Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 286826 |
| ensemblid | ENSG00000183814.16 |
| hgncid | 30830 |
| symbol | LIN9 |
| name | lin-9 DREAM MuvB core complex component |
| refseq_nuc | NM_001366245.2 |
| refseq_prot | NP_001353174.1 |
| ensembl_nuc | ENST00000681046.1 |
| ensembl_prot | ENSP00000505590.1 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 226231157 |
| end | 226309164 |
| strand | - |
| ver | v1.2 |
| region | chr1:226231157-226309164 |
| region5000 | chr1:226226157-226314164 |
| regionname0 | LIN9_chr1_226231157_226309164 |
| regionname5000 | LIN9_chr1_226226157_226314164 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 542 | 361 | 76 | 69 | 162 | 8 | 44 | 125 | LIN9_chr1_226226157_226314164 | LIN9 | MAELD others(537): Show |
chr1 | 226226157 | 226314164 |
| a0002 | 0/0 | 542 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | MAELD others(537): Show |
chr1 | 226226157 | 226314164 |
| a0003 | 0/0 | 542 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | MAELD others(537): Show |
chr1 | 226226157 | 226314164 |
| a0004 | 0/0 | 542 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | MAELD others(537): Show |
chr1 | 226226157 | 226314164 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1626 | 260 | 56 | 49 | 121 | 5 | 28 | LIN9_chr1_226226157_226314164 | LIN9 | ATGGC others(1621): Show |
chr1 | 226226157 | 226314164 | ||
| a0001c0002 | 1/0 | 1626 | 99 | 20 | 19 | 40 | 3 | 16 | LIN9_chr1_226226157_226314164 | LIN9 | ATGGC others(1621): Show |
chr1 | 226226157 | 226314164 | ||
| a0001c0004 | 0/0 | 1626 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | ATGGC others(1621): Show |
chr1 | 226226157 | 226314164 | ||
| a0001c0007 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | ATGGC others(1621): Show |
chr1 | 226226157 | 226314164 | ||
| a0002c0003 | 0/0 | 1626 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | ATGGC others(1621): Show |
chr1 | 226226157 | 226314164 | ||
| a0003c0005 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | ATGGC others(1621): Show |
chr1 | 226226157 | 226314164 | ||
| a0004c0006 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | ATGGC others(1621): Show |
chr1 | 226226157 | 226314164 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2998 | 212 | 56 | 44 | 83 | 3 | 25 | LIN9_chr1_226226157_226314164 | LIN9 | GAAAA others(2993): Show |
chr1 | 226226157 | 226314164 |
| a0001c0001t0003 | 0/0 | 2998 | 45 | 0 | 5 | 35 | 2 | 3 | LIN9_chr1_226226157_226314164 | LIN9 | GAAAA others(2993): Show |
chr1 | 226226157 | 226314164 |
| a0001c0001t0005 | 0/0 | 2998 | 2 | 0 | 0 | 2 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | GAAAA others(2993): Show |
chr1 | 226226157 | 226314164 |
| a0001c0001t0006 | 0/0 | 2998 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | GAAAA others(2993): Show |
chr1 | 226226157 | 226314164 |
| a0001c0002t0001 | 0/0 | 2998 | 2 | 1 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | GAAAA others(2993): Show |
chr1 | 226226157 | 226314164 |
| a0001c0002t0002 | 1/0 | 2998 | 93 | 19 | 16 | 38 | 3 | 16 | LIN9_chr1_226226157_226314164 | LIN9 | GAAAA others(2993): Show |
chr1 | 226226157 | 226314164 |
| a0001c0002t0004 | 0/0 | 2998 | 3 | 0 | 3 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | GAAAA others(2993): Show |
chr1 | 226226157 | 226314164 |
| a0001c0002t0007 | 0/0 | 2998 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | GAAAA others(2993): Show |
chr1 | 226226157 | 226314164 |
| a0001c0004t0002 | 0/0 | 2998 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | GAAAA others(2993): Show |
chr1 | 226226157 | 226314164 |
| a0001c0007t0001 | 0/0 | 2998 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | GAAAA others(2993): Show |
chr1 | 226226157 | 226314164 |
| a0002c0003t0002 | 0/0 | 2998 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | GAAAA others(2993): Show |
chr1 | 226226157 | 226314164 |
| a0003c0005t0001 | 0/0 | 2998 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | GAAAA others(2993): Show |
chr1 | 226226157 | 226314164 |
| a0004c0006t0001 | 0/0 | 2998 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | GAAAA others(2993): Show |
chr1 | 226226157 | 226314164 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0315 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0005g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0001t0006g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0308 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0004g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0004g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0004g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0002t0007g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0004t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0001c0007t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0002c0003t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0003c0005t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| a0004c0006t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | GBR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0156 | EUR | GBR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0171 | EUR | FIN | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0159 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0132 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0145 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0174 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG00621 | hp2 | a0001 | c0002 | t0007 | g0197 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0190 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0137 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0077 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01069 | hp1 | a0001 | c0002 | t0004 | g0149 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01071 | hp1 | a0001 | c0002 | t0004 | g0150 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0179 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0086 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01106 | hp2 | a0001 | c0004 | t0002 | g0133 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0290 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0294 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0289 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0120 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01169 | hp1 | a0001 | c0002 | t0002 | g0291 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01192 | hp1 | a0002 | c0003 | t0002 | g0147 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0181 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0136 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0157 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0139 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0141 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0205 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0140 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0239 | EUR | IBS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0142 | EUR | IBS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0293 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0072 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02027 | hp2 | a0003 | c0005 | t0001 | g0094 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0295 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0155 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0196 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0185 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0193 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0203 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0074 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CDX | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | CDX | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0285 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0288 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02273 | hp2 | a0001 | c0002 | t0004 | g0281 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0286 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0135 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0206 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0198 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0199 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0187 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0161 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0306 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0130 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | ESN | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0287 | AFR | ESN | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | ESN | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | ESN | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0357 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03041 | hp2 | a0001 | c0002 | t0002 | g0163 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | ESN | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0283 | AFR | ESN | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0284 | AFR | MSL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0143 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0282 | AFR | MSL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0170 | AFR | MSL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | MSL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0091 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0144 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0183 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ESN | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0195 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | STU | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0356 | SAS | STU | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0360 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0359 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0117 | SAS | BEB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0208 | SAS | BEB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | BEB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | BEB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0358 | SAS | BEB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | BEB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0105 | SAS | BEB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0207 | SAS | BEB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0186 | SAS | BEB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | STU | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0184 | SAS | STU | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | STU | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | STU | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | STU | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | STU | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0176 | EAS | CHB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | CHB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | CHB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | YRI | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | YRI | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0166 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0177 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0175 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18945 | hp2 | a0001 | c0001 | t0005 | g0055 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18946 | hp1 | a0001 | c0002 | t0002 | g0131 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0178 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0167 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0162 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0362 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18963 | hp2 | a0001 | c0001 | t0006 | g0038 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0173 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0172 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0204 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18979 | hp2 | a0004 | c0006 | t0001 | g0363 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18995 | hp2 | a0001 | c0002 | t0002 | g0189 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19001 | hp2 | a0001 | c0002 | t0002 | g0180 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0152 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0182 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19012 | hp2 | a0001 | c0001 | t0005 | g0044 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0201 | AFR | LWK | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0188 | AFR | LWK | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | LWK | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0154 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19056 | hp2 | a0001 | c0002 | t0002 | g0164 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0151 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19076 | hp2 | a0001 | c0002 | t0002 | g0158 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19080 | hp2 | a0001 | c0007 | t0001 | g0037 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0153 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0165 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0192 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | YRI | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | YRI | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ASW | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ASW | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0073 | EUR | TSI | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0317 | EUR | TSI | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | GIH | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | GIH | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0138 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0361 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0292 | AFR | MSL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0146 | AFR | USA | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0200 | AFR | USA | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | USA | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | USA | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | LWK | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | LWK | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0315 | REF | REF | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0308 | REF | REF | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:226233456 | T | G | 1 | a0002 | 1 | HG01192.hp1 | missense_variant | MODERATE | c.1313A>C | p.Glu438Ala | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 13/15 | 1338/2998 | 1313/1629 | 438/542 | chr1 | 226233456 | |||
| chr1:226266247 | A | G | 1 | a0003 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.902T>C | p.Leu301Ser | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 9/15 | 927/2998 | 902/1629 | 301/542 | chr1 | 226266247 | |||
| chr1:226277828 | T | G | 1 | a0004 | 1 | NA18979.hp2 | missense_variant | MODERATE | c.629A>C | p.Lys210Thr | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/15 | 654/2998 | 629/1629 | 210/542 | chr1 | 226277828 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:226233494 | T | C | 1 | a0001c0004 | 1 | HG01106.hp2 | synonymous_variant | LOW | c.1275A>G | p.Ala425Ala | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 13/15 | 1300/2998 | 1275/1629 | 425/542 | chr1 | 226233494 | |||
| chr1:226286431 | G | A | 4 | a0001c0001 a0001c0007 a0003c0005 others(1): Show |
262 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(259): Show |
synonymous_variant | LOW | c.426C>T | p.Phe142Phe | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/15 | 451/2998 | 426/1629 | 142/542 | chr1 | 226286431 | |||
| chr1:226301177 | T | C | 1 | a0001c0007 | 1 | NA19080.hp2 | synonymous_variant | LOW | c.60A>G | p.Leu20Leu | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/15 | 85/2998 | 60/1629 | 20/542 | chr1 | 226301177 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:226231234 | A | T | 1 | a0001c0001t0005 | 2 | NA18945.hp2 NA19012.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1267T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 15/15 | 1267 | chr1 | 226231234 | ||||||
| chr1:226231465 | G | C | 8 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(5): Show |
264 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(261): Show |
3_prime_UTR_variant | MODIFIER | c.*1036C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 15/15 | 1036 | chr1 | 226231465 | ||||||
| chr1:226231536 | C | G | 8 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(5): Show |
264 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(261): Show |
3_prime_UTR_variant | MODIFIER | c.*965G>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 15/15 | 965 | chr1 | 226231536 | ||||||
| chr1:226231709 | A | G | 1 | a0001c0002t0004 | 3 | HG01069.hp1 HG01071.hp1 HG02273.hp2 |
3_prime_UTR_variant | MODIFIER | c.*792T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 15/15 | 792 | chr1 | 226231709 | ||||||
| chr1:226232249 | A | C | 1 | a0001c0001t0006 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*252T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 15/15 | 252 | chr1 | 226232249 | ||||||
| chr1:226232339 | T | C | 3 | a0001c0001t0003 a0001c0001t0005 a0001c0002t0007 |
48 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*162A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 15/15 | 162 | chr1 | 226232339 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:226232711 | T | C | 3 | a0001c0001t0001g0230 a0001c0001t0001g0239 a0001c0001t0001g0280 |
3 | HG01109.hp2 HG01243.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1524-105A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 14/14 | chr1 | 226232711 | |||||||
| chr1:226232803 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1524-197G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 14/14 | chr1 | 226232803 | |||||||
| chr1:226232835 | C | G | 218 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(215): Show |
219 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.1524-229G>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 14/14 | chr1 | 226232835 | |||||||
| chr1:226232920 | T | C | 1 | a0001c0001t0001g0300 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1523+176A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 14/14 | chr1 | 226232920 | |||||||
| chr1:226232953 | G | A | 2 | a0001c0001t0001g0327 a0001c0001t0001g0338 |
2 | NA18612.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1523+143C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 14/14 | chr1 | 226232953 | |||||||
| chr1:226233021 | A | G | 123 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(120): Show |
123 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1523+75T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 14/14 | chr1 | 226233021 | |||||||
| chr1:226233674 | AAC | A | 3 | a0001c0001t0003g0047 a0001c0001t0003g0051 a0001c0001t0003g0113 |
3 | NA18960.hp1 NA18977.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1246-153_1246-152d others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226233674 | |||||||
| chr1:226233913 | T | A | 1 | a0001c0001t0001g0097 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1246-390A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226233913 | |||||||
| chr1:226233931 | A | G | 1 | a0001c0001t0001g0300 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1246-408T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226233931 | |||||||
| chr1:226233979 | T | C | 264 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(261): Show |
264 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.1246-456A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226233979 | |||||||
| chr1:226234015 | T | G | 2 | a0001c0002t0002g0146 a0001c0002t0002g0188 |
2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1246-492A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226234015 | |||||||
| chr1:226234182 | T | C | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1246-659A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226234182 | |||||||
| chr1:226234219 | C | T | 1 | a0001c0002t0002g0203 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1246-696G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226234219 | |||||||
| chr1:226234531 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1246-1008G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226234531 | |||||||
| chr1:226234701 | AG | A | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0312 others(1): Show |
4 | HG02630.hp1 NA19240.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1246-1179delC | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226234701 | |||||||
| chr1:226234893 | A | AT | 10 | a0001c0001t0001g0217 a0001c0001t0001g0221 a0001c0001t0001g0296 others(7): Show |
10 | HG02055.hp1 HG02809.hp1 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.1246-1371dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226234893 | |||||||
| chr1:226234893 | A | ATTTT | 12 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(9): Show |
12 | HG01069.hp2 HG01074.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.1246-1374_1246-137 others(8): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226234893 | |||||||
| chr1:226234893 | A | ATTTTT | 79 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0016 others(76): Show |
79 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.1246-1375_1246-137 others(9): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226234893 | |||||||
| chr1:226234893 | A | ATTTTTT | 8 | a0001c0001t0001g0049 a0001c0001t0001g0057 a0001c0001t0001g0125 others(5): Show |
8 | HG00673.hp2 HG02027.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.1246-1376_1246-137 others(10): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226234893 | |||||||
| chr1:226234893 | AT | A | 95 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0087 others(92): Show |
95 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.1246-1371delA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226234893 | |||||||
