Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 58472 |
| ensemblid | ENSG00000137767.14 |
| hgncid | 20390 |
| symbol | SQOR |
| name | sulfide quinone oxidoreductase |
| refseq_nuc | NM_021199.4 |
| refseq_prot | NP_067022.1 |
| ensembl_nuc | ENST00000260324.12 |
| ensembl_prot | ENSP00000260324.7 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 45635029 |
| end | 45691281 |
| strand | + |
| ver | v1.2 |
| region | chr15:45635029-45691281 |
| region5000 | chr15:45630029-45696281 |
| regionname0 | SQOR_chr15_45635029_45691281 |
| regionname5000 | SQOR_chr15_45630029_45696281 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 450 | 234 | 66 | 43 | 87 | 8 | 28 | 65 | SQOR_chr15_45630029_45696281 | SQOR | MVPLV others(445): Show |
chr15 | 45630029 | 45696281 |
| a0002 | 0/0 | 450 | 90 | 5 | 16 | 57 | 2 | 10 | 43 | SQOR_chr15_45630029_45696281 | SQOR | MVPLV others(445): Show |
chr15 | 45630029 | 45696281 |
| a0003 | 0/0 | 450 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | SQOR_chr15_45630029_45696281 | SQOR | MVPLV others(445): Show |
chr15 | 45630029 | 45696281 |
| a0004 | 0/0 | 450 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | MVPLV others(445): Show |
chr15 | 45630029 | 45696281 |
| a0005 | 0/0 | 450 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | MVPLV others(445): Show |
chr15 | 45630029 | 45696281 |
| a0006 | 0/0 | 450 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | MVPLV others(445): Show |
chr15 | 45630029 | 45696281 |
| a0007 | 0/0 | 450 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | MVPLV others(445): Show |
chr15 | 45630029 | 45696281 |
| a0008 | 0/0 | 450 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | MVPLV others(445): Show |
chr15 | 45630029 | 45696281 |
| a0009 | 0/0 | 450 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | MVPLV others(445): Show |
chr15 | 45630029 | 45696281 |
| a0010 | 0/0 | 450 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | MVPLV others(445): Show |
chr15 | 45630029 | 45696281 |
| a0011 | 0/0 | 450 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | MVPLV others(445): Show |
chr15 | 45630029 | 45696281 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1350 | 213 | 59 | 38 | 86 | 5 | 23 | SQOR_chr15_45630029_45696281 | SQOR | ATGGT others(1345): Show |
chr15 | 45630029 | 45696281 | ||
| a0001c0003 | 0/0 | 1350 | 16 | 3 | 5 | 1 | 3 | 4 | SQOR_chr15_45630029_45696281 | SQOR | ATGGT others(1345): Show |
chr15 | 45630029 | 45696281 | ||
| a0001c0007 | 0/0 | 1350 | 3 | 3 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | ATGGT others(1345): Show |
chr15 | 45630029 | 45696281 | ||
| a0001c0013 | 0/0 | 1350 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | ATGGT others(1345): Show |
chr15 | 45630029 | 45696281 | ||
| a0001c0016 | 0/0 | 1350 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | ATGGT others(1345): Show |
chr15 | 45630029 | 45696281 | ||
| a0002c0002 | 0/0 | 1350 | 85 | 5 | 11 | 57 | 2 | 10 | SQOR_chr15_45630029_45696281 | SQOR | ATGGT others(1345): Show |
chr15 | 45630029 | 45696281 | ||
| a0002c0004 | 0/0 | 1350 | 5 | 0 | 5 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | ATGGT others(1345): Show |
chr15 | 45630029 | 45696281 | ||
| a0003c0005 | 0/0 | 1350 | 4 | 0 | 0 | 4 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | ATGGT others(1345): Show |
chr15 | 45630029 | 45696281 | ||
| a0004c0006 | 0/0 | 1350 | 3 | 2 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | ATGGT others(1345): Show |
chr15 | 45630029 | 45696281 | ||
| a0005c0008 | 0/0 | 1350 | 3 | 3 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | ATGGT others(1345): Show |
chr15 | 45630029 | 45696281 | ||
| a0006c0015 | 0/0 | 1350 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | ATGGT others(1345): Show |
chr15 | 45630029 | 45696281 | ||
| a0007c0011 | 0/0 | 1350 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | ATGGT others(1345): Show |
chr15 | 45630029 | 45696281 | ||
| a0008c0012 | 0/0 | 1350 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | ATGGT others(1345): Show |
chr15 | 45630029 | 45696281 | ||
| a0009c0014 | 0/0 | 1350 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | ATGGT others(1345): Show |
chr15 | 45630029 | 45696281 | ||
| a0010c0009 | 0/0 | 1350 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | ATGGT others(1345): Show |
chr15 | 45630029 | 45696281 | ||
| a0011c0010 | 0/0 | 1350 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | ATGGT others(1345): Show |
chr15 | 45630029 | 45696281 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1701 | 200 | 48 | 36 | 86 | 5 | 23 | SQOR_chr15_45630029_45696281 | SQOR | AGTCC others(1696): Show |
chr15 | 45630029 | 45696281 |
| a0001c0001t0002 | 0/0 | 1701 | 5 | 3 | 2 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | AGTCC others(1696): Show |
chr15 | 45630029 | 45696281 |
| a0001c0001t0003 | 0/0 | 1701 | 5 | 5 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | AGTCC others(1696): Show |
chr15 | 45630029 | 45696281 |
| a0001c0001t0004 | 0/0 | 1701 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | AGTCC others(1696): Show |
chr15 | 45630029 | 45696281 |
| a0001c0001t0007 | 0/0 | 1701 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | AGTCC others(1696): Show |
chr15 | 45630029 | 45696281 |
| a0001c0001t0008 | 0/0 | 1701 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | AGTCC others(1696): Show |
chr15 | 45630029 | 45696281 |
| a0001c0003t0001 | 0/0 | 1701 | 16 | 3 | 5 | 1 | 3 | 4 | SQOR_chr15_45630029_45696281 | SQOR | AGTCC others(1696): Show |
chr15 | 45630029 | 45696281 |
| a0001c0007t0001 | 0/0 | 1701 | 3 | 3 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | AGTCC others(1696): Show |
chr15 | 45630029 | 45696281 |
| a0001c0013t0001 | 0/0 | 1701 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | AGTCC others(1696): Show |
chr15 | 45630029 | 45696281 |
| a0001c0016t0001 | 0/0 | 1701 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | AGTCC others(1696): Show |
chr15 | 45630029 | 45696281 |
| a0002c0002t0001 | 0/0 | 1701 | 80 | 5 | 9 | 56 | 1 | 9 | SQOR_chr15_45630029_45696281 | SQOR | AGTCC others(1696): Show |
chr15 | 45630029 | 45696281 |
| a0002c0002t0005 | 0/0 | 1701 | 4 | 0 | 2 | 0 | 1 | 1 | SQOR_chr15_45630029_45696281 | SQOR | AGTCC others(1696): Show |
chr15 | 45630029 | 45696281 |
| a0002c0002t0006 | 0/0 | 1701 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | AGTCC others(1696): Show |
chr15 | 45630029 | 45696281 |
| a0002c0004t0001 | 0/0 | 1701 | 5 | 0 | 5 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | AGTCC others(1696): Show |
chr15 | 45630029 | 45696281 |
| a0003c0005t0001 | 0/0 | 1701 | 4 | 0 | 0 | 4 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | AGTCC others(1696): Show |
chr15 | 45630029 | 45696281 |
| a0004c0006t0001 | 0/0 | 1701 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | AGTCC others(1696): Show |
chr15 | 45630029 | 45696281 |
| a0004c0006t0004 | 0/0 | 1701 | 2 | 2 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | AGTCC others(1696): Show |
chr15 | 45630029 | 45696281 |
| a0005c0008t0001 | 0/0 | 1701 | 3 | 3 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | AGTCC others(1696): Show |
chr15 | 45630029 | 45696281 |
| a0006c0015t0001 | 0/0 | 1701 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | AGTCC others(1696): Show |
chr15 | 45630029 | 45696281 |
| a0007c0011t0004 | 0/0 | 1701 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | AGTCC others(1696): Show |
chr15 | 45630029 | 45696281 |
| a0008c0012t0001 | 0/0 | 1701 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | AGTCC others(1696): Show |
chr15 | 45630029 | 45696281 |
| a0009c0014t0001 | 0/0 | 1701 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | AGTCC others(1696): Show |
chr15 | 45630029 | 45696281 |
| a0010c0009t0001 | 0/0 | 1701 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | AGTCC others(1696): Show |
chr15 | 45630029 | 45696281 |
| a0011c0010t0001 | 0/0 | 1701 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | AGTCC others(1696): Show |
chr15 | 45630029 | 45696281 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0086 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0097 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0003g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0004g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0007g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0001t0008g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0003t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0007t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0007t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0013t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0001c0016t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0005g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0005g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0005g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0005g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0002t0006g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0004t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0004t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0004t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0004t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0002c0004t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0003c0005t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0003c0005t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0003c0005t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0003c0005t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0004c0006t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0004c0006t0004g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0004c0006t0004g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0005c0008t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0005c0008t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0005c0008t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0006c0015t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0007c0011t0004g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0008c0012t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0009c0014t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0010c0009t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| a0011c0010t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0245 | EUR | GBR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0093 | EUR | GBR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | GBR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0141 | EUR | GBR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00323 | hp1 | a0001 | c0003 | t0001 | g0267 | EUR | FIN | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0085 | EUR | FIN | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0200 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00423 | hp1 | a0006 | c0015 | t0001 | g0234 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0260 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0231 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0212 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0039 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0222 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01069 | hp2 | a0002 | c0002 | t0005 | g0032 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01074 | hp1 | a0002 | c0004 | t0001 | g0249 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0268 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0066 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01106 | hp1 | a0001 | c0003 | t0001 | g0266 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01109 | hp2 | a0004 | c0006 | t0001 | g0311 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0073 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0327 | AMR | PUR | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01255 | hp1 | a0002 | c0004 | t0001 | g0040 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01257 | hp2 | a0002 | c0004 | t0001 | g0248 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01258 | hp1 | a0002 | c0004 | t0001 | g0250 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01346 | hp2 | a0002 | c0002 | t0005 | g0033 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0221 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0075 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01433 | hp1 | a0001 | c0003 | t0001 | g0059 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01433 | hp2 | a0001 | c0003 | t0001 | g0281 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | IBS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01517 | hp2 | a0001 | c0003 | t0001 | g0080 | EUR | IBS | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01884 | hp1 | a0001 | c0007 | t0001 | g0150 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0178 | AMR | PEL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0170 | AMR | PEL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0084 | AMR | PEL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01981 | hp1 | a0002 | c0004 | t0001 | g0279 | AMR | PEL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02055 | hp1 | a0007 | c0011 | t0004 | g0322 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0217 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0070 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02145 | hp2 | a0001 | c0001 | t0008 | g0328 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CDX | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CDX | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02165 | hp1 | a0008 | c0012 | t0001 | g0253 | EAS | CDX | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CDX | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0318 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0317 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02523 | hp2 | a0002 | c0002 | t0006 | g0171 | EAS | KHV | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02647 | hp2 | a0001 | c0003 | t0001 | g0220 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0271 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02683 | hp2 | a0001 | c0003 | t0001 | g0069 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02698 | hp1 | a0001 | c0003 | t0001 | g0257 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0102 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0106 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0105 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02809 | hp2 | a0005 | c0008 | t0001 | g0094 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02886 | hp2 | a0001 | c0003 | t0001 | g0121 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02896 | hp1 | a0004 | c0006 | t0004 | g0320 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02897 | hp1 | a0004 | c0006 | t0004 | g0319 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ESN | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02965 | hp2 | a0001 | c0007 | t0001 | g0006 | AFR | ESN | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0233 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0026 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0155 | AFR | ESN | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03195 | hp1 | a0009 | c0014 | t0001 | g0115 | AFR | ESN | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0312 | AFR | ESN | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0313 | AFR | MSL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0187 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03486 | hp2 | a0005 | c0008 | t0001 | g0229 | AFR | MSL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03490 | hp1 | a0001 | c0003 | t0001 | g0258 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03516 | hp1 | a0001 | c0007 | t0001 | g0006 | AFR | ESN | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | MSL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0142 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0136 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0020 | SAS | PJL | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | BEB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | BEB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0264 | SAS | BEB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03834 | hp2 | a0001 | c0016 | t0001 | g0256 | SAS | BEB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0244 | SAS | BEB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | STU | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | STU | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | STU | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | STU | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG04228 | hp1 | a0002 | c0002 | t0005 | g0031 | SAS | STU | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | STU | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | CHB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | YRI | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18906 | hp2 | a0005 | c0008 | t0001 | g0326 | AFR | YRI | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0238 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0237 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18962 | hp2 | a0010 | c0009 | t0001 | g0050 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18967 | hp1 | a0011 | c0010 | t0001 | g0282 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0296 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18982 | hp1 | a0003 | c0005 | t0001 | g0306 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18984 | hp2 | a0003 | c0005 | t0001 | g0307 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0302 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19012 | hp2 | a0003 | c0005 | t0001 | g0163 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | LWK | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | LWK | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0315 | AFR | LWK | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | LWK | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19060 | hp1 | a0001 | c0003 | t0001 | g0174 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19066 | hp2 | a0003 | c0005 | t0001 | g0290 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0284 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0087 | AFR | ASW | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ASW | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA20805 | hp1 | a0002 | c0002 | t0005 | g0048 | EUR | TSI | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0309 | EUR | TSI | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | GIH | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | GIH | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0314 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0092 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG02559 | hp2 | a0001 | c0013 | t0001 | g0117 | AFR | ACB | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0321 | AFR | USA | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | USA | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | USA | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | USA | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | LWK | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | LWK | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0086 | REF | REF | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0097 | REF | REF | SQOR_chr15_45630029_45696281 | SQOR | chr15 | 45630029 | 45696281 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:45635106 | C | T | 1 | a0001 | 6 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(3): Show |
splice_region_variant | LOW | c.-20C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/10 | chr15 | 45635106 | |||||||
| chr15:45658958 | G | A | 1 | a0010 | 1 | NA18962.hp2 | missense_variant | MODERATE | c.35G>A | p.Arg12His | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/10 | 132/1701 | 35/1353 | 12/450 | chr15 | 45658958 | |||
| chr15:45659038 | G | A | 1 | a0011 | 1 | NA18967.hp1 | missense_variant | MODERATE | c.115G>A | p.Ala39Thr | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/10 | 212/1701 | 115/1353 | 39/450 | chr15 | 45659038 | |||
| chr15:45659090 | T | C | 1 | a0004 | 3 | HG01109.hp2 HG02896.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.167T>C | p.Ile56Thr | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/10 | 264/1701 | 167/1353 | 56/450 | chr15 | 45659090 | |||
| chr15:45673634 | C | T | 1 | a0005 | 3 | HG02809.hp2 HG03486.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.487C>T | p.His163Tyr | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/10 | 584/1701 | 487/1353 | 163/450 | chr15 | 45673634 | |||
| chr15:45673697 | G | A | 2 | a0004 a0007 |
4 | HG01109.hp2 HG02055.hp1 HG02896.hp1 others(1): Show |
missense_variant | MODERATE | c.550G>A | p.Asp184Asn | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/10 | 647/1701 | 550/1353 | 184/450 | chr15 | 45673697 | |||
| chr15:45676133 | C | G | 1 | a0003 | 4 | NA18982.hp1 NA18984.hp2 NA19012.hp2 others(1): Show |
missense_variant | MODERATE | c.687C>G | p.Phe229Leu | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/10 | 784/1701 | 687/1353 | 229/450 | chr15 | 45676133 | |||
| chr15:45676237 | T | C | 1 | a0002 | 90 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(87): Show |
missense_variant | MODERATE | c.791T>C | p.Ile264Thr | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/10 | 888/1701 | 791/1353 | 264/450 | chr15 | 45676237 | |||
| chr15:45682649 | G | A | 1 | a0008 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.1036G>A | p.Ala346Thr | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/10 | 1133/1701 | 1036/1353 | 346/450 | chr15 | 45682649 | |||
| chr15:45689118 | C | T | 1 | a0006 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.1196C>T | p.Pro399Leu | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/10 | 1293/1701 | 1196/1353 | 399/450 | chr15 | 45689118 | |||
| chr15:45691002 | G | A | 1 | a0009 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.1325G>A | p.Arg442His | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 10/10 | 1422/1701 | 1325/1353 | 442/450 | chr15 | 45691002 | |||
| chr15:45691280 | G | C | 1 | a0002 | 1 | HG02523.hp2 | splice_region_variant | LOW | c.*250G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 10/10 | chr15 | 45691280 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:45673630 | C | T | 1 | a0001c0016 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.483C>T | p.Phe161Phe | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/10 | 580/1701 | 483/1353 | 161/450 | chr15 | 45673630 | |||
| chr15:45689098 | G | A | 1 | a0001c0007 | 3 | HG01884.hp1 HG02965.hp2 HG03516.hp1 |
synonymous_variant | LOW | c.1176G>A | p.Glu392Glu | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/10 | 1273/1701 | 1176/1353 | 392/450 | chr15 | 45689098 | |||
| chr15:45689119 | G | A | 2 | a0001c0003 a0002c0004 |
21 | HG00099.hp2 HG00323.hp1 HG01074.hp1 others(18): Show |
synonymous_variant | LOW | c.1197G>A | p.Pro399Pro | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/10 | 1294/1701 | 1197/1353 | 399/450 | chr15 | 45689119 | |||
| chr15:45690994 | G | A | 1 | a0001c0013 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.1317G>A | p.Ala439Ala | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 10/10 | 1414/1701 | 1317/1353 | 439/450 | chr15 | 45690994 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:45635034 | A | G | 1 | a0001c0001t0008 | 1 | HG02145.hp2 | 5_prime_UTR_variant | MODIFIER | c.-92A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/10 | 23890 | chr15 | 45635034 | ||||||
| chr15:45658910 | G | C | 3 | a0001c0001t0004 a0004c0006t0004 a0007c0011t0004 |
4 | HG02055.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-14G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/10 | 14 | chr15 | 45658910 | ||||||
| chr15:45691078 | G | T | 1 | a0002c0002t0005 | 4 | HG01069.hp2 HG01346.hp2 HG04228.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*48G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 10/10 | 48 | chr15 | 45691078 | ||||||
| chr15:45691235 | T | C | 2 | a0001c0001t0002 a0001c0001t0007 |
6 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*205T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 10/10 | 205 | chr15 | 45691235 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:45635126 | C | T | 1 | a0001c0001t0008g0328 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-18+18C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45635126 | |||||||
| chr15:45635335 | A | G | 17 | a0001c0001t0001g0316 a0001c0001t0001g0323 a0001c0001t0001g0324 others(14): Show |
17 | HG01109.hp2 HG01243.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.-18+227A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45635335 | |||||||
| chr15:45635354 | G | C | 1 | a0001c0001t0008g0328 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-18+246G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45635354 | |||||||
| chr15:45635513 | T | C | 1 | a0004c0006t0001g0311 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-18+405T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45635513 | |||||||
| chr15:45635680 | T | C | 1 | a0004c0006t0001g0311 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-18+572T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45635680 | |||||||
| chr15:45635705 | T | C | 1 | a0001c0001t0001g0011 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-18+597T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45635705 | |||||||
| chr15:45635761 | T | A | 1 | a0002c0002t0001g0012 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-18+653T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45635761 | |||||||
| chr15:45635809 | G | A | 1 | a0002c0002t0001g0013 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-18+701G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45635809 | |||||||
| chr15:45635830 | A | ACTCT | 68 | a0001c0001t0001g0010 a0001c0001t0001g0261 a0001c0001t0001g0262 others(65): Show |
69 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.-18+724_-18+727dup others(4): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45635830 | ||||||
| chr15:45635987 | C | T | 1 | a0002c0002t0001g0260 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-18+879C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45635987 | |||||||
| chr15:45635997 | A | C | 32 | a0001c0001t0001g0232 a0001c0001t0001g0235 a0001c0001t0001g0240 others(29): Show |
33 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.-18+889A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45635997 | |||||||
