Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 837 |
| ensemblid | ENSG00000196954.14 |
| hgncid | 1505 |
| symbol | CASP4 |
| name | caspase 4 |
| refseq_nuc | NM_001225.4 |
| refseq_prot | NP_001216.1 |
| ensembl_nuc | ENST00000444739.7 |
| ensembl_prot | ENSP00000388566.2 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 104942866 |
| end | 104968574 |
| strand | - |
| ver | v1.2 |
| region | chr11:104942866-104968574 |
| region5000 | chr11:104937866-104973574 |
| regionname0 | CASP4_chr11_104942866_104968574 |
| regionname5000 | CASP4_chr11_104937866_104973574 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 377 | 340 | 81 | 66 | 137 | 12 | 42 | 111 | CASP4_chr11_104937866_104973574 | CASP4 | MAEGN others(372): Show |
chr11 | 104937866 | 104973574 |
| a0002 | 0/0 | 377 | 11 | 6 | 5 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | MAEGN others(372): Show |
chr11 | 104937866 | 104973574 |
| a0003 | 0/0 | 377 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | MAEGN others(372): Show |
chr11 | 104937866 | 104973574 |
| a0004 | 0/0 | 377 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | MAEGN others(372): Show |
chr11 | 104937866 | 104973574 |
| a0005 | 0/0 | 377 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | MAEGN others(372): Show |
chr11 | 104937866 | 104973574 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1131 | 305 | 60 | 62 | 135 | 11 | 36 | CASP4_chr11_104937866_104973574 | CASP4 | ATGGC others(1126): Show |
chr11 | 104937866 | 104973574 | ||
| a0001c0002 | 1/0 | 1131 | 20 | 18 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | ATGGC others(1126): Show |
chr11 | 104937866 | 104973574 | ||
| a0001c0003 | 0/0 | 1131 | 13 | 1 | 3 | 2 | 1 | 6 | CASP4_chr11_104937866_104973574 | CASP4 | ATGGC others(1126): Show |
chr11 | 104937866 | 104973574 | ||
| a0001c0009 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | ATGGC others(1126): Show |
chr11 | 104937866 | 104973574 | ||
| a0001c0010 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | ATGGC others(1126): Show |
chr11 | 104937866 | 104973574 | ||
| a0002c0004 | 0/0 | 1131 | 9 | 6 | 3 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | ATGGC others(1126): Show |
chr11 | 104937866 | 104973574 | ||
| a0002c0006 | 0/0 | 1131 | 2 | 0 | 2 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | ATGGC others(1126): Show |
chr11 | 104937866 | 104973574 | ||
| a0003c0005 | 0/0 | 1131 | 5 | 4 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | ATGGC others(1126): Show |
chr11 | 104937866 | 104973574 | ||
| a0004c0008 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | ATGGC others(1126): Show |
chr11 | 104937866 | 104973574 | ||
| a0005c0007 | 0/0 | 1131 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | ATGGC others(1126): Show |
chr11 | 104937866 | 104973574 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1296 | 292 | 48 | 61 | 135 | 11 | 36 | CASP4_chr11_104937866_104973574 | CASP4 | ACTCT others(1291): Show |
chr11 | 104937866 | 104973574 |
| a0001c0001t0002 | 0/0 | 1296 | 6 | 6 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | AGTCT others(1291): Show |
chr11 | 104937866 | 104973574 |
| a0001c0001t0003 | 0/0 | 1296 | 2 | 2 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | ACTCT others(1291): Show |
chr11 | 104937866 | 104973574 |
| a0001c0001t0004 | 0/0 | 1296 | 3 | 3 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | ACTCT others(1291): Show |
chr11 | 104937866 | 104973574 |
| a0001c0001t0005 | 0/0 | 1296 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | AGTCT others(1291): Show |
chr11 | 104937866 | 104973574 |
| a0001c0001t0006 | 0/0 | 1296 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | ATTCT others(1291): Show |
chr11 | 104937866 | 104973574 |
| a0001c0002t0001 | 1/0 | 1296 | 19 | 17 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | ACTCT others(1291): Show |
chr11 | 104937866 | 104973574 |
| a0001c0002t0002 | 0/0 | 1296 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | AGTCT others(1291): Show |
chr11 | 104937866 | 104973574 |
| a0001c0003t0001 | 0/0 | 1296 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | ACTCT others(1291): Show |
chr11 | 104937866 | 104973574 |
| a0001c0003t0002 | 0/0 | 1296 | 12 | 1 | 3 | 1 | 1 | 6 | CASP4_chr11_104937866_104973574 | CASP4 | AGTCT others(1291): Show |
chr11 | 104937866 | 104973574 |
| a0001c0009t0001 | 0/0 | 1296 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | ACTCT others(1291): Show |
chr11 | 104937866 | 104973574 |
| a0001c0010t0001 | 0/0 | 1296 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | ACTCT others(1291): Show |
chr11 | 104937866 | 104973574 |
| a0002c0004t0003 | 0/0 | 1296 | 7 | 4 | 3 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | ACTCT others(1291): Show |
chr11 | 104937866 | 104973574 |
| a0002c0004t0005 | 0/0 | 1296 | 2 | 2 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | AGTCT others(1291): Show |
chr11 | 104937866 | 104973574 |
| a0002c0006t0001 | 0/0 | 1296 | 2 | 0 | 2 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | ACTCT others(1291): Show |
chr11 | 104937866 | 104973574 |
| a0003c0005t0001 | 0/0 | 1296 | 5 | 4 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | ACTCT others(1291): Show |
chr11 | 104937866 | 104973574 |
| a0004c0008t0001 | 0/0 | 1296 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | ACTCT others(1291): Show |
chr11 | 104937866 | 104973574 |
| a0005c0007t0001 | 0/0 | 1296 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | ACTCT others(1291): Show |
chr11 | 104937866 | 104973574 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 29 | 0 | 7 | 18 | 2 | 2 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0002 | 0/0 | 25 | 1 | 6 | 13 | 1 | 4 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0005 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 2 | 2 | 1 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0008 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 1 | 2 | 1 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0016 | 0/0 | 4 | 2 | 0 | 2 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0026 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0072 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0004g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0005g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0001t0006g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0002t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0002t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0002t0001g0025 | 1/0 | 3 | 1 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0002t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0002t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0003t0002g0010 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0003t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0003t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0003t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0003t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0003t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0003t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0003t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0009t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0001c0010t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0002c0004t0003g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0002c0004t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0002c0004t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0002c0004t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0002c0004t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0002c0004t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0002c0004t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0002c0004t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0002c0006t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0003c0005t0001g0011 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0003c0005t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0004c0008t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| a0005c0007t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | GBR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0151 | EUR | GBR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | GBR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | FIN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0077 | EUR | FIN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG00323 | hp2 | a0001 | c0003 | t0002 | g0199 | EUR | FIN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG00639 | hp2 | a0001 | c0003 | t0002 | g0010 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG00738 | hp2 | a0002 | c0006 | t0001 | g0031 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0192 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01099 | hp1 | a0002 | c0006 | t0001 | g0031 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01106 | hp1 | a0002 | c0004 | t0003 | g0032 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01106 | hp2 | a0001 | c0003 | t0002 | g0010 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01109 | hp1 | a0002 | c0004 | t0003 | g0057 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01175 | hp1 | a0002 | c0004 | t0003 | g0032 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01243 | hp2 | a0003 | c0005 | t0001 | g0011 | AMR | PUR | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0025 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01496 | hp2 | a0001 | c0003 | t0002 | g0010 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0079 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0132 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02055 | hp2 | a0003 | c0005 | t0001 | g0011 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02132 | hp2 | a0001 | c0003 | t0002 | g0202 | EAS | KHV | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0064 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02165 | hp1 | a0001 | c0003 | t0001 | g0088 | EAS | CDX | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CDX | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0044 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0046 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0162 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02615 | hp1 | a0004 | c0008 | t0001 | g0139 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02622 | hp1 | a0002 | c0004 | t0003 | g0054 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0130 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0046 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0044 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0129 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02809 | hp1 | a0002 | c0004 | t0003 | g0059 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0204 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02818 | hp2 | a0003 | c0005 | t0001 | g0011 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02922 | hp1 | a0003 | c0005 | t0001 | g0063 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02965 | hp2 | a0002 | c0004 | t0003 | g0058 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03017 | hp2 | a0001 | c0003 | t0002 | g0200 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | MSL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0161 | AFR | MSL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03225 | hp2 | a0002 | c0004 | t0005 | g0197 | AFR | MSL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03453 | hp2 | a0002 | c0004 | t0005 | g0203 | AFR | MSL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0206 | AFR | MSL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0188 | AFR | ESN | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0185 