| chr1:226234907 | T | C | 1 | a0001c0001t0001g0273 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1246-1384A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226234907 | |||||||
| chr1:226235179 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1246-1656C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226235179 | |||||||
| chr1:226235255 | G | A | 5 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(2): Show |
5 | HG03017.hp1 HG03834.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.1246-1732C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226235255 | |||||||
| chr1:226235322 | C | CA | 31 | a0001c0001t0001g0013 a0001c0001t0001g0070 a0001c0001t0001g0128 others(28): Show |
31 | HG02040.hp1 HG02451.hp2 HG02630.hp1 others(28): Show |
intron_variant | MODIFIER | c.1246-1800dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226235322 | |||||||
| chr1:226235322 | C | CAA | 188 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(185): Show |
188 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.1246-1801_1246-180 others(6): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226235322 | |||||||
| chr1:226235322 | C | CAAA | 22 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0064 others(19): Show |
22 | HG00609.hp1 HG01168.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.1246-1802_1246-180 others(7): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226235322 | |||||||
| chr1:226235322 | CAAAA | C | 18 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(15): Show |
18 | HG02055.hp2 HG02145.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.1246-1803_1246-180 others(8): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226235322 | |||||||
| chr1:226235449 | T | C | 350 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(347): Show |
351 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.1246-1926A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226235449 | |||||||
| chr1:226235483 | C | T | 119 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(116): Show |
119 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.1246-1960G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226235483 | |||||||
| chr1:226235559 | T | C | 1 | a0001c0002t0002g0286 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1246-2036A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226235559 | |||||||
| chr1:226235569 | C | G | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0312 others(1): Show |
4 | HG02630.hp1 NA19240.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1246-2046G>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226235569 | |||||||
| chr1:226235871 | C | T | 262 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(259): Show |
262 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.1246-2348G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226235871 | |||||||
| chr1:226236389 | A | G | 1 | a0001c0002t0002g0183 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1245+2582T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226236389 | |||||||
| chr1:226236437 | T | C | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1245+2534A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226236437 | |||||||
| chr1:226236444 | CTTTA | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0003g0046 |
3 | NA19005.hp1 NA19054.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1245+2523_1245+252 others(8): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226236444 | |||||||
| chr1:226236581 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0025 |
2 | HG01255.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1245+2390C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226236581 | |||||||
| chr1:226236754 | G | C | 1 | a0001c0001t0001g0306 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1245+2217C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226236754 | |||||||
| chr1:226236776 | C | A | 120 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(117): Show |
120 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.1245+2195G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226236776 | |||||||
| chr1:226236819 | C | T | 1 | a0001c0002t0002g0144 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1245+2152G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226236819 | |||||||
| chr1:226236933 | G | A | 99 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0087 others(96): Show |
99 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.1245+2038C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226236933 | |||||||
| chr1:226237103 | T | A | 1 | a0001c0001t0001g0123 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1245+1868A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226237103 | |||||||
| chr1:226237317 | A | T | 1 | a0001c0001t0001g0123 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1245+1654T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226237317 | |||||||
| chr1:226237359 | G | A | 15 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(12): Show |
15 | HG02040.hp1 HG03704.hp1 NA18941.hp2 others(12): Show |
intron_variant | MODIFIER | c.1245+1612C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226237359 | |||||||
| chr1:226237360 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1245+1611G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226237360 | |||||||
| chr1:226237619 | C | T | 1 | a0001c0002t0002g0203 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1245+1352G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226237619 | |||||||
| chr1:226237632 | C | CA | 105 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0087 others(102): Show |
106 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.1245+1338dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226237632 | |||||||
| chr1:226237632 | CA | C | 45 | a0001c0001t0001g0004 a0001c0001t0001g0129 a0001c0001t0001g0209 others(42): Show |
45 | HG00609.hp1 HG01168.hp2 HG01516.hp2 others(42): Show |
intron_variant | MODIFIER | c.1245+1338delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226237632 | |||||||
| chr1:226237776 | C | T | 1 | a0001c0002t0002g0205 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1245+1195G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226237776 | |||||||
| chr1:226237919 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1245+1052G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226237919 | |||||||
| chr1:226237940 | A | C | 5 | a0001c0002t0002g0163 a0001c0002t0002g0198 a0001c0002t0002g0200 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1245+1031T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226237940 | |||||||
| chr1:226237952 | CA | C | 258 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(255): Show |
258 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(255): Show |
intron_variant | MODIFIER | c.1245+1018delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226237952 | |||||||
| chr1:226238089 | C | G | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1245+882G>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226238089 | |||||||
| chr1:226238151 | A | G | 5 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0001c0001t0001g0320 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1245+820T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226238151 | |||||||
| chr1:226238588 | A | T | 17 | a0001c0001t0001g0004 a0001c0001t0001g0296 a0001c0001t0001g0297 others(14): Show |
17 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1245+383T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226238588 | |||||||
| chr1:226238609 | C | T | 1 | a0001c0002t0002g0172 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1245+362G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226238609 | |||||||
| chr1:226238636 | T | A | 260 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(257): Show |
260 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(257): Show |
intron_variant | MODIFIER | c.1245+335A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226238636 | |||||||
| chr1:226238942 | A | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0040 others(2): Show |
5 | HG00438.hp1 HG01346.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1245+29T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226238942 | |||||||
| chr1:226239338 | A | G | 3 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0092 |
3 | HG00673.hp2 HG02074.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1120-242T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226239338 | |||||||
| chr1:226239602 | AAT | A | 4 | a0001c0001t0003g0046 a0001c0001t0003g0052 a0001c0001t0005g0044 others(1): Show |
4 | HG02165.hp2 NA18945.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.1120-508_1120-507d others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226239602 | |||||||
| chr1:226239612 | T | C | 122 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(119): Show |
122 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.1120-516A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226239612 | |||||||
| chr1:226239728 | C | T | 1 | a0001c0001t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1120-632G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226239728 | |||||||
| chr1:226239828 | A | G | 1 | a0001c0001t0003g0060 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1120-732T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226239828 | |||||||
| chr1:226239951 | T | C | 1 | a0001c0001t0003g0077 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1120-855A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226239951 | |||||||
| chr1:226240265 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1120-1169C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226240265 | |||||||
| chr1:226240294 | G | A | 1 | a0001c0002t0002g0169 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1120-1198C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226240294 | |||||||
| chr1:226240386 | G | GT | 7 | a0001c0001t0001g0362 a0001c0002t0002g0007 a0001c0002t0002g0166 others(4): Show |
7 | HG01891.hp2 HG03471.hp2 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.1120-1291dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226240386 | |||||||
| chr1:226240386 | GT | G | 243 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(240): Show |
243 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(240): Show |
intron_variant | MODIFIER | c.1120-1291delA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226240386 | |||||||
| chr1:226240425 | G | A | 1 | a0003c0005t0001g0094 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1120-1329C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226240425 | |||||||
| chr1:226240502 | C | T | 1 | a0001c0001t0001g0300 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1120-1406G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226240502 | |||||||
| chr1:226240640 | T | C | 5 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0001c0001t0001g0320 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1120-1544A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226240640 | |||||||
| chr1:226240998 | T | C | 7 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(4): Show |
7 | HG01106.hp1 HG02257.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1120-1902A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226240998 | |||||||
| chr1:226241124 | A | G | 1 | a0001c0001t0003g0113 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1120-2028T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226241124 | |||||||
| chr1:226241214 | G | A | 5 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0001c0001t0001g0320 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1120-2118C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226241214 | |||||||
| chr1:226241235 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1120-2139G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226241235 | |||||||
| chr1:226241313 | A | G | 1 | a0001c0001t0001g0019 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1120-2217T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226241313 | |||||||
| chr1:226241362 | A | C | 1 | a0001c0001t0001g0325 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1120-2266T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226241362 | |||||||
| chr1:226241629 | C | T | 1 | a0001c0002t0002g0131 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1120-2533G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226241629 | |||||||
| chr1:226241674 | C | T | 1 | a0001c0001t0001g0274 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1120-2578G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226241674 | |||||||
| chr1:226241724 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1120-2628C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226241724 | |||||||
| chr1:226241750 | C | T | 5 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0001c0001t0001g0320 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1120-2654G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226241750 | |||||||
| chr1:226241824 | C | T | 1 | a0001c0002t0002g0208 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1120-2728G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226241824 | |||||||
| chr1:226241857 | C | CA | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1120-2762dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226241857 | |||||||
| chr1:226241892 | T | C | 5 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0001c0001t0001g0320 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1120-2796A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226241892 | |||||||
| chr1:226242679 | C | T | 13 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(10): Show |
13 | HG01074.hp2 HG01099.hp2 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.1120-3583G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226242679 | |||||||
| chr1:226242727 | C | T | 1 | a0001c0001t0001g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1120-3631G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226242727 | |||||||
| chr1:226242908 | T | TTAA | 263 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(260): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.1120-3815_1120-381 others(7): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226242908 | |||||||
| chr1:226242943 | G | C | 1 | a0001c0001t0001g0263 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1120-3847C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226242943 | |||||||
| chr1:226243065 | G | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0296 a0001c0001t0001g0297 others(14): Show |
17 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1120-3969C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226243065 | |||||||
| chr1:226243153 | T | C | 1 | a0001c0001t0001g0030 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1120-4057A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226243153 | |||||||
| chr1:226243379 | A | C | 3 | a0001c0001t0003g0047 a0001c0001t0003g0051 a0001c0001t0003g0113 |
3 | NA18960.hp1 NA18977.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1120-4283T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226243379 | |||||||
| chr1:226243484 | C | G | 4 | a0001c0001t0001g0043 a0001c0001t0001g0057 a0001c0001t0001g0067 others(1): Show |
4 | HG02622.hp1 HG02895.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1120-4388G>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226243484 | |||||||
| chr1:226243682 | C | T | 2 | a0001c0001t0001g0302 a0001c0001t0001g0316 |
2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1120-4586G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226243682 | |||||||
| chr1:226243695 | C | CA | 61 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0049 others(58): Show |
61 | HG00621.hp2 HG00673.hp2 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.1120-4600dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226243695 | |||||||
| chr1:226243695 | CA | C | 10 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0097 others(7): Show |
10 | HG01256.hp1 HG02630.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1120-4600delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226243695 | |||||||
| chr1:226243735 | A | C | 221 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(218): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.1120-4639T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226243735 | |||||||
| chr1:226243876 | A | AATT | 262 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(259): Show |
262 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.1120-4783_1120-478 others(7): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226243876 | |||||||
| chr1:226243899 | G | C | 20 | a0001c0002t0002g0001 a0001c0002t0002g0135 a0001c0002t0002g0136 others(17): Show |
21 | HG00544.hp1 HG00738.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1120-4803C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226243899 | |||||||
| chr1:226243931 | G | A | 1 | a0001c0001t0001g0300 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1120-4835C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226243931 | |||||||
| chr1:226244000 | G | A | 1 | a0001c0001t0001g0210 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1120-4904C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226244000 | |||||||
| chr1:226244026 | T | C | 1 | a0001c0002t0002g0175 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1120-4930A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226244026 | |||||||
| chr1:226244166 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1120-5070C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226244166 | |||||||
| chr1:226244281 | A | C | 1 | a0001c0001t0001g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1120-5185T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226244281 | |||||||
| chr1:226244304 | T | C | 216 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1120-5208A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226244304 | |||||||
| chr1:226244416 | A | G | 5 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0001c0001t0001g0320 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1120-5320T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226244416 | |||||||
| chr1:226244819 | C | T | 1 | a0001c0002t0002g0194 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1120-5723G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226244819 | |||||||
| chr1:226244820 | G | A | 259 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(256): Show |
259 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(256): Show |
intron_variant | MODIFIER | c.1120-5724C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226244820 | |||||||
| chr1:226244881 | G | A | 2 | a0001c0002t0002g0136 a0001c0002t0002g0137 |
2 | HG00738.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1120-5785C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226244881 | |||||||
| chr1:226245428 | TC | T | 259 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(256): Show |
259 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(256): Show |
intron_variant | MODIFIER | c.1119+5410delG | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226245428 | |||||||
| chr1:226245429 | C | T | 57 | a0001c0001t0001g0030 a0001c0001t0001g0160 a0001c0001t0003g0156 others(54): Show |
57 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.1119+5410G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226245429 | |||||||
| chr1:226245430 | C | T | 260 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(257): Show |
260 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(257): Show |
intron_variant | MODIFIER | c.1119+5409G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226245430 | |||||||
| chr1:226245431 | C | T | 260 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(257): Show |
260 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(257): Show |
intron_variant | MODIFIER | c.1119+5408G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226245431 | |||||||
| chr1:226245484 | A | T | 1 | a0001c0001t0001g0009 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1119+5355T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226245484 | |||||||
| chr1:226245551 | G | T | 236 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(233): Show |
236 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.1119+5288C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226245551 | |||||||
| chr1:226245598 | T | A | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1119+5241A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226245598 | |||||||
| chr1:226245675 | CCTCT | C | 259 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(256): Show |
259 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(256): Show |
intron_variant | MODIFIER | c.1119+5160_1119+516 others(8): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226245675 | |||||||
| chr1:226245724 | C | T | 2 | a0001c0002t0002g0165 a0001c0002t0002g0173 |
2 | NA18965.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1119+5115G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226245724 | |||||||
| chr1:226245751 | C | T | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG00735.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1119+5088G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226245751 | |||||||
| chr1:226245993 | G | A | 6 | a0001c0001t0001g0214 a0001c0001t0001g0217 a0001c0001t0001g0218 others(3): Show |
6 | NA18941.hp2 NA18966.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.1119+4846C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226245993 | |||||||
| chr1:226246007 | T | C | 219 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(216): Show |
219 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(216): Show |
intron_variant | MODIFIER | c.1119+4832A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226246007 | |||||||
