Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 124801 |
| ensemblid | ENSG00000161654.10 |
| hgncid | 26407 |
| symbol | LSM12 |
| name | LSM12 homolog |
| refseq_nuc | NM_001371445.1 |
| refseq_prot | NP_001358374.1 |
| ensembl_nuc | ENST00000293406.8 |
| ensembl_prot | ENSP00000293406.3 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 44034328 |
| end | 44066671 |
| strand | - |
| ver | v1.2 |
| region | chr17:44034328-44066671 |
| region5000 | chr17:44029328-44071671 |
| regionname0 | LSM12_chr17_44034328_44066671 |
| regionname5000 | LSM12_chr17_44029328_44071671 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 195 | 294 | 84 | 62 | 114 | 8 | 24 | 82 | LSM12_chr17_44029328_44071671 | LSM12 | MAAPP others(190): Show |
chr17 | 44029328 | 44071671 |
| a0002 | 0/0 | 195 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | MAAPP others(190): Show |
chr17 | 44029328 | 44071671 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 585 | 290 | 80 | 62 | 114 | 8 | 24 | LSM12_chr17_44029328_44071671 | LSM12 | ATGGC others(580): Show |
chr17 | 44029328 | 44071671 | ||
| a0001c0003 | 0/0 | 585 | 4 | 4 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | ATGGC others(580): Show |
chr17 | 44029328 | 44071671 | ||
| a0002c0002 | 0/0 | 585 | 4 | 4 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | ATGGC others(580): Show |
chr17 | 44029328 | 44071671 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2553 | 190 | 38 | 37 | 94 | 4 | 17 | LSM12_chr17_44029328_44071671 | LSM12 | GCCGT others(2548): Show |
chr17 | 44029328 | 44071671 |
| a0001c0001t0002 | 0/0 | 2554 | 44 | 18 | 12 | 8 | 2 | 4 | LSM12_chr17_44029328_44071671 | LSM12 | GCCGT others(2549): Show |
chr17 | 44029328 | 44071671 |
| a0001c0001t0003 | 1/0 | 2552 | 20 | 8 | 5 | 3 | 1 | 2 | LSM12_chr17_44029328_44071671 | LSM12 | GCCGT others(2547): Show |
chr17 | 44029328 | 44071671 |
| a0001c0001t0004 | 0/0 | 2553 | 7 | 0 | 6 | 0 | 1 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | GCCGT others(2548): Show |
chr17 | 44029328 | 44071671 |
| a0001c0001t0005 | 0/0 | 2551 | 7 | 0 | 0 | 7 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | GCCGT others(2546): Show |
chr17 | 44029328 | 44071671 |
| a0001c0001t0006 | 0/0 | 2553 | 4 | 3 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | GCCGT others(2548): Show |
chr17 | 44029328 | 44071671 |
| a0001c0001t0007 | 0/0 | 2553 | 4 | 4 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | GCCGT others(2548): Show |
chr17 | 44029328 | 44071671 |
| a0001c0001t0008 | 0/0 | 2553 | 4 | 4 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | GCGGT others(2548): Show |
chr17 | 44029328 | 44071671 |
| a0001c0001t0009 | 0/0 | 2549 | 3 | 3 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | GCCGT others(2544): Show |
chr17 | 44029328 | 44071671 |
| a0001c0001t0010 | 0/0 | 2553 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | GCCGT others(2548): Show |
chr17 | 44029328 | 44071671 |
| a0001c0001t0011 | 0/1 | 2553 | 1 | 0 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | GCCGT others(2548): Show |
chr17 | 44029328 | 44071671 |
| a0001c0001t0012 | 0/0 | 2554 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | GCCGT others(2549): Show |
chr17 | 44029328 | 44071671 |
| a0001c0001t0013 | 0/0 | 2554 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 | GCCGT others(2549): Show |
chr17 | 44029328 | 44071671 |
| a0001c0001t0014 | 0/0 | 2554 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | GCCGT others(2549): Show |
chr17 | 44029328 | 44071671 |
| a0001c0001t0015 | 0/0 | 2531 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | GCCGT others(2526): Show |
chr17 | 44029328 | 44071671 |
| a0001c0001t0016 | 0/0 | 2553 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | GCCGT others(2548): Show |
chr17 | 44029328 | 44071671 |
| a0001c0003t0002 | 0/0 | 2554 | 4 | 4 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | GCCGT others(2549): Show |
chr17 | 44029328 | 44071671 |
| a0002c0002t0003 | 0/0 | 2552 | 4 | 4 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | GCCGT others(2547): Show |
chr17 | 44029328 | 44071671 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 1 | 2 | 2 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 4 | 1 | 1 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0004 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0006 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0003g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0003g0158 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0004g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0004g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0005g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0005g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0005g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0006g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0007g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0007g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0007g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0008g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0008g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0008g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0009g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0009g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0009g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0010g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0011g0202 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0012g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0013g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0014g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0015g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0001t0016g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0003t0002g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0003t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0001c0003t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0002c0002t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0002c0002t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0002c0002t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| a0002c0002t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0017 | EUR | GBR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0013 | EUR | GBR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0079 | EUR | FIN | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | FIN | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0252 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0247 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0259 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0208 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0146 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0243 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0181 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0260 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01169 | hp2 | a0001 | c0001 | t0006 | g0154 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0175 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01257 | hp1 | a0001 | c0001 | t0012 | g0201 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0148 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0147 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0013 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0248 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0151 | EUR | IBS | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02129 | hp2 | a0001 | c0001 | t0016 | g0262 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02145 | hp2 | a0001 | c0001 | t0007 | g0032 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CDX | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02257 | hp1 | a0002 | c0002 | t0003 | g0027 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0246 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02258 | hp1 | a0001 | c0001 | t0010 | g0231 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0255 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02630 | hp1 | a0002 | c0002 | t0003 | g0030 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0244 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0152 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02723 | hp1 | a0001 | c0001 | t0008 | g0018 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0034 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0254 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0144 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0156 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02886 | hp2 | a0001 | c0003 | t0002 | g0011 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02965 | hp2 | a0001 | c0001 | t0009 | g0102 | AFR | ESN | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0238 | AFR | ESN | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02970 | hp2 | a0001 | c0001 | t0014 | g0035 | AFR | ESN | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0257 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0236 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0038 | AFR | MSL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03098 | hp2 | a0001 | c0001 | t0009 | g0103 | AFR | MSL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0134 | AFR | ESN | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | ESN | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | ESN | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | ESN | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03209 | hp1 | a0001 | c0003 | t0002 | g0108 | AFR | MSL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03209 | hp2 | a0001 | c0001 | t0009 | g0115 | AFR | MSL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0264 | AFR | MSL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03225 | hp2 | a0001 | c0003 | t0002 | g0109 | AFR | MSL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03453 | hp2 | a0002 | c0002 | t0003 | g0025 | AFR | MSL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | ESN | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | ESN | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0239 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03669 | hp2 | a0001 | c0001 | t0013 | g0186 | SAS | PJL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | STU | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | STU | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | BEB | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0037 | SAS | BEB | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0191 | SAS | BEB | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | STU | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | YRI | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | YRI | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | YRI | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | YRI | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18941 | hp2 | a0001 | c0001 | t0005 | g0107 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18951 | hp1 | a0001 | c0001 | t0005 | g0165 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18952 | hp2 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18972 | hp1 | a0001 | c0001 | t0005 | g0174 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18988 | hp2 | a0001 | c0001 | t0015 | g0261 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19000 | hp2 | a0001 | c0001 | t0005 | g0192 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0258 | AFR | LWK | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | LWK | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | LWK | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19043 | hp2 | a0001 | c0001 | t0008 | g0018 | AFR | LWK | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19058 | hp2 | a0001 | c0001 | t0005 | g0106 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19062 | hp2 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19240 | hp1 | a0002 | c0002 | t0003 | g0026 | AFR | YRI | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0033 | AFR | YRI | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ASW | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ASW | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0017 | EUR | TSI | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0195 | EUR | TSI | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | CLM | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0256 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0240 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03471 | hp1 | a0001 | c0003 | t0002 | g0011 | AFR | MSL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG03471 | hp2 | a0001 | c0001 | t0008 | g0263 | AFR | MSL | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | USA | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | USA | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | USA | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0157 | AFR | LWK | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | LWK | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0011 | g0202 | REF | REF | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0158 | REF | REF | LSM12_chr17_44029328_44071671 | LSM12 | chr17 | 44029328 | 44071671 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:44036279 | C | G | 1 | a0002 | 4 | HG02257.hp1 HG02630.hp1 HG03453.hp2 others(1): Show |
