0/0 | 3560 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3555): Show |
chr2 | 118083471 | 118115997 |
| a0001c0002t0032 | 0/0 | 3559 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3554): Show |
chr2 | 118083471 | 118115997 |
| a0001c0002t0034 | 0/0 | 3559 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3554): Show |
chr2 | 118083471 | 118115997 |
| a0001c0004t0001 | 0/0 | 3560 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3555): Show |
chr2 | 118083471 | 118115997 |
| a0001c0005t0016 | 0/0 | 3559 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3554): Show |
chr2 | 118083471 | 118115997 |
| a0002c0003t0003 | 0/0 | 3558 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3553): Show |
chr2 | 118083471 | 118115997 |
| a0003c0006t0001 | 0/0 | 3605 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | GTTGT others(3600): Show |
chr2 | 118083471 | 118115997 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 39 | 0 | 9 | 29 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0001g0005 | 0/0 | 17 | 0 | 0 | 14 | 1 | 2 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0001g0011 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0001g0030 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0002g0003 | 0/0 | 26 | 0 | 2 | 24 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0002g0010 | 0/0 | 7 | 4 | 0 | 2 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0002g0012 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0002g0018 | 0/0 | 5 | 1 | 2 | 0 | 0 | 2 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0002g0019 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0002g0020 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0002g0031 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0002g0033 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0002g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0003g0002 | 0/0 | 25 | 0 | 0 | 19 | 2 | 4 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0003g0007 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0003g0016 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0003g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0003g0023 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0003g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0004g0006 | 0/0 | 6 | 5 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0004g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0004g0015 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0004g0017 | 0/0 | 5 | 2 | 2 | 0 | 1 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0004g0021 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0004g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0004g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0004g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0005g0004 | 0/0 | 23 | 0 | 0 | 17 | 2 | 4 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0005g0009 | 0/0 | 7 | 0 | 3 | 0 | 2 | 2 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0005g0029 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0005g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0005g0042 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0005g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0005g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0006g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0006g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0006g0108 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0006g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0006g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0006g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0007g0008 | 0/0 | 9 | 0 | 6 | 0 | 0 | 3 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0007g0024 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0007g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0007g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0008g0014 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0008g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0008g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0009g0027 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0009g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0009g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0009g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0010g0002 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0010g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0010g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0010g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0011g0006 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0011g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0011g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0012g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0012g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0012g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0012g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0012g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0012g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0013g0013 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0014g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0014g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0014g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0014g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0015g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0016g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0017g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0017g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0017g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0017g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0018g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0018g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0018g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0018g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0019g0026 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0020g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0020g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0021g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0021g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0022g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0023g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0024g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0025g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0026g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0027g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0028g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0029g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0030g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0031g0078 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0001t0033g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0002t0004g0032 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0002t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0002t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0002t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0002t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0002t0012g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0002t0032g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0002t0034g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0004t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0001c0005t0016g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0002c0003t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0002c0003t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| a0003c0006t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0017 | EUR | GBR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00099 | hp2 | a0001 | c0001 | t0013 | g0013 | EUR | GBR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00140 | hp1 | a0001 | c0001 | t0011 | g0113 | EUR | GBR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0076 | EUR | GBR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0002 | EUR | FIN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00280 | hp2 | a0001 | c0001 | t0005 | g0009 | EUR | FIN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00323 | hp1 | a0001 | c0001 | t0005 | g0009 | EUR | FIN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00323 | hp2 | a0001 | c0001 | t0011 | g0006 | EUR | FIN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00423 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0149 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00438 | hp2 | a0001 | c0001 | t0010 | g0098 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00544 | hp1 | a0001 | c0001 | t0012 | g0138 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00597 | hp1 | a0001 | c0001 | t0021 | g0083 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0051 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | CHS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0082 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00639 | hp2 | a0001 | c0001 | t0030 | g0001 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00642 | hp2 | a0001 | c0001 | t0025 | g0085 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0093 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0029 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00738 | hp1 | a0001 | c0001 | t0013 | g0013 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00738 | hp2 | a0001 | c0001 | t0022 | g0047 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00741 | hp1 | a0001 | c0001 | t0022 | g0047 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG00741 | hp2 | a0001 | c0001 | t0005 | g0029 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01069 | hp1 | a0001 | c0001 | t0009 | g0036 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01069 | hp2 | a0001 | c0001 | t0010 | g0002 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01070 | hp2 | a0001 | c0001 | t0009 | g0043 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01071 | hp1 | a0001 | c0001 | t0009 | g0043 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01071 | hp2 | a0001 | c0001 | t0009 | g0036 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01074 | hp1 | a0001 | c0001 | t0011 | g0006 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01074 | hp2 | a0001 | c0001 | t0005 | g0009 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01081 | hp2 | a0001 | c0001 | t0007 | g0050 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0017 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0071 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01167 | hp2 | a0001 | c0001 | t0007 | g0008 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01168 | hp2 | a0001 | c0001 | t0012 | g0135 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01169 | hp2 | a0001 | c0001 | t0007 | g0008 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0145 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01192 | hp1 | a0001 | c0001 | t0013 | g0013 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0039 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01243 | hp1 | a0001 | c0001 | t0009 | g0072 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0013 | AMR | PUR | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01255 | hp1 | a0001 | c0001 | t0009 | g0027 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0042 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01257 | hp1 | a0001 | c0001 | t0007 | g0008 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0009 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01261 | hp1 | a0001 | c0001 | t0014 | g0090 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0009 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01346 | hp1 | a0001 | c0001 | t0007 | g0050 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01346 | hp2 | a0001 | c0001 | t0013 | g0013 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0039 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01361 | hp1 | a0001 | c0001 | t0011 | g0006 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01361 | hp2 | a0001 | c0001 | t0007 | g0008 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01433 | hp1 | a0001 | c0001 | t0007 | g0008 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0017 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01515 | hp1 | a0001 | c0001 | t0013 | g0013 | EUR | IBS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0004 | EUR | IBS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0004 | EUR | IBS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0006 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0073 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0014 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01934 | hp2 | a0001 | c0001 | t0007 | g0146 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01981 | hp2 | a0001 | c0001 | t0011 | g0006 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01993 | hp1 | a0001 | c0001 | t0014 | g0022 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0088 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02015 | hp2 | a0001 | c0001 | t0017 | g0048 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02027 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02074 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02083 | hp1 | a0001 | c0001 | t0005 | g0042 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02129 | hp1 | a0001 | c0001 | t0010 | g0089 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0058 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02132 