| chr1:226246067 | A | G | 3 | a0001c0002t0002g0176 a0001c0002t0002g0182 a0001c0002t0002g0196 |
3 | HG02071.hp1 NA18612.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1119+4772T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226246067 | |||||||
| chr1:226246563 | A | G | 1 | a0001c0002t0002g0189 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1119+4276T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226246563 | |||||||
| chr1:226246618 | T | TA | 6 | a0001c0001t0001g0018 a0001c0001t0001g0220 a0001c0001t0001g0228 others(3): Show |
6 | HG01928.hp1 HG01993.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1119+4220dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226246618 | |||||||
| chr1:226246725 | G | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0296 a0001c0001t0001g0297 others(14): Show |
17 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1119+4114C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226246725 | |||||||
| chr1:226246780 | G | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0296 a0001c0001t0001g0297 others(14): Show |
17 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1119+4059C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226246780 | |||||||
| chr1:226246792 | C | CA | 10 | a0001c0002t0001g0134 a0001c0002t0002g0007 a0001c0002t0002g0148 others(7): Show |
10 | HG01106.hp2 HG02622.hp2 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.1119+4046dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226246792 | |||||||
| chr1:226246792 | CA | C | 246 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(243): Show |
247 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.1119+4046delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226246792 | |||||||
| chr1:226246792 | CAA | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0228 a0001c0001t0001g0252 others(3): Show |
6 | HG01257.hp1 HG01928.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1119+4045_1119+404 others(6): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226246792 | |||||||
| chr1:226246968 | TATTCCGT others(5): Show |
T | 1 | a0001c0001t0001g0030 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1119+3859_1119+387 others(16): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226246968 | |||||||
| chr1:226247669 | T | C | 1 | a0001c0001t0003g0012 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1119+3170A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226247669 | |||||||
| chr1:226247674 | C | CT | 144 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(141): Show |
144 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1119+3164dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226247674 | |||||||
| chr1:226247728 | G | C | 125 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(122): Show |
125 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.1119+3111C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226247728 | |||||||
| chr1:226247900 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1119+2939C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226247900 | |||||||
| chr1:226248188 | C | T | 1 | a0001c0002t0002g0204 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1119+2651G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226248188 | |||||||
| chr1:226248346 | A | T | 1 | a0001c0001t0001g0357 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1119+2493T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226248346 | |||||||
| chr1:226248427 | A | T | 3 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0301 |
3 | HG02055.hp2 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1119+2412T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226248427 | |||||||
| chr1:226248437 | T | TGCAATTA others(14): Show |
1 | a0001c0001t0003g0112 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1119+2381_1119+240 others(25): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226248437 | |||||||
| chr1:226248469 | C | G | 97 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0223 others(94): Show |
97 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.1119+2370G>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226248469 | |||||||
| chr1:226249040 | G | C | 1 | a0001c0002t0002g0167 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1119+1799C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226249040 | |||||||
| chr1:226249075 | G | A | 1 | a0001c0001t0003g0076 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1119+1764C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226249075 | |||||||
| chr1:226249209 | A | G | 1 | a0001c0002t0001g0361 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1119+1630T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226249209 | |||||||
| chr1:226249511 | T | TA | 6 | a0001c0001t0001g0030 a0001c0001t0001g0256 a0001c0001t0001g0257 others(3): Show |
6 | HG02109.hp2 HG02451.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1119+1327dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226249511 | |||||||
| chr1:226249525 | T | C | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1119+1314A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226249525 | |||||||
| chr1:226249607 | C | A | 1 | a0001c0001t0001g0042 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1119+1232G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226249607 | |||||||
| chr1:226250170 | GA | G | 22 | a0001c0001t0001g0097 a0001c0001t0001g0209 a0001c0001t0001g0210 others(19): Show |
22 | HG02040.hp1 HG02300.hp1 HG03017.hp2 others(19): Show |
intron_variant | MODIFIER | c.1119+668delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226250170 | |||||||
| chr1:226250276 | C | A | 119 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(116): Show |
119 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.1119+563G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226250276 | |||||||
| chr1:226250536 | T | C | 23 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0296 others(20): Show |
23 | HG02055.hp2 HG02145.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.1119+303A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226250536 | |||||||
| chr1:226250748 | T | C | 316 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(313): Show |
316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.1119+91A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226250748 | |||||||
| chr1:226250753 | A | T | 1 | a0002c0003t0002g0147 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1119+86T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226250753 | |||||||
| chr1:226250776 | T | C | 1 | a0001c0002t0002g0170 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1119+63A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226250776 | |||||||
| chr1:226250783 | TCTCA | T | 14 | a0001c0001t0001g0223 a0001c0001t0001g0248 a0001c0001t0001g0249 others(11): Show |
14 | HG00735.hp1 HG02056.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.1119+52_1119+55del others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226250783 | |||||||
| chr1:226250796 | A | AAATTAGA others(36): Show |
1 | a0001c0002t0002g0153 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1119_1119+42dupGGT others(40): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226250796 | |||||||
| chr1:226251020 | A | G | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1039-101T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226251020 | |||||||
| chr1:226251131 | A | C | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1039-212T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226251131 | |||||||
| chr1:226251202 | C | T | 1 | a0001c0001t0001g0357 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1039-283G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226251202 | |||||||
| chr1:226251216 | A | G | 1 | a0001c0002t0002g0130 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1039-297T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226251216 | |||||||
| chr1:226251229 | A | AT | 127 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(124): Show |
127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1039-311dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226251229 | |||||||
| chr1:226251517 | G | A | 1 | a0001c0002t0002g0317 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1039-598C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226251517 | |||||||
| chr1:226251656 | T | A | 47 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(44): Show |
47 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.1039-737A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226251656 | |||||||
| chr1:226251695 | C | T | 1 | a0001c0001t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1039-776G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226251695 | |||||||
| chr1:226252281 | A | AAAAT | 17 | a0001c0001t0001g0223 a0001c0001t0001g0227 a0001c0001t0001g0228 others(14): Show |
17 | HG01928.hp1 HG02004.hp2 HG02300.hp1 others(14): Show |
intron_variant | MODIFIER | c.1039-1366_1039-136 others(8): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252281 | |||||||
| chr1:226252281 | AAAAT | A | 122 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(119): Show |
122 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.1039-1366_1039-136 others(8): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252281 | |||||||
| chr1:226252298 | A | G | 2 | a0001c0001t0001g0209 a0001c0001t0001g0213 |
2 | NA18984.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1039-1379T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252298 | |||||||
| chr1:226252302 | A | G | 15 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(12): Show |
15 | HG02040.hp1 HG03704.hp1 NA18941.hp2 others(12): Show |
intron_variant | MODIFIER | c.1039-1383T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252302 | |||||||
| chr1:226252306 | A | G | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1039-1387T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252306 | |||||||
| chr1:226252310 | A | G | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1039-1391T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252310 | |||||||
| chr1:226252314 | A | AAATG | 9 | a0001c0001t0001g0296 a0001c0001t0001g0298 a0001c0001t0001g0299 others(6): Show |
9 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1039-1396_1039-139 others(8): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252314 | |||||||
| chr1:226252314 | A | G | 36 | a0001c0001t0001g0004 a0001c0001t0001g0126 a0001c0001t0001g0127 others(33): Show |
36 | HG02040.hp1 HG02145.hp2 HG02486.hp1 others(33): Show |
intron_variant | MODIFIER | c.1039-1395T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252314 | |||||||
| chr1:226252318 | A | AAATAAAT others(1): Show |
7 | a0001c0002t0002g0161 a0001c0002t0002g0162 a0001c0002t0002g0182 others(4): Show |
7 | HG00639.hp1 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.1039-1400_1039-139 others(12): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252318 | |||||||
| chr1:226252318 | A | AAATG | 48 | a0001c0001t0001g0160 a0001c0001t0003g0156 a0001c0001t0003g0191 others(45): Show |
48 | HG00099.hp2 HG00280.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.1039-1403_1039-140 others(8): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252318 | |||||||
| chr1:226252318 | A | AAATGAAT others(1): Show |
3 | a0001c0001t0001g0297 a0001c0002t0002g0285 a0001c0002t0002g0295 |
3 | HG02055.hp1 HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1039-1407_1039-140 others(12): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252318 | |||||||
| chr1:226252318 | A | G | 55 | a0001c0001t0001g0004 a0001c0001t0001g0087 a0001c0001t0001g0088 others(52): Show |
55 | HG01069.hp1 HG01071.hp1 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.1039-1399T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252318 | |||||||
| chr1:226252322 | G | A | 88 | a0001c0001t0001g0009 a0001c0001t0001g0223 a0001c0001t0001g0224 others(85): Show |
88 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.1039-1403C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252322 | |||||||
| chr1:226252335 | A | G | 1 | a0001c0001t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1039-1416T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252335 | |||||||
| chr1:226252695 | AGGTGTGG others(8): Show |
A | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1039-1791_1039-177 others(19): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252695 | |||||||
| chr1:226252861 | G | A | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1039-1942C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252861 | |||||||
| chr1:226252923 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1039-2004C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252923 | |||||||
| chr1:226252953 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1039-2034G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252953 | |||||||
| chr1:226252965 | T | C | 3 | a0001c0002t0002g0145 a0001c0002t0002g0158 a0001c0002t0002g0192 |
3 | HG00544.hp1 NA19076.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1039-2046A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252965 | |||||||
| chr1:226253067 | A | C | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1039-2148T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226253067 | |||||||
| chr1:226253127 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1039-2208C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226253127 | |||||||
| chr1:226253265 | C | CA | 198 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(195): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1039-2347dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226253265 | |||||||
| chr1:226253265 | C | CAA | 17 | a0001c0001t0001g0108 a0001c0001t0001g0302 a0001c0001t0001g0303 others(14): Show |
17 | HG02145.hp2 HG02486.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1039-2348_1039-234 others(6): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226253265 | |||||||
| chr1:226253265 | CA | C | 6 | a0001c0001t0001g0240 a0001c0001t0001g0271 a0001c0001t0001g0277 others(3): Show |
6 | HG00639.hp2 HG00738.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.1039-2347delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226253265 | |||||||
| chr1:226253347 | C | T | 1 | a0001c0001t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1039-2428G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226253347 | |||||||
| chr1:226253492 | C | T | 96 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0223 others(93): Show |
96 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.1039-2573G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226253492 | |||||||
| chr1:226253549 | C | T | 2 | a0001c0001t0001g0079 a0001c0001t0001g0084 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1039-2630G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226253549 | |||||||
| chr1:226253767 | T | G | 1 | a0001c0001t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1039-2848A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226253767 | |||||||
| chr1:226253828 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1039-2909A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226253828 | |||||||
| chr1:226254031 | A | C | 1 | a0001c0002t0002g0194 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1039-3112T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226254031 | |||||||
| chr1:226254057 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1039-3138C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226254057 | |||||||
| chr1:226254184 | C | T | 97 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0087 others(94): Show |
97 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.1039-3265G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226254184 | |||||||
| chr1:226254326 | C | A | 1 | a0001c0001t0001g0279 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1039-3407G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226254326 | |||||||
| chr1:226254542 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1039-3623G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226254542 | |||||||
| chr1:226254686 | C | T | 6 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(3): Show |
6 | HG02055.hp2 HG02809.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1039-3767G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226254686 | |||||||
| chr1:226254694 | G | A | 139 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(136): Show |
139 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.1039-3775C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226254694 | |||||||
| chr1:226254836 | G | A | 22 | a0001c0001t0001g0004 a0001c0001t0001g0296 a0001c0001t0001g0297 others(19): Show |
22 | HG02055.hp2 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.1039-3917C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226254836 | |||||||
| chr1:226254910 | C | CA | 26 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0035 others(23): Show |
26 | HG00597.hp1 HG00741.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.1039-3992dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226254910 | |||||||
| chr1:226254910 | CA | C | 14 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0031 others(11): Show |
14 | HG00639.hp2 HG01069.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.1039-3992delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226254910 | |||||||
| chr1:226255195 | T | C | 1 | a0001c0001t0001g0236 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1039-4276A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226255195 | |||||||
| chr1:226256058 | T | C | 19 | a0001c0001t0001g0004 a0001c0001t0001g0126 a0001c0001t0001g0127 others(16): Show |
19 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.1039-5139A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226256058 | |||||||
| chr1:226256153 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1039-5234G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226256153 | |||||||
| chr1:226256176 | A | G | 1 | a0001c0002t0002g0208 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1039-5257T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226256176 | |||||||
| chr1:226256524 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1039-5605G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226256524 | |||||||
| chr1:226256552 | A | AAT | 23 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(20): Show |
23 | HG02040.hp1 HG02074.hp2 HG03688.hp2 others(20): Show |
intron_variant | MODIFIER | c.1039-5635_1039-563 others(6): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226256552 | |||||||
| chr1:226256560 | T | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0266 others(1): Show |
4 | HG00735.hp2 HG01433.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-5641A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226256560 | |||||||
| chr1:226256569 | A | T | 19 | a0001c0001t0001g0028 a0001c0001t0001g0121 a0001c0001t0001g0122 others(16): Show |
19 | HG00099.hp1 HG00544.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1039-5650T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226256569 | |||||||
| chr1:226256571 | T | A | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1039-5652A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226256571 | |||||||
| chr1:226256651 | T | C | 1 | a0001c0001t0001g0273 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1039-5732A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226256651 | |||||||
| chr1:226256675 | C | T | 1 | a0001c0001t0001g0216 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1039-5756G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226256675 | |||||||
| chr1:226256949 | A | C | 1 | a0001c0001t0001g0210 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1039-6030T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226256949 | |||||||
| chr1:226257245 | T | C | 239 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(236): Show |
239 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.1039-6326A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257245 | |||||||
| chr1:226257659 | GA | G | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1039-6741delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257659 | |||||||
| chr1:226257827 | C | A | 116 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(113): Show |
116 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1039-6908G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257827 | |||||||
| chr1:226257879 | T | A | 1 | a0001c0001t0001g0274 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1039-6960A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257879 | |||||||
| chr1:226257915 | G | A | 1 | a0001c0001t0001g0274 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1039-6996C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257915 | |||||||
| chr1:226257918 | T | C | 1 | a0001c0001t0001g0274 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1039-6999A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257918 | |||||||
| chr1:226257919 | C | T | 1 | a0001c0001t0001g0274 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1039-7000G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257919 | |||||||
| chr1:226257920 | A | T | 1 | a0001c0001t0001g0274 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1039-7001T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257920 | |||||||
| chr1:226257930 | T | G | 1 | a0001c0001t0001g0274 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1039-7011A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257930 | |||||||
| chr1:226257934 | A | G | 1 | a0001c0001t0001g0274 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1039-7015T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257934 | |||||||
| chr1:226257937 | A | C | 1 | a0001c0001t0001g0274 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1039-7018T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257937 | |||||||
