Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55278 |
| ensemblid | ENSG00000130348.11 |
| hgncid | 21020 |
| symbol | QRSL1 |
| name | glutaminyl-tRNA amidotransferase subunit QRSL1 |
| refseq_nuc | NM_018292.5 |
| refseq_prot | NP_060762.3 |
| ensembl_nuc | ENST00000369046.8 |
| ensembl_prot | ENSP00000358042.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 106629578 |
| end | 106668417 |
| strand | + |
| ver | v1.2 |
| region | chr6:106629578-106668417 |
| region5000 | chr6:106624578-106673417 |
| regionname0 | QRSL1_chr6_106629578_106668417 |
| regionname5000 | QRSL1_chr6_106624578_106673417 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 528 | 358 | 68 | 66 | 178 | 13 | 31 | 139 | QRSL1_chr6_106624578_106673417 | QRSL1 | MLGRS others(523): Show |
chr6 | 106624578 | 106673417 |
| a0002 | 0/0 | 528 | 43 | 20 | 6 | 15 | 1 | 1 | 14 | QRSL1_chr6_106624578_106673417 | QRSL1 | MLGRS others(523): Show |
chr6 | 106624578 | 106673417 |
| a0003 | 0/0 | 528 | 16 | 0 | 0 | 14 | 0 | 2 | 12 | QRSL1_chr6_106624578_106673417 | QRSL1 | MLGRS others(523): Show |
chr6 | 106624578 | 106673417 |
| a0004 | 0/0 | 528 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | MLGRS others(523): Show |
chr6 | 106624578 | 106673417 |
| a0005 | 0/0 | 283 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | MLGRS others(278): Show |
chr6 | 106624578 | 106673417 |
| a0006 | 0/0 | 528 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | MLGRS others(523): Show |
chr6 | 106624578 | 106673417 |
| a0007 | 0/0 | 290 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | MLGRS others(285): Show |
chr6 | 106624578 | 106673417 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1584 | 257 | 44 | 41 | 145 | 5 | 21 | QRSL1_chr6_106624578_106673417 | QRSL1 | ATGCT others(1579): Show |
chr6 | 106624578 | 106673417 | ||
| a0001c0002 | 0/1 | 1584 | 92 | 16 | 24 | 33 | 8 | 10 | QRSL1_chr6_106624578_106673417 | QRSL1 | ATGCT others(1579): Show |
chr6 | 106624578 | 106673417 | ||
| a0001c0005 | 0/0 | 1584 | 4 | 4 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | ATGCT others(1579): Show |
chr6 | 106624578 | 106673417 | ||
| a0001c0006 | 0/0 | 1584 | 3 | 2 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | ATGCT others(1579): Show |
chr6 | 106624578 | 106673417 | ||
| a0001c0008 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | ATGCT others(1579): Show |
chr6 | 106624578 | 106673417 | ||
| a0001c0009 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | ATGCT others(1579): Show |
chr6 | 106624578 | 106673417 | ||
| a0002c0003 | 0/0 | 1584 | 43 | 20 | 6 | 15 | 1 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | ATGCT others(1579): Show |
chr6 | 106624578 | 106673417 | ||
| a0003c0004 | 0/0 | 1584 | 16 | 0 | 0 | 14 | 0 | 2 | QRSL1_chr6_106624578_106673417 | QRSL1 | ATGCT others(1579): Show |
chr6 | 106624578 | 106673417 | ||
| a0004c0007 | 0/0 | 1584 | 2 | 0 | 2 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | ATGCT others(1579): Show |
chr6 | 106624578 | 106673417 | ||
| a0005c0011 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | ATGCT others(1579): Show |
chr6 | 106624578 | 106673417 | ||
| a0006c0012 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | ATGCT others(1579): Show |
chr6 | 106624578 | 106673417 | ||
| a0007c0010 | 0/0 | 1634 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | ATGCT others(1629): Show |
chr6 | 106624578 | 106673417 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4106 | 124 | 30 | 24 | 49 | 4 | 16 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4101): Show |
chr6 | 106624578 | 106673417 |
| a0001c0001t0002 | 0/0 | 4103 | 22 | 0 | 0 | 22 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4098): Show |
chr6 | 106624578 | 106673417 |
| a0001c0001t0003 | 0/0 | 4106 | 55 | 13 | 8 | 34 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4101): Show |
chr6 | 106624578 | 106673417 |
| a0001c0001t0005 | 0/0 | 4106 | 42 | 0 | 7 | 35 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4101): Show |
chr6 | 106624578 | 106673417 |
| a0001c0001t0007 | 0/0 | 4106 | 9 | 0 | 1 | 2 | 1 | 5 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4101): Show |
chr6 | 106624578 | 106673417 |
| a0001c0001t0013 | 0/0 | 4105 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4100): Show |
chr6 | 106624578 | 106673417 |
| a0001c0001t0017 | 0/0 | 4106 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4101): Show |
chr6 | 106624578 | 106673417 |
| a0001c0001t0018 | 0/0 | 4106 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4101): Show |
chr6 | 106624578 | 106673417 |
| a0001c0001t0020 | 0/0 | 4106 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4101): Show |
chr6 | 106624578 | 106673417 |
| a0001c0001t0022 | 0/0 | 4106 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4101): Show |
chr6 | 106624578 | 106673417 |
| a0001c0002t0004 | 0/1 | 4103 | 54 | 4 | 16 | 20 | 5 | 8 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4098): Show |
chr6 | 106624578 | 106673417 |
| a0001c0002t0006 | 0/0 | 4105 | 22 | 0 | 6 | 12 | 2 | 2 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4100): Show |
chr6 | 106624578 | 106673417 |
| a0001c0002t0008 | 0/0 | 4103 | 9 | 7 | 1 | 0 | 1 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4098): Show |
chr6 | 106624578 | 106673417 |
| a0001c0002t0011 | 0/0 | 4103 | 3 | 3 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4098): Show |
chr6 | 106624578 | 106673417 |
| a0001c0002t0012 | 0/0 | 4103 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4098): Show |
chr6 | 106624578 | 106673417 |
| a0001c0002t0014 | 0/0 | 4103 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4098): Show |
chr6 | 106624578 | 106673417 |
| a0001c0002t0016 | 0/0 | 4105 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4100): Show |
chr6 | 106624578 | 106673417 |
| a0001c0002t0021 | 0/0 | 4105 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4100): Show |
chr6 | 106624578 | 106673417 |
| a0001c0005t0010 | 0/0 | 4106 | 4 | 4 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4101): Show |
chr6 | 106624578 | 106673417 |
| a0001c0006t0001 | 0/0 | 4106 | 3 | 2 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4101): Show |
chr6 | 106624578 | 106673417 |
| a0001c0008t0006 | 0/0 | 4105 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4100): Show |
chr6 | 106624578 | 106673417 |
| a0001c0009t0013 | 0/0 | 4105 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4100): Show |
chr6 | 106624578 | 106673417 |
| a0002c0003t0001 | 0/0 | 4106 | 9 | 2 | 5 | 0 | 1 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4101): Show |
chr6 | 106624578 | 106673417 |
| a0002c0003t0002 | 0/0 | 4103 | 29 | 14 | 1 | 14 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4098): Show |
chr6 | 106624578 | 106673417 |
| a0002c0003t0009 | 0/0 | 4103 | 4 | 3 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4098): Show |
chr6 | 106624578 | 106673417 |
| a0002c0003t0015 | 0/0 | 4106 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4101): Show |
chr6 | 106624578 | 106673417 |
| a0003c0004t0002 | 0/0 | 4103 | 15 | 0 | 0 | 13 | 0 | 2 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4098): Show |
chr6 | 106624578 | 106673417 |
| a0003c0004t0019 | 0/0 | 4103 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4098): Show |
chr6 | 106624578 | 106673417 |
| a0004c0007t0001 | 0/0 | 4106 | 2 | 0 | 2 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4101): Show |
chr6 | 106624578 | 106673417 |
| a0005c0011t0012 | 0/0 | 4103 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4098): Show |
chr6 | 106624578 | 106673417 |
| a0006c0012t0002 | 0/0 | 4103 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4098): Show |
chr6 | 106624578 | 106673417 |
| a0007c0010t0005 | 0/0 | 4156 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | AGTGA others(4151): Show |
chr6 | 106624578 | 106673417 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 2 | 2 | 1 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0042 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0002g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0011 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0005g0001 | 0/0 | 14 | 0 | 0 | 14 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0005g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0005g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0005g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0005g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0005g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0005g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0005g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0005g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0005g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0005g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0005g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0005g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0005g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0005g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0005g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0005g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0005g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0005g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0005g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0005g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0007g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0007g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0007g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0007g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0007g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0007g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0007g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0007g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0013g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0017g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0018g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0020g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0001t0022g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0002 | 0/0 | 7 | 0 | 3 | 0 | 1 | 3 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0145 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0004g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0006g0007 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0006g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0006g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0006g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0006g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0006g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0006g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0006g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0006g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0006g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0006g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0006g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0006g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0006g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0006g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0006g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0006g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0006g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0008g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0008g0036 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0008g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0008g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0008g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0008g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0008g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0011g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0012g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0014g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0016g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0002t0021g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0005t0010g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0005t0010g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0006t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0006t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0006t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0008t0006g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0001c0009t0013g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0002c0003t0001g0013 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0002c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0002c0003t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0002c0003t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0002c0003t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0002c0003t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0002c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0002c0003t0002g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0002c0003t0002g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0002c0003t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0002c0003t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0002c0003t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0002c0003t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0002c0003t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0002c0003t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0002c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0002c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0002c0003t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0002c0003t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0002c0003t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0002c0003t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0002c0003t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0002c0003t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0002c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0002c0003t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0002c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0002c0003t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0002c0003t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0002c0003t0009g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0002c0003t0009g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0002c0003t0015g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0003c0004t0002g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0003c0004t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0003c0004t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0003c0004t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0003c0004t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0003c0004t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0003c0004t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0003c0004t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0003c0004t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0003c0004t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0003c0004t0019g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0004c0007t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0004c0007t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0005c0011t0012g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0006c0012t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| a0007c0010t0005g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0004 | g0128 | EUR | GBR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00140 | hp2 | a0001 | c0002 | t0008 | g0036 | EUR | GBR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00280 | hp1 | a0001 | c0002 | t0004 | g0133 | EUR | FIN | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00280 | hp2 | a0002 | c0003 | t0001 | g0056 | EUR | FIN | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | FIN | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00323 | hp2 | a0001 | c0002 | t0004 | g0002 | EUR | FIN | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00408 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | CHS | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00423 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | CHS | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | CHS | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | CHS | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00438 | hp2 | a0001 | c0002 | t0006 | g0101 | EAS | CHS | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00558 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | CHS | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | CHS | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00597 | hp2 | a0001 | c0001 | t0005 | g0303 | EAS | CHS | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00609 | hp1 | a0001 | c0001 | t0005 | g0022 | EAS | CHS | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | CHS | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00639 | hp1 | a0002 | c0003 | t0001 | g0013 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00639 | hp2 | a0001 | c0002 | t0004 | g0030 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00642 | hp2 | a0001 | c0001 | t0020 | g0009 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00733 | hp1 | a0001 | c0002 | t0004 | g0002 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00735 | hp2 | a0001 | c0002 | t0014 | g0160 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00738 | hp1 | a0001 | c0002 | t0004 | g0002 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00738 | hp2 | a0001 | c0002 | t0006 | g0093 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00741 | hp1 | a0001 | c0002 | t0008 | g0036 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01070 | hp2 | a0001 | c0002 | t0006 | g0027 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01071 | hp1 | a0001 | c0002 | t0004 | g0002 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01074 | hp2 | a0001 | c0002 | t0004 | g0137 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01106 | hp1 | a0001 | c0002 | t0006 | g0027 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01106 | hp2 | a0002 | c0003 | t0001 | g0013 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01167 | hp2 | a0001 | c0002 | t0004 | g0134 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01168 | hp2 | a0001 | c0002 | t0004 | g0117 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0273 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0245 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01192 | hp2 | a0002 | c0003 | t0001 | g0277 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01243 | hp1 | a0001 | c0006 | t0001 | g0217 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01243 | hp2 | a0004 | c0007 | t0001 | g0077 | AMR | PUR | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0258 | AMR | CLM | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01255 | hp2 | a0002 | c0003 | t0001 | g0060 | AMR | CLM | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0045 | AMR | CLM | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01261 | hp2 | a0001 | c0001 | t0007 | g0152 | AMR | CLM | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01358 | hp1 | a0001 | c0001 | t0005 | g0048 | AMR | CLM | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01361 | hp1 | a0002 | c0003 | t0001 | g0059 | AMR | CLM | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01433 | hp2 | a0001 | c0002 | t0006 | g0091 | AMR | CLM | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01496 | hp1 | a0001 | c0001 | t0005 | g0099 | AMR | CLM | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0264 | AMR | CLM | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0194 | EUR | IBS | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01516 | hp2 | a0001 | c0002 | t0006 | g0097 | EUR | IBS | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01517 | hp1 | a0001 | c0002 | t0004 | g0130 | EUR | IBS | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0195 | EUR | IBS | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01884 | hp1 | a0002 | c0003 | t0002 | g0064 | AFR | ACB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0266 | AFR | ACB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01891 | hp1 | a0002 | c0003 | t0002 | g0023 | AFR | ACB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01891 | hp2 | a0001 | c0002 | t0016 | g0074 | AFR | ACB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01934 | hp1 | a0001 | c0002 | t0004 | g0129 | AMR | PEL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01943 | hp1 | a0001 | c0001 | t0005 | g0299 | AMR | PEL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01943 | hp2 | a0001 | c0002 | t0004 | g0131 | AMR | PEL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01952 | hp1 | a0001 | c0001 | t0005 | g0049 | AMR | PEL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01952 | hp2 | a0004 | c0007 | t0001 | g0078 | AMR | PEL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01978 | hp1 | a0001 | c0002 | t0004 | g0120 | AMR | PEL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01978 | hp2 | a0001 | c0002 | t0004 | g0276 | AMR | PEL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01981 | hp1 | a0001 | c0002 | t0004 | g0136 | AMR | PEL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0259 | AMR | PEL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01993 | hp1 | a0001 | c0002 | t0006 | g0094 | AMR | PEL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01993 | hp2 | a0001 | c0001 | t0005 | g0048 | AMR | PEL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02004 | hp1 | a0001 | c0001 | t0005 | g0049 | AMR | PEL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PEL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0318 | EAS | KHV | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02040 | hp2 | a0001 | c0002 | t0006 | g0028 | EAS | KHV | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02055 | hp1 | a0002 | c0003 | t0001 | g0100 | AFR | ACB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0267 | AFR | ACB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | KHV | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | KHV | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02074 | hp1 | a0001 | c0001 | t0005 | g0314 | EAS | KHV | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02074 | hp2 | a0003 | c0004 | t0002 | g0278 | EAS | KHV | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02080 | hp1 | a0001 | c0001 | t0005 | g0022 | EAS | KHV | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02129 | hp1 | a0001 | c0002 | t0021 | g0007 | EAS | KHV | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | KHV | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02132 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | KHV | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02135 | hp2 | a0002 | c0003 | t0002 | g0058 | EAS | KHV | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0263 | AFR | ACB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02148 | hp1 | a0002 | c0003 | t0002 | g0068 | AMR | PEL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02148 | hp2 | a0001 | c0002 | t0004 | g0132 | AMR | PEL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CDX | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02165 | hp2 | a0001 | c0002 | t0004 | g0159 | EAS | CDX | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02257 | hp1 | a0001 | c0009 | t0013 | g0080 | AFR | ACB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02273 | hp1 | a0001 | c0002 | t0004 | g0030 | AMR | PEL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02273 | hp2 | a0001 | c0001 | t0005 | g0310 | AMR | PEL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02280 | hp1 | a0002 | c0003 | t0002 | g0103 | AFR | ACB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0257 | AFR | ACB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02300 | hp1 | a0001 | c0002 | t0004 | g0242 | AMR | PEL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02300 | hp2 | a0001 | c0002 | t0006 | g0098 | AMR | PEL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02451 | hp1 | a0001 | c0002 | t0008 | g0082 | AFR | ACB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02451 | hp2 | a0002 | c0003 | t0002 | g0008 | AFR | ACB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02523 | hp1 | a0001 | c0002 | t0004 | g0118 | EAS | KHV | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02523 | hp2 | a0001 | c0002 | t0006 | g0102 | EAS | KHV | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02572 | hp2 | a0002 | c0003 | t0002 | g0054 | AFR | GWD | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02602 | hp2 | a0001 | c0001 | t0007 | g0241 | SAS | PJL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0250 | AFR | GWD | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02615 | hp2 | a0002 | c0003 | t0009 | g0020 | AFR | GWD | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02622 | hp2 | a0001 | c0002 | t0011 | g0019 | AFR | GWD | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02647 | hp1 | a0001 | c0002 | t0004 | g0032 | AFR | GWD | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02683 | hp1 | a0002 | c0003 | t0001 | g0286 | SAS | PJL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02698 | hp1 | a0001 | c0002 | t0006 | g0086 | SAS | PJL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02698 | hp2 | a0001 | c0001 | t0007 | g0034 | SAS | PJL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0254 | AFR | GWD | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02723 | hp2 | a0001 | c0002 | t0011 | g0019 | AFR | GWD | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02735 | hp1 | a0001 | c0001 | t0007 | g0233 | SAS | PJL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02735 | hp2 | a0001 | c0002 | t0004 | g0002 | SAS | PJL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02809 | hp1 | a0006 | c0012 | t0002 | g0071 | AFR | GWD | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02809 | hp2 | a0002 | c0003 | t0002 | g0053 | AFR | GWD | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02818 | hp1 | a0001 | c0005 | t0010 | g0021 | AFR | GWD | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02895 | hp1 | a0001 | c0005 | t0010 | g0021 | AFR | GWD | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02895 | hp2 | a0001 | c0002 | t0012 | g0234 | AFR | GWD | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02897 | hp2 | a0001 | c0005 | t0010 | g0284 | AFR | GWD | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02922 | hp1 | a0001 | c0002 | t0008 | g0026 | AFR | ESN | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02965 | hp1 | a0002 | c0003 | t0009 | g0020 | AFR | ESN | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02965 | hp2 | a0001 | c0002 | t0011 | g0019 | AFR | ESN | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02970 | hp1 | a0002 | c0003 | t0002 | g0012 | AFR | ESN | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02970 | hp2 | a0001 | c0002 | t0008 | g0083 | AFR | ESN | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02976 | hp1 | a0001 | c0006 | t0001 | g0222 | AFR | ESN | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02976 | hp2 | a0001 | c0002 | t0008 | g0104 | AFR | ESN | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03017 | hp1 | a0001 | c0002 | t0004 | g0002 | SAS | PJL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03017 | hp2 | a0001 | c0002 | t0004 | g0121 | SAS | PJL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | MSL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | MSL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03130 | hp1 | a0002 | c0003 | t0002 | g0008 | AFR | ESN | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0268 | AFR | ESN | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03139 | hp2 | a0002 | c0003 | t0002 | g0012 | AFR | ESN | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03195 | hp2 | a0001 | c0002 | t0008 | g0085 | AFR | ESN | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0319 | AFR | MSL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03209 | hp2 | a0001 | c0002 | t0008 | g0084 | AFR | MSL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | MSL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03225 | hp2 | a0001 | c0002 | t0008 | g0026 | AFR | MSL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | MSL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03486 | hp1 | a0002 | c0003 | t0009 | g0020 | AFR | MSL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0270 | AFR | MSL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03490 | hp2 | a0001 | c0001 | t0007 | g0034 | SAS | PJL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03516 | hp1 | a0002 | c0003 | t0002 | g0052 | AFR | ESN | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0271 | AFR | MSL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03688 | hp1 | a0001 | c0002 | t0004 | g0124 | SAS | STU | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | STU | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03704 | hp1 | a0001 | c0002 | t0004 | g0122 | SAS | PJL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | BEB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | BEB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03834 | hp2 | a0001 | c0002 | t0004 | g0002 | SAS | BEB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | BEB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03927 | hp2 | a0003 | c0004 | t0002 | g0285 | SAS | BEB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | BEB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG04115 | hp1 | a0001 | c0002 | t0004 | g0139 | SAS | STU | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | STU | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG04184 | hp1 | a0001 | c0001 | t0007 | g0151 | SAS | BEB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG04199 | hp1 | a0001 | c0002 | t0006 | g0095 | SAS | STU | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG04199 | hp2 | a0003 | c0004 | t0002 | g0287 | SAS | STU | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | STU | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG04204 | hp2 | a0001 | c0002 | t0004 | g0031 | SAS | STU | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18522 | hp1 | a0002 | c0003 | t0002 | g0008 | AFR | YRI | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18522 | hp2 | a0002 | c0003 | t0002 | g0012 | AFR | YRI | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CHB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18747 | hp1 | a0003 | c0004 | t0002 | g0279 | EAS | CHB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18747 | hp2 | a0001 | c0002 | t0004 | g0140 | EAS | CHB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | YRI | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18906 | hp2 | a0002 | c0003 | t0002 | g0023 | AFR | YRI | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18940 | hp2 | a0001 | c0001 | t0007 | g0123 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18941 | hp2 | a0001 | c0002 | t0006 | g0089 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18942 | hp1 | a0001 | c0001 | t0005 | g0308 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18943 | hp2 | a0001 | c0002 | t0004 | g0141 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18945 | hp2 | a0002 | c0003 | t0002 | g0024 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18946 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18947 | hp2 | a0001 | c0002 | t0004 | g0154 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18948 | hp2 | a0001 | c0002 | t0006 | g0090 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18950 | hp2 | a0003 | c0004 | t0002 | g0006 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18952 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18954 | hp1 | a0001 | c0001 | t0005 | g0050 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18961 | hp1 | a0001 | c0002 | t0006 | g0092 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18963 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18966 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18966 | hp2 | a0002 | c0003 | t0002 | g0024 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18967 | hp1 | a0001 | c0002 | t0004 | g0144 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18968 | hp1 | a0001 | c0001 | t0005 | g0311 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18969 | hp1 | a0001 | c0002 | t0004 | g0119 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18969 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18970 | hp2 | a0001 | c0002 | t0004 | g0029 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18971 | hp1 | a0003 | c0004 | t0002 | g0006 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18971 | hp2 | a0001 | c0001 | t0005 | g0315 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18972 | hp1 | a0002 | c0003 | t0002 | g0066 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18973 | hp1 | a0001 | c0002 | t0006 | g0087 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18974 | hp1 | a0001 | c0002 | t0006 | g0096 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18974 | hp2 | a0002 | c0003 | t0002 | g0300 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18977 | hp1 | a0001 | c0002 | t0004 | g0029 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18979 | hp1 | a0003 | c0004 | t0002 | g0288 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0307 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18982 | hp2 | a0001 | c0002 | t0004 | g0116 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18983 | hp1 | a0001 | c0002 | t0006 | g0007 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18985 | hp1 | a0002 | c0003 | t0002 | g0063 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18986 | hp2 | a0001 | c0002 | t0004 | g0155 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18987 | hp2 | a0001 | c0001 | t0013 | g0185 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18988 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18988 | hp2 | a0001 | c0002 | t0004 | g0156 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18989 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18991 | hp2 | a0001 | c0002 | t0004 | g0143 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18995 | hp2 | a0003 | c0004 | t0002 | g0282 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18997 | hp2 | a0002 | c0003 | t0002 | g0069 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18998 | hp2 | a0001 | c0001 | t0005 | g0047 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19001 | hp1 | a0001 | c0002 | t0004 | g0157 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19003 | hp1 | a0001 | c0001 | t0007 | g0127 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19004 | hp2 | a0002 | c0003 | t0002 | g0025 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19005 | hp2 | a0003 | c0004 | t0019 | g0280 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19006 | hp1 | a0001 | c0002 | t0004 | g0125 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19006 | hp2 | a0003 | c0004 | t0002 | g0006 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19007 | hp1 | a0001 | c0002 | t0004 | g0158 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19007 | hp2 | a0001 | c0002 | t0006 | g0007 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19010 | hp1 | a0002 | c0003 | t0002 | g0025 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19012 | hp1 | a0001 | c0001 | t0005 | g0316 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19012 | hp2 | a0002 | c0003 | t0002 | g0061 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0272 | AFR | LWK | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19030 | hp2 | a0001 | c0008 | t0006 | g0298 | AFR | LWK | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19043 | hp1 | a0001 | c0002 | t0004 | g0162 | AFR | LWK | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19043 | hp2 | a0001 | c0006 | t0001 | g0221 | AFR | LWK | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19054 | hp2 | a0001 | c0001 | t0005 | g0301 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19055 | hp2 | a0001 | c0001 | t0017 | g0317 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19057 | hp1 | a0002 | c0003 | t0009 | g0246 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19057 | hp2 | a0001 | c0001 | t0005 | g0312 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19058 | hp1 | a0003 | c0004 | t0002 | g0006 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19060 | hp1 | a0003 | c0004 | t0002 | g0046 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19062 | hp1 | a0001 | c0001 | t0005 | g0050 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19063 | hp1 | a0001 | c0001 | t0005 | g0306 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19064 | hp1 | a0003 | c0004 | t0002 | g0046 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19065 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19066 | hp1 | a0001 | c0002 | t0006 | g0028 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19066 | hp2 | a0002 | c0003 | t0002 | g0067 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19067 | hp1 | a0003 | c0004 | t0002 | g0281 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19067 | hp2 | a0001 | c0001 | t0005 | g0304 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19068 | hp2 | a0001 | c0001 | t0005 | g0305 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19070 | hp1 | a0001 | c0001 | t0005 | g0047 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19074 | hp1 | a0001 | c0001 | t0022 | g0309 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19075 | hp1 | a0007 | c0010 | t0005 | g0313 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19077 | hp2 | a0003 | c0004 | t0002 | g0283 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19078 | hp2 | a0002 | c0003 | t0002 | g0065 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19080 | hp1 | a0001 | c0002 | t0004 | g0115 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19080 | hp2 | a0001 | c0001 | t0005 | g0022 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19081 | hp1 | a0001 | c0002 | t0004 | g0161 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19081 | hp2 | a0002 | c0003 | t0002 | g0055 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19082 | hp1 | a0001 | c0002 | t0004 | g0031 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19082 | hp2 | a0003 | c0004 | t0002 | g0006 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19084 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19086 | hp1 | a0001 | c0002 | t0004 | g0126 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19087 | hp1 | a0001 | c0002 | t0006 | g0088 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19088 | hp2 | a0002 | c0003 | t0002 | g0062 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19089 | hp1 | a0001 | c0001 | t0005 | g0057 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19091 | hp1 | a0001 | c0001 | t0005 | g0302 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19240 | hp1 | a0002 | c0003 | t0002 | g0008 | AFR | YRI | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | YRI | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0249 | AFR | ASW | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA20129 | hp2 | a0002 | c0003 | t0001 | g0013 | AFR | ASW | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA20752 | hp1 | a0001 | c0001 | t0007 | g0153 | EUR | TSI | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA20805 | hp1 | a0001 | c0002 | t0004 | g0135 | EUR | TSI | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA20805 | hp2 | a0001 | c0002 | t0006 | g0007 | EUR | TSI | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01123 | hp1 | a0001 | c0002 | t0004 | g0081 | AMR | CLM | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02109 | hp1 | a0001 | c0002 | t0004 | g0032 | AFR | ACB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02559 | hp1 | a0001 | c0005 | t0010 | g0021 | AFR | ACB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG02559 | hp2 | a0005 | c0011 | t0012 | g0138 | AFR | ACB | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03471 | hp1 | a0001 | c0001 | t0018 | g0148 | AFR | MSL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| HG03471 | hp2 | a0001 | c0002 | t0004 | g0142 | AFR | MSL | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0269 | AFR | USA | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA20300 | hp2 | a0002 | c0003 | t0015 | g0275 | AFR | USA | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | LWK | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | LWK | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0004 | g0145 | REF | REF | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0042 | REF | REF | QRSL1_chr6_106624578_106673417 | QRSL1 | chr6 | 106624578 | 106673417 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:106640356 | C | T | 2 | a0002 a0006 |
44 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(41): Show |