missense_variant | MODERATE | c.517G>C | p.Val173Leu | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 5/5 | 601/2552 | 517/588 | 173/195 | chr17 | 44036279 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:44037523 | T | C | 1 | a0001c0003 | 4 | HG02886.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
synonymous_variant | LOW | c.384A>G | p.Lys128Lys | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 4/5 | 468/2552 | 384/588 | 128/195 | chr17 | 44037523 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:44034360 | GCCGA | G | 1 | a0001c0001t0009 | 3 | HG02965.hp2 HG03098.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1844_*1847delTCGG | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 5/5 | 1844 | chr17 | 44034360 | ||||||
| chr17:44034464 | C | A | 1 | a0001c0001t0013 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1744G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 5/5 | 1744 | chr17 | 44034464 | ||||||
| chr17:44034466 | C | T | 2 | a0001c0001t0004 a0001c0001t0012 |
8 | HG00099.hp2 HG00735.hp1 HG01071.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1742G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 5/5 | 1742 | chr17 | 44034466 | ||||||
| chr17:44034966 | G | A | 2 | a0001c0001t0007 a0001c0001t0014 |
5 | HG02145.hp2 HG02723.hp2 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1242C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 5/5 | 1242 | chr17 | 44034966 | ||||||
| chr17:44035139 | A | G | 1 | a0001c0001t0010 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1069T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 5/5 | 1069 | chr17 | 44035139 | ||||||
| chr17:44035270 | ACT | A | 1 | a0001c0001t0005 | 7 | NA18941.hp2 NA18951.hp1 NA18952.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*936_*937delAG | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 5/5 | 936 | chr17 | 44035270 | ||||||
| chr17:44035677 | C | CA | 10 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(7): Show |
222 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(219): Show |
3_prime_UTR_variant | MODIFIER | c.*530dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 5/5 | 530 | chr17 | 44035677 | ||||||
| chr17:44035677 | C | CAA | 5 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0013 others(2): Show |
51 | HG00099.hp1 HG00639.hp1 HG00738.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*529_*530dupTT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 5/5 | 530 | chr17 | 44035677 | ||||||
| chr17:44035711 | A | C | 1 | a0001c0001t0006 | 4 | HG01169.hp2 HG02717.hp1 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*497T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 5/5 | 497 | chr17 | 44035711 | ||||||
| chr17:44066608 | CGGCGGCG others(15): Show |
C | 1 | a0001c0001t0015 | 1 | NA18988.hp2 | 5_prime_UTR_variant | MODIFIER | c.-43_-22delCGCTGCTG others(14): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/5 | 22 | chr17 | 44066608 | ||||||
| chr17:44066656 | G | A | 1 | a0001c0001t0016 | 1 | HG02129.hp2 | 5_prime_UTR_variant | MODIFIER | c.-69C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/5 | 69 | chr17 | 44066656 | ||||||
| chr17:44066669 | G | C | 1 | a0001c0001t0008 | 4 | HG02723.hp1 HG03225.hp1 HG03471.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-82C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/5 | 82 | chr17 | 44066669 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:44036439 | T | C | 23 | a0001c0001t0001g0251 a0001c0001t0002g0016 a0001c0001t0002g0017 others(20): Show |
25 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.496-139A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 4/4 | chr17 | 44036439 | |||||||
| chr17:44036440 | T | C | 1 | a0001c0001t0002g0244 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.496-140A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 4/4 | chr17 | 44036440 | |||||||
| chr17:44036689 | G | GA | 101 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(98): Show |
115 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.496-390dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 4/4 | chr17 | 44036689 | |||||||
| chr17:44036772 | C | T | 1 | a0001c0001t0002g0244 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.496-472G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 4/4 | chr17 | 44036772 | |||||||
| chr17:44036830 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.496-530G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 4/4 | chr17 | 44036830 | |||||||
| chr17:44037029 | G | A | 3 | a0001c0001t0009g0102 a0001c0001t0009g0103 a0001c0001t0009g0115 |
3 | HG02965.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.495+383C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 4/4 | chr17 | 44037029 | |||||||
| chr17:44037091 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.495+321C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 4/4 | chr17 | 44037091 | |||||||
| chr17:44037304 | T | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(99): Show |
116 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.495+108A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 4/4 | chr17 | 44037304 | |||||||
| chr17:44037600 | G | C | 2 | a0001c0001t0001g0142 a0001c0001t0001g0219 |
2 | NA18966.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.369-62C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44037600 | |||||||
| chr17:44037660 | C | G | 1 | a0001c0001t0002g0021 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.369-122G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44037660 | |||||||
| chr17:44037740 | A | G | 1 | a0001c0001t0010g0231 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.369-202T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44037740 | |||||||
| chr17:44037818 | C | T | 6 | a0001c0001t0002g0008 a0001c0001t0002g0236 a0001c0001t0002g0237 others(3): Show |
8 | HG02451.hp2 HG02486.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.369-280G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44037818 | |||||||
| chr17:44037915 | A | G | 3 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0095 |
3 | HG02559.hp1 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.369-377T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44037915 | |||||||
| chr17:44037933 | C | G | 2 | a0001c0001t0001g0081 a0001c0001t0001g0121 |
2 | HG03239.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.369-395G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44037933 | |||||||
| chr17:44037977 | G | T | 4 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
4 | HG01243.hp2 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.369-439C>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44037977 | |||||||
| chr17:44038010 | T | C | 4 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0002g0111 others(1): Show |
4 | HG02258.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.369-472A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038010 | |||||||
| chr17:44038012 | G | A | 4 | a0002c0002t0003g0025 a0002c0002t0003g0026 a0002c0002t0003g0027 others(1): Show |
4 | HG02257.hp1 HG02630.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.369-474C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038012 | |||||||
| chr17:44038070 | C | A | 13 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0045 others(10): Show |
15 | HG01243.hp1 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.369-532G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038070 | |||||||
| chr17:44038094 | A | T | 1 | a0001c0001t0003g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.369-556T>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038094 | |||||||
| chr17:44038102 | G | A | 1 | a0002c0002t0003g0026 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.369-564C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038102 | |||||||
| chr17:44038278 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.369-740C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038278 | |||||||
| chr17:44038338 | A | G | 6 | a0001c0001t0002g0008 a0001c0001t0002g0236 a0001c0001t0002g0237 others(3): Show |
8 | HG02451.hp2 HG02486.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.369-800T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038338 | |||||||
| chr17:44038351 | G | A | 1 | a0001c0001t0002g0096 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.369-813C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038351 | |||||||
| chr17:44038355 | C | CA | 13 | a0001c0001t0001g0053 a0001c0001t0001g0060 a0001c0001t0001g0177 others(10): Show |
13 | HG02647.hp1 HG02723.hp2 HG02970.hp2 others(10): Show |
intron_variant | MODIFIER | c.369-818dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038355 | |||||||
| chr17:44038383 | G | T | 5 | a0001c0001t0001g0040 a0001c0001t0001g0132 a0001c0001t0001g0133 others(2): Show |
5 | HG02109.hp2 HG02976.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.369-845C>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038383 | |||||||
| chr17:44038660 | AAG | A | 34 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0166 others(31): Show |
38 | HG00438.hp1 HG00597.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.369-1124_369-1123d others(4): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038660 | |||||||
| chr17:44038688 | C | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(209): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.369-1150G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038688 | |||||||
| chr17:44038731 | G | C | 6 | a0001c0001t0008g0018 a0001c0001t0008g0263 a0001c0001t0008g0264 others(3): Show |
8 | HG02723.hp1 HG02886.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.369-1193C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038731 | |||||||
| chr17:44038767 | T | C | 1 | a0001c0001t0002g0256 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.369-1229A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038767 | |||||||
| chr17:44038783 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.369-1245A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038783 | |||||||
| chr17:44038896 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.368+1251A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038896 | |||||||
| chr17:44038941 | C | A | 1 | a0001c0001t0001g0036 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.368+1206G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038941 | |||||||
| chr17:44038953 | T | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.368+1194A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038953 | |||||||
| chr17:44038967 | G | A | 20 | a0001c0001t0001g0251 a0001c0001t0002g0016 a0001c0001t0002g0017 others(17): Show |
22 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.368+1180C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44038967 | |||||||
| chr17:44039222 | T | C | 3 | a0001c0001t0008g0018 a0001c0001t0008g0263 a0001c0001t0008g0264 |
4 | HG02723.hp1 HG03225.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.368+925A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44039222 | |||||||
| chr17:44039268 | T | C | 1 | a0001c0001t0003g0024 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.368+879A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44039268 | |||||||
| chr17:44039306 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.368+841G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44039306 | |||||||
| chr17:44039319 | T | C | 2 | a0001c0001t0007g0032 a0001c0001t0007g0033 |
2 | HG02145.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.368+828A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44039319 | |||||||
| chr17:44039353 | C | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0019 others(75): Show |
88 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.368+794G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44039353 | |||||||
| chr17:44039365 | C | CT | 97 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(94): Show |
116 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.368+781dupA | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44039365 | |||||||
| chr17:44039365 | C | CTT | 57 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0040 others(54): Show |
60 | HG00438.hp1 HG00597.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.368+780_368+781dup others(2): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44039365 | |||||||
| chr17:44039365 | C | CTTT | 6 | a0001c0001t0001g0136 a0001c0001t0001g0228 a0001c0001t0002g0183 others(3): Show |
7 | HG01891.hp1 HG02135.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.368+779_368+781dup others(3): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44039365 | |||||||
| chr17:44039365 | CT | C | 25 | a0001c0001t0001g0031 a0001c0001t0001g0052 a0001c0001t0001g0056 others(22): Show |
28 | HG00099.hp1 HG01069.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.368+781delA | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44039365 | |||||||
| chr17:44039365 | CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0014g0035 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.368+765_368+781del others(17): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44039365 | |||||||