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03540 | hp2 | a0001 | c0009 | t0001 | g0068 | AFR | GWD | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | MSL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | STU | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | STU | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG04115 | hp1 | a0001 | c0003 | t0002 | g0010 | SAS | STU | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | STU | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | STU | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG04204 | hp2 | a0001 | c0003 | t0002 | g0010 | SAS | STU | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG04228 | hp1 | a0001 | c0003 | t0002 | g0198 | SAS | STU | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG04228 | hp2 | a0001 | c0003 | t0002 | g0201 | SAS | STU | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | YRI | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | YRI | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | YRI | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | LWK | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | LWK | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19085 | hp1 | a0005 | c0007 | t0001 | g0107 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0183 | AFR | YRI | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | YRI | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ASW | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA20129 | hp2 | a0001 | c0003 | t0002 | g0196 | AFR | ASW | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | GIH | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA20905 | hp2 | a0001 | c0003 | t0002 | g0195 | SAS | GIH | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02559 | hp1 | a0002 | c0004 | t0003 | g0060 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | USA | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | USA | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA21309 | hp1 | a0003 | c0005 | t0001 | g0011 | AFR | LWK | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| NA21309 | hp2 | a0001 | c0010 | t0001 | g0048 | AFR | LWK | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0072 | REF | REF | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0025 | REF | REF | CASP4_chr11_104937866_104973574 | CASP4 | chr11 | 104937866 | 104973574 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:104947132 | C | T | 1 | a0004 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.986G>A | p.Cys329Tyr | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/9 | 1035/1296 | 986/1134 | 329/377 | chr11 | 104947132 | |||
| chr11:104948606 | C | A | 1 | a0003 | 5 | HG01243.hp2 HG02055.hp2 HG02818.hp2 others(2): Show |
missense_variant | MODERATE | c.852G>T | p.Glu284Asp | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 6/9 | 901/1296 | 852/1134 | 284/377 | chr11 | 104948606 | |||
| chr11:104948670 | C | T | 1 | a0005 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.788G>A | p.Arg263His | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 6/9 | 837/1296 | 788/1134 | 263/377 | chr11 | 104948670 | |||
| chr11:104954870 | C | T | 1 | a0002 | 11 | HG00738.hp2 HG01099.hp1 HG01106.hp1 others(8): Show |
missense_variant | MODERATE | c.139G>A | p.Asp47Asn | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/9 | 188/1296 | 139/1134 | 47/377 | chr11 | 104954870 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:104948600 | T | C | 8 | a0001c0001 a0001c0003 a0001c0009 others(5): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
synonymous_variant | LOW | c.858A>G | p.Leu286Leu | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 6/9 | 907/1296 | 858/1134 | 286/377 | chr11 | 104948600 | |||
| chr11:104949706 | T | G | 1 | a0001c0009 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.618A>C | p.Val206Val | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/9 | 667/1296 | 618/1134 | 206/377 | chr11 | 104949706 | |||
| chr11:104954871 | G | A | 1 | a0001c0010 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.138C>T | p.Tyr46Tyr | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/9 | 187/1296 | 138/1134 | 46/377 | chr11 | 104954871 | |||
| chr11:104954922 | C | T | 1 | a0001c0003 | 13 | HG00323.hp2 HG00639.hp2 HG01106.hp2 others(10): Show |
synonymous_variant | LOW | c.87G>A | p.Leu29Leu | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/9 | 136/1296 | 87/1134 | 29/377 | chr11 | 104954922 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:104942869 | G | A | 4 | a0001c0001t0003 a0001c0001t0005 a0002c0004t0003 others(1): Show |
12 | HG01070.hp2 HG01106.hp1 HG01109.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*110C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 9/9 | 1884 | chr11 | 104942869 | ||||||
| chr11:104968537 | T | A | 1 | a0001c0001t0004 | 3 | HG02451.hp2 HG02630.hp1 HG03516.hp2 |
5_prime_UTR_variant | MODIFIER | c.-12A>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/9 | 12 | chr11 | 104968537 | ||||||
| chr11:104968573 | G | A | 1 | a0001c0001t0006 | 1 | HG03486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-48C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/9 | 48 | chr11 | 104968573 | ||||||
| chr11:104968573 | G | C | 5 | a0001c0001t0002 a0001c0001t0005 a0001c0002t0002 others(2): Show |
22 | HG00323.hp2 HG00639.hp2 HG01070.hp2 others(19): Show |
5_prime_UTR_variant | MODIFIER | c.-48C>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/9 | 48 | chr11 | 104968573 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:104943004 | G | A | 1 | a0001c0001t0001g0033 | 2 | HG03239.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.*6-31C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104943004 | |||||||
| chr11:104943055 | C | G | 1 | a0001c0001t0001g0083 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.*6-82G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104943055 | |||||||
| chr11:104943160 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(98): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.*6-187G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104943160 | |||||||
| chr11:104943247 | G | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG00099.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.*6-274C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104943247 | |||||||
| chr11:104943303 | G | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(3): Show |
14 | HG00621.hp2 HG02486.hp1 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.*6-330C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104943303 | |||||||
| chr11:104943480 | G | C | 1 | a0001c0001t0001g0176 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.*6-507C>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104943480 | |||||||
| chr11:104943559 | T | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(98): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.*6-586A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104943559 | |||||||
| chr11:104943574 | C | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.*6-601G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104943574 | |||||||
| chr11:104943686 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.*6-713C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104943686 | |||||||
| chr11:104943748 | A | G | 10 | a0001c0001t0003g0079 a0001c0001t0005g0192 a0002c0004t0003g0032 others(7): Show |
11 | HG01070.hp2 HG01106.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.*6-775T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104943748 | |||||||
| chr11:104943796 | T | C | 2 | a0001c0001t0001g0070 a0001c0001t0001g0078 |
2 | HG01099.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.*6-823A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104943796 | |||||||
| chr11:104943811 | A | G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0102 |
2 | HG01256.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.*6-838T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104943811 | |||||||
| chr11:104943836 | C | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0096 |
3 | HG02165.hp2 NA19062.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.*6-863G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104943836 | |||||||
| chr11:104943989 | C | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(189): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.*5+759G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104943989 | |||||||
| chr11:104944005 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0002g0194 |
2 | HG02895.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.*5+743G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944005 | |||||||
| chr11:104944344 | G | GTCTCTC | 4 | a0002c0004t0003g0032 a0002c0004t0003g0054 a0002c0004t0003g0057 others(1): Show |
5 | HG01106.hp1 HG01109.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.*5+398_*5+403dupGA others(4): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944344 | |||||||
| chr11:104944344 | GTC | G | 36 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(33): Show |
62 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.*5+402_*5+403delGA | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944344 | |||||||
| chr11:104944358 | CTCTCTCT others(7): Show |
C | 1 | a0001c0001t0001g0114 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.*5+376_*5+389delCA others(12): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944358 | |||||||
| chr11:104944366 | C | CTG | 32 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0020 others(29): Show |
48 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.*5+381_*5+382insCA | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944366 | |||||||
| chr11:104944366 | C | CTGTG | 5 | a0001c0001t0001g0049 a0001c0001t0001g0109 a0001c0001t0002g0194 others(2): Show |
5 | HG00673.hp2 HG02615.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.*5+381_*5+382insCA others(2): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944366 | |||||||
| chr11:104944366 | C | G | 1 | a0001c0002t0001g0183 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.*5+382G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944366 | |||||||
| chr11:104944368 | C | CTCTCTCT others(11): Show |
1 | a0001c0001t0003g0064 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.*5+379_*5+380insCA others(16): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944368 | |||||||
| chr11:104944368 | C | CTCTCTCT others(1): Show |
5 | a0001c0001t0003g0079 a0001c0001t0005g0192 a0002c0004t0003g0058 others(2): Show |
5 | HG01070.hp2 HG01891.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.*5+379_*5+380insCA others(6): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944368 | |||||||
| chr11:104944368 | C | CTCTG | 3 | a0001c0002t0001g0044 a0001c0002t0001g0161 a0001c0002t0001g0185 |
3 | HG02258.hp2 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.*5+379_*5+380insCA others(2): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944368 | |||||||
| chr11:104944368 | C | CTG | 3 | a0001c0002t0001g0129 a0001c0002t0001g0130 a0002c0006t0001g0031 |
4 | HG00738.hp2 HG01099.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.*5+378_*5+379dupCA | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944368 | |||||||
| chr11:104944368 | C | CTGTG | 3 | a0001c0002t0001g0015 a0001c0002t0001g0017 a0001c0002t0001g0132 |
8 | HG01884.hp1 HG02055.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.*5+376_*5+379dupCA others(2): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944368 | |||||||
| chr11:104944368 | C | G | 40 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0020 others(37): Show |