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02135 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0075 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02155 | hp1 | a0001 | c0001 | t0010 | g0007 | EAS | CDX | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CDX | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02257 | hp2 | a0001 | c0002 | t0004 | g0032 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0006 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0114 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02273 | hp2 | a0001 | c0001 | t0007 | g0008 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02293 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0112 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02523 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02523 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | KHV | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02572 | hp1 | a0001 | c0002 | t0004 | g0032 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0006 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0057 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0004 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02615 | hp1 | a0001 | c0001 | t0008 | g0014 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02615 | hp2 | a0001 | c0001 | t0014 | g0080 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0121 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0006 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02630 | hp1 | a0001 | c0001 | t0024 | g0079 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0118 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02647 | hp2 | a0001 | c0002 | t0004 | g0152 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02698 | hp1 | a0001 | c0004 | t0001 | g0001 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0006 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02735 | hp2 | a0001 | c0001 | t0005 | g0004 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0070 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02809 | hp1 | a0001 | c0002 | t0004 | g0032 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02818 | hp1 | a0001 | c0001 | t0016 | g0028 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02886 | hp1 | a0001 | c0001 | t0016 | g0028 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02895 | hp1 | a0001 | c0001 | t0027 | g0161 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0035 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0148 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ESN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0124 | AFR | ESN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | ESN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | ESN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | ESN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0049 | AFR | ESN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0021 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0049 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03098 | hp1 | a0001 | c0001 | t0012 | g0142 | AFR | MSL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03130 | hp2 | a0001 | c0002 | t0012 | g0137 | AFR | ESN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | ESN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | MSL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03209 | hp2 | a0001 | c0001 | t0016 | g0028 | AFR | MSL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | MSL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03239 | hp2 | a0001 | c0001 | t0007 | g0008 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0014 | AFR | MSL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0104 | AFR | MSL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03490 | hp2 | a0001 | c0001 | t0005 | g0117 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03491 | hp1 | a0001 | c0001 | t0005 | g0110 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0029 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03516 | hp2 | a0001 | c0002 | t0004 | g0154 | AFR | ESN | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0077 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0105 | AFR | GWD | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0106 | AFR | MSL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03579 | hp2 | a0001 | c0005 | t0016 | g0109 | AFR | MSL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03654 | hp2 | a0001 | c0001 | t0005 | g0126 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0160 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0123 | SAS | STU | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03688 | hp2 | a0001 | c0001 | t0011 | g0120 | SAS | STU | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03704 | hp2 | a0001 | c0001 | t0021 | g0095 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03710 | hp1 | a0001 | c0001 | t0007 | g0008 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03710 | hp2 | a0001 | c0001 | t0019 | g0026 | SAS | PJL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03831 | hp1 | a0001 | c0001 | t0018 | g0136 | SAS | BEB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03831 | hp2 | a0001 | c0001 | t0019 | g0026 | SAS | BEB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03834 | hp1 | a0001 | c0001 | t0005 | g0004 | SAS | BEB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0021 | SAS | BEB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0140 | SAS | BEB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03927 | hp2 | a0001 | c0001 | t0005 | g0004 | SAS | BEB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03942 | hp1 | a0001 | c0001 | t0019 | g0026 | SAS | BEB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0096 | SAS | STU | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG04115 | hp2 | a0001 | c0001 | t0007 | g0024 | SAS | STU | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0007 | SAS | STU | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG04228 | hp2 | a0001 | c0001 | t0005 | g0009 | SAS | STU | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0074 | AFR | YRI | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | YRI | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | CHB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0115 | AFR | YRI | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0014 | AFR | YRI | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18946 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18947 | hp2 | a0001 | c0001 | t0020 | g0004 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18950 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18954 | hp1 | a0001 | c0001 | t0017 | g0143 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18968 | hp2 | a0003 | c0006 | t0001 | g0116 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18969 | hp1 | a0001 | c0001 | t0012 | g0010 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18970 | hp1 | a0001 | c0001 | t0023 | g0007 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18971 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18978 | hp1 | a0001 | c0001 | t0006 | g0119 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18980 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18981 | hp1 | a0001 | c0001 | t0012 | g0048 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18982 | hp1 | a0001 | c0001 | t0026 | g0097 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18983 | hp1 | a0001 | c0001 | t0029 | g0001 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18984 | hp1 | a0001 | c0001 | t0018 | g0107 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18984 | hp2 | a0001 | c0001 | t0010 | g0007 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18986 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18991 | hp2 | a0001 | c0001 | t0017 | g0156 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18992 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18993 | hp2 | a0001 | c0001 | t0020 | g0004 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18997 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19002 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19004 | hp1 | a0001 | c0001 | t0028 | g0007 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19004 | hp2 | a0001 | c0001 | t0033 | g0024 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19005 | hp2 | a0001 | c0001 | t0015 | g0001 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19006 | hp1 | a0001 | c0001 | t0014 | g0101 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19006 | hp2 | a0001 | c0001 | t0020 | g0009 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19030 | hp1 | a0001 | c0002 | t0004 | g0151 | AFR | LWK | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19030 | hp2 | a0001 | c0002 | t0034 | g0150 | AFR | LWK | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | LWK | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0081 | AFR | LWK | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19054 | hp1 | a0001 | c0001 | t0018 | g0003 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19055 | hp1 | a0001 | c0001 | t0018 | g0127 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19055 | hp2 | a0001 | c0001 | t0006 | g0061 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19056 | hp1 | a0001 | c0001 | t0010 | g0007 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19056 | hp2 | a0002 | c0003 | t0003 | g0094 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19057 | hp1 | a0001 | c0001 | t0015 | g0001 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19057 | hp2 | a0001 | c0001 | t0005 | g0041 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19067 | hp1 | a0001 | c0001 | t0007 | g0024 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19067 | hp2 | a0001 | c0001 | t0017 | g0129 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19072 | hp1 | a0001 | c0001 | t0015 | g0001 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19074 | hp1 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19079 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19081 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19082 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19086 | hp1 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19086 | hp2 | a0002 | c0003 | t0003 | g0087 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19087 | hp2 | a0001 | c0001 | t0015 | g0001 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19089 | hp1 | a0001 | c0001 | t0006 | g0125 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19090 | hp1 | a0001 | c0001 | t0005 | g0041 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | YRI | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0038 | AFR | YRI | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA20129 | hp1 | a0001 | c0001 | t0012 | g0141 | AFR | ASW | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | ASW | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA20752 | hp1 | a0001 | c0001 | t0007 | g0024 | EUR | TSI | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0002 | EUR | TSI | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | TSI | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA20805 | hp2 | a0001 | c0001 | t0011 | g0006 | EUR | TSI | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA20905 | hp1 | a0001 | c0001 | t0005 | g0009 | SAS | GIH | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA20905 | hp2 | a0001 | c0001 | t0007 | g0008 | SAS | GIH | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0133 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02109 | hp2 | a0001 | c0001 | t0009 | g0027 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02486 | hp1 | a0001 | c0001 | t0008 | g0014 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02559 | hp1 | a0001 | c0001 | t0008 | g0014 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | ACB | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0069 | AFR | MSL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG03471 | hp2 | a0001 | c0002 | t0032 | g0092 | AFR | MSL | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | USA | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0122 | AFR | USA | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA20300 | hp1 | a0001 | c0002 | t0004 | g0153 | AFR | USA | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA20300 | hp2 | a0001 | c0001 | t0009 | g0027 | AFR | USA | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | LWK | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0111 | AFR | LWK | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0031 | g0078 | REF | REF | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0006 | g0108 | REF | REF | INSIG2_chr2_118083471_118115997 | INSIG2 | chr2 | 118083471 | 118115997 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:118106800 | T | TGGTGGAC others(38): Show |
1 | a0003 | 1 | NA18968.hp2 | disruptive_inframe_insertion | MODERATE | c.435_479dupGTGGACTT others(37): Show |
p.Gly160_Ile161insTr others(43): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 4/6 | 689/3562 | 480/678 | 160/225 | INFO_REALIGN_3_PRIME | chr2 | 118106800 | ||
| chr2:118108299 | G | A | 1 | a0002 | 2 | NA19056.hp2 NA19086.hp2 |
missense_variant | MODERATE | c.655G>A | p.Ala219Thr | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 864/3562 | 655/678 | 219/225 | chr2 | 118108299 | |||