| chr17:44039405 | C | T | 2 | a0001c0001t0007g0034 a0001c0001t0007g0038 |
2 | HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.368+742G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44039405 | |||||||
| chr17:44039430 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.368+717C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44039430 | |||||||
| chr17:44039482 | C | T | 3 | a0001c0001t0003g0146 a0001c0001t0003g0147 a0001c0001t0003g0148 |
3 | HG01106.hp1 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.368+665G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44039482 | |||||||
| chr17:44040003 | C | G | 5 | a0001c0001t0007g0032 a0001c0001t0007g0033 a0001c0001t0007g0034 others(2): Show |
5 | HG02145.hp2 HG02723.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.368+144G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44040003 | |||||||
| chr17:44040011 | T | A | 1 | a0001c0001t0001g0153 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.368+136A>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44040011 | |||||||
| chr17:44040081 | T | A | 1 | a0001c0001t0007g0038 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.368+66A>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44040081 | |||||||
| chr17:44040091 | C | T | 2 | a0001c0001t0006g0144 a0001c0001t0006g0152 |
2 | HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.368+56G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44040091 | |||||||
| chr17:44040099 | C | A | 1 | a0001c0001t0007g0038 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.368+48G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44040099 | |||||||
| chr17:44040118 | G | A | 6 | a0001c0001t0002g0008 a0001c0001t0002g0236 a0001c0001t0002g0237 others(3): Show |
8 | HG02451.hp2 HG02486.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.368+29C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 3/4 | chr17 | 44040118 | |||||||
| chr17:44040403 | A | G | 6 | a0001c0001t0002g0008 a0001c0001t0002g0236 a0001c0001t0002g0237 others(3): Show |
8 | HG02451.hp2 HG02486.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.259-147T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44040403 | |||||||
| chr17:44040449 | G | GTTCC | 5 | a0001c0001t0007g0032 a0001c0001t0007g0033 a0001c0001t0007g0034 others(2): Show |
5 | HG02145.hp2 HG02723.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-197_259-194dup others(4): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44040449 | |||||||
| chr17:44040479 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.259-223A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44040479 | |||||||
| chr17:44040488 | T | C | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02145.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.259-232A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44040488 | |||||||
| chr17:44040681 | A | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0045 others(10): Show |
15 | HG01243.hp1 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.259-425T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44040681 | |||||||
| chr17:44040819 | C | CA | 10 | a0001c0001t0001g0127 a0001c0001t0001g0163 a0001c0001t0001g0164 others(7): Show |
10 | HG00280.hp2 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.259-564dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44040819 | |||||||
| chr17:44040819 | C | CAA | 16 | a0001c0001t0001g0251 a0001c0001t0002g0016 a0001c0001t0002g0017 others(13): Show |
18 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.259-565_259-564dup others(2): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44040819 | |||||||
| chr17:44040938 | G | A | 2 | a0001c0001t0001g0133 a0001c0001t0003g0041 |
2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.259-682C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44040938 | |||||||
| chr17:44040996 | C | A | 1 | a0001c0001t0008g0264 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.259-740G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44040996 | |||||||
| chr17:44041020 | T | TACAC | 4 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0002g0111 others(1): Show |
4 | HG02258.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-768_259-765dup others(4): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041020 | |||||||
| chr17:44041020 | T | TACACAC | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0002g0043 others(1): Show |
4 | HG02145.hp1 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-770_259-765dup others(6): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041020 | |||||||
| chr17:44041127 | C | T | 1 | a0001c0001t0003g0037 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.259-871G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041127 | |||||||
| chr17:44041273 | TA | T | 39 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0049 others(36): Show |
40 | HG00621.hp2 HG00639.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.259-1018delT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041273 | |||||||
| chr17:44041273 | TAAA | T | 20 | a0001c0001t0001g0005 a0001c0001t0001g0143 a0001c0001t0001g0162 others(17): Show |
22 | HG00639.hp2 HG01099.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.259-1020_259-1018d others(5): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041273 | |||||||
| chr17:44041273 | TAAAAA | T | 39 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0040 others(36): Show |
47 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.259-1022_259-1018d others(7): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041273 | |||||||
| chr17:44041273 | TAAAAAAA | T | 15 | a0001c0001t0001g0022 a0001c0001t0001g0126 a0001c0001t0001g0127 others(12): Show |
15 | HG00558.hp1 HG01123.hp1 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.259-1024_259-1018d others(9): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041273 | |||||||
| chr17:44041277 | AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0006g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.259-1032_259-1022d others(13): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041277 | |||||||
| chr17:44041279 | A | C | 1 | a0001c0001t0001g0142 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.259-1023T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041279 | |||||||
| chr17:44041279 | AAAAAAAA others(2): Show |
A | 10 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0150 others(7): Show |
10 | HG01081.hp2 HG02040.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.259-1032_259-1024d others(11): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041279 | |||||||
| chr17:44041279 | AAAAAAAA others(10): Show |
A | 1 | a0001c0001t0001g0161 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.259-1040_259-1024d others(19): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041279 | |||||||
| chr17:44041279 | AAAAAAAA others(16): Show |
A | 1 | a0001c0001t0001g0222 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.259-1046_259-1024d others(25): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041279 | |||||||
| chr17:44041280 | A | AC | 3 | a0001c0001t0001g0160 a0001c0001t0001g0164 a0001c0001t0003g0148 |
3 | HG01257.hp2 HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.259-1025_259-1024i others(3): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041280 | |||||||
| chr17:44041281 | AAAAAAAC | A | 25 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(22): Show |
31 | HG00597.hp1 HG00738.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.259-1032_259-1026d others(9): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041281 | |||||||
| chr17:44041282 | A | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0160 a0001c0001t0001g0162 others(4): Show |
7 | HG01257.hp2 HG01258.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.259-1026T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041282 | |||||||
| chr17:44041283 | AAAAAC | A | 34 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0019 others(31): Show |
43 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.259-1032_259-1028d others(7): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041283 | |||||||
| chr17:44041283 | AAAAACAA others(10): Show |
A | 1 | a0001c0001t0008g0264 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.259-1044_259-1028d others(19): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041283 | |||||||
| chr17:44041284 | A | AAAC | 10 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0241 others(7): Show |
12 | HG00099.hp1 HG00738.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.259-1029_259-1028i others(5): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041284 | |||||||
| chr17:44041284 | A | C | 23 | a0001c0001t0001g0005 a0001c0001t0001g0140 a0001c0001t0001g0143 others(20): Show |
25 | HG00621.hp2 HG01169.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.259-1028T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041284 | |||||||
| chr17:44041284 | AAAACAAA others(3): Show |
A | 1 | a0001c0001t0001g0052 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.259-1038_259-1029d others(12): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041284 | |||||||
| chr17:44041285 | AAACAAAC | A | 7 | a0001c0001t0001g0056 a0001c0001t0001g0076 a0001c0001t0001g0080 others(4): Show |
7 | HG01109.hp2 HG01175.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.259-1036_259-1030d others(9): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041285 | |||||||
| chr17:44041285 | AAACAAAC others(2): Show |
A | 7 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0081 others(4): Show |
7 | HG02132.hp2 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.259-1038_259-1030d others(11): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041285 | |||||||
| chr17:44041285 | AAACAAAC others(4): Show |
A | 1 | a0001c0001t0001g0119 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.259-1040_259-1030d others(13): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041285 | |||||||
| chr17:44041285 | AAACAAAC others(6): Show |
A | 8 | a0001c0001t0001g0085 a0001c0001t0001g0116 a0001c0001t0001g0117 others(5): Show |
8 | HG00735.hp2 HG02698.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.259-1042_259-1030d others(15): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041285 | |||||||
| chr17:44041286 | A | ACAAAC | 3 | a0001c0001t0001g0251 a0001c0001t0002g0258 a0001c0001t0003g0242 |
3 | HG01993.hp2 NA18984.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.259-1031_259-1030i others(7): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041286 | |||||||
| chr17:44041286 | A | C | 52 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0040 others(49): Show |
55 | HG00408.hp1 HG00558.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.259-1030T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041286 | |||||||
| chr17:44041290 | A | C | 130 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.259-1034T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041290 | |||||||
| chr17:44041290 | AAC | A | 15 | a0001c0001t0001g0051 a0001c0001t0001g0063 a0001c0001t0001g0068 others(12): Show |
16 | HG00639.hp1 HG01496.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.259-1036_259-1035d others(4): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041290 | |||||||
| chr17:44041290 | AACACAC | A | 3 | a0001c0001t0003g0024 a0002c0002t0003g0025 a0002c0002t0003g0027 |
3 | HG00741.hp1 HG02257.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.259-1040_259-1035d others(8): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041290 | |||||||
| chr17:44041290 | AACACACA others(5): Show |
A | 1 | a0001c0001t0001g0118 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.259-1046_259-1035d others(14): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041290 | |||||||
| chr17:44041294 | C | A | 33 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0019 others(30): Show |
42 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.259-1038G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041294 | |||||||
| chr17:44041296 | C | A | 7 | a0001c0001t0001g0056 a0001c0001t0001g0076 a0001c0001t0001g0080 others(4): Show |
7 | HG01109.hp2 HG01175.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.259-1040G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041296 | |||||||
| chr17:44041298 | C | A | 8 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(5): Show |
8 | HG02132.hp2 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.259-1042G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041298 | |||||||
| chr17:44041300 | C | A | 1 | a0001c0001t0001g0119 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.259-1044G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041300 | |||||||
| chr17:44041302 | C | A | 8 | a0001c0001t0001g0085 a0001c0001t0001g0116 a0001c0001t0001g0117 others(5): Show |
8 | HG00735.hp2 HG02698.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.259-1046G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041302 | |||||||
| chr17:44041318 | C | A | 3 | a0001c0003t0002g0011 a0001c0003t0002g0108 a0001c0003t0002g0109 |