57 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.*5+380G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944368 | |||||||
| chr11:104944368 | CTG | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(7): Show |
13 | HG01433.hp2 HG01891.hp2 HG03704.hp1 others(10): Show |
intron_variant | MODIFIER | c.*5+378_*5+379delCA | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944368 | |||||||
| chr11:104944368 | CTGTG | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(92): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.*5+376_*5+379delCA others(2): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944368 | |||||||
| chr11:104944370 | G | C | 2 | a0001c0001t0001g0041 a0001c0001t0001g0164 |
3 | HG02647.hp1 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.*5+378C>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944370 | |||||||
| chr11:104944372 | G | C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 |
4 | NA18982.hp1 NA19005.hp2 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.*5+376C>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944372 | |||||||
| chr11:104944374 | G | C | 6 | a0001c0001t0001g0061 a0001c0001t0001g0103 a0001c0001t0001g0106 others(3): Show |
6 | HG01993.hp2 HG02572.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.*5+374C>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944374 | |||||||
| chr11:104944444 | A | G | 1 | a0001c0001t0001g0155 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.*5+304T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944444 | |||||||
| chr11:104944518 | C | A | 36 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0020 others(33): Show |
53 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.*5+230G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944518 | |||||||
| chr11:104944618 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0040 |
4 | HG01891.hp2 HG03239.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.*5+130G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944618 | |||||||
| chr11:104944621 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.*5+127G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944621 | |||||||
| chr11:104944645 | A | G | 4 | a0001c0001t0001g0006 a0001c0001t0001g0042 a0001c0001t0001g0133 others(1): Show |
11 | HG00408.hp2 NA18941.hp2 NA18975.hp1 others(8): Show |
intron_variant | MODIFIER | c.*5+103T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 8/8 | chr11 | 104944645 | |||||||
| chr11:104944968 | C | A | 1 | a0001c0001t0001g0045 | 2 | HG00733.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1036-117G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104944968 | |||||||
| chr11:104945041 | T | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(189): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.1036-190A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945041 | |||||||
| chr11:104945056 | T | G | 1 | a0001c0001t0001g0071 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1036-205A>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945056 | |||||||
| chr11:104945072 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1036-221T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945072 | |||||||
| chr11:104945209 | A | T | 1 | a0001c0001t0001g0040 | 2 | HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1036-358T>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945209 | |||||||
| chr11:104945252 | C | CTT | 10 | a0001c0001t0003g0064 a0001c0001t0003g0079 a0001c0001t0005g0192 others(7): Show |
11 | HG01070.hp2 HG01106.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1036-403_1036-402d others(4): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945252 | |||||||
| chr11:104945252 | CTTT | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.1036-404_1036-402d others(5): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945252 | |||||||
| chr11:104945252 | CTTTT | C | 9 | a0001c0001t0001g0041 a0001c0001t0001g0080 a0001c0001t0001g0097 others(6): Show |
10 | HG01169.hp1 HG01256.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1036-405_1036-402d others(6): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945252 | |||||||
| chr11:104945293 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(98): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1036-442G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945293 | |||||||
| chr11:104945309 | A | G | 10 | a0001c0001t0003g0079 a0001c0001t0005g0192 a0002c0004t0003g0032 others(7): Show |
11 | HG01070.hp2 HG01106.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1036-458T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945309 | |||||||
| chr11:104945546 | G | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1036-695C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945546 | |||||||
| chr11:104945595 | T | G | 1 | a0001c0001t0002g0205 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1036-744A>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945595 | |||||||
| chr11:104945599 | A | G | 1 | a0001c0001t0001g0033 | 2 | HG03239.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1036-748T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945599 | |||||||
| chr11:104945634 | C | T | 1 | a0001c0001t0001g0036 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1036-783G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945634 | |||||||
| chr11:104945647 | G | T | 1 | a0001c0002t0001g0185 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1036-796C>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945647 | |||||||
| chr11:104945798 | T | G | 1 | a0001c0001t0001g0104 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1036-947A>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945798 | |||||||
| chr11:104945832 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1036-981A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945832 | |||||||
| chr11:104945851 | C | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(200): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.1036-1000G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945851 | |||||||
| chr11:104945926 | A | C | 1 | a0001c0001t0001g0154 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1036-1075T>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945926 | |||||||
| chr11:104945932 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1036-1081G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945932 | |||||||
| chr11:104945956 | C | T | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG02451.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1036-1105G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945956 | |||||||
| chr11:104945994 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1035+1089T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104945994 | |||||||
| chr11:104946040 | T | G | 1 | a0001c0001t0001g0141 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1035+1043A>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104946040 | |||||||
| chr11:104946190 | T | C | 40 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0020 others(37): Show |
58 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.1035+893A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104946190 | |||||||
| chr11:104946530 | T | C | 10 | a0001c0001t0003g0079 a0001c0001t0005g0192 a0002c0004t0003g0032 others(7): Show |
11 | HG01070.hp2 HG01106.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1035+553A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104946530 | |||||||
| chr11:104946696 | C | G | 1 | a0001c0001t0003g0064 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1035+387G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104946696 | |||||||
| chr11:104946710 | C | A | 1 | a0001c0001t0001g0173 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1035+373G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104946710 | |||||||
| chr11:104946754 | C | T | 1 | a0001c0001t0001g0033 | 2 | HG03239.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1035+329G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104946754 | |||||||
| chr11:104946771 | C | T | 35 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(32): Show |
61 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.1035+312G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 7/8 | chr11 | 104946771 | |||||||
| chr11:104947566 | A | G | 36 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(33): Show |
62 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.926-374T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 6/8 | chr11 | 104947566 | |||||||
| chr11:104947584 | A | C | 1 | a0001c0001t0001g0055 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.926-392T>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 6/8 | chr11 | 104947584 | |||||||
| chr11:104947643 | A | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0040 |
4 | HG01891.hp2 HG03239.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.926-451T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 6/8 | chr11 | 104947643 | |||||||
| chr11:104947734 | G | A | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(200): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.926-542C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 6/8 | chr11 | 104947734 | |||||||
| chr11:104947863 | C | A | 3 | a0001c0001t0001g0163 a0001c0001t0002g0189 a0001c0001t0002g0190 |
3 | HG02965.hp1 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.925+670G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 6/8 | chr11 | 104947863 | |||||||
| chr11:104948103 | T | C | 1 | a0002c0004t0003g0057 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.925+430A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 6/8 | chr11 | 104948103 | |||||||
| chr11:104948195 | G | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.925+338C>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 6/8 | chr11 | 104948195 | |||||||
| chr11:104948300 | A | G | 1 | a0001c0001t0001g0182 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.925+233T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 6/8 | chr11 | 104948300 | |||||||
| chr11:104948389 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.925+144C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 6/8 | chr11 | 104948389 | |||||||
| chr11:104948708 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.782-32C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104948708 | |||||||
| chr11:104948798 | A | T | 1 | a0005c0007t0001g0107 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.782-122T>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104948798 | |||||||
| chr11:104948815 | G | GAAACAGA others(1): Show |
172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(169): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.782-140_782-139ins others(8): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104948815 | |||||||
| chr11:104948815 | G | GAAACAGA others(3): Show |
8 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0065 others(5): Show |
20 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.782-140_782-139ins others(10): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104948815 | |||||||
| chr11:104948817 | G | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(177): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.782-141C>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104948817 | |||||||
| chr11:104948817 | G | GACACAC | 10 | a0001c0002t0001g0015 a0001c0002t0001g0044 a0001c0002t0001g0129 others(7): Show |
15 | HG00738.hp2 HG01099.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.782-142_782-141ins others(6): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104948817 | |||||||