| chr15:45636197 | C | T | 1 | a0004c0006t0001g0311 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-18+1089C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45636197 | |||||||
| chr15:45636406 | C | CT | 67 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0025 others(64): Show |
70 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.-18+1314dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45636406 | ||||||
| chr15:45636406 | CT | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0143 others(77): Show |
86 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.-18+1314delT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45636406 | ||||||
| chr15:45636440 | T | C | 6 | a0001c0001t0001g0018 a0002c0002t0001g0014 a0002c0002t0001g0015 others(3): Show |
6 | HG00408.hp1 HG00438.hp2 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+1332T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45636440 | |||||||
| chr15:45636498 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-18+1390G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45636498 | |||||||
| chr15:45636504 | A | G | 49 | a0001c0001t0001g0010 a0001c0001t0001g0263 a0001c0001t0001g0265 others(46): Show |
50 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.-18+1396A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45636504 | |||||||
| chr15:45636618 | G | A | 1 | a0001c0001t0003g0312 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-18+1510G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45636618 | |||||||
| chr15:45636635 | C | T | 1 | a0002c0002t0001g0231 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-18+1527C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45636635 | |||||||
| chr15:45636853 | A | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0143 others(97): Show |
107 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.-18+1745A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45636853 | |||||||
| chr15:45636869 | C | T | 1 | a0002c0002t0001g0142 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-18+1761C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45636869 | |||||||
| chr15:45636988 | C | CT | 6 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0230 others(3): Show |
6 | HG00140.hp2 HG01243.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+1894dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45636988 | ||||||
| chr15:45636988 | CT | C | 14 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(11): Show |
15 | HG01169.hp2 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-18+1894delT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45636988 | ||||||
| chr15:45637226 | T | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0143 others(75): Show |
84 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.-18+2118T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45637226 | |||||||
| chr15:45637294 | G | C | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-18+2186G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45637294 | |||||||
| chr15:45637544 | G | A | 1 | a0001c0001t0001g0263 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-18+2436G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45637544 | |||||||
| chr15:45637778 | C | T | 2 | a0001c0003t0001g0257 a0001c0003t0001g0258 |
2 | HG02698.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.-18+2670C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45637778 | |||||||
| chr15:45637869 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-18+2761C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45637869 | |||||||
| chr15:45637873 | C | A | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-18+2765C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45637873 | |||||||
| chr15:45637991 | G | C | 1 | a0002c0002t0001g0020 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-18+2883G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45637991 | |||||||
| chr15:45638155 | C | CA | 6 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(3): Show |
6 | HG02895.hp2 HG03710.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+3054dupA | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45638155 | ||||||
| chr15:45638349 | T | G | 1 | a0002c0002t0001g0157 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-18+3241T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638349 | |||||||
| chr15:45638350 | G | A | 1 | a0002c0002t0001g0157 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-18+3242G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638350 | |||||||
| chr15:45638353 | A | T | 1 | a0002c0002t0001g0157 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-18+3245A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638353 | |||||||
| chr15:45638407 | C | T | 2 | a0002c0002t0001g0327 a0005c0008t0001g0326 |
2 | HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-18+3299C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638407 | |||||||
| chr15:45638450 | C | T | 2 | a0001c0001t0003g0317 a0001c0001t0003g0318 |
2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.-18+3342C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638450 | |||||||
| chr15:45638451 | G | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0027 others(2): Show |
6 | HG02451.hp1 HG02896.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+3343G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638451 | |||||||
| chr15:45638524 | G | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(156): Show |
167 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.-18+3416G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638524 | |||||||
| chr15:45638585 | G | C | 2 | a0002c0002t0001g0327 a0005c0008t0001g0326 |
2 | HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-18+3477G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638585 | |||||||
| chr15:45638588 | G | A | 1 | a0002c0002t0001g0158 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-18+3480G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638588 | |||||||
| chr15:45638595 | G | A | 2 | a0001c0001t0001g0228 a0005c0008t0001g0229 |
2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-18+3487G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638595 | |||||||
| chr15:45638632 | G | A | 1 | a0001c0001t0001g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-18+3524G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638632 | |||||||
| chr15:45638647 | C | A | 4 | a0001c0001t0004g0321 a0004c0006t0004g0319 a0004c0006t0004g0320 others(1): Show |
4 | HG02055.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+3539C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638647 | |||||||
| chr15:45638648 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-18+3540G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638648 | |||||||
| chr15:45638756 | G | A | 7 | a0001c0001t0001g0030 a0001c0001t0001g0034 a0001c0001t0001g0140 others(4): Show |
7 | HG00140.hp2 HG01069.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+3648G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638756 | |||||||
| chr15:45638779 | G | A | 1 | a0001c0001t0001g0001 | 3 | HG00738.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-18+3671G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638779 | |||||||
| chr15:45638792 | C | G | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-18+3684C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45638792 | |||||||
| chr15:45639125 | T | C | 1 | a0001c0001t0001g0030 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-18+4017T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45639125 | |||||||
| chr15:45639448 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-18+4340C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45639448 | |||||||
| chr15:45639476 | A | G | 3 | a0001c0001t0001g0137 a0001c0016t0001g0256 a0002c0002t0001g0136 |
3 | HG02074.hp2 HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-18+4368A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45639476 | |||||||
| chr15:45639494 | C | G | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-18+4386C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45639494 | |||||||
| chr15:45639586 | T | C | 3 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0325 |
3 | HG02717.hp2 HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-18+4478T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45639586 | |||||||
| chr15:45639589 | G | A | 1 | a0004c0006t0001g0311 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-18+4481G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45639589 | |||||||
| chr15:45639609 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-18+4501T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45639609 | |||||||
| chr15:45640463 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG00140.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-18+5355C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45640463 | |||||||
| chr15:45640497 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-18+5389C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45640497 | |||||||
| chr15:45640520 | T | G | 2 | a0001c0001t0001g0228 a0005c0008t0001g0229 |
2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-18+5412T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45640520 | |||||||
| chr15:45640673 | C | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(186): Show |
198 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.-18+5565C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45640673 | |||||||
| chr15:45640739 | G | C | 1 | a0002c0002t0001g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-18+5631G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45640739 | |||||||
| chr15:45640981 | G | A | 53 | a0001c0001t0001g0010 a0001c0001t0001g0263 a0001c0001t0001g0265 others(50): Show |
54 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.-18+5873G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45640981 | |||||||
| chr15:45641077 | T | G | 6 | a0001c0001t0003g0312 a0001c0001t0003g0313 a0001c0001t0003g0314 others(3): Show |
6 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+5969T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45641077 | |||||||
| chr15:45641098 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-18+5990G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45641098 | |||||||
| chr15:45641109 | T | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0143 others(81): Show |
90 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.-18+6001T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45641109 | |||||||
| chr15:45641329 | T | G | 1 | a0004c0006t0001g0311 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-18+6221T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45641329 | |||||||
| chr15:45641675 | G | A | 1 | a0001c0001t0001g0036 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-18+6567G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45641675 | |||||||
| chr15:45641878 | C | G | 2 | a0002c0002t0001g0224 a0002c0002t0001g0225 |
2 | NA18949.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.-18+6770C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45641878 | |||||||
| chr15:45641894 | C | T | 13 | a0001c0001t0001g0024 a0001c0001t0001g0123 a0001c0001t0001g0126 others(10): Show |
13 | HG00673.hp1 HG01517.hp1 NA18612.hp1 others(10): Show |
intron_variant | MODIFIER | c.-18+6786C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45641894 | |||||||
| chr15:45641954 | C | T | 1 | a0001c0001t0001g0310 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-18+6846C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45641954 | |||||||
| chr15:45641956 | A | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(155): Show |
166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+6848A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45641956 | |||||||
| chr15:45642028 | C | T | 1 | a0001c0001t0001g0309 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-18+6920C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642028 | |||||||
| chr15:45642404 | G | A | 1 | a0002c0002t0001g0159 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-18+7296G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642404 | |||||||
| chr15:45642506 | G | T | 49 | a0001c0001t0001g0010 a0001c0001t0001g0263 a0001c0001t0001g0265 others(46): Show |
50 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.-18+7398G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642506 | |||||||
| chr15:45642547 | A | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(155): Show |
166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+7439A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642547 | |||||||
| chr15:45642579 | T | C | 30 | a0001c0001t0001g0232 a0001c0001t0001g0235 a0001c0001t0001g0240 others(27): Show |
31 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.-18+7471T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642579 | |||||||
| chr15:45642612 | A | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(155): Show |
166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+7504A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642612 | |||||||
| chr15:45642642 | G | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(155): Show |
166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+7534G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642642 | |||||||
| chr15:45642671 | C | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(155): Show |
166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+7563C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642671 | |||||||
| chr15:45642689 | C | T | 6 | a0001c0001t0003g0312 a0001c0001t0003g0313 a0001c0001t0003g0314 others(3): Show |
6 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+7581C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642689 | |||||||
| chr15:45642723 | A | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(149): Show |
160 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.-18+7615A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642723 | |||||||
| chr15:45642723 | A | G | 6 | a0001c0001t0003g0312 a0001c0001t0003g0313 a0001c0001t0003g0314 others(3): Show |
6 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+7615A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642723 | |||||||
| chr15:45642782 | C | A | 1 | a0001c0001t0001g0262 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-18+7674C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642782 | |||||||
| chr15:45642809 | C | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(155): Show |
166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+7701C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642809 | |||||||
| chr15:45642823 | T | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(155): Show |
166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+7715T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642823 | |||||||
| chr15:45642826 | G | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(155): Show |
166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+7718G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642826 | |||||||
| chr15:45642876 | T | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(155): Show |
166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+7768T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642876 | |||||||
| chr15:45642958 | T | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(186): Show |
198 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.-18+7850T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642958 | |||||||
| chr15:45642961 | C | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(155): Show |
166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+7853C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642961 | |||||||
| chr15:45642974 | G | C | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-18+7866G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45642974 | |||||||
| chr15:45643027 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-18+7919C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45643027 | |||||||
| chr15:45643053 | C | T | 4 | a0001c0001t0001g0223 a0001c0001t0002g0008 a0002c0002t0001g0221 others(1): Show |
5 | HG00642.hp2 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+7945C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45643053 | |||||||
| chr15:45643088 | G | T | 1 | a0001c0003t0001g0121 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-18+7980G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45643088 | |||||||
| chr15:45643152 | T | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(155): Show |
166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+8044T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45643152 | |||||||
| chr15:45643174 | C | A | 1 | a0001c0001t0002g0037 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-18+8066C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45643174 | |||||||
| chr15:45643195 | C | A | 55 | a0001c0001t0001g0010 a0001c0001t0001g0263 a0001c0001t0001g0265 others(52): Show |
56 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.-18+8087C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45643195 | |||||||
| chr15:45643262 | C | G | 3 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0003t0001g0220 |
3 | HG02258.hp1 HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-18+8154C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45643262 | |||||||
| chr15:45643321 | A | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(156): Show |
167 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.-18+8213A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45643321 | |||||||
| chr15:45643557 | C | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(155): Show |
166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+8449C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45643557 | |||||||
| chr15:45643579 | G | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(155): Show |
166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+8471G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45643579 | |||||||
| chr15:45643618 | C | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(155): Show |
166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+8510C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45643618 | |||||||
| chr15:45643895 | T | C | 1 | a0001c0001t0003g0312 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-18+8787T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45643895 | |||||||
| chr15:45643896 | A | T | 2 | a0002c0002t0001g0327 a0005c0008t0001g0326 |
2 | HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-18+8788A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45643896 | |||||||
| chr15:45643929 | T | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(155): Show |
166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+8821T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45643929 | |||||||
| chr15:45644018 | C | A | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02895.hp2 HG02897.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-18+8910C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644018 | |||||||
| chr15:45644036 | G | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(155): Show |
166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+8928G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644036 | |||||||
| chr15:45644068 | G | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(155): Show |
166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+8960G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644068 | |||||||
| chr15:45644094 | T | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(154): Show |
165 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.-18+8986T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644094 | |||||||
| chr15:45644147 | A | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(155): Show |
166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+9039A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644147 | |||||||
| chr15:45644148 | C | T | 1 | a0001c0003t0001g0258 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-18+9040C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644148 | |||||||
| chr15:45644173 | T | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(154): Show |
165 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.-18+9065T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644173 | |||||||
| chr15:45644191 | G | A | 7 | a0001c0001t0001g0030 a0001c0001t0001g0138 a0001c0001t0001g0140 others(4): Show |
7 | HG00140.hp2 HG01069.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+9083G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644191 | |||||||
| chr15:45644305 | T | C | 3 | a0001c0001t0001g0137 a0001c0016t0001g0256 a0002c0002t0001g0136 |
3 | HG02074.hp2 HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-18+9197T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644305 | |||||||
| chr15:45644389 | A | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(155): Show |
166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+9281A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644389 | |||||||
| chr15:45644391 | G | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(156): Show |
167 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.-18+9283G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644391 | |||||||
| chr15:45644417 | T | A | 2 | a0004c0006t0004g0319 a0004c0006t0004g0320 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-18+9309T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644417 | |||||||
| chr15:45644434 | G | T | 30 | a0001c0001t0001g0232 a0001c0001t0001g0235 a0001c0001t0001g0240 others(27): Show |
31 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.-18+9326G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644434 | |||||||
| chr15:45644547 | G | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(155): Show |
166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+9439G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644547 | |||||||
| chr15:45644658 | G | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(155): Show |
166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+9550G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644658 | |||||||
| chr15:45644664 | G | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(186): Show |
198 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.-18+9556G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644664 | |||||||
| chr15:45644666 | A | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(155): Show |
166 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18+9558A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644666 | |||||||
| chr15:45644734 | T | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(186): Show |
198 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.-18+9626T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644734 | |||||||
| chr15:45644751 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-18+9643A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644751 | |||||||
| chr15:45644785 | G | GAGCTGCC others(13): Show |
1 | a0001c0001t0001g0160 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-18+9678_-18+9697d others(22): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45644785 | ||||||
| chr15:45644938 | C | G | 30 | a0001c0001t0001g0232 a0001c0001t0001g0235 a0001c0001t0001g0240 others(27): Show |
31 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.-18+9830C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45644938 | |||||||
| chr15:45645174 | C | T | 1 | a0002c0002t0001g0142 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-18+10066C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45645174 | |||||||
| chr15:45645279 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-18+10171A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45645279 | |||||||
| chr15:45645324 | C | T | 2 | a0001c0001t0003g0314 a0001c0001t0007g0315 |
2 | HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-18+10216C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45645324 | |||||||
| chr15:45645330 | A | G | 1 | a0001c0001t0001g0030 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-18+10222A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45645330 | |||||||
| chr15:45645386 | T | G | 1 | a0001c0001t0001g0262 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-18+10278T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45645386 | |||||||
| chr15:45645427 | C | A | 41 | a0001c0001t0001g0010 a0001c0001t0001g0161 a0001c0001t0001g0162 others(38): Show |
42 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.-18+10319C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45645427 | |||||||
| chr15:45645434 | G | A | 30 | a0001c0001t0001g0232 a0001c0001t0001g0235 a0001c0001t0001g0240 others(27): Show |
31 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.-18+10326G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45645434 | |||||||
| chr15:45645452 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-18+10344G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45645452 | |||||||
| chr15:45645498 | A | G | 30 | a0001c0001t0001g0232 a0001c0001t0001g0235 a0001c0001t0001g0240 others(27): Show |
31 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.-18+10390A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45645498 | |||||||
| chr15:45645653 | T | A | 2 | a0001c0001t0003g0314 a0001c0001t0007g0315 |
2 | HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-18+10545T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45645653 | |||||||
| chr15:45645705 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-18+10597C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45645705 | |||||||
| chr15:45645752 | T | C | 1 | a0001c0001t0003g0312 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-18+10644T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45645752 | |||||||
| chr15:45645973 | C | G | 1 | a0001c0001t0001g0227 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-18+10865C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45645973 | |||||||
| chr15:45645993 | C | G | 1 | a0001c0001t0001g0299 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-18+10885C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45645993 | |||||||