4 | HG02886.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-1062G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041318 | |||||||
| chr17:44041324 | C | A | 3 | a0001c0001t0007g0034 a0001c0001t0007g0038 a0001c0001t0014g0035 |
3 | HG02723.hp2 HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.259-1068G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041324 | |||||||
| chr17:44041326 | C | A | 3 | a0001c0001t0002g0258 a0001c0001t0007g0032 a0001c0001t0007g0033 |
3 | HG02145.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.259-1070G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041326 | |||||||
| chr17:44041326 | CACACACA others(1): Show |
C | 5 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0007g0034 others(2): Show |
5 | HG02145.hp1 HG02723.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-1078_259-1071d others(10): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041326 | |||||||
| chr17:44041328 | C | A | 16 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0095 others(13): Show |
16 | HG00438.hp1 HG00741.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.259-1072G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041328 | |||||||
| chr17:44041328 | C | CACACACA others(5): Show |
1 | a0001c0001t0002g0255 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.259-1073_259-1072i others(14): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041328 | |||||||
| chr17:44041328 | CACACAA | C | 3 | a0001c0001t0001g0055 a0001c0001t0007g0032 a0001c0001t0007g0033 |
3 | HG01243.hp2 HG02145.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.259-1078_259-1073d others(8): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041328 | |||||||
| chr17:44041330 | C | A | 127 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(124): Show |
145 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.259-1074G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041330 | |||||||
| chr17:44041330 | CACAA | C | 3 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0095 |
3 | HG02559.hp1 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.259-1078_259-1075d others(6): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041330 | |||||||
| chr17:44041332 | C | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0200 |
2 | HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.259-1076G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041332 | |||||||
| chr17:44041332 | CAA | C | 6 | a0001c0001t0001g0046 a0001c0001t0001g0049 a0001c0001t0001g0100 others(3): Show |
6 | HG01192.hp2 HG02895.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.259-1078_259-1077d others(4): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041332 | |||||||
| chr17:44041334 | A | AACAC | 3 | a0001c0001t0001g0059 a0001c0001t0002g0016 a0001c0001t0002g0253 |
4 | HG03579.hp2 NA19064.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-1082_259-1079d others(6): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041334 | |||||||
| chr17:44041334 | A | AACACAC | 10 | a0001c0001t0002g0017 a0001c0001t0002g0241 a0001c0001t0002g0245 others(7): Show |
10 | HG00099.hp1 HG00738.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.259-1084_259-1079d others(8): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041334 | |||||||
| chr17:44041334 | A | C | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(142): Show |
165 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.259-1078T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041334 | |||||||
| chr17:44041336 | C | A | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0003g0037 |
3 | HG02145.hp1 HG03540.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.259-1080G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041336 | |||||||
| chr17:44041879 | C | CTGGAGAC others(28): Show |
1 | a0001c0001t0001g0172 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.259-1658_259-1624d others(37): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44041879 | |||||||
| chr17:44042024 | C | T | 8 | a0001c0001t0001g0051 a0001c0001t0001g0061 a0001c0001t0001g0074 others(5): Show |
8 | HG00438.hp2 HG02165.hp1 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.259-1768G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042024 | |||||||
| chr17:44042039 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(242): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.259-1783A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042039 | |||||||
| chr17:44042055 | G | A | 1 | a0001c0001t0002g0238 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.259-1799C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042055 | |||||||
| chr17:44042057 | C | T | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(240): Show |
273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.259-1801G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042057 | |||||||
| chr17:44042058 | A | G | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(256): Show |
292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.259-1802T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042058 | |||||||
| chr17:44042060 | G | C | 8 | a0001c0001t0001g0051 a0001c0001t0001g0061 a0001c0001t0001g0074 others(5): Show |
8 | HG00438.hp2 HG02165.hp1 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.259-1804C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042060 | |||||||
| chr17:44042240 | T | C | 1 | a0001c0001t0002g0021 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.259-1984A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042240 | |||||||
| chr17:44042495 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.259-2239C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042495 | |||||||
| chr17:44042502 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.259-2246G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042502 | |||||||
| chr17:44042566 | AT | A | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.259-2311delA | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042566 | |||||||
| chr17:44042587 | C | T | 5 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0177 others(2): Show |
5 | NA18957.hp2 NA18988.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-2331G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042587 | |||||||
| chr17:44042603 | C | CGCCCAGG others(8): Show |
246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.259-2348_259-2347i others(17): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042603 | |||||||
| chr17:44042626 | G | C | 1 | a0001c0001t0001g0046 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.259-2370C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042626 | |||||||
| chr17:44042710 | G | A | 88 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(85): Show |
102 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.259-2454C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042710 | |||||||
| chr17:44042721 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.259-2465G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042721 | |||||||
| chr17:44042782 | T | C | 21 | a0001c0001t0001g0251 a0001c0001t0002g0016 a0001c0001t0002g0017 others(18): Show |
23 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.259-2526A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042782 | |||||||
| chr17:44042915 | C | T | 1 | a0001c0001t0002g0111 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.259-2659G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042915 | |||||||
| chr17:44042954 | C | A | 2 | a0001c0003t0002g0108 a0001c0003t0002g0109 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.259-2698G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44042954 | |||||||
| chr17:44043089 | G | C | 4 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
4 | HG01243.hp2 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-2833C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44043089 | |||||||
| chr17:44043125 | G | C | 2 | a0001c0001t0001g0075 a0001c0001t0001g0084 |
2 | HG00438.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.259-2869C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44043125 | |||||||
| chr17:44043311 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.259-3055A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44043311 | |||||||
| chr17:44043315 | G | A | 1 | a0001c0001t0002g0021 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.259-3059C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44043315 | |||||||
| chr17:44043406 | G | A | 1 | a0001c0001t0008g0264 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.259-3150C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44043406 | |||||||
| chr17:44043548 | C | CT | 121 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(118): Show |
137 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.259-3293dupA | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44043548 | |||||||
| chr17:44043806 | T | TA | 11 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0197 others(8): Show |
11 | HG00621.hp2 HG01257.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.259-3551dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44043806 | |||||||
| chr17:44043847 | G | A | 3 | a0001c0001t0008g0018 a0001c0001t0008g0263 a0001c0001t0008g0264 |
4 | HG02723.hp1 HG03225.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-3591C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44043847 | |||||||
| chr17:44043921 | G | A | 1 | a0001c0001t0002g0021 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.259-3665C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44043921 | |||||||
| chr17:44043947 | C | A | 1 | a0001c0001t0002g0021 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.259-3691G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44043947 | |||||||
| chr17:44044022 | C | T | 3 | a0001c0001t0002g0243 a0001c0001t0002g0259 a0001c0001t0002g0260 |
3 | HG01081.hp1 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.259-3766G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44044022 | |||||||
| chr17:44044260 | A | C | 1 | a0001c0001t0002g0090 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.259-4004T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44044260 | |||||||
| chr17:44044322 | A | G | 1 | a0001c0001t0003g0024 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.259-4066T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44044322 | |||||||
| chr17:44044328 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.259-4072A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44044328 | |||||||
| chr17:44044353 | C | G | 1 | a0001c0001t0002g0258 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.259-4097G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44044353 | |||||||
| chr17:44044440 | A | T | 1 | a0001c0001t0004g0181 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.259-4184T>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44044440 | |||||||
| chr17:44044712 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(242): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.259-4456A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44044712 | |||||||
| chr17:44045000 | G | C | 3 | a0001c0001t0001g0180 a0001c0001t0001g0199 a0001c0001t0001g0206 |
3 | NA18947.hp2 NA18992.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.259-4744C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045000 | |||||||
| chr17:44045033 | T | C | 1 | a0001c0001t0001g0072 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.259-4777A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045033 | |||||||
| chr17:44045051 | A | G | 32 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0040 others(29): Show |
34 | HG00558.hp1 HG01106.hp1 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.259-4795T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045051 | |||||||
| chr17:44045067 | G | A | 2 | a0001c0001t0002g0016 a0001c0001t0002g0253 |
3 | NA19064.hp1 NA19080.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.259-4811C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045067 | |||||||
| chr17:44045185 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.259-4929C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045185 | |||||||
| chr17:44045263 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.259-5007A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045263 | |||||||
| chr17:44045300 | A | G | 23 | a0001c0001t0001g0251 a0001c0001t0002g0016 a0001c0001t0002g0017 others(20): Show |
25 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.259-5044T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045300 | |||||||
| chr17:44045304 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0200 |
2 | HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.259-5048C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045304 | |||||||
| chr17:44045593 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.259-5337G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045593 | |||||||
| chr17:44045604 | T | G | 1 | a0001c0001t0001g0228 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.259-5348A>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045604 | |||||||
| chr17:44045605 | C | A | 1 | a0001c0001t0001g0228 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.259-5349G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045605 | |||||||