| chr11:104948817 | G | GACACACA others(1): Show |
1 | a0001c0002t0001g0017 | 3 | HG03098.hp1 HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.782-142_782-141ins others(8): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104948817 | |||||||
| chr11:104948819 | G | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(200): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.782-143C>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104948819 | |||||||
| chr11:104948837 | C | CACACA | 7 | a0001c0001t0003g0079 a0001c0001t0005g0192 a0002c0004t0003g0054 others(4): Show |
7 | HG01070.hp2 HG01109.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.782-162_782-161ins others(5): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104948837 | |||||||
| chr11:104948862 | T | C | 40 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0020 others(37): Show |
58 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.782-186A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104948862 | |||||||
| chr11:104948988 | A | T | 1 | a0001c0001t0003g0064 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.782-312T>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104948988 | |||||||
| chr11:104949039 | C | G | 1 | a0001c0001t0003g0064 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.782-363G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104949039 | |||||||
| chr11:104949210 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.781+333G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104949210 | |||||||
| chr11:104949298 | G | C | 1 | a0001c0001t0001g0179 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.781+245C>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104949298 | |||||||
| chr11:104949320 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.781+223G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104949320 | |||||||
| chr11:104949330 | TTACTGTG others(2): Show |
T | 9 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0038 others(6): Show |
20 | HG00609.hp1 HG00609.hp2 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.781+204_781+212del others(9): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104949330 | |||||||
| chr11:104949436 | A | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.781+107T>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104949436 | |||||||
| chr11:104949481 | C | G | 1 | a0001c0001t0001g0147 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.781+62G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 5/8 | chr11 | 104949481 | |||||||
| chr11:104950026 | A | G | 3 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0187 |
3 | HG00741.hp1 HG01346.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.547-249T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950026 | |||||||
| chr11:104950158 | A | G | 1 | a0001c0001t0001g0040 | 2 | HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.547-381T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950158 | |||||||
| chr11:104950219 | CTT | C | 11 | a0001c0002t0001g0015 a0001c0002t0001g0017 a0001c0002t0001g0044 others(8): Show |
18 | HG00738.hp2 HG01099.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.547-444_547-443del others(2): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950219 | |||||||
| chr11:104950232 | G | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(189): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.547-455C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950232 | |||||||
| chr11:104950481 | T | C | 2 | a0003c0005t0001g0011 a0003c0005t0001g0063 |
5 | HG01243.hp2 HG02055.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.546+444A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950481 | |||||||
| chr11:104950545 | C | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(58): Show |
117 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.546+380G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950545 | |||||||
| chr11:104950647 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.546+278A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950647 | |||||||
| chr11:104950649 | C | T | 1 | a0001c0001t0001g0033 | 2 | HG03239.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.546+276G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950649 | |||||||
| chr11:104950797 | T | TACAC | 6 | a0001c0001t0001g0101 a0001c0001t0001g0172 a0001c0001t0001g0173 others(3): Show |
6 | HG02132.hp2 HG03017.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.546+124_546+127dup others(4): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950797 | |||||||
| chr11:104950797 | T | TACACAC | 54 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(51): Show |
105 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.546+122_546+127dup others(6): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950797 | |||||||
| chr11:104950797 | T | TACACACA others(1): Show |
75 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(72): Show |
145 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.546+120_546+127dup others(8): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950797 | |||||||
| chr11:104950797 | T | TACACACA others(3): Show |
13 | a0001c0001t0001g0082 a0001c0001t0001g0092 a0001c0001t0001g0105 others(10): Show |
13 | HG02027.hp1 HG02698.hp2 HG02738.hp1 others(10): Show |
intron_variant | MODIFIER | c.546+118_546+127dup others(10): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950797 | |||||||
| chr11:104950797 | T | TACACACA others(5): Show |
22 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(19): Show |
41 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.546+116_546+127dup others(12): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950797 | |||||||
| chr11:104950797 | T | TACACACA others(7): Show |
4 | a0001c0001t0001g0041 a0001c0001t0001g0083 a0001c0001t0001g0126 others(1): Show |
5 | HG00558.hp2 HG02451.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.546+114_546+127dup others(14): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950797 | |||||||
| chr11:104950797 | T | TACACACA others(9): Show |
1 | a0001c0001t0001g0090 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.546+112_546+127dup others(16): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950797 | |||||||
| chr11:104950797 | TAC | T | 17 | a0001c0001t0003g0079 a0001c0001t0005g0192 a0001c0002t0001g0015 others(14): Show |
24 | HG01070.hp2 HG01106.hp1 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.546+126_546+127del others(2): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950797 | |||||||
| chr11:104950797 | TACAC | T | 3 | a0001c0002t0001g0129 a0001c0002t0001g0130 a0002c0006t0001g0031 |
4 | HG00738.hp2 HG01099.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.546+124_546+127del others(4): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950797 | |||||||
| chr11:104950801 | C | A | 1 | a0001c0001t0001g0155 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.546+124G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950801 | |||||||
| chr11:104950823 | C | CACACACA others(6): Show |
1 | a0001c0001t0001g0074 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.546+101_546+102ins others(13): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950823 | |||||||
| chr11:104950907 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.546+18G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950907 | |||||||
| chr11:104950908 | G | A | 1 | a0001c0001t0001g0035 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.546+17C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 4/8 | chr11 | 104950908 | |||||||
| chr11:104951305 | A | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.373-207T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 3/8 | chr11 | 104951305 | |||||||
| chr11:104951316 | GCCTTTTC others(5): Show |
G | 3 | a0001c0001t0001g0163 a0001c0001t0002g0189 a0001c0001t0002g0190 |
3 | HG02965.hp1 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.373-230_373-219del others(12): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 3/8 | chr11 | 104951316 | |||||||
| chr11:104951425 | T | C | 3 | a0001c0002t0001g0129 a0001c0002t0001g0130 a0002c0006t0001g0031 |
4 | HG00738.hp2 HG01099.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.373-327A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 3/8 | chr11 | 104951425 | |||||||
| chr11:104951450 | C | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(140): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.373-352G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 3/8 | chr11 | 104951450 | |||||||
| chr11:104951451 | G | A | 9 | a0001c0001t0003g0079 a0001c0001t0005g0192 a0002c0004t0003g0032 others(6): Show |
10 | HG01070.hp2 HG01106.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.373-353C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 3/8 | chr11 | 104951451 | |||||||
| chr11:104951511 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.372+385A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 3/8 | chr11 | 104951511 | |||||||
| chr11:104952074 | C | T | 1 | a0002c0006t0001g0031 | 2 | HG00738.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.263-69G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104952074 | |||||||
| chr11:104952175 | G | T | 6 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(3): Show |
14 | HG00621.hp2 HG02486.hp1 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.263-170C>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104952175 | |||||||
| chr11:104952264 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.263-259G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104952264 | |||||||
| chr11:104952273 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.263-268A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104952273 | |||||||
| chr11:104952580 | CAAAATCC others(49): Show |
C | 1 | a0001c0001t0001g0051 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.263-631_263-576del others(56): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104952580 | |||||||
| chr11:104952641 | A | T | 1 | a0001c0001t0001g0051 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.263-636T>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104952641 | |||||||
| chr11:104952658 | C | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0167 a0001c0001t0001g0170 |
5 | HG01175.hp2 HG01934.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.263-653G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104952658 | |||||||
| chr11:104952693 | T | TTTTTTTT others(48): Show |
1 | a0001c0001t0001g0051 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.263-689_263-688ins others(55): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104952693 | |||||||
| chr11:104952746 | A | G | 9 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(6): Show |
18 | HG00621.hp2 HG01891.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.263-741T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104952746 | |||||||
| chr11:104952790 | C | G | 6 | a0001c0001t0001g0092 a0001c0001t0001g0098 a0001c0001t0001g0099 others(3): Show |
6 | HG01192.hp2 HG01261.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.263-785G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104952790 | |||||||
| chr11:104952886 | A | T | 1 | a0001c0009t0001g0068 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.263-881T>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104952886 | |||||||
| chr11:104952940 | G | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0062 a0001c0002t0001g0017 |
5 | HG03098.hp1 HG03130.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.263-935C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104952940 | |||||||