| chr2:118110997 | A | G | 1 | a0001 | 1 | HG02895.hp1 | splice_region_variant | LOW | c.*2675A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | chr2 | 118110997 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:118103297 | T | C | 1 | a0001c0004 | 1 | HG02698.hp1 | synonymous_variant | LOW | c.345T>C | p.Phe115Phe | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/6 | 554/3562 | 345/678 | 115/225 | chr2 | 118103297 | |||
| chr2:118107180 | A | G | 1 | a0001c0002 | 10 | HG02257.hp2 HG02572.hp1 HG02647.hp2 others(7): Show |
synonymous_variant | LOW | c.627A>G | p.Gln209Gln | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 5/6 | 836/3562 | 627/678 | 209/225 | chr2 | 118107180 | |||
| chr2:118108307 | A | G | 1 | a0001c0005 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.663A>G | p.Lys221Lys | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 872/3562 | 663/678 | 221/225 | chr2 | 118108307 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:118088485 | G | A | 1 | a0001c0001t0019 | 3 | HG03710.hp2 HG03831.hp2 HG03942.hp1 |
5_prime_UTR_variant | MODIFIER | c.-195G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/6 | 8072 | chr2 | 118088485 | ||||||
| chr2:118096518 | A | AT | 7 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0012 others(4): Show |
110 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(107): Show |
5_prime_UTR_variant | MODIFIER | c.-26dupT | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/6 | 25 | INFO_REALIGN_3_PRIME | chr2 | 118096518 | |||||
| chr2:118096518 | AT | A | 12 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0014 others(9): Show |
78 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(75): Show |
5_prime_UTR_variant | MODIFIER | c.-26delT | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/6 | 26 | INFO_REALIGN_3_PRIME | chr2 | 118096518 | |||||
| chr2:118108424 | G | C | 2 | a0001c0001t0010 a0001c0001t0023 |
8 | HG00438.hp2 HG01069.hp2 HG02129.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*102G>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 102 | chr2 | 118108424 | ||||||
| chr2:118108457 | G | GA | 9 | a0001c0001t0001 a0001c0001t0015 a0001c0001t0017 others(6): Show |
105 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*136dupA | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 137 | INFO_REALIGN_3_PRIME | chr2 | 118108457 | |||||
| chr2:118108816 | A | C | 1 | a0001c0001t0013 | 5 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*494A>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 494 | chr2 | 118108816 | ||||||
| chr2:118108935 | C | T | 1 | a0001c0002t0034 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*613C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 613 | chr2 | 118108935 | ||||||
| chr2:118108936 | G | A | 3 | a0001c0001t0008 a0001c0001t0009 a0001c0001t0024 |
18 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*614G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 614 | chr2 | 118108936 | ||||||
| chr2:118109215 | C | T | 1 | a0001c0001t0011 | 7 | HG00140.hp1 HG00323.hp2 HG01074.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*893C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 893 | chr2 | 118109215 | ||||||
| chr2:118109660 | C | G | 2 | a0001c0001t0016 a0001c0005t0016 |
4 | HG02818.hp1 HG02886.hp1 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1338C>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 1338 | chr2 | 118109660 | ||||||
| chr2:118110437 | TGAG | T | 30 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(27): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*2132_*2134delAGG | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 2132 | INFO_REALIGN_3_PRIME | chr2 | 118110437 | |||||
| chr2:118110469 | T | C | 6 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0020 others(3): Show |
51 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*2147T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 2147 | chr2 | 118110469 | ||||||
| chr2:118110626 | T | C | 1 | a0001c0001t0030 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2304T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 2304 | chr2 | 118110626 | ||||||
| chr2:118110654 | T | C | 1 | a0001c0001t0015 | 4 | NA19005.hp2 NA19057.hp1 NA19072.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2332T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 2332 | chr2 | 118110654 | ||||||
| chr2:118110682 | A | G | 1 | a0001c0001t0028 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2360A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 2360 | chr2 | 118110682 | ||||||
| chr2:118110730 | T | C | 1 | a0001c0002t0032 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2408T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 2408 | chr2 | 118110730 | ||||||
| chr2:118110813 | AAAC | A | 5 | a0001c0001t0007 a0001c0001t0020 a0001c0001t0022 others(2): Show |
22 | HG00738.hp2 HG00741.hp1 HG01081.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2494_*2496delCAA | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 6/6 | 2494 | INFO_REALIGN_3_PRIME | chr2 | 118110813 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:118088569 | C | G | 1 | a0001c0001t0027g0161 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-139+28C>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118088569 | |||||||
| chr2:118088732 | C | T | 1 | a0001c0001t0004g0160 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-139+191C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118088732 | |||||||
| chr2:118088881 | G | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0025 others(21): Show |
84 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.-139+340G>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118088881 | |||||||
| chr2:118089262 | A | G | 1 | a0001c0001t0002g0159 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-139+721A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118089262 | |||||||
| chr2:118089309 | T | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(80): Show |
204 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.-139+768T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118089309 | |||||||
| chr2:118089392 | G | C | 1 | a0001c0001t0006g0069 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-139+851G>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118089392 | |||||||
| chr2:118089394 | T | G | 2 | a0001c0001t0004g0021 a0001c0001t0004g0070 |
5 | HG00642.hp1 HG02293.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.-139+853T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118089394 | |||||||
| chr2:118089446 | G | A | 2 | a0001c0001t0008g0014 a0001c0001t0008g0106 |
7 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-139+905G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118089446 | |||||||
| chr2:118089470 | C | G | 6 | a0001c0001t0002g0033 a0001c0001t0002g0052 a0001c0001t0002g0155 others(3): Show |
9 | HG00621.hp2 HG02027.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.-139+929C>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118089470 | |||||||
| chr2:118089530 | A | G | 3 | a0001c0001t0004g0104 a0001c0001t0006g0069 a0001c0001t0006g0105 |
3 | HG03471.hp1 HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-139+989A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118089530 | |||||||
| chr2:118089734 | AAG | A | 5 | a0001c0002t0004g0032 a0001c0002t0004g0151 a0001c0002t0004g0152 others(2): Show |
7 | HG02257.hp2 HG02572.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-139+1196_-139+119 others(6): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118089734 | ||||||
| chr2:118089760 | A | G | 1 | a0001c0002t0034g0150 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-139+1219A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118089760 | |||||||
| chr2:118089804 | A | G | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG03654.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-139+1263A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118089804 | |||||||
| chr2:118090113 | G | C | 2 | a0001c0001t0002g0040 a0001c0001t0018g0107 |
3 | NA18968.hp1 NA18984.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-139+1572G>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118090113 | |||||||
| chr2:118090227 | A | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(174): Show |
434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.-139+1686A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118090227 | |||||||
| chr2:118090265 | G | A | 33 | a0001c0001t0001g0030 a0001c0001t0004g0006 a0001c0001t0004g0015 others(30): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.-139+1724G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118090265 | |||||||
| chr2:118090311 | G | T | 1 | a0001c0001t0009g0043 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-139+1770G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118090311 | |||||||
| chr2:118090319 | G | C | 45 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0012 others(42): Show |
110 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.-139+1778G>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118090319 | |||||||
| chr2:118090367 | T | C | 5 | a0001c0002t0004g0032 a0001c0002t0004g0151 a0001c0002t0004g0152 others(2): Show |
7 | HG02257.hp2 HG02572.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-139+1826T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118090367 | |||||||
| chr2:118090848 | G | A | 2 | a0001c0001t0004g0071 a0001c0001t0009g0072 |
2 | HG01109.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-139+2307G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118090848 | |||||||
| chr2:118090915 | C | G | 1 | a0001c0001t0005g0126 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-139+2374C>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118090915 | |||||||
| chr2:118091248 | G | A | 1 | a0001c0001t0018g0127 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-139+2707G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118091248 | |||||||
| chr2:118091302 | G | C | 1 | a0001c0001t0002g0044 | 2 | NA18972.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.-139+2761G>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118091302 | |||||||
| chr2:118091306 | C | G | 2 | a0001c0001t0004g0071 a0001c0001t0009g0072 |
2 | HG01109.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-139+2765C>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118091306 | |||||||
| chr2:118091408 | C | T | 1 | a0001c0002t0034g0150 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-139+2867C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118091408 | |||||||
| chr2:118091437 | G | C | 33 | a0001c0001t0001g0030 a0001c0001t0004g0006 a0001c0001t0004g0015 others(30): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.-139+2896G>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118091437 | |||||||
| chr2:118091542 | T | G | 1 | a0001c0001t0002g0155 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-139+3001T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118091542 | |||||||
| chr2:118091629 | CTTTTA | C | 1 | a0001c0001t0001g0025 | 3 | HG01168.hp1 HG01169.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.-139+3093_-139+309 others(9): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118091629 | ||||||
| chr2:118091663 | T | A | 1 | a0001c0001t0002g0155 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-139+3122T>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118091663 | |||||||
| chr2:118091673 | T | A | 1 | a0001c0001t0002g0155 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-139+3132T>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118091673 | |||||||
| chr2:118091782 | A | G | 1 | a0001c0001t0004g0039 | 2 | HG01192.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.-139+3241A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118091782 | |||||||
| chr2:118091854 | A | G | 1 | a0001c0001t0006g0125 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-139+3313A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118091854 | |||||||
| chr2:118092176 | G | A | 4 | a0001c0001t0003g0035 a0001c0001t0004g0035 a0001c0001t0004g0073 others(1): Show |
4 | HG01891.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-139+3635G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118092176 | |||||||
| chr2:118092274 | A | G | 2 | a0001c0001t0004g0021 a0001c0001t0004g0070 |
5 | HG00642.hp1 HG02293.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.-139+3733A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118092274 | |||||||
| chr2:118092577 | T | C | 3 | a0001c0001t0003g0022 a0001c0001t0003g0075 a0001c0001t0014g0022 |
5 | HG01981.hp1 HG01993.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.-138-3842T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118092577 | |||||||
| chr2:118092592 | G | A | 2 | a0001c0001t0005g0029 a0001c0001t0005g0110 |
4 | HG00735.hp2 HG00741.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.-138-3827G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118092592 | |||||||
| chr2:118092643 | A | G | 45 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0012 others(42): Show |
110 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.-138-3776A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118092643 | |||||||
| chr2:118092811 | TGATGAGG others(140): Show |
T | 8 | a0001c0001t0003g0035 a0001c0001t0004g0013 a0001c0001t0004g0035 others(5): Show |
12 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.-138-3605_-138-345 others(4): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118092811 | ||||||
| chr2:118092814 | T | G | 2 | a0001c0001t0003g0023 a0001c0001t0004g0039 |
3 | HG01192.hp2 HG01358.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-138-3605T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118092814 | |||||||