| chr17:44045744 | G | A | 1 | a0001c0001t0002g0236 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.259-5488C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045744 | |||||||
| chr17:44045749 | T | C | 1 | a0001c0001t0002g0021 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.259-5493A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045749 | |||||||
| chr17:44045760 | A | G | 1 | a0001c0001t0002g0021 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.259-5504T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045760 | |||||||
| chr17:44045887 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.259-5631C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045887 | |||||||
| chr17:44045936 | C | CT | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(220): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.259-5681dupA | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045936 | |||||||
| chr17:44045936 | C | CTT | 19 | a0001c0001t0001g0044 a0001c0001t0001g0075 a0001c0001t0001g0076 others(16): Show |
20 | HG00438.hp2 HG01169.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.259-5682_259-5681d others(4): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045936 | |||||||
| chr17:44045936 | C | CTTTTTTT others(1699): Show |
1 | a0001c0001t0001g0085 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.259-5681_259-5680i others(1708): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045936 | |||||||
| chr17:44045936 | CT | C | 6 | a0001c0001t0002g0008 a0001c0001t0002g0236 a0001c0001t0002g0237 others(3): Show |
8 | HG02451.hp2 HG02486.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.259-5681delA | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44045936 | |||||||
| chr17:44046227 | G | A | 1 | a0001c0001t0002g0255 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.259-5971C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046227 | |||||||
| chr17:44046569 | T | C | 1 | a0001c0001t0002g0244 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.259-6313A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046569 | |||||||
| chr17:44046613 | A | G | 1 | a0001c0001t0002g0244 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.259-6357T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046613 | |||||||
| chr17:44046638 | C | T | 1 | a0001c0001t0003g0024 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.259-6382G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046638 | |||||||
| chr17:44046709 | C | CA | 10 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0069 others(7): Show |
10 | HG01169.hp1 HG01192.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.259-6454dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046709 | |||||||
| chr17:44046709 | C | CAAAAAAA others(1699): Show |
1 | a0001c0001t0001g0124 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.259-6454_259-6453i others(1708): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046709 | |||||||
| chr17:44046742 | GTTTTCTT others(5): Show |
G | 1 | a0001c0001t0010g0231 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.259-6498_259-6487d others(14): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046742 | |||||||
| chr17:44046747 | CTTTTTTT others(6): Show |
C | 7 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0229 others(4): Show |
7 | HG02145.hp1 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.259-6504_259-6492d others(15): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046747 | |||||||
| chr17:44046759 | C | CT | 7 | a0001c0001t0001g0057 a0001c0001t0001g0060 a0001c0001t0001g0069 others(4): Show |
7 | HG01978.hp2 HG02135.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.259-6504dupA | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046759 | |||||||
| chr17:44046759 | C | T | 1 | a0001c0001t0002g0090 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.259-6503G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046759 | |||||||
| chr17:44046759 | CT | C | 138 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(135): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.259-6504delA | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046759 | |||||||
| chr17:44046759 | CTTTTTTT others(5): Show |
C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0169 a0001c0001t0001g0171 others(2): Show |
5 | HG02523.hp1 HG02523.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.259-6515_259-6504d others(14): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046759 | |||||||
| chr17:44046760 | T | C | 3 | a0001c0001t0001g0149 a0001c0001t0001g0172 a0001c0001t0002g0090 |
3 | HG01123.hp1 NA18957.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.259-6504A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046760 | |||||||
| chr17:44046808 | G | A | 3 | a0001c0003t0002g0011 a0001c0003t0002g0108 a0001c0003t0002g0109 |
4 | HG02886.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-6552C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046808 | |||||||
| chr17:44046875 | C | T | 3 | a0001c0001t0001g0004 a0001c0001t0001g0058 a0001c0001t0001g0059 |
5 | HG01243.hp1 HG02280.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-6619G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046875 | |||||||
| chr17:44046939 | C | A | 1 | a0001c0001t0001g0053 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.259-6683G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44046939 | |||||||
| chr17:44047010 | G | A | 8 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0229 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.259-6754C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44047010 | |||||||
| chr17:44047061 | A | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(242): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.259-6805T>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44047061 | |||||||
| chr17:44047448 | C | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0125 |
2 | NA18957.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.259-7192G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44047448 | |||||||
| chr17:44047742 | G | GT | 24 | a0001c0001t0001g0060 a0001c0001t0001g0116 a0001c0001t0001g0132 others(21): Show |
26 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.259-7487dupA | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44047742 | |||||||
| chr17:44047769 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02145.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.259-7513C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44047769 | |||||||
| chr17:44047846 | G | T | 1 | a0001c0001t0002g0176 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.259-7590C>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44047846 | |||||||
| chr17:44047860 | A | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(89): Show |
107 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.259-7604T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44047860 | |||||||
| chr17:44047879 | G | A | 1 | a0001c0001t0002g0239 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.259-7623C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44047879 | |||||||
| chr17:44048018 | A | AAC | 15 | a0001c0001t0001g0170 a0001c0001t0001g0213 a0001c0001t0001g0217 others(12): Show |
15 | HG00741.hp1 HG01069.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.259-7764_259-7763d others(4): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048018 | |||||||
| chr17:44048018 | A | AACAC | 17 | a0001c0001t0001g0002 a0001c0001t0001g0142 a0001c0001t0001g0171 others(14): Show |
17 | HG00280.hp2 HG01169.hp2 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.259-7766_259-7763d others(6): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048018 | |||||||
| chr17:44048018 | AAC | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(52): Show |
61 | HG00099.hp2 HG00438.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.259-7764_259-7763d others(4): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048018 | |||||||
| chr17:44048018 | AACAC | A | 37 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0040 others(34): Show |
37 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.259-7766_259-7763d others(6): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048018 | |||||||
| chr17:44048018 | AACACAC | A | 16 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0073 others(13): Show |
16 | HG00558.hp1 HG00741.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.259-7768_259-7763d others(8): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048018 | |||||||
| chr17:44048018 | AACACACA others(1): Show |
A | 16 | a0001c0001t0001g0004 a0001c0001t0001g0045 a0001c0001t0001g0046 others(13): Show |
19 | HG01243.hp1 HG02129.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.259-7770_259-7763d others(10): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048018 | |||||||
| chr17:44048018 | AACACACA others(3): Show |
A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0019 others(55): Show |
67 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.259-7772_259-7763d others(12): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048018 | |||||||
| chr17:44048018 | AACACACA others(5): Show |
A | 20 | a0001c0001t0001g0003 a0001c0001t0001g0085 a0001c0001t0001g0092 others(17): Show |
20 | HG00597.hp2 HG00735.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.259-7774_259-7763d others(14): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048018 | |||||||
| chr17:44048018 | AACACACA others(7): Show |
A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0160 a0001c0001t0001g0161 others(6): Show |
11 | HG02280.hp2 HG02486.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.259-7776_259-7763d others(16): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048018 | |||||||
| chr17:44048018 | AACACACA others(9): Show |
A | 1 | a0001c0001t0002g0008 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.259-7778_259-7763d others(18): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048018 | |||||||
| chr17:44048231 | C | T | 1 | a0001c0001t0002g0021 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.259-7975G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048231 | |||||||
| chr17:44048280 | G | A | 2 | a0001c0001t0002g0043 a0001c0001t0003g0042 |
2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.259-8024C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048280 | |||||||
| chr17:44048341 | G | A | 6 | a0001c0001t0002g0008 a0001c0001t0002g0236 a0001c0001t0002g0237 others(3): Show |
8 | HG02451.hp2 HG02486.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.259-8085C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048341 | |||||||
| chr17:44048481 | C | CA | 15 | a0001c0001t0001g0045 a0001c0001t0001g0066 a0001c0001t0001g0099 others(12): Show |
15 | HG01109.hp2 HG01978.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.259-8226dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048481 | |||||||
| chr17:44048481 | CA | C | 16 | a0001c0001t0001g0039 a0001c0001t0001g0051 a0001c0001t0001g0053 others(13): Show |
16 | HG01123.hp1 HG01256.hp1 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.259-8226delT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048481 | |||||||
| chr17:44048892 | T | C | 2 | a0001c0001t0003g0147 a0001c0001t0003g0148 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.259-8636A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44048892 | |||||||
| chr17:44049010 | G | A | 1 | a0001c0001t0003g0037 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.259-8754C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049010 | |||||||
| chr17:44049065 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.259-8809G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049065 | |||||||
| chr17:44049123 | G | A | 1 | a0001c0001t0008g0264 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.259-8867C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049123 | |||||||
| chr17:44049141 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.259-8885T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049141 | |||||||
| chr17:44049191 | A | C | 37 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0229 others(34): Show |
39 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.259-8935T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049191 | |||||||
| chr17:44049220 | C | T | 5 | a0001c0001t0007g0032 a0001c0001t0007g0033 a0001c0001t0007g0034 others(2): Show |
5 | HG02145.hp2 HG02723.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-8964G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049220 | |||||||
| chr17:44049221 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.259-8965C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049221 | |||||||
| chr17:44049233 | C | A | 1 | a0001c0001t0001g0105 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.259-8977G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049233 | |||||||
| chr17:44049312 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.259-9056A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049312 | |||||||
| chr17:44049370 | T | C | 1 | a0001c0001t0002g0256 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.259-9114A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049370 | |||||||