| chr11:104952976 | A | G | 1 | a0001c0001t0003g0064 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.263-971T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104952976 | |||||||
| chr11:104953070 | T | C | 3 | a0001c0001t0001g0047 a0001c0001t0001g0062 a0001c0002t0001g0017 |
5 | HG03098.hp1 HG03130.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.263-1065A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104953070 | |||||||
| chr11:104953110 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.263-1105G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104953110 | |||||||
| chr11:104953469 | A | G | 6 | a0001c0001t0001g0040 a0001c0001t0002g0189 a0001c0001t0002g0190 others(3): Show |
7 | HG01070.hp2 HG01891.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.262+1278T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104953469 | |||||||
| chr11:104953578 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.262+1169A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104953578 | |||||||
| chr11:104953646 | C | G | 1 | a0001c0001t0001g0163 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.262+1101G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104953646 | |||||||
| chr11:104953653 | G | C | 3 | a0001c0001t0001g0041 a0001c0001t0001g0163 a0001c0001t0001g0164 |
4 | HG02647.hp1 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.262+1094C>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104953653 | |||||||
| chr11:104953676 | T | A | 3 | a0001c0001t0001g0040 a0001c0001t0002g0189 a0001c0001t0002g0190 |
4 | HG01891.hp2 HG02965.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.262+1071A>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104953676 | |||||||
| chr11:104953753 | T | A | 1 | a0001c0001t0001g0110 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.262+994A>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104953753 | |||||||
| chr11:104953755 | C | T | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0002t0002g0204 |
3 | HG02451.hp1 HG02809.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.262+992G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104953755 | |||||||
| chr11:104953758 | G | A | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0002t0002g0204 |
3 | HG02451.hp1 HG02809.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.262+989C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104953758 | |||||||
| chr11:104953792 | A | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0128 |
3 | NA18953.hp2 NA18982.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.262+955T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104953792 | |||||||
| chr11:104953896 | T | A | 2 | a0001c0002t0001g0161 a0001c0002t0001g0162 |
2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.262+851A>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104953896 | |||||||
| chr11:104954120 | G | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(146): Show |
248 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.262+627C>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104954120 | |||||||
| chr11:104954139 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.262+608C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104954139 | |||||||
| chr11:104954200 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.262+547A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104954200 | |||||||
| chr11:104954396 | T | C | 1 | a0001c0001t0003g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.262+351A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104954396 | |||||||
| chr11:104954465 | A | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(97): Show |
177 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.262+282T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104954465 | |||||||
| chr11:104954482 | T | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0056 |
4 | HG02280.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.262+265A>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104954482 | |||||||
| chr11:104954521 | A | G | 3 | a0001c0001t0001g0041 a0001c0001t0001g0163 a0001c0001t0001g0164 |
4 | HG02647.hp1 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.262+226T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104954521 | |||||||
| chr11:104954742 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG03579.hp1 | splice_region_variant&intron_variant | LOW | c.262+5G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 2/8 | chr11 | 104954742 | |||||||
| chr11:104955164 | C | G | 3 | a0001c0001t0002g0193 a0001c0001t0002g0194 a0001c0001t0005g0192 |
3 | HG01070.hp2 HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.8-163G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104955164 | |||||||
| chr11:104955247 | A | G | 6 | a0001c0001t0001g0040 a0001c0001t0002g0189 a0001c0001t0002g0190 others(3): Show |
7 | HG01070.hp2 HG01891.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.8-246T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104955247 | |||||||
| chr11:104955348 | C | G | 43 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0027 others(40): Show |
64 | HG00140.hp2 HG00280.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.8-347G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104955348 | |||||||
| chr11:104955379 | C | G | 2 | a0001c0001t0001g0153 a0001c0001t0001g0156 |
2 | NA18966.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.8-378G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104955379 | |||||||
| chr11:104955565 | ATAAAT | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(97): Show |
177 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.8-569_8-565delATTT others(1): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104955565 | |||||||
| chr11:104955877 | A | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.8-876T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104955877 | |||||||
| chr11:104955897 | G | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
262 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.8-896C>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104955897 | |||||||
| chr11:104955999 | C | T | 9 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0134 others(6): Show |
13 | HG02056.hp2 HG03490.hp1 NA18963.hp1 others(10): Show |
intron_variant | MODIFIER | c.8-998G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104955999 | |||||||
| chr11:104956102 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.8-1101A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104956102 | |||||||
| chr11:104956229 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.8-1228C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104956229 | |||||||
| chr11:104956431 | C | T | 1 | a0001c0002t0001g0129 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.8-1430G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104956431 | |||||||
| chr11:104956454 | T | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0157 others(2): Show |
14 | HG01243.hp2 HG02055.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.8-1453A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104956454 | |||||||
| chr11:104956490 | T | A | 2 | a0001c0002t0001g0044 a0001c0002t0001g0185 |
3 | HG02258.hp2 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.8-1489A>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104956490 | |||||||
| chr11:104956815 | G | A | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0002t0002g0204 |
3 | HG02451.hp1 HG02809.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.8-1814C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104956815 | |||||||
| chr11:104956855 | T | C | 3 | a0001c0001t0001g0040 a0001c0001t0002g0189 a0001c0001t0002g0190 |
4 | HG01891.hp2 HG02965.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-1854A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104956855 | |||||||
| chr11:104956985 | C | A | 1 | a0001c0001t0001g0148 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.8-1984G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104956985 | |||||||
| chr11:104957116 | G | T | 1 | a0001c0001t0001g0040 | 2 | HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.8-2115C>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957116 | |||||||
| chr11:104957148 | C | T | 3 | a0001c0001t0001g0087 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | HG00621.hp1 HG02165.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.8-2147G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957148 | |||||||
| chr11:104957176 | T | C | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG02451.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.8-2175A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957176 | |||||||
| chr11:104957177 | C | A | 1 | a0001c0001t0001g0075 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.8-2176G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957177 | |||||||
| chr11:104957242 | G | GTAGTGTT others(30): Show |
1 | a0001c0001t0001g0065 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.8-2278_8-2242dupTT others(35): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957242 | |||||||
| chr11:104957334 | G | A | 24 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0030 others(21): Show |
39 | HG01243.hp2 HG01433.hp2 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.8-2333C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957334 | |||||||
| chr11:104957369 | A | C | 32 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0027 others(29): Show |
51 | HG00140.hp2 HG00280.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.8-2368T>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957369 | |||||||
| chr11:104957380 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(53): Show |
110 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.8-2379C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957380 | |||||||
| chr11:104957452 | G | C | 16 | a0001c0001t0001g0007 a0001c0001t0001g0061 a0001c0001t0001g0067 others(13): Show |
21 | HG00140.hp2 HG00280.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.8-2451C>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957452 | |||||||
| chr11:104957472 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.8-2471A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957472 | |||||||
| chr11:104957518 | GCTATAAT others(7): Show |
G | 4 | a0001c0001t0001g0033 a0001c0001t0001g0047 a0001c0001t0001g0062 others(1): Show |
7 | HG03098.hp1 HG03130.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.8-2531_8-2518delTG others(12): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957518 | |||||||
| chr11:104957579 | A | T | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(100): Show |
180 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.8-2578T>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957579 | |||||||
| chr11:104957804 | C | CA | 3 | a0001c0001t0001g0120 a0001c0001t0001g0146 a0001c0001t0001g0147 |
3 | HG02027.hp1 HG04184.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.8-2804dupT | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957804 | |||||||
| chr11:104957806 | C | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
240 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.8-2805G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957806 | |||||||
| chr11:104957857 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0157 others(2): Show |
14 | HG01243.hp2 HG02055.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.8-2856C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957857 | |||||||