missense_variant | MODERATE | c.32C>T | p.Ala11Val | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 2/11 | 136/4106 | 32/1587 | 11/528 | chr6 | 106640356 | |||
| chr6:106652485 | A | ACCCCAGG others(43): Show |
1 | a0007 | 1 | NA19075.hp1 | frameshift_variant | HIGH | c.753_802dupCCCCAGGG others(42): Show |
p.Leu268fs | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 7/11 | 907/4106 | 803/1587 | 268/528 | INFO_REALIGN_3_PRIME | chr6 | 106652485 | ||
| chr6:106652521 | A | G | 1 | a0003 | 16 | HG02074.hp2 HG03927.hp2 HG04199.hp2 others(13): Show |
missense_variant | MODERATE | c.788A>G | p.Asn263Ser | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 7/11 | 892/4106 | 788/1587 | 263/528 | chr6 | 106652521 | |||
| chr6:106654730 | G | T | 1 | a0005 | 1 | HG02559.hp2 | stop_gained&splice_region_variant | HIGH | c.850G>T | p.Glu284* | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 8/11 | 954/4106 | 850/1587 | 284/528 | chr6 | 106654730 | |||
| chr6:106655635 | G | T | 1 | a0004 | 2 | HG01243.hp2 HG01952.hp2 |
missense_variant | MODERATE | c.1063G>T | p.Val355Leu | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/11 | 1167/4106 | 1063/1587 | 355/528 | chr6 | 106655635 | |||
| chr6:106663113 | G | A | 1 | a0006 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.1294G>A | p.Glu432Lys | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 10/11 | 1398/4106 | 1294/1587 | 432/528 | chr6 | 106663113 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:106640893 | G | A | 1 | a0001c0005 | 4 | HG02559.hp1 HG02818.hp1 HG02895.hp1 others(1): Show |
synonymous_variant | LOW | c.255G>A | p.Glu85Glu | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 3/11 | 359/4106 | 255/1587 | 85/528 | chr6 | 106640893 | |||
| chr6:106649184 | G | A | 1 | a0001c0006 | 3 | HG01243.hp1 HG02976.hp1 NA19043.hp2 |
synonymous_variant | LOW | c.540G>A | p.Ser180Ser | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/11 | 644/4106 | 540/1587 | 180/528 | chr6 | 106649184 | |||
| chr6:106652329 | G | A | 1 | a0001c0008 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.678G>A | p.Ser226Ser | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 6/11 | 782/4106 | 678/1587 | 226/528 | chr6 | 106652329 | |||
| chr6:106652522 | T | C | 1 | a0001c0009 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.789T>C | p.Asn263Asn | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 7/11 | 893/4106 | 789/1587 | 263/528 | chr6 | 106652522 | |||
| chr6:106665840 | G | A | 5 | a0001c0002 a0001c0005 a0001c0008 others(2): Show |
98 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
synonymous_variant | LOW | c.1425G>A | p.Leu475Leu | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 11/11 | 1529/4106 | 1425/1587 | 475/528 | chr6 | 106665840 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:106629627 | G | A | 5 | a0001c0001t0007 a0001c0002t0004 a0001c0002t0012 others(2): Show |
65 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(62): Show |
5_prime_UTR_variant | MODIFIER | c.-55G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/11 | 55 | chr6 | 106629627 | ||||||
| chr6:106629642 | C | T | 1 | a0001c0001t0022 | 1 | NA19074.hp1 | 5_prime_UTR_variant | MODIFIER | c.-40C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/11 | 40 | chr6 | 106629642 | ||||||
| chr6:106629675 | G | A | 5 | a0001c0001t0003 a0001c0002t0011 a0001c0002t0016 others(2): Show |
64 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(61): Show |
5_prime_UTR_variant | MODIFIER | c.-7G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/11 | 7 | chr6 | 106629675 | ||||||
| chr6:106666078 | C | G | 6 | a0001c0002t0004 a0001c0002t0008 a0001c0002t0011 others(3): Show |
68 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*76C>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 11/11 | 76 | chr6 | 106666078 | ||||||
| chr6:106666085 | G | A | 1 | a0001c0001t0017 | 1 | NA19055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*83G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 11/11 | 83 | chr6 | 106666085 | ||||||
| chr6:106666088 | C | T | 4 | a0001c0002t0006 a0001c0002t0016 a0001c0002t0021 others(1): Show |
25 | HG00438.hp2 HG00738.hp2 HG01070.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*86C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 11/11 | 86 | chr6 | 106666088 | ||||||
| chr6:106666092 | T | A | 4 | a0001c0002t0006 a0001c0002t0016 a0001c0002t0021 others(1): Show |
25 | HG00438.hp2 HG00738.hp2 HG01070.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*90T>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 11/11 | 90 | chr6 | 106666092 | ||||||
| chr6:106666141 | G | A | 1 | a0001c0002t0014 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*139G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 11/11 | 139 | chr6 | 106666141 | ||||||
| chr6:106666416 | TAC | T | 7 | a0001c0002t0004 a0001c0002t0008 a0001c0002t0011 others(4): Show |
72 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*416_*417delCA | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 11/11 | 416 | INFO_REALIGN_3_PRIME | chr6 | 106666416 | |||||
| chr6:106666486 | A | G | 6 | a0001c0002t0004 a0001c0002t0008 a0001c0002t0011 others(3): Show |
68 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*484A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 11/11 | 484 | chr6 | 106666486 | ||||||
| chr6:106666711 | G | A | 1 | a0001c0005t0010 | 4 | HG02559.hp1 HG02818.hp1 HG02895.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*709G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 11/11 | 709 | chr6 | 106666711 | ||||||
| chr6:106666960 | T | G | 1 | a0001c0002t0021 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*958T>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 11/11 | 958 | chr6 | 106666960 | ||||||
| chr6:106666998 | G | T | 1 | a0002c0003t0015 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*996G>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 11/11 | 996 | chr6 | 106666998 | ||||||
| chr6:106667296 | A | C | 1 | a0001c0001t0020 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1294A>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 11/11 | 1294 | chr6 | 106667296 | ||||||
| chr6:106667322 | G | A | 2 | a0001c0002t0012 a0005c0011t0012 |
2 | HG02559.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1320G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 11/11 | 1320 | chr6 | 106667322 | ||||||
| chr6:106667350 | A | C | 4 | a0001c0001t0005 a0001c0001t0017 a0001c0001t0022 others(1): Show |
45 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1348A>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 11/11 | 1348 | chr6 | 106667350 | ||||||
| chr6:106667509 | G | T | 4 | a0001c0001t0005 a0001c0001t0017 a0001c0001t0022 others(1): Show |
45 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1507G>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 11/11 | 1507 | chr6 | 106667509 | ||||||
| chr6:106667519 | A | G | 6 | a0001c0002t0004 a0001c0002t0008 a0001c0002t0011 others(3): Show |
68 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*1517A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 11/11 | 1517 | chr6 | 106667519 | ||||||
| chr6:106667526 | C | G | 1 | a0001c0005t0010 | 4 | HG02559.hp1 HG02818.hp1 HG02895.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1524C>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 11/11 | 1524 | chr6 | 106667526 | ||||||
| chr6:106667956 | TA | T | 13 | a0001c0001t0013 a0001c0002t0004 a0001c0002t0006 others(10): Show |
99 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*1963delA | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 11/11 | 1963 | INFO_REALIGN_3_PRIME | chr6 | 106667956 | |||||
| chr6:106667957 | A | T | 1 | a0004c0007t0001 | 2 | HG01243.hp2 HG01952.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1955A>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 11/11 | 1955 | chr6 | 106667957 | ||||||
| chr6:106667963 | AAAG | A | 6 | a0001c0001t0002 a0002c0003t0002 a0002c0003t0009 others(3): Show |
72 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1963_*1965delAGA | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 11/11 | 1963 | INFO_REALIGN_3_PRIME | chr6 | 106667963 | |||||
| chr6:106667964 | A | G | 1 | a0001c0001t0001 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1962A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 11/11 | 1962 | chr6 | 106667964 | ||||||
| chr6:106668013 | C | G | 1 | a0003c0004t0019 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2011C>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 11/11 | 2011 | chr6 | 106668013 | ||||||
| chr6:106668095 | A | AAAT | 1 | a0001c0005t0010 | 4 | HG02559.hp1 HG02818.hp1 HG02895.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2101_*2103dupATA | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 11/11 | 2104 | INFO_REALIGN_3_PRIME | chr6 | 106668095 | |||||
| chr6:106668241 | G | A | 1 | a0001c0001t0018 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2239G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 11/11 | 2239 | chr6 | 106668241 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:106629722 | C | T | 1 | a0001c0001t0003g0319 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.24+17C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106629722 | |||||||
| chr6:106629770 | A | G | 1 | a0001c0001t0003g0318 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.24+65A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106629770 | |||||||
| chr6:106629969 | AG | A | 25 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0047 others(22): Show |
44 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.24+266delG | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 106629969 | ||||||
| chr6:106630156 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.24+451T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106630156 | |||||||
| chr6:106630280 | A | C | 24 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(21): Show |
31 | HG02074.hp2 HG02257.hp2 HG02559.hp1 others(28): Show |
intron_variant | MODIFIER | c.24+575A>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106630280 | |||||||
| chr6:106630297 | T | C | 1 | a0001c0001t0003g0319 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.24+592T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106630297 | |||||||
| chr6:106630310 | A | C | 1 | a0002c0003t0001g0277 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.24+605A>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106630310 | |||||||
| chr6:106630334 | C | T | 1 | a0001c0002t0004g0276 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.24+629C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106630334 | |||||||
| chr6:106630349 | A | G | 1 | a0001c0008t0006g0298 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.24+644A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106630349 | |||||||
| chr6:106630380 | CTT | C | 24 | a0001c0001t0005g0057 a0002c0003t0001g0013 a0002c0003t0001g0056 others(21): Show |
31 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.24+679_24+680delTT | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 106630380 | ||||||
| chr6:106630471 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.24+766T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106630471 | |||||||
| chr6:106630783 | G | A | 1 | a0006c0012t0002g0071 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.24+1078G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106630783 | |||||||
| chr6:106630796 | C | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.24+1091C>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106630796 | |||||||
| chr6:106630931 | T | C | 1 | a0001c0002t0016g0074 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.24+1226T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106630931 | |||||||
| chr6:106631001 | T | C | 1 | a0001c0001t0001g0075 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.24+1296T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106631001 | |||||||
| chr6:106631106 | G | T | 43 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(40): Show |
64 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.24+1401G>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106631106 | |||||||
| chr6:106631112 | G | C | 1 | a0001c0001t0005g0299 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.24+1407G>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106631112 | |||||||
| chr6:106631175 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.24+1470A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106631175 | |||||||
| chr6:106631181 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.24+1476A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106631181 | |||||||
| chr6:106631217 | C | T | 1 | a0001c0001t0003g0319 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.24+1512C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106631217 | |||||||
| chr6:106631255 | T | C | 4 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0004c0007t0001g0077 others(1): Show |
4 | HG00733.hp2 HG01243.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.24+1550T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106631255 | |||||||
| chr6:106631322 | T | G | 2 | a0001c0001t0003g0043 a0001c0001t0003g0244 |
3 | HG00423.hp2 NA18978.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.24+1617T>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106631322 | |||||||
| chr6:106631418 | G | T | 1 | a0002c0003t0015g0275 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.24+1713G>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106631418 | |||||||
| chr6:106631432 | T | A | 1 | a0001c0009t0013g0080 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.24+1727T>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106631432 | |||||||
| chr6:106631488 | T | C | 4 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0004c0007t0001g0077 others(1): Show |
4 | HG00733.hp2 HG01243.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.24+1783T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106631488 | |||||||
| chr6:106631523 | G | A | 1 | a0002c0003t0015g0275 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.24+1818G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106631523 | |||||||
| chr6:106631638 | T | C | 1 | a0001c0002t0004g0081 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.24+1933T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106631638 | |||||||
| chr6:106631662 | T | TA | 70 | a0001c0001t0005g0057 a0001c0001t0005g0099 a0001c0002t0006g0007 others(67): Show |
92 | HG00280.hp2 HG00438.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.24+1957_24+1958ins others(1): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106631662 | |||||||
| chr6:106631663 | T | A | 105 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0289 others(102): Show |
146 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.24+1958T>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106631663 | |||||||
| chr6:106631671 | A | G | 1 | a0001c0001t0003g0319 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.24+1966A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106631671 | |||||||
| chr6:106631672 | A | T | 4 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0004c0007t0001g0077 others(1): Show |
4 | HG00733.hp2 HG01243.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.24+1967A>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106631672 | |||||||
| chr6:106631685 | C | T | 43 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(40): Show |
64 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.24+1980C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106631685 | |||||||
| chr6:106631806 | T | G | 5 | a0002c0003t0002g0012 a0002c0003t0002g0023 a0002c0003t0002g0052 others(2): Show |
8 | HG01891.hp1 HG02572.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.24+2101T>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106631806 | |||||||
| chr6:106631932 | C | G | 1 | a0001c0001t0001g0079 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.24+2227C>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106631932 | |||||||
| chr6:106631938 | C | T | 1 | a0003c0004t0002g0288 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.24+2233C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106631938 | |||||||
| chr6:106631943 | C | T | 1 | a0002c0003t0002g0054 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.24+2238C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106631943 | |||||||
| chr6:106631947 | A | G | 1 | a0001c0002t0004g0242 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.24+2242A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106631947 | |||||||
| chr6:106631982 | A | G | 1 | a0001c0001t0007g0241 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.24+2277A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106631982 | |||||||
| chr6:106632144 | G | A | 3 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 |
3 | NA18952.hp2 NA18978.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.24+2439G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106632144 | |||||||
| chr6:106632350 | C | T | 1 | a0003c0004t0002g0287 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.24+2645C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106632350 | |||||||
| chr6:106632370 | A | T | 1 | a0001c0001t0001g0240 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.24+2665A>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106632370 | |||||||
| chr6:106632539 | A | G | 43 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(40): Show |
64 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.24+2834A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106632539 | |||||||
| chr6:106632573 | AG | A | 7 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(4): Show |
7 | NA18952.hp2 NA18978.hp2 NA19003.hp2 others(4): Show |
intron_variant | MODIFIER | c.24+2869delG | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106632573 | |||||||
| chr6:106632579 | T | C | 9 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(6): Show |
9 | HG02257.hp2 HG02647.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.24+2874T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106632579 | |||||||
| chr6:106632581 | A | G | 1 | a0001c0001t0003g0274 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.24+2876A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106632581 | |||||||
| chr6:106632583 | A | G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0235 a0001c0001t0001g0243 |
5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.24+2878A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106632583 | |||||||
| chr6:106632740 | G | A | 1 | a0002c0003t0015g0275 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.24+3035G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106632740 | |||||||
| chr6:106632762 | G | A | 43 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0003g0003 others(40): Show |
64 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.24+3057G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106632762 | |||||||
| chr6:106632822 | T | G | 4 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0004c0007t0001g0077 others(1): Show |
4 | HG00733.hp2 HG01243.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.24+3117T>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106632822 | |||||||
| chr6:106632841 | A | T | 1 | a0001c0002t0012g0234 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.24+3136A>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106632841 | |||||||
| chr6:106632906 | C | T | 2 | a0001c0001t0003g0272 a0001c0001t0003g0273 |
2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.24+3201C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106632906 | |||||||
| chr6:106633012 | C | T | 1 | a0001c0001t0003g0319 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.24+3307C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106633012 | |||||||
| chr6:106633033 | C | T | 1 | a0002c0003t0015g0275 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.24+3328C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106633033 | |||||||
| chr6:106633113 | C | T | 24 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0047 others(21): Show |
43 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.24+3408C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106633113 | |||||||