| chr17:44049475 | G | A | 2 | a0001c0001t0001g0204 a0001c0001t0001g0225 |
2 | HG01099.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.259-9219C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049475 | |||||||
| chr17:44049524 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.259-9268G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049524 | |||||||
| chr17:44049577 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.259-9321T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049577 | |||||||
| chr17:44049648 | G | A | 3 | a0001c0003t0002g0011 a0001c0003t0002g0108 a0001c0003t0002g0109 |
4 | HG02886.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-9392C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049648 | |||||||
| chr17:44049726 | T | C | 1 | a0001c0001t0001g0221 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.259-9470A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049726 | |||||||
| chr17:44049758 | G | A | 1 | a0001c0001t0003g0024 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.259-9502C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049758 | |||||||
| chr17:44049960 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.259-9704C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049960 | |||||||
| chr17:44049976 | C | G | 3 | a0001c0001t0003g0146 a0001c0001t0003g0147 a0001c0001t0003g0148 |
3 | HG01106.hp1 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.259-9720G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44049976 | |||||||
| chr17:44050202 | C | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(74): Show |
90 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.259-9946G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44050202 | |||||||
| chr17:44050275 | A | AT | 83 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0019 others(80): Show |
93 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.259-10020dupA | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44050275 | |||||||
| chr17:44050333 | CT | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(84): Show |
99 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.259-10078delA | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44050333 | |||||||
| chr17:44050516 | A | AT | 11 | a0001c0001t0001g0044 a0001c0001t0001g0073 a0001c0001t0001g0097 others(8): Show |
13 | HG01346.hp2 HG02145.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.259-10261dupA | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44050516 | |||||||
| chr17:44050667 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.259-10411G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44050667 | |||||||
| chr17:44050706 | A | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.259-10450T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44050706 | |||||||
| chr17:44050719 | C | T | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0097 |
3 | NA18972.hp2 NA18984.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.259-10463G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44050719 | |||||||
| chr17:44050904 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.259-10648C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44050904 | |||||||
| chr17:44050969 | A | T | 1 | a0001c0001t0008g0264 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.259-10713T>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44050969 | |||||||
| chr17:44051033 | G | C | 1 | a0001c0001t0001g0251 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.259-10777C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051033 | |||||||
| chr17:44051040 | G | T | 6 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0068 others(3): Show |
6 | HG01192.hp1 HG01934.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-10784C>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051040 | |||||||
| chr17:44051187 | A | T | 1 | a0001c0001t0002g0255 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.259-10931T>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051187 | |||||||
| chr17:44051389 | C | CA | 17 | a0001c0001t0001g0022 a0001c0001t0002g0008 a0001c0001t0002g0016 others(14): Show |
20 | HG01169.hp2 HG01256.hp2 HG02083.hp2 others(17): Show |
intron_variant | MODIFIER | c.259-11134dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051389 | |||||||
| chr17:44051389 | C | CAA | 16 | a0001c0001t0001g0251 a0001c0001t0002g0017 a0001c0001t0002g0243 others(13): Show |
17 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.259-11135_259-1113 others(6): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051389 | |||||||
| chr17:44051389 | C | CAAA | 9 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0002g0111 others(6): Show |
9 | HG00738.hp2 HG02451.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.259-11136_259-1113 others(7): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051389 | |||||||
| chr17:44051389 | CAAAAAAA others(1): Show |
C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(79): Show |
94 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.259-11141_259-1113 others(12): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051389 | |||||||
| chr17:44051389 | CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0001g0167 a0001c0001t0001g0207 a0001c0001t0001g0210 |
3 | HG00597.hp1 HG01943.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.259-11143_259-1113 others(14): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051389 | |||||||
| chr17:44051389 | CAAAAAAA others(4): Show |
C | 80 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(77): Show |
93 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.259-11144_259-1113 others(15): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051389 | |||||||
| chr17:44051389 | CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0001g0172 a0001c0001t0002g0043 a0001c0001t0005g0106 |
3 | HG03139.hp1 NA18957.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.259-11145_259-1113 others(16): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051389 | |||||||
| chr17:44051389 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0003g0042 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.259-11146_259-1113 others(17): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051389 | |||||||
| chr17:44051527 | T | C | 20 | a0001c0001t0001g0251 a0001c0001t0002g0016 a0001c0001t0002g0017 others(17): Show |
22 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.259-11271A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051527 | |||||||
| chr17:44051791 | T | C | 3 | a0001c0001t0008g0018 a0001c0001t0008g0263 a0001c0001t0008g0264 |
4 | HG02723.hp1 HG03225.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-11535A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051791 | |||||||
| chr17:44051818 | A | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0095 |
3 | HG02559.hp1 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.259-11562T>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051818 | |||||||
| chr17:44051826 | G | A | 20 | a0001c0001t0001g0251 a0001c0001t0002g0016 a0001c0001t0002g0017 others(17): Show |
22 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.259-11570C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051826 | |||||||
| chr17:44051840 | G | A | 5 | a0001c0001t0007g0032 a0001c0001t0007g0033 a0001c0001t0007g0034 others(2): Show |
5 | HG02145.hp2 HG02723.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-11584C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051840 | |||||||
| chr17:44051879 | G | A | 2 | a0001c0001t0003g0028 a0001c0001t0003g0157 |
2 | HG02622.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.259-11623C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051879 | |||||||
| chr17:44051880 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.259-11624C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051880 | |||||||
| chr17:44051895 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.259-11639C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051895 | |||||||
| chr17:44051896 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.259-11640A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051896 | |||||||
| chr17:44051898 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.259-11642T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051898 | |||||||
| chr17:44051899 | C | G | 1 | a0001c0001t0001g0105 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.259-11643G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051899 | |||||||
| chr17:44051910 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.259-11654G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051910 | |||||||
| chr17:44051911 | C | G | 1 | a0001c0001t0001g0105 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.259-11655G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051911 | |||||||
| chr17:44051999 | C | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(209): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.259-11743G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44051999 | |||||||
| chr17:44052115 | T | G | 1 | a0001c0001t0001g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.258+11686A>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44052115 | |||||||
| chr17:44052190 | C | A | 1 | a0001c0001t0008g0264 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.258+11611G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44052190 | |||||||
| chr17:44052230 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.258+11571A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44052230 | |||||||
| chr17:44052257 | C | T | 1 | a0001c0001t0002g0244 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.258+11544G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44052257 | |||||||
| chr17:44052260 | C | CA | 14 | a0001c0001t0001g0036 a0001c0001t0001g0066 a0001c0001t0001g0100 others(11): Show |
14 | HG00558.hp2 HG01099.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.258+11540dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44052260 | |||||||
| chr17:44052270 | A | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0067 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.258+11531T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44052270 | |||||||
| chr17:44052489 | T | A | 8 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0229 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.258+11312A>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44052489 | |||||||
| chr17:44052556 | C | T | 1 | a0001c0001t0003g0028 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.258+11245G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44052556 | |||||||
| chr17:44052557 | G | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(84): Show |
99 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.258+11244C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44052557 | |||||||
| chr17:44052642 | C | G | 1 | a0001c0001t0001g0228 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.258+11159G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44052642 | |||||||
| chr17:44052766 | A | T | 1 | a0001c0001t0002g0245 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.258+11035T>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44052766 | |||||||
| chr17:44052817 | AT | A | 4 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
4 | HG01243.hp2 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+10983delA | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44052817 | |||||||
| chr17:44052850 | A | G | 3 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0010g0231 |
3 | HG02258.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.258+10951T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44052850 | |||||||
| chr17:44053183 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.258+10618C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44053183 | |||||||
| chr17:44053215 | A | G | 3 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0010g0231 |
3 | HG02258.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.258+10586T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44053215 | |||||||
| chr17:44053234 | A | G | 5 | a0001c0001t0007g0032 a0001c0001t0007g0033 a0001c0001t0007g0034 others(2): Show |
5 | HG02145.hp2 HG02723.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+10567T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44053234 | |||||||
| chr17:44053244 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.258+10557A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44053244 | |||||||
| chr17:44053293 | G | A | 1 | a0001c0001t0003g0037 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.258+10508C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44053293 | |||||||
| chr17:44053575 | G | A | 3 | a0001c0001t0001g0137 a0001c0001t0001g0233 a0001c0001t0002g0138 |
3 | HG02055.hp2 HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.258+10226C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44053575 | |||||||
| chr17:44053695 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.258+10106A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44053695 | |||||||