| chr1:226257939 | T | C | 1 | a0001c0001t0001g0274 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1039-7020A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257939 | |||||||
| chr1:226257946 | G | A | 1 | a0001c0001t0001g0274 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1039-7027C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257946 | |||||||
| chr1:226257950 | G | A | 59 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(56): Show |
59 | HG00423.hp1 HG00609.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.1039-7031C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257950 | |||||||
| chr1:226257957 | GTCCCATC others(6): Show |
G | 1 | a0001c0001t0001g0274 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1039-7051_1039-703 others(17): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257957 | |||||||
| chr1:226257971 | G | C | 1 | a0001c0001t0001g0274 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1039-7052C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257971 | |||||||
| chr1:226258007 | A | C | 1 | a0001c0001t0001g0347 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1039-7088T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258007 | |||||||
| chr1:226258008 | C | A | 1 | a0001c0001t0001g0347 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1039-7089G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258008 | |||||||
| chr1:226258050 | G | A | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0312 others(1): Show |
4 | HG02630.hp1 NA19240.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-7131C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258050 | |||||||
| chr1:226258102 | TA | T | 3 | a0001c0001t0003g0047 a0001c0001t0003g0051 a0001c0001t0003g0113 |
3 | NA18960.hp1 NA18977.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1039-7184delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258102 | |||||||
| chr1:226258123 | G | A | 13 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(10): Show |
13 | HG01074.hp2 HG01099.hp2 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.1039-7204C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258123 | |||||||
| chr1:226258175 | A | AAAAC | 26 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0298 others(23): Show |
27 | HG00544.hp1 HG00738.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.1039-7260_1039-725 others(8): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258175 | |||||||
| chr1:226258175 | A | AAAACAAA others(1): Show |
7 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(4): Show |
7 | HG02559.hp1 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1039-7264_1039-725 others(12): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258175 | |||||||
| chr1:226258175 | AAAAC | A | 24 | a0001c0001t0001g0057 a0001c0001t0001g0128 a0001c0001t0001g0129 others(21): Show |
24 | HG02040.hp1 HG02080.hp1 HG02622.hp1 others(21): Show |
intron_variant | MODIFIER | c.1039-7260_1039-725 others(8): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258175 | |||||||
| chr1:226258175 | AAAACAAA others(1): Show |
A | 123 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(120): Show |
123 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.1039-7264_1039-725 others(12): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258175 | |||||||
| chr1:226258175 | AAAACAAA others(5): Show |
A | 96 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0223 others(93): Show |
96 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.1039-7268_1039-725 others(16): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258175 | |||||||
| chr1:226258192 | AAACAAAC others(4): Show |
A | 1 | a0001c0001t0001g0347 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1039-7284_1039-727 others(15): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258192 | |||||||
| chr1:226258362 | G | A | 1 | a0001c0002t0002g0130 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1038+7171C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258362 | |||||||
| chr1:226258468 | C | CA | 29 | a0001c0001t0001g0030 a0001c0001t0001g0115 a0001c0001t0001g0125 others(26): Show |
29 | HG00621.hp1 HG01978.hp2 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.1038+7064dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258468 | |||||||
| chr1:226258662 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1038+6871C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258662 | |||||||
| chr1:226258666 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1038+6867C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258666 | |||||||
| chr1:226258894 | C | A | 1 | a0001c0002t0002g0282 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1038+6639G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258894 | |||||||
| chr1:226258894 | C | CA | 99 | a0001c0001t0001g0009 a0001c0001t0001g0160 a0001c0001t0001g0224 others(96): Show |
99 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1038+6638dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258894 | |||||||
| chr1:226258894 | C | CAA | 69 | a0001c0001t0001g0223 a0001c0001t0001g0225 a0001c0001t0001g0226 others(66): Show |
69 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1038+6637_1038+663 others(6): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258894 | |||||||
| chr1:226258894 | C | CAAA | 15 | a0001c0001t0001g0004 a0001c0001t0001g0227 a0001c0001t0001g0230 others(12): Show |
15 | HG00738.hp2 HG00741.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1038+6636_1038+663 others(7): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258894 | |||||||
| chr1:226258894 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1038+6627_1038+663 others(16): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258894 | |||||||
| chr1:226258894 | CAAAAAAA others(1): Show |
C | 33 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0022 others(30): Show |
33 | HG00438.hp1 HG00673.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.1038+6631_1038+663 others(12): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258894 | |||||||
| chr1:226258894 | CAAAAAAA others(2): Show |
C | 88 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(85): Show |
88 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.1038+6630_1038+663 others(13): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258894 | |||||||
| chr1:226258894 | CAAAAAAA others(7): Show |
C | 4 | a0001c0001t0001g0219 a0001c0001t0001g0221 a0001c0001t0001g0356 others(1): Show |
4 | HG01516.hp2 HG03688.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.1038+6625_1038+663 others(18): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258894 | |||||||
| chr1:226258894 | CAAAAAAA others(8): Show |
C | 16 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(13): Show |
16 | HG02040.hp1 HG03017.hp2 HG03704.hp1 others(13): Show |
intron_variant | MODIFIER | c.1038+6624_1038+663 others(19): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258894 | |||||||
| chr1:226258894 | CAAAAAAA others(9): Show |
C | 1 | a0001c0002t0002g0206 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1038+6623_1038+663 others(20): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258894 | |||||||
| chr1:226258972 | A | AT | 119 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(116): Show |
119 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.1038+6560dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258972 | |||||||
| chr1:226258992 | A | C | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1038+6541T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258992 | |||||||
| chr1:226258998 | TCTTGCTC others(6): Show |
T | 1 | a0001c0001t0001g0021 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+6522_1038+653 others(17): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258998 | |||||||
| chr1:226259083 | C | T | 5 | a0001c0002t0002g0163 a0001c0002t0002g0198 a0001c0002t0002g0200 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1038+6450G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226259083 | |||||||
| chr1:226259149 | G | A | 1 | a0001c0002t0002g0170 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1038+6384C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226259149 | |||||||
| chr1:226259179 | C | T | 5 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0001c0001t0001g0320 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1038+6354G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226259179 | |||||||
| chr1:226259207 | G | A | 2 | a0001c0001t0001g0252 a0001c0001t0001g0276 |
2 | NA18975.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1038+6326C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226259207 | |||||||
| chr1:226259255 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1038+6278G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226259255 | |||||||
| chr1:226259533 | G | A | 1 | a0001c0001t0001g0356 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1038+6000C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226259533 | |||||||
| chr1:226259649 | A | G | 1 | a0001c0002t0002g0207 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1038+5884T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226259649 | |||||||
| chr1:226259945 | A | AAATT | 240 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(237): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.1038+5587_1038+558 others(8): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226259945 | |||||||
| chr1:226260565 | A | C | 3 | a0001c0002t0002g0001 a0001c0002t0002g0135 a0001c0002t0002g0143 |
4 | HG02602.hp2 HG02698.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+4968T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260565 | |||||||
| chr1:226260618 | G | A | 1 | a0001c0002t0002g0162 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1038+4915C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260618 | |||||||
| chr1:226260628 | G | GT | 24 | a0001c0001t0001g0009 a0001c0001t0001g0216 a0001c0001t0001g0226 others(21): Show |
24 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.1038+4904dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260628 | |||||||
| chr1:226260628 | G | GTT | 7 | a0001c0001t0001g0209 a0001c0001t0001g0212 a0001c0001t0001g0213 others(4): Show |
7 | HG03017.hp2 HG03927.hp1 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.1038+4903_1038+490 others(6): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260628 | |||||||
| chr1:226260628 | G | GTTT | 12 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0214 others(9): Show |
12 | HG02040.hp1 HG03041.hp2 HG03688.hp2 others(9): Show |
intron_variant | MODIFIER | c.1038+4902_1038+490 others(7): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260628 | |||||||
| chr1:226260628 | G | GTTTTTTT others(3): Show |
1 | a0001c0001t0001g0302 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1038+4895_1038+490 others(14): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260628 | |||||||
| chr1:226260628 | G | GTTTTTTT others(12): Show |
3 | a0001c0001t0001g0303 a0001c0001t0001g0309 a0001c0001t0001g0310 |
3 | HG02559.hp1 HG02886.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1038+4886_1038+490 others(23): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260628 | |||||||
| chr1:226260628 | G | GTTTTTTT others(13): Show |
3 | a0001c0001t0001g0304 a0001c0001t0001g0306 a0001c0001t0001g0311 |
3 | HG02572.hp2 HG02647.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1038+4885_1038+490 others(24): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260628 | |||||||
| chr1:226260628 | G | GTTTTTTT others(22): Show |
1 | a0001c0001t0001g0305 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1038+4876_1038+490 others(33): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260628 | |||||||
| chr1:226260628 | GT | G | 84 | a0001c0001t0001g0223 a0001c0001t0001g0225 a0001c0001t0001g0227 others(81): Show |
84 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.1038+4904delA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260628 | |||||||
| chr1:226260628 | GTT | G | 26 | a0001c0001t0001g0251 a0001c0001t0001g0256 a0001c0001t0001g0257 others(23): Show |
27 | HG00544.hp1 HG01167.hp2 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.1038+4903_1038+490 others(6): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260628 | |||||||
| chr1:226260628 | GTTTT | G | 6 | a0001c0001t0001g0013 a0001c0001t0001g0126 a0001c0001t0001g0127 others(3): Show |
6 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1038+4901_1038+490 others(8): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260628 | |||||||
| chr1:226260628 | GTTTTT | G | 25 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0030 others(22): Show |
25 | HG00423.hp1 HG00438.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.1038+4900_1038+490 others(9): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260628 | |||||||
| chr1:226260628 | GTTTTTT | G | 92 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0014 others(89): Show |
92 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1038+4899_1038+490 others(10): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260628 | |||||||
| chr1:226260628 | GTTTTTTT | G | 7 | a0001c0001t0001g0021 a0001c0001t0001g0088 a0001c0001t0001g0296 others(4): Show |
7 | HG01081.hp2 HG02809.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1038+4898_1038+490 others(11): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260628 | |||||||
| chr1:226260630 | T | G | 3 | a0001c0002t0004g0149 a0001c0002t0004g0150 a0001c0002t0004g0281 |
3 | HG01069.hp1 HG01071.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1038+4903A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260630 | |||||||
| chr1:226260636 | T | G | 4 | a0001c0001t0001g0013 a0001c0001t0001g0126 a0001c0001t0001g0127 others(1): Show |
4 | HG01192.hp1 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1038+4897A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260636 | |||||||
| chr1:226260637 | T | G | 25 | a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0057 others(22): Show |
25 | HG00423.hp1 HG00438.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.1038+4896A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260637 | |||||||
| chr1:226260638 | T | G | 90 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0014 others(87): Show |
90 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.1038+4895A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260638 | |||||||
| chr1:226260639 | T | G | 4 | a0001c0001t0001g0021 a0001c0001t0001g0088 a0001c0001t0003g0083 others(1): Show |
4 | HG01081.hp2 NA18945.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+4894A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260639 | |||||||
| chr1:226260645 | T | G | 1 | a0001c0001t0003g0060 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1038+4888A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260645 | |||||||
| chr1:226260692 | C | T | 121 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(118): Show |
121 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.1038+4841G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260692 | |||||||
| chr1:226260706 | A | G | 262 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(259): Show |
262 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.1038+4827T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260706 | |||||||
| chr1:226260730 | C | T | 1 | a0001c0001t0003g0060 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1038+4803G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260730 | |||||||
| chr1:226260745 | C | T | 4 | a0001c0001t0001g0225 a0001c0001t0001g0229 a0001c0001t0001g0268 others(1): Show |
4 | HG00738.hp2 HG01993.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+4788G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260745 | |||||||
| chr1:226260836 | G | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0296 a0001c0001t0001g0297 others(14): Show |
17 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1038+4697C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260836 | |||||||
| chr1:226261111 | T | C | 19 | a0001c0001t0001g0004 a0001c0001t0001g0126 a0001c0001t0001g0127 others(16): Show |
19 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.1038+4422A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226261111 | |||||||
| chr1:226261133 | C | G | 1 | a0001c0002t0002g0157 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1038+4400G>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226261133 | |||||||
| chr1:226261138 | TA | T | 22 | a0001c0001t0001g0013 a0001c0001t0001g0042 a0001c0001t0001g0043 others(19): Show |
22 | HG01256.hp2 HG01258.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.1038+4394delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226261138 | |||||||
| chr1:226261520 | A | G | 2 | a0001c0001t0003g0072 a0001c0001t0003g0073 |
2 | HG01993.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1038+4013T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226261520 | |||||||
| chr1:226261533 | T | G | 1 | a0001c0001t0001g0021 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+4000A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226261533 | |||||||
| chr1:226261655 | T | A | 1 | a0001c0001t0001g0021 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+3878A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226261655 | |||||||
| chr1:226261741 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1038+3792C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226261741 | |||||||
| chr1:226261927 | T | C | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1038+3606A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226261927 | |||||||
| chr1:226262130 | G | T | 1 | a0001c0001t0001g0021 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+3403C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226262130 | |||||||
| chr1:226262163 | T | C | 75 | a0001c0001t0001g0087 a0001c0001t0001g0224 a0001c0001t0001g0225 others(72): Show |
75 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1038+3370A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226262163 | |||||||
| chr1:226262235 | T | C | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG00735.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1038+3298A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226262235 | |||||||
| chr1:226262246 | G | A | 8 | a0001c0002t0002g0164 a0001c0002t0002g0165 a0001c0002t0002g0166 others(5): Show |
8 | NA18939.hp1 NA18941.hp1 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1038+3287C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226262246 | |||||||
| chr1:226262289 | T | A | 1 | a0001c0001t0001g0021 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+3244A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226262289 | |||||||
| chr1:226262293 | A | T | 1 | a0001c0001t0001g0021 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+3240T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226262293 | |||||||
| chr1:226262295 | T | G | 1 | a0001c0001t0001g0021 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+3238A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226262295 | |||||||
| chr1:226262532 | G | T | 1 | a0001c0001t0001g0021 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+3001C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226262532 | |||||||
| chr1:226263093 | T | G | 1 | a0001c0001t0001g0021 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+2440A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226263093 | |||||||
| chr1:226263340 | G | A | 6 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(3): Show |
6 | HG02055.hp2 HG02809.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1038+2193C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226263340 | |||||||
| chr1:226263374 | G | T | 1 | a0001c0001t0001g0231 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1038+2159C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226263374 | |||||||
| chr1:226263676 | A | G | 3 | a0001c0001t0001g0230 a0001c0001t0001g0239 a0001c0001t0001g0280 |
3 | HG01109.hp2 HG01243.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1038+1857T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226263676 | |||||||
| chr1:226263747 | A | G | 5 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0001c0001t0001g0320 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1038+1786T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226263747 | |||||||
| chr1:226263801 | G | A | 1 | a0001c0002t0002g0169 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1038+1732C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226263801 | |||||||
| chr1:226263914 | C | T | 17 | a0001c0001t0001g0004 a0001c0001t0001g0296 a0001c0001t0001g0297 others(14): Show |
17 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1038+1619G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226263914 | |||||||
| chr1:226263999 | A | C | 4 | a0001c0001t0001g0356 a0001c0001t0001g0357 a0001c0001t0001g0358 others(1): Show |
4 | HG03017.hp2 HG03688.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.1038+1534T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226263999 | |||||||
| chr1:226263999 | A | T | 15 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(12): Show |
15 | HG02040.hp1 HG03704.hp1 NA18941.hp2 others(12): Show |
intron_variant | MODIFIER | c.1038+1534T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226263999 | |||||||
| chr1:226264078 | A | C | 1 | a0001c0001t0001g0021 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+1455T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226264078 | |||||||
| chr1:226264097 | A | C | 1 | a0001c0001t0001g0021 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+1436T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226264097 | |||||||
| chr1:226264148 | C | T | 8 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(5): Show |
8 | HG02559.hp1 HG02572.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1038+1385G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226264148 | |||||||
| chr1:226264206 | C | G | 1 | a0001c0001t0001g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1038+1327G>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226264206 | |||||||