| chr6:106633135 | C | T | 1 | a0001c0001t0007g0233 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.24+3430C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106633135 | |||||||
| chr6:106633147 | G | A | 295 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(292): Show |
393 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.24+3442G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106633147 | |||||||
| chr6:106633159 | T | C | 6 | a0001c0001t0002g0014 a0001c0001t0002g0110 a0001c0001t0002g0111 others(3): Show |
8 | HG00438.hp1 HG02071.hp2 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.24+3454T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106633159 | |||||||
| chr6:106633381 | C | T | 296 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(293): Show |
394 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(391): Show |
intron_variant | MODIFIER | c.24+3676C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106633381 | |||||||
| chr6:106633426 | C | T | 1 | a0001c0001t0003g0319 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.24+3721C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106633426 | |||||||
| chr6:106633524 | C | T | 1 | a0002c0003t0015g0275 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.24+3819C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106633524 | |||||||
| chr6:106633776 | A | T | 41 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(38): Show |
62 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.24+4071A>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106633776 | |||||||
| chr6:106633948 | TA | T | 148 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0210 others(145): Show |
210 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.24+4257delA | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 106633948 | ||||||
| chr6:106633989 | G | A | 43 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(40): Show |
64 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.24+4284G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106633989 | |||||||
| chr6:106634277 | A | G | 2 | a0002c0003t0002g0008 a0002c0003t0002g0103 |
5 | HG02280.hp1 HG02451.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.24+4572A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106634277 | |||||||
| chr6:106634671 | T | G | 1 | a0001c0002t0004g0115 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.24+4966T>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106634671 | |||||||
| chr6:106634795 | C | G | 41 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(38): Show |
62 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.24+5090C>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106634795 | |||||||
| chr6:106634885 | G | A | 9 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(6): Show |
9 | HG02257.hp2 HG02647.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.24+5180G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106634885 | |||||||
| chr6:106635168 | A | G | 1 | a0001c0002t0006g0102 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.25-5181A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106635168 | |||||||
| chr6:106635303 | A | G | 41 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(38): Show |
62 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.25-5046A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106635303 | |||||||
| chr6:106635320 | G | C | 1 | a0001c0001t0003g0319 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.25-5029G>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106635320 | |||||||
| chr6:106635444 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.25-4905G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106635444 | |||||||
| chr6:106635489 | A | G | 2 | a0002c0003t0002g0068 a0002c0003t0002g0069 |
2 | HG02148.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.25-4860A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106635489 | |||||||
| chr6:106635501 | A | T | 5 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0269 others(2): Show |
5 | HG02055.hp2 HG03139.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.25-4848A>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106635501 | |||||||
| chr6:106635534 | G | C | 6 | a0001c0002t0008g0026 a0001c0002t0008g0082 a0001c0002t0008g0083 others(3): Show |
7 | HG02451.hp1 HG02922.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.25-4815G>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106635534 | |||||||
| chr6:106635641 | G | A | 1 | a0002c0003t0009g0246 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.25-4708G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106635641 | |||||||
| chr6:106635649 | C | G | 1 | a0001c0001t0001g0109 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.25-4700C>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106635649 | |||||||
| chr6:106635743 | C | T | 83 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(80): Show |
107 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.25-4606C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106635743 | |||||||
| chr6:106635820 | G | A | 3 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0002c0003t0015g0275 |
3 | HG03453.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.25-4529G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106635820 | |||||||
| chr6:106635886 | A | G | 3 | a0001c0001t0003g0266 a0001c0001t0003g0272 a0001c0001t0003g0273 |
3 | HG01175.hp1 HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.25-4463A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106635886 | |||||||
| chr6:106635943 | C | T | 15 | a0001c0001t0001g0208 a0001c0001t0002g0010 a0001c0001t0002g0014 others(12): Show |
22 | HG00438.hp1 HG00621.hp2 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.25-4406C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106635943 | |||||||
| chr6:106635983 | T | C | 4 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0004c0007t0001g0077 others(1): Show |
4 | HG00733.hp2 HG01243.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.25-4366T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106635983 | |||||||
| chr6:106636296 | C | T | 1 | a0001c0002t0004g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.25-4053C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106636296 | |||||||
| chr6:106636317 | A | C | 1 | a0001c0002t0016g0074 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.25-4032A>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106636317 | |||||||
| chr6:106636318 | C | CT | 32 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0073 others(29): Show |
37 | HG00438.hp2 HG00735.hp2 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.25-4010dupT | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 106636318 | ||||||
| chr6:106636318 | CT | C | 6 | a0001c0001t0001g0236 a0001c0001t0003g0247 a0001c0002t0004g0116 others(3): Show |
6 | HG00280.hp2 HG01168.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.25-4010delT | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 106636318 | ||||||
| chr6:106636353 | G | A | 1 | a0001c0001t0003g0319 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.25-3996G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106636353 | |||||||
| chr6:106636432 | T | C | 1 | a0001c0001t0003g0248 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.25-3917T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106636432 | |||||||
| chr6:106636437 | T | C | 1 | a0001c0001t0003g0248 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.25-3912T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106636437 | |||||||
| chr6:106636445 | C | T | 1 | a0001c0001t0003g0248 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.25-3904C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106636445 | |||||||
| chr6:106636446 | A | G | 1 | a0001c0001t0003g0248 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.25-3903A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106636446 | |||||||
| chr6:106636469 | C | T | 12 | a0001c0001t0003g0261 a0001c0001t0003g0262 a0001c0001t0003g0265 others(9): Show |
12 | HG02165.hp2 HG02523.hp1 NA18947.hp2 others(9): Show |
intron_variant | MODIFIER | c.25-3880C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106636469 | |||||||
| chr6:106636526 | G | A | 4 | a0001c0001t0001g0035 a0001c0001t0001g0051 a0001c0001t0001g0163 others(1): Show |
5 | HG01258.hp1 HG01433.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.25-3823G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106636526 | |||||||
| chr6:106636566 | G | A | 1 | a0002c0003t0015g0275 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.25-3783G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106636566 | |||||||
| chr6:106636603 | G | A | 1 | a0001c0001t0003g0319 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.25-3746G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106636603 | |||||||
| chr6:106636625 | A | G | 42 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(39): Show |
59 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.25-3724A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106636625 | |||||||
| chr6:106636670 | T | A | 1 | a0001c0002t0016g0074 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.25-3679T>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106636670 | |||||||
| chr6:106636836 | T | C | 130 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(127): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.25-3513T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106636836 | |||||||
| chr6:106636931 | ACTTTGTG others(1): Show |
A | 30 | a0001c0001t0003g0319 a0001c0001t0005g0001 a0001c0001t0005g0022 others(27): Show |
49 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.25-3414_25-3407del others(8): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 106636931 | ||||||
| chr6:106637066 | G | A | 72 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0047 others(69): Show |
110 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.25-3283G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106637066 | |||||||
| chr6:106637089 | T | A | 26 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0047 others(23): Show |
45 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.25-3260T>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106637089 | |||||||
| chr6:106637113 | G | A | 1 | a0001c0001t0005g0301 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.25-3236G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106637113 | |||||||
| chr6:106637140 | G | T | 3 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0240 |
3 | HG00621.hp1 NA18960.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.25-3209G>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106637140 | |||||||
| chr6:106637169 | G | C | 1 | a0001c0001t0001g0164 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.25-3180G>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106637169 | |||||||
| chr6:106637325 | C | T | 4 | a0001c0001t0003g0319 a0001c0002t0016g0074 a0002c0003t0001g0100 others(1): Show |
4 | HG01891.hp2 HG02055.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.25-3024C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106637325 | |||||||
| chr6:106637375 | G | A | 1 | a0001c0009t0013g0080 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.25-2974G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106637375 | |||||||
| chr6:106637386 | A | T | 13 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(10): Show |
13 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.25-2963A>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106637386 | |||||||
| chr6:106637484 | C | CTA | 30 | a0002c0003t0001g0013 a0002c0003t0001g0056 a0002c0003t0001g0059 others(27): Show |
42 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.25-2862_25-2861dup others(2): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 106637484 | ||||||
| chr6:106637489 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.25-2860G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106637489 | |||||||
| chr6:106637524 | A | G | 2 | a0001c0001t0001g0202 a0001c0001t0001g0211 |
2 | HG03927.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.25-2825A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106637524 | |||||||
| chr6:106637630 | T | G | 3 | a0002c0003t0002g0012 a0002c0003t0002g0023 a0002c0003t0002g0052 |
6 | HG01891.hp1 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.25-2719T>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106637630 | |||||||
| chr6:106637699 | T | C | 37 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(34): Show |
54 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.25-2650T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106637699 | |||||||
| chr6:106637731 | G | A | 122 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(119): Show |
159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.25-2618G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106637731 | |||||||
| chr6:106637752 | G | A | 1 | a0001c0002t0006g0086 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.25-2597G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106637752 | |||||||
| chr6:106637801 | A | C | 30 | a0002c0003t0001g0013 a0002c0003t0001g0056 a0002c0003t0001g0059 others(27): Show |
42 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.25-2548A>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106637801 | |||||||
| chr6:106638021 | T | C | 9 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(6): Show |
9 | HG02257.hp2 HG02647.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.25-2328T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106638021 | |||||||
| chr6:106638103 | G | A | 122 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(119): Show |
159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.25-2246G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106638103 | |||||||
| chr6:106638238 | C | T | 1 | a0003c0004t0002g0285 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.25-2111C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106638238 | |||||||
| chr6:106638305 | C | CT | 149 | a0001c0001t0001g0231 a0001c0001t0005g0001 a0001c0001t0005g0022 others(146): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.25-2035dupT | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 106638305 | ||||||
| chr6:106638344 | GCC | G | 3 | a0001c0001t0001g0289 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02257.hp2 HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.25-2003_25-2002del others(2): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 106638344 | ||||||
| chr6:106638371 | C | T | 14 | a0001c0005t0010g0021 a0001c0005t0010g0284 a0001c0008t0006g0298 others(11): Show |
21 | HG02074.hp2 HG02559.hp1 HG02818.hp1 others(18): Show |
intron_variant | MODIFIER | c.25-1978C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106638371 | |||||||
| chr6:106638381 | C | T | 1 | a0002c0003t0002g0053 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.25-1968C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106638381 | |||||||
| chr6:106638588 | A | G | 196 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(193): Show |
269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.25-1761A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106638588 | |||||||
| chr6:106638636 | A | G | 33 | a0001c0002t0006g0007 a0001c0002t0006g0027 a0001c0002t0006g0028 others(30): Show |
44 | HG00438.hp2 HG00738.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.25-1713A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106638636 | |||||||
| chr6:106638650 | G | A | 1 | a0003c0004t0002g0287 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.25-1699G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106638650 | |||||||
| chr6:106638679 | G | A | 3 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 |
3 | HG00642.hp1 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.25-1670G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106638679 | |||||||
| chr6:106638685 | G | A | 32 | a0002c0003t0001g0013 a0002c0003t0001g0056 a0002c0003t0001g0059 others(29): Show |
44 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.25-1664G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106638685 | |||||||
| chr6:106638709 | G | T | 26 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0047 others(23): Show |
45 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.25-1640G>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106638709 | |||||||
| chr6:106638796 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.25-1553A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106638796 | |||||||
| chr6:106638844 | A | G | 19 | a0001c0002t0006g0007 a0001c0002t0006g0027 a0001c0002t0006g0028 others(16): Show |
23 | HG00438.hp2 HG00738.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.25-1505A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106638844 | |||||||
| chr6:106638940 | A | G | 23 | a0001c0001t0001g0017 a0001c0001t0001g0070 a0001c0001t0001g0076 others(20): Show |
26 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.25-1409A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106638940 | |||||||
| chr6:106638980 | T | C | 1 | a0001c0002t0004g0119 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.25-1369T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106638980 | |||||||
| chr6:106639049 | G | C | 1 | a0001c0009t0013g0080 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.25-1300G>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106639049 | |||||||
| chr6:106639111 | G | GTTTTTTT others(3): Show |
1 | a0001c0001t0001g0295 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.25-1234_25-1233ins others(10): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 106639111 | ||||||
| chr6:106639111 | G | GTTTTTTT others(7): Show |
1 | a0001c0002t0016g0074 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.25-1234_25-1233ins others(14): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 106639111 | ||||||
| chr6:106639116 | G | GT | 15 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(12): Show |
20 | HG00423.hp2 HG01192.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.25-1231dupT | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 106639116 | ||||||
| chr6:106639116 | G | GTT | 2 | a0001c0001t0003g0003 a0001c0001t0003g0273 |
3 | HG00609.hp2 HG01175.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.25-1232_25-1231dup others(2): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 106639116 | ||||||
| chr6:106639116 | G | GTTTTTTT | 7 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0303 others(4): Show |
8 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(5): Show |
intron_variant | MODIFIER | c.25-1231_25-1230ins others(7): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 106639116 | ||||||
| chr6:106639116 | G | GTTTTTTT others(1): Show |
12 | a0001c0001t0005g0001 a0001c0001t0005g0047 a0001c0001t0005g0048 others(9): Show |
16 | HG00408.hp2 HG00423.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.25-1231_25-1230ins others(8): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 106639116 | ||||||
| chr6:106639116 | G | GTTTTTTT others(2): Show |
11 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0047 others(8): Show |
15 | HG01952.hp1 HG02132.hp2 NA18946.hp2 others(12): Show |
intron_variant | MODIFIER | c.25-1231_25-1230ins others(9): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 106639116 | ||||||
| chr6:106639116 | G | GTTTTTTT others(3): Show |
3 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0299 |
3 | HG01943.hp1 HG02080.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.25-1231_25-1230ins others(10): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 106639116 | ||||||
| chr6:106639116 | G | T | 10 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(7): Show |
10 | HG01891.hp2 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.25-1233G>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106639116 | |||||||
| chr6:106639116 | GTTGTTTT others(3): Show |
G | 2 | a0001c0001t0005g0001 a0001c0001t0005g0305 |
2 | NA18969.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.25-1230_25-1221del others(10): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 106639116 | ||||||
| chr6:106639118 | TG | T | 7 | a0001c0001t0003g0249 a0001c0001t0003g0250 a0001c0001t0003g0252 others(4): Show |
7 | HG02132.hp1 HG02615.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.25-1230delG | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106639118 | |||||||