| chr15:45646115 | T | G | 1 | a0001c0001t0001g0262 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-18+11007T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45646115 | |||||||
| chr15:45646163 | G | T | 1 | a0001c0001t0001g0262 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-18+11055G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45646163 | |||||||
| chr15:45646312 | C | A | 7 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0325 others(4): Show |
7 | HG02055.hp1 HG02717.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+11204C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45646312 | |||||||
| chr15:45646441 | T | A | 1 | a0001c0001t0001g0010 | 2 | NA18947.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.-18+11333T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45646441 | |||||||
| chr15:45646463 | A | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0143 others(88): Show |
98 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.-18+11355A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45646463 | |||||||
| chr15:45646470 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-18+11362C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45646470 | |||||||
| chr15:45646654 | T | A | 4 | a0001c0001t0004g0321 a0004c0006t0004g0319 a0004c0006t0004g0320 others(1): Show |
4 | HG02055.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+11546T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45646654 | |||||||
| chr15:45646849 | C | G | 1 | a0001c0001t0001g0298 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-18+11741C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45646849 | |||||||
| chr15:45646885 | T | A | 49 | a0001c0001t0001g0010 a0001c0001t0001g0161 a0001c0001t0001g0263 others(46): Show |
50 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.-18+11777T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45646885 | |||||||
| chr15:45647077 | A | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(198): Show |
211 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.-17-11830A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45647077 | |||||||
| chr15:45647091 | A | G | 25 | a0001c0001t0001g0263 a0001c0001t0001g0285 a0001c0001t0001g0286 others(22): Show |
25 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.-17-11816A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45647091 | |||||||
| chr15:45647141 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-17-11766C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45647141 | |||||||
| chr15:45647164 | G | A | 3 | a0001c0001t0001g0038 a0002c0002t0001g0039 a0002c0004t0001g0040 |
3 | HG00639.hp2 HG01255.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-17-11743G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45647164 | |||||||
| chr15:45647328 | C | CT | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
172 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.-17-11563dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45647328 | ||||||
| chr15:45647328 | C | CTT | 15 | a0001c0001t0001g0215 a0001c0001t0001g0232 a0001c0001t0001g0235 others(12): Show |
16 | HG00423.hp1 HG02080.hp1 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.-17-11564_-17-1156 others(6): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45647328 | ||||||
| chr15:45647328 | C | CTTT | 19 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 others(16): Show |
19 | HG00099.hp1 HG00639.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.-17-11565_-17-1156 others(7): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45647328 | ||||||
| chr15:45647494 | A | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(179): Show |
191 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.-17-11413A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45647494 | |||||||
| chr15:45647565 | A | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(179): Show |
191 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.-17-11342A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45647565 | |||||||
| chr15:45647642 | C | T | 1 | a0001c0001t0003g0312 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-17-11265C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45647642 | |||||||
| chr15:45647650 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-11257C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45647650 | |||||||
| chr15:45647779 | G | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0143 others(70): Show |
79 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.-17-11128G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45647779 | |||||||
| chr15:45647780 | G | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0143 others(70): Show |
79 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.-17-11127G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45647780 | |||||||
| chr15:45648153 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-10754A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45648153 | |||||||
| chr15:45648167 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-10740G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45648167 | |||||||
| chr15:45648174 | T | A | 8 | a0001c0001t0003g0312 a0001c0001t0003g0313 a0001c0001t0003g0314 others(5): Show |
8 | HG01243.hp2 HG02109.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17-10733T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45648174 | |||||||
| chr15:45648198 | C | T | 2 | a0001c0001t0003g0317 a0001c0001t0003g0318 |
2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.-17-10709C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45648198 | |||||||
| chr15:45648399 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-10508A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45648399 | |||||||
| chr15:45648409 | C | G | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-10498C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45648409 | |||||||
| chr15:45648472 | A | T | 32 | a0001c0001t0001g0232 a0001c0001t0001g0235 a0001c0001t0001g0240 others(29): Show |
33 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.-17-10435A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45648472 | |||||||
| chr15:45648502 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-17-10405C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45648502 | |||||||
| chr15:45648534 | G | T | 1 | a0001c0001t0001g0214 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-17-10373G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45648534 | |||||||
| chr15:45648628 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-10279G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45648628 | |||||||
| chr15:45648707 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-10200C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45648707 | |||||||
| chr15:45648764 | G | A | 31 | a0001c0001t0001g0232 a0001c0001t0001g0235 a0001c0001t0001g0240 others(28): Show |
32 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.-17-10143G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45648764 | |||||||
| chr15:45648830 | T | C | 4 | a0002c0002t0001g0164 a0002c0002t0001g0165 a0002c0002t0001g0224 others(1): Show |
4 | NA18949.hp2 NA18986.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-10077T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45648830 | |||||||
| chr15:45648854 | C | A | 1 | a0001c0001t0001g0041 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-17-10053C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45648854 | |||||||
| chr15:45648984 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-9923T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45648984 | |||||||
| chr15:45649119 | A | C | 17 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0027 others(14): Show |
18 | HG00735.hp2 HG01081.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.-17-9788A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649119 | |||||||
| chr15:45649170 | G | A | 2 | a0002c0002t0001g0327 a0005c0008t0001g0326 |
2 | HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-17-9737G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649170 | |||||||
| chr15:45649267 | C | T | 1 | a0002c0002t0001g0213 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-17-9640C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649267 | |||||||
| chr15:45649373 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-17-9534G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649373 | |||||||
| chr15:45649485 | C | T | 1 | a0001c0001t0001g0283 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-17-9422C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649485 | |||||||
| chr15:45649491 | T | C | 27 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0027 others(24): Show |
28 | HG00735.hp2 HG01081.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.-17-9416T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649491 | |||||||
| chr15:45649497 | A | G | 1 | a0001c0003t0001g0121 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-17-9410A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649497 | |||||||
| chr15:45649512 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-9395G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649512 | |||||||
| chr15:45649616 | A | G | 1 | a0001c0001t0002g0022 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-17-9291A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649616 | |||||||
| chr15:45649646 | A | AT | 16 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(13): Show |
17 | HG01169.hp2 HG01884.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.-17-9253dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45649646 | ||||||
| chr15:45649749 | C | G | 1 | a0001c0001t0001g0111 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-17-9158C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649749 | |||||||
| chr15:45649785 | A | T | 1 | a0001c0001t0001g0283 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-17-9122A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649785 | |||||||
| chr15:45649785 | AT | A | 3 | a0001c0001t0001g0301 a0002c0002t0001g0300 a0002c0002t0001g0302 |
3 | HG00423.hp2 NA18992.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-17-9116delT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45649785 | ||||||
| chr15:45649812 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG00735.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.-17-9095G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649812 | |||||||
| chr15:45649813 | A | G | 30 | a0001c0001t0001g0010 a0001c0001t0001g0110 a0001c0001t0001g0161 others(27): Show |
31 | HG00323.hp1 HG01081.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.-17-9094A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649813 | |||||||
| chr15:45649829 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-9078T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649829 | |||||||
| chr15:45649831 | T | A | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-9076T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649831 | |||||||
| chr15:45649844 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-9063T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649844 | |||||||
| chr15:45649851 | T | C | 2 | a0001c0001t0001g0029 a0004c0006t0001g0311 |
2 | HG01109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-17-9056T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649851 | |||||||
| chr15:45649865 | G | A | 11 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0027 others(8): Show |
12 | HG02257.hp2 HG02280.hp2 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.-17-9042G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45649865 | |||||||
| chr15:45650001 | G | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 |
3 | HG02965.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-17-8906G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650001 | |||||||
| chr15:45650005 | G | A | 1 | a0001c0001t0001g0303 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-17-8902G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650005 | |||||||
| chr15:45650068 | C | T | 1 | a0002c0002t0001g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-17-8839C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650068 | |||||||
| chr15:45650098 | C | A | 15 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(12): Show |
16 | HG01169.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.-17-8809C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650098 | |||||||
| chr15:45650119 | A | C | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-8788A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650119 | |||||||
| chr15:45650141 | C | CT | 11 | a0001c0001t0001g0104 a0001c0001t0001g0107 a0001c0001t0001g0108 others(8): Show |
11 | HG00621.hp1 HG00673.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.-17-8758dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45650141 | ||||||
| chr15:45650198 | G | T | 1 | a0001c0001t0001g0103 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-17-8709G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650198 | |||||||
| chr15:45650224 | C | G | 14 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0027 others(11): Show |
15 | HG01255.hp2 HG02145.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.-17-8683C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650224 | |||||||
| chr15:45650232 | T | A | 15 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0243 others(12): Show |
17 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-8675T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650232 | |||||||
| chr15:45650315 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-8592G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650315 | |||||||
| chr15:45650351 | G | A | 1 | a0002c0002t0001g0300 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-17-8556G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650351 | |||||||
| chr15:45650369 | C | T | 1 | a0011c0010t0001g0282 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-17-8538C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650369 | |||||||
| chr15:45650373 | C | T | 1 | a0002c0002t0001g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-17-8534C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650373 | |||||||
| chr15:45650498 | G | A | 1 | a0001c0001t0002g0022 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-17-8409G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650498 | |||||||
| chr15:45650571 | G | C | 3 | a0001c0001t0001g0116 a0001c0001t0003g0312 a0009c0014t0001g0115 |
3 | HG03195.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-17-8336G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650571 | |||||||
| chr15:45650585 | C | T | 75 | a0001c0001t0001g0002 a0001c0001t0001g0099 a0001c0001t0001g0100 others(72): Show |
79 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.-17-8322C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650585 | |||||||
| chr15:45650588 | T | C | 3 | a0004c0006t0004g0319 a0004c0006t0004g0320 a0007c0011t0004g0322 |
3 | HG02055.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-17-8319T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650588 | |||||||
| chr15:45650754 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-8153T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650754 | |||||||
| chr15:45650849 | G | T | 3 | a0004c0006t0004g0319 a0004c0006t0004g0320 a0007c0011t0004g0322 |
3 | HG02055.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-17-8058G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650849 | |||||||
| chr15:45650885 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-8022C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650885 | |||||||
| chr15:45650901 | C | G | 1 | a0001c0003t0001g0102 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-17-8006C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650901 | |||||||
| chr15:45650952 | C | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0243 others(12): Show |
17 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-7955C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650952 | |||||||
| chr15:45650980 | G | A | 1 | a0001c0001t0004g0321 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-17-7927G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650980 | |||||||
| chr15:45650991 | C | G | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-7916C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650991 | |||||||
| chr15:45650998 | C | T | 1 | a0001c0003t0001g0121 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-17-7909C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650998 | |||||||
| chr15:45650999 | G | A | 1 | a0002c0002t0001g0098 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-17-7908G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45650999 | |||||||
| chr15:45651032 | G | A | 1 | a0001c0001t0003g0313 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-17-7875G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651032 | |||||||
| chr15:45651052 | A | C | 1 | a0002c0002t0001g0013 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-17-7855A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651052 | |||||||
| chr15:45651055 | G | C | 1 | a0001c0001t0001g0265 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-17-7852G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651055 | |||||||
| chr15:45651200 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-17-7707G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651200 | |||||||
| chr15:45651213 | T | G | 2 | a0001c0001t0001g0235 a0006c0015t0001g0234 |
2 | HG00423.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.-17-7694T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651213 | |||||||
| chr15:45651270 | G | A | 3 | a0004c0006t0004g0319 a0004c0006t0004g0320 a0007c0011t0004g0322 |
3 | HG02055.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-17-7637G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651270 | |||||||
| chr15:45651335 | C | T | 1 | a0001c0001t0008g0328 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-17-7572C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651335 | |||||||
| chr15:45651402 | G | A | 1 | a0002c0002t0001g0045 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-17-7505G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651402 | |||||||
| chr15:45651492 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 |
3 | HG02965.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-17-7415C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651492 | |||||||
| chr15:45651518 | T | C | 325 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(322): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.-17-7389T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651518 | |||||||
| chr15:45651519 | G | T | 15 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0027 others(12): Show |
16 | HG01255.hp2 HG02145.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-17-7388G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651519 | |||||||
| chr15:45651555 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-7352C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651555 | |||||||
| chr15:45651556 | G | A | 1 | a0001c0003t0001g0174 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-17-7351G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651556 | |||||||
| chr15:45651812 | A | G | 15 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0243 others(12): Show |
17 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-7095A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651812 | |||||||
| chr15:45651845 | A | ATTCTTCT others(29): Show |
2 | a0001c0003t0001g0257 a0001c0003t0001g0258 |
2 | HG02698.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.-17-7047_-17-7012d others(38): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45651845 | ||||||
| chr15:45651874 | T | C | 3 | a0004c0006t0004g0319 a0004c0006t0004g0320 a0007c0011t0004g0322 |
3 | HG02055.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-17-7033T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651874 | |||||||
| chr15:45651883 | T | A | 1 | a0004c0006t0001g0311 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-17-7024T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651883 | |||||||
| chr15:45651896 | T | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0243 others(12): Show |
17 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-7011T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651896 | |||||||
| chr15:45651925 | G | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0243 others(12): Show |
17 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-6982G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651925 | |||||||
| chr15:45651975 | C | T | 1 | a0001c0003t0001g0093 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-17-6932C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45651975 | |||||||
| chr15:45652000 | G | A | 15 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0243 others(12): Show |
17 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-6907G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652000 | |||||||
| chr15:45652019 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-17-6888G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652019 | |||||||
| chr15:45652030 | C | T | 1 | a0002c0004t0001g0040 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-17-6877C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652030 | |||||||
| chr15:45652165 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-6742C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652165 | |||||||
| chr15:45652169 | C | T | 2 | a0001c0001t0001g0091 a0002c0002t0001g0092 |
2 | HG01496.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-17-6738C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652169 | |||||||
| chr15:45652173 | C | T | 15 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(12): Show |
16 | HG01169.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.-17-6734C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652173 | |||||||
| chr15:45652174 | G | A | 15 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0243 others(12): Show |
17 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-6733G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652174 | |||||||
| chr15:45652327 | T | C | 1 | a0004c0006t0001g0311 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-17-6580T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652327 | |||||||
| chr15:45652396 | G | A | 92 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(89): Show |
96 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.-17-6511G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652396 | |||||||
| chr15:45652427 | C | A | 1 | a0005c0008t0001g0094 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-6480C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652427 | |||||||
| chr15:45652485 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-6422G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652485 | |||||||
| chr15:45652488 | C | G | 15 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(12): Show |
16 | HG01169.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.-17-6419C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652488 | |||||||
| chr15:45652494 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-17-6413C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652494 | |||||||
| chr15:45652504 | G | A | 15 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0243 others(12): Show |
17 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-6403G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652504 | |||||||
| chr15:45652510 | T | C | 1 | a0002c0002t0001g0221 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-17-6397T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652510 | |||||||
| chr15:45652619 | T | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
199 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.-17-6288T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652619 | |||||||
| chr15:45652638 | C | CT | 34 | a0001c0001t0001g0018 a0001c0001t0001g0088 a0001c0001t0001g0089 others(31): Show |
35 | HG00408.hp1 HG01106.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.-17-6243dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45652638 | ||||||
| chr15:45652638 | C | CTT | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0025 others(89): Show |
97 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.-17-6244_-17-6243d others(4): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45652638 | ||||||
| chr15:45652638 | C | CTTT | 20 | a0001c0001t0001g0035 a0001c0001t0001g0095 a0001c0001t0001g0101 others(17): Show |
20 | HG00621.hp2 HG00741.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-17-6245_-17-6243d others(5): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45652638 | ||||||
| chr15:45652638 | CT | C | 45 | a0001c0001t0001g0010 a0001c0001t0001g0046 a0001c0001t0001g0049 others(42): Show |
46 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.-17-6243delT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45652638 | ||||||
| chr15:45652638 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-6252_-17-6243d others(12): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45652638 | ||||||
| chr15:45652672 | C | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0243 others(12): Show |
17 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-6235C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652672 | |||||||
| chr15:45652673 | G | A | 1 | a0001c0013t0001g0117 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-17-6234G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652673 | |||||||
| chr15:45652776 | A | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0243 others(12): Show |
17 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-6131A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652776 | |||||||
| chr15:45652846 | C | A | 95 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(92): Show |
99 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.-17-6061C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652846 | |||||||
| chr15:45652921 | C | G | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0034 others(108): Show |
117 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-17-5986C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652921 | |||||||
| chr15:45652937 | C | T | 3 | a0004c0006t0004g0319 a0004c0006t0004g0320 a0007c0011t0004g0322 |