| chr17:44053724 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.258+10077C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44053724 | |||||||
| chr17:44054196 | T | C | 1 | a0001c0001t0003g0041 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.258+9605A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44054196 | |||||||
| chr17:44054511 | G | A | 1 | a0001c0001t0008g0264 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.258+9290C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44054511 | |||||||
| chr17:44054822 | C | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0062 a0001c0001t0001g0112 |
3 | HG00558.hp2 NA18951.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.258+8979G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44054822 | |||||||
| chr17:44054909 | G | C | 1 | a0001c0001t0001g0097 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.258+8892C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44054909 | |||||||
| chr17:44054910 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.258+8891G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44054910 | |||||||
| chr17:44055000 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0130 |
2 | HG00558.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.258+8801C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44055000 | |||||||
| chr17:44055385 | G | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0019 others(76): Show |
89 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.258+8416C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44055385 | |||||||
| chr17:44055507 | C | A | 1 | a0001c0001t0001g0097 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.258+8294G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44055507 | |||||||
| chr17:44055507 | C | CA | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(88): Show |
103 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.258+8293dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44055507 | |||||||
| chr17:44055507 | C | CAA | 10 | a0001c0001t0001g0061 a0001c0001t0001g0088 a0001c0001t0001g0092 others(7): Show |
10 | HG02559.hp1 HG03098.hp2 HG03195.hp1 others(7): Show |
intron_variant | MODIFIER | c.258+8292_258+8293d others(4): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44055507 | |||||||
| chr17:44055507 | CA | C | 6 | a0001c0001t0001g0040 a0001c0001t0001g0132 a0001c0001t0001g0133 others(3): Show |
6 | HG02109.hp2 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.258+8293delT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44055507 | |||||||
| chr17:44055672 | C | T | 21 | a0001c0001t0001g0251 a0001c0001t0002g0016 a0001c0001t0002g0017 others(18): Show |
23 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.258+8129G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44055672 | |||||||
| chr17:44055680 | T | TATATATA others(26): Show |
1 | a0001c0001t0006g0156 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.258+8088_258+8120d others(35): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44055680 | |||||||
| chr17:44055682 | T | TATATATA others(15): Show |
2 | a0001c0001t0002g0021 a0001c0001t0002g0258 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.258+8097_258+8118d others(24): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44055682 | |||||||
| chr17:44055691 | A | AAT | 3 | a0001c0001t0001g0169 a0001c0001t0001g0234 a0001c0001t0002g0145 |
3 | HG03516.hp2 NA18952.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.258+8108_258+8109d others(4): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44055691 | |||||||
| chr17:44055721 | TA | T | 10 | a0001c0001t0001g0036 a0001c0001t0001g0062 a0001c0001t0001g0063 others(7): Show |
10 | HG00558.hp2 HG00673.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.258+8079delT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44055721 | |||||||
| chr17:44055978 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.258+7823C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44055978 | |||||||
| chr17:44055992 | G | A | 3 | a0001c0001t0008g0018 a0001c0001t0008g0263 a0001c0001t0008g0264 |
4 | HG02723.hp1 HG03225.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+7809C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44055992 | |||||||
| chr17:44056030 | A | G | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.258+7771T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44056030 | |||||||
| chr17:44056100 | T | G | 2 | a0002c0002t0003g0026 a0002c0002t0003g0027 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.258+7701A>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44056100 | |||||||
| chr17:44056219 | C | T | 1 | a0001c0001t0014g0035 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.258+7582G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44056219 | |||||||
| chr17:44056295 | C | CA | 9 | a0001c0001t0001g0036 a0001c0001t0001g0116 a0001c0001t0001g0125 others(6): Show |
9 | HG00558.hp1 HG00558.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.258+7505dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44056295 | |||||||
| chr17:44056449 | T | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.258+7352A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44056449 | |||||||
| chr17:44056573 | G | A | 3 | a0001c0001t0008g0018 a0001c0001t0008g0263 a0001c0001t0008g0264 |
4 | HG02723.hp1 HG03225.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+7228C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44056573 | |||||||
| chr17:44056663 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.258+7138T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44056663 | |||||||
| chr17:44056700 | G | GA | 9 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0171 others(6): Show |
9 | HG02145.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.258+7100dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44056700 | |||||||
| chr17:44056701 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.258+7100T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44056701 | |||||||
| chr17:44056703 | A | G | 5 | a0001c0001t0007g0032 a0001c0001t0007g0033 a0001c0001t0007g0034 others(2): Show |
5 | HG02145.hp2 HG02723.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+7098T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44056703 | |||||||
| chr17:44056864 | G | A | 3 | a0001c0001t0001g0057 a0001c0001t0001g0091 a0001c0001t0001g0101 |
3 | NA18960.hp1 NA18989.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.258+6937C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44056864 | |||||||
| chr17:44057156 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.258+6645A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44057156 | |||||||
| chr17:44057157 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.258+6644G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44057157 | |||||||
| chr17:44057181 | G | A | 3 | a0001c0003t0002g0011 a0001c0003t0002g0108 a0001c0003t0002g0109 |
4 | HG02886.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+6620C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44057181 | |||||||
| chr17:44057391 | G | A | 1 | a0001c0001t0002g0255 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.258+6410C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44057391 | |||||||
| chr17:44057437 | C | G | 8 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0229 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.258+6364G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44057437 | |||||||
| chr17:44057499 | C | G | 78 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(75): Show |
91 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.258+6302G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44057499 | |||||||
| chr17:44057607 | A | C | 1 | a0001c0001t0001g0061 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.258+6194T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44057607 | |||||||
| chr17:44057715 | C | A | 4 | a0002c0002t0003g0025 a0002c0002t0003g0026 a0002c0002t0003g0027 others(1): Show |
4 | HG02257.hp1 HG02630.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+6086G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44057715 | |||||||
| chr17:44057727 | A | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.258+6074T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44057727 | |||||||
| chr17:44057728 | T | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.258+6073A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44057728 | |||||||
| chr17:44057734 | G | A | 1 | a0001c0001t0002g0256 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.258+6067C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44057734 | |||||||
| chr17:44057943 | T | TA | 119 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
135 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.258+5857dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44057943 | |||||||
| chr17:44058036 | A | C | 1 | a0001c0001t0002g0111 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.258+5765T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058036 | |||||||
| chr17:44058110 | G | A | 1 | a0001c0001t0002g0244 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.258+5691C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058110 | |||||||
| chr17:44058163 | G | C | 1 | a0001c0001t0002g0021 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.258+5638C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058163 | |||||||
| chr17:44058192 | G | A | 1 | a0001c0001t0003g0028 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.258+5609C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058192 | |||||||
| chr17:44058251 | AAAT | A | 4 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+5547_258+5549d others(5): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058251 | |||||||
| chr17:44058292 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.258+5509T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058292 | |||||||
| chr17:44058490 | C | G | 5 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(2): Show |
5 | HG02080.hp2 HG02523.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+5311G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058490 | |||||||
| chr17:44058559 | G | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | NA18943.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.258+5242C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058559 | |||||||
| chr17:44058701 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.258+5100C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058701 | |||||||
| chr17:44058817 | A | C | 3 | a0001c0001t0009g0102 a0001c0001t0009g0103 a0001c0001t0009g0115 |
3 | HG02965.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.258+4984T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058817 | |||||||
| chr17:44058823 | A | G | 3 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0010g0231 |
3 | HG02258.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.258+4978T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058823 | |||||||
| chr17:44058837 | A | G | 1 | a0001c0001t0003g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.258+4964T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058837 | |||||||
| chr17:44058838 | A | G | 3 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0010g0231 |
3 | HG02258.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.258+4963T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058838 | |||||||
| chr17:44058894 | G | C | 5 | a0001c0001t0007g0032 a0001c0001t0007g0033 a0001c0001t0007g0034 others(2): Show |
5 | HG02145.hp2 HG02723.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+4907C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058894 | |||||||
| chr17:44058926 | C | T | 1 | a0001c0001t0001g0060 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.258+4875G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058926 | |||||||
| chr17:44058985 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.258+4816T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44058985 | |||||||
| chr17:44059066 | T | C | 1 | a0001c0001t0016g0262 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.258+4735A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44059066 | |||||||
| chr17:44059102 | G | A | 2 | a0001c0001t0003g0028 a0001c0001t0003g0157 |
2 | HG02622.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.258+4699C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44059102 | |||||||
| chr17:44059207 | C | T | 21 | a0001c0001t0001g0251 a0001c0001t0002g0016 a0001c0001t0002g0017 others(18): Show |
23 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.258+4594G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44059207 | |||||||
| chr17:44059378 | C | A | 3 | a0001c0001t0009g0102 a0001c0001t0009g0103 a0001c0001t0009g0115 |
3 | HG02965.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.258+4423G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44059378 | |||||||
| chr17:44059418 | A | C | 1 | a0001c0001t0001g0141 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.258+4383T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44059418 | |||||||
| chr17:44059493 | G | A | 1 | a0001c0001t0002g0256 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.258+4308C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44059493 | |||||||