| chr6:106639119 | G | GT | 57 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(54): Show |
68 | HG00438.hp1 HG00597.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.25-1203dupT | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 106639119 | ||||||
| chr6:106639119 | G | GTT | 20 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0070 others(17): Show |
20 | HG00544.hp1 HG00642.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.25-1204_25-1203dup others(2): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 106639119 | ||||||
| chr6:106639119 | G | T | 186 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(183): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.25-1230G>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106639119 | |||||||
| chr6:106639121 | T | TTTTTG | 6 | a0002c0003t0001g0060 a0002c0003t0001g0100 a0002c0003t0001g0286 others(3): Show |
6 | HG01255.hp2 HG01884.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.25-1224_25-1223ins others(5): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 106639121 | ||||||
| chr6:106639122 | T | TTTTG | 22 | a0001c0009t0013g0080 a0002c0003t0001g0013 a0002c0003t0001g0056 others(19): Show |
27 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.25-1224_25-1223ins others(4): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 106639122 | ||||||
| chr6:106639124 | T | TTG | 87 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(84): Show |
112 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.25-1224_25-1223ins others(2): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 106639124 | ||||||
| chr6:106639129 | T | G | 1 | a0002c0003t0002g0058 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.25-1220T>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106639129 | |||||||
| chr6:106639130 | T | G | 2 | a0002c0003t0001g0060 a0002c0003t0001g0286 |
2 | HG01255.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.25-1219T>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106639130 | |||||||
| chr6:106639131 | T | G | 37 | a0001c0002t0006g0007 a0001c0002t0006g0027 a0001c0002t0006g0028 others(34): Show |
50 | HG00280.hp2 HG00438.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.25-1218T>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106639131 | |||||||
| chr6:106639132 | T | G | 1 | a0001c0001t0001g0166 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.25-1217T>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106639132 | |||||||
| chr6:106639133 | T | G | 2 | a0001c0002t0004g0143 a0002c0003t0002g0061 |
2 | NA18991.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.25-1216T>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106639133 | |||||||
| chr6:106639134 | T | G | 55 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(52): Show |
69 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.25-1215T>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106639134 | |||||||
| chr6:106639136 | T | G | 1 | a0001c0001t0001g0166 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.25-1213T>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106639136 | |||||||
| chr6:106639138 | T | G | 15 | a0001c0005t0010g0021 a0001c0005t0010g0284 a0001c0008t0006g0298 others(12): Show |
22 | HG02074.hp2 HG02559.hp1 HG02818.hp1 others(19): Show |
intron_variant | MODIFIER | c.25-1211T>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106639138 | |||||||
| chr6:106639187 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.25-1162G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106639187 | |||||||
| chr6:106639188 | C | T | 30 | a0002c0003t0001g0013 a0002c0003t0001g0056 a0002c0003t0001g0059 others(27): Show |
42 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.25-1161C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106639188 | |||||||
| chr6:106639206 | A | G | 56 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(53): Show |
70 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.25-1143A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106639206 | |||||||
| chr6:106639665 | T | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.25-684T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106639665 | |||||||
| chr6:106639696 | C | A | 5 | a0001c0001t0001g0033 a0001c0001t0001g0146 a0001c0001t0001g0147 others(2): Show |
6 | HG02258.hp2 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.25-653C>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106639696 | |||||||
| chr6:106639747 | A | G | 80 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(77): Show |
100 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.25-602A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106639747 | |||||||
| chr6:106639765 | T | C | 48 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(45): Show |
70 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.25-584T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106639765 | |||||||
| chr6:106639944 | G | A | 9 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(6): Show |
9 | HG02257.hp2 HG02647.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.25-405G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106639944 | |||||||
| chr6:106639995 | G | A | 32 | a0002c0003t0001g0013 a0002c0003t0001g0056 a0002c0003t0001g0059 others(29): Show |
44 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.25-354G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106639995 | |||||||
| chr6:106640080 | T | A | 1 | a0001c0001t0001g0167 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.25-269T>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106640080 | |||||||
| chr6:106640124 | G | T | 1 | a0002c0003t0002g0069 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.25-225G>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106640124 | |||||||
| chr6:106640278 | C | A | 1 | a0001c0002t0004g0242 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.25-71C>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 1/10 | chr6 | 106640278 | |||||||
| chr6:106640710 | T | A | 112 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(109): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.185-113T>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 2/10 | chr6 | 106640710 | |||||||
| chr6:106640974 | C | T | 1 | a0001c0001t0005g0314 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.283+53C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 3/10 | chr6 | 106640974 | |||||||
| chr6:106641011 | CTAAT | C | 19 | a0001c0002t0006g0007 a0001c0002t0006g0027 a0001c0002t0006g0028 others(16): Show |
23 | HG00438.hp2 HG00738.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.283+93_283+96delAT others(2): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr6 | 106641011 | ||||||
| chr6:106641052 | TG | T | 9 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(6): Show |
9 | HG02257.hp2 HG02647.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.283+132delG | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 3/10 | chr6 | 106641052 | |||||||
| chr6:106641186 | A | G | 21 | a0001c0002t0006g0007 a0001c0002t0006g0027 a0001c0002t0006g0028 others(18): Show |
25 | HG00438.hp2 HG00738.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.283+265A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 3/10 | chr6 | 106641186 | |||||||
| chr6:106641300 | C | T | 1 | a0001c0009t0013g0080 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.283+379C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 3/10 | chr6 | 106641300 | |||||||
| chr6:106641394 | A | G | 5 | a0003c0004t0002g0006 a0003c0004t0002g0046 a0003c0004t0002g0282 others(2): Show |
10 | NA18950.hp2 NA18971.hp1 NA18979.hp1 others(7): Show |
intron_variant | MODIFIER | c.283+473A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 3/10 | chr6 | 106641394 | |||||||
| chr6:106641413 | G | C | 1 | a0001c0002t0004g0120 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.283+492G>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 3/10 | chr6 | 106641413 | |||||||
| chr6:106641414 | T | G | 90 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(87): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.283+493T>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 3/10 | chr6 | 106641414 | |||||||
| chr6:106641544 | A | T | 48 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(45): Show |
70 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.283+623A>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 3/10 | chr6 | 106641544 | |||||||
| chr6:106641598 | C | T | 26 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0047 others(23): Show |
45 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.283+677C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 3/10 | chr6 | 106641598 | |||||||
| chr6:106641709 | T | C | 58 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(55): Show |
74 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.283+788T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 3/10 | chr6 | 106641709 | |||||||
| chr6:106641965 | A | G | 56 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(53): Show |
70 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.284-1029A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 3/10 | chr6 | 106641965 | |||||||
| chr6:106642120 | G | A | 2 | a0001c0002t0004g0121 a0001c0002t0004g0122 |
2 | HG03017.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.284-874G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 3/10 | chr6 | 106642120 | |||||||
| chr6:106642247 | T | C | 112 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(109): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.284-747T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 3/10 | chr6 | 106642247 | |||||||
| chr6:106642292 | G | C | 1 | a0001c0001t0003g0319 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.284-702G>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 3/10 | chr6 | 106642292 | |||||||
| chr6:106642347 | C | T | 32 | a0002c0003t0001g0013 a0002c0003t0001g0056 a0002c0003t0001g0059 others(29): Show |
44 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.284-647C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 3/10 | chr6 | 106642347 | |||||||
| chr6:106642348 | G | A | 78 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(75): Show |
96 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.284-646G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 3/10 | chr6 | 106642348 | |||||||
| chr6:106642352 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.284-642C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 3/10 | chr6 | 106642352 | |||||||
| chr6:106642353 | G | A | 112 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(109): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.284-641G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 3/10 | chr6 | 106642353 | |||||||
| chr6:106642355 | C | T | 80 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(77): Show |
100 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.284-639C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 3/10 | chr6 | 106642355 | |||||||
| chr6:106642356 | G | A | 48 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(45): Show |
70 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.284-638G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 3/10 | chr6 | 106642356 | |||||||
| chr6:106642494 | A | G | 138 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0047 others(135): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.284-500A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 3/10 | chr6 | 106642494 | |||||||
| chr6:106642518 | C | G | 112 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(109): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.284-476C>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 3/10 | chr6 | 106642518 | |||||||
| chr6:106642562 | A | G | 2 | a0001c0005t0010g0021 a0001c0005t0010g0284 |
4 | HG02559.hp1 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-432A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 3/10 | chr6 | 106642562 | |||||||
| chr6:106642697 | T | A | 1 | a0002c0003t0009g0246 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.284-297T>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 3/10 | chr6 | 106642697 | |||||||
| chr6:106642739 | C | A | 58 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(55): Show |
74 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.284-255C>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 3/10 | chr6 | 106642739 | |||||||
| chr6:106642832 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.284-162G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 3/10 | chr6 | 106642832 | |||||||
| chr6:106642840 | C | T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.284-154C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 3/10 | chr6 | 106642840 | |||||||
| chr6:106643173 | G | A | 3 | a0001c0001t0003g0249 a0001c0001t0003g0250 a0001c0001t0003g0263 |
3 | HG02145.hp2 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.380+83G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106643173 | |||||||
| chr6:106643223 | T | C | 1 | a0001c0009t0013g0080 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.380+133T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106643223 | |||||||
| chr6:106643324 | G | A | 112 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(109): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.380+234G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106643324 | |||||||
| chr6:106643345 | T | G | 112 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(109): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.380+255T>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106643345 | |||||||
| chr6:106643350 | A | G | 26 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0047 others(23): Show |
45 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.380+260A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106643350 | |||||||
| chr6:106643446 | G | A | 32 | a0002c0003t0001g0013 a0002c0003t0001g0056 a0002c0003t0001g0059 others(29): Show |
44 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.380+356G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106643446 | |||||||
| chr6:106643446 | G | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | NA18948.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.380+356G>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106643446 | |||||||
| chr6:106643477 | C | T | 1 | a0001c0002t0004g0142 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.380+387C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106643477 | |||||||
| chr6:106643509 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.380+419G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106643509 | |||||||
| chr6:106643637 | G | A | 1 | a0001c0009t0013g0080 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.380+547G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106643637 | |||||||
| chr6:106643680 | CA | C | 33 | a0002c0003t0001g0013 a0002c0003t0001g0056 a0002c0003t0001g0059 others(30): Show |
45 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.380+605delA | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 106643680 | ||||||
| chr6:106643730 | A | G | 6 | a0002c0003t0002g0025 a0002c0003t0002g0067 a0002c0003t0002g0068 others(3): Show |
7 | HG02148.hp1 NA18974.hp2 NA18997.hp2 others(4): Show |
intron_variant | MODIFIER | c.380+640A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106643730 | |||||||
| chr6:106643816 | G | T | 1 | a0001c0002t0004g0141 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.380+726G>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106643816 | |||||||
| chr6:106643865 | T | G | 1 | a0001c0008t0006g0298 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.380+775T>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106643865 | |||||||
| chr6:106643974 | C | T | 2 | a0001c0001t0001g0191 a0001c0002t0004g0140 |
2 | NA18747.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.380+884C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106643974 | |||||||
| chr6:106644072 | A | G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0235 a0001c0001t0001g0243 |
5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.380+982A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106644072 | |||||||
| chr6:106644108 | A | G | 112 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(109): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.380+1018A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106644108 | |||||||
| chr6:106644188 | C | T | 5 | a0003c0004t0002g0006 a0003c0004t0002g0046 a0003c0004t0002g0282 others(2): Show |
10 | NA18950.hp2 NA18971.hp1 NA18979.hp1 others(7): Show |
intron_variant | MODIFIER | c.380+1098C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106644188 | |||||||
| chr6:106644499 | TTTTG | T | 32 | a0002c0003t0001g0013 a0002c0003t0001g0056 a0002c0003t0001g0059 others(29): Show |
44 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.380+1425_380+1428d others(6): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 106644499 | ||||||
| chr6:106644623 | C | T | 32 | a0002c0003t0001g0013 a0002c0003t0001g0056 a0002c0003t0001g0059 others(29): Show |
44 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.380+1533C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106644623 | |||||||
| chr6:106644645 | C | T | 5 | a0001c0001t0001g0033 a0001c0001t0001g0146 a0001c0001t0001g0147 others(2): Show |
6 | HG02258.hp2 HG02717.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.380+1555C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106644645 | |||||||
| chr6:106644661 | C | T | 1 | a0001c0002t0004g0139 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.380+1571C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106644661 | |||||||
| chr6:106644910 | A | C | 58 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(55): Show |
74 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.380+1820A>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106644910 | |||||||
| chr6:106644948 | A | G | 1 | a0001c0001t0007g0153 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.380+1858A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106644948 | |||||||
| chr6:106644986 | A | G | 79 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(76): Show |
99 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.380+1896A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106644986 | |||||||
| chr6:106644999 | T | C | 1 | a0001c0002t0016g0074 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.380+1909T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106644999 | |||||||
| chr6:106645017 | A | G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0235 a0001c0001t0001g0243 |
5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.380+1927A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106645017 | |||||||
| chr6:106645024 | G | GT | 9 | a0001c0001t0005g0048 a0001c0001t0005g0049 a0001c0001t0005g0050 others(6): Show |
12 | HG01358.hp1 HG01496.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.380+1941dupT | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 106645024 | ||||||
| chr6:106645047 | C | T | 26 | a0002c0003t0001g0013 a0002c0003t0001g0056 a0002c0003t0001g0059 others(23): Show |
33 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.380+1957C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106645047 | |||||||
| chr6:106645048 | A | G | 19 | a0001c0002t0006g0007 a0001c0002t0006g0027 a0001c0002t0006g0028 others(16): Show |
23 | HG00438.hp2 HG00738.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.380+1958A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106645048 | |||||||
| chr6:106645118 | T | C | 1 | a0001c0002t0006g0087 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.380+2028T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106645118 | |||||||
| chr6:106645423 | T | G | 1 | a0001c0001t0003g0319 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.380+2333T>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106645423 | |||||||
| chr6:106645479 | A | G | 3 | a0002c0003t0002g0012 a0002c0003t0002g0023 a0002c0003t0002g0052 |
6 | HG01891.hp1 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.380+2389A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106645479 | |||||||
| chr6:106645526 | G | C | 9 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(6): Show |
9 | HG02257.hp2 HG02647.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.380+2436G>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106645526 | |||||||