3 | HG02055.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-17-5970C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652937 | |||||||
| chr15:45652971 | A | T | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-5936A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45652971 | |||||||
| chr15:45653003 | C | CAATTTTA others(5): Show |
1 | a0001c0001t0001g0046 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-17-5903_-17-5892d others(14): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45653003 | ||||||
| chr15:45653008 | T | G | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0034 others(108): Show |
117 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-17-5899T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653008 | |||||||
| chr15:45653098 | C | G | 1 | a0002c0002t0001g0159 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-17-5809C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653098 | |||||||
| chr15:45653176 | A | G | 1 | a0001c0001t0007g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-17-5731A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653176 | |||||||
| chr15:45653246 | CG | C | 29 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0143 others(26): Show |
29 | HG00621.hp2 HG01109.hp1 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.-17-5660delG | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653246 | |||||||
| chr15:45653260 | G | A | 1 | a0001c0001t0001g0286 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-17-5647G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653260 | |||||||
| chr15:45653276 | C | T | 96 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(93): Show |
100 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.-17-5631C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653276 | |||||||
| chr15:45653315 | C | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
152 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.-17-5592C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653315 | |||||||
| chr15:45653372 | A | G | 33 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0027 others(30): Show |
35 | HG01169.hp2 HG01255.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.-17-5535A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653372 | |||||||
| chr15:45653387 | ACT | A | 15 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0027 others(12): Show |
16 | HG01255.hp2 HG02145.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-17-5517_-17-5516d others(4): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45653387 | ||||||
| chr15:45653455 | T | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(152): Show |
162 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.-17-5452T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653455 | |||||||
| chr15:45653456 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-17-5451G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653456 | |||||||
| chr15:45653513 | C | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0169 |
2 | NA18993.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-17-5394C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653513 | |||||||
| chr15:45653558 | A | G | 13 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0112 others(10): Show |
13 | HG00735.hp2 HG01081.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.-17-5349A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653558 | |||||||
| chr15:45653614 | G | A | 99 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(96): Show |
103 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.-17-5293G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653614 | |||||||
| chr15:45653639 | G | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0034 others(108): Show |
117 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-17-5268G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653639 | |||||||
| chr15:45653659 | C | T | 5 | a0001c0001t0001g0210 a0001c0001t0001g0308 a0002c0002t0001g0159 others(2): Show |
5 | HG00621.hp1 HG02015.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-5248C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653659 | |||||||
| chr15:45653663 | C | T | 1 | a0002c0002t0001g0133 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-17-5244C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653663 | |||||||
| chr15:45653696 | G | T | 13 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0027 others(10): Show |
14 | HG01255.hp2 HG02145.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-17-5211G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653696 | |||||||
| chr15:45653702 | C | A | 14 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0027 others(11): Show |
15 | HG01255.hp2 HG02145.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.-17-5205C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653702 | |||||||
| chr15:45653898 | C | T | 1 | a0002c0002t0001g0327 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-17-5009C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653898 | |||||||
| chr15:45653933 | C | G | 42 | a0001c0001t0001g0010 a0001c0001t0001g0161 a0001c0001t0001g0162 others(39): Show |
43 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.-17-4974C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45653933 | |||||||
| chr15:45654039 | T | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0243 others(12): Show |
17 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-4868T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654039 | |||||||
| chr15:45654044 | C | A | 1 | a0002c0002t0001g0105 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-17-4863C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654044 | |||||||
| chr15:45654071 | A | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(84): Show |
92 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-17-4836A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654071 | |||||||
| chr15:45654115 | C | CA | 7 | a0001c0001t0001g0041 a0001c0001t0001g0057 a0001c0001t0001g0058 others(4): Show |
7 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-4773dupA | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45654115 | ||||||
| chr15:45654115 | CA | C | 20 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0056 others(17): Show |
20 | HG00735.hp2 HG01081.hp1 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.-17-4773delA | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45654115 | ||||||
| chr15:45654115 | CAA | C | 80 | a0001c0001t0001g0002 a0001c0001t0001g0100 a0001c0001t0001g0119 others(77): Show |
84 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.-17-4774_-17-4773d others(4): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45654115 | ||||||
| chr15:45654124 | A | AAAC | 15 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(12): Show |
16 | HG01169.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.-17-4781_-17-4780i others(5): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45654124 | ||||||
| chr15:45654124 | A | AAC | 72 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(69): Show |
76 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.-17-4782_-17-4781i others(4): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45654124 | ||||||
| chr15:45654130 | A | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(84): Show |
92 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-17-4777A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654130 | |||||||
| chr15:45654135 | G | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(84): Show |
92 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-17-4772G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654135 | |||||||
| chr15:45654210 | C | T | 1 | a0002c0002t0001g0085 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-17-4697C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654210 | |||||||
| chr15:45654216 | T | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(84): Show |
92 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-17-4691T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654216 | |||||||
| chr15:45654243 | G | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0243 others(12): Show |
17 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-4664G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654243 | |||||||
| chr15:45654419 | A | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(85): Show |
93 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.-17-4488A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654419 | |||||||
| chr15:45654433 | T | C | 4 | a0001c0003t0001g0266 a0001c0003t0001g0267 a0001c0003t0001g0268 others(1): Show |
4 | HG00323.hp1 HG01081.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-4474T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654433 | |||||||
| chr15:45654529 | T | C | 5 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0218 others(2): Show |
5 | HG01884.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-4378T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654529 | |||||||
| chr15:45654653 | G | A | 15 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0243 others(12): Show |
17 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-4254G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654653 | |||||||
| chr15:45654672 | T | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(84): Show |
92 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-17-4235T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654672 | |||||||
| chr15:45654692 | C | T | 1 | a0002c0002t0001g0173 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-17-4215C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654692 | |||||||
| chr15:45654779 | T | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(83): Show |
91 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.-17-4128T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654779 | |||||||
| chr15:45654884 | T | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(84): Show |
92 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-17-4023T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654884 | |||||||
| chr15:45654885 | G | A | 72 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0025 others(69): Show |
75 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.-17-4022G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654885 | |||||||
| chr15:45654930 | G | T | 43 | a0001c0001t0001g0010 a0001c0001t0001g0104 a0001c0001t0001g0161 others(40): Show |
44 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.-17-3977G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45654930 | |||||||
| chr15:45655008 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(84): Show |
92 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-17-3899C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655008 | |||||||
| chr15:45655027 | G | T | 27 | a0001c0001t0001g0183 a0001c0001t0001g0195 a0001c0001t0001g0196 others(24): Show |
29 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.-17-3880G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655027 | |||||||
| chr15:45655195 | C | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0243 others(12): Show |
17 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17-3712C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655195 | |||||||
| chr15:45655212 | G | A | 2 | a0002c0002t0001g0017 a0002c0002t0001g0260 |
2 | HG00408.hp1 HG00438.hp2 |
intron_variant | MODIFIER | c.-17-3695G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655212 | |||||||
| chr15:45655421 | G | A | 71 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0025 others(68): Show |
74 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.-17-3486G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655421 | |||||||
| chr15:45655427 | A | G | 1 | a0001c0001t0007g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-17-3480A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655427 | |||||||
| chr15:45655517 | G | T | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-17-3390G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655517 | |||||||
| chr15:45655586 | G | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(87): Show |
95 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.-17-3321G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655586 | |||||||
| chr15:45655631 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-17-3276A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655631 | |||||||
| chr15:45655646 | G | A | 3 | a0001c0001t0002g0008 a0002c0002t0001g0221 a0002c0002t0001g0222 |
4 | HG00642.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-3261G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655646 | |||||||
| chr15:45655681 | C | CT | 7 | a0001c0001t0001g0089 a0001c0001t0001g0261 a0001c0001t0004g0321 others(4): Show |
7 | HG01884.hp1 HG02055.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-3212dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45655681 | ||||||
| chr15:45655681 | C | CTT | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(138): Show |
149 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.-17-3213_-17-3212d others(4): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45655681 | ||||||
| chr15:45655681 | C | CTTT | 45 | a0001c0001t0001g0010 a0001c0001t0001g0104 a0001c0001t0001g0161 others(42): Show |
46 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.-17-3214_-17-3212d others(5): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45655681 | ||||||
| chr15:45655746 | C | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0029 others(77): Show |
84 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.-17-3161C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655746 | |||||||
| chr15:45655769 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG00140.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-17-3138C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655769 | |||||||
| chr15:45655776 | C | T | 3 | a0001c0003t0001g0267 a0001c0003t0001g0268 a0001c0003t0001g0281 |
3 | HG00323.hp1 HG01081.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-17-3131C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655776 | |||||||
| chr15:45655841 | G | C | 3 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0003g0314 |
3 | HG02109.hp1 HG02109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-17-3066G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655841 | |||||||
| chr15:45655879 | A | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0019 others(81): Show |
88 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.-17-3028A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655879 | |||||||
| chr15:45655892 | G | A | 3 | a0001c0001t0001g0034 a0001c0003t0001g0121 a0002c0002t0001g0045 |
3 | HG01361.hp1 HG02886.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.-17-3015G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655892 | |||||||
| chr15:45655953 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-17-2954A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655953 | |||||||
| chr15:45655971 | C | T | 38 | a0001c0001t0001g0010 a0001c0001t0001g0088 a0001c0001t0001g0104 others(35): Show |
39 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.-17-2936C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655971 | |||||||
| chr15:45655986 | A | AT | 22 | a0001c0001t0001g0046 a0001c0001t0001g0111 a0001c0001t0001g0144 others(19): Show |
22 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.-17-2908dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45655986 | ||||||
| chr15:45655999 | T | C | 1 | a0001c0001t0004g0321 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-17-2908T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45655999 | |||||||
| chr15:45655999 | TC | T | 23 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0101 others(20): Show |
25 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.-17-2904delC | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45655999 | ||||||
| chr15:45656000 | C | T | 153 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(150): Show |
160 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.-17-2907C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45656000 | |||||||
| chr15:45656104 | C | G | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(198): Show |
210 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.-17-2803C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45656104 | |||||||
| chr15:45656110 | A | G | 13 | a0001c0001t0001g0029 a0001c0001t0001g0101 a0001c0001t0001g0118 others(10): Show |
13 | HG01255.hp2 HG02145.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-17-2797A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45656110 | |||||||
| chr15:45656186 | G | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
225 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.-17-2721G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45656186 | |||||||
| chr15:45656335 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-17-2572C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45656335 | |||||||
| chr15:45656336 | T | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(216): Show |
228 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.-17-2571T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45656336 | |||||||
| chr15:45656356 | G | A | 8 | a0001c0001t0001g0232 a0001c0001t0001g0259 a0001c0003t0001g0220 others(5): Show |
8 | HG02647.hp2 HG02698.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17-2551G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45656356 | |||||||
| chr15:45656456 | AT | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(133): Show |
142 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.-17-2437delT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45656456 | ||||||
| chr15:45656525 | C | G | 2 | a0001c0001t0001g0005 a0001c0001t0001g0139 |
3 | NA18954.hp2 NA19007.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-17-2382C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45656525 | |||||||
| chr15:45656536 | T | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(221): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.-17-2371T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45656536 | |||||||
| chr15:45656731 | C | T | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(226): Show |
238 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.-17-2176C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45656731 | |||||||
| chr15:45656863 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-17-2044G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45656863 | |||||||
| chr15:45656880 | C | CT | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(220): Show |
232 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.-17-2026dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45656880 | ||||||
| chr15:45656917 | G | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(129): Show |
138 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.-17-1990G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45656917 | |||||||
| chr15:45656944 | A | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(223): Show |
235 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.-17-1963A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45656944 | |||||||
| chr15:45656961 | C | T | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(218): Show |
230 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.-17-1946C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45656961 | |||||||
| chr15:45657056 | T | C | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(226): Show |
238 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.-17-1851T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657056 | |||||||
| chr15:45657107 | C | CA | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(223): Show |
235 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.-17-1800_-17-1799i others(3): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657107 | |||||||
| chr15:45657192 | T | G | 1 | a0001c0001t0003g0312 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-17-1715T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657192 | |||||||
| chr15:45657240 | C | G | 57 | a0001c0001t0001g0010 a0001c0001t0001g0104 a0001c0001t0001g0144 others(54): Show |
59 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.-17-1667C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657240 | |||||||
| chr15:45657252 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-1655G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657252 | |||||||
| chr15:45657265 | A | AT | 19 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0243 others(16): Show |
21 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-1631dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45657265 | ||||||
| chr15:45657265 | A | ATT | 107 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0021 others(104): Show |
111 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.-17-1632_-17-1631d others(4): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45657265 | ||||||
| chr15:45657265 | A | ATTT | 25 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(22): Show |
26 | HG00741.hp1 HG01099.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.-17-1633_-17-1631d others(5): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45657265 | ||||||
| chr15:45657265 | A | ATTTT | 76 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(73): Show |
78 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.-17-1634_-17-1631d others(6): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45657265 | ||||||
| chr15:45657288 | A | T | 10 | a0001c0001t0001g0029 a0001c0001t0001g0101 a0001c0001t0001g0118 others(7): Show |
10 | HG01255.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-1619A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657288 | |||||||
| chr15:45657470 | T | C | 11 | a0001c0001t0001g0018 a0001c0001t0001g0060 a0001c0001t0001g0061 others(8): Show |
11 | HG00408.hp1 HG00438.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.-17-1437T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657470 | |||||||
| chr15:45657528 | C | G | 1 | a0001c0001t0001g0095 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-17-1379C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657528 | |||||||
| chr15:45657646 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-17-1261A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657646 | |||||||
| chr15:45657676 | T | C | 26 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0027 others(23): Show |
27 | HG00408.hp1 HG00438.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.-17-1231T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657676 | |||||||
| chr15:45657688 | C | T | 123 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0021 others(120): Show |
127 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.-17-1219C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657688 | |||||||
| chr15:45657745 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-17-1162C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657745 | |||||||
| chr15:45657785 | T | A | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(223): Show |
235 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.-17-1122T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657785 | |||||||
| chr15:45657940 | A | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(223): Show |
235 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.-17-967A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657940 | |||||||
| chr15:45657944 | A | C | 1 | a0001c0001t0001g0167 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-17-963A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657944 | |||||||
| chr15:45657961 | A | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(223): Show |
235 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.-17-946A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45657961 | |||||||
| chr15:45658061 | G | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
238 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.-17-846G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658061 | |||||||
| chr15:45658075 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-17-832G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658075 | |||||||
| chr15:45658169 | A | G | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(226): Show |
238 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.-17-738A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658169 | |||||||
| chr15:45658193 | C | A | 1 | a0001c0001t0001g0167 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-17-714C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658193 | |||||||
| chr15:45658193 | C | T | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
234 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.-17-714C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658193 | |||||||
| chr15:45658203 | C | A | 1 | a0001c0001t0001g0167 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-17-704C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658203 | |||||||
| chr15:45658237 | G | A | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
234 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.-17-670G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658237 | |||||||
| chr15:45658283 | C | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0095 a0001c0001t0001g0101 others(39): Show |
45 | HG00639.hp1 HG00738.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.-17-624C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658283 | |||||||
| chr15:45658286 | T | A | 2 | a0001c0001t0001g0028 a0005c0008t0001g0094 |
2 | HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-17-621T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658286 | |||||||
| chr15:45658325 | C | G | 18 | a0001c0001t0001g0001 a0001c0001t0001g0232 a0001c0001t0001g0243 others(15): Show |
20 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.-17-582C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658325 | |||||||
| chr15:45658330 | C | T | 54 | a0001c0001t0001g0010 a0001c0001t0001g0104 a0001c0001t0001g0130 others(51): Show |
56 | HG00323.hp1 HG00438.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.-17-577C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658330 | |||||||
| chr15:45658371 | G | A | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(221): Show |