| chr1:226264389 | T | C | 1 | a0001c0002t0002g0178 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1038+1144A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226264389 | |||||||
| chr1:226264502 | A | C | 1 | a0001c0001t0001g0021 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+1031T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226264502 | |||||||
| chr1:226264574 | A | C | 1 | a0001c0001t0001g0021 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+959T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226264574 | |||||||
| chr1:226264587 | T | A | 1 | a0001c0001t0001g0021 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+946A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226264587 | |||||||
| chr1:226264675 | A | C | 1 | a0001c0001t0001g0021 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+858T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226264675 | |||||||
| chr1:226264860 | A | C | 1 | a0001c0001t0001g0021 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+673T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226264860 | |||||||
| chr1:226264946 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1038+587T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226264946 | |||||||
| chr1:226265201 | A | G | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1038+332T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226265201 | |||||||
| chr1:226265348 | G | T | 2 | a0001c0002t0002g0165 a0001c0002t0002g0173 |
2 | NA18965.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1038+185C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226265348 | |||||||
| chr1:226265880 | T | C | 223 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(220): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.937-246A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 9/14 | chr1 | 226265880 | |||||||
| chr1:226265899 | G | C | 1 | a0001c0002t0004g0281 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.937-265C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 9/14 | chr1 | 226265899 | |||||||
| chr1:226265917 | T | C | 240 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(237): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.937-283A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 9/14 | chr1 | 226265917 | |||||||
| chr1:226265969 | G | A | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.936+244C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 9/14 | chr1 | 226265969 | |||||||
| chr1:226266110 | T | C | 2 | a0001c0001t0001g0209 a0001c0001t0001g0213 |
2 | NA18984.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.936+103A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 9/14 | chr1 | 226266110 | |||||||
| chr1:226266155 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.936+58T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 9/14 | chr1 | 226266155 | |||||||
| chr1:226266161 | T | C | 1 | a0001c0001t0003g0105 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.936+52A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 9/14 | chr1 | 226266161 | |||||||
| chr1:226266530 | T | C | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.817-198A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226266530 | |||||||
| chr1:226266685 | T | C | 1 | a0001c0001t0001g0357 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.817-353A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226266685 | |||||||
| chr1:226266777 | AT | A | 96 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0223 others(93): Show |
96 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.817-446delA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226266777 | |||||||
| chr1:226266843 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.817-511C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226266843 | |||||||
| chr1:226267023 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.817-691C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267023 | |||||||
| chr1:226267055 | T | C | 1 | a0001c0002t0002g0132 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.817-723A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267055 | |||||||
| chr1:226267164 | G | C | 4 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0062 others(1): Show |
4 | NA18962.hp1 NA19064.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+793C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267164 | |||||||
| chr1:226267230 | G | GAT | 107 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(104): Show |
107 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.816+725_816+726dup others(2): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267230 | |||||||
| chr1:226267230 | G | GATAT | 23 | a0001c0001t0001g0020 a0001c0001t0001g0087 a0001c0001t0001g0088 others(20): Show |
23 | HG00741.hp1 HG01071.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.816+723_816+726dup others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267230 | |||||||
| chr1:226267230 | G | GATATAT | 6 | a0001c0001t0001g0034 a0001c0001t0001g0125 a0001c0001t0001g0356 others(3): Show |
6 | HG02148.hp2 HG02300.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.816+721_816+726dup others(6): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267230 | |||||||
| chr1:226267230 | GAT | G | 23 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(20): Show |
23 | HG01109.hp1 HG01167.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.816+725_816+726del others(2): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267230 | |||||||
| chr1:226267230 | GATAT | G | 99 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0128 others(96): Show |
99 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.816+723_816+726del others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267230 | |||||||
| chr1:226267310 | T | TTATGTAT others(5): Show |
5 | a0001c0001t0001g0017 a0001c0001t0001g0098 a0001c0001t0001g0115 others(2): Show |
5 | HG01071.hp2 HG01099.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.816+646_816+647ins others(12): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267310 | |||||||
| chr1:226267310 | T | TTATGTAT others(9): Show |
50 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(47): Show |
50 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.816+646_816+647ins others(16): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267310 | |||||||
| chr1:226267310 | T | TTATGTAT others(13): Show |
5 | a0001c0001t0001g0020 a0001c0001t0001g0065 a0001c0001t0001g0087 others(2): Show |
5 | HG01255.hp2 HG01978.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+646_816+647ins others(20): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267310 | |||||||
| chr1:226267318 | A | ATATGTAT others(9): Show |
98 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0075 others(95): Show |
98 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.816+623_816+638dup others(16): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267318 | |||||||
| chr1:226267318 | A | ATATGTAT others(13): Show |
95 | a0001c0001t0001g0004 a0001c0001t0001g0068 a0001c0001t0001g0069 others(92): Show |
95 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.816+619_816+638dup others(20): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267318 | |||||||
| chr1:226267318 | A | ATATGTAT others(17): Show |
8 | a0001c0001t0001g0126 a0001c0001t0001g0237 a0001c0001t0001g0241 others(5): Show |
8 | HG00609.hp1 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.816+615_816+638dup others(24): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267318 | |||||||
| chr1:226267318 | A | G | 60 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(57): Show |
60 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.816+639T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267318 | |||||||
| chr1:226267422 | C | CA | 116 | a0001c0001t0001g0008 a0001c0001t0001g0030 a0001c0001t0001g0070 others(113): Show |
116 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.816+534dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267422 | |||||||
| chr1:226267422 | C | CAA | 114 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.816+533_816+534dup others(2): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267422 | |||||||
| chr1:226267500 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.816+457G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267500 | |||||||
| chr1:226267736 | G | A | 1 | a0001c0002t0002g0130 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.816+221C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267736 | |||||||
| chr1:226268233 | C | T | 7 | a0001c0002t0002g0161 a0001c0002t0002g0169 a0001c0002t0002g0181 others(4): Show |
7 | HG00639.hp1 HG01192.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.683-143G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226268233 | |||||||
| chr1:226268823 | A | G | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.683-733T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226268823 | |||||||
| chr1:226268865 | C | T | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0312 others(1): Show |
4 | HG02630.hp1 NA19240.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-775G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226268865 | |||||||
| chr1:226269184 | A | T | 1 | a0001c0001t0001g0302 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.683-1094T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226269184 | |||||||
| chr1:226269301 | G | A | 3 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0301 |
3 | HG02055.hp2 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.683-1211C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226269301 | |||||||
| chr1:226269445 | G | C | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0312 others(1): Show |
4 | HG02630.hp1 NA19240.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-1355C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226269445 | |||||||
| chr1:226269473 | CAA | C | 51 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(48): Show |
51 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.683-1385_683-1384d others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226269473 | |||||||
| chr1:226269873 | G | T | 1 | a0001c0002t0002g0192 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.683-1783C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226269873 | |||||||
| chr1:226269993 | G | A | 3 | a0001c0001t0003g0076 a0001c0001t0003g0083 a0001c0001t0003g0118 |
3 | HG02074.hp2 NA18954.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.683-1903C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226269993 | |||||||
| chr1:226270253 | G | T | 1 | a0001c0001t0001g0306 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.683-2163C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226270253 | |||||||
| chr1:226270334 | T | A | 47 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(44): Show |
47 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.683-2244A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226270334 | |||||||
| chr1:226270488 | A | C | 2 | a0001c0002t0002g0161 a0001c0002t0002g0190 |
2 | HG00639.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.683-2398T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226270488 | |||||||
| chr1:226270601 | C | T | 1 | a0001c0002t0002g0148 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.683-2511G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226270601 | |||||||
| chr1:226270702 | G | A | 8 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0017 others(5): Show |
8 | NA18943.hp2 NA18950.hp2 NA18972.hp1 others(5): Show |
intron_variant | MODIFIER | c.683-2612C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226270702 | |||||||
| chr1:226270810 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.683-2720C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226270810 | |||||||
| chr1:226270824 | C | CA | 57 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0023 others(54): Show |
57 | HG00438.hp1 HG00673.hp1 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.683-2735dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226270824 | |||||||
| chr1:226270824 | CA | C | 12 | a0001c0001t0001g0111 a0001c0001t0001g0334 a0001c0001t0001g0356 others(9): Show |
12 | HG01069.hp1 HG01192.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.683-2735delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226270824 | |||||||
| chr1:226270824 | CAAAA | C | 11 | a0001c0002t0002g0283 a0001c0002t0002g0284 a0001c0002t0002g0285 others(8): Show |
11 | HG01109.hp1 HG01167.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.683-2738_683-2735d others(6): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226270824 | |||||||
| chr1:226270834 | A | T | 1 | a0001c0001t0001g0217 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.683-2744T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226270834 | |||||||
| chr1:226270984 | C | G | 22 | a0001c0001t0001g0004 a0001c0001t0001g0296 a0001c0001t0001g0297 others(19): Show |
22 | HG02055.hp2 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.683-2894G>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226270984 | |||||||
| chr1:226271146 | T | C | 1 | a0001c0001t0001g0223 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.683-3056A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226271146 | |||||||
| chr1:226271162 | T | C | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.683-3072A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226271162 | |||||||
| chr1:226271335 | C | T | 8 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(5): Show |
8 | HG02559.hp1 HG02572.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.683-3245G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226271335 | |||||||
| chr1:226271792 | A | T | 1 | a0001c0001t0001g0296 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.683-3702T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226271792 | |||||||
| chr1:226271876 | G | A | 261 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(258): Show |
261 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.683-3786C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226271876 | |||||||
| chr1:226272021 | C | CT | 216 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.683-3932dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226272021 | |||||||
| chr1:226272051 | CT | C | 27 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0296 others(24): Show |
27 | HG02055.hp2 HG02145.hp2 HG02273.hp1 others(24): Show |
intron_variant | MODIFIER | c.683-3962delA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226272051 | |||||||
| chr1:226272381 | C | CT | 8 | a0001c0001t0001g0223 a0001c0001t0001g0322 a0001c0001t0003g0047 others(5): Show |
8 | HG01167.hp2 HG02886.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.683-4292dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226272381 | |||||||
| chr1:226272399 | A | T | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0312 others(1): Show |
4 | HG02630.hp1 NA19240.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-4309T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226272399 | |||||||
| chr1:226272465 | G | C | 22 | a0001c0001t0001g0004 a0001c0001t0001g0296 a0001c0001t0001g0297 others(19): Show |
22 | HG02055.hp2 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.683-4375C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226272465 | |||||||
| chr1:226272487 | G | C | 256 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(253): Show |
256 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.683-4397C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226272487 | |||||||
| chr1:226272539 | C | CT | 6 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0002t0002g0005 others(3): Show |
6 | NA18945.hp1 NA18946.hp1 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.683-4450dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226272539 | |||||||
| chr1:226272539 | CT | C | 30 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(27): Show |
30 | HG01069.hp1 HG01071.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.683-4450delA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226272539 | |||||||
| chr1:226272539 | CTT | C | 8 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0319 others(5): Show |
8 | HG02486.hp1 HG02818.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.683-4451_683-4450d others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226272539 | |||||||
| chr1:226272539 | CTTT | C | 95 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0223 others(92): Show |
95 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.683-4452_683-4450d others(5): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226272539 | |||||||
| chr1:226272558 | T | A | 2 | a0001c0001t0001g0358 a0001c0001t0001g0359 |
2 | HG03704.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.683-4468A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226272558 | |||||||
| chr1:226272559 | T | A | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.683-4469A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226272559 | |||||||
| chr1:226272760 | C | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0067 a0001c0001t0001g0100 |
3 | HG02895.hp1 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.683-4670G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226272760 | |||||||
| chr1:226272771 | C | T | 4 | a0001c0001t0003g0076 a0001c0001t0003g0083 a0001c0001t0003g0101 others(1): Show |
4 | HG02074.hp2 NA18954.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-4681G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226272771 | |||||||
| chr1:226272924 | ACTGT | A | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.683-4838_683-4835d others(6): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226272924 | |||||||
| chr1:226273256 | A | AT | 145 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(142): Show |
145 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.682+4518dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226273256 | |||||||
| chr1:226273256 | A | ATT | 12 | a0001c0001t0001g0042 a0001c0001t0001g0063 a0001c0001t0001g0122 others(9): Show |
12 | HG00423.hp1 HG01168.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.682+4517_682+4518d others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226273256 | |||||||
| chr1:226273256 | AT | A | 18 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(15): Show |
18 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(15): Show |
intron_variant | MODIFIER | c.682+4518delA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226273256 | |||||||
| chr1:226273281 | G | A | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.682+4494C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226273281 | |||||||
| chr1:226273509 | T | C | 4 | a0001c0002t0002g0136 a0001c0002t0002g0137 a0001c0002t0002g0138 others(1): Show |
4 | HG00738.hp1 HG01123.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.682+4266A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226273509 | |||||||
| chr1:226273681 | A | C | 1 | a0001c0001t0003g0102 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.682+4094T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226273681 | |||||||
| chr1:226273798 | A | G | 2 | a0001c0001t0001g0240 a0001c0001t0001g0264 |
2 | HG00639.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.682+3977T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226273798 | |||||||
| chr1:226273834 | C | CT | 155 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(152): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.682+3940dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226273834 | |||||||
| chr1:226273899 | G | A | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.682+3876C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226273899 | |||||||
| chr1:226274060 | T | G | 1 | a0001c0002t0002g0154 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.682+3715A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226274060 | |||||||
| chr1:226274111 | G | A | 1 | a0001c0001t0003g0078 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.682+3664C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226274111 | |||||||
| chr1:226274671 | TC | T | 96 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0223 others(93): Show |
96 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.682+3103delG | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226274671 | |||||||
| chr1:226274735 | G | A | 8 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(5): Show |
8 | HG02559.hp1 HG02572.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.682+3040C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226274735 | |||||||
| chr1:226275110 | T | C | 2 | a0001c0002t0002g0146 a0001c0002t0002g0188 |
2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.682+2665A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275110 | |||||||
| chr1:226275252 | G | T | 92 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(89): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.682+2523C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275252 | |||||||
| chr1:226275254 | T | C | 8 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(5): Show |
8 | HG02559.hp1 HG02572.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.682+2521A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275254 | |||||||
| chr1:226275390 | T | TTTA | 5 | a0001c0002t0002g0144 a0001c0002t0002g0145 a0001c0002t0002g0158 others(2): Show |
5 | HG00544.hp1 HG02683.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.682+2384_682+2385i others(5): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275390 | |||||||
| chr1:226275467 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG02109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.682+2308C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275467 | |||||||
| chr1:226275487 | A | G | 1 | a0001c0002t0002g0171 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.682+2288T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275487 | |||||||