| chr17:44059658 | T | C | 1 | a0001c0001t0008g0263 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.258+4143A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44059658 | |||||||
| chr17:44059744 | AAGCCCTT others(9): Show |
A | 3 | a0001c0003t0002g0011 a0001c0003t0002g0108 a0001c0003t0002g0109 |
4 | HG02886.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+4041_258+4056d others(18): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44059744 | |||||||
| chr17:44059837 | C | G | 3 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0010g0231 |
3 | HG02258.hp1 HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.258+3964G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44059837 | |||||||
| chr17:44059939 | C | T | 5 | a0001c0001t0007g0032 a0001c0001t0007g0033 a0001c0001t0007g0034 others(2): Show |
5 | HG02145.hp2 HG02723.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+3862G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44059939 | |||||||
| chr17:44059979 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.258+3822T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44059979 | |||||||
| chr17:44060090 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.258+3711C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44060090 | |||||||
| chr17:44060365 | A | G | 1 | a0001c0001t0002g0098 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.258+3436T>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44060365 | |||||||
| chr17:44060744 | C | G | 2 | a0001c0001t0007g0032 a0001c0001t0007g0033 |
2 | HG02145.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.258+3057G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44060744 | |||||||
| chr17:44060922 | CCTCT | C | 21 | a0001c0001t0001g0251 a0001c0001t0002g0016 a0001c0001t0002g0017 others(18): Show |
23 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.258+2875_258+2878d others(6): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44060922 | |||||||
| chr17:44061024 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.258+2777G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44061024 | |||||||
| chr17:44061070 | C | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(93): Show |
111 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.258+2731G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44061070 | |||||||
| chr17:44061105 | G | A | 1 | a0001c0001t0002g0096 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.258+2696C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44061105 | |||||||
| chr17:44061241 | C | T | 5 | a0001c0001t0007g0032 a0001c0001t0007g0033 a0001c0001t0007g0034 others(2): Show |
5 | HG02145.hp2 HG02723.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+2560G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44061241 | |||||||
| chr17:44061317 | CA | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(242): Show |
275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.258+2483delT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44061317 | |||||||
| chr17:44061506 | T | A | 1 | a0001c0001t0001g0129 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.258+2295A>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44061506 | |||||||
| chr17:44061542 | A | C | 3 | a0001c0001t0001g0004 a0001c0001t0001g0058 a0001c0001t0001g0059 |
5 | HG01243.hp1 HG02280.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+2259T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44061542 | |||||||
| chr17:44061875 | G | A | 7 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 others(4): Show |
7 | HG02040.hp1 NA18944.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.258+1926C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44061875 | |||||||
| chr17:44061889 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.258+1912G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44061889 | |||||||
| chr17:44061990 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(91): Show |
108 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.258+1811C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44061990 | |||||||
| chr17:44062091 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.258+1710C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44062091 | |||||||
| chr17:44062095 | G | A | 21 | a0001c0001t0001g0251 a0001c0001t0002g0016 a0001c0001t0002g0017 others(18): Show |
23 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.258+1706C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44062095 | |||||||
| chr17:44062108 | G | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0223 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.258+1693C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44062108 | |||||||
| chr17:44062200 | C | T | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG00597.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.258+1601G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44062200 | |||||||
| chr17:44062221 | C | CA | 94 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(91): Show |
108 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.258+1579dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44062221 | |||||||
| chr17:44062221 | C | CAA | 6 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(3): Show |
6 | HG00639.hp2 HG01175.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.258+1578_258+1579d others(4): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44062221 | |||||||
| chr17:44062221 | CA | C | 14 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(11): Show |
14 | HG01243.hp2 HG01256.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.258+1579delT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44062221 | |||||||
| chr17:44062286 | TA | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(84): Show |
99 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.258+1514delT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44062286 | |||||||
| chr17:44062412 | G | A | 1 | a0001c0001t0002g0258 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.258+1389C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44062412 | |||||||
| chr17:44062609 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.258+1192C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44062609 | |||||||
| chr17:44062770 | C | A | 1 | a0001c0001t0014g0035 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.258+1031G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44062770 | |||||||
| chr17:44062860 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.258+941A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44062860 | |||||||
| chr17:44062890 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.258+911C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44062890 | |||||||
| chr17:44062898 | C | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(91): Show |
108 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.258+903G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44062898 | |||||||
| chr17:44062971 | G | A | 9 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0229 others(6): Show |
9 | HG02145.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.258+830C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44062971 | |||||||
| chr17:44063025 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
2 | NA18962.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.258+776G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44063025 | |||||||
| chr17:44063220 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.258+581G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44063220 | |||||||
| chr17:44063254 | G | C | 3 | a0001c0001t0002g0243 a0001c0001t0002g0259 a0001c0001t0002g0260 |
3 | HG01081.hp1 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.258+547C>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44063254 | |||||||
| chr17:44063448 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02145.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.258+353C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 2/4 | chr17 | 44063448 | |||||||
| chr17:44064004 | T | C | 1 | a0001c0001t0002g0021 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.125-70A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44064004 | |||||||
| chr17:44064254 | ACT | A | 88 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(85): Show |
102 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.125-322_125-321del others(2): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44064254 | |||||||
| chr17:44064270 | C | G | 7 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(4): Show |
7 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.125-336G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44064270 | |||||||
| chr17:44064286 | C | G | 1 | a0001c0001t0001g0046 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.125-352G>C | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44064286 | |||||||
| chr17:44064570 | C | CA | 9 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0229 others(6): Show |
9 | HG02145.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.125-637dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44064570 | |||||||
| chr17:44064732 | C | CA | 6 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(3): Show |
6 | HG00621.hp1 HG02135.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.125-799dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44064732 | |||||||
| chr17:44064732 | CA | C | 11 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0040 others(8): Show |
11 | HG01069.hp1 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.125-799delT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44064732 | |||||||
| chr17:44064815 | G | T | 6 | a0001c0001t0002g0008 a0001c0001t0002g0236 a0001c0001t0002g0237 others(3): Show |
8 | HG02451.hp2 HG02486.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.125-881C>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44064815 | |||||||
| chr17:44064865 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.125-931C>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44064865 | |||||||
| chr17:44065145 | C | CA | 16 | a0001c0001t0001g0022 a0001c0001t0001g0116 a0001c0001t0001g0117 others(13): Show |
16 | HG00558.hp1 HG00597.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.125-1212dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44065145 | |||||||
| chr17:44065270 | T | TA | 5 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0005g0015 others(2): Show |
7 | HG01975.hp1 HG02723.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.124+1193dupT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44065270 | |||||||
| chr17:44065378 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.124+1086A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44065378 | |||||||
| chr17:44065439 | TA | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(102): Show |
119 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.124+1024delT | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44065439 | |||||||
| chr17:44065439 | TAA | T | 33 | a0001c0001t0001g0031 a0001c0001t0001g0036 a0001c0001t0001g0251 others(30): Show |
37 | HG00099.hp1 HG00558.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.124+1023_124+1024d others(4): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44065439 | |||||||
| chr17:44065439 | TAAA | T | 12 | a0001c0001t0002g0241 a0001c0001t0002g0243 a0001c0001t0003g0009 others(9): Show |
13 | HG00741.hp1 HG01109.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.124+1022_124+1024d others(5): Show |
LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44065439 | |||||||
| chr17:44065567 | T | C | 6 | a0001c0001t0002g0008 a0001c0001t0002g0236 a0001c0001t0002g0237 others(3): Show |
8 | HG02451.hp2 HG02486.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.124+897A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44065567 | |||||||
| chr17:44065758 | A | C | 1 | a0001c0001t0001g0022 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.124+706T>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44065758 | |||||||
| chr17:44065810 | C | T | 1 | a0001c0001t0002g0021 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.124+654G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44065810 | |||||||
| chr17:44065864 | C | A | 6 | a0001c0001t0002g0008 a0001c0001t0002g0236 a0001c0001t0002g0237 others(3): Show |
8 | HG02451.hp2 HG02486.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.124+600G>T | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44065864 | |||||||
| chr17:44065884 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.124+580G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44065884 | |||||||
| chr17:44065888 | T | C | 22 | a0001c0001t0001g0251 a0001c0001t0002g0016 a0001c0001t0002g0017 others(19): Show |
24 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.124+576A>G | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44065888 | |||||||
| chr17:44066295 | C | T | 1 | a0001c0001t0001g0019 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.124+169G>A | LSM12 | ENSG00000161654.10 | transcript | ENST00000293406.8 | protein_coding | 1/4 | chr17 | 44066295 |