| chr6:106645663 | C | T | 1 | a0001c0001t0002g0209 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.380+2573C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106645663 | |||||||
| chr6:106645668 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.380+2578G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106645668 | |||||||
| chr6:106645687 | T | G | 48 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(45): Show |
59 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.380+2597T>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106645687 | |||||||
| chr6:106645710 | C | T | 1 | a0001c0009t0013g0080 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.380+2620C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106645710 | |||||||
| chr6:106645877 | G | A | 196 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(193): Show |
269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.380+2787G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106645877 | |||||||
| chr6:106645955 | G | A | 1 | a0001c0002t0004g0154 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.380+2865G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106645955 | |||||||
| chr6:106646137 | C | T | 80 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(77): Show |
100 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.381-2888C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106646137 | |||||||
| chr6:106646199 | A | T | 26 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0047 others(23): Show |
45 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.381-2826A>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106646199 | |||||||
| chr6:106646207 | A | G | 32 | a0002c0003t0001g0013 a0002c0003t0001g0056 a0002c0003t0001g0059 others(29): Show |
44 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.381-2818A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106646207 | |||||||
| chr6:106646282 | G | C | 48 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(45): Show |
70 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.381-2743G>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106646282 | |||||||
| chr6:106646288 | A | G | 1 | a0001c0001t0003g0319 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.381-2737A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106646288 | |||||||
| chr6:106646357 | AG | A | 3 | a0001c0001t0003g0249 a0001c0001t0003g0250 a0001c0001t0003g0263 |
3 | HG02145.hp2 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.381-2667delG | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106646357 | |||||||
| chr6:106646385 | G | T | 7 | a0001c0001t0003g0011 a0001c0001t0003g0045 a0001c0001t0003g0245 others(4): Show |
11 | HG01192.hp1 HG01255.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.381-2640G>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106646385 | |||||||
| chr6:106646422 | A | T | 48 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(45): Show |
70 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.381-2603A>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106646422 | |||||||
| chr6:106646483 | C | G | 19 | a0001c0002t0006g0007 a0001c0002t0006g0027 a0001c0002t0006g0028 others(16): Show |
23 | HG00438.hp2 HG00738.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.381-2542C>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106646483 | |||||||
| chr6:106646648 | T | TA | 81 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(78): Show |
104 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.381-2369dupA | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 106646648 | ||||||
| chr6:106646649 | A | T | 9 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(6): Show |
9 | HG02257.hp2 HG02647.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.381-2376A>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106646649 | |||||||
| chr6:106646738 | G | T | 1 | a0006c0012t0002g0071 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.381-2287G>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106646738 | |||||||
| chr6:106646751 | G | A | 1 | a0002c0003t0001g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.381-2274G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106646751 | |||||||
| chr6:106646794 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.381-2231C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106646794 | |||||||
| chr6:106646860 | C | G | 32 | a0002c0003t0001g0013 a0002c0003t0001g0056 a0002c0003t0001g0059 others(29): Show |
44 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.381-2165C>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106646860 | |||||||
| chr6:106646888 | C | T | 1 | a0006c0012t0002g0071 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.381-2137C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106646888 | |||||||
| chr6:106646914 | G | A | 53 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(50): Show |
75 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.381-2111G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106646914 | |||||||
| chr6:106646968 | C | T | 4 | a0002c0003t0002g0012 a0002c0003t0002g0023 a0002c0003t0002g0052 others(1): Show |
7 | HG01891.hp1 HG02572.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.381-2057C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106646968 | |||||||
| chr6:106647003 | G | A | 1 | a0001c0002t0016g0074 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.381-2022G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106647003 | |||||||
| chr6:106647027 | C | CA | 6 | a0001c0001t0001g0070 a0001c0001t0001g0169 a0001c0001t0001g0225 others(3): Show |
6 | HG01175.hp2 HG02258.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.381-1970dupA | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 106647027 | ||||||
| chr6:106647027 | CA | C | 66 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0109 others(63): Show |
86 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.381-1970delA | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 106647027 | ||||||
| chr6:106647027 | CAA | C | 82 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0018 others(79): Show |
122 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.381-1971_381-1970d others(4): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 106647027 | ||||||
| chr6:106647027 | CAAA | C | 16 | a0001c0001t0001g0195 a0001c0001t0001g0236 a0001c0001t0001g0289 others(13): Show |
18 | HG01517.hp2 HG02257.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.381-1972_381-1970d others(5): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 106647027 | ||||||
| chr6:106647027 | CAAAA | C | 51 | a0001c0001t0007g0127 a0001c0002t0004g0002 a0001c0002t0004g0029 others(48): Show |
65 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.381-1973_381-1970d others(6): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 106647027 | ||||||
| chr6:106647027 | CAAAAA | C | 23 | a0001c0002t0004g0122 a0001c0002t0004g0137 a0001c0002t0004g0157 others(20): Show |
27 | HG00438.hp2 HG00738.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.381-1974_381-1970d others(7): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 106647027 | ||||||
| chr6:106647027 | CAAAAAAA others(1): Show |
C | 9 | a0003c0004t0002g0006 a0003c0004t0002g0046 a0003c0004t0002g0279 others(6): Show |
14 | HG03927.hp2 HG04199.hp2 NA18747.hp1 others(11): Show |
intron_variant | MODIFIER | c.381-1977_381-1970d others(10): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 106647027 | ||||||
| chr6:106647027 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0005g0312 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.381-1979_381-1970d others(12): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 106647027 | ||||||
| chr6:106647027 | CAAAAAAA others(4): Show |
C | 4 | a0002c0003t0002g0008 a0002c0003t0002g0103 a0002c0003t0009g0020 others(1): Show |
9 | HG02280.hp1 HG02451.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.381-1980_381-1970d others(13): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 106647027 | ||||||
| chr6:106647027 | CAAAAAAA others(5): Show |
C | 26 | a0002c0003t0001g0013 a0002c0003t0001g0059 a0002c0003t0001g0060 others(23): Show |
33 | HG00639.hp1 HG01106.hp2 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.381-1981_381-1970d others(14): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 106647027 | ||||||
| chr6:106647027 | CAAAAAAA others(6): Show |
C | 2 | a0002c0003t0001g0056 a0002c0003t0002g0069 |
2 | HG00280.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.381-1982_381-1970d others(15): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 106647027 | ||||||
| chr6:106647175 | C | T | 3 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0005g0304 |
3 | HG01516.hp1 HG01517.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.381-1850C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106647175 | |||||||
| chr6:106647319 | G | A | 1 | a0001c0002t0016g0074 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.381-1706G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106647319 | |||||||
| chr6:106647443 | G | C | 1 | a0001c0002t0006g0101 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.381-1582G>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106647443 | |||||||
| chr6:106647490 | C | T | 26 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0047 others(23): Show |
45 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.381-1535C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106647490 | |||||||
| chr6:106647508 | A | G | 1 | a0002c0003t0002g0103 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.381-1517A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106647508 | |||||||
| chr6:106647534 | G | T | 1 | a0001c0001t0005g0304 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.381-1491G>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106647534 | |||||||
| chr6:106647540 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.381-1485T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106647540 | |||||||
| chr6:106647556 | C | CA | 36 | a0001c0001t0001g0172 a0001c0001t0001g0289 a0001c0001t0001g0290 others(33): Show |
43 | HG00438.hp2 HG00738.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.381-1453dupA | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 106647556 | ||||||
| chr6:106647556 | C | CAAA | 56 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(53): Show |
72 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.381-1455_381-1453d others(5): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 106647556 | ||||||
| chr6:106647556 | CA | C | 27 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0047 others(24): Show |
46 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.381-1453delA | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 106647556 | ||||||
| chr6:106647573 | G | A | 20 | a0001c0002t0006g0007 a0001c0002t0006g0027 a0001c0002t0006g0028 others(17): Show |
24 | HG00438.hp2 HG00738.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.381-1452G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106647573 | |||||||
| chr6:106647575 | G | A | 20 | a0001c0002t0006g0007 a0001c0002t0006g0027 a0001c0002t0006g0028 others(17): Show |
24 | HG00438.hp2 HG00738.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.381-1450G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106647575 | |||||||
| chr6:106647649 | C | CT | 173 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(170): Show |
235 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(232): Show |
intron_variant | MODIFIER | c.381-1357dupT | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 106647649 | ||||||
| chr6:106647649 | C | CTT | 64 | a0001c0001t0001g0033 a0001c0001t0001g0040 a0001c0001t0001g0041 others(61): Show |
82 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.381-1358_381-1357d others(4): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 106647649 | ||||||
| chr6:106647649 | C | CTTT | 51 | a0001c0001t0005g0047 a0001c0001t0005g0308 a0001c0002t0004g0002 others(48): Show |
67 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.381-1359_381-1357d others(5): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 106647649 | ||||||
| chr6:106647649 | C | CTTTT | 6 | a0001c0002t0004g0136 a0001c0002t0004g0139 a0001c0002t0004g0141 others(3): Show |
6 | HG01981.hp1 HG02970.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.381-1360_381-1357d others(6): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 106647649 | ||||||
| chr6:106647744 | G | A | 26 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0047 others(23): Show |
45 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.381-1281G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106647744 | |||||||
| chr6:106647748 | T | TCACACCA others(317): Show |
1 | a0002c0003t0001g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.381-1265_381-1264i others(326): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 106647748 | ||||||
| chr6:106647748 | T | TCACACCA others(318): Show |
1 | a0002c0003t0015g0275 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.381-1265_381-1264i others(327): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 106647748 | ||||||
| chr6:106647757 | T | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.381-1268T>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106647757 | |||||||
| chr6:106647811 | C | G | 1 | a0001c0001t0005g0304 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.381-1214C>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106647811 | |||||||
| chr6:106647813 | G | C | 1 | a0001c0001t0005g0304 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.381-1212G>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106647813 | |||||||
| chr6:106647859 | C | G | 19 | a0001c0002t0006g0007 a0001c0002t0006g0027 a0001c0002t0006g0028 others(16): Show |
23 | HG00438.hp2 HG00738.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.381-1166C>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106647859 | |||||||
| chr6:106647892 | C | A | 1 | a0001c0001t0001g0243 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.381-1133C>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106647892 | |||||||
| chr6:106648017 | G | C | 1 | a0001c0001t0005g0304 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.381-1008G>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106648017 | |||||||
| chr6:106648018 | C | G | 1 | a0001c0001t0005g0304 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.381-1007C>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106648018 | |||||||
| chr6:106648068 | C | G | 1 | a0001c0001t0005g0304 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.381-957C>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106648068 | |||||||
| chr6:106648069 | G | C | 1 | a0001c0001t0005g0304 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.381-956G>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106648069 | |||||||
| chr6:106648157 | G | A | 1 | a0001c0002t0004g0128 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.381-868G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106648157 | |||||||
| chr6:106648239 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.381-786T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106648239 | |||||||
| chr6:106648282 | G | A | 1 | a0001c0001t0007g0123 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.381-743G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106648282 | |||||||
| chr6:106648287 | T | TCGTCTCA others(3): Show |
1 | a0001c0001t0005g0304 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.381-737_381-728dup others(10): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 106648287 | ||||||
| chr6:106648432 | G | A | 2 | a0001c0001t0001g0164 a0001c0002t0004g0129 |
2 | HG01934.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.381-593G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106648432 | |||||||
| chr6:106648546 | C | T | 21 | a0001c0002t0006g0007 a0001c0002t0006g0027 a0001c0002t0006g0028 others(18): Show |
25 | HG00438.hp2 HG00738.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.381-479C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106648546 | |||||||
| chr6:106648749 | C | A | 9 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(6): Show |
9 | HG02257.hp2 HG02647.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.381-276C>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106648749 | |||||||
| chr6:106648931 | A | G | 6 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(3): Show |
6 | HG00558.hp2 NA18965.hp2 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.381-94A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106648931 | |||||||
| chr6:106648978 | A | C | 80 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(77): Show |
100 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.381-47A>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 4/10 | chr6 | 106648978 | |||||||
| chr6:106649218 | T | C | 1 | a0001c0002t0006g0101 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.557+17T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/10 | chr6 | 106649218 | |||||||
| chr6:106649248 | AAC | A | 78 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(75): Show |
96 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.557+49_557+50delCA | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 106649248 | ||||||
| chr6:106649398 | TTAAAA | T | 32 | a0002c0003t0001g0013 a0002c0003t0001g0056 a0002c0003t0001g0059 others(29): Show |
44 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.557+201_557+205del others(5): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 106649398 | ||||||
| chr6:106649475 | G | A | 78 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(75): Show |
96 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.557+274G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/10 | chr6 | 106649475 | |||||||
| chr6:106649833 | A | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | NA18978.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.557+632A>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/10 | chr6 | 106649833 | |||||||
| chr6:106649997 | T | A | 1 | a0001c0002t0004g0140 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.557+796T>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/10 | chr6 | 106649997 | |||||||
| chr6:106650108 | C | T | 56 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(53): Show |
70 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.557+907C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/10 | chr6 | 106650108 | |||||||
| chr6:106650212 | T | G | 80 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(77): Show |
100 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.557+1011T>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/10 | chr6 | 106650212 | |||||||
| chr6:106650244 | G | A | 1 | a0001c0002t0004g0130 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.557+1043G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/10 | chr6 | 106650244 | |||||||
| chr6:106650334 | G | C | 1 | a0001c0001t0001g0040 | 2 | NA19065.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.557+1133G>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/10 | chr6 | 106650334 | |||||||
| chr6:106650335 | T | A | 1 | a0001c0001t0001g0040 | 2 | NA19065.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.557+1134T>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/10 | chr6 | 106650335 | |||||||
| chr6:106650524 | TATTTTTG others(12): Show |
T | 34 | a0001c0005t0010g0021 a0001c0005t0010g0284 a0002c0003t0001g0013 others(31): Show |
48 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(45): Show |
intron_variant | MODIFIER | c.557+1324_557+1342d others(21): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/10 | chr6 | 106650524 | |||||||
| chr6:106650525 | ATTTTTGA others(12): Show |
A | 253 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(250): Show |
336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.557+1358_557+1376d others(21): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 106650525 | ||||||
| chr6:106650629 | C | T | 19 | a0001c0002t0006g0007 a0001c0002t0006g0027 a0001c0002t0006g0028 others(16): Show |
23 | HG00438.hp2 HG00738.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.557+1428C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/10 | chr6 | 106650629 | |||||||