| chr1:226275491 | C | T | 1 | a0001c0001t0001g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.682+2284G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275491 | |||||||
| chr1:226275515 | G | T | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0312 others(1): Show |
4 | HG02630.hp1 NA19240.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.682+2260C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275515 | |||||||
| chr1:226275548 | T | A | 1 | a0001c0002t0002g0293 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.682+2227A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275548 | |||||||
| chr1:226275687 | G | A | 1 | a0001c0001t0001g0325 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.682+2088C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275687 | |||||||
| chr1:226275691 | C | CA | 23 | a0001c0001t0001g0014 a0001c0001t0001g0107 a0001c0001t0001g0114 others(20): Show |
23 | HG01109.hp2 HG01516.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.682+2083dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275691 | |||||||
| chr1:226275692 | AG | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0215 a0001c0001t0001g0233 others(2): Show |
5 | HG00609.hp1 HG01081.hp1 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.682+2082delC | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275692 | |||||||
| chr1:226275693 | G | A | 255 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(252): Show |
255 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.682+2082C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275693 | |||||||
| chr1:226275693 | GA | G | 17 | a0001c0002t0001g0361 a0001c0002t0002g0001 a0001c0002t0002g0136 others(14): Show |
18 | HG00544.hp1 HG00738.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.682+2081delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275693 | |||||||
| chr1:226275721 | G | GA | 22 | a0001c0001t0001g0325 a0001c0002t0001g0361 a0001c0002t0002g0001 others(19): Show |
23 | HG00544.hp1 HG00738.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.682+2053dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275721 | |||||||
| chr1:226275740 | G | A | 96 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0223 others(93): Show |
96 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.682+2035C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275740 | |||||||
| chr1:226275755 | C | T | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0312 others(1): Show |
4 | HG02630.hp1 NA19240.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.682+2020G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275755 | |||||||
| chr1:226276604 | T | C | 1 | a0001c0002t0002g0285 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.682+1171A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226276604 | |||||||
| chr1:226276666 | G | A | 1 | a0001c0002t0002g0183 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.682+1109C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226276666 | |||||||
| chr1:226276728 | T | C | 1 | a0001c0002t0002g0130 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.682+1047A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226276728 | |||||||
| chr1:226276806 | A | G | 1 | a0001c0001t0001g0242 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.682+969T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226276806 | |||||||
| chr1:226276838 | C | A | 38 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(35): Show |
38 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.682+937G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226276838 | |||||||
| chr1:226277004 | A | G | 1 | a0001c0002t0002g0161 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.682+771T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226277004 | |||||||
| chr1:226277110 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.682+665C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226277110 | |||||||
| chr1:226277216 | G | GA | 17 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0066 others(14): Show |
17 | HG01978.hp1 HG02257.hp1 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.682+558dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226277216 | |||||||
| chr1:226277230 | A | C | 97 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0223 others(94): Show |
97 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.682+545T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226277230 | |||||||
| chr1:226277360 | T | C | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.682+415A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226277360 | |||||||
| chr1:226277584 | C | CT | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.682+190dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226277584 | |||||||
| chr1:226278018 | A | G | 1 | a0001c0001t0003g0051 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.525-86T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226278018 | |||||||
| chr1:226278069 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.525-137A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226278069 | |||||||
| chr1:226278113 | T | G | 1 | a0001c0001t0001g0277 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.525-181A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226278113 | |||||||
| chr1:226278199 | C | A | 1 | a0001c0001t0003g0077 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.525-267G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226278199 | |||||||
| chr1:226278649 | T | C | 263 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(260): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.525-717A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226278649 | |||||||
| chr1:226278658 | T | C | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.525-726A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226278658 | |||||||
| chr1:226278666 | A | G | 1 | a0001c0001t0001g0300 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.525-734T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226278666 | |||||||
| chr1:226278728 | G | A | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.525-796C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226278728 | |||||||
| chr1:226278823 | C | CA | 141 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(138): Show |
141 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.525-892dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226278823 | |||||||
| chr1:226278893 | G | A | 1 | a0001c0001t0001g0310 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.525-961C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226278893 | |||||||
| chr1:226278957 | T | TA | 123 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0021 others(120): Show |
123 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.525-1026dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226278957 | |||||||
| chr1:226278957 | T | TAA | 13 | a0001c0001t0001g0040 a0001c0001t0001g0209 a0001c0001t0001g0210 others(10): Show |
13 | HG01433.hp1 HG01928.hp1 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.525-1027_525-1026d others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226278957 | |||||||
| chr1:226279002 | C | A | 5 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0062 others(2): Show |
5 | HG01106.hp2 NA18962.hp1 NA19064.hp2 others(2): Show |
intron_variant | MODIFIER | c.525-1070G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226279002 | |||||||
| chr1:226279039 | T | C | 2 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
2 | HG03491.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.525-1107A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226279039 | |||||||
| chr1:226279301 | T | C | 24 | a0001c0001t0001g0004 a0001c0001t0001g0126 a0001c0001t0001g0127 others(21): Show |
24 | HG02055.hp2 HG02145.hp2 HG02486.hp1 others(21): Show |
intron_variant | MODIFIER | c.525-1369A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226279301 | |||||||
| chr1:226279440 | C | T | 1 | a0001c0001t0003g0061 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.525-1508G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226279440 | |||||||
| chr1:226279608 | C | CA | 132 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0057 others(129): Show |
133 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.525-1677dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226279608 | |||||||
| chr1:226279608 | C | CAA | 27 | a0001c0001t0001g0008 a0001c0001t0001g0126 a0001c0001t0001g0127 others(24): Show |
27 | HG00544.hp2 HG00741.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.525-1678_525-1677d others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226279608 | |||||||
| chr1:226279608 | C | CAAA | 6 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0305 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.525-1679_525-1677d others(5): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226279608 | |||||||
| chr1:226279609 | A | C | 4 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0062 others(1): Show |
4 | NA18962.hp1 NA19064.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.525-1677T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226279609 | |||||||
| chr1:226279769 | G | GA | 119 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(116): Show |
119 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.525-1838dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226279769 | |||||||
| chr1:226279769 | GA | G | 6 | a0001c0001t0001g0229 a0001c0001t0001g0337 a0001c0001t0001g0338 others(3): Show |
6 | HG02258.hp1 HG03834.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.525-1838delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226279769 | |||||||
| chr1:226279821 | A | C | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.525-1889T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226279821 | |||||||
| chr1:226279967 | C | T | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.525-2035G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226279967 | |||||||
| chr1:226280254 | T | C | 1 | a0001c0002t0002g0143 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.525-2322A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226280254 | |||||||
| chr1:226280347 | G | A | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.525-2415C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226280347 | |||||||
| chr1:226280495 | C | A | 75 | a0001c0001t0001g0160 a0001c0001t0001g0224 a0001c0001t0001g0225 others(72): Show |
75 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.525-2563G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226280495 | |||||||
| chr1:226280495 | C | T | 1 | a0001c0001t0003g0086 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.525-2563G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226280495 | |||||||
| chr1:226280944 | A | G | 4 | a0001c0001t0003g0047 a0001c0001t0003g0051 a0001c0001t0003g0082 others(1): Show |
4 | NA18960.hp1 NA18977.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.525-3012T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226280944 | |||||||
| chr1:226281049 | A | T | 1 | a0001c0002t0002g0195 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.525-3117T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226281049 | |||||||
| chr1:226281131 | T | C | 14 | a0001c0002t0002g0282 a0001c0002t0002g0283 a0001c0002t0002g0284 others(11): Show |
14 | HG01109.hp1 HG01167.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.525-3199A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226281131 | |||||||
| chr1:226281414 | TTAA | T | 98 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0160 others(95): Show |
98 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.525-3485_525-3483d others(5): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226281414 | |||||||
| chr1:226281498 | T | C | 1 | a0001c0002t0002g0169 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.525-3566A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226281498 | |||||||
| chr1:226281632 | T | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0097 |
2 | NA19055.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.525-3700A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226281632 | |||||||
| chr1:226281673 | T | G | 4 | a0001c0001t0001g0356 a0001c0001t0001g0357 a0001c0001t0001g0358 others(1): Show |
4 | HG03017.hp2 HG03688.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.525-3741A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226281673 | |||||||
| chr1:226282526 | A | G | 20 | a0001c0002t0002g0001 a0001c0002t0002g0135 a0001c0002t0002g0136 others(17): Show |
21 | HG00544.hp1 HG00738.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.524+3807T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226282526 | |||||||
| chr1:226282538 | C | T | 3 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 |
3 | HG02486.hp1 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.524+3795G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226282538 | |||||||
| chr1:226282586 | C | T | 4 | a0001c0001t0001g0228 a0001c0001t0001g0231 a0001c0001t0001g0232 others(1): Show |
4 | HG01081.hp1 HG01346.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.524+3747G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226282586 | |||||||
| chr1:226282673 | T | C | 224 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(221): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.524+3660A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226282673 | |||||||
| chr1:226282863 | A | T | 358 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(355): Show |
359 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.524+3470T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226282863 | |||||||
| chr1:226283278 | A | AT | 72 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0126 others(69): Show |
72 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.524+3054dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226283278 | |||||||
| chr1:226283278 | A | ATT | 97 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(94): Show |
97 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.524+3053_524+3054d others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226283278 | |||||||
| chr1:226283278 | A | ATTT | 45 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(42): Show |
45 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.524+3052_524+3054d others(5): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226283278 | |||||||
| chr1:226283547 | A | G | 2 | a0001c0002t0002g0151 a0001c0002t0002g0153 |
2 | NA19070.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.524+2786T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226283547 | |||||||
| chr1:226283593 | G | A | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.524+2740C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226283593 | |||||||
| chr1:226283891 | G | A | 1 | a0001c0002t0002g0185 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.524+2442C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226283891 | |||||||
| chr1:226283925 | G | C | 52 | a0001c0002t0001g0134 a0001c0002t0002g0005 a0001c0002t0002g0006 others(49): Show |
52 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.524+2408C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226283925 | |||||||
| chr1:226283951 | A | AAG | 6 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(3): Show |
6 | HG02055.hp2 HG02809.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.524+2380_524+2381d others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226283951 | |||||||
| chr1:226284126 | C | T | 1 | a0001c0002t0002g0151 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.524+2207G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226284126 | |||||||
| chr1:226284136 | G | A | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.524+2197C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226284136 | |||||||
| chr1:226284463 | C | T | 4 | a0001c0002t0002g0136 a0001c0002t0002g0137 a0001c0002t0002g0138 others(1): Show |
4 | HG00738.hp1 HG01123.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.524+1870G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226284463 | |||||||
| chr1:226284598 | C | A | 2 | a0001c0001t0001g0244 a0001c0001t0001g0278 |
2 | HG00438.hp2 HG00597.hp1 |
intron_variant | MODIFIER | c.524+1735G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226284598 | |||||||
| chr1:226284698 | T | C | 2 | a0001c0001t0001g0302 a0001c0001t0001g0316 |
2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.524+1635A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226284698 | |||||||
| chr1:226284831 | T | C | 262 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(259): Show |
262 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.524+1502A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226284831 | |||||||
| chr1:226284890 | C | T | 262 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(259): Show |
262 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.524+1443G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226284890 | |||||||
| chr1:226284926 | AGTTTCAC others(10): Show |
A | 1 | a0001c0001t0003g0191 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.524+1390_524+1406d others(19): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226284926 | |||||||
| chr1:226284937 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.524+1396A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226284937 | |||||||
| chr1:226284945 | T | A | 1 | a0001c0001t0003g0191 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.524+1388A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226284945 | |||||||
| chr1:226284948 | A | C | 1 | a0001c0001t0003g0191 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.524+1385T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226284948 | |||||||
| chr1:226284949 | A | C | 1 | a0001c0001t0003g0191 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.524+1384T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226284949 | |||||||
| chr1:226285024 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.524+1309G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226285024 | |||||||
| chr1:226285150 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.524+1183G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226285150 | |||||||
| chr1:226285173 | T | C | 2 | a0001c0001t0001g0302 a0001c0001t0001g0316 |
2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.524+1160A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226285173 | |||||||
| chr1:226285425 | A | G | 1 | a0001c0001t0001g0320 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.524+908T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226285425 | |||||||
| chr1:226285595 | A | G | 124 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(121): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.524+738T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226285595 | |||||||
| chr1:226285949 | T | G | 3 | a0001c0002t0004g0149 a0001c0002t0004g0150 a0001c0002t0004g0281 |
3 | HG01069.hp1 HG01071.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.524+384A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226285949 | |||||||
| chr1:226285986 | T | G | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.524+347A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226285986 | |||||||
| chr1:226286646 | G | A | 1 | a0001c0001t0003g0085 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.399-188C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 5/14 | chr1 | 226286646 | |||||||
| chr1:226286727 | C | T | 1 | a0001c0001t0001g0350 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.399-269G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 5/14 | chr1 | 226286727 | |||||||
| chr1:226286778 | A | G | 222 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(219): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.399-320T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 5/14 | chr1 | 226286778 | |||||||
| chr1:226287008 | T | C | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG00735.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.399-550A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 5/14 | chr1 | 226287008 | |||||||
| chr1:226287405 | T | C | 2 | a0001c0002t0002g0146 a0001c0002t0002g0188 |
2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.398+259A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 5/14 | chr1 | 226287405 | |||||||
| chr1:226287879 | G | T | 28 | a0001c0001t0001g0004 a0001c0001t0001g0126 a0001c0001t0001g0127 others(25): Show |
28 | HG02055.hp2 HG02145.hp2 HG02486.hp1 others(25): Show |
intron_variant | MODIFIER | c.265-82C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226287879 | |||||||
| chr1:226287981 | C | CT | 27 | a0001c0001t0001g0004 a0001c0001t0001g0079 a0001c0001t0001g0126 others(24): Show |
27 | HG01109.hp1 HG01256.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.265-185dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226287981 | |||||||
| chr1:226288062 | C | T | 1 | a0001c0001t0001g0024 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.265-265G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226288062 | |||||||
| chr1:226288131 | C | A | 1 | a0001c0004t0002g0133 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.265-334G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226288131 | |||||||
| chr1:226288298 | A | G | 2 | a0001c0002t0002g0136 a0001c0002t0002g0137 |
2 | HG00738.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.265-501T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226288298 | |||||||
| chr1:226288628 | A | G | 6 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(3): Show |
6 | HG02055.hp2 HG02809.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.265-831T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226288628 | |||||||
| chr1:226288746 | A | ATGT | 318 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(315): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.265-950_265-949ins others(3): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226288746 | |||||||