| chr2:118092859 | A | AGAT | 3 | a0001c0001t0001g0001 a0001c0001t0002g0046 a0001c0001t0009g0027 |
6 | HG01255.hp1 HG02109.hp2 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.-138-3536_-138-353 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118092859 | ||||||
| chr2:118092880 | T | G | 1 | a0001c0001t0020g0004 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-138-3539T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118092880 | |||||||
| chr2:118092883 | T | G | 33 | a0001c0001t0001g0030 a0001c0001t0004g0006 a0001c0001t0004g0015 others(30): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.-138-3536T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118092883 | |||||||
| chr2:118092889 | CGAGGAGA others(65): Show |
C | 5 | a0001c0002t0004g0032 a0001c0002t0004g0151 a0001c0002t0004g0152 others(2): Show |
7 | HG02257.hp2 HG02572.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-138-3484_-138-341 others(76): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118092889 | ||||||
| chr2:118092893 | G | A | 45 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0012 others(42): Show |
110 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.-138-3526G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118092893 | |||||||
| chr2:118092933 | A | G | 2 | a0001c0001t0004g0071 a0001c0001t0009g0072 |
2 | HG01109.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-138-3486A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118092933 | |||||||
| chr2:118092946 | T | G | 3 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0063 |
3 | HG00408.hp2 NA18951.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-138-3473T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118092946 | |||||||
| chr2:118092946 | TGAGGAGG others(68): Show |
T | 1 | a0001c0001t0005g0126 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-138-3427_-138-335 others(79): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118092946 | ||||||
| chr2:118092949 | G | T | 3 | a0001c0001t0009g0043 a0001c0001t0030g0001 a0001c0002t0032g0092 |
4 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.-138-3470G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118092949 | |||||||
| chr2:118093003 | A | AGAT | 38 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0018 others(35): Show |
91 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.-138-3404_-138-340 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093003 | ||||||
| chr2:118093015 | T | G | 12 | a0001c0001t0003g0035 a0001c0001t0004g0013 a0001c0001t0004g0035 others(9): Show |
17 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-138-3404T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093015 | |||||||
| chr2:118093015 | TGAG | T | 38 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0018 others(35): Show |
91 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.-138-3379_-138-337 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093015 | ||||||
| chr2:118093018 | G | T | 7 | a0001c0001t0002g0012 a0001c0001t0002g0045 a0001c0001t0002g0128 others(4): Show |
17 | HG00621.hp2 HG00642.hp1 HG02293.hp2 others(14): Show |
intron_variant | MODIFIER | c.-138-3401G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093018 | |||||||
| chr2:118093038 | AGGAGAGT others(1343): Show |
A | 2 | a0001c0001t0002g0012 a0001c0001t0002g0130 |
8 | HG02717.hp2 HG02818.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-138-3352_-138-200 others(4): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093038 | ||||||
| chr2:118093078 | A | AGAT | 2 | a0001c0001t0005g0042 a0001c0001t0006g0006 |
5 | HG01884.hp2 HG02083.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-138-3317_-138-331 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093078 | ||||||
| chr2:118093078 | AGATGATG others(2): Show |
A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(85): Show |
211 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.-138-3323_-138-331 others(13): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093078 | ||||||
| chr2:118093106 | G | A | 43 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0018 others(40): Show |
101 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.-138-3313G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093106 | |||||||
| chr2:118093120 | C | A | 1 | a0001c0001t0004g0039 | 2 | HG01192.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.-138-3299C>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093120 | |||||||
| chr2:118093145 | A | AGAT | 6 | a0001c0001t0005g0004 a0001c0001t0008g0014 a0001c0001t0008g0049 others(3): Show |
13 | HG01515.hp2 HG01517.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-138-3253_-138-325 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093145 | ||||||
| chr2:118093209 | A | AGAT | 3 | a0001c0001t0001g0001 a0001c0001t0006g0069 a0001c0001t0006g0105 |
5 | HG02040.hp2 HG02056.hp2 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.-138-3172_-138-317 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093209 | ||||||
| chr2:118093209 | A | AGATGAT | 5 | a0001c0001t0004g0021 a0001c0001t0004g0070 a0001c0001t0016g0028 others(2): Show |
8 | HG00642.hp1 HG02293.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.-138-3175_-138-317 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093209 | ||||||
| chr2:118093209 | AGAT | A | 47 | a0001c0001t0001g0030 a0001c0001t0003g0035 a0001c0001t0003g0082 others(44): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.-138-3172_-138-317 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093209 | ||||||
| chr2:118093209 | AGATGAT | A | 13 | a0001c0001t0001g0005 a0001c0001t0001g0056 a0001c0001t0001g0147 others(10): Show |
25 | HG00438.hp1 HG00597.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.-138-3175_-138-317 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093209 | ||||||
| chr2:118093209 | AGATGATG others(5): Show |
A | 2 | a0001c0001t0004g0071 a0001c0001t0009g0072 |
2 | HG01109.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-138-3181_-138-317 others(16): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093209 | ||||||
| chr2:118093209 | AGATGATG others(11): Show |
A | 43 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0018 others(40): Show |
102 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.-138-3187_-138-317 others(22): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093209 | ||||||
| chr2:118093239 | T | A | 1 | a0001c0001t0002g0155 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-138-3180T>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093239 | |||||||
| chr2:118093288 | AGAT | A | 43 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0016 others(40): Show |
91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.-138-3119_-138-311 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093288 | ||||||
| chr2:118093297 | T | G | 5 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0084 others(2): Show |
6 | HG02083.hp2 NA18953.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-138-3122T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093297 | |||||||
| chr2:118093297 | T | TGAG | 2 | a0001c0001t0004g0039 a0001c0002t0034g0150 |
3 | HG01192.hp2 HG01358.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-138-3120_-138-311 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093297 | ||||||
| chr2:118093300 | T | G | 31 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0016 others(28): Show |
66 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.-138-3119T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093300 | |||||||
| chr2:118093300 | T | TGAG | 12 | a0001c0001t0001g0147 a0001c0001t0004g0015 a0001c0001t0004g0051 others(9): Show |
24 | HG00438.hp1 HG00597.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.-138-3094_-138-309 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093300 | ||||||
| chr2:118093300 | T | TGAGGAG | 17 | a0001c0001t0001g0030 a0001c0001t0004g0006 a0001c0001t0004g0015 others(14): Show |
38 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.-138-3097_-138-309 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093300 | ||||||
| chr2:118093300 | T | TGATGAG | 14 | a0001c0001t0005g0004 a0001c0001t0005g0009 a0001c0001t0005g0029 others(11): Show |
47 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.-138-3117_-138-311 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093300 | ||||||
| chr2:118093300 | TGAG | T | 33 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(30): Show |
104 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.-138-3094_-138-309 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093300 | ||||||
| chr2:118093300 | TGAGGAG | T | 5 | a0001c0001t0004g0071 a0001c0001t0008g0049 a0001c0001t0009g0072 others(2): Show |
5 | HG01109.hp1 HG01243.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-138-3097_-138-309 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093300 | ||||||
| chr2:118093303 | G | T | 2 | a0001c0001t0002g0003 a0001c0001t0002g0020 |
2 | NA18975.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.-138-3116G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093303 | |||||||
| chr2:118093306 | G | T | 3 | a0001c0002t0004g0032 a0001c0002t0004g0151 a0001c0002t0004g0152 |
5 | HG02257.hp2 HG02572.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-138-3113G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093306 | |||||||
| chr2:118093319 | GAGGAGGA others(66): Show |
G | 9 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0084 others(6): Show |
10 | HG02083.hp2 HG03471.hp1 HG03471.hp2 others(7): Show |
intron_variant | MODIFIER | c.-138-3094_-138-302 others(77): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093319 | ||||||
| chr2:118093353 | AAAAGCAA others(62): Show |
A | 1 | a0001c0001t0003g0002 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-138-3062_-138-299 others(73): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093353 | ||||||
| chr2:118093363 | AGAT | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0147 others(90): Show |
226 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.-138-3029_-138-302 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093363 | ||||||
| chr2:118093363 | AGATGAT | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(73): Show |
188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.-138-3032_-138-302 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093363 | ||||||
| chr2:118093433 | A | AGAT | 4 | a0001c0001t0004g0015 a0001c0001t0004g0112 a0001c0001t0004g0115 others(1): Show |
6 | HG02451.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-138-2965_-138-296 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093433 | ||||||
| chr2:118093433 | AGATGATG others(63): Show |
A | 33 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0016 others(30): Show |
75 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.-138-2962_-138-289 others(74): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093433 | ||||||
| chr2:118093433 | AGATGATG others(69): Show |
A | 29 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(26): Show |
94 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.-138-2962_-138-288 others(80): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093433 | ||||||
| chr2:118093433 | AGATGATG others(72): Show |
A | 3 | a0001c0001t0001g0001 a0001c0001t0004g0071 a0001c0001t0009g0072 |
3 | HG01109.hp1 HG01243.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.-138-2962_-138-288 others(83): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093433 | ||||||
| chr2:118093433 | AGATGATG others(75): Show |
A | 1 | a0001c0001t0001g0005 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-138-2963_-138-288 others(86): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093433 | ||||||
| chr2:118093436 | TGATGATG others(54): Show |
T | 3 | a0001c0001t0004g0013 a0001c0001t0006g0077 a0001c0001t0013g0013 |
7 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.-138-2962_-138-290 others(65): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093436 | ||||||
| chr2:118093439 | TGATGATG others(51): Show |
T | 8 | a0001c0001t0003g0035 a0001c0001t0004g0035 a0001c0001t0004g0039 others(5): Show |
10 | HG00140.hp2 HG01069.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.-138-2962_-138-290 others(62): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093439 | ||||||
| chr2:118093442 | TGATGATG others(48): Show |
T | 1 | a0001c0001t0009g0027 | 3 | HG01255.hp1 HG02109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-138-2962_-138-290 others(59): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093442 | ||||||
| chr2:118093497 | AGAT | A | 5 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0084 others(2): Show |
6 | HG02083.hp2 NA18953.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-138-2884_-138-288 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093497 | ||||||
| chr2:118093497 | AGATGAT | A | 17 | a0001c0001t0001g0147 a0001c0001t0003g0002 a0001c0001t0004g0051 others(14): Show |
31 | HG00438.hp1 HG00597.hp2 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-138-2887_-138-288 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093497 | ||||||
| chr2:118093497 | AGATGATG others(5): Show |
A | 34 | a0001c0001t0001g0030 a0001c0001t0004g0006 a0001c0001t0004g0015 others(31): Show |
91 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.-138-2893_-138-288 others(16): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093497 | ||||||
| chr2:118093497 | AGATGATG others(8): Show |
A | 43 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0018 others(40): Show |