| chr6:106650659 | T | C | 1 | a0001c0002t0004g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.557+1458T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/10 | chr6 | 106650659 | |||||||
| chr6:106650721 | G | C | 32 | a0002c0003t0001g0013 a0002c0003t0001g0056 a0002c0003t0001g0059 others(29): Show |
44 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.558-1488G>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/10 | chr6 | 106650721 | |||||||
| chr6:106650809 | G | A | 1 | a0001c0001t0007g0152 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.558-1400G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/10 | chr6 | 106650809 | |||||||
| chr6:106650946 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.558-1263G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/10 | chr6 | 106650946 | |||||||
| chr6:106650990 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.558-1219A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/10 | chr6 | 106650990 | |||||||
| chr6:106651084 | C | A | 14 | a0001c0001t0002g0010 a0001c0001t0002g0014 a0001c0001t0002g0016 others(11): Show |
21 | HG00438.hp1 HG00621.hp2 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.558-1125C>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/10 | chr6 | 106651084 | |||||||
| chr6:106651114 | T | C | 58 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(55): Show |
74 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.558-1095T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/10 | chr6 | 106651114 | |||||||
| chr6:106651152 | G | A | 19 | a0001c0002t0006g0007 a0001c0002t0006g0027 a0001c0002t0006g0028 others(16): Show |
23 | HG00438.hp2 HG00738.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.558-1057G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/10 | chr6 | 106651152 | |||||||
| chr6:106651160 | G | A | 112 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(109): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.558-1049G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/10 | chr6 | 106651160 | |||||||
| chr6:106651218 | G | T | 1 | a0001c0001t0001g0231 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.558-991G>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/10 | chr6 | 106651218 | |||||||
| chr6:106651316 | A | G | 19 | a0001c0002t0006g0007 a0001c0002t0006g0027 a0001c0002t0006g0028 others(16): Show |
23 | HG00438.hp2 HG00738.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.558-893A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/10 | chr6 | 106651316 | |||||||
| chr6:106651376 | A | G | 1 | a0001c0002t0004g0143 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.558-833A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/10 | chr6 | 106651376 | |||||||
| chr6:106651403 | C | T | 2 | a0002c0003t0001g0100 a0002c0003t0015g0275 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.558-806C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/10 | chr6 | 106651403 | |||||||
| chr6:106651472 | A | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.558-737A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/10 | chr6 | 106651472 | |||||||
| chr6:106651627 | G | GT | 5 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0219 others(2): Show |
5 | HG02109.hp2 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.558-581dupT | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 106651627 | ||||||
| chr6:106651714 | G | A | 112 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(109): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.558-495G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/10 | chr6 | 106651714 | |||||||
| chr6:106651979 | T | C | 34 | a0001c0005t0010g0021 a0001c0005t0010g0284 a0002c0003t0001g0013 others(31): Show |
48 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(45): Show |
intron_variant | MODIFIER | c.558-230T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 5/10 | chr6 | 106651979 | |||||||
| chr6:106652608 | C | T | 32 | a0002c0003t0001g0013 a0002c0003t0001g0056 a0002c0003t0001g0059 others(29): Show |
44 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.849+26C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 7/10 | chr6 | 106652608 | |||||||
| chr6:106652689 | A | G | 1 | a0002c0003t0002g0053 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.849+107A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 7/10 | chr6 | 106652689 | |||||||
| chr6:106653311 | G | A | 32 | a0002c0003t0001g0013 a0002c0003t0001g0056 a0002c0003t0001g0059 others(29): Show |
44 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.849+729G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 7/10 | chr6 | 106653311 | |||||||
| chr6:106653388 | C | G | 56 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(53): Show |
70 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.849+806C>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 7/10 | chr6 | 106653388 | |||||||
| chr6:106653765 | C | T | 32 | a0002c0003t0001g0013 a0002c0003t0001g0056 a0002c0003t0001g0059 others(29): Show |
44 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.850-965C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 7/10 | chr6 | 106653765 | |||||||
| chr6:106653817 | C | A | 1 | a0001c0002t0004g0121 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.850-913C>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 7/10 | chr6 | 106653817 | |||||||
| chr6:106653823 | C | CA | 9 | a0001c0001t0001g0168 a0001c0001t0002g0111 a0001c0001t0002g0114 others(6): Show |
9 | HG00438.hp1 HG00597.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.850-888dupA | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 106653823 | ||||||
| chr6:106653823 | CA | C | 39 | a0001c0001t0001g0220 a0001c0001t0001g0293 a0001c0001t0005g0312 others(36): Show |
51 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.850-888delA | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 106653823 | ||||||
| chr6:106654120 | G | A | 1 | a0001c0002t0008g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.850-610G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 7/10 | chr6 | 106654120 | |||||||
| chr6:106654123 | G | A | 82 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0047 others(79): Show |
115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.850-607G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 7/10 | chr6 | 106654123 | |||||||
| chr6:106654147 | C | G | 56 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(53): Show |
70 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.850-583C>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 7/10 | chr6 | 106654147 | |||||||
| chr6:106654209 | G | T | 32 | a0002c0003t0001g0013 a0002c0003t0001g0056 a0002c0003t0001g0059 others(29): Show |
44 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.850-521G>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 7/10 | chr6 | 106654209 | |||||||
| chr6:106654242 | C | T | 9 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(6): Show |
9 | HG02257.hp2 HG02647.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.850-488C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 7/10 | chr6 | 106654242 | |||||||
| chr6:106654262 | A | G | 1 | a0001c0002t0006g0086 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.850-468A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 7/10 | chr6 | 106654262 | |||||||
| chr6:106654266 | C | T | 26 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0047 others(23): Show |
45 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.850-464C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 7/10 | chr6 | 106654266 | |||||||
| chr6:106654267 | G | A | 1 | a0001c0001t0003g0319 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.850-463G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 7/10 | chr6 | 106654267 | |||||||
| chr6:106654358 | A | C | 1 | a0001c0008t0006g0298 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.850-372A>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 7/10 | chr6 | 106654358 | |||||||
| chr6:106654404 | CATATATG others(3): Show |
C | 2 | a0001c0005t0010g0021 a0001c0005t0010g0284 |
4 | HG02559.hp1 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-311_850-302del others(10): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 106654404 | ||||||
| chr6:106654453 | G | A | 3 | a0001c0001t0003g0266 a0001c0001t0003g0272 a0001c0001t0003g0273 |
3 | HG01175.hp1 HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.850-277G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 7/10 | chr6 | 106654453 | |||||||
| chr6:106654467 | TATTTTCC others(2): Show |
T | 56 | a0001c0001t0007g0123 a0001c0001t0007g0127 a0001c0002t0004g0002 others(53): Show |
70 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.850-261_850-253del others(9): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 106654467 | ||||||
| chr6:106654518 | A | G | 26 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0047 others(23): Show |
45 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.850-212A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 7/10 | chr6 | 106654518 | |||||||
| chr6:106654522 | T | G | 2 | a0002c0003t0002g0008 a0002c0003t0002g0103 |
5 | HG02280.hp1 HG02451.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.850-208T>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 7/10 | chr6 | 106654522 | |||||||
| chr6:106654725 | A | G | 1 | a0001c0002t0004g0276 | 1 | HG01978.hp2 | splice_region_variant&intron_variant | LOW | c.850-5A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 7/10 | chr6 | 106654725 | |||||||
| chr6:106655108 | T | C | 1 | a0001c0001t0001g0177 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1042+186T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 8/10 | chr6 | 106655108 | |||||||
| chr6:106655282 | A | G | 50 | a0001c0001t0001g0176 a0001c0001t0001g0183 a0001c0001t0003g0003 others(47): Show |
72 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.1043-333A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 8/10 | chr6 | 106655282 | |||||||
| chr6:106655514 | C | CA | 86 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0167 others(83): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.1043-82dupA | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 106655514 | ||||||
| chr6:106655514 | CA | C | 26 | a0001c0001t0003g0045 a0001c0001t0005g0308 a0001c0001t0005g0312 others(23): Show |
36 | HG00438.hp2 HG00738.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.1043-82delA | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 106655514 | ||||||
| chr6:106655604 | C | T | 30 | a0002c0003t0001g0013 a0002c0003t0001g0056 a0002c0003t0001g0059 others(27): Show |
42 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.1043-11C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 8/10 | chr6 | 106655604 | |||||||
| chr6:106655979 | T | G | 1 | a0001c0002t0004g0128 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1160+247T>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106655979 | |||||||
| chr6:106656178 | A | G | 4 | a0001c0002t0004g0081 a0001c0002t0004g0117 a0001c0002t0004g0133 others(1): Show |
4 | HG00280.hp1 HG01123.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160+446A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106656178 | |||||||
| chr6:106656180 | A | G | 21 | a0001c0002t0006g0007 a0001c0002t0006g0027 a0001c0002t0006g0028 others(18): Show |
25 | HG00438.hp2 HG00738.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.1160+448A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106656180 | |||||||
| chr6:106656263 | G | A | 1 | a0001c0001t0018g0148 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1160+531G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106656263 | |||||||
| chr6:106656326 | T | C | 1 | a0001c0001t0001g0172 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1160+594T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106656326 | |||||||
| chr6:106656452 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1160+720C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106656452 | |||||||
| chr6:106656498 | C | T | 26 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0047 others(23): Show |
45 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1160+766C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106656498 | |||||||
| chr6:106656499 | T | C | 138 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0047 others(135): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.1160+767T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106656499 | |||||||
| chr6:106656631 | G | A | 6 | a0002c0003t0001g0013 a0002c0003t0001g0056 a0002c0003t0001g0059 others(3): Show |
8 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.1160+899G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106656631 | |||||||
| chr6:106656845 | C | T | 48 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(45): Show |
70 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1160+1113C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106656845 | |||||||
| chr6:106656846 | G | A | 2 | a0001c0005t0010g0021 a0001c0005t0010g0284 |
4 | HG02559.hp1 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1160+1114G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106656846 | |||||||
| chr6:106656889 | T | C | 5 | a0001c0001t0005g0048 a0001c0001t0005g0049 a0001c0001t0005g0099 others(2): Show |
7 | HG01358.hp1 HG01496.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.1160+1157T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106656889 | |||||||
| chr6:106657003 | C | T | 82 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(79): Show |
105 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1160+1271C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106657003 | |||||||
| chr6:106657114 | C | A | 1 | a0001c0008t0006g0298 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1160+1382C>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106657114 | |||||||
| chr6:106657135 | G | C | 1 | a0001c0001t0001g0223 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1160+1403G>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106657135 | |||||||
| chr6:106657147 | C | T | 288 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(285): Show |
385 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(382): Show |
intron_variant | MODIFIER | c.1160+1415C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106657147 | |||||||
| chr6:106657194 | G | A | 1 | a0001c0001t0003g0319 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1160+1462G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106657194 | |||||||
| chr6:106657224 | G | T | 1 | a0001c0001t0001g0193 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1160+1492G>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106657224 | |||||||
| chr6:106657268 | C | CA | 27 | a0001c0001t0001g0163 a0001c0001t0001g0216 a0001c0001t0005g0001 others(24): Show |
45 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1160+1549dupA | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 106657268 | ||||||
| chr6:106657319 | T | A | 1 | a0001c0008t0006g0298 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1160+1587T>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106657319 | |||||||
| chr6:106657319 | T | TA | 20 | a0001c0002t0006g0007 a0001c0002t0006g0027 a0001c0002t0006g0028 others(17): Show |
24 | HG00438.hp2 HG00738.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.1160+1588dupA | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 106657319 | ||||||
| chr6:106657486 | A | T | 32 | a0002c0003t0001g0013 a0002c0003t0001g0056 a0002c0003t0001g0059 others(29): Show |
44 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.1160+1754A>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106657486 | |||||||
| chr6:106657490 | A | G | 21 | a0002c0003t0001g0013 a0002c0003t0001g0056 a0002c0003t0001g0059 others(18): Show |
25 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.1160+1758A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106657490 | |||||||
| chr6:106657536 | C | T | 1 | a0001c0008t0006g0298 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1160+1804C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106657536 | |||||||
| chr6:106657570 | G | A | 1 | a0001c0001t0001g0037 | 2 | HG00741.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.1160+1838G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106657570 | |||||||
| chr6:106657615 | T | G | 1 | a0001c0001t0002g0114 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1160+1883T>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106657615 | |||||||
| chr6:106657683 | A | G | 2 | a0001c0001t0001g0176 a0001c0001t0001g0183 |
2 | NA18612.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.1160+1951A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106657683 | |||||||
| chr6:106657700 | G | A | 1 | a0001c0001t0002g0204 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1160+1968G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106657700 | |||||||
| chr6:106657769 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1160+2037G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106657769 | |||||||
| chr6:106657771 | T | C | 30 | a0002c0003t0001g0013 a0002c0003t0001g0056 a0002c0003t0001g0059 others(27): Show |
42 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.1160+2039T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106657771 | |||||||
| chr6:106657945 | C | T | 4 | a0001c0001t0001g0168 a0001c0001t0001g0199 a0001c0005t0010g0021 others(1): Show |
6 | HG01123.hp2 HG02559.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1160+2213C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106657945 | |||||||
| chr6:106657969 | C | T | 1 | a0001c0001t0003g0319 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1160+2237C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106657969 | |||||||
| chr6:106657983 | G | A | 9 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(6): Show |
9 | HG02257.hp2 HG02647.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1160+2251G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106657983 | |||||||
| chr6:106658200 | C | T | 30 | a0002c0003t0001g0013 a0002c0003t0001g0056 a0002c0003t0001g0059 others(27): Show |
42 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.1160+2468C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106658200 | |||||||
| chr6:106658612 | T | C | 1 | a0001c0002t0016g0074 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1160+2880T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106658612 | |||||||
| chr6:106658621 | G | T | 1 | a0001c0001t0002g0207 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1160+2889G>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106658621 | |||||||
| chr6:106658933 | C | T | 1 | a0001c0009t0013g0080 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1160+3201C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106658933 | |||||||
| chr6:106658951 | A | G | 11 | a0003c0004t0002g0006 a0003c0004t0002g0046 a0003c0004t0002g0278 others(8): Show |
16 | HG02074.hp2 HG03927.hp2 HG04199.hp2 others(13): Show |
intron_variant | MODIFIER | c.1160+3219A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106658951 | |||||||
| chr6:106658956 | C | CT | 32 | a0002c0003t0001g0013 a0002c0003t0001g0056 a0002c0003t0001g0059 others(29): Show |
44 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.1160+3233dupT | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 106658956 | ||||||
| chr6:106658956 | CT | C | 25 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0269 others(22): Show |
29 | HG00438.hp2 HG00738.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.1160+3233delT | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 106658956 | ||||||
| chr6:106659171 | A | G | 78 | a0001c0002t0004g0002 a0001c0002t0004g0029 a0001c0002t0004g0030 others(75): Show |
98 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.1160+3439A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106659171 | |||||||
| chr6:106659188 | C | T | 1 | a0001c0001t0003g0244 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1160+3456C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106659188 | |||||||
| chr6:106659212 | C | A | 1 | a0001c0002t0006g0090 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1160+3480C>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106659212 | |||||||
| chr6:106659236 | G | A | 54 | a0001c0002t0004g0002 a0001c0002t0004g0029 a0001c0002t0004g0030 others(51): Show |