| chr1:226288752 | T | C | 99 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0223 others(96): Show |
99 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.265-955A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226288752 | |||||||
| chr1:226288821 | T | C | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.265-1024A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226288821 | |||||||
| chr1:226288964 | C | T | 116 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(113): Show |
116 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.265-1167G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226288964 | |||||||
| chr1:226289112 | G | A | 1 | a0001c0001t0003g0059 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.265-1315C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289112 | |||||||
| chr1:226289234 | CA | C | 99 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0223 others(96): Show |
99 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.265-1438delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289234 | |||||||
| chr1:226289330 | A | C | 7 | a0001c0001t0001g0225 a0001c0001t0001g0229 a0001c0001t0001g0230 others(4): Show |
7 | HG00738.hp2 HG01109.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.265-1533T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289330 | |||||||
| chr1:226289334 | T | TTG | 7 | a0001c0001t0001g0108 a0001c0001t0001g0126 a0001c0001t0001g0127 others(4): Show |
7 | HG01167.hp2 HG01192.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.265-1539_265-1538d others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289334 | |||||||
| chr1:226289551 | C | T | 1 | a0001c0002t0002g0002 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.265-1754G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289551 | |||||||
| chr1:226289606 | C | T | 2 | a0001c0001t0001g0227 a0001c0001t0001g0269 |
2 | HG02004.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.265-1809G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289606 | |||||||
| chr1:226289834 | C | CG | 20 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0093 others(17): Show |
20 | HG00438.hp1 HG00741.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.265-2038dupC | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289834 | |||||||
| chr1:226289834 | C | CGG | 30 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(27): Show |
30 | HG00408.hp1 HG01081.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.265-2039_265-2038d others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289834 | |||||||
| chr1:226289834 | C | CGGA | 40 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0001g0231 others(37): Show |
40 | HG00621.hp1 HG00738.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.265-2038_265-2037i others(5): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289834 | |||||||
| chr1:226289834 | C | CGGG | 23 | a0001c0001t0001g0020 a0001c0001t0001g0035 a0001c0001t0001g0079 others(20): Show |
23 | HG00280.hp1 HG01071.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.265-2040_265-2038d others(5): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289834 | |||||||
| chr1:226289834 | C | CGGGG | 34 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0019 others(31): Show |
34 | HG00280.hp2 HG00621.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.265-2041_265-2038d others(6): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289834 | |||||||
| chr1:226289834 | CGGGGGGG others(6): Show |
C | 3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 |
3 | HG03017.hp1 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.265-2050_265-2038d others(15): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289834 | |||||||
| chr1:226289835 | G | GGA | 21 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0239 others(18): Show |
21 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.265-2039_265-2038i others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289835 | |||||||
| chr1:226289836 | G | GA | 5 | a0001c0001t0001g0333 a0001c0001t0001g0343 a0001c0001t0001g0344 others(2): Show |
5 | HG00609.hp2 NA18949.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.265-2040_265-2039i others(3): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289836 | |||||||
| chr1:226289840 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.265-2043C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289840 | |||||||
| chr1:226289840 | G | C | 3 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0278 |
3 | HG00438.hp2 HG00597.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.265-2043C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289840 | |||||||
| chr1:226289841 | G | C | 1 | a0001c0001t0001g0013 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.265-2044C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289841 | |||||||
| chr1:226289841 | G | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0017 |
2 | NA18989.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.265-2044C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289841 | |||||||
| chr1:226289843 | G | GGGGGT | 22 | a0001c0001t0001g0049 a0001c0001t0001g0325 a0001c0001t0001g0334 others(19): Show |
22 | HG00423.hp1 HG00609.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.265-2047_265-2046i others(7): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289843 | |||||||
| chr1:226289843 | G | T | 1 | a0001c0001t0001g0016 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.265-2046C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289843 | |||||||
| chr1:226289844 | G | GGGGGGGG others(6): Show |
1 | a0001c0001t0001g0209 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.265-2048_265-2047i others(15): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289844 | |||||||
| chr1:226289844 | G | GGGGGGGG others(4): Show |
3 | a0001c0001t0001g0210 a0001c0001t0001g0218 a0001c0001t0001g0222 |
3 | NA18966.hp2 NA18990.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.265-2048_265-2047i others(13): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289844 | |||||||
| chr1:226289844 | G | GGGGGGGG others(3): Show |
2 | a0001c0001t0001g0211 a0001c0001t0001g0220 |
2 | HG02040.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.265-2048_265-2047i others(12): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289844 | |||||||
| chr1:226289844 | G | GGGGGGGG others(3): Show |
2 | a0001c0001t0001g0356 a0001c0001t0001g0358 |
2 | HG03688.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.265-2048_265-2047i others(12): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289844 | |||||||
| chr1:226289844 | G | GGGGT | 18 | a0001c0001t0001g0011 a0001c0001t0001g0106 a0001c0001t0001g0107 others(15): Show |
18 | HG00099.hp2 HG00741.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.265-2048_265-2047i others(6): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289844 | |||||||
| chr1:226289845 | G | GGGGGGGG others(3): Show |
1 | a0001c0001t0001g0213 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.265-2049_265-2048i others(12): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289845 | |||||||
| chr1:226289845 | G | GGGGGGGG others(3): Show |
1 | a0001c0001t0001g0357 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.265-2049_265-2048i others(12): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289845 | |||||||
| chr1:226289845 | GT | G | 6 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0031 others(3): Show |
6 | HG01074.hp2 HG01433.hp1 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.265-2049delA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289845 | |||||||
| chr1:226289846 | T | G | 183 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(180): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.265-2049A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289846 | |||||||
| chr1:226289847 | G | GT | 3 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0002t0002g0285 |
3 | HG02257.hp1 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.265-2051_265-2050i others(3): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289847 | |||||||
| chr1:226289847 | G | T | 10 | a0001c0001t0001g0337 a0001c0001t0001g0340 a0001c0001t0001g0341 others(7): Show |
10 | NA18946.hp2 NA18949.hp1 NA18973.hp1 others(7): Show |
intron_variant | MODIFIER | c.265-2050C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289847 | |||||||
| chr1:226289856 | T | G | 1 | a0001c0001t0003g0102 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.265-2059A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289856 | |||||||
| chr1:226289867 | G | A | 4 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0062 others(1): Show |
4 | NA18962.hp1 NA19064.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.265-2070C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289867 | |||||||
| chr1:226289921 | G | A | 304 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(301): Show |
304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.265-2124C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289921 | |||||||
| chr1:226290136 | C | T | 4 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(1): Show |
4 | HG02109.hp2 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.265-2339G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226290136 | |||||||
| chr1:226290333 | C | CT | 25 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0095 others(22): Show |
25 | HG02027.hp2 HG02055.hp2 HG02071.hp1 others(22): Show |
intron_variant | MODIFIER | c.265-2537dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226290333 | |||||||
| chr1:226290333 | CT | C | 98 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0217 others(95): Show |
98 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.265-2537delA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226290333 | |||||||
| chr1:226290372 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.265-2575C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226290372 | |||||||
| chr1:226290402 | A | G | 1 | a0001c0002t0002g0193 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.265-2605T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226290402 | |||||||
| chr1:226290452 | T | C | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.265-2655A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226290452 | |||||||
| chr1:226290498 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.265-2701C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226290498 | |||||||
| chr1:226290650 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.265-2853G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226290650 | |||||||
| chr1:226290655 | T | C | 1 | a0001c0001t0001g0335 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.265-2858A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226290655 | |||||||
| chr1:226290680 | G | C | 358 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(355): Show |
359 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.265-2883C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226290680 | |||||||
| chr1:226290702 | G | C | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.265-2905C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226290702 | |||||||
| chr1:226290783 | G | A | 1 | a0001c0001t0001g0213 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.265-2986C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226290783 | |||||||
| chr1:226290920 | C | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0067 a0001c0001t0001g0100 |
3 | HG02895.hp1 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.265-3123G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226290920 | |||||||
| chr1:226291025 | G | C | 97 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0223 others(94): Show |
97 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.265-3228C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226291025 | |||||||
| chr1:226291133 | C | A | 1 | a0001c0001t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.265-3336G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226291133 | |||||||
| chr1:226291231 | G | C | 99 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0087 others(96): Show |
99 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.265-3434C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226291231 | |||||||
| chr1:226291324 | C | T | 1 | a0001c0001t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.265-3527G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226291324 | |||||||
| chr1:226291461 | A | T | 1 | a0001c0001t0001g0035 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.265-3664T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226291461 | |||||||
| chr1:226291544 | CTA | C | 5 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.265-3749_265-3748d others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226291544 | |||||||
| chr1:226291878 | T | C | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG00735.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.264+3964A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226291878 | |||||||
| chr1:226291879 | G | C | 1 | a0001c0001t0001g0272 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.264+3963C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226291879 | |||||||
| chr1:226291964 | A | C | 1 | a0001c0001t0001g0013 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.264+3878T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226291964 | |||||||
| chr1:226292250 | T | G | 1 | a0001c0002t0002g0204 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.264+3592A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226292250 | |||||||
| chr1:226292387 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.264+3455A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226292387 | |||||||
| chr1:226292455 | G | C | 1 | a0001c0001t0001g0336 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.264+3387C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226292455 | |||||||
| chr1:226292625 | T | A | 1 | a0001c0001t0001g0245 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.264+3217A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226292625 | |||||||
| chr1:226292626 | A | T | 3 | a0001c0002t0004g0149 a0001c0002t0004g0150 a0001c0002t0004g0281 |
3 | HG01069.hp1 HG01071.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.264+3216T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226292626 | |||||||
| chr1:226292633 | AT | A | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.264+3208delA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226292633 | |||||||
| chr1:226292634 | T | A | 1 | a0001c0001t0001g0300 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.264+3208A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226292634 | |||||||
| chr1:226293261 | T | C | 2 | a0001c0001t0003g0032 a0001c0001t0003g0033 |
2 | NA19012.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.264+2581A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226293261 | |||||||
| chr1:226293345 | A | C | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.264+2497T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226293345 | |||||||
| chr1:226293395 | G | A | 1 | a0001c0001t0003g0105 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.264+2447C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226293395 | |||||||
| chr1:226293773 | G | A | 12 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0303 others(9): Show |
12 | HG02559.hp1 HG02572.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.264+2069C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226293773 | |||||||
| chr1:226293983 | G | A | 5 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(2): Show |
5 | HG03017.hp1 HG03834.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.264+1859C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226293983 | |||||||
| chr1:226294087 | C | T | 1 | a0001c0002t0002g0294 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.264+1755G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226294087 | |||||||
| chr1:226294277 | CA | C | 253 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(250): Show |
253 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(250): Show |
intron_variant | MODIFIER | c.264+1564delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226294277 | |||||||
| chr1:226294429 | A | G | 14 | a0001c0001t0001g0004 a0001c0001t0001g0296 a0001c0001t0001g0297 others(11): Show |
14 | HG02055.hp2 HG02145.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.264+1413T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226294429 | |||||||
| chr1:226294441 | A | G | 263 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(260): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.264+1401T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226294441 | |||||||
| chr1:226294464 | C | T | 52 | a0001c0001t0003g0156 a0001c0002t0002g0005 a0001c0002t0002g0006 others(49): Show |
52 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.264+1378G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226294464 | |||||||
| chr1:226294536 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.264+1306G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226294536 | |||||||
| chr1:226294576 | A | C | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG00735.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.264+1266T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226294576 | |||||||
| chr1:226294580 | A | C | 222 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(219): Show |
222 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.264+1262T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226294580 | |||||||
| chr1:226294582 | A | C | 14 | a0001c0002t0002g0282 a0001c0002t0002g0283 a0001c0002t0002g0284 others(11): Show |
14 | HG01109.hp1 HG01167.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.264+1260T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226294582 | |||||||
| chr1:226294588 | A | C | 235 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(232): Show |
236 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.264+1254T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226294588 | |||||||
| chr1:226294589 | A | C | 1 | a0001c0001t0001g0079 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.264+1253T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226294589 | |||||||
| chr1:226294721 | A | C | 5 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0001c0001t0001g0320 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.264+1121T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226294721 | |||||||
| chr1:226294817 | T | G | 98 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(95): Show |
98 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.264+1025A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226294817 | |||||||
| chr1:226294869 | G | A | 21 | a0001c0002t0001g0361 a0001c0002t0002g0001 a0001c0002t0002g0135 others(18): Show |
22 | HG00544.hp1 HG00738.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.264+973C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226294869 | |||||||
| chr1:226295221 | G | A | 19 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(16): Show |
19 | HG01099.hp1 HG01106.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.264+621C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226295221 | |||||||
| chr1:226295236 | G | C | 14 | a0001c0001t0001g0223 a0001c0001t0001g0248 a0001c0001t0001g0249 others(11): Show |
14 | HG00735.hp1 HG02056.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.264+606C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226295236 | |||||||
| chr1:226295282 | T | C | 14 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(11): Show |
14 | HG02040.hp1 NA18941.hp2 NA18949.hp2 others(11): Show |
intron_variant | MODIFIER | c.264+560A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226295282 | |||||||
| chr1:226295418 | C | T | 4 | a0001c0001t0001g0356 a0001c0001t0001g0357 a0001c0001t0001g0358 others(1): Show |
4 | HG03017.hp2 HG03688.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.264+424G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226295418 | |||||||
| chr1:226295453 | T | A | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.264+389A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226295453 | |||||||
| chr1:226295484 | A | T | 215 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(212): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.264+358T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226295484 | |||||||
| chr1:226295689 | A | T | 2 | a0001c0001t0001g0327 a0001c0001t0001g0338 |
2 | NA18612.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.264+153T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226295689 | |||||||
| chr1:226296112 | A | G | 1 | a0001c0001t0001g0326 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.160-166T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 3/14 | chr1 | 226296112 | |||||||
| chr1:226296151 | T | C | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.160-205A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 3/14 | chr1 | 226296151 | |||||||
| chr1:226296225 | G | A | 1 | a0002c0003t0002g0147 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.160-279C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 3/14 | chr1 | 226296225 | |||||||
| chr1:226296421 | C | T | 1 | a0001c0002t0002g0161 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.160-475G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 3/14 | chr1 | 226296421 | |||||||
| chr1:226296573 | T | A | 1 | a0001c0002t0002g0182 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.160-627A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 3/14 | chr1 | 226296573 | |||||||
| chr1:226296605 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.160-659C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 3/14 | chr1 | 226296605 | |||||||