| chr11:104957906 | A | G | 8 | a0002c0004t0003g0032 a0002c0004t0003g0054 a0002c0004t0003g0057 others(5): Show |
10 | HG00738.hp2 HG01099.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.8-2905T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104957906 | |||||||
| chr11:104958010 | T | C | 27 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0033 others(24): Show |
44 | HG00140.hp2 HG00280.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.8-3009A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958010 | |||||||
| chr11:104958044 | A | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0049 a0001c0001t0001g0056 |
4 | HG02280.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-3043T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958044 | |||||||
| chr11:104958128 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.8-3127T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958128 | |||||||
| chr11:104958226 | G | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
238 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.8-3225C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958226 | |||||||
| chr11:104958435 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(127): Show |
224 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.8-3434T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958435 | |||||||
| chr11:104958698 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.8-3697G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958698 | |||||||
| chr11:104958757 | T | A | 1 | a0001c0001t0001g0033 | 2 | HG03239.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.8-3756A>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958757 | |||||||
| chr11:104958822 | G | A | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0002t0002g0204 |
3 | HG02451.hp1 HG02809.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.8-3821C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958822 | |||||||
| chr11:104958833 | C | T | 23 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0061 others(20): Show |
37 | HG00140.hp2 HG00280.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.8-3832G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958833 | |||||||
| chr11:104958842 | T | A | 1 | a0001c0010t0001g0048 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.8-3841A>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958842 | |||||||
| chr11:104958911 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.8-3910T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958911 | |||||||
| chr11:104958960 | C | CA | 8 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0026 others(5): Show |
16 | HG00423.hp1 HG00609.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.8-3960dupT | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958960 | |||||||
| chr11:104958960 | C | CAA | 8 | a0001c0003t0001g0088 a0001c0003t0002g0010 a0001c0003t0002g0195 others(5): Show |
13 | HG00639.hp2 HG00738.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.8-3961_8-3960dupTT | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958960 | |||||||
| chr11:104958960 | CA | C | 11 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0056 others(8): Show |
12 | HG01070.hp2 HG01169.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.8-3960delT | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958960 | |||||||
| chr11:104958960 | CAA | C | 15 | a0001c0001t0001g0019 a0001c0001t0001g0037 a0001c0001t0001g0052 others(12): Show |
18 | HG01952.hp2 HG02055.hp1 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.8-3961_8-3960delTT | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958960 | |||||||
| chr11:104958960 | CAAA | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(72): Show |
148 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.8-3962_8-3960delTT others(1): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958960 | |||||||
| chr11:104958960 | CAAAA | C | 28 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0028 others(25): Show |
45 | HG00140.hp2 HG00735.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.8-3963_8-3960delTT others(2): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958960 | |||||||
| chr11:104958960 | CAAAAAAA | C | 6 | a0002c0004t0003g0032 a0002c0004t0003g0054 a0002c0004t0003g0058 others(3): Show |
7 | HG01106.hp1 HG01175.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.8-3966_8-3960delTT others(5): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958960 | |||||||
| chr11:104958960 | CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0001g0041 a0001c0001t0001g0163 a0001c0001t0001g0164 |
4 | HG02647.hp1 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-3969_8-3960delTT others(8): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958960 | |||||||
| chr11:104958984 | A | G | 2 | a0001c0001t0002g0189 a0001c0001t0002g0190 |
2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.8-3983T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104958984 | |||||||
| chr11:104959193 | T | C | 33 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0040 others(30): Show |
42 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.8-4192A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959193 | |||||||
| chr11:104959259 | T | A | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.8-4258A>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959259 | |||||||
| chr11:104959316 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.8-4315T>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959316 | |||||||
| chr11:104959324 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.8-4323T>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959324 | |||||||
| chr11:104959329 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.8-4328T>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959329 | |||||||
| chr11:104959333 | CAGGCACC others(22): Show |
C | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.8-4361_8-4333delAT others(27): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959333 | |||||||
| chr11:104959365 | C | A | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.8-4364G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959365 | |||||||
| chr11:104959366 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.8-4365T>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959366 | |||||||
| chr11:104959367 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.8-4366G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959367 | |||||||
| chr11:104959368 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.8-4367A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959368 | |||||||
| chr11:104959370 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.8-4369T>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959370 | |||||||
| chr11:104959372 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.8-4371T>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959372 | |||||||
| chr11:104959382 | T | C | 27 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0033 others(24): Show |
44 | HG00140.hp2 HG00280.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.8-4381A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959382 | |||||||
| chr11:104959414 | G | A | 29 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0019 others(26): Show |
40 | HG01081.hp2 HG01243.hp1 HG02027.hp1 others(37): Show |
intron_variant | MODIFIER | c.8-4413C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959414 | |||||||
| chr11:104959532 | A | C | 3 | a0001c0001t0002g0193 a0001c0001t0002g0194 a0001c0001t0005g0192 |
3 | HG01070.hp2 HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.8-4531T>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959532 | |||||||
| chr11:104959542 | T | G | 3 | a0001c0001t0001g0040 a0001c0001t0002g0189 a0001c0001t0002g0190 |
4 | HG01891.hp2 HG02965.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-4541A>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959542 | |||||||
| chr11:104959734 | A | T | 2 | a0003c0005t0001g0011 a0003c0005t0001g0063 |
5 | HG01243.hp2 HG02055.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.8-4733T>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959734 | |||||||
| chr11:104959800 | T | A | 27 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0033 others(24): Show |
44 | HG00140.hp2 HG00280.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.8-4799A>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959800 | |||||||
| chr11:104959827 | G | A | 7 | a0002c0004t0003g0032 a0002c0004t0003g0054 a0002c0004t0003g0057 others(4): Show |
8 | HG01106.hp1 HG01109.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.8-4826C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959827 | |||||||
| chr11:104959864 | C | A | 3 | a0001c0001t0001g0040 a0001c0001t0002g0189 a0001c0001t0002g0190 |
4 | HG01891.hp2 HG02965.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-4863G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959864 | |||||||
| chr11:104959886 | C | G | 1 | a0001c0001t0001g0091 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.8-4885G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959886 | |||||||
| chr11:104959947 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.8-4946G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959947 | |||||||
| chr11:104959948 | G | A | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0002t0002g0204 |
3 | HG02451.hp1 HG02809.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.8-4947C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959948 | |||||||
| chr11:104959980 | G | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0084 others(4): Show |
16 | HG01243.hp2 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.8-4979C>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104959980 | |||||||
| chr11:104960074 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.8-5073G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960074 | |||||||
| chr11:104960088 | C | A | 1 | a0001c0001t0001g0033 | 2 | HG03239.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.8-5087G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960088 | |||||||
| chr11:104960111 | G | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
245 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.8-5110C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960111 | |||||||
| chr11:104960115 | A | G | 16 | a0001c0001t0001g0007 a0001c0001t0001g0061 a0001c0001t0001g0067 others(13): Show |
21 | HG00140.hp2 HG00280.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.8-5114T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960115 | |||||||
| chr11:104960168 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.8-5167A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960168 | |||||||
| chr11:104960332 | T | C | 4 | a0001c0001t0001g0033 a0001c0001t0001g0047 a0001c0001t0001g0062 others(1): Show |
7 | HG03098.hp1 HG03130.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.8-5331A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960332 | |||||||
| chr11:104960412 | C | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(5): Show |
16 | HG00621.hp2 HG02145.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.8-5411G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960412 | |||||||
| chr11:104960445 | AT | A | 7 | a0002c0004t0003g0032 a0002c0004t0003g0054 a0002c0004t0003g0057 others(4): Show |
8 | HG01106.hp1 HG01109.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.8-5445delA | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960445 | |||||||
| chr11:104960623 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.8-5622G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960623 | |||||||