102 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.-138-2896_-138-288 others(19): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093497 | ||||||
| chr2:118093533 | T | C | 1 | a0001c0001t0004g0149 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-138-2886T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093533 | |||||||
| chr2:118093543 | T | C | 42 | a0001c0001t0001g0030 a0001c0001t0001g0147 a0001c0001t0004g0006 others(39): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.-138-2876T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093543 | |||||||
| chr2:118093576 | AGATGAT | A | 8 | a0001c0001t0001g0147 a0001c0001t0004g0051 a0001c0001t0004g0149 others(5): Show |
19 | HG00438.hp1 HG00597.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-138-2831_-138-282 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093576 | ||||||
| chr2:118093588 | T | G | 16 | a0001c0001t0001g0001 a0001c0001t0001g0055 a0001c0001t0003g0035 others(13): Show |
25 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.-138-2831T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093588 | |||||||
| chr2:118093588 | TGATGAG | T | 2 | a0001c0001t0004g0006 a0001c0001t0005g0004 |
3 | HG02735.hp1 NA18946.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-138-2828_-138-282 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093588 | ||||||
| chr2:118093591 | T | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(110): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.-138-2828T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093591 | |||||||
| chr2:118093591 | T | TGAG | 42 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0018 others(39): Show |
101 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.-138-2806_-138-280 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093591 | ||||||
| chr2:118093594 | G | T | 3 | a0001c0001t0004g0071 a0001c0001t0009g0027 a0001c0001t0009g0072 |
5 | HG01109.hp1 HG01243.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.-138-2825G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093594 | |||||||
| chr2:118093633 | A | T | 1 | a0001c0001t0019g0026 | 2 | HG03710.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-138-2786A>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093633 | |||||||
| chr2:118093651 | A | AGAT | 3 | a0001c0001t0004g0071 a0001c0001t0009g0027 a0001c0001t0009g0072 |
5 | HG01109.hp1 HG01243.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.-138-2756_-138-275 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093651 | ||||||
| chr2:118093651 | AGAT | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0034 others(42): Show |
98 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.-138-2756_-138-275 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093651 | ||||||
| chr2:118093660 | T | TGAG | 24 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(21): Show |
85 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.-138-2757_-138-275 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093660 | ||||||
| chr2:118093660 | T | TGAGGAG | 4 | a0001c0001t0001g0001 a0001c0001t0004g0021 a0001c0001t0004g0070 others(1): Show |
7 | HG00642.hp1 HG02293.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-138-2757_-138-275 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093660 | ||||||
| chr2:118093663 | T | G | 44 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(41): Show |
125 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.-138-2756T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093663 | |||||||
| chr2:118093663 | T | TGAG | 15 | a0001c0001t0001g0001 a0001c0001t0003g0002 a0001c0001t0003g0023 others(12): Show |
22 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.-138-2731_-138-272 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093663 | ||||||
| chr2:118093663 | T | TGAGGAG | 6 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0053 others(3): Show |
8 | HG02056.hp2 HG02257.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.-138-2734_-138-272 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093663 | ||||||
| chr2:118093663 | T | TGATGATG others(8): Show |
1 | a0001c0001t0004g0145 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-138-2754_-138-275 others(19): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093663 | ||||||
| chr2:118093663 | TGAG | T | 7 | a0001c0001t0002g0155 a0001c0001t0005g0004 a0001c0001t0008g0014 others(4): Show |
12 | HG00621.hp2 HG01891.hp2 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.-138-2731_-138-272 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093663 | ||||||
| chr2:118093663 | TGAGGAG | T | 12 | a0001c0001t0003g0035 a0001c0001t0004g0013 a0001c0001t0004g0035 others(9): Show |
18 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.-138-2734_-138-272 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093663 | ||||||
| chr2:118093666 | G | T | 2 | a0001c0001t0004g0160 a0003c0006t0001g0116 |
2 | HG03669.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.-138-2753G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093666 | |||||||
| chr2:118093733 | G | C | 2 | a0001c0001t0004g0071 a0001c0001t0009g0072 |
2 | HG01109.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-138-2686G>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093733 | |||||||
| chr2:118093741 | TGAA | T | 41 | a0001c0001t0001g0030 a0001c0001t0001g0147 a0001c0001t0004g0006 others(38): Show |
110 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.-138-2676_-138-267 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093741 | ||||||
| chr2:118093744 | A | T | 1 | a0001c0001t0005g0148 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-138-2675A>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093744 | |||||||
| chr2:118093805 | TGAA | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(76): Show |
197 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-138-2612_-138-261 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093805 | ||||||
| chr2:118093848 | A | AGAT | 14 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0034 others(11): Show |
26 | HG00438.hp1 HG00597.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.-138-2556_-138-255 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093848 | ||||||
| chr2:118093848 | AGAT | A | 35 | a0001c0001t0001g0030 a0001c0001t0004g0006 a0001c0001t0004g0015 others(32): Show |
95 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.-138-2556_-138-255 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093848 | ||||||
| chr2:118093860 | T | G | 1 | a0001c0001t0008g0106 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-138-2559T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093860 | |||||||
| chr2:118093863 | T | G | 55 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0018 others(52): Show |
133 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.-138-2556T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093863 | |||||||
| chr2:118093863 | T | TGAG | 4 | a0001c0001t0005g0148 a0001c0001t0006g0081 a0001c0001t0008g0014 others(1): Show |
9 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-138-2534_-138-253 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093863 | ||||||
| chr2:118093863 | TGAG | T | 7 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0034 others(4): Show |
8 | HG00099.hp1 HG01106.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.-138-2534_-138-253 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093863 | ||||||
| chr2:118093866 | G | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(62): Show |
173 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.-138-2553G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093866 | |||||||
| chr2:118093923 | A | AGAT | 3 | a0001c0001t0004g0145 a0001c0001t0007g0008 a0001c0001t0007g0050 |
3 | HG01175.hp1 HG01257.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.-138-2478_-138-247 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093923 | ||||||
| chr2:118093923 | AGAT | A | 8 | a0001c0001t0003g0035 a0001c0001t0004g0013 a0001c0001t0004g0035 others(5): Show |
8 | HG01243.hp2 HG01891.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-138-2478_-138-247 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093923 | ||||||
| chr2:118093923 | AGATGAT | A | 8 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0016 others(5): Show |
14 | HG00423.hp1 HG00597.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-138-2481_-138-247 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093923 | ||||||
| chr2:118093938 | T | G | 1 | a0001c0001t0004g0076 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-138-2481T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093938 | |||||||
| chr2:118093938 | T | TGAGGAG | 2 | a0001c0001t0006g0081 a0001c0001t0009g0036 |
3 | HG01069.hp1 HG01071.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-138-2479_-138-247 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093938 | ||||||
| chr2:118093938 | TGATGAG | T | 47 | a0001c0001t0001g0030 a0001c0001t0003g0002 a0001c0001t0003g0007 others(44): Show |
126 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.-138-2478_-138-247 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093938 | ||||||
| chr2:118093938 | TGATGAGG others(2): Show |
T | 8 | a0001c0001t0004g0121 a0001c0001t0006g0006 a0001c0001t0006g0111 others(5): Show |
11 | HG00438.hp2 HG01069.hp2 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.-138-2478_-138-247 others(13): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093938 | ||||||
| chr2:118093938 | TGATGAGG others(5): Show |
T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(21): Show |
67 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.-138-2478_-138-246 others(16): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093938 | ||||||
| chr2:118093941 | T | G | 10 | a0001c0001t0004g0039 a0001c0001t0004g0076 a0001c0001t0004g0122 others(7): Show |
12 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.-138-2478T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093941 | |||||||
| chr2:118093941 | T | TGAG | 14 | a0001c0001t0001g0147 a0001c0001t0004g0013 a0001c0001t0004g0021 others(11): Show |
31 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.-138-2447_-138-244 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093941 | ||||||
| chr2:118093941 | T | TGAGGAG | 6 | a0001c0001t0003g0035 a0001c0001t0004g0035 a0001c0001t0004g0073 others(3): Show |
6 | HG01891.hp1 HG02896.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-138-2450_-138-244 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093941 | ||||||
| chr2:118093941 | TGAG | T | 6 | a0001c0001t0004g0015 a0001c0001t0004g0112 a0001c0001t0006g0015 others(3): Show |
9 | HG02257.hp2 HG02451.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-138-2447_-138-244 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093941 | ||||||
| chr2:118093941 | TGAGGAG | T | 10 | a0001c0001t0002g0010 a0001c0001t0002g0132 a0001c0001t0002g0134 others(7): Show |
16 | HG01070.hp2 HG01071.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-138-2450_-138-244 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093941 | ||||||
| chr2:118093941 | TGAGGAGG others(2): Show |
T | 40 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0018 others(37): Show |
95 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.-138-2453_-138-244 others(13): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093941 | ||||||
| chr2:118093941 | TGAGGAGG others(5): Show |
T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0034 others(6): Show |
30 | HG00621.hp1 HG00639.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.-138-2456_-138-244 others(16): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093941 | ||||||
| chr2:118093944 | G | T | 1 | a0001c0002t0034g0150 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-138-2475G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093944 | |||||||
| chr2:118093950 | G | T | 4 | a0001c0001t0002g0010 a0001c0001t0002g0132 a0001c0001t0002g0134 others(1): Show |
7 | HG02055.hp1 HG02145.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-138-2469G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093950 | |||||||
| chr2:118093953 | G | T | 43 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0018 others(40): Show |
102 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.-138-2466G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093953 | |||||||
| chr2:118093956 | G | GGAGAGTT others(207): Show |
1 | a0001c0001t0004g0122 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-138-2460_-138-245 others(218): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093956 | ||||||
| chr2:118093956 | G | T | 43 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0018 others(40): Show |
102 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.-138-2463G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093956 | |||||||
| chr2:118093959 | G | T | 43 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0018 others(40): Show |
98 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.-138-2460G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093959 | |||||||
| chr2:118093962 | G | T | 1 | a0001c0001t0002g0003 | 2 | NA18942.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.-138-2457G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093962 | |||||||
| chr2:118093967 | A | AGAGTTCT others(353): Show |
1 | a0001c0001t0005g0029 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-138-2451_-138-245 others(364): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118093967 | ||||||