233 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.-17-536G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658371 | |||||||
| chr15:45658484 | G | T | 2 | a0001c0001t0001g0101 a0001c0001t0001g0154 |
2 | HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-17-423G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658484 | |||||||
| chr15:45658521 | C | CACTG | 3 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0325 |
3 | HG02717.hp2 HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-17-385_-17-382dup others(4): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 45658521 | ||||||
| chr15:45658521 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-17-386C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658521 | |||||||
| chr15:45658653 | A | G | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(220): Show |
233 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.-17-254A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658653 | |||||||
| chr15:45658663 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-244A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658663 | |||||||
| chr15:45658687 | C | A | 204 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(201): Show |
211 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.-17-220C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658687 | |||||||
| chr15:45658717 | C | T | 202 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(199): Show |
209 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.-17-190C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658717 | |||||||
| chr15:45658760 | C | T | 81 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0034 others(78): Show |
84 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.-17-147C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658760 | |||||||
| chr15:45658860 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-17-47C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658860 | |||||||
| chr15:45658866 | T | G | 51 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0061 others(48): Show |
52 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.-17-41T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658866 | |||||||
| chr15:45658873 | C | G | 1 | a0001c0001t0001g0056 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-17-34C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 1/9 | chr15 | 45658873 | |||||||
| chr15:45659195 | C | CGTGT | 4 | a0001c0001t0004g0321 a0004c0006t0004g0319 a0004c0006t0004g0320 others(1): Show |
4 | HG02055.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+50_234+53dupTG others(2): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr15 | 45659195 | ||||||
| chr15:45659209 | T | A | 1 | a0001c0001t0001g0110 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.234+52T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45659209 | |||||||
| chr15:45659211 | A | AGT | 4 | a0001c0001t0001g0029 a0001c0001t0001g0316 a0001c0003t0001g0102 others(1): Show |
4 | HG02647.hp2 HG02723.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+71_234+72dupGT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr15 | 45659211 | ||||||
| chr15:45659211 | A | T | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(116): Show |
124 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.234+54A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45659211 | |||||||
| chr15:45659215 | T | A | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(115): Show |
123 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.234+58T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45659215 | |||||||
| chr15:45659273 | T | C | 169 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(166): Show |
176 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(173): Show |
intron_variant | MODIFIER | c.234+116T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45659273 | |||||||
| chr15:45659293 | G | A | 6 | a0001c0001t0001g0179 a0001c0001t0001g0299 a0002c0002t0001g0189 others(3): Show |
6 | NA18982.hp1 NA18984.hp2 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.234+136G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45659293 | |||||||
| chr15:45659353 | A | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(216): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.234+196A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45659353 | |||||||
| chr15:45659462 | A | G | 1 | a0001c0001t0001g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.234+305A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45659462 | |||||||
| chr15:45659512 | C | T | 11 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0062 others(8): Show |
13 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.234+355C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45659512 | |||||||
| chr15:45659523 | T | C | 1 | a0001c0001t0002g0037 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.234+366T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45659523 | |||||||
| chr15:45659540 | C | G | 42 | a0001c0001t0001g0002 a0001c0001t0001g0107 a0001c0001t0001g0108 others(39): Show |
46 | HG00597.hp1 HG00609.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.234+383C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45659540 | |||||||
| chr15:45659613 | T | C | 8 | a0001c0001t0001g0101 a0001c0001t0001g0228 a0001c0001t0001g0261 others(5): Show |
8 | HG01109.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.234+456T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45659613 | |||||||
| chr15:45659715 | A | G | 4 | a0001c0001t0001g0113 a0001c0001t0001g0246 a0001c0001t0001g0247 others(1): Show |
4 | HG00639.hp1 HG01106.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+558A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45659715 | |||||||
| chr15:45659781 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.234+624C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45659781 | |||||||
| chr15:45659797 | T | G | 1 | a0007c0011t0004g0322 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.234+640T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45659797 | |||||||
| chr15:45659837 | CTTTGAGA others(4): Show |
C | 1 | a0001c0001t0001g0291 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.234+682_234+692del others(11): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr15 | 45659837 | ||||||
| chr15:45659962 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.234+805G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45659962 | |||||||
| chr15:45660229 | G | C | 1 | a0001c0001t0001g0068 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.234+1072G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45660229 | |||||||
| chr15:45660264 | A | G | 49 | a0001c0001t0001g0029 a0001c0001t0001g0127 a0001c0001t0001g0151 others(46): Show |
49 | HG00323.hp2 HG00621.hp1 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.234+1107A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45660264 | |||||||
| chr15:45660279 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.234+1122C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45660279 | |||||||
| chr15:45660335 | A | G | 13 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0166 others(10): Show |
13 | HG00323.hp1 HG01081.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.234+1178A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45660335 | |||||||
| chr15:45660455 | G | A | 5 | a0001c0001t0001g0060 a0001c0001t0001g0091 a0001c0001t0001g0146 others(2): Show |
5 | HG01496.hp2 HG02451.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+1298G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45660455 | |||||||
| chr15:45660474 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.234+1317A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45660474 | |||||||
| chr15:45660630 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.235-1325A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45660630 | |||||||
| chr15:45660946 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.235-1009C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45660946 | |||||||
| chr15:45660950 | G | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0043 others(3): Show |
7 | HG01169.hp2 HG02257.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.235-1005G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45660950 | |||||||
| chr15:45660961 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.235-994C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45660961 | |||||||
| chr15:45661278 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0288 |
2 | HG00438.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.235-677G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661278 | |||||||
| chr15:45661289 | T | TA | 3 | a0002c0002t0001g0083 a0005c0008t0001g0094 a0007c0011t0004g0322 |
3 | HG02055.hp1 HG02809.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.235-666_235-665ins others(1): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | |||||||
| chr15:45661289 | T | TAA | 61 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0044 others(58): Show |
64 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.235-666_235-665ins others(2): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | |||||||
| chr15:45661289 | T | TAAA | 31 | a0001c0001t0001g0018 a0001c0001t0001g0034 a0001c0001t0001g0042 others(28): Show |
32 | HG00621.hp2 HG00735.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.235-666_235-665ins others(3): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | |||||||
| chr15:45661289 | T | TAAAA | 6 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0029 others(3): Show |
6 | HG01257.hp2 HG01981.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.235-666_235-665ins others(4): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | |||||||
| chr15:45661289 | T | TAAAAA | 4 | a0001c0001t0001g0046 a0001c0001t0001g0210 a0001c0001t0001g0261 others(1): Show |
4 | HG03669.hp2 HG06807.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-666_235-665ins others(5): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | |||||||
| chr15:45661289 | T | TAAAAAA | 14 | a0001c0001t0001g0024 a0001c0001t0001g0051 a0001c0001t0001g0052 others(11): Show |
14 | HG00639.hp1 HG01243.hp1 HG02293.hp1 others(11): Show |
intron_variant | MODIFIER | c.235-666_235-665ins others(6): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | |||||||
| chr15:45661289 | T | TAAAAAAA | 6 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0049 others(3): Show |
6 | HG00558.hp2 HG01106.hp2 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.235-666_235-665ins others(7): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | |||||||
| chr15:45661289 | T | TAAAAAAA others(3): Show |
3 | a0001c0001t0001g0123 a0001c0001t0001g0167 a0001c0001t0001g0301 |
3 | HG00423.hp2 NA18993.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.235-666_235-665ins others(10): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | |||||||
| chr15:45661289 | T | TAAAAAAA others(8): Show |
2 | a0001c0001t0001g0168 a0001c0001t0001g0202 |
2 | NA18984.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.235-666_235-665ins others(15): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | |||||||
| chr15:45661289 | T | TAAAAAAA others(9): Show |
8 | a0001c0001t0001g0114 a0001c0001t0001g0140 a0001c0001t0001g0141 others(5): Show |
8 | HG00140.hp2 HG01081.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.235-666_235-665ins others(16): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | |||||||
| chr15:45661289 | T | TAAAAAAA others(10): Show |
8 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0081 others(5): Show |
8 | HG00438.hp1 HG01070.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.235-666_235-665ins others(17): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | |||||||
| chr15:45661289 | T | TAAAAAAA others(15): Show |
1 | a0001c0003t0001g0121 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.235-666_235-665ins others(22): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | |||||||
| chr15:45661289 | T | TAGAA | 29 | a0001c0001t0001g0151 a0001c0001t0001g0176 a0001c0001t0001g0182 others(26): Show |
29 | HG00323.hp2 HG00621.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.235-666_235-665ins others(4): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | |||||||
| chr15:45661289 | T | TAGAAA | 9 | a0001c0001t0001g0127 a0001c0001t0001g0175 a0001c0001t0001g0192 others(6): Show |
9 | HG01099.hp2 HG01346.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.235-666_235-665ins others(5): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | |||||||
| chr15:45661289 | T | TAGAAAAA others(9): Show |
1 | a0001c0001t0001g0101 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.235-666_235-665ins others(16): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | |||||||
| chr15:45661289 | TTAAAA | T | 16 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0166 others(13): Show |
16 | HG00099.hp2 HG00323.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.235-665_235-661del others(5): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | |||||||
| chr15:45661289 | TTAAAAAA others(2): Show |
T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0043 others(3): Show |
7 | HG01169.hp2 HG02257.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.235-665_235-657del others(9): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661289 | |||||||
| chr15:45661290 | T | A | 193 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(190): Show |
197 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.235-665T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661290 | |||||||
| chr15:45661290 | T | TA | 13 | a0001c0001t0001g0061 a0001c0001t0001g0067 a0001c0001t0001g0076 others(10): Show |
13 | HG00140.hp1 HG00741.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.235-641dupA | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr15 | 45661290 | ||||||
| chr15:45661290 | TA | T | 26 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0107 others(23): Show |
28 | HG00609.hp2 HG01496.hp1 HG01952.hp2 others(25): Show |
intron_variant | MODIFIER | c.235-641delA | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr15 | 45661290 | ||||||
| chr15:45661343 | A | G | 6 | a0001c0001t0001g0232 a0001c0001t0001g0242 a0001c0001t0001g0323 others(3): Show |
6 | HG02559.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.235-612A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661343 | |||||||
| chr15:45661363 | T | C | 2 | a0001c0003t0001g0080 a0001c0003t0001g0093 |
2 | HG00099.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.235-592T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661363 | |||||||
| chr15:45661468 | T | G | 1 | a0001c0003t0001g0069 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.235-487T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661468 | |||||||
| chr15:45661557 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.235-398A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661557 | |||||||
| chr15:45661594 | A | T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0056 |
2 | NA18960.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.235-361A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661594 | |||||||
| chr15:45661799 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0210 |
3 | HG02165.hp2 HG02523.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.235-156C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661799 | |||||||
| chr15:45661810 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0043 others(1): Show |
5 | HG01169.hp2 HG02896.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.235-145C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 2/9 | chr15 | 45661810 | |||||||
| chr15:45662136 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.405+11A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45662136 | |||||||
| chr15:45662144 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.405+19A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45662144 | |||||||
| chr15:45662157 | A | G | 1 | a0005c0008t0001g0094 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.405+32A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45662157 | |||||||
| chr15:45662278 | G | C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0043 others(3): Show |
7 | HG01169.hp2 HG02257.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.405+153G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45662278 | |||||||
| chr15:45662280 | A | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0043 others(3): Show |
7 | HG01169.hp2 HG02257.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.405+155A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45662280 | |||||||
| chr15:45662288 | A | G | 6 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0043 others(3): Show |
7 | HG01169.hp2 HG02257.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.405+163A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45662288 | |||||||
| chr15:45662359 | C | G | 28 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0081 others(25): Show |
28 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.405+234C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45662359 | |||||||
| chr15:45662608 | G | A | 26 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0081 others(23): Show |
26 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.405+483G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45662608 | |||||||
| chr15:45662812 | A | C | 1 | a0005c0008t0001g0229 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.405+687A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45662812 | |||||||
| chr15:45663156 | T | C | 1 | a0001c0003t0001g0073 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.405+1031T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45663156 | |||||||
| chr15:45663303 | C | T | 55 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0043 others(52): Show |
56 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.405+1178C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45663303 | |||||||
| chr15:45663634 | G | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0107 a0001c0001t0001g0108 others(26): Show |
31 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.405+1509G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45663634 | |||||||
| chr15:45663733 | C | G | 1 | a0001c0001t0001g0057 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.405+1608C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45663733 | |||||||
| chr15:45663775 | T | TA | 5 | a0001c0001t0001g0130 a0001c0001t0001g0137 a0001c0001t0001g0291 others(2): Show |
5 | HG02074.hp2 NA18967.hp2 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.405+1658dupA | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45663775 | ||||||
| chr15:45663908 | T | C | 33 | a0001c0001t0001g0151 a0001c0001t0001g0175 a0001c0001t0001g0176 others(30): Show |
33 | HG00323.hp2 HG00621.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.405+1783T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45663908 | |||||||
| chr15:45663936 | A | T | 1 | a0001c0001t0001g0089 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.405+1811A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45663936 | |||||||
| chr15:45663937 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.405+1812C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45663937 | |||||||
| chr15:45663982 | C | T | 4 | a0004c0006t0001g0311 a0004c0006t0004g0319 a0004c0006t0004g0320 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.405+1857C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45663982 | |||||||
| chr15:45663994 | A | C | 25 | a0001c0001t0001g0038 a0001c0001t0001g0054 a0001c0001t0001g0088 others(22): Show |
25 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.405+1869A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45663994 | |||||||
| chr15:45664138 | A | G | 7 | a0001c0001t0001g0179 a0001c0001t0001g0196 a0001c0001t0001g0198 others(4): Show |
7 | HG00597.hp1 NA18956.hp2 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.405+2013A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45664138 | |||||||
| chr15:45664194 | T | C | 1 | a0001c0001t0001g0273 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.405+2069T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45664194 | |||||||
| chr15:45664195 | A | G | 2 | a0001c0001t0001g0154 a0005c0008t0001g0326 |
2 | HG02280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.405+2070A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45664195 | |||||||
| chr15:45664240 | T | A | 1 | a0001c0001t0001g0226 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.405+2115T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45664240 | |||||||
| chr15:45664584 | G | A | 4 | a0004c0006t0001g0311 a0004c0006t0004g0319 a0004c0006t0004g0320 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.405+2459G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45664584 | |||||||
| chr15:45664595 | C | T | 1 | a0001c0001t0002g0022 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.405+2470C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45664595 | |||||||
| chr15:45664607 | C | A | 6 | a0001c0001t0001g0232 a0001c0001t0001g0242 a0001c0001t0001g0323 others(3): Show |
6 | HG02559.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.405+2482C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45664607 | |||||||
| chr15:45664614 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.405+2489A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45664614 | |||||||
| chr15:45664654 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.405+2529G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45664654 | |||||||
| chr15:45664690 | G | T | 24 | a0001c0001t0001g0038 a0001c0001t0001g0088 a0001c0001t0001g0123 others(21): Show |
24 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.405+2565G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45664690 | |||||||
| chr15:45664704 | G | C | 1 | a0002c0002t0001g0092 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.405+2579G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45664704 | |||||||
| chr15:45664940 | G | T | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.405+2815G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45664940 | |||||||
| chr15:45665040 | G | A | 1 | a0001c0001t0001g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.405+2915G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45665040 | |||||||
| chr15:45665085 | G | C | 1 | a0001c0001t0001g0023 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.405+2960G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45665085 | |||||||
| chr15:45665308 | C | T | 1 | a0002c0002t0001g0012 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.405+3183C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45665308 | |||||||
| chr15:45665321 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.405+3196A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45665321 | |||||||
| chr15:45665343 | A | G | 2 | a0001c0001t0001g0116 a0009c0014t0001g0115 |
2 | HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.405+3218A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45665343 | |||||||
| chr15:45665537 | AT | A | 178 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0018 others(175): Show |
184 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.405+3415delT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45665537 | ||||||
| chr15:45665584 | C | CT | 15 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0036 others(12): Show |
16 | HG00423.hp1 HG01169.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.405+3475dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45665584 | ||||||
| chr15:45665584 | CT | C | 7 | a0001c0001t0001g0030 a0001c0001t0001g0232 a0002c0002t0001g0083 others(4): Show |
7 | HG01109.hp2 HG02055.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.405+3475delT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45665584 | ||||||
| chr15:45665704 | C | T | 1 | a0002c0002t0001g0083 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.405+3579C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45665704 | |||||||
| chr15:45665740 | C | T | 1 | a0002c0002t0001g0200 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.405+3615C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45665740 | |||||||
| chr15:45665750 | A | T | 1 | a0001c0001t0001g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.405+3625A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45665750 | |||||||
| chr15:45665752 | T | A | 87 | a0001c0001t0001g0018 a0001c0001t0001g0101 a0001c0001t0001g0151 others(84): Show |
90 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.405+3627T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45665752 | |||||||
| chr15:45665775 | G | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0088 others(46): Show |
51 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.405+3650G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45665775 | |||||||
| chr15:45665862 | G | A | 1 | a0005c0008t0001g0094 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.405+3737G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45665862 | |||||||
| chr15:45665924 | A | T | 1 | a0001c0001t0001g0199 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.405+3799A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45665924 | |||||||
| chr15:45665999 | G | A | 2 | a0005c0008t0001g0094 a0005c0008t0001g0229 |
2 | HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.405+3874G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45665999 | |||||||
| chr15:45666033 | G | C | 1 | a0001c0001t0001g0072 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.406-3895G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666033 | |||||||
| chr15:45666204 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.406-3724A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666204 | |||||||
| chr15:45666329 | C | G | 1 | a0001c0001t0001g0072 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.406-3599C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666329 | |||||||
| chr15:45666342 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.406-3586G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666342 | |||||||
| chr15:45666511 | G | A | 87 | a0001c0001t0001g0018 a0001c0001t0001g0101 a0001c0001t0001g0151 others(84): Show |
90 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.406-3417G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666511 | |||||||