| chr11:104960626 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.8-5625G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960626 | |||||||
| chr11:104960775 | T | A | 1 | a0001c0001t0001g0123 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.8-5774A>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960775 | |||||||
| chr11:104960807 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0090 a0001c0001t0001g0126 others(1): Show |
11 | HG00558.hp2 HG00609.hp2 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.8-5806G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960807 | |||||||
| chr11:104960808 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0090 a0001c0001t0001g0126 others(1): Show |
11 | HG00558.hp2 HG00609.hp2 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.8-5807G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960808 | |||||||
| chr11:104960811 | C | A | 1 | a0001c0001t0001g0149 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.8-5810G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960811 | |||||||
| chr11:104960863 | A | G | 1 | a0001c0003t0002g0198 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.8-5862T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960863 | |||||||
| chr11:104960946 | C | T | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0002t0002g0204 |
3 | HG02451.hp1 HG02809.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.8-5945G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104960946 | |||||||
| chr11:104961115 | T | C | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG02451.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.8-6114A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961115 | |||||||
| chr11:104961127 | G | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
244 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.8-6126C>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961127 | |||||||
| chr11:104961205 | C | T | 1 | a0001c0001t0006g0206 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.8-6204G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961205 | |||||||
| chr11:104961214 | T | A | 3 | a0001c0001t0001g0040 a0001c0001t0002g0189 a0001c0001t0002g0190 |
4 | HG01891.hp2 HG02965.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-6213A>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961214 | |||||||
| chr11:104961276 | A | G | 5 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0049 others(2): Show |
7 | HG01433.hp2 HG02280.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.8-6275T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961276 | |||||||
| chr11:104961336 | C | A | 1 | a0001c0001t0001g0150 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.8-6335G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961336 | |||||||
| chr11:104961384 | GTGTC | G | 6 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(3): Show |
14 | HG00621.hp2 HG02486.hp1 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.8-6387_8-6384delGA others(2): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961384 | |||||||
| chr11:104961400 | C | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0055 |
3 | HG01433.hp2 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.8-6399G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961400 | |||||||
| chr11:104961465 | CTTGTCTG others(2): Show |
C | 3 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0157 |
9 | HG02109.hp1 HG02280.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.8-6473_8-6465delTA others(7): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961465 | |||||||
| chr11:104961475 | G | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0157 |
9 | HG02109.hp1 HG02280.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.8-6474C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961475 | |||||||
| chr11:104961524 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.8-6523T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961524 | |||||||
| chr11:104961531 | G | T | 1 | a0001c0001t0001g0035 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.8-6530C>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961531 | |||||||
| chr11:104961620 | C | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
245 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.8-6619G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961620 | |||||||
| chr11:104961738 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.8-6737A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961738 | |||||||
| chr11:104961950 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.7+6569G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961950 | |||||||
| chr11:104961985 | C | T | 1 | a0002c0006t0001g0031 | 2 | HG00738.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.7+6534G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104961985 | |||||||
| chr11:104962164 | T | C | 14 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0158 others(11): Show |
18 | HG00323.hp2 HG00639.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.7+6355A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104962164 | |||||||
| chr11:104962417 | G | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG01256.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.7+6102C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104962417 | |||||||
| chr11:104962436 | C | T | 1 | a0001c0002t0002g0204 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.7+6083G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104962436 | |||||||
| chr11:104962597 | A | G | 5 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0049 others(2): Show |
7 | HG01433.hp2 HG02280.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.7+5922T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104962597 | |||||||
| chr11:104962848 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.7+5671G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104962848 | |||||||
| chr11:104962849 | A | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
262 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.7+5670T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104962849 | |||||||
| chr11:104963012 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(88): Show |
160 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.7+5507C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104963012 | |||||||
| chr11:104963047 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0056 |
3 | HG02280.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.7+5472G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104963047 | |||||||
| chr11:104963117 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7+5402C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104963117 | |||||||
| chr11:104963127 | C | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(6): Show |
17 | HG00621.hp2 HG02145.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.7+5392G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104963127 | |||||||
| chr11:104963288 | A | G | 39 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(36): Show |
55 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.7+5231T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104963288 | |||||||
| chr11:104963355 | C | A | 2 | a0001c0001t0001g0047 a0001c0002t0001g0017 |
4 | HG03098.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+5164G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104963355 | |||||||
| chr11:104963389 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.7+5130G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104963389 | |||||||
| chr11:104963490 | C | A | 9 | a0001c0003t0002g0010 a0001c0003t0002g0195 a0001c0003t0002g0196 others(6): Show |
13 | HG00323.hp2 HG00639.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.7+5029G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104963490 | |||||||
| chr11:104963570 | C | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(5): Show |
17 | HG01243.hp2 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.7+4949G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104963570 | |||||||
| chr11:104963616 | C | T | 35 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(32): Show |
51 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.7+4903G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104963616 | |||||||
| chr11:104963638 | A | G | 6 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(3): Show |
14 | HG00621.hp2 HG02486.hp1 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.7+4881T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104963638 | |||||||
| chr11:104963653 | T | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
161 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.7+4866A>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104963653 | |||||||
| chr11:104963662 | C | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(5): Show |
17 | HG01243.hp2 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.7+4857G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104963662 | |||||||
| chr11:104963696 | C | T | 4 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0163 others(1): Show |
6 | HG01891.hp2 HG02647.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+4823G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104963696 | |||||||
| chr11:104964053 | T | C | 14 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(11): Show |
24 | HG00621.hp2 HG01433.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.7+4466A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104964053 | |||||||
| chr11:104964070 | TATA | T | 6 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(3): Show |
14 | HG00621.hp2 HG02486.hp1 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.7+4446_7+4448delTA others(1): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104964070 | |||||||
| chr11:104964080 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.7+4439T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104964080 | |||||||
| chr11:104964189 | G | C | 38 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(35): Show |
53 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.7+4330C>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104964189 | |||||||
| chr11:104964222 | A | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(5): Show |
17 | HG01243.hp2 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.7+4297T>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104964222 | |||||||
| chr11:104964237 | C | A | 2 | a0001c0001t0002g0189 a0001c0001t0002g0190 |
2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.7+4282G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104964237 | |||||||
| chr11:104964336 | C | T | 33 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(30): Show |
48 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.7+4183G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104964336 | |||||||
| chr11:104964405 | A | C | 12 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(9): Show |
21 | HG00621.hp2 HG01433.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.7+4114T>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104964405 | |||||||
| chr11:104964524 | A | C | 7 | a0001c0001t0002g0191 a0002c0004t0003g0032 a0002c0004t0003g0057 others(4): Show |
9 | HG00738.hp2 HG01099.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.7+3995T>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104964524 | |||||||
| chr11:104964572 | T | C | 1 | a0001c0001t0001g0045 | 2 | HG00733.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.7+3947A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104964572 | |||||||