| chr2:118093969 | G | A | 1 | a0001c0001t0005g0029 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-138-2450G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118093969 | |||||||
| chr2:118094010 | A | AGAT | 60 | a0001c0001t0002g0003 a0001c0001t0002g0031 a0001c0001t0003g0002 others(57): Show |
139 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.-138-2371_-138-236 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094010 | ||||||
| chr2:118094010 | A | AGATGAT | 21 | a0001c0001t0001g0030 a0001c0001t0002g0003 a0001c0001t0002g0010 others(18): Show |
38 | HG00544.hp1 HG01257.hp2 HG01258.hp2 others(35): Show |
intron_variant | MODIFIER | c.-138-2374_-138-236 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094010 | ||||||
| chr2:118094010 | A | AGATGATG others(2): Show |
21 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0018 others(18): Show |
52 | HG00609.hp1 HG00609.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.-138-2377_-138-236 others(13): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094010 | ||||||
| chr2:118094010 | A | AGATGATG others(5): Show |
8 | a0001c0001t0002g0003 a0001c0001t0002g0018 a0001c0001t0002g0128 others(5): Show |
9 | HG00738.hp2 HG00741.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.-138-2380_-138-236 others(16): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094010 | ||||||
| chr2:118094010 | AGAT | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(42): Show |
124 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.-138-2371_-138-236 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094010 | ||||||
| chr2:118094010 | AGATGAT | A | 4 | a0001c0001t0001g0056 a0001c0001t0004g0015 a0001c0001t0009g0043 others(1): Show |
5 | HG01070.hp2 HG01071.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.-138-2374_-138-236 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094010 | ||||||
| chr2:118094013 | T | TGATGATG others(353): Show |
1 | a0001c0001t0005g0029 | 2 | HG00735.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-138-2319_-138-231 others(364): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094013 | ||||||
| chr2:118094013 | T | TGATGATG others(347): Show |
1 | a0001c0001t0004g0017 | 2 | HG00099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.-138-2316_-138-231 others(358): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094013 | ||||||
| chr2:118094013 | T | TGATGATG others(353): Show |
1 | a0001c0001t0004g0017 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-138-2316_-138-231 others(364): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094013 | ||||||
| chr2:118094013 | T | TGATGATG others(356): Show |
1 | a0001c0001t0004g0124 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-138-2316_-138-231 others(367): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094013 | ||||||
| chr2:118094025 | T | G | 10 | a0001c0001t0004g0013 a0001c0001t0004g0039 a0001c0001t0004g0074 others(7): Show |
18 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.-138-2394T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094025 | |||||||
| chr2:118094028 | T | G | 13 | a0001c0001t0003g0035 a0001c0001t0004g0013 a0001c0001t0004g0035 others(10): Show |
21 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.-138-2391T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094028 | |||||||
| chr2:118094031 | T | G | 13 | a0001c0001t0003g0035 a0001c0001t0004g0013 a0001c0001t0004g0035 others(10): Show |
21 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.-138-2388T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094031 | |||||||
| chr2:118094034 | T | G | 13 | a0001c0001t0003g0035 a0001c0001t0004g0013 a0001c0001t0004g0035 others(10): Show |
21 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.-138-2385T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094034 | |||||||
| chr2:118094037 | T | G | 13 | a0001c0001t0003g0035 a0001c0001t0004g0013 a0001c0001t0004g0035 others(10): Show |
21 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.-138-2382T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094037 | |||||||
| chr2:118094040 | T | G | 13 | a0001c0001t0003g0035 a0001c0001t0004g0013 a0001c0001t0004g0035 others(10): Show |
21 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.-138-2379T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094040 | |||||||
| chr2:118094043 | T | G | 11 | a0001c0001t0003g0035 a0001c0001t0004g0035 a0001c0001t0004g0039 others(8): Show |
19 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.-138-2376T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094043 | |||||||
| chr2:118094045 | ATGAT | A | 11 | a0001c0001t0003g0035 a0001c0001t0004g0035 a0001c0001t0004g0039 others(8): Show |
19 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.-138-2373_-138-237 others(8): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094045 | |||||||
| chr2:118094049 | T | A | 1 | a0001c0001t0004g0122 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-138-2370T>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094049 | |||||||
| chr2:118094051 | G | A | 1 | a0001c0001t0002g0139 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-138-2368G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094051 | |||||||
| chr2:118094078 | T | C | 1 | a0001c0001t0004g0122 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-138-2341T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094078 | |||||||
| chr2:118094079 | G | A | 1 | a0001c0001t0004g0122 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-138-2340G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094079 | |||||||
| chr2:118094089 | AGAT | A | 3 | a0001c0001t0003g0023 a0001c0001t0003g0082 a0001c0001t0027g0161 |
6 | HG00639.hp1 HG01884.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-138-2315_-138-231 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094089 | ||||||
| chr2:118094092 | T | TGATGATG others(350): Show |
1 | a0001c0001t0005g0110 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-138-2319_-138-231 others(361): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094092 | ||||||
| chr2:118094092 | T | TGATGATG others(356): Show |
1 | a0001c0001t0005g0126 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-138-2316_-138-231 others(367): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094092 | ||||||
| chr2:118094092 | T | TGATGATG others(124): Show |
1 | a0001c0001t0004g0122 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-138-2313_-138-231 others(135): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094092 | ||||||
| chr2:118094101 | T | G | 27 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0016 others(24): Show |
64 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.-138-2318T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094101 | |||||||
| chr2:118094101 | TGATGAGG others(2): Show |
T | 3 | a0001c0001t0004g0104 a0001c0001t0006g0069 a0001c0001t0006g0105 |
3 | HG03471.hp1 HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-138-2315_-138-230 others(13): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094101 | ||||||
| chr2:118094101 | TGATGAGG others(5): Show |
T | 29 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(26): Show |
96 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.-138-2315_-138-230 others(16): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094101 | ||||||
| chr2:118094104 | T | G | 78 | a0001c0001t0001g0030 a0001c0001t0001g0147 a0001c0001t0002g0010 others(75): Show |
194 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-138-2315T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094104 | |||||||
| chr2:118094104 | T | TGAG | 3 | a0001c0001t0004g0122 a0001c0001t0005g0110 a0001c0001t0005g0126 |
3 | HG03491.hp1 HG03654.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-138-2293_-138-229 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094104 | ||||||
| chr2:118094104 | TGAGGAG | T | 14 | a0001c0001t0003g0035 a0001c0001t0004g0013 a0001c0001t0004g0035 others(11): Show |
23 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.-138-2296_-138-229 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094104 | ||||||
| chr2:118094107 | G | T | 1 | a0001c0001t0002g0031 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-138-2312G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094107 | |||||||
| chr2:118094169 | A | T | 1 | a0001c0001t0002g0155 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-138-2250A>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094169 | |||||||
| chr2:118094179 | T | G | 9 | a0001c0001t0001g0001 a0001c0001t0002g0010 a0001c0001t0003g0035 others(6): Show |
10 | HG00609.hp1 HG01891.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-138-2240T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094179 | |||||||
| chr2:118094182 | G | T | 2 | a0001c0001t0004g0021 a0001c0001t0004g0070 |
4 | HG00642.hp1 HG02738.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-138-2237G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094182 | |||||||
| chr2:118094233 | A | AGAT | 112 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(109): Show |
276 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.-138-2153_-138-215 others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | ||||||
| chr2:118094233 | A | AGATGAT | 27 | a0001c0001t0001g0001 a0001c0001t0001g0065 a0001c0001t0001g0099 others(24): Show |
43 | HG00408.hp1 HG00438.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.-138-2156_-138-215 others(10): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | ||||||
| chr2:118094233 | A | AGATGATG others(2): Show |
4 | a0001c0001t0001g0001 a0001c0001t0004g0017 a0001c0001t0007g0008 others(1): Show |
6 | HG00099.hp1 HG01106.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.-138-2159_-138-215 others(13): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | ||||||
| chr2:118094233 | A | AGATGATG others(5): Show |
1 | a0001c0002t0034g0150 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-138-2162_-138-215 others(16): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | ||||||
| chr2:118094233 | A | AGATGATG others(356): Show |
1 | a0001c0001t0004g0121 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-138-2151_-138-215 others(367): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | ||||||
| chr2:118094233 | A | AGATGATG others(359): Show |
1 | a0001c0001t0004g0015 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-138-2151_-138-215 others(370): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | ||||||
| chr2:118094233 | A | AGATGATG others(362): Show |
4 | a0001c0001t0004g0015 a0001c0001t0004g0112 a0001c0001t0004g0115 others(1): Show |
7 | HG02451.hp1 HG02486.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-138-2151_-138-215 others(373): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | ||||||
| chr2:118094233 | A | AGATGATG others(362): Show |
1 | a0001c0001t0009g0043 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-138-2151_-138-215 others(373): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | ||||||
| chr2:118094233 | A | AGATGATG others(359): Show |
1 | a0001c0001t0005g0004 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-138-2151_-138-215 others(370): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | ||||||
| chr2:118094233 | A | AGATGATG others(359): Show |
12 | a0001c0001t0005g0004 a0001c0001t0005g0009 a0001c0001t0005g0041 others(9): Show |
37 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.-138-2151_-138-215 others(370): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | ||||||
| chr2:118094233 | A | AGATGATG others(359): Show |
1 | a0001c0001t0006g0118 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-138-2151_-138-215 others(370): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | ||||||
| chr2:118094233 | A | AGATGATG others(362): Show |
9 | a0001c0001t0001g0030 a0001c0001t0004g0006 a0001c0001t0004g0123 others(6): Show |
22 | HG00140.hp1 HG00323.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.-138-2151_-138-215 others(373): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | ||||||
| chr2:118094233 | A | AGATGATG others(365): Show |
1 | a0001c0001t0004g0017 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-138-2151_-138-215 others(376): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | ||||||
| chr2:118094233 | A | AGATGATG others(365): Show |
2 | a0001c0001t0004g0114 a0001c0001t0006g0006 |
2 | HG02258.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-138-2151_-138-215 others(376): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | ||||||
| chr2:118094233 | A | AGATGATG others(356): Show |
1 | a0001c0001t0005g0004 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-138-2151_-138-215 others(367): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | ||||||
| chr2:118094233 | A | T | 1 | a0001c0001t0003g0002 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-138-2186A>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094233 | |||||||
| chr2:118094233 | AGATGATG others(2): Show |
A | 1 | a0001c0001t0009g0027 | 3 | HG01255.hp1 HG02109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-138-2159_-138-215 others(13): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094233 | ||||||
| chr2:118094269 | A | T | 1 | a0001c0001t0003g0002 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-138-2150A>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094269 | |||||||
| chr2:118094278 | C | A | 1 | a0001c0001t0009g0027 | 3 | HG01255.hp1 HG02109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-138-2141C>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094278 | |||||||