| chr15:45666555 | A | G | 1 | a0002c0002t0001g0187 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.406-3373A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666555 | |||||||
| chr15:45666651 | A | G | 52 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0088 others(49): Show |
54 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.406-3277A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666651 | |||||||
| chr15:45666774 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.406-3154T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666774 | |||||||
| chr15:45666789 | T | TCTCTCCC others(13): Show |
38 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0027 others(35): Show |
39 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.406-3102_406-3083d others(22): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45666789 | ||||||
| chr15:45666803 | T | C | 1 | a0002c0002t0001g0083 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.406-3125T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666803 | |||||||
| chr15:45666819 | C | CCCCTCCT others(20): Show |
1 | a0001c0001t0001g0199 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.406-3083_406-3082i others(29): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45666819 | ||||||
| chr15:45666831 | T | TCTCCCCT others(18): Show |
4 | a0001c0001t0001g0095 a0001c0003t0001g0073 a0001c0003t0001g0233 others(1): Show |
4 | HG01169.hp1 HG02698.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.406-3083_406-3082i others(27): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45666831 | ||||||
| chr15:45666836 | C | CCTCCCCT others(13): Show |
6 | a0001c0001t0001g0232 a0001c0001t0001g0242 a0001c0001t0001g0323 others(3): Show |
6 | HG02559.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.406-3077_406-3058d others(22): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45666836 | ||||||
| chr15:45666836 | C | CCTCCCCT others(12): Show |
1 | a0001c0001t0001g0205 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.406-3082_406-3081i others(21): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45666836 | ||||||
| chr15:45666841 | CCTCCCCT others(3): Show |
C | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.406-3082_406-3073d others(12): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45666841 | ||||||
| chr15:45666846 | C | T | 4 | a0001c0001t0001g0095 a0001c0003t0001g0073 a0001c0003t0001g0233 others(1): Show |
4 | HG01169.hp1 HG02698.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.406-3082C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666846 | |||||||
| chr15:45666851 | T | C | 1 | a0001c0001t0001g0205 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.406-3077T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666851 | |||||||
| chr15:45666856 | T | C | 4 | a0001c0001t0001g0095 a0001c0003t0001g0073 a0001c0003t0001g0233 others(1): Show |
4 | HG01169.hp1 HG02698.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.406-3072T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666856 | |||||||
| chr15:45666856 | T | TCTCCC | 18 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0043 others(15): Show |
19 | HG00099.hp2 HG00323.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.406-3052_406-3048d others(7): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45666856 | ||||||
| chr15:45666856 | TCTCCC | T | 90 | a0001c0001t0001g0018 a0001c0001t0001g0151 a0001c0001t0001g0175 others(87): Show |
93 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.406-3052_406-3048d others(7): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45666856 | ||||||
| chr15:45666861 | C | CCTCCCCT others(13): Show |
48 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0088 others(45): Show |
50 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.406-3053_406-3052i others(22): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45666861 | ||||||
| chr15:45666861 | C | CCTCCCCT others(13): Show |
2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.406-3053_406-3052i others(22): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45666861 | ||||||
| chr15:45666861 | C | T | 2 | a0001c0001t0001g0205 a0001c0001t0001g0261 |
2 | HG03669.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.406-3067C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666861 | |||||||
| chr15:45666866 | C | T | 1 | a0002c0002t0005g0048 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.406-3062C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666866 | |||||||
| chr15:45666909 | T | C | 4 | a0001c0001t0001g0090 a0001c0001t0001g0261 a0005c0008t0001g0094 others(1): Show |
4 | HG00738.hp2 HG02809.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.406-3019T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666909 | |||||||
| chr15:45666924 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.406-3004C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666924 | |||||||
| chr15:45666927 | T | C | 1 | a0001c0001t0001g0199 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.406-3001T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666927 | |||||||
| chr15:45666928 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.406-3000C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666928 | |||||||
| chr15:45666939 | T | TCCTTTCT others(12): Show |
10 | a0001c0001t0001g0060 a0001c0001t0001g0063 a0001c0001t0001g0067 others(7): Show |
10 | HG00741.hp1 HG01496.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.406-2985_406-2967d others(21): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45666939 | ||||||
| chr15:45666956 | T | A | 52 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0088 others(49): Show |
54 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.406-2972T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666956 | |||||||
| chr15:45666989 | C | T | 89 | a0001c0001t0001g0018 a0001c0001t0001g0101 a0001c0001t0001g0151 others(86): Show |
92 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.406-2939C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45666989 | |||||||
| chr15:45667011 | C | CCCCT | 84 | a0001c0001t0001g0018 a0001c0001t0001g0151 a0001c0001t0001g0175 others(81): Show |
87 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.406-2900_406-2897d others(6): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45667011 | ||||||
| chr15:45667011 | C | CCCCTCCC others(5): Show |
1 | a0001c0003t0001g0121 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.406-2908_406-2897d others(14): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45667011 | ||||||
| chr15:45667011 | C | CCCCTCCC others(13): Show |
1 | a0001c0001t0001g0101 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.406-2916_406-2897d others(22): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45667011 | ||||||
| chr15:45667011 | CCCCT | C | 6 | a0001c0001t0001g0232 a0001c0001t0001g0242 a0001c0001t0001g0323 others(3): Show |
6 | HG02559.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.406-2900_406-2897d others(6): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45667011 | ||||||
| chr15:45667028 | C | CCCTCCCT others(9): Show |
50 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0088 others(47): Show |
52 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.406-2897_406-2896i others(18): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45667028 | ||||||
| chr15:45667028 | C | CCCTCCCT others(5): Show |
1 | a0001c0001t0001g0206 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.406-2897_406-2896i others(14): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45667028 | ||||||
| chr15:45667028 | C | CCCTCCCT others(1): Show |
3 | a0001c0001t0001g0261 a0005c0008t0001g0094 a0005c0008t0001g0229 |
3 | HG02809.hp2 HG03486.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.406-2897_406-2896i others(10): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45667028 | ||||||
| chr15:45667032 | T | C | 1 | a0002c0002t0001g0012 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.406-2896T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667032 | |||||||
| chr15:45667049 | T | C | 1 | a0002c0002t0001g0012 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.406-2879T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667049 | |||||||
| chr15:45667127 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.406-2801T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667127 | |||||||
| chr15:45667140 | C | T | 1 | a0002c0002t0001g0129 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.406-2788C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667140 | |||||||
| chr15:45667141 | T | C | 1 | a0002c0002t0001g0129 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.406-2787T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667141 | |||||||
| chr15:45667142 | C | T | 1 | a0002c0002t0001g0129 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.406-2786C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667142 | |||||||
| chr15:45667175 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.406-2753T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667175 | |||||||
| chr15:45667255 | A | G | 244 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(241): Show |
252 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.406-2673A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667255 | |||||||
| chr15:45667316 | A | T | 87 | a0001c0001t0001g0018 a0001c0001t0001g0151 a0001c0001t0001g0175 others(84): Show |
90 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.406-2612A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667316 | |||||||
| chr15:45667647 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.406-2281C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667647 | |||||||
| chr15:45667763 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.406-2165G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667763 | |||||||
| chr15:45667764 | T | G | 1 | a0001c0001t0001g0130 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.406-2164T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667764 | |||||||
| chr15:45667765 | T | A | 1 | a0001c0001t0001g0130 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.406-2163T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667765 | |||||||
| chr15:45667768 | C | G | 1 | a0001c0001t0001g0130 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.406-2160C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667768 | |||||||
| chr15:45667769 | A | C | 1 | a0001c0001t0001g0130 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.406-2159A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667769 | |||||||
| chr15:45667778 | A | T | 1 | a0001c0001t0001g0130 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.406-2150A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667778 | |||||||
| chr15:45667837 | G | T | 1 | a0005c0008t0001g0094 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.406-2091G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667837 | |||||||
| chr15:45667859 | C | T | 6 | a0001c0001t0001g0232 a0001c0001t0001g0242 a0001c0001t0001g0323 others(3): Show |
6 | HG02559.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.406-2069C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667859 | |||||||
| chr15:45667918 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.406-2010T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667918 | |||||||
| chr15:45667925 | A | C | 5 | a0001c0001t0001g0262 a0002c0002t0001g0014 a0002c0002t0001g0015 others(2): Show |
5 | HG02717.hp1 HG02809.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.406-2003A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667925 | |||||||
| chr15:45667941 | C | CT | 62 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0021 others(59): Show |
63 | HG00099.hp2 HG00558.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.406-1966dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45667941 | ||||||
| chr15:45667941 | C | CTT | 10 | a0001c0001t0001g0043 a0001c0001t0001g0072 a0001c0001t0001g0095 others(7): Show |
10 | HG01169.hp2 HG01433.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.406-1967_406-1966d others(4): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45667941 | ||||||
| chr15:45667941 | CT | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(144): Show |
152 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.406-1966delT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45667941 | ||||||
| chr15:45667945 | T | C | 1 | a0002c0002t0001g0083 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.406-1983T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667945 | |||||||
| chr15:45667946 | T | C | 88 | a0001c0001t0001g0018 a0001c0001t0001g0151 a0001c0001t0001g0175 others(85): Show |
91 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.406-1982T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667946 | |||||||
| chr15:45667947 | T | C | 2 | a0001c0001t0001g0101 a0001c0001t0001g0261 |
2 | HG02145.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.406-1981T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667947 | |||||||
| chr15:45667948 | T | C | 1 | a0002c0002t0001g0079 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.406-1980T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45667948 | |||||||
| chr15:45668006 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.406-1922G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45668006 | |||||||
| chr15:45668018 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.406-1910C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45668018 | |||||||
| chr15:45668143 | G | A | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0018 others(204): Show |
213 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.406-1785G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45668143 | |||||||
| chr15:45668190 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.406-1738C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45668190 | |||||||
| chr15:45668205 | A | T | 2 | a0004c0006t0004g0319 a0004c0006t0004g0320 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.406-1723A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45668205 | |||||||
| chr15:45668234 | G | A | 1 | a0002c0002t0001g0020 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.406-1694G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45668234 | |||||||
| chr15:45668279 | G | A | 1 | a0011c0010t0001g0282 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.406-1649G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45668279 | |||||||
| chr15:45668350 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.406-1578A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45668350 | |||||||
| chr15:45668591 | C | T | 6 | a0001c0001t0001g0232 a0001c0001t0001g0242 a0001c0001t0001g0323 others(3): Show |
6 | HG02559.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.406-1337C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45668591 | |||||||
| chr15:45668608 | A | G | 1 | a0002c0002t0001g0014 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.406-1320A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45668608 | |||||||
| chr15:45668626 | G | A | 1 | a0001c0003t0001g0102 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.406-1302G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45668626 | |||||||
| chr15:45668699 | C | T | 12 | a0001c0001t0001g0060 a0001c0001t0001g0063 a0001c0001t0001g0067 others(9): Show |
12 | HG00741.hp1 HG01496.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.406-1229C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45668699 | |||||||
| chr15:45668703 | C | T | 2 | a0005c0008t0001g0094 a0005c0008t0001g0229 |
2 | HG02809.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.406-1225C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45668703 | |||||||
| chr15:45668927 | G | A | 1 | a0002c0004t0001g0249 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.406-1001G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45668927 | |||||||
| chr15:45668960 | A | G | 1 | a0002c0002t0001g0087 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.406-968A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45668960 | |||||||
| chr15:45669160 | A | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0219 a0001c0001t0003g0317 others(1): Show |
4 | HG02257.hp2 HG02258.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.406-768A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45669160 | |||||||
| chr15:45669162 | T | A | 1 | a0001c0001t0001g0180 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.406-766T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45669162 | |||||||
| chr15:45669175 | T | A | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.406-753T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45669175 | |||||||
| chr15:45669176 | T | A | 4 | a0001c0001t0001g0261 a0002c0002t0001g0159 a0005c0008t0001g0094 others(1): Show |
4 | HG02809.hp2 HG03486.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.406-752T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45669176 | |||||||
| chr15:45669178 | A | AT | 93 | a0001c0001t0001g0018 a0001c0001t0001g0101 a0001c0001t0001g0151 others(90): Show |
96 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.406-741dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45669178 | ||||||
| chr15:45669178 | A | ATT | 55 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0088 others(52): Show |
57 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.406-742_406-741dup others(2): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 45669178 | ||||||
| chr15:45669178 | A | T | 1 | a0002c0002t0001g0159 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.406-750A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45669178 | |||||||
| chr15:45669206 | A | G | 3 | a0001c0001t0001g0153 a0001c0007t0001g0006 a0001c0007t0001g0150 |
4 | HG01884.hp1 HG02965.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.406-722A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45669206 | |||||||
| chr15:45669413 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.406-515C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45669413 | |||||||
| chr15:45669756 | C | T | 3 | a0001c0001t0001g0261 a0005c0008t0001g0094 a0005c0008t0001g0229 |
3 | HG02809.hp2 HG03486.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.406-172C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45669756 | |||||||
| chr15:45669794 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.406-134C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45669794 | |||||||
| chr15:45669843 | A | G | 5 | a0001c0003t0001g0073 a0001c0003t0001g0266 a0001c0003t0001g0267 others(2): Show |
5 | HG00323.hp1 HG01081.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.406-85A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45669843 | |||||||
| chr15:45669885 | C | T | 3 | a0001c0001t0001g0252 a0001c0001t0001g0254 a0001c0001t0001g0255 |
3 | NA18942.hp2 NA18978.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.406-43C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 3/9 | chr15 | 45669885 | |||||||
| chr15:45669986 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG00738.hp2 | splice_region_variant&intron_variant | LOW | c.459+5C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45669986 | |||||||
| chr15:45670084 | C | G | 1 | a0001c0001t0001g0104 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.459+103C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45670084 | |||||||
| chr15:45670094 | C | A | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.459+113C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45670094 | |||||||
| chr15:45670158 | T | C | 1 | a0002c0002t0005g0048 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.459+177T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45670158 | |||||||
| chr15:45670389 | G | A | 1 | a0005c0008t0001g0094 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.459+408G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45670389 | |||||||
| chr15:45670402 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.459+421G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45670402 | |||||||
| chr15:45670429 | A | G | 208 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0018 others(205): Show |
214 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.459+448A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45670429 | |||||||
| chr15:45670507 | T | G | 1 | a0001c0003t0001g0102 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.459+526T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45670507 | |||||||
| chr15:45670546 | T | G | 1 | a0001c0001t0001g0259 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.459+565T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45670546 | |||||||
| chr15:45670679 | C | T | 1 | a0002c0002t0001g0177 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.459+698C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45670679 | |||||||
| chr15:45670854 | T | A | 12 | a0001c0001t0001g0060 a0001c0001t0001g0063 a0001c0001t0001g0067 others(9): Show |
12 | HG00741.hp1 HG01496.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.459+873T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45670854 | |||||||
| chr15:45671064 | A | C | 1 | a0001c0001t0001g0052 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.459+1083A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45671064 | |||||||
| chr15:45671068 | T | A | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.459+1087T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45671068 | |||||||
| chr15:45671308 | C | A | 1 | a0001c0001t0008g0328 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.459+1327C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45671308 | |||||||
| chr15:45671413 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.459+1432C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45671413 | |||||||
| chr15:45671442 | A | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0018 others(207): Show |
216 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.459+1461A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45671442 | |||||||
| chr15:45671589 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.459+1608C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45671589 | |||||||
| chr15:45671595 | C | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0018 others(161): Show |
170 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.459+1614C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45671595 | |||||||
| chr15:45671840 | A | G | 26 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0027 others(23): Show |
27 | HG00099.hp2 HG00323.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.460-1767A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45671840 | |||||||
| chr15:45672014 | C | T | 4 | a0002c0002t0001g0165 a0005c0008t0001g0094 a0005c0008t0001g0229 others(1): Show |
4 | HG02809.hp2 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-1593C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45672014 | |||||||
| chr15:45672063 | C | T | 5 | a0001c0001t0001g0261 a0001c0001t0004g0321 a0005c0008t0001g0094 others(2): Show |
5 | HG02809.hp2 HG03486.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.460-1544C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45672063 | |||||||
| chr15:45672069 | C | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0210 others(1): Show |
4 | HG00558.hp1 HG02165.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-1538C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45672069 | |||||||
| chr15:45672105 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0316 |
2 | HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.460-1502T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45672105 | |||||||
| chr15:45672381 | A | C | 1 | a0002c0002t0001g0172 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.460-1226A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45672381 | |||||||
| chr15:45672534 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.460-1073A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45672534 | |||||||
| chr15:45672612 | T | C | 5 | a0001c0001t0001g0261 a0001c0001t0004g0321 a0005c0008t0001g0094 others(2): Show |
5 | HG02809.hp2 HG03486.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.460-995T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45672612 | |||||||
| chr15:45672675 | A | T | 3 | a0005c0008t0001g0094 a0005c0008t0001g0229 a0005c0008t0001g0326 |
3 | HG02809.hp2 HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.460-932A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45672675 | |||||||
| chr15:45672950 | C | CAG | 167 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0018 others(164): Show |
173 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.460-656_460-655dup others(2): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr15 | 45672950 | ||||||
| chr15:45673243 | A | G | 52 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0088 others(49): Show |
54 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.460-364A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45673243 | |||||||
| chr15:45673316 | G | A | 1 | a0002c0002t0001g0142 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.460-291G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45673316 | |||||||
| chr15:45673443 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.460-164C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45673443 | |||||||
| chr15:45673487 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.460-120G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 4/9 | chr15 | 45673487 | |||||||
| chr15:45673903 | C | T | 52 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0088 others(49): Show |
54 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.654+102C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45673903 | |||||||
| chr15:45674069 | T | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0184 a0001c0001t0001g0191 others(5): Show |
10 | HG00609.hp2 HG01496.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.654+268T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45674069 | |||||||
| chr15:45674087 | C | T | 1 | a0011c0010t0001g0282 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.654+286C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45674087 | |||||||
| chr15:45674158 | T | C | 12 | a0001c0001t0001g0025 a0001c0001t0001g0232 a0001c0001t0001g0242 others(9): Show |