| chr11:104964952 | G | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(9): Show |
21 | HG00621.hp2 HG01433.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.7+3567C>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104964952 | |||||||
| chr11:104965128 | T | G | 1 | a0001c0001t0001g0187 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.7+3391A>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104965128 | |||||||
| chr11:104965166 | C | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(46): Show |
89 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.7+3353G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104965166 | |||||||
| chr11:104965373 | C | G | 1 | a0001c0001t0001g0087 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.7+3146G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104965373 | |||||||
| chr11:104965467 | T | G | 17 | a0001c0001t0001g0158 a0001c0001t0002g0189 a0001c0001t0002g0190 others(14): Show |
21 | HG00323.hp2 HG00639.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.7+3052A>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104965467 | |||||||
| chr11:104965527 | G | A | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0002t0002g0204 |
3 | HG02451.hp1 HG02809.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.7+2992C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104965527 | |||||||
| chr11:104965536 | A | G | 4 | a0001c0001t0002g0193 a0001c0001t0002g0194 a0001c0001t0005g0192 others(1): Show |
4 | HG01070.hp2 HG02886.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+2983T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104965536 | |||||||
| chr11:104965551 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.7+2968G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104965551 | |||||||
| chr11:104965640 | G | T | 2 | a0001c0002t0001g0161 a0001c0002t0001g0162 |
2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.7+2879C>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104965640 | |||||||
| chr11:104965721 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.7+2798G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104965721 | |||||||
| chr11:104965737 | A | G | 4 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0049 others(1): Show |
6 | HG02280.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+2782T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104965737 | |||||||
| chr11:104965785 | A | G | 40 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(37): Show |
56 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.7+2734T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104965785 | |||||||
| chr11:104966072 | G | C | 3 | a0001c0001t0001g0033 a0001c0001t0001g0047 a0001c0002t0001g0017 |
6 | HG03098.hp1 HG03130.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.7+2447C>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966072 | |||||||
| chr11:104966101 | C | A | 1 | a0001c0001t0001g0029 | 2 | HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.7+2418G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966101 | |||||||
| chr11:104966110 | G | A | 8 | a0001c0003t0002g0010 a0001c0003t0002g0195 a0001c0003t0002g0196 others(5): Show |
12 | HG00323.hp2 HG00639.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.7+2409C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966110 | |||||||
| chr11:104966140 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0160 |
4 | HG01109.hp2 HG01123.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+2379G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966140 | |||||||
| chr11:104966271 | A | C | 1 | a0001c0010t0001g0048 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.7+2248T>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966271 | |||||||
| chr11:104966307 | T | A | 1 | a0001c0002t0002g0204 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.7+2212A>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966307 | |||||||
| chr11:104966315 | C | CCGAT | 38 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(35): Show |
54 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.7+2203_7+2204insAT others(2): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966315 | |||||||
| chr11:104966430 | C | G | 39 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(36): Show |
55 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.7+2089G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966430 | |||||||
| chr11:104966517 | G | A | 3 | a0001c0001t0002g0193 a0001c0001t0002g0194 a0001c0001t0005g0192 |
3 | HG01070.hp2 HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.7+2002C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966517 | |||||||
| chr11:104966588 | A | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(35): Show |
54 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.7+1931T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966588 | |||||||
| chr11:104966597 | G | T | 25 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0061 others(22): Show |
39 | HG00140.hp2 HG00280.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.7+1922C>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966597 | |||||||
| chr11:104966630 | A | C | 1 | a0001c0001t0001g0034 | 2 | HG03831.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.7+1889T>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966630 | |||||||
| chr11:104966660 | C | T | 14 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(11): Show |
24 | HG00621.hp2 HG01433.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.7+1859G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966660 | |||||||
| chr11:104966821 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.7+1698G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966821 | |||||||
| chr11:104966867 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.7+1652G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966867 | |||||||
| chr11:104966982 | T | C | 1 | a0002c0004t0005g0203 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.7+1537A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104966982 | |||||||
| chr11:104967253 | C | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG00099.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.7+1266G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967253 | |||||||
| chr11:104967303 | C | T | 3 | a0001c0001t0001g0021 a0001c0003t0002g0195 a0001c0003t0002g0196 |
5 | HG00099.hp1 HG00140.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.7+1216G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967303 | |||||||
| chr11:104967450 | G | A | 1 | a0001c0002t0002g0204 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.7+1069C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967450 | |||||||
| chr11:104967488 | G | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
261 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.7+1031C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967488 | |||||||
| chr11:104967496 | G | C | 3 | a0002c0004t0003g0058 a0002c0004t0003g0059 a0002c0004t0003g0060 |
3 | HG02559.hp1 HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.7+1023C>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967496 | |||||||
| chr11:104967502 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7+1017C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967502 | |||||||
| chr11:104967536 | A | G | 1 | a0001c0001t0002g0189 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.7+983T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967536 | |||||||
| chr11:104967547 | T | A | 1 | a0002c0004t0005g0203 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.7+972A>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967547 | |||||||
| chr11:104967580 | T | A | 1 | a0001c0002t0002g0204 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.7+939A>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967580 | |||||||
| chr11:104967623 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.7+896G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967623 | |||||||
| chr11:104967627 | A | G | 6 | a0002c0004t0003g0032 a0002c0004t0003g0057 a0002c0004t0003g0058 others(3): Show |
8 | HG00738.hp2 HG01099.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.7+892T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967627 | |||||||
| chr11:104967744 | C | T | 63 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(60): Show |
96 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.7+775G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967744 | |||||||
| chr11:104967842 | A | G | 4 | a0001c0001t0002g0191 a0001c0001t0002g0193 a0001c0001t0002g0194 others(1): Show |
4 | HG01070.hp2 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+677T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967842 | |||||||
| chr11:104967843 | C | T | 14 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(11): Show |
24 | HG00621.hp2 HG01433.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.7+676G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967843 | |||||||
| chr11:104967883 | TTCTGTGT others(36): Show |
T | 1 | a0001c0001t0001g0158 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.7+593_7+635delCCAT others(39): Show |
CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967883 | |||||||
| chr11:104967996 | G | A | 5 | a0001c0001t0001g0020 a0001c0001t0001g0153 a0001c0001t0001g0154 others(2): Show |
7 | HG03490.hp1 NA18966.hp1 NA18993.hp2 others(4): Show |
intron_variant | MODIFIER | c.7+523C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104967996 | |||||||
| chr11:104968026 | A | G | 1 | a0002c0006t0001g0031 | 2 | HG00738.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.7+493T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104968026 | |||||||
| chr11:104968112 | C | T | 2 | a0001c0001t0002g0189 a0001c0001t0002g0190 |
2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.7+407G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104968112 | |||||||
| chr11:104968153 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0056 |
3 | HG02280.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.7+366G>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104968153 | |||||||
| chr11:104968210 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.7+309C>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104968210 | |||||||
| chr11:104968211 | C | A | 1 | a0001c0001t0001g0157 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.7+308G>T | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104968211 | |||||||
| chr11:104968227 | G | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(9): Show |
21 | HG00621.hp2 HG01433.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.7+292C>A | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104968227 | |||||||
| chr11:104968391 | A | C | 2 | a0001c0001t0002g0189 a0001c0001t0002g0190 |
2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.7+128T>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104968391 | |||||||
| chr11:104968423 | T | C | 2 | a0001c0001t0001g0047 a0001c0002t0001g0017 |
4 | HG03098.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+96A>G | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104968423 | |||||||
| chr11:104968426 | C | G | 2 | a0001c0001t0001g0047 a0001c0002t0001g0017 |
4 | HG03098.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+93G>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104968426 | |||||||
| chr11:104968495 | A | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
262 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.7+24T>C | CASP4 | ENSG00000196954.14 | transcript | ENST00000444739.7 | protein_coding | 1/8 | chr11 | 104968495 |