| chr2:118094315 | TGATGATG others(45): Show |
T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0064 a0001c0001t0001g0066 others(1): Show |
9 | NA18942.hp1 NA18951.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-138-2092_-138-204 others(56): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094315 | ||||||
| chr2:118094367 | A | AGATGATG others(5): Show |
123 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(120): Show |
302 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.-138-2041_-138-203 others(16): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094367 | ||||||
| chr2:118094367 | A | AGATGATG others(8): Show |
40 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0065 others(37): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-138-2044_-138-203 others(19): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094367 | ||||||
| chr2:118094367 | A | AGATGATG others(11): Show |
6 | a0001c0001t0002g0003 a0001c0001t0003g0035 a0001c0001t0004g0035 others(3): Show |
6 | HG01891.hp1 HG01975.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-138-2047_-138-203 others(22): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094367 | ||||||
| chr2:118094367 | A | AGATGATG others(17): Show |
3 | a0001c0002t0004g0032 a0001c0002t0004g0151 a0001c0002t0004g0152 |
5 | HG02257.hp2 HG02572.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-138-2030_-138-202 others(28): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094367 | ||||||
| chr2:118094367 | A | AGATGATG others(20): Show |
1 | a0001c0002t0004g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-138-2030_-138-202 others(31): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094367 | ||||||
| chr2:118094367 | A | AGATGATG others(368): Show |
2 | a0001c0001t0005g0004 a0001c0001t0006g0125 |
3 | NA18946.hp2 NA18971.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.-138-2030_-138-202 others(379): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094367 | ||||||
| chr2:118094367 | A | AGATGATG others(8): Show |
1 | a0001c0001t0004g0017 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-138-2039_-138-203 others(19): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 118094367 | ||||||
| chr2:118094871 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-138-1548C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094871 | |||||||
| chr2:118094971 | C | G | 1 | a0001c0001t0002g0144 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-138-1448C>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118094971 | |||||||
| chr2:118095253 | G | A | 1 | a0001c0001t0002g0131 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-138-1166G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118095253 | |||||||
| chr2:118095278 | C | G | 2 | a0001c0001t0001g0011 a0001c0001t0004g0038 |
9 | HG02145.hp1 HG02257.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-138-1141C>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118095278 | |||||||
| chr2:118096228 | C | T | 1 | a0001c0001t0009g0036 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-138-191C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118096228 | |||||||
| chr2:118096229 | G | A | 1 | a0001c0002t0034g0150 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-138-190G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118096229 | |||||||
| chr2:118096271 | T | C | 1 | a0001c0001t0002g0046 | 2 | NA18948.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-138-148T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 1/5 | chr2 | 118096271 | |||||||
| chr2:118096935 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.244+135C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118096935 | |||||||
| chr2:118096936 | G | C | 1 | a0001c0001t0002g0132 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.244+136G>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118096936 | |||||||
| chr2:118097137 | A | G | 2 | a0001c0002t0004g0153 a0001c0002t0004g0154 |
2 | HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.244+337A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118097137 | |||||||
| chr2:118097150 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0004g0038 |
9 | HG02145.hp1 HG02257.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.244+350C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118097150 | |||||||
| chr2:118097172 | A | AT | 176 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(173): Show |
433 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(430): Show |
intron_variant | MODIFIER | c.244+374dupT | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 118097172 | ||||||
| chr2:118097348 | G | A | 33 | a0001c0001t0001g0030 a0001c0001t0004g0006 a0001c0001t0004g0015 others(30): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.244+548G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118097348 | |||||||
| chr2:118097365 | C | T | 3 | a0001c0001t0002g0045 a0001c0001t0017g0129 a0001c0001t0017g0143 |
4 | NA18954.hp1 NA18969.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.244+565C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118097365 | |||||||
| chr2:118097633 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.244+833T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118097633 | |||||||
| chr2:118097867 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.244+1067G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118097867 | |||||||
| chr2:118098231 | C | T | 9 | a0001c0001t0001g0147 a0001c0001t0004g0051 a0001c0001t0004g0149 others(6): Show |
21 | HG00438.hp1 HG00597.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.244+1431C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118098231 | |||||||
| chr2:118098351 | G | A | 33 | a0001c0001t0001g0030 a0001c0001t0004g0006 a0001c0001t0004g0015 others(30): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.244+1551G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118098351 | |||||||
| chr2:118098580 | G | A | 4 | a0001c0001t0001g0147 a0001c0001t0007g0008 a0001c0001t0007g0050 others(1): Show |
13 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.244+1780G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118098580 | |||||||
| chr2:118098728 | C | T | 1 | a0001c0001t0005g0126 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.244+1928C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118098728 | |||||||
| chr2:118098891 | A | G | 1 | a0001c0001t0014g0101 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.244+2091A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118098891 | |||||||
| chr2:118099007 | T | C | 3 | a0001c0002t0004g0032 a0001c0002t0004g0151 a0001c0002t0004g0152 |
5 | HG02257.hp2 HG02572.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.244+2207T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118099007 | |||||||
| chr2:118099035 | A | G | 6 | a0001c0001t0003g0100 a0001c0002t0004g0032 a0001c0002t0004g0151 others(3): Show |
8 | HG02257.hp2 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.244+2235A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118099035 | |||||||
| chr2:118099191 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.244+2391G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118099191 | |||||||
| chr2:118099338 | A | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(84): Show |
210 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.244+2538A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118099338 | |||||||
| chr2:118099492 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.244+2692T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118099492 | |||||||
| chr2:118099618 | A | G | 1 | a0001c0001t0004g0124 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.244+2818A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118099618 | |||||||
| chr2:118099705 | G | T | 1 | a0001c0001t0001g0099 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.244+2905G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118099705 | |||||||
| chr2:118099712 | C | G | 10 | a0001c0001t0003g0035 a0001c0001t0004g0013 a0001c0001t0004g0035 others(7): Show |
16 | HG00099.hp2 HG00738.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.244+2912C>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118099712 | |||||||
| chr2:118099784 | G | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(84): Show |
210 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.244+2984G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118099784 | |||||||
| chr2:118099950 | C | T | 32 | a0001c0001t0001g0030 a0001c0001t0004g0006 a0001c0001t0004g0015 others(29): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.244+3150C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118099950 | |||||||
| chr2:118100007 | G | A | 3 | a0001c0002t0004g0032 a0001c0002t0004g0151 a0001c0002t0004g0152 |
5 | HG02257.hp2 HG02572.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.245-3190G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100007 | |||||||
| chr2:118100019 | T | C | 1 | a0001c0001t0003g0037 | 2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.245-3178T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100019 | |||||||
| chr2:118100073 | T | A | 3 | a0001c0001t0003g0023 a0001c0001t0003g0082 a0001c0001t0027g0161 |
6 | HG00639.hp1 HG01884.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.245-3124T>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100073 | |||||||
| chr2:118100130 | A | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(173): Show |
433 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(430): Show |
intron_variant | MODIFIER | c.245-3067A>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100130 | |||||||
| chr2:118100172 | G | A | 1 | a0001c0001t0021g0083 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.245-3025G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100172 | |||||||
| chr2:118100175 | A | C | 2 | a0001c0001t0012g0141 a0001c0001t0012g0142 |
2 | HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.245-3022A>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100175 | |||||||
| chr2:118100184 | T | C | 2 | a0001c0001t0012g0141 a0001c0001t0012g0142 |
2 | HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.245-3013T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100184 | |||||||
| chr2:118100185 | G | C | 2 | a0001c0001t0012g0141 a0001c0001t0012g0142 |
2 | HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.245-3012G>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100185 | |||||||
| chr2:118100186 | A | T | 2 | a0001c0001t0012g0141 a0001c0001t0012g0142 |
2 | HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.245-3011A>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100186 | |||||||
| chr2:118100187 | A | C | 2 | a0001c0001t0012g0141 a0001c0001t0012g0142 |
2 | HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.245-3010A>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100187 | |||||||
| chr2:118100217 | G | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(172): Show |
432 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(429): Show |
intron_variant | MODIFIER | c.245-2980G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100217 | |||||||
| chr2:118100373 | C | CT | 70 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0025 others(67): Show |
181 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.245-2801dupT | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 118100373 | ||||||
| chr2:118100373 | C | CTT | 31 | a0001c0001t0001g0005 a0001c0001t0001g0064 a0001c0001t0001g0065 others(28): Show |
65 | HG00597.hp1 HG00597.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.245-2802_245-2801d others(4): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 118100373 | ||||||
| chr2:118100373 | C | CTTT | 5 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0004g0149 others(2): Show |
6 | HG00438.hp1 HG00438.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.245-2803_245-2801d others(5): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 118100373 | ||||||
| chr2:118100373 | CT | C | 34 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0012 others(31): Show |
92 | HG00140.hp1 HG00544.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.245-2801delT | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 118100373 | ||||||
| chr2:118100373 | CTT | C | 7 | a0001c0001t0002g0018 a0001c0001t0002g0130 a0001c0001t0002g0133 others(4): Show |
12 | HG00738.hp2 HG00741.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.245-2802_245-2801d others(4): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 118100373 | ||||||
| chr2:118100415 | G | A | 50 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(47): Show |
130 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.245-2782G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100415 | |||||||
| chr2:118100448 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.245-2749G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100448 | |||||||
| chr2:118100488 | C | A | 1 | a0001c0001t0004g0071 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.245-2709C>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100488 | |||||||
| chr2:118100495 | C | G | 1 | a0001c0002t0034g0150 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.245-2702C>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100495 | |||||||
| chr2:118100519 | C | T | 5 | a0001c0002t0004g0032 a0001c0002t0004g0151 a0001c0002t0004g0152 others(2): Show |