| chr1:226296867 | A | T | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.159+852T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 3/14 | chr1 | 226296867 | |||||||
| chr1:226297240 | T | C | 12 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0303 others(9): Show |
12 | HG02559.hp1 HG02572.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.159+479A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 3/14 | chr1 | 226297240 | |||||||
| chr1:226297490 | C | G | 1 | a0001c0001t0001g0042 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.159+229G>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 3/14 | chr1 | 226297490 | |||||||
| chr1:226297571 | T | C | 1 | a0001c0002t0002g0282 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.159+148A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 3/14 | chr1 | 226297571 | |||||||
| chr1:226297626 | A | AT | 224 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(221): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.159+92dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 3/14 | chr1 | 226297626 | |||||||
| chr1:226298255 | C | A | 1 | a0001c0002t0002g0183 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.65-442G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226298255 | |||||||
| chr1:226298364 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.65-551G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226298364 | |||||||
| chr1:226298511 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.65-698A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226298511 | |||||||
| chr1:226298631 | T | C | 264 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(261): Show |
264 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(261): Show |
intron_variant | MODIFIER | c.65-818A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226298631 | |||||||
| chr1:226298658 | C | T | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.65-845G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226298658 | |||||||
| chr1:226298730 | A | G | 264 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(261): Show |
264 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.65-917T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226298730 | |||||||
| chr1:226298731 | C | T | 8 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(5): Show |
8 | HG02040.hp1 NA18949.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.65-918G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226298731 | |||||||
| chr1:226298803 | C | G | 3 | a0001c0002t0002g0284 a0001c0002t0002g0292 a0001c0002t0002g0293 |
3 | HG01891.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.65-990G>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226298803 | |||||||
| chr1:226298820 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.65-1007C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226298820 | |||||||
| chr1:226298843 | G | A | 1 | a0001c0001t0003g0076 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.65-1030C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226298843 | |||||||
| chr1:226298909 | A | G | 1 | a0001c0001t0001g0358 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.65-1096T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226298909 | |||||||
| chr1:226299049 | A | G | 1 | a0001c0001t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.65-1236T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226299049 | |||||||
| chr1:226299186 | C | T | 96 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0003 others(93): Show |
97 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.65-1373G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226299186 | |||||||
| chr1:226299383 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.65-1570T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226299383 | |||||||
| chr1:226299484 | G | A | 1 | a0001c0002t0002g0184 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.65-1671C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226299484 | |||||||
| chr1:226299504 | CA | C | 209 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0079 others(206): Show |
210 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.64+1668delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226299504 | |||||||
| chr1:226299745 | C | A | 8 | a0001c0001t0001g0340 a0001c0001t0001g0341 a0001c0001t0001g0342 others(5): Show |
8 | NA18946.hp2 NA18973.hp1 NA18983.hp2 others(5): Show |
intron_variant | MODIFIER | c.64+1428G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226299745 | |||||||
| chr1:226299843 | T | C | 2 | a0001c0001t0003g0091 a0001c0001t0003g0120 |
2 | HG01168.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.64+1330A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226299843 | |||||||
| chr1:226299907 | T | C | 1 | a0001c0001t0003g0112 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.64+1266A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226299907 | |||||||
| chr1:226299926 | C | CT | 18 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(15): Show |
18 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(15): Show |
intron_variant | MODIFIER | c.64+1246dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226299926 | |||||||
| chr1:226299989 | A | C | 1 | a0001c0001t0001g0088 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.64+1184T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226299989 | |||||||
| chr1:226300001 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.64+1172G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226300001 | |||||||
| chr1:226300181 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.64+992C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226300181 | |||||||
| chr1:226300594 | G | A | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.64+579C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226300594 | |||||||
| chr1:226300831 | G | A | 25 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0148 others(22): Show |
25 | HG00408.hp1 HG01109.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.64+342C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226300831 | |||||||
| chr1:226300855 | A | AAAAC | 8 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(5): Show |
8 | HG02559.hp1 HG02572.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.64+314_64+317dupGT others(2): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226300855 | |||||||
| chr1:226300929 | T | C | 1 | a0001c0001t0003g0117 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.64+244A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226300929 | |||||||
| chr1:226301125 | A | G | 98 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0087 others(95): Show |
98 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.64+48T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226301125 | |||||||
| chr1:226301223 | A | G | 1 | a0001c0002t0002g0186 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.32-18T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226301223 | |||||||
| chr1:226301325 | G | A | 1 | a0001c0002t0002g0185 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.32-120C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226301325 | |||||||
| chr1:226301384 | T | A | 10 | a0001c0001t0001g0337 a0001c0001t0001g0340 a0001c0001t0001g0341 others(7): Show |
10 | NA18946.hp2 NA18949.hp1 NA18973.hp1 others(7): Show |
intron_variant | MODIFIER | c.32-179A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226301384 | |||||||
| chr1:226301684 | C | T | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.32-479G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226301684 | |||||||
| chr1:226301754 | A | G | 231 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(228): Show |
232 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.32-549T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226301754 | |||||||
| chr1:226301940 | G | A | 98 | a0001c0002t0001g0134 a0001c0002t0001g0361 a0001c0002t0002g0001 others(95): Show |
99 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.32-735C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226301940 | |||||||
| chr1:226302052 | G | C | 1 | a0001c0001t0001g0009 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.32-847C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226302052 | |||||||
| chr1:226302227 | T | A | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.32-1022A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226302227 | |||||||
| chr1:226302421 | T | C | 220 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(217): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.32-1216A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226302421 | |||||||
| chr1:226302460 | G | A | 1 | a0001c0002t0002g0208 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.32-1255C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226302460 | |||||||
| chr1:226302547 | C | CA | 73 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0090 others(70): Show |
74 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.32-1343dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226302547 | |||||||
| chr1:226302704 | A | G | 1 | a0001c0002t0002g0317 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.32-1499T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226302704 | |||||||
| chr1:226302978 | ACT | A | 52 | a0001c0001t0001g0160 a0001c0002t0002g0005 a0001c0002t0002g0006 others(49): Show |
52 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.32-1775_32-1774del others(2): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226302978 | |||||||
| chr1:226303307 | T | C | 2 | a0001c0001t0001g0217 a0001c0001t0001g0219 |
2 | NA18972.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.32-2102A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226303307 | |||||||
| chr1:226303437 | T | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0126 a0001c0001t0001g0127 others(8): Show |
11 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.32-2232A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226303437 | |||||||
| chr1:226303529 | G | A | 1 | a0001c0001t0001g0316 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.32-2324C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226303529 | |||||||
| chr1:226303803 | C | T | 5 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0001c0001t0001g0320 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.32-2598G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226303803 | |||||||
| chr1:226303933 | A | G | 1 | a0001c0001t0003g0041 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.32-2728T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226303933 | |||||||
| chr1:226303955 | G | A | 98 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0128 others(95): Show |
98 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.32-2750C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226303955 | |||||||
| chr1:226304376 | T | A | 1 | a0001c0001t0001g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.32-3171A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226304376 | |||||||
| chr1:226304432 | A | C | 93 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0087 others(90): Show |
93 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.32-3227T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226304432 | |||||||
| chr1:226304453 | A | T | 267 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(264): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.32-3248T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226304453 | |||||||
| chr1:226304554 | G | A | 1 | a0001c0002t0002g0185 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.32-3349C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226304554 | |||||||
| chr1:226304558 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.32-3353G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226304558 | |||||||
| chr1:226304560 | G | C | 1 | a0001c0002t0002g0206 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.32-3355C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226304560 | |||||||
| chr1:226304579 | T | C | 89 | a0001c0001t0001g0079 a0001c0001t0001g0084 a0001c0001t0001g0115 others(86): Show |
89 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.32-3374A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226304579 | |||||||
| chr1:226304771 | T | C | 5 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(2): Show |
5 | HG01081.hp2 HG01928.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.32-3566A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226304771 | |||||||
| chr1:226305196 | A | C | 1 | a0001c0001t0003g0012 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.31+3913T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305196 | |||||||
| chr1:226305287 | T | C | 2 | a0001c0001t0003g0091 a0001c0001t0003g0120 |
2 | HG01168.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.31+3822A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305287 | |||||||
| chr1:226305290 | G | A | 1 | a0001c0002t0002g0207 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.31+3819C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305290 | |||||||
| chr1:226305315 | G | A | 1 | a0001c0001t0003g0120 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.31+3794C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305315 | |||||||
| chr1:226305315 | G | GA | 93 | a0001c0001t0001g0009 a0001c0001t0001g0092 a0001c0001t0001g0093 others(90): Show |
93 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.31+3793dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305315 | |||||||
| chr1:226305315 | GA | G | 15 | a0001c0001t0001g0011 a0001c0001t0001g0220 a0001c0001t0001g0221 others(12): Show |
15 | HG00408.hp2 HG01106.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.31+3793delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305315 | |||||||
| chr1:226305315 | GAA | G | 15 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(12): Show |
15 | HG02040.hp1 HG02055.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.31+3792_31+3793del others(2): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305315 | |||||||
| chr1:226305315 | GAAA | G | 10 | a0001c0001t0001g0010 a0001c0001t0001g0296 a0001c0001t0001g0297 others(7): Show |
10 | HG02809.hp1 HG03017.hp2 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.31+3791_31+3793del others(3): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305315 | |||||||
| chr1:226305315 | GAAAAAAA others(8): Show |
G | 1 | a0001c0001t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.31+3779_31+3793del others(15): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305315 | |||||||
| chr1:226305315 | GAAAAAAA others(10): Show |
G | 1 | a0001c0001t0001g0323 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.31+3777_31+3793del others(17): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305315 | |||||||
| chr1:226305330 | A | C | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.31+3779T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305330 | |||||||
| chr1:226305333 | A | C | 1 | a0001c0001t0001g0318 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.31+3776T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305333 | |||||||
| chr1:226305334 | A | C | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.31+3775T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305334 | |||||||
| chr1:226305372 | G | A | 1 | a0001c0002t0002g0002 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.31+3737C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305372 | |||||||
| chr1:226305615 | G | A | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 |
3 | HG02109.hp1 HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.31+3494C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305615 | |||||||
| chr1:226305621 | G | T | 1 | a0001c0001t0001g0223 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.31+3488C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305621 | |||||||
| chr1:226305626 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.31+3483C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305626 | |||||||
| chr1:226305669 | G | C | 1 | a0001c0001t0001g0311 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.31+3440C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305669 | |||||||
| chr1:226305688 | G | A | 1 | a0001c0002t0002g0208 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.31+3421C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305688 | |||||||
| chr1:226305728 | T | C | 100 | a0001c0001t0001g0160 a0001c0001t0003g0156 a0001c0001t0003g0191 others(97): Show |
101 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.31+3381A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305728 | |||||||
| chr1:226305967 | T | C | 19 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(16): Show |
19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.31+3142A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305967 | |||||||
| chr1:226305984 | G | A | 9 | a0001c0001t0001g0004 a0001c0001t0001g0296 a0001c0001t0001g0297 others(6): Show |
9 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.31+3125C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305984 | |||||||
| chr1:226306154 | G | A | 96 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0223 others(93): Show |
96 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.31+2955C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226306154 | |||||||
| chr1:226306302 | T | G | 1 | a0001c0001t0001g0360 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.31+2807A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226306302 | |||||||
| chr1:226306323 | C | CA | 7 | a0001c0001t0001g0125 a0001c0001t0001g0280 a0001c0001t0001g0318 others(4): Show |
7 | HG01109.hp2 HG02145.hp2 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.31+2785dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226306323 | |||||||
| chr1:226306373 | C | A | 1 | a0001c0002t0004g0281 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.31+2736G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226306373 | |||||||
| chr1:226306509 | G | A | 14 | a0001c0002t0002g0282 a0001c0002t0002g0283 a0001c0002t0002g0284 others(11): Show |
14 | HG01109.hp1 HG01167.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.31+2600C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226306509 | |||||||
| chr1:226306814 | C | T | 116 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(113): Show |
116 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.31+2295G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226306814 | |||||||
| chr1:226307070 | C | A | 9 | a0001c0001t0001g0004 a0001c0001t0001g0296 a0001c0001t0001g0297 others(6): Show |
9 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.31+2039G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226307070 | |||||||
| chr1:226307361 | G | A | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.31+1748C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226307361 | |||||||
| chr1:226307463 | A | G | 351 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(348): Show |
352 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.31+1646T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226307463 | |||||||
| chr1:226307494 | G | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.31+1615C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226307494 | |||||||
| chr1:226307648 | A | AAATC | 3 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 |
3 | NA18945.hp1 NA18975.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.31+1460_31+1461ins others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226307648 | |||||||
| chr1:226307758 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.31+1351C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226307758 | |||||||
| chr1:226307969 | A | G | 1 | a0001c0001t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.31+1140T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226307969 | |||||||
| chr1:226308185 | C | T | 3 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0317 |
3 | HG02602.hp1 HG03239.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.31+924G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226308185 | |||||||
| chr1:226308406 | G | C | 1 | a0001c0001t0001g0316 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.31+703C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226308406 | |||||||
| chr1:226308551 | G | C | 1 | a0001c0001t0001g0322 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.31+558C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226308551 | |||||||
| chr1:226308695 | C | A | 2 | a0001c0002t0002g0002 a0001c0002t0002g0317 |
2 | HG02602.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.31+414G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226308695 | |||||||
| chr1:226308863 | G | A | 5 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0001c0001t0001g0320 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.31+246C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226308863 | |||||||
| chr1:226308968 | G | A | 33 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0325 others(30): Show |
33 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.31+141C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226308968 | |||||||
| chr1:226309050 | G | C | 5 | a0001c0001t0001g0356 a0001c0001t0001g0357 a0001c0001t0001g0358 others(2): Show |
5 | HG03017.hp2 HG03688.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.31+59C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226309050 | |||||||
| chr1:226309060 | G | A | 1 | a0001c0002t0001g0361 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.31+49C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226309060 | |||||||
| chr1:226309082 | G | A | 2 | a0001c0001t0001g0362 a0004c0006t0001g0363 |
2 | NA18963.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.31+27C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226309082 | |||||||
| chr1:226309083 | G | T | 1 | a0001c0002t0002g0002 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.31+26C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226309083 |