13 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.654+357T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45674158 | |||||||
| chr15:45674174 | C | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0043 others(3): Show |
7 | HG01169.hp2 HG02257.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.654+373C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45674174 | |||||||
| chr15:45674301 | G | A | 11 | a0001c0001t0001g0232 a0001c0001t0001g0242 a0001c0001t0001g0323 others(8): Show |
12 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.654+500G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45674301 | |||||||
| chr15:45674427 | C | T | 19 | a0001c0001t0001g0018 a0001c0001t0001g0067 a0001c0001t0001g0166 others(16): Show |
19 | HG00099.hp2 HG00323.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.654+626C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45674427 | |||||||
| chr15:45674435 | C | T | 8 | a0001c0001t0001g0060 a0001c0001t0001g0063 a0001c0001t0001g0067 others(5): Show |
8 | HG00741.hp1 HG01496.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.654+634C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45674435 | |||||||
| chr15:45674440 | T | TA | 6 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0043 others(3): Show |
7 | HG01169.hp2 HG01243.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.654+654dupA | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr15 | 45674440 | ||||||
| chr15:45674440 | TA | T | 10 | a0001c0001t0001g0025 a0001c0001t0001g0056 a0001c0001t0001g0161 others(7): Show |
10 | HG01069.hp2 HG02293.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.654+654delA | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr15 | 45674440 | ||||||
| chr15:45674455 | A | G | 1 | a0001c0001t0003g0313 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.654+654A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45674455 | |||||||
| chr15:45674620 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.654+819C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45674620 | |||||||
| chr15:45674677 | GA | G | 19 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0036 others(16): Show |
19 | HG00558.hp2 HG00639.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.654+880delA | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr15 | 45674677 | ||||||
| chr15:45674689 | T | G | 1 | a0001c0001t0001g0179 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.654+888T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45674689 | |||||||
| chr15:45674726 | C | A | 1 | a0006c0015t0001g0234 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.654+925C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45674726 | |||||||
| chr15:45674740 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.654+939G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45674740 | |||||||
| chr15:45674816 | G | T | 4 | a0004c0006t0001g0311 a0004c0006t0004g0319 a0004c0006t0004g0320 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.654+1015G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45674816 | |||||||
| chr15:45674926 | C | T | 1 | a0002c0002t0001g0133 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.654+1125C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45674926 | |||||||
| chr15:45675197 | G | A | 1 | a0001c0003t0001g0069 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.655-904G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45675197 | |||||||
| chr15:45675345 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.655-756A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45675345 | |||||||
| chr15:45675399 | A | AT | 89 | a0001c0001t0001g0101 a0001c0001t0001g0215 a0001c0001t0001g0227 others(86): Show |
92 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.655-690dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr15 | 45675399 | ||||||
| chr15:45675402 | T | G | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.655-699T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45675402 | |||||||
| chr15:45675412 | G | T | 89 | a0001c0001t0001g0101 a0001c0001t0001g0215 a0001c0001t0001g0227 others(86): Show |
92 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.655-689G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45675412 | |||||||
| chr15:45675434 | A | T | 1 | a0002c0002t0001g0133 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.655-667A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45675434 | |||||||
| chr15:45675509 | C | T | 16 | a0001c0001t0001g0018 a0001c0001t0001g0166 a0001c0003t0001g0059 others(13): Show |
16 | HG00099.hp2 HG00323.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.655-592C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45675509 | |||||||
| chr15:45675540 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.655-561G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45675540 | |||||||
| chr15:45675592 | C | T | 1 | a0002c0002t0001g0092 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.655-509C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45675592 | |||||||
| chr15:45675651 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.655-450C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45675651 | |||||||
| chr15:45676039 | T | TA | 86 | a0001c0001t0001g0101 a0002c0002t0001g0004 a0002c0002t0001g0007 others(83): Show |
89 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.655-50dupA | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr15 | 45676039 | ||||||
| chr15:45676061 | A | C | 1 | a0001c0001t0001g0101 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.655-40A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45676061 | |||||||
| chr15:45676069 | T | G | 1 | a0005c0008t0001g0229 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.655-32T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 5/9 | chr15 | 45676069 | |||||||
| chr15:45676337 | A | C | 248 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(245): Show |
256 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.864+27A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45676337 | |||||||
| chr15:45676343 | C | T | 1 | a0001c0001t0001g0297 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.864+33C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45676343 | |||||||
| chr15:45676587 | C | T | 4 | a0001c0001t0002g0074 a0005c0008t0001g0094 a0005c0008t0001g0229 others(1): Show |
4 | HG02809.hp2 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.864+277C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45676587 | |||||||
| chr15:45676657 | C | T | 17 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0035 others(14): Show |
17 | HG00735.hp2 HG00738.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.864+347C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45676657 | |||||||
| chr15:45676933 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.864+623C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45676933 | |||||||
| chr15:45676973 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.864+663G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45676973 | |||||||
| chr15:45677006 | A | C | 12 | a0001c0001t0001g0011 a0001c0001t0001g0072 a0001c0001t0001g0145 others(9): Show |
13 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.864+696A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45677006 | |||||||
| chr15:45677039 | T | TA | 102 | a0001c0001t0001g0024 a0001c0001t0001g0036 a0001c0001t0001g0041 others(99): Show |
106 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.864+746dupA | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 45677039 | ||||||
| chr15:45677039 | T | TAA | 6 | a0002c0002t0001g0070 a0002c0002t0001g0142 a0002c0002t0001g0158 others(3): Show |
6 | HG00597.hp2 HG02055.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.864+745_864+746dup others(2): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 45677039 | ||||||
| chr15:45677040 | A | T | 4 | a0001c0001t0001g0261 a0005c0008t0001g0094 a0005c0008t0001g0229 others(1): Show |
4 | HG02809.hp2 HG03486.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.864+730A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45677040 | |||||||
| chr15:45677053 | A | G | 2 | a0005c0008t0001g0094 a0005c0008t0001g0326 |
2 | HG02809.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.864+743A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45677053 | |||||||
| chr15:45677065 | C | A | 4 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0210 others(1): Show |
4 | HG00558.hp1 HG02165.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+755C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45677065 | |||||||
| chr15:45677167 | T | C | 2 | a0001c0001t0001g0241 a0001c0001t0001g0262 |
2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.864+857T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45677167 | |||||||
| chr15:45677177 | TCTTC | T | 43 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0027 others(40): Show |
46 | HG00099.hp2 HG00323.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.864+888_864+891del others(4): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 45677177 | ||||||
| chr15:45677423 | A | G | 2 | a0002c0002t0001g0155 a0002c0002t0001g0327 |
2 | HG01243.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.864+1113A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45677423 | |||||||
| chr15:45677582 | C | T | 16 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0035 others(13): Show |
16 | HG00735.hp2 HG00738.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.864+1272C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45677582 | |||||||
| chr15:45677724 | G | A | 4 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0210 others(1): Show |
4 | HG00558.hp1 HG02165.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+1414G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45677724 | |||||||
| chr15:45677829 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.864+1519T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45677829 | |||||||
| chr15:45677831 | G | A | 2 | a0001c0003t0001g0102 a0001c0003t0001g0220 |
2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.864+1521G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45677831 | |||||||
| chr15:45677867 | A | C | 22 | a0001c0001t0001g0029 a0001c0001t0001g0060 a0001c0001t0001g0063 others(19): Show |
23 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.864+1557A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45677867 | |||||||
| chr15:45677905 | A | G | 1 | a0001c0003t0001g0069 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.864+1595A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45677905 | |||||||
| chr15:45677933 | G | C | 214 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0018 others(211): Show |
220 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.864+1623G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45677933 | |||||||
| chr15:45678014 | CTGTT | C | 23 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0027 others(20): Show |
24 | HG00735.hp2 HG00738.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.864+1709_864+1712d others(6): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 45678014 | ||||||
| chr15:45678115 | T | A | 1 | a0001c0001t0002g0037 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.864+1805T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45678115 | |||||||
| chr15:45678478 | G | A | 21 | a0001c0001t0001g0018 a0001c0003t0001g0059 a0001c0003t0001g0069 others(18): Show |
21 | HG00099.hp2 HG00323.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.864+2168G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45678478 | |||||||
| chr15:45678493 | T | G | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.864+2183T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45678493 | |||||||
| chr15:45678503 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.864+2193C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45678503 | |||||||
| chr15:45678605 | C | T | 2 | a0002c0002t0001g0164 a0002c0002t0001g0236 |
2 | NA18948.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.864+2295C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45678605 | |||||||
| chr15:45678654 | C | T | 3 | a0001c0001t0001g0151 a0001c0001t0001g0175 a0001c0001t0001g0176 |
3 | HG01884.hp2 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.864+2344C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45678654 | |||||||
| chr15:45678656 | G | C | 21 | a0001c0001t0001g0029 a0001c0001t0001g0060 a0001c0001t0001g0063 others(18): Show |
22 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.864+2346G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45678656 | |||||||
| chr15:45678707 | T | G | 1 | a0001c0001t0001g0034 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.864+2397T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45678707 | |||||||
| chr15:45678769 | T | C | 1 | a0002c0002t0001g0157 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.864+2459T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45678769 | |||||||
| chr15:45678885 | T | C | 4 | a0001c0001t0001g0113 a0001c0001t0001g0246 a0001c0001t0001g0247 others(1): Show |
4 | HG00639.hp1 HG01106.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+2575T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45678885 | |||||||
| chr15:45678932 | C | T | 21 | a0001c0001t0001g0018 a0001c0003t0001g0059 a0001c0003t0001g0069 others(18): Show |
21 | HG00099.hp2 HG00323.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.864+2622C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45678932 | |||||||
| chr15:45678983 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.864+2673G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45678983 | |||||||
| chr15:45679469 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.865-3009C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45679469 | |||||||
| chr15:45679557 | C | T | 1 | a0001c0001t0002g0022 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.865-2921C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45679557 | |||||||
| chr15:45679593 | T | C | 247 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(244): Show |
255 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.865-2885T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45679593 | |||||||
| chr15:45679625 | G | T | 1 | a0011c0010t0001g0282 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.865-2853G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45679625 | |||||||
| chr15:45679730 | A | G | 1 | a0008c0012t0001g0253 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.865-2748A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45679730 | |||||||
| chr15:45679847 | C | T | 4 | a0004c0006t0001g0311 a0004c0006t0004g0319 a0004c0006t0004g0320 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.865-2631C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45679847 | |||||||
| chr15:45679968 | T | C | 99 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0027 others(96): Show |
103 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.865-2510T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45679968 | |||||||
| chr15:45679994 | G | A | 324 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(321): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.865-2484G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45679994 | |||||||
| chr15:45680044 | A | G | 47 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(44): Show |
47 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.865-2434A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45680044 | |||||||
| chr15:45680083 | TTTTC | T | 9 | a0002c0002t0001g0157 a0002c0002t0001g0159 a0002c0002t0001g0164 others(6): Show |
9 | HG00621.hp1 HG02683.hp1 HG03927.hp2 others(6): Show |
intron_variant | MODIFIER | c.865-2383_865-2380d others(6): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 45680083 | ||||||
| chr15:45680124 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.865-2354G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45680124 | |||||||
| chr15:45680130 | T | C | 105 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(102): Show |
107 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.865-2348T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45680130 | |||||||
| chr15:45680138 | A | G | 58 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0038 others(55): Show |
60 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.865-2340A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45680138 | |||||||
| chr15:45680415 | T | C | 1 | a0002c0002t0001g0133 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.865-2063T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45680415 | |||||||
| chr15:45680416 | C | T | 1 | a0002c0002t0001g0133 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.865-2062C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45680416 | |||||||
| chr15:45680806 | A | G | 1 | a0001c0001t0001g0054 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.865-1672A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45680806 | |||||||
| chr15:45680918 | G | A | 4 | a0004c0006t0001g0311 a0004c0006t0004g0319 a0004c0006t0004g0320 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.865-1560G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45680918 | |||||||
| chr15:45681067 | C | G | 3 | a0004c0006t0001g0311 a0004c0006t0004g0319 a0004c0006t0004g0320 |
3 | HG01109.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.865-1411C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45681067 | |||||||
| chr15:45681078 | G | A | 1 | a0001c0001t0001g0010 | 2 | NA18947.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.865-1400G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45681078 | |||||||
| chr15:45681087 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.865-1391G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45681087 | |||||||
| chr15:45681089 | G | A | 3 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0193 |
3 | NA18949.hp1 NA18950.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.865-1389G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45681089 | |||||||
| chr15:45681128 | A | G | 1 | a0002c0002t0001g0012 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.865-1350A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45681128 | |||||||
| chr15:45681216 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.865-1262T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45681216 | |||||||
| chr15:45681254 | T | A | 1 | a0002c0002t0001g0221 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.865-1224T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45681254 | |||||||
| chr15:45681305 | G | C | 47 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(44): Show |
47 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.865-1173G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45681305 | |||||||
| chr15:45681312 | C | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0038 others(58): Show |
63 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.865-1166C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45681312 | |||||||
| chr15:45681321 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.865-1157A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45681321 | |||||||
| chr15:45681372 | G | A | 232 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0018 others(229): Show |
239 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.865-1106G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45681372 | |||||||
| chr15:45681508 | C | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0210 others(1): Show |
4 | HG00558.hp1 HG02165.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.865-970C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45681508 | |||||||
| chr15:45681519 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.865-959G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45681519 | |||||||
| chr15:45681728 | C | T | 82 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0027 others(79): Show |
86 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.865-750C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45681728 | |||||||
| chr15:45681981 | G | C | 1 | a0002c0002t0001g0221 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.865-497G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45681981 | |||||||
| chr15:45682048 | T | C | 21 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0036 others(18): Show |
21 | HG00558.hp2 HG00639.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.865-430T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45682048 | |||||||
| chr15:45682145 | T | G | 1 | a0001c0001t0001g0072 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.865-333T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45682145 | |||||||
| chr15:45682225 | G | A | 4 | a0002c0002t0001g0159 a0002c0002t0001g0194 a0002c0002t0001g0211 others(1): Show |
4 | HG00621.hp1 NA18612.hp2 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.865-253G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45682225 | |||||||
| chr15:45682287 | A | G | 1 | a0001c0001t0007g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.865-191A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45682287 | |||||||
| chr15:45682317 | A | G | 1 | a0002c0002t0001g0087 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.865-161A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45682317 | |||||||
| chr15:45682338 | G | A | 50 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(47): Show |
50 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.865-140G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45682338 | |||||||
| chr15:45682395 | A | G | 51 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(48): Show |
51 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.865-83A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45682395 | |||||||
| chr15:45682430 | G | A | 74 | a0001c0001t0001g0030 a0001c0001t0001g0166 a0001c0001t0001g0168 others(71): Show |
77 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.865-48G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45682430 | |||||||
| chr15:45682454 | T | C | 8 | a0001c0001t0001g0101 a0004c0006t0001g0311 a0004c0006t0004g0319 others(5): Show |
8 | HG01109.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.865-24T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 6/9 | chr15 | 45682454 | |||||||
| chr15:45682671 | C | T | 9 | a0001c0001t0001g0060 a0001c0001t0001g0063 a0001c0001t0001g0067 others(6): Show |
9 | HG00741.hp1 HG01496.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1048+10C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45682671 | |||||||
| chr15:45682715 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1048+54A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45682715 | |||||||
| chr15:45682733 | C | A | 3 | a0005c0008t0001g0094 a0005c0008t0001g0229 a0005c0008t0001g0326 |
3 | HG02809.hp2 HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1048+72C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45682733 | |||||||
| chr15:45682899 | C | T | 1 | a0001c0003t0001g0258 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1048+238C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45682899 | |||||||
| chr15:45682914 | C | T | 1 | a0002c0002t0001g0026 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1048+253C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45682914 | |||||||
| chr15:45682990 | C | A | 4 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0210 others(1): Show |
4 | HG00558.hp1 HG02165.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.1048+329C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45682990 | |||||||
| chr15:45683026 | C | CA | 47 | a0001c0001t0001g0029 a0001c0001t0001g0058 a0001c0001t0001g0060 others(44): Show |
47 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.1048+381dupA | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45683026 | ||||||
| chr15:45683026 | C | CAAAAAAA others(22): Show |
1 | a0005c0008t0001g0229 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1048+381_1048+382i others(31): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45683026 | ||||||
| chr15:45683026 | C | CAAAAAAA others(24): Show |
2 | a0005c0008t0001g0094 a0005c0008t0001g0326 |
2 | HG02809.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1048+381_1048+382i others(33): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45683026 | ||||||
| chr15:45683026 | CA | C | 47 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(44): Show |
48 | HG00558.hp2 HG00639.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.1048+381delA | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45683026 | ||||||
| chr15:45683057 | A | C | 1 | a0005c0008t0001g0229 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1048+396A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683057 | |||||||
| chr15:45683068 | G | A | 17 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0035 others(14): Show |
17 | HG00735.hp2 HG00738.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.1048+407G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683068 | |||||||
| chr15:45683072 | A | G | 2 | a0001c0001t0001g0029 a0001c0001t0001g0316 |
2 | HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1048+411A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683072 | |||||||
| chr15:45683153 | G | T | 3 | a0005c0008t0001g0094 a0005c0008t0001g0229 a0005c0008t0001g0326 |
3 | HG02809.hp2 HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1048+492G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683153 | |||||||
| chr15:45683177 | A | G | 2 | a0001c0001t0001g0095 a0001c0001t0001g0149 |
2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1048+516A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683177 | |||||||
| chr15:45683206 | GCT | G | 20 | a0001c0003t0001g0059 a0001c0003t0001g0069 a0001c0003t0001g0073 others(17): Show |
20 | HG00099.hp2 HG00323.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1048+550_1048+551d others(4): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45683206 | ||||||
| chr15:45683215 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1048+554A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683215 | |||||||
| chr15:45683222 | T | C | 9 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0210 others(6): Show |
9 | HG00558.hp1 HG01109.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1048+561T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683222 | |||||||