7 | HG02257.hp2 HG02572.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.245-2678C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100519 | |||||||
| chr2:118100966 | ATAACT | A | 4 | a0001c0001t0004g0015 a0001c0001t0004g0112 a0001c0001t0004g0115 others(1): Show |
8 | HG02451.hp1 HG02486.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.245-2227_245-2223d others(7): Show |
INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 118100966 | ||||||
| chr2:118100977 | G | T | 2 | a0001c0001t0002g0020 a0001c0001t0012g0138 |
6 | HG00544.hp1 NA18961.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.245-2220G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118100977 | |||||||
| chr2:118101192 | A | G | 1 | a0001c0001t0005g0148 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.245-2005A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118101192 | |||||||
| chr2:118101248 | C | T | 1 | a0001c0001t0003g0091 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.245-1949C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118101248 | |||||||
| chr2:118101460 | G | T | 5 | a0001c0001t0002g0019 a0001c0001t0002g0040 a0001c0001t0002g0044 others(2): Show |
11 | NA18959.hp1 NA18968.hp1 NA18972.hp1 others(8): Show |
intron_variant | MODIFIER | c.245-1737G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118101460 | |||||||
| chr2:118101583 | TG | T | 2 | a0001c0001t0004g0021 a0001c0001t0004g0070 |
5 | HG00642.hp1 HG02293.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.245-1609delG | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 118101583 | ||||||
| chr2:118101980 | G | A | 7 | a0001c0001t0004g0038 a0001c0001t0007g0008 a0001c0001t0007g0024 others(4): Show |
20 | HG00738.hp2 HG00741.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.245-1217G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118101980 | |||||||
| chr2:118102066 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.245-1131G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118102066 | |||||||
| chr2:118102088 | G | A | 1 | a0001c0001t0005g0126 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.245-1109G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118102088 | |||||||
| chr2:118102137 | G | C | 3 | a0001c0001t0004g0145 a0001c0001t0016g0028 a0001c0005t0016g0109 |
5 | HG01175.hp1 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.245-1060G>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118102137 | |||||||
| chr2:118102550 | T | C | 1 | a0001c0001t0005g0148 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.245-647T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118102550 | |||||||
| chr2:118102695 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0065 |
4 | HG01255.hp2 HG01257.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.245-502G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118102695 | |||||||
| chr2:118102786 | A | G | 2 | a0001c0001t0002g0157 a0001c0001t0002g0158 |
2 | NA18981.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.245-411A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118102786 | |||||||
| chr2:118102851 | G | A | 1 | a0001c0001t0017g0156 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.245-346G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118102851 | |||||||
| chr2:118102879 | GA | G | 8 | a0001c0001t0004g0015 a0001c0001t0004g0112 a0001c0001t0004g0115 others(5): Show |
12 | HG02451.hp1 HG02486.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.245-316delA | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 118102879 | ||||||
| chr2:118102895 | C | T | 74 | a0001c0001t0003g0035 a0001c0001t0004g0006 a0001c0001t0004g0013 others(71): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.245-302C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118102895 | |||||||
| chr2:118102964 | A | G | 2 | a0001c0002t0032g0092 a0001c0002t0034g0150 |
2 | HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.245-233A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118102964 | |||||||
| chr2:118102985 | G | A | 6 | a0001c0001t0007g0008 a0001c0001t0007g0024 a0001c0001t0007g0050 others(3): Show |
18 | HG00738.hp2 HG00741.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.245-212G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | chr2 | 118102985 | |||||||
| chr2:118103080 | G | GT | 6 | a0001c0001t0001g0062 a0001c0001t0004g0145 a0001c0001t0016g0028 others(3): Show |
8 | HG01175.hp1 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.245-104dupT | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 118103080 | ||||||
| chr2:118103808 | T | C | 1 | a0001c0002t0032g0092 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.369+487T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118103808 | |||||||
| chr2:118103859 | A | G | 25 | a0001c0001t0002g0003 a0001c0001t0002g0018 a0001c0001t0002g0019 others(22): Show |
69 | HG00544.hp1 HG00609.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.369+538A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118103859 | |||||||
| chr2:118104170 | G | A | 1 | a0001c0001t0003g0082 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.369+849G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118104170 | |||||||
| chr2:118104389 | G | T | 3 | a0001c0001t0004g0145 a0001c0001t0016g0028 a0001c0005t0016g0109 |
5 | HG01175.hp1 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.369+1068G>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118104389 | |||||||
| chr2:118104517 | A | T | 1 | a0001c0001t0009g0036 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.369+1196A>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118104517 | |||||||
| chr2:118104521 | A | T | 8 | a0001c0001t0008g0014 a0001c0001t0008g0049 a0001c0001t0008g0106 others(5): Show |
17 | HG01070.hp2 HG01071.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.369+1200A>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118104521 | |||||||
| chr2:118104557 | A | G | 19 | a0001c0001t0003g0035 a0001c0001t0003g0096 a0001c0001t0004g0013 others(16): Show |
36 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.369+1236A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118104557 | |||||||
| chr2:118104621 | A | G | 2 | a0001c0001t0004g0051 a0001c0001t0004g0149 |
3 | HG00438.hp1 HG00597.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.369+1300A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118104621 | |||||||
| chr2:118104690 | A | G | 1 | a0001c0001t0003g0088 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.369+1369A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118104690 | |||||||
| chr2:118104776 | G | C | 7 | a0001c0002t0004g0032 a0001c0002t0004g0151 a0001c0002t0004g0152 others(4): Show |
9 | HG02257.hp2 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.369+1455G>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118104776 | |||||||
| chr2:118104780 | G | A | 1 | a0001c0002t0034g0150 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.369+1459G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118104780 | |||||||
| chr2:118104819 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.369+1498A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118104819 | |||||||
| chr2:118104888 | T | G | 22 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0104 others(19): Show |
39 | HG00140.hp1 HG00323.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.369+1567T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118104888 | |||||||
| chr2:118104916 | T | C | 15 | a0001c0001t0004g0038 a0001c0001t0007g0008 a0001c0001t0007g0024 others(12): Show |
38 | HG00738.hp2 HG00741.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.369+1595T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118104916 | |||||||
| chr2:118105036 | T | G | 58 | a0001c0001t0003g0035 a0001c0001t0004g0006 a0001c0001t0004g0013 others(55): Show |
109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.370-1701T>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118105036 | |||||||
| chr2:118105064 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.370-1673G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118105064 | |||||||
| chr2:118105109 | T | C | 92 | a0001c0001t0002g0003 a0001c0001t0002g0018 a0001c0001t0002g0019 others(89): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.370-1628T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118105109 | |||||||
| chr2:118105243 | A | G | 2 | a0001c0001t0004g0121 a0001c0001t0004g0122 |
2 | HG02622.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.370-1494A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118105243 | |||||||
| chr2:118105323 | G | A | 8 | a0001c0001t0008g0014 a0001c0001t0008g0049 a0001c0001t0008g0106 others(5): Show |
18 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.370-1414G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118105323 | |||||||
| chr2:118105345 | T | C | 1 | a0001c0001t0006g0061 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.370-1392T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118105345 | |||||||
| chr2:118105545 | G | A | 1 | a0001c0001t0010g0089 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.370-1192G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118105545 | |||||||
| chr2:118105564 | A | G | 6 | a0001c0002t0004g0032 a0001c0002t0004g0151 a0001c0002t0004g0152 others(3): Show |
8 | HG02257.hp2 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.370-1173A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118105564 | |||||||
| chr2:118105822 | C | T | 1 | a0001c0001t0005g0041 | 2 | NA19057.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.370-915C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118105822 | |||||||
| chr2:118106100 | G | C | 1 | a0001c0001t0004g0121 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.370-637G>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118106100 | |||||||
| chr2:118106194 | G | A | 21 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0104 others(18): Show |
38 | HG00140.hp1 HG00323.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.370-543G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118106194 | |||||||
| chr2:118106298 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(111): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.370-439C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 3/5 | chr2 | 118106298 | |||||||
| chr2:118107300 | T | C | 1 | a0001c0001t0004g0057 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.636+111T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 5/5 | chr2 | 118107300 | |||||||
| chr2:118107327 | A | G | 1 | a0001c0001t0004g0057 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.636+138A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 5/5 | chr2 | 118107327 | |||||||
| chr2:118107412 | A | G | 2 | a0002c0003t0003g0087 a0002c0003t0003g0094 |
2 | NA19056.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.636+223A>G | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 5/5 | chr2 | 118107412 | |||||||
| chr2:118107557 | A | C | 1 | a0001c0001t0007g0146 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.636+368A>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 5/5 | chr2 | 118107557 | |||||||
| chr2:118107558 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.636+369C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 5/5 | chr2 | 118107558 | |||||||
| chr2:118107864 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.637-417G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 5/5 | chr2 | 118107864 | |||||||
| chr2:118107872 | A | C | 3 | a0001c0001t0004g0017 a0001c0001t0004g0039 a0001c0001t0004g0123 |
8 | HG00099.hp1 HG01106.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.637-409A>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 5/5 | chr2 | 118107872 | |||||||
| chr2:118107947 | T | C | 1 | a0001c0001t0003g0086 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.637-334T>C | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 5/5 | chr2 | 118107947 | |||||||
| chr2:118107981 | C | T | 7 | a0001c0001t0003g0035 a0001c0001t0004g0013 a0001c0001t0004g0035 others(4): Show |
11 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.637-300C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 5/5 | chr2 | 118107981 | |||||||
| chr2:118108052 | C | T | 3 | a0001c0001t0004g0145 a0001c0001t0016g0028 a0001c0005t0016g0109 |
5 | HG01175.hp1 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-229C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 5/5 | chr2 | 118108052 | |||||||
| chr2:118108086 | C | T | 7 | a0001c0001t0003g0035 a0001c0001t0004g0013 a0001c0001t0004g0035 others(4): Show |
11 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.637-195C>T | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 5/5 | chr2 | 118108086 | |||||||
| chr2:118108093 | G | A | 29 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0104 others(26): Show |
48 | HG00140.hp1 HG00323.hp2 HG01074.hp1 others(45): Show |
intron_variant | MODIFIER | c.637-188G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 5/5 | chr2 | 118108093 | |||||||
| chr2:118108179 | TA | T | 3 | a0001c0001t0003g0016 a0001c0001t0003g0093 a0001c0001t0012g0135 |
7 | HG00735.hp1 HG01167.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.637-101delA | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 5/5 | chr2 | 118108179 | |||||||
| chr2:118108238 | G | A | 8 | a0001c0001t0008g0014 a0001c0001t0008g0049 a0001c0001t0008g0106 others(5): Show |
18 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.637-43G>A | INSIG2 | ENSG00000125629.16 | transcript | ENST00000245787.9 | protein_coding | 5/5 | chr2 | 118108238 |