68 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.1160+3504G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106659236 | |||||||
| chr6:106659257 | G | A | 32 | a0002c0003t0001g0013 a0002c0003t0001g0056 a0002c0003t0001g0059 others(29): Show |
44 | HG00280.hp2 HG00639.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.1160+3525G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106659257 | |||||||
| chr6:106659261 | T | A | 71 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(68): Show |
87 | HG00323.hp1 HG00408.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.1160+3529T>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106659261 | |||||||
| chr6:106659315 | A | C | 56 | a0001c0002t0004g0002 a0001c0002t0004g0029 a0001c0002t0004g0030 others(53): Show |
72 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.1160+3583A>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106659315 | |||||||
| chr6:106659345 | A | G | 1 | a0001c0001t0007g0123 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1160+3613A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106659345 | |||||||
| chr6:106659438 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1161-3542C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106659438 | |||||||
| chr6:106659439 | T | G | 71 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(68): Show |
87 | HG00323.hp1 HG00408.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.1161-3541T>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106659439 | |||||||
| chr6:106659447 | G | A | 1 | a0001c0002t0016g0074 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1161-3533G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106659447 | |||||||
| chr6:106659465 | C | CA | 27 | a0001c0001t0001g0174 a0001c0001t0001g0181 a0001c0001t0001g0184 others(24): Show |
29 | HG01358.hp1 HG01433.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.1161-3500dupA | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 106659465 | ||||||
| chr6:106659722 | G | A | 26 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0047 others(23): Show |
45 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1161-3258G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106659722 | |||||||
| chr6:106659742 | A | G | 26 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0047 others(23): Show |
45 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1161-3238A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106659742 | |||||||
| chr6:106659862 | G | A | 1 | a0002c0003t0002g0064 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1161-3118G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106659862 | |||||||
| chr6:106659964 | C | T | 2 | a0002c0003t0001g0100 a0002c0003t0015g0275 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1161-3016C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106659964 | |||||||
| chr6:106660010 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1161-2970T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106660010 | |||||||
| chr6:106660179 | A | G | 2 | a0001c0002t0004g0081 a0001c0002t0004g0134 |
2 | HG01123.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.1161-2801A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106660179 | |||||||
| chr6:106660227 | C | T | 26 | a0001c0001t0002g0010 a0001c0001t0002g0014 a0001c0001t0002g0016 others(23): Show |
38 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.1161-2753C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106660227 | |||||||
| chr6:106660253 | C | T | 1 | a0001c0002t0004g0154 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1161-2727C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106660253 | |||||||
| chr6:106660330 | AC | A | 28 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0047 others(25): Show |
47 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.1161-2642delC | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 106660330 | ||||||
| chr6:106660332 | C | G | 7 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0171 others(4): Show |
9 | HG02056.hp2 HG02071.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.1161-2648C>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106660332 | |||||||
| chr6:106660333 | C | G | 9 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(6): Show |
9 | HG02257.hp2 HG02647.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1161-2647C>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106660333 | |||||||
| chr6:106660334 | C | G | 4 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(1): Show |
4 | HG00642.hp1 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1161-2646C>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106660334 | |||||||
| chr6:106660334 | C | T | 19 | a0001c0002t0006g0007 a0001c0002t0006g0027 a0001c0002t0006g0028 others(16): Show |
23 | HG00438.hp2 HG00738.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.1161-2646C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106660334 | |||||||
| chr6:106660336 | C | A | 1 | a0001c0001t0003g0247 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1161-2644C>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106660336 | |||||||
| chr6:106660556 | T | C | 3 | a0001c0001t0003g0245 a0001c0001t0003g0258 a0001c0001t0003g0259 |
3 | HG01192.hp1 HG01255.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1161-2424T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106660556 | |||||||
| chr6:106660604 | CT | C | 5 | a0001c0002t0004g0030 a0001c0002t0004g0129 a0001c0002t0004g0131 others(2): Show |
6 | HG00639.hp2 HG01934.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1161-2363delT | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 106660604 | ||||||
| chr6:106660699 | G | A | 3 | a0002c0003t0001g0100 a0002c0003t0015g0275 a0003c0004t0002g0278 |
3 | HG02055.hp1 HG02074.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1161-2281G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106660699 | |||||||
| chr6:106660714 | C | T | 1 | a0001c0001t0003g0252 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1161-2266C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106660714 | |||||||
| chr6:106660834 | G | A | 1 | a0003c0004t0002g0287 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1161-2146G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106660834 | |||||||
| chr6:106660916 | C | T | 1 | a0001c0002t0006g0095 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1161-2064C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106660916 | |||||||
| chr6:106660938 | A | T | 3 | a0001c0001t0003g0249 a0001c0001t0003g0250 a0001c0001t0003g0263 |
3 | HG02145.hp2 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1161-2042A>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106660938 | |||||||
| chr6:106660969 | T | A | 1 | a0001c0002t0004g0118 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1161-2011T>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106660969 | |||||||
| chr6:106661101 | A | ATTTGT | 25 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0047 others(22): Show |
44 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1161-1860_1161-185 others(9): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 106661101 | ||||||
| chr6:106661120 | G | GT | 66 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(63): Show |
80 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.1161-1851dupT | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 106661120 | ||||||
| chr6:106661125 | T | G | 85 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(82): Show |
104 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1161-1855T>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106661125 | |||||||
| chr6:106661196 | C | T | 1 | a0001c0001t0003g0319 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1161-1784C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106661196 | |||||||
| chr6:106661259 | G | A | 1 | a0001c0002t0004g0126 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1161-1721G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106661259 | |||||||
| chr6:106661275 | G | A | 19 | a0001c0002t0006g0007 a0001c0002t0006g0027 a0001c0002t0006g0028 others(16): Show |
23 | HG00438.hp2 HG00738.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.1161-1705G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106661275 | |||||||
| chr6:106661314 | A | C | 2 | a0001c0002t0016g0074 a0001c0009t0013g0080 |
2 | HG01891.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1161-1666A>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106661314 | |||||||
| chr6:106661323 | G | T | 1 | a0001c0001t0001g0196 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1161-1657G>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106661323 | |||||||
| chr6:106661336 | C | T | 26 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0047 others(23): Show |
45 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1161-1644C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106661336 | |||||||
| chr6:106661351 | G | A | 1 | a0001c0009t0013g0080 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1161-1629G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106661351 | |||||||
| chr6:106661361 | G | C | 1 | a0007c0010t0005g0313 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1161-1619G>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106661361 | |||||||
| chr6:106661362 | C | G | 1 | a0007c0010t0005g0313 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1161-1618C>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106661362 | |||||||
| chr6:106661391 | A | G | 315 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(312): Show |
415 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(412): Show |
intron_variant | MODIFIER | c.1161-1589A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106661391 | |||||||
| chr6:106661525 | T | A | 54 | a0001c0002t0004g0002 a0001c0002t0004g0029 a0001c0002t0004g0030 others(51): Show |
68 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.1161-1455T>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106661525 | |||||||
| chr6:106661591 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1161-1389G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106661591 | |||||||
| chr6:106661596 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1161-1384T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106661596 | |||||||
| chr6:106661686 | CT | C | 11 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(8): Show |
12 | HG00642.hp1 HG01070.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1161-1259delT | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 106661686 | ||||||
| chr6:106661686 | CTTT | C | 9 | a0001c0001t0001g0167 a0001c0001t0001g0174 a0001c0001t0003g0251 others(6): Show |
9 | HG01175.hp1 HG01884.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.1161-1261_1161-125 others(7): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 106661686 | ||||||
| chr6:106661686 | CTTTT | C | 44 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0106 others(41): Show |
51 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.1161-1262_1161-125 others(8): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 106661686 | ||||||
| chr6:106661686 | CTTTTT | C | 113 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(110): Show |
157 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.1161-1263_1161-125 others(9): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 106661686 | ||||||
| chr6:106661686 | CTTTTTT | C | 71 | a0001c0001t0001g0172 a0001c0001t0001g0228 a0001c0001t0001g0289 others(68): Show |
102 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.1161-1264_1161-125 others(10): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 106661686 | ||||||
| chr6:106661686 | CTTTTTTT | C | 21 | a0001c0001t0005g0305 a0001c0002t0004g0131 a0001c0002t0004g0134 others(18): Show |
26 | HG00738.hp2 HG01070.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.1161-1265_1161-125 others(11): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 106661686 | ||||||
| chr6:106661686 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0007g0152 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1161-1268_1161-125 others(14): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 106661686 | ||||||
| chr6:106661686 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0007g0233 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1161-1269_1161-125 others(15): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 106661686 | ||||||
| chr6:106661686 | CTTTTTTT others(11): Show |
C | 24 | a0002c0003t0002g0008 a0002c0003t0002g0012 a0002c0003t0002g0023 others(21): Show |
34 | HG01884.hp1 HG01891.hp1 HG02135.hp2 others(31): Show |
intron_variant | MODIFIER | c.1161-1276_1161-125 others(22): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 106661686 | ||||||
| chr6:106661753 | C | G | 1 | a0001c0001t0001g0181 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1161-1227C>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106661753 | |||||||
| chr6:106661792 | A | G | 26 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0047 others(23): Show |
45 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1161-1188A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106661792 | |||||||
| chr6:106661798 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1161-1182G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106661798 | |||||||
| chr6:106661884 | T | C | 77 | a0001c0002t0004g0002 a0001c0002t0004g0029 a0001c0002t0004g0030 others(74): Show |
97 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.1161-1096T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106661884 | |||||||
| chr6:106661953 | C | T | 4 | a0001c0001t0002g0010 a0001c0001t0002g0203 a0001c0001t0002g0206 others(1): Show |
7 | NA18940.hp1 NA18950.hp1 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.1161-1027C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106661953 | |||||||
| chr6:106662090 | T | C | 26 | a0002c0003t0001g0100 a0002c0003t0002g0008 a0002c0003t0002g0012 others(23): Show |
36 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(33): Show |
intron_variant | MODIFIER | c.1161-890T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106662090 | |||||||
| chr6:106662094 | T | C | 1 | a0001c0008t0006g0298 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1161-886T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106662094 | |||||||
| chr6:106662147 | C | T | 56 | a0001c0002t0004g0002 a0001c0002t0004g0029 a0001c0002t0004g0030 others(53): Show |
72 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.1161-833C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106662147 | |||||||
| chr6:106662221 | GCTGT | G | 5 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0219 others(2): Show |
5 | HG02109.hp2 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1161-756_1161-753d others(6): Show |
QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 106662221 | ||||||
| chr6:106662255 | G | A | 1 | a0001c0002t0006g0092 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1161-725G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106662255 | |||||||
| chr6:106662461 | C | T | 1 | a0001c0002t0006g0102 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1161-519C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106662461 | |||||||
| chr6:106662489 | CT | C | 103 | a0001c0002t0004g0002 a0001c0002t0004g0029 a0001c0002t0004g0030 others(100): Show |
133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1161-476delT | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 106662489 | ||||||
| chr6:106662504 | T | C | 1 | a0002c0003t0002g0064 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1161-476T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106662504 | |||||||
| chr6:106662776 | T | C | 2 | a0001c0005t0010g0021 a0001c0005t0010g0284 |
4 | HG02559.hp1 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1161-204T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 9/10 | chr6 | 106662776 | |||||||
| chr6:106663209 | T | G | 32 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0011 others(29): Show |
49 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.1366+24T>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 10/10 | chr6 | 106663209 | |||||||
| chr6:106663234 | G | A | 1 | a0003c0004t0002g0279 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1366+49G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 10/10 | chr6 | 106663234 | |||||||
| chr6:106663461 | C | A | 1 | a0001c0001t0005g0306 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1366+276C>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 10/10 | chr6 | 106663461 | |||||||
| chr6:106663939 | C | G | 1 | a0001c0001t0003g0254 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1366+754C>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 10/10 | chr6 | 106663939 | |||||||
| chr6:106664001 | G | A | 9 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(6): Show |
9 | HG02257.hp2 HG02647.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1366+816G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 10/10 | chr6 | 106664001 | |||||||
| chr6:106664041 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1366+856C>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 10/10 | chr6 | 106664041 | |||||||
| chr6:106664431 | C | A | 2 | a0001c0002t0006g0093 a0001c0009t0013g0080 |
2 | HG00738.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1366+1246C>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 10/10 | chr6 | 106664431 | |||||||
| chr6:106664761 | G | A | 3 | a0001c0005t0010g0021 a0001c0005t0010g0284 a0002c0003t0009g0020 |
7 | HG02559.hp1 HG02615.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1367-1021G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 10/10 | chr6 | 106664761 | |||||||
| chr6:106664845 | A | G | 26 | a0001c0001t0005g0001 a0001c0001t0005g0022 a0001c0001t0005g0047 others(23): Show |
45 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1367-937A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 10/10 | chr6 | 106664845 | |||||||
| chr6:106664905 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1367-877T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 10/10 | chr6 | 106664905 | |||||||
| chr6:106665052 | G | A | 1 | a0006c0012t0002g0071 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1367-730G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 10/10 | chr6 | 106665052 | |||||||
| chr6:106665096 | T | C | 1 | a0001c0002t0016g0074 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1367-686T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 10/10 | chr6 | 106665096 | |||||||
| chr6:106665180 | G | T | 1 | a0001c0001t0001g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1367-602G>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 10/10 | chr6 | 106665180 | |||||||
| chr6:106665261 | A | T | 4 | a0001c0002t0006g0027 a0001c0002t0006g0091 a0001c0002t0006g0094 others(1): Show |
5 | HG01070.hp2 HG01106.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.1367-521A>T | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 10/10 | chr6 | 106665261 | |||||||
| chr6:106665528 | T | G | 21 | a0001c0002t0006g0007 a0001c0002t0006g0027 a0001c0002t0006g0028 others(18): Show |
25 | HG00438.hp2 HG00738.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.1367-254T>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 10/10 | chr6 | 106665528 | |||||||
| chr6:106665546 | T | C | 5 | a0001c0002t0004g0154 a0001c0002t0004g0155 a0001c0002t0004g0156 others(2): Show |
5 | NA18947.hp2 NA18986.hp2 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.1367-236T>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 10/10 | chr6 | 106665546 | |||||||
| chr6:106665634 | A | G | 54 | a0001c0002t0004g0002 a0001c0002t0004g0029 a0001c0002t0004g0030 others(51): Show |
68 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.1367-148A>G | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 10/10 | chr6 | 106665634 | |||||||
| chr6:106665724 | G | C | 1 | a0006c0012t0002g0071 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1367-58G>C | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 10/10 | chr6 | 106665724 | |||||||
| chr6:106665743 | G | A | 17 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0038 others(14): Show |
20 | HG00741.hp2 HG01099.hp2 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.1367-39G>A | QRSL1 | ENSG00000130348.11 | transcript | ENST00000369046.8 | protein_coding | 10/10 | chr6 | 106665743 |