| chr15:45683245 | G | A | 3 | a0005c0008t0001g0094 a0005c0008t0001g0229 a0005c0008t0001g0326 |
3 | HG02809.hp2 HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1048+584G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683245 | |||||||
| chr15:45683308 | C | T | 2 | a0002c0002t0001g0017 a0002c0002t0001g0260 |
2 | HG00408.hp1 HG00438.hp2 |
intron_variant | MODIFIER | c.1048+647C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683308 | |||||||
| chr15:45683314 | A | T | 2 | a0002c0002t0001g0017 a0002c0002t0001g0260 |
2 | HG00408.hp1 HG00438.hp2 |
intron_variant | MODIFIER | c.1048+653A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683314 | |||||||
| chr15:45683319 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1048+658G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683319 | |||||||
| chr15:45683327 | T | G | 153 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(150): Show |
160 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1048+666T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683327 | |||||||
| chr15:45683350 | G | C | 72 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(69): Show |
73 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.1048+689G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683350 | |||||||
| chr15:45683391 | A | C | 1 | a0001c0001t0001g0138 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1048+730A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683391 | |||||||
| chr15:45683629 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1048+968A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683629 | |||||||
| chr15:45683679 | A | G | 4 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0119 others(1): Show |
4 | HG00741.hp1 HG02698.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1048+1018A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683679 | |||||||
| chr15:45683799 | G | T | 1 | a0002c0002t0001g0092 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1048+1138G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683799 | |||||||
| chr15:45683854 | A | ATG | 9 | a0001c0001t0001g0232 a0001c0001t0001g0242 a0001c0001t0001g0261 others(6): Show |
9 | HG02559.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1048+1211_1048+121 others(6): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45683854 | ||||||
| chr15:45683877 | T | C | 1 | a0005c0008t0001g0229 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1048+1216T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683877 | |||||||
| chr15:45683890 | A | T | 11 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0072 others(8): Show |
11 | HG01884.hp2 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1048+1229A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683890 | |||||||
| chr15:45683892 | TTTTG | T | 70 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(67): Show |
71 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.1048+1255_1048+125 others(8): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45683892 | ||||||
| chr15:45683892 | TTTTGTTT others(5): Show |
T | 1 | a0001c0001t0001g0023 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1048+1247_1048+125 others(16): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45683892 | ||||||
| chr15:45683896 | G | T | 1 | a0001c0001t0001g0101 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1048+1235G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683896 | |||||||
| chr15:45683958 | C | G | 19 | a0001c0003t0001g0059 a0001c0003t0001g0069 a0001c0003t0001g0073 others(16): Show |
19 | HG00099.hp2 HG00323.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.1048+1297C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45683958 | |||||||
| chr15:45684005 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1048+1344A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45684005 | |||||||
| chr15:45684078 | AT | A | 68 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(65): Show |
68 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.1048+1425delT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45684078 | ||||||
| chr15:45684204 | C | T | 1 | a0002c0002t0001g0020 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1048+1543C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45684204 | |||||||
| chr15:45684220 | A | G | 1 | a0002c0002t0005g0031 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1048+1559A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45684220 | |||||||
| chr15:45684306 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1048+1645G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45684306 | |||||||
| chr15:45684309 | A | G | 19 | a0001c0001t0001g0029 a0001c0001t0001g0060 a0001c0001t0001g0063 others(16): Show |
19 | HG00741.hp1 HG01496.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1048+1648A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45684309 | |||||||
| chr15:45684421 | A | C | 22 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(19): Show |
22 | HG00558.hp2 HG00639.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.1048+1760A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45684421 | |||||||
| chr15:45684459 | T | A | 5 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0210 others(2): Show |
5 | HG00558.hp1 HG02165.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.1048+1798T>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45684459 | |||||||
| chr15:45684498 | T | G | 72 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(69): Show |
72 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.1048+1837T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45684498 | |||||||
| chr15:45684592 | T | TTC | 135 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0030 others(132): Show |
140 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.1048+1951_1048+195 others(6): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45684592 | ||||||
| chr15:45684592 | TTC | T | 72 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(69): Show |
72 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.1048+1951_1048+195 others(6): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45684592 | ||||||
| chr15:45684592 | TTCTC | T | 3 | a0001c0001t0001g0151 a0001c0001t0001g0175 a0001c0001t0001g0176 |
3 | HG01884.hp2 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1048+1949_1048+195 others(8): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45684592 | ||||||
| chr15:45684592 | TTCTCTC | T | 3 | a0002c0002t0001g0047 a0002c0002t0001g0213 a0002c0002t0006g0171 |
3 | HG00609.hp1 HG02523.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1048+1947_1048+195 others(10): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45684592 | ||||||
| chr15:45684614 | T | C | 1 | a0001c0001t0001g0305 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1048+1953T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45684614 | |||||||
| chr15:45684916 | C | G | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1048+2255C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45684916 | |||||||
| chr15:45685106 | A | G | 1 | a0002c0002t0001g0244 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1048+2445A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45685106 | |||||||
| chr15:45685114 | C | G | 5 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0210 others(2): Show |
5 | HG00558.hp1 HG02165.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.1048+2453C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45685114 | |||||||
| chr15:45685150 | C | T | 1 | a0002c0002t0001g0013 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1048+2489C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45685150 | |||||||
| chr15:45685162 | C | T | 69 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(66): Show |
69 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.1048+2501C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45685162 | |||||||
| chr15:45685294 | T | TCCCA | 4 | a0004c0006t0001g0311 a0004c0006t0004g0319 a0004c0006t0004g0320 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1048+2634_1048+263 others(8): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45685294 | ||||||
| chr15:45685360 | T | C | 71 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(68): Show |
71 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.1048+2699T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45685360 | |||||||
| chr15:45685431 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0043 others(1): Show |
5 | HG01169.hp2 HG02896.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1048+2770C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45685431 | |||||||
| chr15:45685484 | C | G | 5 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0210 others(2): Show |
5 | HG00558.hp1 HG02165.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.1048+2823C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45685484 | |||||||
| chr15:45685554 | C | T | 68 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(65): Show |
68 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.1049-2783C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45685554 | |||||||
| chr15:45685680 | C | A | 21 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(18): Show |
21 | HG00558.hp2 HG00639.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.1049-2657C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45685680 | |||||||
| chr15:45685767 | G | A | 1 | a0002c0002t0001g0157 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1049-2570G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45685767 | |||||||
| chr15:45685994 | C | G | 76 | a0001c0001t0001g0030 a0001c0001t0001g0166 a0001c0001t0001g0168 others(73): Show |
79 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.1049-2343C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45685994 | |||||||
| chr15:45686077 | C | A | 1 | a0001c0001t0001g0138 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1049-2260C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45686077 | |||||||
| chr15:45686100 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0219 |
2 | HG02258.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1049-2237C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45686100 | |||||||
| chr15:45686152 | A | AAT | 36 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0025 others(33): Show |
38 | HG00735.hp2 HG00738.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.1049-2170_1049-216 others(6): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45686152 | ||||||
| chr15:45686152 | A | AATAT | 76 | a0001c0001t0001g0030 a0001c0001t0001g0166 a0001c0001t0001g0168 others(73): Show |
79 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.1049-2172_1049-216 others(8): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45686152 | ||||||
| chr15:45686194 | C | T | 61 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(58): Show |
62 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.1049-2143C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45686194 | |||||||
| chr15:45686195 | G | A | 61 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(58): Show |
62 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.1049-2142G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45686195 | |||||||
| chr15:45686256 | A | G | 7 | a0001c0001t0001g0029 a0001c0001t0001g0232 a0001c0001t0001g0242 others(4): Show |
7 | HG02559.hp2 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1049-2081A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45686256 | |||||||
| chr15:45686323 | C | T | 61 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(58): Show |
62 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.1049-2014C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45686323 | |||||||
| chr15:45686437 | C | A | 1 | a0001c0001t0007g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1049-1900C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45686437 | |||||||
| chr15:45686439 | A | G | 8 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0210 others(5): Show |
8 | HG00558.hp1 HG02055.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.1049-1898A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45686439 | |||||||
| chr15:45686446 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1049-1891C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45686446 | |||||||
| chr15:45686448 | G | A | 117 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0025 others(114): Show |
122 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1049-1889G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45686448 | |||||||
| chr15:45686648 | C | A | 78 | a0001c0001t0001g0030 a0001c0001t0001g0166 a0001c0001t0001g0168 others(75): Show |
81 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1049-1689C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45686648 | |||||||
| chr15:45686716 | C | T | 1 | a0002c0002t0001g0026 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1049-1621C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45686716 | |||||||
| chr15:45686765 | A | G | 1 | a0005c0008t0001g0326 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1049-1572A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45686765 | |||||||
| chr15:45686974 | A | C | 1 | a0001c0001t0007g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1049-1363A>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45686974 | |||||||
| chr15:45687048 | C | T | 2 | a0001c0001t0001g0110 a0005c0008t0001g0229 |
2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1049-1289C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45687048 | |||||||
| chr15:45687080 | G | A | 1 | a0001c0001t0004g0321 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1049-1257G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45687080 | |||||||
| chr15:45687127 | G | A | 8 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0210 others(5): Show |
8 | HG00558.hp1 HG02055.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.1049-1210G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45687127 | |||||||
| chr15:45687493 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1049-844G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45687493 | |||||||
| chr15:45687590 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1049-747C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45687590 | |||||||
| chr15:45687593 | G | GA | 68 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(65): Show |
69 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.1049-737dupA | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45687593 | ||||||
| chr15:45687742 | G | A | 5 | a0001c0001t0002g0008 a0001c0001t0002g0022 a0001c0001t0002g0037 others(2): Show |
6 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1049-595G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45687742 | |||||||
| chr15:45687743 | TTCTG | T | 80 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0030 others(77): Show |
84 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.1049-578_1049-575d others(6): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45687743 | ||||||
| chr15:45687946 | TG | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0210 others(1): Show |
4 | HG00558.hp1 HG02165.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.1049-387delG | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 45687946 | ||||||
| chr15:45687965 | T | C | 8 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0210 others(5): Show |
8 | HG00558.hp1 HG02055.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.1049-372T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45687965 | |||||||
| chr15:45688177 | C | T | 32 | a0001c0001t0001g0029 a0001c0001t0001g0110 a0001c0001t0001g0232 others(29): Show |
32 | HG00099.hp2 HG00323.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.1049-160C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45688177 | |||||||
| chr15:45688178 | G | A | 1 | a0001c0001t0001g0021 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1049-159G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45688178 | |||||||
| chr15:45688194 | A | G | 69 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(66): Show |
70 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1049-143A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 7/9 | chr15 | 45688194 | |||||||
| chr15:45688515 | C | CT | 6 | a0001c0001t0001g0259 a0002c0002t0001g0156 a0003c0005t0001g0307 others(3): Show |
6 | HG02055.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1116+125dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 45688515 | ||||||
| chr15:45688515 | C | CTT | 9 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0027 others(6): Show |
10 | HG00558.hp1 HG01169.hp2 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.1116+124_1116+125d others(4): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 45688515 | ||||||
| chr15:45688560 | G | A | 1 | a0002c0002t0001g0136 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1116+156G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 8/9 | chr15 | 45688560 | |||||||
| chr15:45688749 | A | G | 182 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(179): Show |
188 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1117-290A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 8/9 | chr15 | 45688749 | |||||||
| chr15:45688760 | G | A | 14 | a0001c0001t0001g0011 a0001c0001t0001g0060 a0001c0001t0001g0063 others(11): Show |
14 | HG00741.hp1 HG01496.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1117-279G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 8/9 | chr15 | 45688760 | |||||||
| chr15:45688889 | T | C | 1 | a0005c0008t0001g0326 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1117-150T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 8/9 | chr15 | 45688889 | |||||||
| chr15:45688919 | C | T | 69 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(66): Show |
70 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1117-120C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 8/9 | chr15 | 45688919 | |||||||
| chr15:45689417 | C | CT | 14 | a0001c0001t0001g0127 a0001c0001t0001g0144 a0001c0001t0001g0149 others(11): Show |
14 | HG00642.hp2 HG02015.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1295+218dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 45689417 | ||||||
| chr15:45689417 | CT | C | 28 | a0001c0001t0001g0044 a0001c0001t0001g0167 a0001c0001t0002g0008 others(25): Show |
29 | HG00099.hp2 HG00323.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1295+218delT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 45689417 | ||||||
| chr15:45689426 | T | G | 6 | a0001c0001t0001g0024 a0001c0001t0001g0036 a0001c0001t0001g0046 others(3): Show |
6 | NA18959.hp1 NA18962.hp2 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1295+209T>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45689426 | |||||||
| chr15:45689482 | A | G | 3 | a0004c0006t0004g0319 a0004c0006t0004g0320 a0007c0011t0004g0322 |
3 | HG02055.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1295+265A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45689482 | |||||||
| chr15:45689535 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1295+318A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45689535 | |||||||
| chr15:45689643 | C | A | 74 | a0001c0001t0001g0030 a0001c0001t0001g0166 a0001c0001t0001g0168 others(71): Show |
77 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.1295+426C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45689643 | |||||||
| chr15:45689661 | C | A | 1 | a0001c0001t0001g0195 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1295+444C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45689661 | |||||||
| chr15:45689662 | C | T | 74 | a0001c0001t0001g0030 a0001c0001t0001g0166 a0001c0001t0001g0168 others(71): Show |
77 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.1295+445C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45689662 | |||||||
| chr15:45689671 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1295+454C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45689671 | |||||||
| chr15:45689710 | G | A | 1 | a0001c0001t0003g0313 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1295+493G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45689710 | |||||||
| chr15:45689951 | A | G | 8 | a0001c0001t0001g0029 a0001c0001t0001g0232 a0001c0001t0001g0242 others(5): Show |
8 | HG02559.hp2 HG02717.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1295+734A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45689951 | |||||||
| chr15:45690064 | G | A | 4 | a0001c0001t0001g0019 a0001c0001t0001g0100 a0001c0001t0001g0210 others(1): Show |
4 | HG00558.hp1 HG02165.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.1295+847G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690064 | |||||||
| chr15:45690081 | C | T | 69 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(66): Show |
70 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1295+864C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690081 | |||||||
| chr15:45690082 | C | CT | 114 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0025 others(111): Show |
119 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.1296-875dupT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 45690082 | ||||||
| chr15:45690082 | C | CTT | 7 | a0001c0001t0001g0072 a0001c0001t0001g0101 a0001c0001t0001g0240 others(4): Show |
7 | HG02145.hp1 HG02615.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1296-876_1296-875d others(4): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 45690082 | ||||||
| chr15:45690082 | C | CTTT | 39 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(36): Show |
40 | HG00558.hp1 HG00558.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.1296-877_1296-875d others(5): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 45690082 | ||||||
| chr15:45690082 | C | CTTTT | 28 | a0001c0001t0001g0029 a0001c0001t0001g0110 a0001c0001t0001g0232 others(25): Show |
28 | HG00099.hp2 HG00323.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.1295+878_1296-875d others(6): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 45690082 | ||||||
| chr15:45690082 | CT | C | 15 | a0001c0001t0001g0011 a0001c0001t0001g0060 a0001c0001t0001g0063 others(12): Show |
15 | HG00741.hp1 HG01496.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1296-875delT | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 45690082 | ||||||
| chr15:45690119 | C | CCACCCAG others(9): Show |
69 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(66): Show |
70 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1296-853_1296-852i others(18): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 45690119 | ||||||
| chr15:45690121 | C | A | 69 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(66): Show |
70 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1296-852C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690121 | |||||||
| chr15:45690140 | G | C | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1296-833G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690140 | |||||||
| chr15:45690159 | G | A | 2 | a0001c0007t0001g0006 a0001c0007t0001g0150 |
3 | HG01884.hp1 HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1296-814G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690159 | |||||||
| chr15:45690348 | G | A | 1 | a0009c0014t0001g0115 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1296-625G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690348 | |||||||
| chr15:45690390 | T | C | 68 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(65): Show |
69 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.1296-583T>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690390 | |||||||
| chr15:45690397 | C | A | 69 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(66): Show |
70 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1296-576C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690397 | |||||||
| chr15:45690408 | C | A | 68 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(65): Show |
69 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.1296-565C>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690408 | |||||||
| chr15:45690542 | G | T | 1 | a0009c0014t0001g0115 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1296-431G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690542 | |||||||
| chr15:45690583 | A | G | 1 | a0001c0001t0004g0321 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1296-390A>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690583 | |||||||
| chr15:45690587 | G | A | 70 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(67): Show |
71 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.1296-386G>A | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690587 | |||||||
| chr15:45690609 | C | T | 69 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(66): Show |
70 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1296-364C>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690609 | |||||||
| chr15:45690663 | A | T | 1 | a0001c0001t0001g0111 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1296-310A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690663 | |||||||
| chr15:45690664 | T | TCCTGA | 69 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(66): Show |
70 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1296-306_1296-305i others(7): Show |
SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 45690664 | ||||||
| chr15:45690683 | G | C | 69 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(66): Show |
70 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1296-290G>C | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690683 | |||||||
| chr15:45690767 | A | T | 21 | a0001c0003t0001g0059 a0001c0003t0001g0069 a0001c0003t0001g0073 others(18): Show |
21 | HG00099.hp2 HG00323.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1296-206A>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690767 | |||||||
| chr15:45690806 | G | T | 23 | a0001c0001t0001g0110 a0001c0003t0001g0059 a0001c0003t0001g0069 others(20): Show |
23 | HG00099.hp2 HG00323.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.1296-167G>T | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690806 | |||||||
| chr15:45690909 | C | G | 1 | a0005c0008t0001g0326 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1296-64C>G | SQOR | ENSG00000137767.14 | transcript | ENST00000260324.12 | protein_coding | 9/9 | chr15 | 45690909 |